PCDH15 (protocadherin related 15) - Rat Genome Database

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Gene: PCDH15 (protocadherin related 15) Homo sapiens
Analyze
Symbol: PCDH15
Name: protocadherin related 15
RGD ID: 1353280
HGNC Page HGNC:14674
Description: Predicted to enable calcium ion binding activity. Involved in equilibrioception; photoreceptor cell maintenance; and sensory perception of light stimulus. Acts upstream of or within sensory perception of sound. Located in extracellular space; photoreceptor outer segment; and synapse. Implicated in Usher syndrome type 1D; Usher syndrome type 1F; and autosomal recessive nonsyndromic deafness 23.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: cadherin-related family member 15; CDHR15; DFNB23; DKFZp667A1711; protocadherin 15; protocadherin-15; protocadherin-related 15; USH1F
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381053,802,771 - 55,627,942 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1053,802,771 - 55,627,942 (-)EnsemblGRCh38hg38GRCh38
GRCh371055,562,531 - 57,387,702 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361055,250,866 - 56,231,057 (-)NCBINCBI36Build 36hg18NCBI36
Build 341055,250,865 - 56,231,057NCBI
Celera1048,825,500 - 49,824,287 (-)NCBICelera
Cytogenetic Map10q21.1NCBI
HuRef1049,544,130 - 50,545,244 (-)NCBIHuRef
CHM1_11055,844,015 - 56,842,749 (-)NCBICHM1_1
T2T-CHM13v2.01054,651,649 - 56,479,356 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. Mechanotransduction by hair cells: models, molecules, and mechanisms. Gillespie PG and Muller U, Cell. 2009 Oct 2;139(1):33-44. doi: 10.1016/j.cell.2009.09.010.
2. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
3. Sensing sound: molecules that orchestrate mechanotransduction by hair cells. Kazmierczak P and Muller U, Trends Neurosci. 2012 Apr;35(4):220-9. doi: 10.1016/j.tins.2011.10.007. Epub 2011 Dec 15.
4. Characterization of the Kyoto circling (KCI) rat carrying a spontaneous nonsense mutation in the protocadherin 15 (Pcdh15) gene. Naoi K, etal., Exp Anim. 2009 Jan;58(1):1-10.
5. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
6. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
7. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
8. RGD HPO Phenotype Annotation Pipeline RGD automated import pipeline for human HPO-to-gene-to-disease annotations
9. Photoreceptor degeneration: genetic and mechanistic dissection of a complex trait. Wright AF, etal., Nat Rev Genet. 2010 Apr;11(4):273-84. doi: 10.1038/nrg2717.
Additional References at PubMed
PMID:8889548   PMID:11138007   PMID:11398101   PMID:11487575   PMID:12711741   PMID:14570705   PMID:15028842   PMID:15537665   PMID:15660226   PMID:16369489   PMID:16385451   PMID:16679490  
PMID:16807332   PMID:16887306   PMID:16963483   PMID:17277737   PMID:17706913   PMID:17903293   PMID:18384968   PMID:18395802   PMID:18463160   PMID:18484607   PMID:18519826   PMID:18719945  
PMID:19107147   PMID:19183343   PMID:19240061   PMID:19375528   PMID:19606495   PMID:19683999   PMID:19816713   PMID:19913121   PMID:20142502   PMID:20182759   PMID:20201926   PMID:20301442  
PMID:20301607   PMID:20379614   PMID:20498078   PMID:20513143   PMID:20538994   PMID:20628086   PMID:20801516   PMID:20966902   PMID:21117948   PMID:21173574   PMID:21174530   PMID:21203349  
PMID:21234346   PMID:21281516   PMID:21873635   PMID:21940737   PMID:22135276   PMID:22363448   PMID:22424883   PMID:22542470   PMID:22690115   PMID:22718019   PMID:22815625   PMID:23144817  
PMID:23207014   PMID:23217710   PMID:23376485   PMID:23400010   PMID:23443030   PMID:23451239   PMID:23767834   PMID:23776407   PMID:24025145   PMID:24164807   PMID:24239741   PMID:24618850  
PMID:24625443   PMID:24667918   PMID:24797007   PMID:24940003   PMID:24965255   PMID:25114259   PMID:25258483   PMID:25307757   PMID:25404053   PMID:25462672   PMID:25467981   PMID:25520874  
PMID:25575603   PMID:25692141   PMID:25804404   PMID:25930172   PMID:26011067   PMID:26166082   PMID:26279247   PMID:26338283   PMID:26343869   PMID:26445815   PMID:26483173   PMID:26687479  
PMID:26791358   PMID:26841241   PMID:27058588   PMID:27275418   PMID:27429853   PMID:27440999   PMID:27583663   PMID:27610647   PMID:27745870   PMID:27766948   PMID:27867666   PMID:27918536  
PMID:28056266   PMID:28238533   PMID:28263850   PMID:28281779   PMID:28292353   PMID:29301965   PMID:29692870   PMID:30029624   PMID:30057206   PMID:31937901   PMID:32835555   PMID:32963095  
PMID:35637313   PMID:37198144   PMID:38697112   PMID:39187782   PMID:39298473  


Genomics

Comparative Map Data
PCDH15
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381053,802,771 - 55,627,942 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1053,802,771 - 55,627,942 (-)EnsemblGRCh38hg38GRCh38
GRCh371055,562,531 - 57,387,702 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361055,250,866 - 56,231,057 (-)NCBINCBI36Build 36hg18NCBI36
Build 341055,250,865 - 56,231,057NCBI
Celera1048,825,500 - 49,824,287 (-)NCBICelera
Cytogenetic Map10q21.1NCBI
HuRef1049,544,130 - 50,545,244 (-)NCBIHuRef
CHM1_11055,844,015 - 56,842,749 (-)NCBICHM1_1
T2T-CHM13v2.01054,651,649 - 56,479,356 (-)NCBIT2T-CHM13v2.0
Pcdh15
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391072,932,003 - 74,485,663 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1072,935,174 - 74,485,569 (+)EnsemblGRCm39 Ensembl
GRCm381073,096,277 - 74,649,831 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1073,099,342 - 74,649,737 (+)EnsemblGRCm38mm10GRCm38
MGSCv371073,284,615 - 74,112,482 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361073,667,153 - 74,076,383 (+)NCBIMGSCv36mm8
Celera1074,887,647 - 75,712,367 (+)NCBICelera
Cytogenetic Map10B5.3NCBI
cM Map1037.43NCBI
Pcdh15
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr82013,996,383 - 15,495,206 (-)NCBIGRCr8
mRatBN7.22013,997,094 - 15,496,446 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl2013,963,565 - 15,494,719 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx2014,715,022 - 15,411,013 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.02014,069,984 - 14,766,014 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.02014,542,552 - 15,238,564 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.02014,952,213 - 15,334,745 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl2014,952,213 - 15,334,745 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.02017,138,580 - 17,521,597 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Rnor_5.02018,712,995 - 19,021,206 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.42014,507,804 - 15,240,479 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera2015,459,406 - 16,139,466 (-)NCBICelera
Cytogenetic Map20p12-p11NCBI
Pcdh15
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554258,428,680 - 8,899,028 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554258,443,523 - 9,203,177 (-)NCBIChiLan1.0ChiLan1.0
PCDH15
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2866,121,235 - 67,901,123 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11066,126,557 - 67,907,741 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01050,452,290 - 52,236,538 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11052,661,035 - 54,456,043 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1052,666,969 - 53,536,611 (-)Ensemblpanpan1.1panPan2
PCDH15
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12633,426,728 - 34,589,208 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2633,719,839 - 34,588,017 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2633,735,217 - 34,473,542 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02635,380,608 - 36,116,590 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2635,248,142 - 36,113,521 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12633,285,817 - 34,023,503 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02632,872,620 - 33,606,715 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02634,074,758 - 34,812,730 (+)NCBIUU_Cfam_GSD_1.0
Pcdh15
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440721373,974,985 - 74,439,013 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936910141,917 - 602,089 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936910233,800 - 602,145 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
PCDH15
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.11495,530,168 - 96,388,032 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.214103,931,584 - 104,873,398 (+)NCBISscrofa10.2Sscrofa10.2susScr3
PCDH15
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1975,642,985 - 77,415,370 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl976,726,627 - 77,398,716 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604836,564,791 - 38,363,879 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Pcdh15
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247919,195,902 - 9,990,131 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247919,042,311 - 9,992,341 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in PCDH15
2716 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_001384140.1(PCDH15):c.2897G>C (p.Arg966Thr) single nucleotide variant PCDH15-related disorder [RCV004537877]|Usher syndrome type 1F [RCV001829495]|not provided [RCV000519130] Chr10:53961864 [GRCh38]
Chr10:55721624 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3718-2A>G single nucleotide variant Usher syndrome type 1F [RCV000005215] Chr10:53857265 [GRCh38]
Chr10:55617025 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.7C>T (p.Arg3Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV000770851]|Rare genetic deafness [RCV000824737]|Usher syndrome type 1F [RCV000005216]|not provided [RCV000808283] Chr10:54664256 [GRCh38]
Chr10:56424016 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|conflicting interpretations of pathogenicity|conflicting data from submitters
NM_001384140.1(PCDH15):c.1088del (p.Leu363fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003472980]|Usher syndrome type 1D [RCV001198734]|Usher syndrome type 1F [RCV000005217]|not provided [RCV001381510] Chr10:54213946 [GRCh38]
Chr10:55973706 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.733C>T (p.Arg245Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV000477806]|Autosomal recessive nonsyndromic hearing loss 23 [RCV001004803]|PCDH15-related disorder [RCV004734497]|Rare genetic deafness [RCV000824735]|Usher syndrome type 1 [RCV000218809]|Usher syndrome type 1D [RCV001030749]|Usher syndrome type 1F [RCV000005218]|Usher syndrome type 1G [RCV000055970]|not provided [RCV000269122] Chr10:54317414 [GRCh38]
Chr10:56077174 [GRCh37]
Chr10:10q21.1		 pathogenic|not provided
PCDH15, 3-BP DEL, 5601AAC deletion USHER SYNDROME, TYPE ID/F, DIGENIC [RCV000005220]|Usher syndrome type 1F [RCV000005219] Chr10:10q21-q22 pathogenic
NM_001384140.1(PCDH15):c.785G>A (p.Gly262Asp) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV000005221] Chr10:54317362 [GRCh38]
Chr10:56077122 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.400C>G (p.Arg134Gly) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV000005222]|Rare genetic deafness [RCV000211736]|Usher syndrome type 1F [RCV003234893] Chr10:54369194 [GRCh38]
Chr10:56128954 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|conflicting interpretations of pathogenicity|conflicting data from submitters
PCDH15, 1-BP DEL, 16T deletion USHER SYNDROME, TYPE ID/F, DIGENIC [RCV000005223] Chr10:10q21-q22 pathogenic
NM_001384140.1(PCDH15):c.1940C>G (p.Ser647Ter) single nucleotide variant Usher syndrome type 1F [RCV000005224] Chr10:54090041 [GRCh38]
Chr10:55849801 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.1583T>A (p.Val528Asp) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV000005225]|Usher syndrome type 1F [RCV002513133]|not provided [RCV001851963] Chr10:54183451 [GRCh38]
Chr10:55943211 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.*16A>C single nucleotide variant not provided [RCV001545196] Chr10:53806563 [GRCh38]
Chr10:55566323 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2277T>C (p.Phe759=) single nucleotide variant not provided [RCV000729920] Chr10:54023141 [GRCh38]
Chr10:55782901 [GRCh37]
Chr10:10q21.1		 conflicting interpretations of pathogenicity|uncertain significance
NM_033056.4(PCDH15):c.5265T>G (p.Pro1755=) single nucleotide variant not provided [RCV002189322] Chr10:53822461 [GRCh38]
Chr10:55582221 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.394dup (p.Glu132fs) duplication Usher syndrome type 1G [RCV000055969] Chr10:54369199..54369200 [GRCh38]
Chr10:56128959..56128960 [GRCh37]
Chr10:10q21.1		 pathogenic|not provided
NM_001384140.1(PCDH15):c.1306-4123C>T single nucleotide variant Usher syndrome type 1F [RCV001533760]|not provided [RCV001517122]|not specified [RCV000037006] Chr10:54189391 [GRCh38]
Chr10:55949151 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4671+1046A>G single nucleotide variant PCDH15-related disorder [RCV004534782]|not provided [RCV000882213]|not specified [RCV000037007] Chr10:53809510 [GRCh38]
Chr10:55569270 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.4671+1114A>C single nucleotide variant not provided [RCV000968660]|not specified [RCV000037008] Chr10:53809442 [GRCh38]
Chr10:55569202 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4671+1164_4671+1167del deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003155051]|not specified [RCV000037009] Chr10:53809389..53809392 [GRCh38]
Chr10:55569149..55569152 [GRCh37]
Chr10:10q21.1		 pathogenic|uncertain significance
NM_001384140.1(PCDH15):c.4671+1344A>C single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001787824]|Usher syndrome type 1F [RCV001533684]|not provided [RCV001522643]|not specified [RCV000037010] Chr10:53809212 [GRCh38]
Chr10:55568972 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4672-1699G>A single nucleotide variant not provided [RCV000965135]|not specified [RCV000037011] Chr10:53808829 [GRCh38]
Chr10:55568589 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.4672-1637G>A single nucleotide variant not provided [RCV000882834]|not specified [RCV000037012] Chr10:53808767 [GRCh38]
Chr10:55568527 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.1028G>A (p.Arg343Lys) single nucleotide variant PCDH15-related disorder [RCV004734556]|not provided [RCV001038798]|not specified [RCV000039692] Chr10:54214006 [GRCh38]
Chr10:55973766 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.1039C>T (p.Leu347Phe) single nucleotide variant Usher syndrome type 1 [RCV001105070]|Usher syndrome type 1F [RCV001449930]|not provided [RCV000969899]|not specified [RCV000039693] Chr10:54213995 [GRCh38]
Chr10:55973755 [GRCh37]
Chr10:10q21.1		 benign|likely benign|uncertain significance
NM_001384140.1(PCDH15):c.1121C>T (p.Pro374Leu) single nucleotide variant Usher syndrome type 1F [RCV001835651]|not provided [RCV001852830]|not specified [RCV000039694] Chr10:54195867 [GRCh38]
Chr10:55955627 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1138G>A (p.Gly380Ser) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002490548]|Usher syndrome type 1 [RCV000407693]|Usher syndrome type 1F [RCV000988364]|not provided [RCV000086940]|not specified [RCV000039695] Chr10:54195850 [GRCh38]
Chr10:54195850..54195851 [GRCh38]
Chr10:55955610 [GRCh37]
Chr10:55955610..55955611 [GRCh37]
Chr10:10q21.1		 benign|likely benign|not provided
NM_001384140.1(PCDH15):c.1169A>G (p.Asn390Ser) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001578651]|Inborn genetic diseases [RCV003298077]|Usher syndrome type 1 [RCV001103159]|Usher syndrome type 1F [RCV001578652]|not provided [RCV001340857]|not specified [RCV000039696] Chr10:54195819 [GRCh38]
Chr10:55955579 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1181A>G (p.Tyr394Cys) single nucleotide variant Inborn genetic diseases [RCV003298078]|PCDH15-related disorder [RCV004534839]|not provided [RCV000925884]|not specified [RCV000039697] Chr10:54195807 [GRCh38]
Chr10:55955567 [GRCh37]
Chr10:10q21.1		 benign|likely benign|uncertain significance
NM_001384140.1(PCDH15):c.1263T>C (p.Thr421=) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002483009]|Usher syndrome type 1 [RCV000293259]|Usher syndrome type 1F [RCV001276783]|not provided [RCV000086941]|not specified [RCV000039698] Chr10:54195725 [GRCh38]
Chr10:55955485 [GRCh37]
Chr10:10q21.1		 benign|likely benign|not provided
NM_001384140.1(PCDH15):c.1304A>C (p.Asp435Ala) single nucleotide variant Usher syndrome type 1 [RCV000333000]|Usher syndrome type 1F [RCV000988363]|not provided [RCV001517123]|not specified [RCV000039699] Chr10:54195684 [GRCh38]
Chr10:55955444 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.1339G>A (p.Asp447Asn) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002496639]|Usher syndrome type 1 [RCV001108337]|Usher syndrome type 1F [RCV001275402]|not provided [RCV000755595]|not specified [RCV000039700] Chr10:54185235 [GRCh38]
Chr10:55944995 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1360G>A (p.Val454Ile) single nucleotide variant Usher syndrome type 1 [RCV000327397]|Usher syndrome type 1F [RCV001275401]|not provided [RCV000588827]|not specified [RCV000039701] Chr10:54185214 [GRCh38]
Chr10:55944974 [GRCh37]
Chr10:10q21.1		 benign|uncertain significance
NM_001384140.1(PCDH15):c.1362C>T (p.Val454=) single nucleotide variant Usher syndrome type 1 [RCV000272282]|Usher syndrome type 1F [RCV001831683]|not provided [RCV000963503]|not specified [RCV000039702] Chr10:54185212 [GRCh38]
Chr10:55944972 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.157+3A>G single nucleotide variant Usher syndrome type 1 [RCV000316372]|Usher syndrome type 1F [RCV001276792]|not provided [RCV001523423]|not specified [RCV000039703] Chr10:54527809 [GRCh38]
Chr10:56287569 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.1653G>A (p.Gly551=) single nucleotide variant not provided [RCV001515822]|not specified [RCV000039704] Chr10:54153231 [GRCh38]
Chr10:55912991 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.16del (p.Tyr6fs) deletion Rare genetic deafness [RCV000824736]|USHER SYNDROME, TYPE ID/F, DIGENIC [RCV000005223]|Usher syndrome type 1 [RCV000219366]|Usher syndrome type 1F [RCV000039705]|not provided [RCV001008080] Chr10:54664247 [GRCh38]
Chr10:56424007 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|not provided
NM_001384140.1(PCDH15):c.1702G>A (p.Ala568Thr) single nucleotide variant Usher syndrome type 1 [RCV001106126]|not provided [RCV000888746]|not specified [RCV000039706] Chr10:54153182 [GRCh38]
Chr10:55912942 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity
NM_001384140.1(PCDH15):c.1910A>G (p.Asn637Ser) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001787835]|Usher syndrome type 1 [RCV000346480]|Usher syndrome type 1F [RCV001275397]|not provided [RCV000992504]|not specified [RCV000039707] Chr10:54132882 [GRCh38]
Chr10:55892642 [GRCh37]
Chr10:10q21.1		 benign|uncertain significance
NM_001384140.1(PCDH15):c.1998-2A>G single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003473288]|Rare genetic deafness [RCV000824733]|Usher syndrome type 1F [RCV000039708]|not provided [RCV001379283] Chr10:54079426 [GRCh38]
Chr10:55839186 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.2424G>C (p.Lys808Asn) single nucleotide variant Usher syndrome type 1F [RCV001273395]|not provided [RCV000734148]|not specified [RCV000039709] Chr10:54022994 [GRCh38]
Chr10:55782754 [GRCh37]
Chr10:10q21.1		 conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.2439T>A (p.Asp813Glu) single nucleotide variant Usher syndrome type 1F [RCV001274797]|not specified [RCV000039710] Chr10:54022979 [GRCh38]
Chr10:55782739 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.243G>A (p.Val81=) single nucleotide variant Usher syndrome type 1 [RCV000261127]|Usher syndrome type 1F [RCV001275407]|not provided [RCV000587293]|not specified [RCV000039711] Chr10:54378857 [GRCh38]
Chr10:56138617 [GRCh37]
Chr10:10q21.1		 benign|likely benign|uncertain significance
NM_001384140.1(PCDH15):c.2563C>T (p.Arg855Trp) single nucleotide variant PCDH15-related disorder [RCV004541127]|Usher syndrome type 1 [RCV000259703]|Usher syndrome type 1F [RCV001273393]|not provided [RCV000658086]|not specified [RCV000039712] Chr10:54020380 [GRCh38]
Chr10:55780140 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.2625G>A (p.Ser875=) single nucleotide variant Usher syndrome type 1 [RCV000309900]|Usher syndrome type 1F [RCV001274795]|not provided [RCV000950187]|not specified [RCV000039713] Chr10:54020318 [GRCh38]
Chr10:55780078 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance|conflicting data from submitters
NM_001384140.1(PCDH15):c.2717C>T (p.Pro906Leu) single nucleotide variant Inborn genetic diseases [RCV002513554]|Usher syndrome type 1F [RCV000665604]|not provided [RCV001244960]|not specified [RCV000039714] Chr10:54020226 [GRCh38]
Chr10:55779986 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2786G>A (p.Arg929Gln) single nucleotide variant Usher syndrome type 1 [RCV000350263]|Usher syndrome type 1F [RCV001274793]|not provided [RCV001522645]|not specified [RCV000039715] Chr10:53995731 [GRCh38]
Chr10:55755491 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.2885G>A (p.Arg962His) single nucleotide variant PCDH15-related disorder [RCV004534840]|Usher syndrome type 1 [RCV000378203]|Usher syndrome type 1F [RCV000664561]|not provided [RCV000973447]|not specified [RCV000039716] Chr10:53961876 [GRCh38]
Chr10:55721636 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.2885G>T (p.Arg962Leu) single nucleotide variant PCDH15-related disorder [RCV004534841]|Usher syndrome type 1 [RCV000273097]|Usher syndrome type 1F [RCV001273392]|not provided [RCV000723804]|not specified [RCV000039717] Chr10:53961876 [GRCh38]
Chr10:55721636 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.2990A>G (p.Glu997Gly) single nucleotide variant Inborn genetic diseases [RCV001266721]|not provided [RCV000881441]|not specified [RCV000039718] Chr10:53961771 [GRCh38]
Chr10:55721531 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.2992C>G (p.Pro998Ala) single nucleotide variant Usher syndrome type 1F [RCV000671480]|not provided [RCV001212794]|not specified [RCV000039719] Chr10:53961769 [GRCh38]
Chr10:55721529 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3018G>T (p.Val1006=) single nucleotide variant Usher syndrome type 1 [RCV000327217]|Usher syndrome type 1F [RCV001449927]|not provided [RCV000840674]|not specified [RCV000039720] Chr10:53959836 [GRCh38]
Chr10:55719596 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.3131C>T (p.Pro1044Leu) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001334391]|Inborn genetic diseases [RCV004018893]|Usher syndrome type 1F [RCV001831684]|not provided [RCV001050722]|not specified [RCV000039721] Chr10:53940967 [GRCh38]
Chr10:55700727 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.330C>T (p.Asn110=) single nucleotide variant not provided [RCV000726890]|not specified [RCV000039722] Chr10:54369264 [GRCh38]
Chr10:56129024 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.3316C>T (p.Arg1106Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV000515240]|Autosomal recessive nonsyndromic hearing loss 23 [RCV003473289]|Rare genetic deafness [RCV000824731]|Usher syndrome [RCV003389450]|Usher syndrome type 1F [RCV000039723]|not provided [RCV001386496] Chr10:53938872 [GRCh38]
Chr10:55698632 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|conflicting interpretations of pathogenicity|conflicting data from submitters
NM_001384140.1(PCDH15):c.3373+3A>G single nucleotide variant not specified [RCV000039724] Chr10:53938812 [GRCh38]
Chr10:55698572 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3374-4C>T single nucleotide variant Usher syndrome type 1 [RCV001108250]|Usher syndrome type 1F [RCV001274791]|not provided [RCV000956827]|not specified [RCV000039725] Chr10:53903374 [GRCh38]
Chr10:55663134 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.343G>A (p.Val115Met) single nucleotide variant Inborn genetic diseases [RCV002513555]|PCDH15-related disorder [RCV004534842]|not provided [RCV000839729]|not specified [RCV000039726] Chr10:54369251 [GRCh38]
Chr10:56129011 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.3502-14dup duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV001787837]|Usher syndrome type 1F [RCV001787836]|not provided [RCV000590635]|not specified [RCV000039727] Chr10:53866870..53866871 [GRCh38]
Chr10:55626630..55626631 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3502-8C>T single nucleotide variant PCDH15-related disorder [RCV004534843]|Usher syndrome type 1 [RCV000407955]|Usher syndrome type 1F [RCV001826581]|not provided [RCV000761719]|not specified [RCV000039728] Chr10:53866865 [GRCh38]
Chr10:55626625 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.3532G>A (p.Val1178Ile) single nucleotide variant Usher syndrome type 1 [RCV001106031]|not provided [RCV000886091]|not specified [RCV000039729] Chr10:53866827 [GRCh38]
Chr10:55626587 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity
NM_001384140.1(PCDH15):c.3585T>C (p.Phe1195=) single nucleotide variant not provided [RCV001467895]|not specified [RCV000039730] Chr10:53866774 [GRCh38]
Chr10:55626534 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3718-19C>A single nucleotide variant Usher syndrome type 1F [RCV001533690]|not provided [RCV000587424]|not specified [RCV000039731] Chr10:53857282 [GRCh38]
Chr10:55617042 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.3719T>A (p.Val1240Asp) single nucleotide variant not provided [RCV003727610]|not specified [RCV000039732] Chr10:53857262 [GRCh38]
Chr10:55617022 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3795A>T (p.Glu1265Asp) single nucleotide variant Usher syndrome type 1 [RCV000347883]|Usher syndrome type 1F [RCV001274790]|not provided [RCV000956825]|not specified [RCV000039733] Chr10:53857186 [GRCh38]
Chr10:55616946 [GRCh37]
Chr10:10q21.1		 benign|uncertain significance
NM_001384140.1(PCDH15):c.3817C>A (p.Arg1273Ser) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV000763655]|Usher syndrome type 1 [RCV001104870]|Usher syndrome type 1D [RCV001810408]|Usher syndrome type 1F [RCV001449585]|not provided [RCV000727028]|not specified [RCV000039734] Chr10:53840486 [GRCh38]
Chr10:55600246 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.3984-20C>T single nucleotide variant Usher syndrome type 1F [RCV001533689]|not provided [RCV001523599]|not specified [RCV000039735] Chr10:53831553 [GRCh38]
Chr10:55591313 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4024C>A (p.Gln1342Lys) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002496640]|Usher syndrome type 1 [RCV001104869]|Usher syndrome type 1F [RCV000671678]|not provided [RCV000514851]|not specified [RCV000039736] Chr10:53831493 [GRCh38]
Chr10:55591253 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity
NM_001384140.1(PCDH15):c.4080G>A (p.Val1360=) single nucleotide variant PCDH15-related disorder [RCV004541128]|Usher syndrome type 1 [RCV000296351]|Usher syndrome type 1F [RCV001272409]|not provided [RCV000912149]|not specified [RCV000039737] Chr10:53831437 [GRCh38]
Chr10:55591197 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4103A>G (p.Glu1368Gly) single nucleotide variant Inborn genetic diseases [RCV002513556]|Usher syndrome type 1 [RCV001104868]|not provided [RCV000963253]|not specified [RCV000039738] Chr10:53831414 [GRCh38]
Chr10:55591174 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.4334C>G (p.Ala1445Gly) single nucleotide variant PCDH15-related disorder [RCV004541129]|Usher syndrome type 1 [RCV000361500]|Usher syndrome type 1F [RCV001274788]|not provided [RCV000889224]|not specified [RCV000039739] Chr10:53827426 [GRCh38]
Chr10:55587186 [GRCh37]
Chr10:10q21.1		 benign|likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4343A>G (p.Tyr1448Cys) single nucleotide variant Usher syndrome type 1F [RCV001831685]|not specified [RCV000039740] Chr10:53827417 [GRCh38]
Chr10:55587177 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4581C>A (p.Pro1527=) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001787838]|Usher syndrome type 1 [RCV000304409]|Usher syndrome type 1F [RCV001274785]|not provided [RCV001522644]|not specified [RCV000039741] Chr10:53823145 [GRCh38]
Chr10:55582905 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_033056.4(PCDH15):c.4592A>G (p.Glu1531Gly) single nucleotide variant not specified [RCV000039742] Chr10:53823134 [GRCh38]
Chr10:55582894 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4850A>G (p.Asn1617Ser) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002490549]|Usher syndrome type 1 [RCV000350911]|Usher syndrome type 1F [RCV001526752]|not provided [RCV000514010]|not specified [RCV000039743] Chr10:53822876 [GRCh38]
Chr10:55582636 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.475-3C>T single nucleotide variant Usher syndrome type 1 [RCV000345244]|Usher syndrome type 1F [RCV001276791]|not provided [RCV000948373]|not specified [RCV000039744] Chr10:54346487 [GRCh38]
Chr10:56106247 [GRCh37]
Chr10:10q21.1		 benign|likely benign|uncertain significance
NM_033056.4(PCDH15):c.4783A>C (p.Ile1595Leu) single nucleotide variant Usher syndrome type 1 [RCV000345143]|Usher syndrome type 1F [RCV001831686]|not provided [RCV000928675]|not specified [RCV000039745] Chr10:53822943 [GRCh38]
Chr10:55582703 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.4884T>C (p.Thr1628=) single nucleotide variant Usher syndrome type 1F [RCV001831687]|not provided [RCV000881153]|not specified [RCV000039746] Chr10:53822842 [GRCh38]
Chr10:55582602 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity
NM_033056.4(PCDH15):c.5245CCT[3] (p.Pro1752del) microsatellite Hearing loss, autosomal recessive [RCV004577721]|PCDH15-related disorder [RCV004534844]|Retinitis pigmentosa-deafness syndrome [RCV000360567]|Usher syndrome type 1F [RCV001826582]|not provided [RCV000415971]|not specified [RCV000039747] Chr10:53822470..53822472 [GRCh38]
Chr10:55582230..55582232 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_033056.4(PCDH15):c.5269_5280del (p.Ser1757_Pro1760del) deletion not provided [RCV001243117]|not specified [RCV000039748] Chr10:53822446..53822457 [GRCh38]
Chr10:55582206..55582217 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.5278C>A (p.Pro1760Thr) single nucleotide variant Usher syndrome type 1F [RCV001831688]|not provided [RCV001312814]|not specified [RCV000039749] Chr10:53822448 [GRCh38]
Chr10:55582208 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5283T>A (p.Ala1761=) single nucleotide variant Usher syndrome type 1 [RCV000264922]|Usher syndrome type 1F [RCV001826583]|not provided [RCV001497321]|not specified [RCV000039750] Chr10:53822443 [GRCh38]
Chr10:55582203 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.5286T>A (p.Pro1762=) single nucleotide variant Usher syndrome type 1 [RCV000405593]|Usher syndrome type 1F [RCV001274781]|not provided [RCV000879272]|not specified [RCV000039751] Chr10:53822440 [GRCh38]
Chr10:55582200 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_033056.4(PCDH15):c.5281GCTCCT[1] (p.1761AP[1]) microsatellite Hearing loss, autosomal recessive [RCV004577722]|PCDH15-related disorder [RCV004541130]|Retinitis pigmentosa-deafness syndrome [RCV000363120]|Usher syndrome type 1D [RCV001810409]|Usher syndrome type 1F [RCV001449922]|not provided [RCV000910500]|not specified [RCV000039752] Chr10:53822434..53822439 [GRCh38]
Chr10:55582194..55582199 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_033056.4(PCDH15):c.5296_5304dup (p.Ala1766_Pro1768dup) duplication not provided [RCV000734418]|not specified [RCV000039753] Chr10:53822421..53822422 [GRCh38]
Chr10:55582181..55582182 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.5327_5335del (p.Leu1776_Cys1778del) deletion not provided [RCV001824285]|not specified [RCV000039754] Chr10:53822391..53822399 [GRCh38]
Chr10:55582151..55582159 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_033056.4(PCDH15):c.5346T>A (p.Ser1782=) single nucleotide variant not specified [RCV000039755] Chr10:53822380 [GRCh38]
Chr10:55582140 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5353T>C (p.Ser1785Pro) single nucleotide variant Inborn genetic diseases [RCV004018894]|PCDH15-related disorder [RCV004541131]|Usher syndrome type 1 [RCV000280214]|Usher syndrome type 1F [RCV001274780]|not provided [RCV000901705]|not specified [RCV000039756] Chr10:53822373 [GRCh38]
Chr10:55582133 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.5359C>T (p.Pro1787Ser) single nucleotide variant Usher syndrome type 1 [RCV000343313]|Usher syndrome type 1F [RCV000169021]|not provided [RCV000992510]|not specified [RCV000039757] Chr10:53822367 [GRCh38]
Chr10:55582127 [GRCh37]
Chr10:10q21.1		 benign|likely benign|uncertain significance
NM_033056.4(PCDH15):c.5398G>A (p.Val1800Ile) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002477117]|PCDH15-related disorder [RCV004534845]|Usher syndrome type 1 [RCV001105924]|Usher syndrome type 1F [RCV000169085]|not provided [RCV000896182]|not specified [RCV000039758] Chr10:53822328 [GRCh38]
Chr10:55582088 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity
NM_033056.4(PCDH15):c.5414C>T (p.Pro1805Leu) single nucleotide variant PCDH15-related disorder [RCV004534846]|Usher syndrome type 1 [RCV001105923]|Usher syndrome type 1F [RCV001831689]|not provided [RCV000971054]|not specified [RCV000039759] Chr10:53822312 [GRCh38]
Chr10:55582072 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.546A>G (p.Gly182=) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001578790]|Usher syndrome type 1 [RCV000398758]|Usher syndrome type 1F [RCV001275404]|not provided [RCV000992511]|not specified [RCV000039760] Chr10:54346413 [GRCh38]
Chr10:56106173 [GRCh37]
Chr10:10q21.1		 benign|likely benign|uncertain significance
NM_033056.4(PCDH15):c.5550C>A (p.Thr1850=) single nucleotide variant Usher syndrome type 1 [RCV001104786]|not provided [RCV000881359]|not specified [RCV000039761] Chr10:53822176 [GRCh38]
Chr10:55581936 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity
NM_033056.4(PCDH15):c.5565C>T (p.Ala1855=) single nucleotide variant Usher syndrome type 1 [RCV000381540]|Usher syndrome type 1F [RCV001831690]|not provided [RCV000727222]|not specified [RCV000039762] Chr10:53822161 [GRCh38]
Chr10:55581921 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.55T>G (p.Ser19Ala) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001787839]|Usher syndrome type 1 [RCV000321670]|Usher syndrome type 1F [RCV001276793]|not provided [RCV000586437]|not specified [RCV000039763] Chr10:54664208 [GRCh38]
Chr10:56423968 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_033056.4(PCDH15):c.5598AAC[1] (p.Thr1869del) microsatellite Autosomal recessive nonsyndromic hearing loss 23 [RCV002490550]|USHER SYNDROME, TYPE ID/F, DIGENIC [RCV002277128]|Usher syndrome type 1 [RCV000215699]|Usher syndrome type 1F [RCV001272395]|not provided [RCV000514811]|not specified [RCV000039764] Chr10:53822123..53822125 [GRCh38]
Chr10:55581883..55581885 [GRCh37]
Chr10:10q21.1		 pathogenic|benign|conflicting interpretations of pathogenicity|not provided
NM_033056.4(PCDH15):c.5603C>T (p.Thr1868Met) single nucleotide variant Usher syndrome type 1 [RCV001104784]|not provided [RCV000909077]|not specified [RCV000039765] Chr10:53822123 [GRCh38]
Chr10:55581883 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_033056.4(PCDH15):c.5707A>G (p.Ile1903Val) single nucleotide variant Usher syndrome type 1 [RCV000300657]|Usher syndrome type 1F [RCV001274778]|not provided [RCV000992512]|not specified [RCV000039766] Chr10:53822019 [GRCh38]
Chr10:55581779 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_033056.4(PCDH15):c.5726G>A (p.Arg1909His) single nucleotide variant Usher syndrome type 1F [RCV000671807]|not provided [RCV001548684]|not specified [RCV000039767] Chr10:53822000 [GRCh38]
Chr10:55581760 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.593C>T (p.Pro198Leu) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002504908]|Inborn genetic diseases [RCV004018895]|Usher syndrome type 1 [RCV000378841]|Usher syndrome type 1F [RCV001276789]|not provided [RCV001248205] Chr10:54346366 [GRCh38]
Chr10:56106126 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.607A>G (p.Thr203Ala) single nucleotide variant Inborn genetic diseases [RCV002513557]|Usher syndrome type 1F [RCV001826584]|not specified [RCV000039769] Chr10:54329694 [GRCh38]
Chr10:56089454 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.706-8C>T single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001787840]|Usher syndrome type 1 [RCV000275968]|Usher syndrome type 1F [RCV001276787]|not provided [RCV001513890]|not specified [RCV000039770] Chr10:54317449 [GRCh38]
Chr10:56077209 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.947C>T (p.Pro316Leu) single nucleotide variant not specified [RCV000039772] Chr10:54236861 [GRCh38]
Chr10:55996621 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.960A>G (p.Pro320=) single nucleotide variant Usher syndrome type 1 [RCV000365159]|Usher syndrome type 1F [RCV001276785]|not provided [RCV000992513]|not specified [RCV000039773] Chr10:54236848 [GRCh38]
Chr10:55996608 [GRCh37]
Chr10:10q21.1		 benign|uncertain significance
GRCh38/hg38 10q21.1(chr10:53477144-54916701)x3 copy number gain See cases [RCV000051627] Chr10:53477144..54916701 [GRCh38]
Chr10:55236904..56676461 [GRCh37]
Chr10:54906910..56346467 [NCBI36]
Chr10:10q21.1		 uncertain significance
GRCh38/hg38 10q11.21-21.2(chr10:42335305-60284876)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052506]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052506]|See cases [RCV000052506] Chr10:42335305..60284876 [GRCh38]
Chr10:42830753..62044634 [GRCh37]
Chr10:42150759..61714640 [NCBI36]
Chr10:10q11.21-21.2		 pathogenic
GRCh38/hg38 10q21.1(chr10:54287239-57268543)x1 copy number loss See cases [RCV000052510] Chr10:54287239..57268543 [GRCh38]
Chr10:56046999..59028303 [GRCh37]
Chr10:55717005..58698309 [NCBI36]
Chr10:10q21.1		 pathogenic
NM_033056.3(PCDH15):c.4532G>A (p.Arg1511Lys) single nucleotide variant Malignant melanoma [RCV000068979] Chr10:53823194 [GRCh38]
Chr10:55582954 [GRCh37]
Chr10:55252960 [NCBI36]
Chr10:10q21.1		 not provided
NM_033056.3(PCDH15):c.4374C>T (p.Phe1458=) single nucleotide variant Malignant melanoma [RCV000068980] Chr10:53823352 [GRCh38]
Chr10:55583112 [GRCh37]
Chr10:55253118 [NCBI36]
Chr10:10q21.1		 not provided
NM_033056.3(PCDH15):c.3786A>T (p.Lys1262Asn) single nucleotide variant Malignant melanoma [RCV000068981] Chr10:53857195 [GRCh38]
Chr10:55616955 [GRCh37]
Chr10:55286961 [NCBI36]
Chr10:10q21.1		 not provided
NM_033056.3(PCDH15):c.5568G>A (p.Glu1856=) single nucleotide variant Malignant melanoma [RCV000062044] Chr10:53822158 [GRCh38]
Chr10:55581918 [GRCh37]
Chr10:55251924 [NCBI36]
Chr10:10q21.1		 not provided
NM_001384140.1(PCDH15):c.3156G>A (p.Gly1052=) single nucleotide variant not provided [RCV003854177] Chr10:53940942 [GRCh38]
Chr10:55700702 [GRCh37]
Chr10:55370708 [NCBI36]
Chr10:10q21.1		 likely benign|not provided
NM_001384140.1(PCDH15):c.3964G>C (p.Asp1322His) single nucleotide variant Usher syndrome type 1F [RCV001829819]|not provided [RCV000658006] Chr10:53840339 [GRCh38]
Chr10:55600099 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.149G>T (p.Ser50Ile) single nucleotide variant not provided [RCV000658085] Chr10:54527820 [GRCh38]
Chr10:56287580 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.3(PCDH15):c.3806+2110T>A single nucleotide variant Lung cancer [RCV000109112] Chr10:53855065 [GRCh38]
Chr10:55614825 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.3(PCDH15):c.2751+5491T>A single nucleotide variant Lung cancer [RCV000109113] Chr10:54014701 [GRCh38]
Chr10:55774461 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.3(PCDH15):c.2221-7402T>G single nucleotide variant Lung cancer [RCV000109114] Chr10:54030599 [GRCh38]
Chr10:55790359 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.3(PCDH15):c.1917+12887C>A single nucleotide variant Lung cancer [RCV000109115] Chr10:54119988 [GRCh38]
Chr10:55879748 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.3(PCDH15):c.1591-12946G>A single nucleotide variant Lung cancer [RCV000109116] Chr10:54166239 [GRCh38]
Chr10:55925999 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.3(PCDH15):c.877-8249C>A single nucleotide variant Lung cancer [RCV000109117] Chr10:54245180 [GRCh38]
Chr10:56004940 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.3(PCDH15):c.877-36912T>A single nucleotide variant Lung cancer [RCV000109118] Chr10:54273843 [GRCh38]
Chr10:56033603 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.3(PCDH15):c.706-283T>C single nucleotide variant Lung cancer [RCV000109119] Chr10:54317724 [GRCh38]
Chr10:56077484 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.3(PCDH15):c.158-10238C>T single nucleotide variant Lung cancer [RCV000109120] Chr10:54389180 [GRCh38]
Chr10:56148940 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.158-16930T>C single nucleotide variant Usher syndrome type 1F [RCV000668795] Chr10:54395872 [GRCh38]
Chr10:56155632 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.3(PCDH15):c.158-32458T>A single nucleotide variant Lung cancer [RCV000109122] Chr10:54411400 [GRCh38]
Chr10:56171160 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.3(PCDH15):c.157+59112A>G single nucleotide variant Lung cancer [RCV000109123] Chr10:54468700 [GRCh38]
Chr10:56228460 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.3(PCDH15):c.91+44681G>A single nucleotide variant Lung cancer [RCV000109124] Chr10:54619491 [GRCh38]
Chr10:56379251 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.3(PCDH15):c.-28-17504C>T single nucleotide variant Lung cancer [RCV000109125] Chr10:54681794 [GRCh38]
Chr10:56441554 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.3(PCDH15):c.-29+57025C>T single nucleotide variant Lung cancer [RCV000109126] Chr10:54743900 [GRCh38]
Chr10:56503660 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2361TGT[2] (p.Val790del) microsatellite Autosomal recessive nonsyndromic hearing loss 23 [RCV000114410]|Usher syndrome type 1F [RCV000675146]|not provided [RCV002514567]|not specified [RCV000220485] Chr10:54023049..54023051 [GRCh38]
Chr10:55782809..55782811 [GRCh37]
Chr10:10q21.1		 pathogenic|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.3936A>G (p.Ala1312=) single nucleotide variant Usher syndrome type 1F [RCV001826770]|not provided [RCV000723701]|not specified [RCV000082314] Chr10:53840367 [GRCh38]
Chr10:55600127 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.949T>A (p.Ser317Thr) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001804834]|PCDH15-related disorder [RCV004734641]|not provided [RCV000657972]|not specified [RCV000082317] Chr10:54236859 [GRCh38]
Chr10:55996619 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.1434C>T (p.Thr478=) single nucleotide variant not provided [RCV001412315] Chr10:54185140 [GRCh38]
Chr10:55944900 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4213C>G (p.Arg1405Gly) single nucleotide variant not specified [RCV000603349] Chr10:53827547 [GRCh38]
Chr10:55587307 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5290_5295del (p.Pro1764_Leu1765del) deletion not provided [RCV001367930] Chr10:53822431..53822436 [GRCh38]
Chr10:55582191..55582196 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.3983+12T>C single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002492483]|Usher syndrome type 1 [RCV000325579]|not provided [RCV001520241]|not specified [RCV000155382] Chr10:53840308 [GRCh38]
Chr10:55600068 [GRCh37]
Chr10:10q21.1		 benign|likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4492-1191G>A single nucleotide variant not provided [RCV000127329] Chr10:53812810 [GRCh38]
Chr10:55572570 [GRCh37]
Chr10:10q21.1		 benign
NM_033056.3:c.+15180G>A single nucleotide variant not provided [RCV000127330] Chr10:10q21.1 benign
NM_033056.3:c.+15212A>C single nucleotide variant not provided [RCV000127331] Chr10:10q21.1 benign
NM_001384140.1(PCDH15):c.4671+1559C>T single nucleotide variant Usher syndrome type 1F [RCV000668969]|not specified [RCV001002355] Chr10:53808997 [GRCh38]
Chr10:55568757 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3717+8G>C single nucleotide variant not provided [RCV000956826]|not specified [RCV000176769] Chr10:53866634 [GRCh38]
Chr10:55626394 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity
NM_033056.3(PCDH15):c.4834_4835insAACA (p.Thr1612Lysfs) insertion not specified [RCV000177751] Chr10:53822891..53822892 [GRCh38]
Chr10:55582651..55582652 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.92-493A>T single nucleotide variant not provided [RCV000513721] Chr10:54528370 [GRCh38]
Chr10:56288130 [GRCh37]
Chr10:10q21.1		 benign|likely benign
GRCh38/hg38 10q11.21-22.2(chr10:42685306-73715908)x3 copy number gain See cases [RCV000134848] Chr10:42685306..73715908 [GRCh38]
Chr10:43180754..75475666 [GRCh37]
Chr10:42500760..75145672 [NCBI36]
Chr10:10q11.21-22.2		 pathogenic
GRCh38/hg38 10q21.1(chr10:53366596-56420041)x4 copy number gain See cases [RCV000137162] Chr10:53366596..56420041 [GRCh38]
Chr10:55126356..58179802 [GRCh37]
Chr10:54796362..57849808 [NCBI36]
Chr10:10q21.1		 uncertain significance
GRCh38/hg38 10q21.1(chr10:53051023-54726415)x1 copy number loss See cases [RCV000137246] Chr10:53051023..54726415 [GRCh38]
Chr10:54810783..56486175 [GRCh37]
Chr10:54480789..56156181 [NCBI36]
Chr10:10q21.1		 uncertain significance
GRCh38/hg38 10q11.23-23.2(chr10:50729367-87147204)x3 copy number gain See cases [RCV000138007] Chr10:50729367..87147204 [GRCh38]
Chr10:52489127..88906961 [GRCh37]
Chr10:52159133..88896941 [NCBI36]
Chr10:10q11.23-23.2		 pathogenic
GRCh38/hg38 10q21.1(chr10:53954459-54098171)x0 copy number loss See cases [RCV000138105] Chr10:53954459..54098171 [GRCh38]
Chr10:55714219..55857931 [GRCh37]
Chr10:55384225..55527937 [NCBI36]
Chr10:10q21.1		 pathogenic
GRCh38/hg38 10q21.1(chr10:53051046-54726547)x1 copy number loss See cases [RCV000138417] Chr10:53051046..54726547 [GRCh38]
Chr10:54810806..56486307 [GRCh37]
Chr10:54480812..56156313 [NCBI36]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2161C>G (p.Leu721Val) single nucleotide variant not provided [RCV000175372] Chr10:54066816 [GRCh38]
Chr10:55826576 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh38/hg38 10q21.1(chr10:53308026-56420041)x3 copy number gain See cases [RCV000139643] Chr10:53308026..56420041 [GRCh38]
Chr10:55067786..58179802 [GRCh37]
Chr10:54737792..57849808 [NCBI36]
Chr10:10q21.1		 likely benign
GRCh38/hg38 10q21.1(chr10:54417212-54436627)x3 copy number gain See cases [RCV000141195] Chr10:54417212..54436627 [GRCh38]
Chr10:56176972..56196387 [GRCh37]
Chr10:55846978..55866393 [NCBI36]
Chr10:10q21.1		 benign
GRCh38/hg38 10q11.21-21.3(chr10:42112187-67400675)x3 copy number gain See cases [RCV000142967] Chr10:42112187..67400675 [GRCh38]
Chr10:42607635..69160433 [GRCh37]
Chr10:41927641..68830439 [NCBI36]
Chr10:10q11.21-21.3		 pathogenic
NM_001384140.1(PCDH15):c.2538C>T (p.Val846=) single nucleotide variant not provided [RCV000929731]|not specified [RCV000155741] Chr10:54020405 [GRCh38]
Chr10:55780165 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1998-13G>A single nucleotide variant not specified [RCV000155871] Chr10:54079437 [GRCh38]
Chr10:55839197 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4367+8G>A single nucleotide variant not provided [RCV001442901]|not specified [RCV000156045] Chr10:53827385 [GRCh38]
Chr10:55587145 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3807-6T>G single nucleotide variant PCDH15-related disorder [RCV004544448]|Usher syndrome type 1F [RCV000668863]|not provided [RCV001246357]|not specified [RCV000156110] Chr10:53840502 [GRCh38]
Chr10:55600262 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_033056.4(PCDH15):c.5048T>G (p.Leu1683Arg) single nucleotide variant Usher syndrome type 1F [RCV001272397]|not provided [RCV002516151]|not specified [RCV000156146] Chr10:53822678 [GRCh38]
Chr10:55582438 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2721T>G (p.Pro907=) single nucleotide variant not provided [RCV000983040]|not specified [RCV000156177] Chr10:54020222 [GRCh38]
Chr10:55779982 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4681_4684dup (p.Ser1562Ter) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003474813]|PCDH15-related disorder [RCV004734739]|Usher syndrome type 1F [RCV001274784]|not provided [RCV001224404]|not specified [RCV000156189] Chr10:53823041..53823042 [GRCh38]
Chr10:55582801..55582802 [GRCh37]
Chr10:10q21.1		 pathogenic|conflicting interpretations of pathogenicity|uncertain significance
NM_033056.4(PCDH15):c.5294_5302del (p.Leu1765_Pro1767del) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV002505164]|PCDH15-related disorder [RCV004544401]|not provided [RCV000888344]|not specified [RCV000153650] Chr10:53822424..53822432 [GRCh38]
Chr10:55582184..55582192 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.679C>T (p.Arg227Cys) single nucleotide variant Usher syndrome type 1F [RCV001276788]|not provided [RCV000726127]|not specified [RCV000156248] Chr10:54329622 [GRCh38]
Chr10:56089382 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4672-1586T>C single nucleotide variant not specified [RCV000156281] Chr10:53808716 [GRCh38]
Chr10:55568476 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4671+1418T>C single nucleotide variant not specified [RCV000156285] Chr10:53809138 [GRCh38]
Chr10:55568898 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3502-14del deletion not provided [RCV001509863]|not specified [RCV000156335] Chr10:53866871 [GRCh38]
Chr10:55626631 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1927C>T (p.Arg643Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002498738]|Autosomal recessive nonsyndromic hearing loss 23 [RCV004567176]|Rare genetic deafness [RCV000824734]|Usher syndrome type 1D [RCV001002687]|Usher syndrome type 1F [RCV000154331]|not provided [RCV001386498] Chr10:54090054 [GRCh38]
Chr10:55849814 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.5557A>C (p.Met1853Leu) single nucleotide variant PCDH15-related disorder [RCV004544404]|Usher syndrome type 1 [RCV001104785]|Usher syndrome type 1F [RCV001826830]|not provided [RCV000879612]|not specified [RCV000154360] Chr10:53822169 [GRCh38]
Chr10:55581929 [GRCh37]
Chr10:10q21.1		 benign|likely benign|uncertain significance
NM_033056.4(PCDH15):c.5280_5342del (p.Ala1761_Pro1781del) deletion PCDH15-related disorder [RCV004535011]|Usher syndrome type 1F [RCV001826854]|not provided [RCV000766307]|not specified [RCV000156548] Chr10:53822384..53822446 [GRCh38]
Chr10:55582144..55582206 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_033056.4(PCDH15):c.5352T>A (p.Pro1784=) single nucleotide variant not specified [RCV000156549] Chr10:53822374 [GRCh38]
Chr10:55582134 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1590+20= single nucleotide variant not specified [RCV000154406] Chr10:54183424 [GRCh38]
Chr10:55943184 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.706-8= single nucleotide variant not specified [RCV000154439] Chr10:54317449 [GRCh38]
Chr10:56077209 [GRCh37]
Chr10:10q21.1		 benign
NM_033056.4(PCDH15):c.5349T>G (p.Pro1783=) single nucleotide variant not specified [RCV000156567] Chr10:53822377 [GRCh38]
Chr10:55582137 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5397C>T (p.Ser1799=) single nucleotide variant not provided [RCV000932824]|not specified [RCV000151621] Chr10:53822329 [GRCh38]
Chr10:55582089 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5358C>A (p.Ile1786=) single nucleotide variant not specified [RCV000151622] Chr10:53822368 [GRCh38]
Chr10:55582128 [GRCh37]
Chr10:10q21.1		 not provided
NM_033056.4(PCDH15):c.5334T>C (p.Cys1778=) single nucleotide variant PCDH15-related disorder [RCV004544360]|not provided [RCV000933745]|not specified [RCV000151623] Chr10:53822392 [GRCh38]
Chr10:55582152 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5260TCTCCTCCT[1] (p.1754SPP[1]) microsatellite not provided [RCV001244893]|not specified [RCV000151624] Chr10:53822449..53822457 [GRCh38]
Chr10:55582209..55582217 [GRCh37]
Chr10:10q21.1		 benign|likely benign|uncertain significance
NM_033056.4(PCDH15):c.5189T>A (p.Ile1730Asn) single nucleotide variant Inborn genetic diseases [RCV003352779]|not provided [RCV001046214]|not specified [RCV000151625] Chr10:53822537 [GRCh38]
Chr10:55582297 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.3501+13A>G single nucleotide variant Usher syndrome type 1F [RCV000668536]|not provided [RCV002055999]|not specified [RCV000151626] Chr10:53903230 [GRCh38]
Chr10:55662990 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2769T>C (p.Pro923=) single nucleotide variant not provided [RCV002056000]|not specified [RCV000151629] Chr10:53995748 [GRCh38]
Chr10:55755508 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2290C>T (p.Arg764Cys) single nucleotide variant Usher syndrome type 1 [RCV001104968]|Usher syndrome type 1F [RCV001273396]|not provided [RCV000712511]|not specified [RCV000151630] Chr10:54023128 [GRCh38]
Chr10:55782888 [GRCh37]
Chr10:10q21.1		 conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.1141C>G (p.Leu381Val) single nucleotide variant Usher syndrome type 1F [RCV001835689]|not provided [RCV002516047]|not specified [RCV000151637] Chr10:54195847 [GRCh38]
Chr10:55955607 [GRCh37]
Chr10:10q21.1		 benign|uncertain significance
NM_001384140.1(PCDH15):c.809T>G (p.Leu270Arg) single nucleotide variant Usher syndrome type 1F [RCV001826810]|not provided [RCV002516049]|not specified [RCV000151639] Chr10:54317338 [GRCh38]
Chr10:56077098 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.734G>A (p.Arg245Gln) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002492560]|PCDH15-related disorder [RCV004734708]|Usher syndrome type 1F [RCV001835690]|not provided [RCV001314166]|not specified [RCV000151640] Chr10:54317413 [GRCh38]
Chr10:56077173 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2379T>C (p.Asp793=) single nucleotide variant not provided [RCV000906652]|not specified [RCV000154572] Chr10:54023039 [GRCh38]
Chr10:55782799 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5422C>A (p.Pro1808Thr) single nucleotide variant Usher syndrome type 1F [RCV001831979]|not specified [RCV000156742] Chr10:53822304 [GRCh38]
Chr10:55582064 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3451G>A (p.Gly1151Arg) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002478466]|Usher syndrome type 1 [RCV001106033]|Usher syndrome type 1F [RCV001273388]|not provided [RCV000757596]|not specified [RCV000156763] Chr10:53903293 [GRCh38]
Chr10:55663053 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.161C>T (p.Thr54Ile) single nucleotide variant PCDH15-related disorder [RCV004535016]|Usher syndrome type 1F [RCV001826856]|not provided [RCV001850170]|not specified [RCV000156775] Chr10:54378939 [GRCh38]
Chr10:56138699 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.470A>G (p.Asn157Ser) single nucleotide variant Usher syndrome type 1F [RCV001826811]|not provided [RCV003114299]|not specified [RCV000151642] Chr10:54369124 [GRCh38]
Chr10:56128884 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4671+1355A>G single nucleotide variant Inborn genetic diseases [RCV002516127]|Usher syndrome type 1D [RCV001198583]|not specified [RCV000155263] Chr10:53809201 [GRCh38]
Chr10:55568961 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4526A>G (p.Gln1509Arg) single nucleotide variant PCDH15-related disorder [RCV004734732]|not provided [RCV004691772]|not specified [RCV000155265] Chr10:53811585 [GRCh38]
Chr10:55571345 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.5614A>G (p.Lys1872Glu) single nucleotide variant Inborn genetic diseases [RCV003258674]|Usher syndrome type 1F [RCV001274779]|not provided [RCV001850125]|not specified [RCV000155266] Chr10:53822112 [GRCh38]
Chr10:55581872 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4974A>C (p.Ser1658=) single nucleotide variant Usher syndrome type 1 [RCV001108158]|not provided [RCV000930978]|not specified [RCV000155267] Chr10:53822752 [GRCh38]
Chr10:55582512 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.4733T>C (p.Val1578Ala) single nucleotide variant PCDH15-related disorder [RCV004734733]|not provided [RCV000757598]|not specified [RCV000155268] Chr10:53822993 [GRCh38]
Chr10:55582753 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3724G>A (p.Val1242Met) single nucleotide variant Usher syndrome type 1 [RCV001106029]|Usher syndrome type 1F [RCV001273382]|not provided [RCV000892246]|not specified [RCV000155269] Chr10:53857257 [GRCh38]
Chr10:55617017 [GRCh37]
Chr10:10q21.1		 benign|likely benign|uncertain significance
NM_001384140.1(PCDH15):c.942A>G (p.Gln314=) single nucleotide variant Usher syndrome type 1 [RCV001105074]|not provided [RCV000981578]|not specified [RCV000155270] Chr10:54236866 [GRCh38]
Chr10:55996626 [GRCh37]
Chr10:10q21.1		 benign|likely benign|uncertain significance
NM_033056.3(PCDH15):c.(?_-15)_(876_?)del deletion Rare genetic deafness [RCV000151618] Chr10:54317271..54664277 [GRCh38]
Chr10:56077031..56424037 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.4671+1595GAA[3] microsatellite not specified [RCV000151619] Chr10:53808950..53808952 [GRCh38]
Chr10:55568710..55568712 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5439A>C (p.Pro1813=) single nucleotide variant Usher syndrome type 1 [RCV001105921]|Usher syndrome type 1F [RCV001449588]|not provided [RCV000918866]|not specified [RCV000151620] Chr10:53822287 [GRCh38]
Chr10:55582047 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.2884C>T (p.Arg962Cys) single nucleotide variant PCDH15-related disorder [RCV004734707]|Usher syndrome type 1 [RCV000343106]|Usher syndrome type 1F [RCV000988360]|not provided [RCV000890106]|not specified [RCV000151628] Chr10:53961877 [GRCh38]
Chr10:55721637 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.2194G>A (p.Ala732Thr) single nucleotide variant Usher syndrome type 1F [RCV001273398]|not provided [RCV001044754]|not specified [RCV000151631] Chr10:54066783 [GRCh38]
Chr10:55826543 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2102C>T (p.Ala701Val) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV000477800]|Usher syndrome type 1F [RCV001273399]|not provided [RCV001245383]|not specified [RCV000151632] Chr10:54066875 [GRCh38]
Chr10:55826635 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2051A>G (p.Tyr684Cys) single nucleotide variant Inborn genetic diseases [RCV003343656]|Usher syndrome type 1F [RCV001273401]|not provided [RCV001245462]|not specified [RCV000151633] Chr10:54079371 [GRCh38]
Chr10:55839131 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1590+17_1590+21del deletion not provided [RCV001519967]|not specified [RCV000151634] Chr10:54183423..54183427 [GRCh38]
Chr10:55943183..55943187 [GRCh37]
Chr10:10q21.1		 likely pathogenic|benign|not provided
NM_001384140.1(PCDH15):c.1256A>G (p.Asn419Ser) single nucleotide variant Usher syndrome type 1 [RCV001103156]|not provided [RCV001071653]|not specified [RCV000151635] Chr10:54195732 [GRCh38]
Chr10:55955492 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.1195A>G (p.Ser399Gly) single nucleotide variant not provided [RCV001461010]|not specified [RCV000151636] Chr10:54195793 [GRCh38]
Chr10:55955553 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.913C>G (p.Gln305Glu) single nucleotide variant Inborn genetic diseases [RCV002516048]|not provided [RCV001047051]|not specified [RCV000151638] Chr10:54236895 [GRCh38]
Chr10:55996655 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.709C>T (p.Arg237Cys) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002483311]|Usher syndrome type 1F [RCV001835691]|not provided [RCV001657859]|not specified [RCV000151641] Chr10:54317438 [GRCh38]
Chr10:56077198 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2435T>C (p.Ile812Thr) single nucleotide variant Usher syndrome type 1 [RCV001104967]|Usher syndrome type 1F [RCV000664808]|not provided [RCV000513885]|not specified [RCV000155383] Chr10:54022983 [GRCh38]
Chr10:55782743 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity
NM_001384140.1(PCDH15):c.4671+1053A>C single nucleotide variant PCDH15-related disorder [RCV004534995]|not provided [RCV000881152]|not specified [RCV000155435] Chr10:53809503 [GRCh38]
Chr10:55569263 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.4671+1223C>T single nucleotide variant not specified [RCV000155673] Chr10:53809333 [GRCh38]
Chr10:55569093 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4672-1607delinsAGT indel not specified [RCV000155736] Chr10:53808737 [GRCh38]
Chr10:55568497 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5805G>T (p.Gly1935=) single nucleotide variant PCDH15-related disorder [RCV004544400]|not provided [RCV000153648] Chr10:53821921 [GRCh38]
Chr10:55581681 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_033056.4(PCDH15):c.4608A>G (p.Val1536=) single nucleotide variant not provided [RCV000153651] Chr10:53823118 [GRCh38]
Chr10:55582878 [GRCh37]
Chr10:10q21.1		 conflicting interpretations of pathogenicity|uncertain significance
NM_033056.4(PCDH15):c.4459T>C (p.Ser1487Pro) single nucleotide variant not provided [RCV000153652] Chr10:53823267 [GRCh38]
Chr10:55583027 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4308GCC[6] (p.Pro1443dup) microsatellite Usher syndrome type 1F [RCV001278195]|not provided [RCV000153653] Chr10:53827437..53827438 [GRCh38]
Chr10:55587197..55587198 [GRCh37]
Chr10:10q21.1		 conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.3679G>A (p.Asp1227Asn) single nucleotide variant not provided [RCV000153654] Chr10:53866680 [GRCh38]
Chr10:55626440 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4671+1087C>T single nucleotide variant not provided [RCV000959106]|not specified [RCV000155264] Chr10:53809469 [GRCh38]
Chr10:55569229 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.-5A>G single nucleotide variant Usher syndrome type 1 [RCV001103250]|Usher syndrome type 1F [RCV001826837]|not provided [RCV000828326]|not specified [RCV000155271] Chr10:54664267 [GRCh38]
Chr10:56424027 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.2619A>G (p.Glu873=) single nucleotide variant Usher syndrome type 1F [RCV001274796]|not provided [RCV000176122] Chr10:54020324 [GRCh38]
Chr10:55780084 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
Single allele deletion Small for gestational age [RCV000161593] Chr10:53975703..54020155 [GRCh38]
Chr10:55735463..55779915 [GRCh37]
Chr10:10q21.1		 not provided
NM_001384140.1(PCDH15):c.3717+1G>A single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003474915]|Usher syndrome type 1F [RCV000169489]|not provided [RCV001850401] Chr10:53866641 [GRCh38]
Chr10:55626401 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.3596C>T (p.Thr1199Ile) single nucleotide variant not provided [RCV000176768] Chr10:53866763 [GRCh38]
Chr10:55626523 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3717+10T>C single nucleotide variant not provided [RCV000176770] Chr10:53866632 [GRCh38]
Chr10:55626392 [GRCh37]
Chr10:10q21.1		 conflicting interpretations of pathogenicity|uncertain significance
NM_033056.3(PCDH15):c.4368-10_4368-9insCTTT insertion not specified [RCV000177750] Chr10:53823367..53823368 [GRCh38]
Chr10:55583127..55583128 [GRCh37]
Chr10:10q21.1		 benign
NM_033056.4(PCDH15):c.5630_5633del (p.Arg1877fs) microsatellite not provided [RCV000177752] Chr10:53822093..53822096 [GRCh38]
Chr10:55581853..55581856 [GRCh37]
Chr10:10q21.1		 conflicting interpretations of pathogenicity|uncertain significance
NM_033056.4(PCDH15):c.5010_5015del (p.1669FS[1]) deletion not provided [RCV000177753] Chr10:53822711..53822716 [GRCh38]
Chr10:55582471..55582476 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2138A>G (p.Asn713Ser) single nucleotide variant Usher syndrome type 1 [RCV000294986]|Usher syndrome type 1F [RCV002519268]|not provided [RCV000267122] Chr10:54066839 [GRCh38]
Chr10:55826599 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.3(PCDH15):c.4368-13_4368-10dup duplication PCDH15-related disorder [RCV004530280]|Usher syndrome type 1F [RCV001274787]|not provided [RCV000965722]|not specified [RCV000221835] Chr10:53823367..53823368 [GRCh38]
Chr10:55583128..55583131 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.3358C>T (p.Arg1120Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003474996]|PCDH15-related disorder [RCV004734863]|Rare genetic deafness [RCV000223562]|Usher syndrome type 1F [RCV001833187]|not provided [RCV000797689] Chr10:53938830 [GRCh38]
Chr10:55698590 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001142763.1:c.-189197_c.610-5166del deletion Usher syndrome type 1D [RCV000210332] Chr10:10q21.1 likely pathogenic
NM_001384140.1(PCDH15):c.2971C>T (p.Arg991Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003474992]|Usher syndrome type 1D [RCV000210315]|Usher syndrome type 1F [RCV000781698]|not provided [RCV001386497] Chr10:53961790 [GRCh38]
Chr10:55721550 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.4599_4602dup (p.Gln1535fs) duplication not provided [RCV002519647]|not specified [RCV000217078] Chr10:53823123..53823124 [GRCh38]
Chr10:55582883..55582884 [GRCh37]
Chr10:10q21.1		 pathogenic|uncertain significance
NM_001384140.1(PCDH15):c.5156A>C (p.Gln1719Pro) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001788082]|Usher syndrome type 1F [RCV000988359]|not provided [RCV000712512]|not specified [RCV000222137] Chr10:53806646 [GRCh38]
Chr10:55566406 [GRCh37]
Chr10:10q21.1		 benign
NM_033056.4(PCDH15):c.4463A>G (p.Asn1488Ser) single nucleotide variant Inborn genetic diseases [RCV002517492]|not provided [RCV001062555]|not specified [RCV000222252] Chr10:53823263 [GRCh38]
Chr10:55583023 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.5033C>T (p.Ser1678Leu) single nucleotide variant Inborn genetic diseases [RCV004658991]|Usher syndrome type 1F [RCV001272399]|not provided [RCV002518185]|not specified [RCV000220123] Chr10:53822693 [GRCh38]
Chr10:55582453 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4812G>T (p.Arg1604Ser) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001822855]|Autosomal recessive nonsyndromic hearing loss 23 [RCV002500691]|Usher syndrome type 1 [RCV000287812]|Usher syndrome type 1F [RCV001272402]|not provided [RCV000839178]|not specified [RCV000215424] Chr10:53822914 [GRCh38]
Chr10:55582674 [GRCh37]
Chr10:10q21.1		 benign|likely benign|uncertain significance
NM_001384140.1(PCDH15):c.5124G>A (p.Lys1708=) single nucleotide variant not provided [RCV000992508]|not specified [RCV000217927] Chr10:53806678 [GRCh38]
Chr10:55566438 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4758G>A (p.Gln1586=) single nucleotide variant not specified [RCV000213894] Chr10:53807044 [GRCh38]
Chr10:55566804 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4671+1109C>T single nucleotide variant PCDH15-related disorder [RCV004530279]|not provided [RCV001722151]|not specified [RCV000220366] Chr10:53809447 [GRCh38]
Chr10:55569207 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity
NM_001384140.1(PCDH15):c.4672-1640A>G single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002485378]|PCDH15-related disorder [RCV004734860]|not provided [RCV000712513]|not specified [RCV000214030] Chr10:53808770 [GRCh38]
Chr10:55568530 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.*14A>G single nucleotide variant not specified [RCV000215680] Chr10:53806565 [GRCh38]
Chr10:55566325 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4801G>A (p.Gly1601Ser) single nucleotide variant PCDH15-related disorder [RCV004541325]|not specified [RCV000218188] Chr10:53807001 [GRCh38]
Chr10:55566761 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity
NM_033056.4(PCDH15):c.5849_5852dup (p.Thr1953fs) duplication Usher syndrome type 1F [RCV000670185]|not provided [RCV002532096] Chr10:53821873..53821874 [GRCh38]
Chr10:55581633..55581634 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2396G>A (p.Arg799His) single nucleotide variant Usher syndrome type 1F [RCV001833214]|not provided [RCV002519646]|not specified [RCV000214105] Chr10:54023022 [GRCh38]
Chr10:55782782 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4640G>A (p.Gly1547Asp) single nucleotide variant not provided [RCV000970000]|not specified [RCV000218241] Chr10:53810587 [GRCh38]
Chr10:55570347 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.158-1G>A single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003474993]|Usher syndrome type 1 [RCV000222386] Chr10:54378943 [GRCh38]
Chr10:56138703 [GRCh37]
Chr10:10q21.1		 pathogenic|no classifications from unflagged records|not provided
NM_001384140.1(PCDH15):c.1606G>C (p.Ala536Pro) single nucleotide variant Inborn genetic diseases [RCV003165545]|Usher syndrome type 1F [RCV001833213]|not provided [RCV000756463]|not specified [RCV000222497] Chr10:54153278 [GRCh38]
Chr10:55913038 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4831_4834dup (p.Thr1612fs) duplication Usher syndrome type 1F [RCV001272401]|not provided [RCV000887967]|not specified [RCV000218422] Chr10:53822891..53822892 [GRCh38]
Chr10:55582651..55582652 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity
NM_001384140.1(PCDH15):c.2691G>C (p.Glu897Asp) single nucleotide variant not specified [RCV000220898] Chr10:54020252 [GRCh38]
Chr10:55780012 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.5082_5089del (p.Ser1694fs) deletion Usher syndrome type 1F [RCV000670609] Chr10:53806713..53806720 [GRCh38]
Chr10:55566473..55566480 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1985A>G (p.Asn662Ser) single nucleotide variant Usher syndrome type 1F [RCV001828083]|not provided [RCV001853476]|not specified [RCV000216223] Chr10:54089996 [GRCh38]
Chr10:55849756 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.5105_5108dup (p.Asp1703_Ser1704insTer) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV002478771]|not provided [RCV004696878]|not specified [RCV000218627] Chr10:53806693..53806694 [GRCh38]
Chr10:55566453..55566454 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.3(PCDH15):c.(?_3374)_(3501_?)del deletion Rare genetic deafness [RCV000218655] Chr10:53903243..53903370 [GRCh38]
Chr10:55663003..55663130 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.1917+13GT[10] microsatellite Autosomal recessive nonsyndromic hearing loss 23 [RCV001788084]|Usher syndrome type 1F [RCV001788083]|not provided [RCV001682928]|not specified [RCV000214489] Chr10:54132841..54132842 [GRCh38]
Chr10:55892601..55892602 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4728_4730dup (p.Thr1577dup) duplication not provided [RCV000992506]|not specified [RCV000221199] Chr10:53807071..53807072 [GRCh38]
Chr10:55566831..55566832 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4891C>T (p.Leu1631=) single nucleotide variant PCDH15-related disorder [RCV004530311]|not provided [RCV000734847]|not specified [RCV000221230] Chr10:53806911 [GRCh38]
Chr10:55566671 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.128T>C (p.Ile43Thr) single nucleotide variant Usher syndrome type 1F [RCV001828082]|not provided [RCV002518184]|not specified [RCV000222910] Chr10:54527841 [GRCh38]
Chr10:56287601 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4672-2A>G single nucleotide variant Usher syndrome type 1F [RCV000670272] Chr10:53807132 [GRCh38]
Chr10:55566892 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5818_5820dup (p.Ile1940dup) duplication Usher syndrome type 1F [RCV000670274]|not provided [RCV001226372]|not specified [RCV001195251] Chr10:53821905..53821906 [GRCh38]
Chr10:55581665..55581666 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4837G>A (p.Gly1613Arg) single nucleotide variant Inborn genetic diseases [RCV004020599]|not specified [RCV000214659] Chr10:53822889 [GRCh38]
Chr10:55582649 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.5435C>T (p.Pro1812Leu) single nucleotide variant PCDH15-related disorder [RCV004530281]|Usher syndrome type 1 [RCV001105922]|not provided [RCV000724949]|not specified [RCV000216469] Chr10:53822291 [GRCh38]
Chr10:55582051 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.1537T>C (p.Ser513Pro) single nucleotide variant not specified [RCV000216573] Chr10:54183497 [GRCh38]
Chr10:55943257 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.3(PCDH15):c.1917+33_1917+34dup microsatellite not provided [RCV001712322]|not specified [RCV000218888] Chr10:54132840..54132841 [GRCh38]
Chr10:55892601..55892602 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.2092-6T>C single nucleotide variant not provided [RCV003669112]|not specified [RCV000214934] Chr10:54066891 [GRCh38]
Chr10:55826651 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5424A>C (p.Pro1808=) single nucleotide variant not provided [RCV001490335]|not specified [RCV000219009] Chr10:53822302 [GRCh38]
Chr10:55582062 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4672-1657del deletion not specified [RCV000223266] Chr10:53808787 [GRCh38]
Chr10:55568547 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4639_4656dup (p.Asp1547_Phe1552dup) duplication Usher syndrome type 1F [RCV000669497] Chr10:53823069..53823070 [GRCh38]
Chr10:55582829..55582830 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.647T>G (p.Leu216Ter) single nucleotide variant Usher syndrome type 1F [RCV000669594] Chr10:54329654 [GRCh38]
Chr10:56089414 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.5743_5766del (p.Leu1915_Glu1922del) deletion Usher syndrome type 1F [RCV000669689] Chr10:53821960..53821983 [GRCh38]
Chr10:55581720..55581743 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4860G>A (p.Thr1620=) single nucleotide variant not provided [RCV000992507]|not specified [RCV000214975] Chr10:53806942 [GRCh38]
Chr10:55566702 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity
NM_001384140.1(PCDH15):c.3444C>T (p.Phe1148=) single nucleotide variant not provided [RCV001396781]|not specified [RCV000219258] Chr10:53903300 [GRCh38]
Chr10:55663060 [GRCh37]
Chr10:10q21.1		 likely benign
GRCh38/hg38 10q21.1(chr10:55172554-55427295)x1 copy number loss See cases [RCV000140021] Chr10:55172554..55427295 [GRCh38]
Chr10:56932314..57187055 [GRCh37]
Chr10:56602320..56857061 [NCBI36]
Chr10:10q21.1		 benign
GRCh38/hg38 10q21.1-21.3(chr10:55287177-67558442)x3 copy number gain See cases [RCV000141179] Chr10:55287177..67558442 [GRCh38]
Chr10:57046937..69318200 [GRCh37]
Chr10:56716943..68988206 [NCBI36]
Chr10:10q21.1-21.3		 pathogenic
GRCh38/hg38 10q21.1(chr10:54935320-55905923)x1 copy number loss See cases [RCV000141799] Chr10:54935320..55905923 [GRCh38]
Chr10:56695080..57665683 [GRCh37]
Chr10:56365086..57335689 [NCBI36]
Chr10:10q21.1		 uncertain significance
GRCh38/hg38 10q21.1(chr10:55427295-55645239)x1 copy number loss See cases [RCV000143346] Chr10:55427295..55645239 [GRCh38]
Chr10:57187055..57404999 [GRCh37]
Chr10:56857061..57075005 [NCBI36]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5364_5373del (p.Pro1789fs) deletion Retinal dystrophy [RCV000225400]|Usher syndrome type 1F [RCV000671752]|not provided [RCV002223824] Chr10:53822353..53822362 [GRCh38]
Chr10:55582113..55582122 [GRCh37]
Chr10:10q21.1		 likely pathogenic|conflicting interpretations of pathogenicity|uncertain significance
NM_033056.4(PCDH15):c.5565C>A (p.Ala1855=) single nucleotide variant Retinal dystrophy [RCV000225513]|Usher syndrome type 1F [RCV000665949]|not provided [RCV001039646] Chr10:53822161 [GRCh38]
Chr10:55581921 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.1789T>C (p.Ser597Pro) single nucleotide variant not provided [RCV001368101] Chr10:54133003 [GRCh38]
Chr10:55892763 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4688_4691dup (p.Lys1565fs) duplication Usher syndrome type 1F [RCV000670365] Chr10:53807110..53807111 [GRCh38]
Chr10:55566870..55566871 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3862T>C (p.Ser1288Pro) single nucleotide variant Usher syndrome type 1F [RCV000669757] Chr10:53840441 [GRCh38]
Chr10:55600201 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4936A>G (p.Met1646Val) single nucleotide variant Usher syndrome type 1F [RCV000669758] Chr10:53822790 [GRCh38]
Chr10:55582550 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5136_5139dup (p.Arg1714delinsLeuTer) microsatellite Usher syndrome type 1F [RCV000668793]|not provided [RCV002532080] Chr10:53822586..53822587 [GRCh38]
Chr10:55582346..55582347 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.5336del (p.Pro1779fs) deletion Usher syndrome type 1F [RCV000668934] Chr10:53822390 [GRCh38]
Chr10:55582150 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5619_5623dup (p.Pro1875fs) duplication Usher syndrome type 1F [RCV000669205] Chr10:53822102..53822103 [GRCh38]
Chr10:55581862..55581863 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4726C>T (p.Gln1576Ter) single nucleotide variant Usher syndrome type 1F [RCV000669259] Chr10:53823000 [GRCh38]
Chr10:55582760 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4671+1577GAA[3] microsatellite Usher syndrome type 1F [RCV000669386] Chr10:53808968..53808970 [GRCh38]
Chr10:55568728..55568730 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5252_5259del (p.Pro1751fs) deletion Usher syndrome type 1F [RCV000669572] Chr10:53822467..53822474 [GRCh38]
Chr10:55582227..55582234 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4383C>A (p.Tyr1461Ter) single nucleotide variant Usher syndrome type 1F [RCV000669959] Chr10:53823343 [GRCh38]
Chr10:55583103 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2751+37C>T single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001788182]|Usher syndrome type 1F [RCV001788181]|not provided [RCV000829540]|not specified [RCV000246098] Chr10:54020155 [GRCh38]
Chr10:55779915 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.2751+43C>G single nucleotide variant not provided [RCV000835831]|not specified [RCV000251219] Chr10:54020149 [GRCh38]
Chr10:55779909 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.195T>C (p.Thr65=) single nucleotide variant not provided [RCV000911023]|not specified [RCV000254238] Chr10:54378905 [GRCh38]
Chr10:56138665 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3010-48G>A single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001788183]|Usher syndrome type 1F [RCV001533753]|not provided [RCV000829541]|not specified [RCV000247389] Chr10:53959892 [GRCh38]
Chr10:55719652 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.400C>T (p.Arg134Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003474975]|Usher syndrome type 1 [RCV003333743]|Usher syndrome type 1F [RCV000240654]|not provided [RCV001381511] Chr10:54369194 [GRCh38]
Chr10:56128954 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|conflicting interpretations of pathogenicity
NM_001384140.1(PCDH15):c.319-31T>C single nucleotide variant Usher syndrome type 1F [RCV001533582]|not provided [RCV000829536]|not specified [RCV000250515] Chr10:54369306 [GRCh38]
Chr10:56129066 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1590+20A>G single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001788180]|Usher syndrome type 1F [RCV001533759]|not provided [RCV000590545]|not specified [RCV000252948] Chr10:54183424 [GRCh38]
Chr10:55943184 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.877-29G>T single nucleotide variant not provided [RCV001530603]|not specified [RCV000248115] Chr10:54236960 [GRCh38]
Chr10:55996720 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_033056.4(PCDH15):c.5177C>T (p.Thr1726Ile) single nucleotide variant Usher syndrome type 1 [RCV000268152]|not provided [RCV001850588] Chr10:53822549 [GRCh38]
Chr10:55582309 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4368-1564A>T single nucleotide variant Usher syndrome type 1 [RCV000339484] Chr10:53821794 [GRCh38]
Chr10:55581554 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.575A>G (p.Gln192Arg) single nucleotide variant Inborn genetic diseases [RCV003258747]|Usher syndrome type 1 [RCV000284389]|Usher syndrome type 1F [RCV001828300]|not provided [RCV001038040]|not specified [RCV000826010] Chr10:54346384 [GRCh38]
Chr10:56106144 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3782A>C (p.Glu1261Ala) single nucleotide variant Usher syndrome type 1 [RCV000399778]|not provided [RCV002520603] Chr10:53857199 [GRCh38]
Chr10:55616959 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4368-1214G>C single nucleotide variant Usher syndrome type 1 [RCV000302319] Chr10:53821444 [GRCh38]
Chr10:55581204 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.1900G>A (p.Val634Ile) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV000763657]|Autosomal recessive nonsyndromic hearing loss 23 [RCV001578793]|PCDH15-related disorder [RCV004734960]|Usher syndrome type 1 [RCV000302330]|Usher syndrome type 1F [RCV001275398]|not provided [RCV000594545]|not specified [RCV000825082] Chr10:54132892 [GRCh38]
Chr10:55892652 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.851C>T (p.Ala284Val) single nucleotide variant Usher syndrome type 1 [RCV000270643] Chr10:54317296 [GRCh38]
Chr10:56077056 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.-180C>T single nucleotide variant Usher syndrome type 1 [RCV000351853] Chr10:54801076 [GRCh38]
Chr10:56560836 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5864T>C (p.Leu1955Pro) single nucleotide variant Inborn genetic diseases [RCV003243061]|Usher syndrome type 1 [RCV000408121]|not provided [RCV002520600] Chr10:53821862 [GRCh38]
Chr10:55581622 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2768C>T (p.Pro923Leu) single nucleotide variant PCDH15-related disorder [RCV004734959]|Usher syndrome type 1 [RCV000306542]|not provided [RCV002059554] Chr10:53995749 [GRCh38]
Chr10:55755509 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.5480G>T (p.Cys1827Phe) single nucleotide variant Usher syndrome type 1 [RCV000328020]|not provided [RCV003231441] Chr10:53822246 [GRCh38]
Chr10:55582006 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1934G>T (p.Gly645Val) single nucleotide variant Usher syndrome type 1 [RCV000400993] Chr10:54090047 [GRCh38]
Chr10:55849807 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.466G>A (p.Val156Met) single nucleotide variant Usher syndrome type 1 [RCV000301069]|Usher syndrome type 1F [RCV001833434]|not provided [RCV002522161]|not specified [RCV001195250] Chr10:54369128 [GRCh38]
Chr10:56128888 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3450C>A (p.Ile1150=) single nucleotide variant Usher syndrome type 1 [RCV000366826]|Usher syndrome type 1F [RCV001273390]|not provided [RCV000963254] Chr10:53903294 [GRCh38]
Chr10:55663054 [GRCh37]
Chr10:10q21.1		 benign|likely benign|uncertain significance
NM_001384140.1(PCDH15):c.-126G>A single nucleotide variant Usher syndrome type 1 [RCV000376297] Chr10:54801022 [GRCh38]
Chr10:56560782 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4749G>A (p.Arg1583=) single nucleotide variant Usher syndrome type 1 [RCV000309831]|Usher syndrome type 1F [RCV001272404]|not provided [RCV001458803]|not specified [RCV000825808] Chr10:53822977 [GRCh38]
Chr10:55582737 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4368-1142G>A single nucleotide variant Usher syndrome type 1 [RCV000310722] Chr10:53821372 [GRCh38]
Chr10:55581132 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5566G>A (p.Glu1856Lys) single nucleotide variant Usher syndrome type 1 [RCV000276333] Chr10:53822160 [GRCh38]
Chr10:55581920 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.594G>A (p.Pro198=) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002502193]|Retinitis pigmentosa [RCV000787858]|Usher syndrome type 1 [RCV000372702]|Usher syndrome type 1F [RCV001828299]|not provided [RCV001367556]|not specified [RCV002509358] Chr10:54346365 [GRCh38]
Chr10:56106125 [GRCh37]
Chr10:10q21.1		 likely pathogenic|uncertain significance
NM_001384140.1(PCDH15):c.-288T>C single nucleotide variant Usher syndrome type 1 [RCV000401198] Chr10:54801184 [GRCh38]
Chr10:56560944 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3195A>G (p.Gln1065=) single nucleotide variant Usher syndrome type 1 [RCV000371325]|not provided [RCV000841000]|not specified [RCV000604640] Chr10:53940903 [GRCh38]
Chr10:55700663 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.5726G>T (p.Arg1909Leu) single nucleotide variant Usher syndrome type 1 [RCV000335914]|not provided [RCV002520601] Chr10:53822000 [GRCh38]
Chr10:55581760 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1098+14A>G single nucleotide variant Usher syndrome type 1 [RCV000359354] Chr10:54213922 [GRCh38]
Chr10:55973682 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1649T>G (p.Val550Gly) single nucleotide variant Inborn genetic diseases [RCV004021477]|Usher syndrome type 1 [RCV000359382]|Usher syndrome type 1F [RCV001828298]|not provided [RCV001044696] Chr10:54153235 [GRCh38]
Chr10:55912995 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4368-1116G>C single nucleotide variant Usher syndrome type 1 [RCV000345702] Chr10:53821346 [GRCh38]
Chr10:55581106 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.466G>C (p.Val156Leu) single nucleotide variant Inborn genetic diseases [RCV004021478]|Usher syndrome type 1 [RCV000314912]|Usher syndrome type 1F [RCV001833433]|not provided [RCV002520607]|not specified [RCV000825428] Chr10:54369128 [GRCh38]
Chr10:56128888 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2807C>T (p.Ala936Val) single nucleotide variant Usher syndrome type 1 [RCV000398960]|Usher syndrome type 1F [RCV001833431]|not provided [RCV001048169] Chr10:53995710 [GRCh38]
Chr10:55755470 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4368-1262G>A single nucleotide variant Usher syndrome type 1 [RCV000263492] Chr10:53821492 [GRCh38]
Chr10:55581252 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2823G>T (p.Lys941Asn) single nucleotide variant Usher syndrome type 1 [RCV000279802]|Usher syndrome type 1F [RCV001828297]|not provided [RCV001051889]|not specified [RCV000826011] Chr10:53995694 [GRCh38]
Chr10:55755454 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1172A>G (p.Gln391Arg) single nucleotide variant Usher syndrome type 1 [RCV000280313]|Usher syndrome type 1F [RCV001833432]|not provided [RCV001289115] Chr10:54195816 [GRCh38]
Chr10:55955576 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3502-10del deletion Hearing loss, autosomal recessive [RCV004577753]|Retinitis pigmentosa-deafness syndrome [RCV000297781]|not provided [RCV001410527] Chr10:53866867 [GRCh38]
Chr10:55626627 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4272A>G (p.Pro1424=) single nucleotide variant Usher syndrome type 1 [RCV000317288]|not provided [RCV000992505] Chr10:53827488 [GRCh38]
Chr10:55587248 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.2539G>A (p.Asp847Asn) single nucleotide variant Usher syndrome type 1 [RCV000374290]|Usher syndrome type 1F [RCV002520604]|not provided [RCV002520605] Chr10:54020404 [GRCh38]
Chr10:55780164 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2581G>A (p.Val861Met) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV000763656]|Autosomal recessive nonsyndromic hearing loss 23 [RCV001578639]|Hearing impairment [RCV001375215]|Usher syndrome type 1 [RCV000322580]|Usher syndrome type 1F [RCV001578640]|not provided [RCV001246481]|not specified [RCV000614926] Chr10:54020362 [GRCh38]
Chr10:55780122 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.665A>G (p.Tyr222Cys) single nucleotide variant Usher syndrome type 1 [RCV000281779]|not provided [RCV002520606] Chr10:54329636 [GRCh38]
Chr10:56089396 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4368-1207C>T single nucleotide variant Usher syndrome type 1 [RCV000390658] Chr10:53821437 [GRCh38]
Chr10:55581197 [GRCh37]
Chr10:10q21.1		 benign|uncertain significance
NM_001384140.1(PCDH15):c.1590+15A>G single nucleotide variant Usher syndrome type 1 [RCV000321593]|not provided [RCV001519968] Chr10:54183429 [GRCh38]
Chr10:55943189 [GRCh37]
Chr10:10q21.1		 benign|likely benign|uncertain significance
NM_033056.4(PCDH15):c.5450C>T (p.Pro1817Leu) single nucleotide variant Inborn genetic diseases [RCV002520602]|Usher syndrome type 1 [RCV000377988]|Usher syndrome type 1F [RCV001833430]|not provided [RCV001244892] Chr10:53822276 [GRCh38]
Chr10:55582036 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5318C>G (p.Pro1773Arg) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002480093]|Usher syndrome type 1 [RCV000391115]|Usher syndrome type 1F [RCV001526739]|not provided [RCV001242453] Chr10:53822408 [GRCh38]
Chr10:55582168 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3501+7G>T single nucleotide variant PCDH15-related disorder [RCV004734958]|Usher syndrome type 1 [RCV000407974]|not provided [RCV000944576] Chr10:53903236 [GRCh38]
Chr10:55662996 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.4892C>A (p.Ala1631Glu) single nucleotide variant Usher syndrome type 1 [RCV000386024]|Usher syndrome type 1F [RCV001835776]|not provided [RCV001049538]|not specified [RCV001000845] Chr10:53822834 [GRCh38]
Chr10:55582594 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4719G>A (p.Leu1573=) single nucleotide variant PCDH15-related disorder [RCV004543047]|Usher syndrome type 1F [RCV001833335]|not provided [RCV000303306] Chr10:53823007 [GRCh38]
Chr10:55582767 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_033056.4(PCDH15):c.4993C>A (p.Pro1665Thr) single nucleotide variant Usher syndrome type 1 [RCV000281198] Chr10:53822733 [GRCh38]
Chr10:55582493 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3009+7G>A single nucleotide variant Usher syndrome type 1F [RCV001273391]|not provided [RCV000270684] Chr10:53961745 [GRCh38]
Chr10:55721505 [GRCh37]
Chr10:10q21.1		 conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.2709A>G (p.Gly903=) single nucleotide variant Usher syndrome type 1 [RCV000271218]|not provided [RCV001502851] Chr10:54020234 [GRCh38]
Chr10:55779994 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.2220+9A>G single nucleotide variant Usher syndrome type 1 [RCV000282135]|not provided [RCV001439631] Chr10:54066748 [GRCh38]
Chr10:55826508 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.1998C>T (p.Thr666=) single nucleotide variant Usher syndrome type 1F [RCV001828238]|not provided [RCV000272286] Chr10:54079424 [GRCh38]
Chr10:55839184 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4294G>C (p.Val1432Leu) single nucleotide variant not provided [RCV000281052] Chr10:53827466 [GRCh38]
Chr10:55587226 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4320G>A (p.Pro1440=) single nucleotide variant Usher syndrome type 1F [RCV001833385]|not provided [RCV000346512] Chr10:53827440 [GRCh38]
Chr10:55587200 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.521A>G (p.Asn174Ser) single nucleotide variant Usher syndrome type 1F [RCV001276790]|not provided [RCV000282912] Chr10:54346438 [GRCh38]
Chr10:56106198 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4202+5G>A single nucleotide variant Retinal dystrophy [RCV001073719]|Usher syndrome type 1 [RCV000263105] Chr10:53831310 [GRCh38]
Chr10:55591070 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4320_4328dup (p.Pro1441_Pro1443dup) duplication See cases [RCV002252079]|not provided [RCV000285613] Chr10:53827431..53827432 [GRCh38]
Chr10:55587191..55587192 [GRCh37]
Chr10:10q21.1		 conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.4672-1564T>C single nucleotide variant Usher syndrome type 1D [RCV001810442]|not provided [RCV000285722] Chr10:53808694 [GRCh38]
Chr10:55568454 [GRCh37]
Chr10:10q21.1		 conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.1548G>A (p.Val516=) single nucleotide variant not provided [RCV000388809] Chr10:54183486 [GRCh38]
Chr10:55943246 [GRCh37]
Chr10:10q21.1		 conflicting interpretations of pathogenicity|uncertain significance
NM_033056.4(PCDH15):c.5653C>T (p.His1885Tyr) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002494938]|Usher syndrome type 1 [RCV000311631] Chr10:53822073 [GRCh38]
Chr10:55581833 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4672-1638C>T single nucleotide variant Inborn genetic diseases [RCV002518981]|not provided [RCV000355783] Chr10:53808768 [GRCh38]
Chr10:55568528 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1205G>C (p.Gly402Ala) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV000763658]|Usher syndrome type 1 [RCV001103157]|Usher syndrome type 1F [RCV001526428]|not provided [RCV000724967]|not specified [RCV000323966] Chr10:54195783 [GRCh38]
Chr10:55955543 [GRCh37]
Chr10:10q21.1		 conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.4671+1633T>A single nucleotide variant not provided [RCV000358392] Chr10:53808923 [GRCh38]
Chr10:55568683 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4368-1481_4368-1478dup duplication Hearing loss, autosomal recessive [RCV004577751]|Retinitis pigmentosa-deafness syndrome [RCV000277198] Chr10:53821707..53821708 [GRCh38]
Chr10:55581467..55581468 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4651GAA[1] (p.Glu1552del) microsatellite not provided [RCV000890061]|not specified [RCV000328385] Chr10:53810571..53810573 [GRCh38]
Chr10:55570331..55570333 [GRCh37]
Chr10:10q21.1		 benign|conflicting interpretations of pathogenicity
NM_001384140.1(PCDH15):c.4368-1239G>A single nucleotide variant Usher syndrome type 1 [RCV000298865] Chr10:53821469 [GRCh38]
Chr10:55581229 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2908G>A (p.Val970Ile) single nucleotide variant Inborn genetic diseases [RCV002521959]|Usher syndrome type 1F [RCV001828237]|not provided [RCV000269198] Chr10:53961853 [GRCh38]
Chr10:55721613 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.131T>C (p.Val44Ala) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001004802]|Usher syndrome type 1F [RCV001275408]|not provided [RCV000522599] Chr10:54527838 [GRCh38]
Chr10:56287598 [GRCh37]
Chr10:10q21.1		 pathogenic|uncertain significance
NM_001384140.1(PCDH15):c.4063C>T (p.Arg1355Trp) single nucleotide variant not provided [RCV001760528] Chr10:53831454 [GRCh38]
Chr10:55591214 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1897G>A (p.Ala633Thr) single nucleotide variant Usher syndrome type 1F [RCV001278998] Chr10:54132895 [GRCh38]
Chr10:55892655 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1306A>G (p.Thr436Ala) single nucleotide variant Inborn genetic diseases [RCV004035480]|Usher syndrome type 1F [RCV001279004]|not provided [RCV001570593] Chr10:54185268 [GRCh38]
Chr10:55945028 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1213C>T (p.Leu405=) single nucleotide variant Usher syndrome type 1F [RCV001279006]|not provided [RCV001472519] Chr10:54195775 [GRCh38]
Chr10:55955535 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.876+7A>G single nucleotide variant Usher syndrome type 1F [RCV001279009]|not provided [RCV002537825] Chr10:54317264 [GRCh38]
Chr10:56077024 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.92-816C>T single nucleotide variant not provided [RCV001547681] Chr10:54528693 [GRCh38]
Chr10:56288453 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4596C>T (p.Asn1532=) single nucleotide variant Usher syndrome type 1F [RCV001278193]|not provided [RCV003679055] Chr10:53823130 [GRCh38]
Chr10:55582890 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4328C>T (p.Pro1443Leu) single nucleotide variant Usher syndrome type 1F [RCV001278194]|not provided [RCV001880249] Chr10:53827432 [GRCh38]
Chr10:55587192 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3502-13dup duplication Usher syndrome type 1F [RCV001278204]|not provided [RCV001451258] Chr10:53866866..53866867 [GRCh38]
Chr10:55626626..55626627 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.3410A>G (p.Glu1137Gly) single nucleotide variant Usher syndrome type 1F [RCV001278205]|not specified [RCV004587101] Chr10:53903334 [GRCh38]
Chr10:55663094 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3382G>A (p.Ala1128Thr) single nucleotide variant Usher syndrome type 1F [RCV001278207]|not provided [RCV001880250] Chr10:53903362 [GRCh38]
Chr10:55663122 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2291G>T (p.Arg764Leu) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002504396]|Inborn genetic diseases [RCV004035467]|Usher syndrome type 1F [RCV001278214]|not provided [RCV001880251] Chr10:54023127 [GRCh38]
Chr10:55782887 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2120T>G (p.Val707Gly) single nucleotide variant not provided [RCV000594906] Chr10:54066857 [GRCh38]
Chr10:55826617 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5847C>G (p.His1949Gln) single nucleotide variant Usher syndrome type 1F [RCV001277663] Chr10:53821879 [GRCh38]
Chr10:55581639 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4728G>A (p.Gln1576=) single nucleotide variant Usher syndrome type 1F [RCV001277672]|not provided [RCV001398080] Chr10:53822998 [GRCh38]
Chr10:55582758 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4316C>T (p.Pro1439Leu) single nucleotide variant Inborn genetic diseases [RCV002526033]|Usher syndrome type 1F [RCV001272407]|not provided [RCV000490047] Chr10:53827444 [GRCh38]
Chr10:55587204 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.5022C>T (p.Ala1674=) single nucleotide variant PCDH15-related disorder [RCV004735638]|not provided [RCV000596008] Chr10:53806780 [GRCh38]
Chr10:55566540 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4311G>A (p.Pro1437=) single nucleotide variant Usher syndrome type 1F [RCV001278197]|not provided [RCV001436436] Chr10:53827449 [GRCh38]
Chr10:55587209 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.3327T>C (p.Ala1109=) single nucleotide variant not specified [RCV000601222] Chr10:53938861 [GRCh38]
Chr10:55698621 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.706-17_706-14del microsatellite Hearing loss, autosomal recessive [RCV004577755]|Retinitis pigmentosa-deafness syndrome [RCV000330997]|not provided [RCV002059555] Chr10:54317455..54317458 [GRCh38]
Chr10:56077215..56077218 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.-155G>C single nucleotide variant Usher syndrome type 1 [RCV000381919] Chr10:54801051 [GRCh38]
Chr10:56560811 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4368-1501dup duplication Hearing loss, autosomal recessive [RCV004577752]|Retinitis pigmentosa-deafness syndrome [RCV000347572] Chr10:53821730..53821731 [GRCh38]
Chr10:55581490..55581491 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5313T>G (p.Ile1771Met) single nucleotide variant Usher syndrome type 1 [RCV000348241]|not provided [RCV003328580] Chr10:53822413 [GRCh38]
Chr10:55582173 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1631T>G (p.Ile544Ser) single nucleotide variant Usher syndrome type 1 [RCV000305930]|not provided [RCV001859785] Chr10:54153253 [GRCh38]
Chr10:55913013 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4368-1360_4368-1359del deletion Hearing loss, autosomal recessive [RCV004577750]|Retinitis pigmentosa-deafness syndrome [RCV000318723] Chr10:53821589..53821590 [GRCh38]
Chr10:55581349..55581350 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4368-1070T>A single nucleotide variant Usher syndrome type 1 [RCV000393038] Chr10:53821300 [GRCh38]
Chr10:55581060 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1220C>T (p.Ser407Phe) single nucleotide variant Hearing loss, autosomal recessive [RCV004577754]|Retinitis pigmentosa-deafness syndrome [RCV000338916] Chr10:54195768 [GRCh38]
Chr10:55955528 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4788T>G (p.Asp1596Glu) single nucleotide variant Inborn genetic diseases [RCV002531678]|not provided [RCV001361291]|not specified [RCV000603812] Chr10:53822938 [GRCh38]
Chr10:55582698 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.4368-1493T>C single nucleotide variant Usher syndrome type 1 [RCV000382218] Chr10:53821723 [GRCh38]
Chr10:55581483 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1306-4086A>T single nucleotide variant not provided [RCV000730083] Chr10:54189354 [GRCh38]
Chr10:55949114 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4671+1392dup duplication not provided [RCV000592495] Chr10:53809163..53809164 [GRCh38]
Chr10:55568923..55568924 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.189A>G (p.Lys63=) single nucleotide variant not provided [RCV000597217] Chr10:54378911 [GRCh38]
Chr10:56138671 [GRCh37]
Chr10:10q21.1		 conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.4671+1449_4671+1457dup duplication not specified [RCV000598786] Chr10:53809098..53809099 [GRCh38]
Chr10:55568858..55568859 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.706-3_717del deletion Usher syndrome type 1F [RCV002232235]|not provided [RCV000593242] Chr10:54317430..54317444 [GRCh38]
Chr10:56077190..56077204 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.2799G>C (p.Gly933=) single nucleotide variant not provided [RCV001392846]|not specified [RCV000588940] Chr10:53995718 [GRCh38]
Chr10:55755478 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4672-4_4672-2dup duplication not provided [RCV000593532] Chr10:53807131..53807132 [GRCh38]
Chr10:55566891..55566892 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4049G>A (p.Arg1350His) single nucleotide variant Usher syndrome type 1F [RCV001278199]|not provided [RCV000591050] Chr10:53831468 [GRCh38]
Chr10:55591228 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2859A>C (p.Ala953=) single nucleotide variant not provided [RCV002065191]|not specified [RCV000602927] Chr10:53995658 [GRCh38]
Chr10:55755418 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1830_1833del (p.Asn610fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003475970]|Usher syndrome type 1F [RCV000409254]|not provided [RCV001861394] Chr10:54132959..54132962 [GRCh38]
Chr10:55892719..55892722 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_033056.4(PCDH15):c.4368-15_4368-2del deletion Usher syndrome type 1F [RCV000409410] Chr10:53823360..53823373 [GRCh38]
Chr10:55583120..55583133 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3023del (p.Ala1008fs) deletion Usher syndrome type 1F [RCV000409420] Chr10:53959831 [GRCh38]
Chr10:55719591 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4671+1468A>G single nucleotide variant not provided [RCV000735055] Chr10:53809088 [GRCh38]
Chr10:55568848 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4227T>A (p.Cys1409Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003475946]|Usher syndrome type 1F [RCV000409923]|not provided [RCV002524620] Chr10:53827533 [GRCh38]
Chr10:55587293 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.3082del (p.His1028fs) deletion Usher syndrome type 1F [RCV000409970]|not provided [RCV002510882] Chr10:53959772 [GRCh38]
Chr10:55719532 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.3211del (p.Ile1071fs) deletion Usher syndrome type 1F [RCV000409990] Chr10:53940887 [GRCh38]
Chr10:55700647 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3885_3889dup (p.Ala1297fs) duplication Usher syndrome type 1F [RCV000410014] Chr10:53840413..53840414 [GRCh38]
Chr10:55600173..55600174 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.901dup (p.Thr301fs) duplication Usher syndrome type 1F [RCV000410045]|not provided [RCV003698784] Chr10:54236906..54236907 [GRCh38]
Chr10:55996666..55996667 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.1006C>T (p.Arg336Ter) single nucleotide variant Usher syndrome type 1F [RCV000410351]|not provided [RCV001386990] Chr10:54214028 [GRCh38]
Chr10:55973788 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.2825del (p.Gly942fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV004567880]|Usher syndrome type 1F [RCV000410518]|not provided [RCV001861381] Chr10:53995692 [GRCh38]
Chr10:55755452 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.1737C>G (p.Tyr579Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003475969]|Childhood onset hearing loss [RCV001328031]|PCDH15-related disorder [RCV004530499]|Retinal dystrophy [RCV001073718]|Usher syndrome type 1F [RCV000410287]|not provided [RCV001050534] Chr10:54153147 [GRCh38]
Chr10:55912907 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.4367+1G>A single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002505994]|Usher syndrome type 1F [RCV000410301] Chr10:53827392 [GRCh38]
Chr10:55587152 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4197_4198insGTAG (p.Arg1400fs) insertion Usher syndrome type 1F [RCV000410395] Chr10:53831319..53831320 [GRCh38]
Chr10:55591079..55591080 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.2624C>A (p.Ser875Ter) single nucleotide variant Usher syndrome type 1F [RCV000410835]|not provided [RCV001865259] Chr10:54020319 [GRCh38]
Chr10:55780079 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.3983+1G>T single nucleotide variant Usher syndrome type 1F [RCV000410951]|not provided [RCV001268370] Chr10:53840319 [GRCh38]
Chr10:55600079 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.1305+1G>A single nucleotide variant Usher syndrome type 1F [RCV000411068]|not provided [RCV003565419] Chr10:54195682 [GRCh38]
Chr10:55955442 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1915C>T (p.Gln639Ter) single nucleotide variant Usher syndrome type 1F [RCV000412275]|not provided [RCV001383685] Chr10:54132877 [GRCh38]
Chr10:55892637 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_033056.4(PCDH15):c.4368-2A>T single nucleotide variant Usher syndrome type 1F [RCV000410459]|not provided [RCV003679000] Chr10:53823360 [GRCh38]
Chr10:55583120 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.1785-2A>C single nucleotide variant Usher syndrome type 1F [RCV000410583] Chr10:54133009 [GRCh38]
Chr10:55892769 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1806T>G (p.Tyr602Ter) single nucleotide variant Usher syndrome type 1F [RCV000410816]|not provided [RCV003669146] Chr10:54132986 [GRCh38]
Chr10:55892746 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.3341del (p.Val1114fs) deletion Usher syndrome type 1F [RCV000410850] Chr10:53938847 [GRCh38]
Chr10:55698607 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1627del (p.Glu543fs) deletion PCDH15-related disorder [RCV004725198]|Usher syndrome type 1F [RCV000410989]|not provided [RCV001039425] Chr10:54153257 [GRCh38]
Chr10:55913017 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.1442T>C (p.Ile481Thr) single nucleotide variant Usher syndrome type 1F [RCV001835950]|not provided [RCV000757597] Chr10:54183592 [GRCh38]
Chr10:55943352 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.594+1G>T single nucleotide variant Usher syndrome type 1F [RCV000411154] Chr10:54346364 [GRCh38]
Chr10:56106124 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4313del (p.Pro1438fs) deletion Usher syndrome type 1F [RCV000411267] Chr10:53827447 [GRCh38]
Chr10:55587207 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001142763.1(PCDH15):c.(?_-1)_(2235+1_2236-1)del deletion Retinal dystrophy [RCV000416294] Chr10:10q21.1 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.416_444del (p.Asp139fs) deletion Usher syndrome type 1F [RCV000411523] Chr10:54369150..54369178 [GRCh38]
Chr10:56128910..56128938 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.157+1G>C single nucleotide variant Usher syndrome type 1F [RCV000411565] Chr10:54527811 [GRCh38]
Chr10:56287571 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3699C>T (p.Ser1233=) single nucleotide variant not provided [RCV000594636] Chr10:53866660 [GRCh38]
Chr10:55626420 [GRCh37]
Chr10:10q21.1		 conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.358_359del (p.Cys120fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003475971]|Usher syndrome type 1F [RCV000411639]|not provided [RCV001861395] Chr10:54369235..54369236 [GRCh38]
Chr10:56128995..56128996 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.333dup (p.His112fs) duplication Usher syndrome type 1F [RCV000411746] Chr10:54369260..54369261 [GRCh38]
Chr10:56129020..56129021 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3653del (p.Phe1218fs) deletion Usher syndrome type 1F [RCV000411967] Chr10:53866706 [GRCh38]
Chr10:55626466 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1770_1771del (p.Pro591fs) deletion Usher syndrome type 1F [RCV000411988] Chr10:54153113..54153114 [GRCh38]
Chr10:55912873..55912874 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4211+2dup duplication Usher syndrome type 1F [RCV000412235]|not provided [RCV002524626] Chr10:53828562..53828563 [GRCh38]
Chr10:55588322..55588323 [GRCh37]
Chr10:10q21.1		 likely pathogenic|uncertain significance
NM_001384140.1(PCDH15):c.2785C>T (p.Arg929Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV000770852]|Usher syndrome type 1F [RCV000412338]|not provided [RCV000811416] Chr10:53995732 [GRCh38]
Chr10:55755492 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.4492-101A>G single nucleotide variant not provided [RCV001571066] Chr10:53811720 [GRCh38]
Chr10:55571480 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3441dup (p.Phe1148fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003475937]|Rare genetic deafness [RCV000826148]|Usher syndrome type 1F [RCV000409226]|not provided [RCV002523845] Chr10:53903302..53903303 [GRCh38]
Chr10:55663062..55663063 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.2487dup (p.Glu830fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003475948]|Usher syndrome type 1F [RCV000411936] Chr10:54022930..54022931 [GRCh38]
Chr10:55782690..55782691 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.2419dup (p.Ile807fs) duplication Rare genetic deafness [RCV000824732]|Usher syndrome type 1F [RCV000412083] Chr10:54022998..54022999 [GRCh38]
Chr10:55782758..55782759 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|conflicting interpretations of pathogenicity
NM_001384140.1(PCDH15):c.3942C>G (p.Asp1314Glu) single nucleotide variant not provided [RCV000728066] Chr10:53840361 [GRCh38]
Chr10:55600121 [GRCh37]
Chr10:10q21.1		 uncertain significance
Single allele deletion Usher syndrome [RCV000504833] Chr10:54069818..54963276 [GRCh38]
Chr10:55829578..56723036 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.475-2204_594+1766del deletion Usher syndrome [RCV000505024] Chr10:54344599..54348688 [GRCh38]
Chr10:56104359..56108448 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.2192A>C (p.Glu731Ala) single nucleotide variant Inborn genetic diseases [RCV004023618]|Usher syndrome type 1F [RCV001829528]|not provided [RCV000520870] Chr10:54066785 [GRCh38]
Chr10:55826545 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh37/hg19 10q11.23-21.1(chr10:52752503-57406199)x3 copy number gain See cases [RCV000449275] Chr10:52752503..57406199 [GRCh37]
Chr10:10q11.23-21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4671+1217C>T single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV000454314] Chr10:53809339 [GRCh38]
Chr10:55569099 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3877C>A (p.Arg1293=) single nucleotide variant not provided [RCV000916890] Chr10:53840426 [GRCh38]
Chr10:55600186 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.3374-16G>A single nucleotide variant not provided [RCV001439527]|not specified [RCV000424595] Chr10:53903386 [GRCh38]
Chr10:55663146 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.19C>A (p.Leu7Ile) single nucleotide variant Usher syndrome type 1F [RCV001833519]|not provided [RCV000432030] Chr10:54664244 [GRCh38]
Chr10:56424004 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1997+1G>A single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003476015]|Usher syndrome type 1F [RCV002307495]|not provided [RCV000427347] Chr10:54089983 [GRCh38]
Chr10:55849743 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.3984-1G>C single nucleotide variant Usher syndrome type 1F [RCV000671775]|not provided [RCV000433340] Chr10:53831534 [GRCh38]
Chr10:55591294 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.4035T>A (p.Tyr1345Ter) single nucleotide variant not provided [RCV000435518] Chr10:53831482 [GRCh38]
Chr10:55591242 [GRCh37]
Chr10:10q21.1		 pathogenic
GRCh37/hg19 10q21.1(chr10:56413465-56560751)x1 copy number loss See cases [RCV000448642] Chr10:56413465..56560751 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh37/hg19 10q21.1(chr10:55199169-56857578)x4 copy number gain See cases [RCV000448303] Chr10:55199169..56857578 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh37/hg19 10p15.3-q26.3(chr10:93297-135378918)x3 copy number gain See cases [RCV000448750] Chr10:93297..135378918 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
NM_001384140.1(PCDH15):c.3857T>A (p.Val1286Glu) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV000477756]|not provided [RCV001700130] Chr10:53840446 [GRCh38]
Chr10:55600206 [GRCh37]
Chr10:10q21.1		 pathogenic|uncertain significance
NM_001384140.1(PCDH15):c.1427C>T (p.Thr476Ile) single nucleotide variant Usher syndrome type 1F [RCV001829386]|not provided [RCV000485440] Chr10:54185147 [GRCh38]
Chr10:55944907 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5278_5286del (p.Pro1760_Pro1762del) deletion PCDH15-related disorder [RCV004541525]|Usher syndrome type 1F [RCV000673254]|not provided [RCV001069767]|not specified [RCV000487227] Chr10:53822440..53822448 [GRCh38]
Chr10:55582200..55582208 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.4462_4469dup (p.Glu1491fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003476195]|Nonsyndromic Deafness [RCV000578330]|Usher syndrome [RCV000578273]|not provided [RCV000498908] Chr10:53823256..53823257 [GRCh38]
Chr10:55583016..55583017 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|uncertain significance
GRCh37/hg19 10q21.1(chr10:55045347-58190685)x3 copy number gain See cases [RCV000510270] Chr10:55045347..58190685 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4249G>A (p.Ala1417Thr) single nucleotide variant not specified [RCV000508416] Chr10:53827511 [GRCh38]
Chr10:55587271 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4368T>A (p.Ile1456=) single nucleotide variant Usher syndrome type 1F [RCV001829451]|not specified [RCV000508490] Chr10:53823358 [GRCh38]
Chr10:55583118 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3127C>T (p.Pro1043Ser) single nucleotide variant Usher syndrome type 1F [RCV001834641]|not provided [RCV000506827] Chr10:53940971 [GRCh38]
Chr10:55700731 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5363TTCCTC[1] (p.1788LP[1]) microsatellite not provided [RCV001239400]|not specified [RCV000507421] Chr10:53822352..53822357 [GRCh38]
Chr10:55582112..55582117 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_033056.4(PCDH15):c.5543G>T (p.Cys1848Phe) single nucleotide variant Usher syndrome type 1F [RCV001834642]|not provided [RCV003654416] Chr10:53822183 [GRCh38]
Chr10:55581943 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143) copy number gain See cases [RCV000511389] Chr10:100027..135427143 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic|uncertain significance
NM_001384140.1(PCDH15):c.3717+2dup duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV004568520]|Usher syndrome type 1F [RCV000669022]|not provided [RCV000808578] Chr10:53866639..53866640 [GRCh38]
Chr10:55626399..55626400 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.5215A>T (p.Lys1739Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002493103]|Usher syndrome type 1F [RCV000669118] Chr10:53806587 [GRCh38]
Chr10:55566347 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4915_4918dup (p.Arg1640fs) duplication Usher syndrome type 1F [RCV000669291]|not provided [RCV002060819] Chr10:53822807..53822808 [GRCh38]
Chr10:55582567..55582568 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.5317_5319del (p.Pro1773del) deletion Usher syndrome type 1F [RCV000670408] Chr10:53822407..53822409 [GRCh38]
Chr10:55582167..55582169 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)x3 copy number gain See cases [RCV000510861] Chr10:100027..135427143 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
NM_033056.4(PCDH15):c.5520dup (p.Val1841fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV002493104]|Usher syndrome type 1F [RCV000669808] Chr10:53822205..53822206 [GRCh38]
Chr10:55581965..55581966 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4864del (p.Ser1622fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV001806066]|not provided [RCV001231107]|not specified [RCV003117858] Chr10:53822862 [GRCh38]
Chr10:55582622 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.4866_4869dup (p.Lys1624fs) duplication Usher syndrome type 1F [RCV000669115] Chr10:53806932..53806933 [GRCh38]
Chr10:55566692..55566693 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3866T>C (p.Ile1289Thr) single nucleotide variant Inborn genetic diseases [RCV003249065] Chr10:53840437 [GRCh38]
Chr10:55600197 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4368-3204C>T single nucleotide variant Usher syndrome type 1F [RCV000672384] Chr10:53823434 [GRCh38]
Chr10:55583194 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3276T>C (p.Asn1092=) single nucleotide variant not provided [RCV002065203]|not specified [RCV000607062] Chr10:53938912 [GRCh38]
Chr10:55698672 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2811G>A (p.Pro937=) single nucleotide variant not provided [RCV001496921]|not specified [RCV000607374] Chr10:53995706 [GRCh38]
Chr10:55755466 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3778G>A (p.Val1260Met) single nucleotide variant Inborn genetic diseases [RCV003280960] Chr10:53857203 [GRCh38]
Chr10:55616963 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3498G>A (p.Val1166=) single nucleotide variant not specified [RCV000604758] Chr10:53903246 [GRCh38]
Chr10:55663006 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.92-18del deletion not provided [RCV001812319] Chr10:54527895 [GRCh38]
Chr10:56287655 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5266_5319del (p.Pro1756_Pro1773del) deletion Usher syndrome type 1F [RCV000672237]|not provided [RCV002531312] Chr10:53822407..53822460 [GRCh38]
Chr10:55582167..55582220 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4671+1642T>C single nucleotide variant PCDH15-related disorder [RCV004543400]|not provided [RCV003420053]|not specified [RCV000606051] Chr10:53808914 [GRCh38]
Chr10:55568674 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.369A>G (p.Lys123=) single nucleotide variant not provided [RCV001489433]|not specified [RCV000601210] Chr10:54369225 [GRCh38]
Chr10:56128985 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4317G>A (p.Pro1439=) single nucleotide variant not provided [RCV000936932]|not specified [RCV000606727] Chr10:53827443 [GRCh38]
Chr10:55587203 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4579C>T (p.Pro1527Ser) single nucleotide variant Inborn genetic diseases [RCV003261576] Chr10:53823147 [GRCh38]
Chr10:55582907 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2385A>G (p.Ala795=) single nucleotide variant not provided [RCV002532733]|not specified [RCV000602493] Chr10:54023033 [GRCh38]
Chr10:55782793 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4247_4258del (p.Gln1416_Leu1419del) deletion Usher syndrome type 1F [RCV000672146] Chr10:53827502..53827513 [GRCh38]
Chr10:55587262..55587273 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1045C>G (p.Leu349Val) single nucleotide variant not specified [RCV000609629] Chr10:54213989 [GRCh38]
Chr10:55973749 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4671+1344_4671+1345delinsCC indel not provided [RCV001613394]|not specified [RCV000612456] Chr10:53809211..53809212 [GRCh38]
Chr10:55568971..55568972 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1102G>A (p.Glu368Lys) single nucleotide variant Inborn genetic diseases [RCV004025021]|not specified [RCV000610050] Chr10:54195886 [GRCh38]
Chr10:55955646 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2936T>C (p.Phe979Ser) single nucleotide variant Inborn genetic diseases [RCV002532732]|Usher syndrome type 1F [RCV001829694]|not provided [RCV001071709]|not specified [RCV000610079] Chr10:53961825 [GRCh38]
Chr10:55721585 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4677G>A (p.Lys1559=) single nucleotide variant not provided [RCV000732333]|not specified [RCV000615549] Chr10:53823049 [GRCh38]
Chr10:55582809 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_033056.4(PCDH15):c.4568G>A (p.Ser1523Asn) single nucleotide variant not specified [RCV000615987] Chr10:53823158 [GRCh38]
Chr10:55582918 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4314G>A (p.Pro1438=) single nucleotide variant not provided [RCV002062189]|not specified [RCV000610156] Chr10:53827446 [GRCh38]
Chr10:55587206 [GRCh37]
Chr10:10q21.1		 likely benign
NC_000010.10:g.43611191_61663279inv inversion Pediatric metastatic thyroid tumour [RCV000585841] Chr10:43611191..61663279 [GRCh37]
Chr10:10q11.21-21.2		 likely pathogenic
NM_001384140.1(PCDH15):c.3521G>A (p.Gly1174Asp) single nucleotide variant Inborn genetic diseases [RCV002531130]|Usher syndrome type 1F [RCV001835875]|not provided [RCV001038859]|not specified [RCV000613222] Chr10:53866838 [GRCh38]
Chr10:55626598 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4810A>C (p.Arg1604=) single nucleotide variant not provided [RCV000597403] Chr10:53822916 [GRCh38]
Chr10:55582676 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4671+1345G>C single nucleotide variant PCDH15-related disorder [RCV004530738]|not provided [RCV001584417]|not specified [RCV000608202] Chr10:53809211 [GRCh38]
Chr10:55568971 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.1784+11T>G single nucleotide variant not provided [RCV003736837]|not specified [RCV000608342] Chr10:54153089 [GRCh38]
Chr10:55912849 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5372C>T (p.Pro1791Leu) single nucleotide variant Usher syndrome type 1F [RCV001834924]|not provided [RCV002531141]|not specified [RCV000611017] Chr10:53822354 [GRCh38]
Chr10:55582114 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4925G>A (p.Gly1642Asp) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002483677]|Usher syndrome type 1F [RCV001829707]|not provided [RCV001868023]|not specified [RCV000608419] Chr10:53822801 [GRCh38]
Chr10:55582561 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3667A>T (p.Ile1223Phe) single nucleotide variant Usher syndrome type 1F [RCV001829706]|not provided [RCV001346729]|not specified [RCV000611050] Chr10:53866692 [GRCh38]
Chr10:55626452 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.92-10C>T single nucleotide variant PCDH15-related disorder [RCV004530732]|not provided [RCV000919727]|not specified [RCV000611349] Chr10:54527887 [GRCh38]
Chr10:56287647 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4671+1438A>C single nucleotide variant PCDH15-related disorder [RCV004530735]|not provided [RCV000965805]|not specified [RCV000614177] Chr10:53809118 [GRCh38]
Chr10:55568878 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.4671+1066_4671+1068del microsatellite not specified [RCV000614275] Chr10:53809488..53809490 [GRCh38]
Chr10:55569248..55569250 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2354A>G (p.Tyr785Cys) single nucleotide variant Usher syndrome type 1F [RCV001829731]|not specified [RCV000609404] Chr10:54023064 [GRCh38]
Chr10:55782824 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.974C>T (p.Ser325Phe) single nucleotide variant Usher syndrome type 1F [RCV001829729]|not provided [RCV002528784]|not specified [RCV000603600] Chr10:54236834 [GRCh38]
Chr10:55996594 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh37/hg19 10q11.21-26.3(chr10:42347406-135534747)x1 copy number loss Poly (ADP-Ribose) polymerase inhibitor response [RCV000626438] Chr10:42347406..135534747 [GRCh37]
Chr10:10q11.21-26.3		 drug response
NM_001384140.1(PCDH15):c.4671+1033dup duplication not specified [RCV000607539] Chr10:53809522..53809523 [GRCh38]
Chr10:55569282..55569283 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3040_3047dup (p.Met1016delinsIleLeuTer) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003471963]|not provided [RCV000596460] Chr10:53959806..53959807 [GRCh38]
Chr10:55719566..55719567 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.3122+3A>G single nucleotide variant Usher syndrome type 1F [RCV001834865]|not provided [RCV000597354]|not specified [RCV000826006] Chr10:53959729 [GRCh38]
Chr10:55719489 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4118C>T (p.Thr1373Ile) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV004568545]|Usher syndrome type 1F [RCV000671939] Chr10:53831399 [GRCh38]
Chr10:55591159 [GRCh37]
Chr10:10q21.1		 likely pathogenic|uncertain significance
NM_033056.4(PCDH15):c.5343del (p.Ser1782fs) deletion Usher syndrome type 1F [RCV000672013]|not provided [RCV000992509] Chr10:53822383 [GRCh38]
Chr10:55582143 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.158-2A>T single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003472143]|Usher syndrome type 1F [RCV000672062]|not provided [RCV001212804] Chr10:54378944 [GRCh38]
Chr10:56138704 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.4368-3205del deletion Usher syndrome type 1F [RCV000672833] Chr10:53823435 [GRCh38]
Chr10:55583195 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4671+1257_4671+1258del deletion Usher syndrome type 1F [RCV000672969] Chr10:53809298..53809299 [GRCh38]
Chr10:55569058..55569059 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.5092C>T (p.Gln1698Ter) single nucleotide variant Usher syndrome type 1F [RCV000664453] Chr10:53806710 [GRCh38]
Chr10:55566470 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4988_4991dup (p.Met1664fs) duplication Usher syndrome type 1F [RCV000664455] Chr10:53806810..53806811 [GRCh38]
Chr10:55566570..55566571 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5838_5841del (p.Lys1946fs) deletion Usher syndrome type 1F [RCV000673146] Chr10:53821885..53821888 [GRCh38]
Chr10:55581645..55581648 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4618del (p.Ser1540fs) deletion Usher syndrome type 1F [RCV000672243] Chr10:53823108 [GRCh38]
Chr10:55582868 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4368-3142TCTTT[3] microsatellite Usher syndrome type 1F [RCV000672745]|not provided [RCV001498263] Chr10:53823362..53823363 [GRCh38]
Chr10:55583122..55583123 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.4955_4963dup (p.Ser1655Ter) duplication Usher syndrome type 1F [RCV000673307] Chr10:53822762..53822763 [GRCh38]
Chr10:55582522..55582523 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5702_5705dup (p.Ile1903fs) duplication Usher syndrome type 1F [RCV000673341] Chr10:53822020..53822021 [GRCh38]
Chr10:55581780..55581781 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5863del (p.Leu1955fs) deletion Usher syndrome type 1F [RCV000670659] Chr10:53821863 [GRCh38]
Chr10:55581623 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4705_4708dup (p.Ile1570fs) duplication Usher syndrome type 1F [RCV000670820]|not provided [RCV001855548] Chr10:53823017..53823018 [GRCh38]
Chr10:55582777..55582778 [GRCh37]
Chr10:10q21.1		 pathogenic|uncertain significance
NM_033056.4(PCDH15):c.5269_5295del (p.Ser1757_Leu1765del) deletion Usher syndrome type 1F [RCV000670872] Chr10:53822431..53822457 [GRCh38]
Chr10:55582191..55582217 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3984-2A>G single nucleotide variant Usher syndrome type 1F [RCV000670875] Chr10:53831535 [GRCh38]
Chr10:55591295 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.5257_5262del (p.Ile1753_Ser1754del) deletion Usher syndrome type 1F [RCV000670952]|not provided [RCV002060822] Chr10:53822464..53822469 [GRCh38]
Chr10:55582224..55582229 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.4409_4413dup (p.Val1472fs) duplication Usher syndrome type 1F [RCV000672638] Chr10:53823312..53823313 [GRCh38]
Chr10:55583072..55583073 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4368-3207_4368-3204del deletion Usher syndrome type 1F [RCV000672639] Chr10:53823434..53823437 [GRCh38]
Chr10:55583194..55583197 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4970_4971del (p.Ser1657fs) microsatellite Usher syndrome type 1F [RCV000671143]|not provided [RCV003660825] Chr10:53822755..53822756 [GRCh38]
Chr10:55582515..55582516 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.157+59097T>C single nucleotide variant Usher syndrome type 1F [RCV000671187] Chr10:54468715 [GRCh38]
Chr10:56228475 [GRCh37]
Chr10:10q21.1		 benign
NM_033056.4(PCDH15):c.4410_4420del (p.Asn1470fs) deletion Usher syndrome type 1F [RCV000671194]|not provided [RCV001383498] Chr10:53823306..53823316 [GRCh38]
Chr10:55583066..55583076 [GRCh37]
Chr10:10q21.1		 pathogenic|uncertain significance
NM_001384140.1(PCDH15):c.4671+1616G>A single nucleotide variant Inborn genetic diseases [RCV002534291]|not provided [RCV000658562]|not specified [RCV001449714] Chr10:53808940 [GRCh38]
Chr10:55568700 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5798_5816dup (p.Asn1939fs) duplication Usher syndrome type 1F [RCV000664851] Chr10:53821909..53821910 [GRCh38]
Chr10:55581669..55581670 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5721_5724dup (p.Arg1909fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV002499186]|PCDH15-related disorder [RCV004535687]|Usher syndrome type 1F [RCV000673478]|not provided [RCV001239240] Chr10:53822001..53822002 [GRCh38]
Chr10:55581761..55581762 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4368-3205G>A single nucleotide variant Usher syndrome type 1F [RCV000664969]|not provided [RCV001355937] Chr10:53823435 [GRCh38]
Chr10:55583195 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.5084_5085del (p.Thr1695fs) microsatellite Usher syndrome type 1F [RCV000665045] Chr10:53806717..53806718 [GRCh38]
Chr10:55566477..55566478 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4127C>A (p.Ala1376Asp) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002499169]|Usher syndrome type 1F [RCV000670158] Chr10:53831390 [GRCh38]
Chr10:55591150 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5617dup (p.Thr1873fs) duplication Usher syndrome type 1F [RCV000670319] Chr10:53822108..53822109 [GRCh38]
Chr10:55581868..55581869 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4621_4624dup (p.Ile1542fs) duplication Usher syndrome type 1F [RCV000670675] Chr10:53823101..53823102 [GRCh38]
Chr10:55582861..55582862 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.274C>T (p.Gln92Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001809740]|Retinal dystrophy [RCV001073252]|Usher syndrome type 1F [RCV000670777]|not provided [RCV003558511] Chr10:54378826 [GRCh38]
Chr10:56138586 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_033056.4(PCDH15):c.4987dup (p.Cys1663fs) duplication Usher syndrome type 1F [RCV000669179]|not provided [RCV002531220] Chr10:53822738..53822739 [GRCh38]
Chr10:55582498..55582499 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4754dup (p.Met1585fs) duplication Usher syndrome type 1F [RCV000669375] Chr10:53822971..53822972 [GRCh38]
Chr10:55582731..55582732 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.139del (p.Asp47fs) deletion Usher syndrome type 1F [RCV000669464]|not provided [RCV001868231] Chr10:54527830 [GRCh38]
Chr10:56287590 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_033056.4(PCDH15):c.4921C>T (p.Gln1641Ter) single nucleotide variant Usher syndrome type 1F [RCV000671437]|not provided [RCV002531284] Chr10:53822805 [GRCh38]
Chr10:55582565 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.3502-2A>G single nucleotide variant Usher syndrome type 1F [RCV000671550]|not provided [RCV003718277] Chr10:53866859 [GRCh38]
Chr10:55626619 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.-5AGA[1] (p.Met1del) microsatellite Usher syndrome type 1F [RCV000671683] Chr10:54664262..54664264 [GRCh38]
Chr10:56424022..56424024 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5347_5363del (p.Pro1783fs) deletion Usher syndrome type 1F [RCV000671747]|not provided [RCV000961061]|not specified [RCV004768541] Chr10:53822363..53822379 [GRCh38]
Chr10:55582123..55582139 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.4368-1896_4368-1893delinsT indel Usher syndrome type 1F [RCV000671848] Chr10:53822123..53822126 [GRCh38]
Chr10:55581883..55581886 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5272CCT[4] (p.Pro1760dup) microsatellite Usher syndrome type 1F [RCV000673560] Chr10:53822445..53822446 [GRCh38]
Chr10:55582205..55582206 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3806+2T>C single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003472159]|Usher syndrome type 1F [RCV000673647]|not provided [RCV001855599] Chr10:53857173 [GRCh38]
Chr10:55616933 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_033056.4(PCDH15):c.5193dup (p.Glu1732Ter) duplication Usher syndrome type 1F [RCV000670136] Chr10:53822532..53822533 [GRCh38]
Chr10:55582292..55582293 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4722del (p.Ser1575fs) deletion Usher syndrome type 1F [RCV000673772] Chr10:53807080 [GRCh38]
Chr10:55566840 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2728G>T (p.Ala910Ser) single nucleotide variant PCDH15-related disorder [RCV004735733]|Usher syndrome type 1D [RCV001810467]|Usher syndrome type 1F [RCV000665239]|not provided [RCV001071361]|not specified [RCV000825424] Chr10:54020215 [GRCh38]
Chr10:55779975 [GRCh37]
Chr10:10q21.1		 conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.299del (p.Gly100fs) deletion Usher syndrome type 1F [RCV000665269] Chr10:54378801 [GRCh38]
Chr10:56138561 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.5349_5359del (p.Pro1784fs) deletion Usher syndrome type 1F [RCV000665276] Chr10:53822367..53822377 [GRCh38]
Chr10:55582127..55582137 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5632_5633del (p.Glu1878fs) microsatellite Usher syndrome type 1F [RCV000667847] Chr10:53822093..53822094 [GRCh38]
Chr10:55581853..55581854 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4504G>A (p.Glu1502Lys) single nucleotide variant Usher syndrome type 1F [RCV000667908] Chr10:53811607 [GRCh38]
Chr10:55571367 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4563_4566dup (p.Ser1523fs) duplication Usher syndrome type 1F [RCV000667960] Chr10:53823159..53823160 [GRCh38]
Chr10:55582919..55582920 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5296_5304del (p.Ala1766_Pro1768del) deletion Usher syndrome type 1F [RCV000670779] Chr10:53822422..53822430 [GRCh38]
Chr10:55582182..55582190 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.323del (p.Pro108fs) deletion Usher syndrome type 1F [RCV000665362] Chr10:54369271 [GRCh38]
Chr10:56129031 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.2091+2T>C single nucleotide variant Usher syndrome type 1F [RCV000665400] Chr10:54079329 [GRCh38]
Chr10:55839089 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.5047_5050dup (p.Lys1684fs) duplication Usher syndrome type 1F [RCV000665522] Chr10:53822675..53822676 [GRCh38]
Chr10:55582435..55582436 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4724_4726dup (p.Ser1575_Gln1576insArg) duplication Usher syndrome type 1F [RCV000668199] Chr10:53822999..53823000 [GRCh38]
Chr10:55582759..55582760 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5257_5268dup (p.Ile1753_Pro1756dup) duplication Usher syndrome type 1F [RCV000668333] Chr10:53822457..53822458 [GRCh38]
Chr10:55582217..55582218 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4561_4565dup (p.Ser1523fs) duplication Usher syndrome type 1F [RCV000671485]|not provided [RCV003767994] Chr10:53823160..53823161 [GRCh38]
Chr10:55582920..55582921 [GRCh37]
Chr10:10q21.1		 pathogenic|uncertain significance
NM_001384140.1(PCDH15):c.3792_3798dup (p.Leu1267fs) duplication Usher syndrome type 1F [RCV000671510] Chr10:53857182..53857183 [GRCh38]
Chr10:55616942..55616943 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3501+1G>T single nucleotide variant Usher syndrome type 1F [RCV000674150] Chr10:53903242 [GRCh38]
Chr10:55663002 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.2751+2T>C single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003472103]|Usher syndrome type 1F [RCV000668602]|not provided [RCV001855503]|not specified [RCV000826014] Chr10:54020190 [GRCh38]
Chr10:55779950 [GRCh37]
Chr10:10q21.1		 likely pathogenic|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.705+1G>A single nucleotide variant Usher syndrome type 1F [RCV000668616] Chr10:54329595 [GRCh38]
Chr10:56089355 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.5806del (p.Ser1936fs) deletion Usher syndrome type 1F [RCV000672390]|not provided [RCV002066979] Chr10:53821920 [GRCh38]
Chr10:55581680 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.5713A>T (p.Lys1905Ter) single nucleotide variant Usher syndrome type 1F [RCV000674489] Chr10:53822013 [GRCh38]
Chr10:55581773 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4367+2T>C single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003472171]|Usher syndrome type 1F [RCV000674498] Chr10:53827391 [GRCh38]
Chr10:55587151 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.3791_3794del (p.Ile1264fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003472172]|Usher syndrome type 1F [RCV000674516] Chr10:53857187..53857190 [GRCh38]
Chr10:55616947..55616950 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.4672-1648_4672-1644dup duplication Usher syndrome type 1F [RCV000674557] Chr10:53808773..53808774 [GRCh38]
Chr10:55568533..55568534 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4211+1del deletion Usher syndrome type 1F [RCV000674589] Chr10:53828564 [GRCh38]
Chr10:55588324 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.4368-1_4369dup duplication Usher syndrome type 1F [RCV000667042] Chr10:53823356..53823357 [GRCh38]
Chr10:55583116..55583117 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4671+1403GAG[5] microsatellite Usher syndrome type 1F [RCV000664440] Chr10:53809141..53809142 [GRCh38]
Chr10:55568901..55568902 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4875_4894del (p.Leu1626fs) deletion PCDH15-related disorder [RCV004735732]|Usher syndrome type 1F [RCV000664564]|not provided [RCV001485739] Chr10:53822832..53822851 [GRCh38]
Chr10:55582592..55582611 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_033056.4(PCDH15):c.5445_5456del (p.Thr1816_Pro1819del) deletion Usher syndrome type 1F [RCV000666091] Chr10:53822270..53822281 [GRCh38]
Chr10:55582030..55582041 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3233-2A>G single nucleotide variant Usher syndrome type 1F [RCV000666101]|not provided [RCV001855452] Chr10:53938957 [GRCh38]
Chr10:55698717 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3374-1G>T single nucleotide variant Usher syndrome type 1F [RCV000674704] Chr10:53903371 [GRCh38]
Chr10:55663131 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.4983_4986dup (p.Cys1663fs) duplication Usher syndrome type 1F [RCV000674707]|not provided [RCV002060829] Chr10:53822739..53822740 [GRCh38]
Chr10:55582499..55582500 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.1917+2T>C single nucleotide variant Usher syndrome type 1F [RCV000674799]|not provided [RCV003768014] Chr10:54132873 [GRCh38]
Chr10:55892633 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1456G>A (p.Gly486Ser) single nucleotide variant Usher syndrome type 1F [RCV000674811]|not specified [RCV004526008] Chr10:54183578 [GRCh38]
Chr10:55943338 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5710_5711del (p.Glu1904fs) deletion Usher syndrome type 1F [RCV000667113] Chr10:53822015..53822016 [GRCh38]
Chr10:55581775..55581776 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4907_4908del (p.Lys1636fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV002499158]|Usher syndrome type 1F [RCV000667172]|not provided [RCV001238927]|not specified [RCV002307583] Chr10:53822818..53822819 [GRCh38]
Chr10:55582578..55582579 [GRCh37]
Chr10:10q21.1		 conflicting interpretations of pathogenicity|uncertain significance
NM_033056.4(PCDH15):c.4813C>T (p.Gln1605Ter) single nucleotide variant Usher syndrome type 1F [RCV000667208] Chr10:53822913 [GRCh38]
Chr10:55582673 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4308GCC[9] (p.Pro1440_Pro1443dup) microsatellite Usher syndrome type 1F [RCV000667211] Chr10:53827437..53827438 [GRCh38]
Chr10:55587197..55587198 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5361_5376del (p.Pro1789fs) deletion Usher syndrome type 1F [RCV000664597] Chr10:53822350..53822365 [GRCh38]
Chr10:55582110..55582125 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4812del (p.Arg1604fs) deletion Usher syndrome type 1F [RCV000664909] Chr10:53822914 [GRCh38]
Chr10:55582674 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5626C>T (p.Gln1876Ter) single nucleotide variant Usher syndrome type 1F [RCV000673593]|not provided [RCV002532149] Chr10:53822100 [GRCh38]
Chr10:55581860 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.5684C>G (p.Ser1895Ter) single nucleotide variant Usher syndrome type 1F [RCV000669235] Chr10:53822042 [GRCh38]
Chr10:55581802 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.5054T>C (p.Val1685Ala) single nucleotide variant Usher syndrome type 1F [RCV000670257] Chr10:53806748 [GRCh38]
Chr10:55566508 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.29del (p.Cys10fs) deletion Usher syndrome type 1F [RCV000672339] Chr10:54664234 [GRCh38]
Chr10:56423994 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4308GCC[2] (p.Pro1441_Pro1443del) microsatellite Autosomal recessive nonsyndromic hearing loss 23 [RCV002485522]|Usher syndrome type 1F [RCV000665102]|not provided [RCV001861741] Chr10:53827438..53827446 [GRCh38]
Chr10:55587198..55587206 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2047C>T (p.Arg683Cys) single nucleotide variant Usher syndrome type 1F [RCV000673903] Chr10:54079375 [GRCh38]
Chr10:55839135 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4671+1617_4671+1637del deletion Usher syndrome type 1F [RCV000667399] Chr10:53808919..53808939 [GRCh38]
Chr10:55568679..55568699 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4708C>T (p.Arg1570Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002507158]|Usher syndrome type 1F [RCV000667404] Chr10:53807094 [GRCh38]
Chr10:55566854 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.145G>T (p.Glu49Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003472126]|Usher syndrome type 1F [RCV000670660]|not provided [RCV003727796] Chr10:54527824 [GRCh38]
Chr10:56287584 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.1305+1G>C single nucleotide variant Usher syndrome type 1F [RCV000670840] Chr10:54195682 [GRCh38]
Chr10:55955442 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4671+1511_4671+1519del deletion Usher syndrome type 1F [RCV000673888] Chr10:53809037..53809045 [GRCh38]
Chr10:55568797..55568805 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4895_4897dup (p.Asn1632_Leu1633insTyr) duplication Usher syndrome type 1F [RCV000673925]|not provided [RCV002532155] Chr10:53822828..53822829 [GRCh38]
Chr10:55582588..55582589 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.5106_5109dup (p.Ser1704Ter) duplication Usher syndrome type 1F [RCV000673986] Chr10:53806692..53806693 [GRCh38]
Chr10:55566452..55566453 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4672-1662del deletion Usher syndrome type 1F [RCV000674038] Chr10:53808792 [GRCh38]
Chr10:55568552 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4114_4119del (p.Tyr1372_Thr1373del) deletion Usher syndrome type 1F [RCV000667434] Chr10:53831398..53831403 [GRCh38]
Chr10:55591158..55591163 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4875_4896del (p.Leu1625fs) deletion Usher syndrome type 1F [RCV000667518]|not provided [RCV003117468] Chr10:53822830..53822851 [GRCh38]
Chr10:55582590..55582611 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.1637_1638del (p.Thr545_Tyr546insTer) microsatellite Usher syndrome type 1F [RCV000667538] Chr10:54153246..54153247 [GRCh38]
Chr10:55913006..55913007 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4671+1077_4671+1082del deletion Usher syndrome type 1F [RCV000667583] Chr10:53809474..53809479 [GRCh38]
Chr10:55569234..55569239 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4305_4310dup (p.Pro1442_Pro1443dup) duplication Usher syndrome type 1F [RCV000667623]|not provided [RCV001855484] Chr10:53827449..53827450 [GRCh38]
Chr10:55587209..55587210 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5061_5067dup (p.Ile1690Ter) duplication Usher syndrome type 1F [RCV000671793]|not provided [RCV002531296] Chr10:53822658..53822659 [GRCh38]
Chr10:55582418..55582419 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.4832del (p.Asn1611fs) deletion Usher syndrome type 1F [RCV000672418] Chr10:53822894 [GRCh38]
Chr10:55582654 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2052C>A (p.Tyr684Ter) single nucleotide variant Usher syndrome type 1F [RCV000672564] Chr10:54079370 [GRCh38]
Chr10:55839130 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4671+1523G>T single nucleotide variant Usher syndrome type 1F [RCV000674158]|not provided [RCV001592855] Chr10:53809033 [GRCh38]
Chr10:55568793 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.5108_5111dup (p.Ser1704fs) duplication Usher syndrome type 1F [RCV000674520] Chr10:53806690..53806691 [GRCh38]
Chr10:55566450..55566451 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5388dup (p.Pro1797fs) duplication Usher syndrome type 1F [RCV000671244] Chr10:53822337..53822338 [GRCh38]
Chr10:55582097..55582098 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1997+1G>T single nucleotide variant Usher syndrome type 1F [RCV000674070] Chr10:54089983 [GRCh38]
Chr10:55849743 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.875C>G (p.Pro292Arg) single nucleotide variant Usher syndrome type 1F [RCV000674085]|not provided [RCV001092481] Chr10:54317272 [GRCh38]
Chr10:56077032 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5472_5495del (p.Ile1825_Ser1832del) deletion Usher syndrome type 1F [RCV000665652]|not provided [RCV002530661] Chr10:53822231..53822254 [GRCh38]
Chr10:55581991..55582014 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3806+1G>C single nucleotide variant Usher syndrome type 1F [RCV000674273] Chr10:53857174 [GRCh38]
Chr10:55616934 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.5003_5007dup (p.Ser1670fs) duplication Usher syndrome type 1F [RCV000667747] Chr10:53822718..53822719 [GRCh38]
Chr10:55582478..55582479 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4671+1355_4671+1359dup duplication Usher syndrome type 1F [RCV000667857] Chr10:53809196..53809197 [GRCh38]
Chr10:55568956..55568957 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4905_4907dup (p.Lys1636dup) duplication Usher syndrome type 1F [RCV000667878]|not provided [RCV001313603] Chr10:53822818..53822819 [GRCh38]
Chr10:55582578..55582579 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5355_5365del (p.Ile1786fs) deletion Usher syndrome type 1F [RCV000672805]|not provided [RCV003679017] Chr10:53822361..53822371 [GRCh38]
Chr10:55582121..55582131 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.5294_5302dup (p.Leu1765_Pro1767dup) duplication Usher syndrome type 1F [RCV000664509] Chr10:53822423..53822424 [GRCh38]
Chr10:55582183..55582184 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4618G>T (p.Glu1540Ter) single nucleotide variant Usher syndrome type 1F [RCV000674743]|not provided [RCV004692070] Chr10:53810609 [GRCh38]
Chr10:55570369 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5274_5278del (p.Pro1759fs) deletion Usher syndrome type 1F [RCV000675009] Chr10:53822448..53822452 [GRCh38]
Chr10:55582208..55582212 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4733_4736dup (p.Leu1580fs) microsatellite PCDH15-related disorder [RCV004735740]|Usher syndrome type 1F [RCV000671488] Chr10:53822989..53822990 [GRCh38]
Chr10:55582749..55582750 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5682dup (p.Ser1895fs) duplication Usher syndrome type 1F [RCV000671545] Chr10:53822043..53822044 [GRCh38]
Chr10:55581803..55581804 [GRCh37]
Chr10:10q21.1		 conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.3731_3734del (p.Asn1244fs) deletion Usher syndrome type 1F [RCV000671600] Chr10:53857247..53857250 [GRCh38]
Chr10:55617007..55617010 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.5363TTCCTC[3] (p.1788LP[3]) microsatellite Usher syndrome type 1F [RCV000671798] Chr10:53822351..53822352 [GRCh38]
Chr10:55582111..55582112 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4546_4553dup (p.Glu1519fs) duplication Usher syndrome type 1F [RCV000671849] Chr10:53823172..53823173 [GRCh38]
Chr10:55582932..55582933 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4792C>T (p.Gln1598Ter) single nucleotide variant Usher syndrome type 1F [RCV000665772]|not provided [RCV002530665] Chr10:53822934 [GRCh38]
Chr10:55582694 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4671+1009G>A single nucleotide variant Usher syndrome type 1F [RCV000674377] Chr10:53809547 [GRCh38]
Chr10:55569307 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1924G>A (p.Asp642Asn) single nucleotide variant Usher syndrome type 1F [RCV000674396] Chr10:54090057 [GRCh38]
Chr10:55849817 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2869-1G>T single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV000770853]|Usher syndrome type 1F [RCV000674501] Chr10:53961893 [GRCh38]
Chr10:55721653 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.5109_5129del (p.Arg1704_Ser1710del) deletion Usher syndrome type 1F [RCV000667994] Chr10:53822597..53822617 [GRCh38]
Chr10:55582357..55582377 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4671+1420del deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV002485542]|Usher syndrome type 1F [RCV000668055] Chr10:53809136 [GRCh38]
Chr10:55568896 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.92-515T>G single nucleotide variant Usher syndrome type 1F [RCV000668059] Chr10:54528392 [GRCh38]
Chr10:56288152 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5014_5022dup (p.Ser1672_Leu1674dup) duplication Usher syndrome type 1F [RCV000673235] Chr10:53822703..53822704 [GRCh38]
Chr10:55582463..55582464 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1591C>T (p.Leu531Phe) single nucleotide variant Usher syndrome type 1D [RCV001810479]|not provided [RCV000945066]|not specified [RCV001844219] Chr10:54153293 [GRCh38]
Chr10:55913053 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4214G>A (p.Arg1405His) single nucleotide variant Usher syndrome type 1F [RCV000664819]|not provided [RCV001241412]|not specified [RCV004525998] Chr10:53827546 [GRCh38]
Chr10:55587306 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.84T>A (p.Tyr28Ter) single nucleotide variant Usher syndrome type 1F [RCV000664985] Chr10:54664179 [GRCh38]
Chr10:56423939 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.5161_5162del (p.Met1721fs) deletion Usher syndrome type 1F [RCV000664989] Chr10:53822564..53822565 [GRCh38]
Chr10:55582324..55582325 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4671+1708_4671+1711dup duplication Usher syndrome type 1F [RCV000672022] Chr10:53808844..53808845 [GRCh38]
Chr10:55568604..55568605 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4769_4771dup (p.Asn1590dup) duplication Usher syndrome type 1F [RCV000666132] Chr10:53822954..53822955 [GRCh38]
Chr10:55582714..55582715 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5029_5032dup (p.Ser1678fs) duplication Usher syndrome type 1F [RCV000666134]|not provided [RCV001170021] Chr10:53822693..53822694 [GRCh38]
Chr10:55582453..55582454 [GRCh37]
Chr10:10q21.1		 likely pathogenic|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.4231_4234dup (p.Thr1412fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV004568569]|Usher syndrome type 1F [RCV000674755] Chr10:53827525..53827526 [GRCh38]
Chr10:55587285..55587286 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4237_4238del (p.Ala1413fs) deletion Usher syndrome type 1F [RCV000668253] Chr10:53827522..53827523 [GRCh38]
Chr10:55587282..55587283 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3122+2T>A single nucleotide variant Usher syndrome type 1F [RCV000668350]|not provided [RCV001378360] Chr10:53959730 [GRCh38]
Chr10:55719490 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.5806_5807del (p.Ser1936fs) deletion Usher syndrome type 1F [RCV000668385] Chr10:53821919..53821920 [GRCh38]
Chr10:55581679..55581680 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4925del (p.Gly1642fs) deletion Usher syndrome type 1F [RCV000668438] Chr10:53822801 [GRCh38]
Chr10:55582561 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4672-1709_4672-1706dup duplication Usher syndrome type 1F [RCV000673866] Chr10:53808835..53808836 [GRCh38]
Chr10:55568595..55568596 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4768_4771dup (p.Arg1591delinsLysTer) duplication Usher syndrome type 1F [RCV000673907]|not provided [RCV001861827] Chr10:53822954..53822955 [GRCh38]
Chr10:55582714..55582715 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4211+1G>A single nucleotide variant Usher syndrome type 1F [RCV000666836] Chr10:53828564 [GRCh38]
Chr10:55588324 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3807-2A>G single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003472082]|Usher syndrome type 1F [RCV000666838] Chr10:53840498 [GRCh38]
Chr10:55600258 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.4671+1550C>T single nucleotide variant Usher syndrome type 1F [RCV000668631] Chr10:53809006 [GRCh38]
Chr10:55568766 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5332dup (p.Cys1778fs) duplication Usher syndrome type 1F [RCV000668779]|not provided [RCV001868225]|not specified [RCV004768530] Chr10:53822393..53822394 [GRCh38]
Chr10:55582153..55582154 [GRCh37]
Chr10:10q21.1		 conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.788C>A (p.Pro263Gln) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV000681533]|Hearing loss, autosomal recessive [RCV001291231] Chr10:54317359 [GRCh38]
Chr10:56077119 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_033056.4(PCDH15):c.4603_4607del (p.Gln1535fs) deletion Usher syndrome type 1F [RCV000674163]|not provided [RCV001387819] Chr10:53823119..53823123 [GRCh38]
Chr10:55582879..55582883 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|uncertain significance
NM_033056.4(PCDH15):c.4973C>A (p.Ser1658Ter) single nucleotide variant Usher syndrome type 1F [RCV000674338]|not provided [RCV003698809] Chr10:53822753 [GRCh38]
Chr10:55582513 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4729_4734dup (p.Thr1577_Gly1578dup) duplication Usher syndrome type 1F [RCV000672487] Chr10:53807067..53807068 [GRCh38]
Chr10:55566827..55566828 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4147del (p.Ile1383fs) deletion Usher syndrome type 1F [RCV000666470] Chr10:53831370 [GRCh38]
Chr10:55591130 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4603C>A (p.Pro1535Thr) single nucleotide variant Usher syndrome type 1F [RCV000675001] Chr10:53810624 [GRCh38]
Chr10:55570384 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5566G>T (p.Glu1856Ter) single nucleotide variant Usher syndrome type 1F [RCV000675002]|not provided [RCV002066985] Chr10:53822160 [GRCh38]
Chr10:55581920 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.4368-3_4379dup duplication Usher syndrome type 1F [RCV000675005] Chr10:53823346..53823347 [GRCh38]
Chr10:55583106..55583107 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.803G>A (p.Cys268Tyr) single nucleotide variant Usher syndrome type 1F [RCV000666523]|not specified [RCV004689835] Chr10:54317344 [GRCh38]
Chr10:56077104 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4607C>T (p.Pro1536Leu) single nucleotide variant Usher syndrome type 1F [RCV000674730] Chr10:53810620 [GRCh38]
Chr10:55570380 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4399_4410dup (p.Arg1467_Asn1470dup) duplication Usher syndrome type 1F [RCV000672780] Chr10:53823315..53823316 [GRCh38]
Chr10:55583075..55583076 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4435CAA[1] (p.Gln1480del) microsatellite Usher syndrome type 1F [RCV000672835] Chr10:53823286..53823288 [GRCh38]
Chr10:55583046..55583048 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4834dup (p.Thr1612fs) duplication Usher syndrome type 1F [RCV000672891] Chr10:53822891..53822892 [GRCh38]
Chr10:55582651..55582652 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4548_4551del (p.Ser1517fs) deletion Usher syndrome type 1F [RCV000672908]|not provided [RCV001062906] Chr10:53823175..53823178 [GRCh38]
Chr10:55582935..55582938 [GRCh37]
Chr10:10q21.1		 pathogenic|uncertain significance
NM_001384140.1(PCDH15):c.4671+1412G>T single nucleotide variant Usher syndrome type 1F [RCV000664443] Chr10:53809144 [GRCh38]
Chr10:55568904 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5463_5489del (p.Pro1823_Pro1831del) deletion Usher syndrome type 1F [RCV000673979]|not provided [RCV002066982] Chr10:53822237..53822263 [GRCh38]
Chr10:55581997..55582023 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.4968_4970dup (p.Ser1658dup) duplication Usher syndrome type 1F [RCV000674110] Chr10:53822755..53822756 [GRCh38]
Chr10:55582515..55582516 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4006_4008dup (p.Asp1336dup) duplication Usher syndrome type 1F [RCV000674112] Chr10:53831508..53831509 [GRCh38]
Chr10:55591268..55591269 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4317_4328dup (p.Pro1440_Pro1443dup) duplication Usher syndrome type 1F [RCV000666588] Chr10:53827431..53827432 [GRCh38]
Chr10:55587191..55587192 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4914del (p.Asp1639fs) deletion Usher syndrome type 1F [RCV000664445] Chr10:53806888 [GRCh38]
Chr10:55566648 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4828_4835del (p.Ser1610fs) deletion Usher syndrome type 1F [RCV000664448] Chr10:53806967..53806974 [GRCh38]
Chr10:55566727..55566734 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4672-1666G>T single nucleotide variant Usher syndrome type 1F [RCV000664449] Chr10:53808796 [GRCh38]
Chr10:55568556 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4671+1297_4671+1300dup duplication Usher syndrome type 1F [RCV000664454] Chr10:53809255..53809256 [GRCh38]
Chr10:55569015..55569016 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.5043_5045dup (p.Asn1682dup) duplication Usher syndrome type 1F [RCV000664456] Chr10:53806756..53806757 [GRCh38]
Chr10:55566516..55566517 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4853_4864dup (p.Lys1618_Ser1621dup) duplication Usher syndrome type 1F [RCV000664562] Chr10:53822861..53822862 [GRCh38]
Chr10:55582621..55582622 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.705+2_705+3insTT insertion Usher syndrome type 1F [RCV000673276] Chr10:54329593..54329594 [GRCh38]
Chr10:56089353..56089354 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5430_5438del (p.Leu1811_Pro1813del) deletion Usher syndrome type 1F [RCV000665848] Chr10:53822288..53822296 [GRCh38]
Chr10:55582048..55582056 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3123-1G>A single nucleotide variant Usher syndrome type 1F [RCV000665959] Chr10:53940976 [GRCh38]
Chr10:55700736 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.5753del (p.Met1918fs) deletion Usher syndrome type 1F [RCV000673504] Chr10:53821973 [GRCh38]
Chr10:55581733 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4556_4557dup (p.Asp1520fs) duplication Usher syndrome type 1F [RCV000666630] Chr10:53823168..53823169 [GRCh38]
Chr10:55582928..55582929 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5308_5310del (p.Asp1770del) deletion Usher syndrome type 1F [RCV000674817] Chr10:53822416..53822418 [GRCh38]
Chr10:55582176..55582178 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5513_5514del (p.Thr1838fs) microsatellite Usher syndrome type 1F [RCV000666319]|not provided [RCV001425523] Chr10:53822212..53822213 [GRCh38]
Chr10:55581972..55581973 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.3983+2dup duplication Usher syndrome type 1F [RCV000666352] Chr10:53840317..53840318 [GRCh38]
Chr10:55600077..55600078 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4645_4656del (p.Ala1549_Glu1552del) deletion Usher syndrome type 1F [RCV000675003] Chr10:53810571..53810582 [GRCh38]
Chr10:55570331..55570342 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5272CCT[1] (p.Pro1759_Pro1760del) microsatellite Usher syndrome type 1F [RCV000666538]|not provided [RCV001868214] Chr10:53822446..53822451 [GRCh38]
Chr10:55582206..55582211 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.1305+1del deletion Usher syndrome type 1F [RCV000667450]|not provided [RCV001379412] Chr10:54195682 [GRCh38]
Chr10:55955442 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4739_4742dup (p.Ser1581fs) duplication Usher syndrome type 1F [RCV000665074] Chr10:53807059..53807060 [GRCh38]
Chr10:55566819..55566820 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.5160TGA[2] (p.Asp1722del) microsatellite Usher syndrome type 1F [RCV000673742] Chr10:53806634..53806636 [GRCh38]
Chr10:55566394..55566396 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5257_5277del (p.Ile1753_Pro1759del) deletion Usher syndrome type 1F [RCV000666606]|not provided [RCV002530693] Chr10:53822449..53822469 [GRCh38]
Chr10:55582209..55582229 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.3416ATC[1] (p.His1140del) microsatellite Usher syndrome type 1F [RCV000667562] Chr10:53903323..53903325 [GRCh38]
Chr10:55663083..55663085 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5357dup (p.Leu1788fs) duplication Usher syndrome type 1F [RCV000667697] Chr10:53822368..53822369 [GRCh38]
Chr10:55582128..55582129 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4211+2T>G single nucleotide variant Usher syndrome type 1F [RCV000667757]|not provided [RCV000793173] Chr10:53828563 [GRCh38]
Chr10:55588323 [GRCh37]
Chr10:10q21.1		 likely pathogenic|conflicting interpretations of pathogenicity
NM_001384140.1(PCDH15):c.1A>G (p.Met1Val) single nucleotide variant Usher syndrome type 1F [RCV000667761]|not provided [RCV001295433]|not specified [RCV004689838] Chr10:54664262 [GRCh38]
Chr10:56424022 [GRCh37]
Chr10:10q21.1		 likely pathogenic|uncertain significance
GRCh37/hg19 10q21.1(chr10:55906378-56353687)x1 copy number loss not provided [RCV000683235] Chr10:55906378..56353687 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh37/hg19 10q21.1(chr10:56309824-56823236)x1 copy number loss not provided [RCV000683237] Chr10:56309824..56823236 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh37/hg19 10q21.1(chr10:55776283-55874295)x1 copy number loss not provided [RCV000683189] Chr10:55776283..55874295 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh37/hg19 10q21.1(chr10:56110143-56361476)x3 copy number gain not provided [RCV000683212] Chr10:56110143..56361476 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh37/hg19 10q21.1(chr10:54794207-56488063)x1 copy number loss not provided [RCV000683264] Chr10:54794207..56488063 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4990dup (p.Met1664fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV000714885]|Usher syndrome type 1F [RCV000714884] Chr10:53806811..53806812 [GRCh38]
Chr10:55566571..55566572 [GRCh37]
Chr10:10q21.1		 likely pathogenic|conflicting interpretations of pathogenicity
NM_001384140.1(PCDH15):c.3661C>T (p.Gln1221Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003472387]|not provided [RCV000806168] Chr10:53866698 [GRCh38]
Chr10:55626458 [GRCh37]
Chr10:10q21.1		 pathogenic|no classifications from unflagged records
GRCh37/hg19 10q21.1(chr10:55559110-55582905)x1 copy number loss not provided [RCV000737120] Chr10:55559110..55582905 [GRCh37]
Chr10:10q21.1		 benign
GRCh37/hg19 10q21.1(chr10:55943184-55991753)x3 copy number gain not provided [RCV000737121] Chr10:55943184..55991753 [GRCh37]
Chr10:10q21.1		 benign
GRCh37/hg19 10q21.1(chr10:56047470-56170113)x3 copy number gain not provided [RCV000737122] Chr10:56047470..56170113 [GRCh37]
Chr10:10q21.1		 benign
GRCh37/hg19 10q21.1(chr10:56233117-56288866)x3 copy number gain not provided [RCV000737123] Chr10:56233117..56288866 [GRCh37]
Chr10:10q21.1		 benign
GRCh37/hg19 10q21.1(chr10:56286068-56288866)x1 copy number loss not provided [RCV000737124] Chr10:56286068..56288866 [GRCh37]
Chr10:10q21.1		 benign
GRCh37/hg19 10q21.1(chr10:56423968-56469288)x3 copy number gain not provided [RCV000737125] Chr10:56423968..56469288 [GRCh37]
Chr10:10q21.1		 benign
GRCh37/hg19 10q21.1(chr10:56441012-56467563)x3 copy number gain not provided [RCV000737126] Chr10:56441012..56467563 [GRCh37]
Chr10:10q21.1		 benign
GRCh37/hg19 10q21.1(chr10:56452411-56480111)x3 copy number gain not provided [RCV000737127] Chr10:56452411..56480111 [GRCh37]
Chr10:10q21.1		 benign
GRCh37/hg19 10q21.1(chr10:56503477-57540235)x3 copy number gain not provided [RCV000737128] Chr10:56503477..57540235 [GRCh37]
Chr10:10q21.1		 benign
GRCh37/hg19 10q21.1(chr10:56523671-56573906)x3 copy number gain not provided [RCV000737129] Chr10:56523671..56573906 [GRCh37]
Chr10:10q21.1		 benign
NC_000010.11:g.(?_53976705)_(54036062_?)del deletion Autism [RCV000754120] Chr10:53976705..54036062 [GRCh38]
Chr10:10q21.1		 likely pathogenic
NC_000010.11:g.(?_54690788)_(54898513_?)del deletion Schizophrenia [RCV000754121] Chr10:54690788..54898513 [GRCh38]
Chr10:10q21.1		 likely pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:98087-135477883)x3 copy number gain not provided [RCV000749465] Chr10:98087..135477883 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
GRCh37/hg19 10p15.3-q26.3(chr10:73232-135524321)x3 copy number gain not provided [RCV000749464] Chr10:73232..135524321 [GRCh37]
Chr10:10p15.3-q26.3		 pathogenic
NM_001384140.1(PCDH15):c.2092-168C>T single nucleotide variant not provided [RCV001708706] Chr10:54067053 [GRCh38]
Chr10:55826813 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.2092-148T>A single nucleotide variant not provided [RCV001667354] Chr10:54067033 [GRCh38]
Chr10:55826793 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.2001G>C (p.Thr667=) single nucleotide variant not provided [RCV001487319] Chr10:54079421 [GRCh38]
Chr10:55839181 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.474+183A>G single nucleotide variant not provided [RCV001645070] Chr10:54368937 [GRCh38]
Chr10:56128697 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.92-501C>T single nucleotide variant not provided [RCV000977221] Chr10:54528378 [GRCh38]
Chr10:56288138 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5646C>T (p.Ile1882=) single nucleotide variant not provided [RCV000941417] Chr10:53822080 [GRCh38]
Chr10:55581840 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1320G>A (p.Glu440=) single nucleotide variant not provided [RCV000941549] Chr10:54185254 [GRCh38]
Chr10:55945014 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3232+10C>T single nucleotide variant not provided [RCV000941638] Chr10:53940856 [GRCh38]
Chr10:55700616 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2527-293C>T single nucleotide variant not provided [RCV001566252] Chr10:54020709 [GRCh38]
Chr10:55780469 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4208A>G (p.Lys1403Arg) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001578696]|Usher syndrome type 1F [RCV001578697]|not provided [RCV001866083] Chr10:53828568 [GRCh38]
Chr10:55588328 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3373+9T>C single nucleotide variant not provided [RCV000978692] Chr10:53938806 [GRCh38]
Chr10:55698566 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1843C>T (p.Arg615Cys) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001578645]|Usher syndrome type 1F [RCV001578646]|not provided [RCV002573244] Chr10:54132949 [GRCh38]
Chr10:55892709 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.10:g.(55839185_55849743)_(55892768_55912859)del deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV000761612] Chr10:54089983..54133008 [GRCh38]
Chr10:55849743..55892768 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.556C>T (p.Gln186Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003473548]|Usher syndrome type 1 [RCV001004340]|Usher syndrome type 1F [RCV002549240]|not provided [RCV003769404] Chr10:54346403 [GRCh38]
Chr10:56106163 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
GRCh37/hg19 10q11.22-21.1(chr10:49390457-60061643)x1 copy number loss not provided [RCV000762699] Chr10:49390457..60061643 [GRCh37]
Chr10:10q11.22-21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1441-102del deletion not provided [RCV001568977] Chr10:54183695 [GRCh38]
Chr10:55943455 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.*144GA[4] microsatellite not provided [RCV001669315] Chr10:53806431..53806432 [GRCh38]
Chr10:55566191..55566192 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.2868+1G>A single nucleotide variant not provided [RCV000994399] Chr10:53995648 [GRCh38]
Chr10:55755408 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.725A>C (p.Asn242Thr) single nucleotide variant Usher syndrome type 1F [RCV001827341]|not provided [RCV001054417] Chr10:54317422 [GRCh38]
Chr10:56077182 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh37/hg19 10q21.1(chr10:55581618-56288162)x6 copy number gain not provided [RCV000994529] Chr10:55581618..56288162 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4367+1949G>A single nucleotide variant not provided [RCV001546692] Chr10:53825444 [GRCh38]
Chr10:55585204 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.876+246T>A single nucleotide variant not provided [RCV001581658] Chr10:54317025 [GRCh38]
Chr10:56076785 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2751+146A>G single nucleotide variant not provided [RCV001577920] Chr10:54020046 [GRCh38]
Chr10:55779806 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.706-106C>A single nucleotide variant not provided [RCV001570543] Chr10:54317547 [GRCh38]
Chr10:56077307 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4671+965G>C single nucleotide variant not provided [RCV001567071] Chr10:53809591 [GRCh38]
Chr10:55569351 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1891G>T (p.Val631Phe) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001578647]|Usher syndrome type 1F [RCV001578648] Chr10:54132901 [GRCh38]
Chr10:55892661 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3832C>A (p.Gln1278Lys) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001578702]|Usher syndrome type 1F [RCV001578703] Chr10:53840471 [GRCh38]
Chr10:55600231 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5847_5848del (p.His1949fs) microsatellite Progressive cone dystrophy (without rod involvement) [RCV000787857] Chr10:53821878..53821879 [GRCh38]
Chr10:55581638..55581639 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.4794G>A (p.Gln1598=) single nucleotide variant Usher syndrome type 1F [RCV001272403]|not provided [RCV000981570] Chr10:53822932 [GRCh38]
Chr10:55582692 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5256T>A (p.Pro1752=) single nucleotide variant not provided [RCV000944592] Chr10:53822470 [GRCh38]
Chr10:55582230 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1440+7A>C single nucleotide variant Usher syndrome type 1F [RCV001275399]|not provided [RCV000900635] Chr10:54185127 [GRCh38]
Chr10:55944887 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.3687G>A (p.Gly1229=) single nucleotide variant not provided [RCV000929269] Chr10:53866672 [GRCh38]
Chr10:55626432 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3900A>G (p.Leu1300=) single nucleotide variant not provided [RCV000925768] Chr10:53840403 [GRCh38]
Chr10:55600163 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.402A>G (p.Arg134=) single nucleotide variant not provided [RCV000927495] Chr10:54369192 [GRCh38]
Chr10:56128952 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2026C>T (p.Leu676=) single nucleotide variant Usher syndrome type 1F [RCV001826929]|not provided [RCV000926833] Chr10:54079396 [GRCh38]
Chr10:55839156 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2014T>C (p.Leu672=) single nucleotide variant not provided [RCV000926834] Chr10:54079408 [GRCh38]
Chr10:55839168 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2262C>T (p.Tyr754=) single nucleotide variant not provided [RCV000928636] Chr10:54023156 [GRCh38]
Chr10:55782916 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4698A>G (p.Pro1566=) single nucleotide variant not provided [RCV000943181] Chr10:53823028 [GRCh38]
Chr10:55582788 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4671+1327T>C single nucleotide variant not provided [RCV000975932] Chr10:53809229 [GRCh38]
Chr10:55568989 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4671+1396A>G single nucleotide variant not provided [RCV000943616] Chr10:53809160 [GRCh38]
Chr10:55568920 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2445C>T (p.Asn815=) single nucleotide variant PCDH15-related disorder [RCV004735892]|Usher syndrome type 1 [RCV001104966]|Usher syndrome type 1F [RCV001826933]|not provided [RCV000927706] Chr10:54022973 [GRCh38]
Chr10:55782733 [GRCh37]
Chr10:10q21.1		 benign|likely benign|uncertain significance
NM_001384140.1(PCDH15):c.1306-4111A>C single nucleotide variant not provided [RCV000944301] Chr10:54189379 [GRCh38]
Chr10:55949139 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4542A>G (p.Thr1514=) single nucleotide variant Usher syndrome type 1F [RCV001272406]|not provided [RCV000903776] Chr10:53823184 [GRCh38]
Chr10:55582944 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4367+2262_4367+2265del microsatellite not provided [RCV000947251] Chr10:53825128..53825131 [GRCh38]
Chr10:55584888..55584891 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1602C>G (p.Val534=) single nucleotide variant not provided [RCV000941857] Chr10:54153282 [GRCh38]
Chr10:55913042 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1441-7C>T single nucleotide variant not provided [RCV000902127] Chr10:54183600 [GRCh38]
Chr10:55943360 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2268G>A (p.Leu756=) single nucleotide variant not provided [RCV000902989] Chr10:54023150 [GRCh38]
Chr10:55782910 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4897T>C (p.Leu1633=) single nucleotide variant not provided [RCV000981031] Chr10:53822829 [GRCh38]
Chr10:55582589 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3450C>T (p.Ile1150=) single nucleotide variant Usher syndrome type 1F [RCV001273389]|not provided [RCV000928337] Chr10:53903294 [GRCh38]
Chr10:55663054 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2868+10A>C single nucleotide variant not provided [RCV000942137] Chr10:53995639 [GRCh38]
Chr10:55755399 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5055A>G (p.Ser1685=) single nucleotide variant not provided [RCV000983601] Chr10:53822671 [GRCh38]
Chr10:55582431 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3502-7C>T single nucleotide variant Usher syndrome type 1F [RCV001278203]|not provided [RCV000927316] Chr10:53866864 [GRCh38]
Chr10:55626624 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4177T>C (p.Leu1393=) single nucleotide variant not provided [RCV000983599] Chr10:53831340 [GRCh38]
Chr10:55591100 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2856T>C (p.Asp952=) single nucleotide variant not provided [RCV000944786] Chr10:53995661 [GRCh38]
Chr10:55755421 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4039G>A (p.Glu1347Lys) single nucleotide variant Usher syndrome type 1F [RCV001828528]|not provided [RCV001071339] Chr10:53831478 [GRCh38]
Chr10:55591238 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.11:g.(?_54346355)_(54378952_?)dup duplication not provided [RCV001033789] Chr10:56106115..56138712 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2001G>A (p.Thr667=) single nucleotide variant Usher syndrome type 1F [RCV001275396]|not provided [RCV001050345] Chr10:54079421 [GRCh38]
Chr10:55839181 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.11:g.(?_53806579)_(54664262_?)del deletion not provided [RCV001033835] Chr10:55566339..56424022 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3984-6A>G single nucleotide variant Usher syndrome [RCV002274123]|not provided [RCV001044214] Chr10:53831539 [GRCh38]
Chr10:55591299 [GRCh37]
Chr10:10q21.1		 pathogenic|uncertain significance
NM_033056.4(PCDH15):c.4644_4689dup (p.Arg1564delinsCysArgProIlePheThrGlnAsnThrSerGlnGluTer) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV002497397]|not provided [RCV001050776] Chr10:53823036..53823037 [GRCh38]
Chr10:55582796..55582797 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.5375C>G (p.Pro1792Arg) single nucleotide variant not provided [RCV001067444] Chr10:53822351 [GRCh38]
Chr10:55582111 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh37/hg19 10q11.23-21.3(chr10:50250603-69256083)x1 copy number loss not provided [RCV001006319] Chr10:50250603..69256083 [GRCh37]
Chr10:10q11.23-21.3		 pathogenic
NM_033056.4(PCDH15):c.5216A>T (p.Asn1739Ile) single nucleotide variant Usher syndrome type 1F [RCV001833657]|not provided [RCV001068076] Chr10:53822510 [GRCh38]
Chr10:55582270 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.944C>T (p.Pro315Leu) single nucleotide variant Usher syndrome type 1 [RCV001105073]|Usher syndrome type 1F [RCV001276786]|not provided [RCV001045508]|not specified [RCV001553688] Chr10:54236864 [GRCh38]
Chr10:55996624 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3501+6C>T single nucleotide variant Usher syndrome type 1F [RCV001832437]|not provided [RCV001046172] Chr10:53903237 [GRCh38]
Chr10:55662997 [GRCh37]
Chr10:10q21.1		 conflicting interpretations of pathogenicity|uncertain significance
NC_000010.11:g.(?_54369120)_(54378942_?)del deletion not provided [RCV001033422] Chr10:56128880..56138702 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.11:g.(?_53903233)_(53903380_?)del deletion not provided [RCV001033448] Chr10:55662993..55663140 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.11:g.(?_53806569)_(54528412_?)del deletion not provided [RCV001032670] Chr10:55566329..56288172 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.11:g.(?_54369110)_(54378952_?)dup duplication not provided [RCV001031877] Chr10:56128870..56138712 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1898C>T (p.Ala633Val) single nucleotide variant Usher syndrome type 1F [RCV001827257]|not provided [RCV001042753] Chr10:54132894 [GRCh38]
Chr10:55892654 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.11:g.(?_53806569)_(54664272_?)del deletion not provided [RCV001032018] Chr10:55566329..56424032 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2869-1G>A single nucleotide variant not provided [RCV001048167] Chr10:53961893 [GRCh38]
Chr10:55721653 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NC_000010.11:g.(?_54527802)_(54664272_?)del deletion not provided [RCV001032062] Chr10:56287562..56424032 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.11:g.(?_53903233)_(54664272_?)del deletion not provided [RCV001032096] Chr10:55662993..56424032 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3700G>A (p.Gly1234Ser) single nucleotide variant Usher syndrome type 1F [RCV001273384]|not provided [RCV001049185] Chr10:53866659 [GRCh38]
Chr10:55626419 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1979T>A (p.Val660Asp) single nucleotide variant Usher syndrome type 1F [RCV001276782]|not provided [RCV001043655] Chr10:54090002 [GRCh38]
Chr10:55849762 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4553A>T (p.Asp1518Val) single nucleotide variant Usher syndrome type 1F [RCV001272405]|not provided [RCV001049631] Chr10:53823173 [GRCh38]
Chr10:55582933 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4671+1206G>T single nucleotide variant not specified [RCV000825429] Chr10:53809350 [GRCh38]
Chr10:55569110 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4308GCC[7] (p.Pro1442_Pro1443dup) microsatellite Autosomal recessive nonsyndromic hearing loss 23 [RCV002493398]|PCDH15-related disorder [RCV004540089]|Usher syndrome type 1F [RCV000768426]|not provided [RCV000891458]|not specified [RCV001195202] Chr10:53827437..53827438 [GRCh38]
Chr10:55587197..55587198 [GRCh37]
Chr10:10q21.1		 likely pathogenic|benign|likely benign|conflicting interpretations of pathogenicity
NM_001384140.1(PCDH15):c.319-251G>T single nucleotide variant not provided [RCV000826709] Chr10:54369526 [GRCh38]
Chr10:56129286 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1475dup (p.Val493fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV004569625]|not provided [RCV000805838] Chr10:54183558..54183559 [GRCh38]
Chr10:55943318..55943319 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_033056.3:c.92-13779_157+41368del deletion Usher syndrome, type 1F [RCV000781936] Chr10:10q21.1 pathogenic
NM_033056.4(PCDH15):c.5486del (p.Pro1829fs) deletion PCDH15-related disorder [RCV000778286]|not provided [RCV002067365] Chr10:53822240 [GRCh38]
Chr10:55582000 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.2196C>T (p.Ala732=) single nucleotide variant not provided [RCV000907987] Chr10:54066781 [GRCh38]
Chr10:55826541 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5481C>T (p.Cys1827=) single nucleotide variant not provided [RCV000928086] Chr10:53822245 [GRCh38]
Chr10:55582005 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3456T>C (p.Gly1152=) single nucleotide variant Usher syndrome type 1 [RCV001106032]|Usher syndrome type 1F [RCV001273387]|not provided [RCV000941532] Chr10:53903288 [GRCh38]
Chr10:55663048 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.4575T>C (p.His1525=) single nucleotide variant Usher syndrome type 1F [RCV001274786]|not provided [RCV000928314] Chr10:53823151 [GRCh38]
Chr10:55582911 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4329A>C (p.Pro1443=) single nucleotide variant not provided [RCV000977223] Chr10:53827431 [GRCh38]
Chr10:55587191 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4733_4734delinsCT (p.Val1578Ala) indel not provided [RCV000980611] Chr10:53822992..53822993 [GRCh38]
Chr10:55582752..55582753 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3522C>A (p.Gly1174=) single nucleotide variant Usher syndrome type 1F [RCV001273385]|not provided [RCV000976453] Chr10:53866837 [GRCh38]
Chr10:55626597 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.969C>A (p.Leu323=) single nucleotide variant Usher syndrome type 1F [RCV001825811]|not provided [RCV000898881] Chr10:54236839 [GRCh38]
Chr10:55996599 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1245G>A (p.Ser415=) single nucleotide variant not provided [RCV000975325] Chr10:54195743 [GRCh38]
Chr10:55955503 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4770T>C (p.Asn1590=) single nucleotide variant Usher syndrome type 1F [RCV001274783]|not provided [RCV000979463] Chr10:53822956 [GRCh38]
Chr10:55582716 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.678T>C (p.Thr226=) single nucleotide variant not provided [RCV000979468] Chr10:54329623 [GRCh38]
Chr10:56089383 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1306-6dup duplication not provided [RCV000941620] Chr10:54185273..54185274 [GRCh38]
Chr10:55945033..55945034 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.3147C>G (p.Ala1049=) single nucleotide variant not provided [RCV000920934] Chr10:53940951 [GRCh38]
Chr10:55700711 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2325G>A (p.Val775=) single nucleotide variant Usher syndrome type 1F [RCV001278213]|not provided [RCV000942125] Chr10:54023093 [GRCh38]
Chr10:55782853 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2223A>G (p.Ala741=) single nucleotide variant PCDH15-related disorder [RCV004530939]|not provided [RCV000886760] Chr10:54023195 [GRCh38]
Chr10:55782955 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4672-1577C>T single nucleotide variant not provided [RCV000943568] Chr10:53808707 [GRCh38]
Chr10:55568467 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.93T>C (p.Asp31=) single nucleotide variant not provided [RCV000981276] Chr10:54527876 [GRCh38]
Chr10:56287636 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4881A>C (p.Thr1627=) single nucleotide variant not provided [RCV000941866] Chr10:53822845 [GRCh38]
Chr10:55582605 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.297C>G (p.Thr99=) single nucleotide variant Usher syndrome type 1F [RCV001832161]|not provided [RCV000941868] Chr10:54378803 [GRCh38]
Chr10:56138563 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3489A>G (p.Val1163=) single nucleotide variant not provided [RCV000978417] Chr10:53903255 [GRCh38]
Chr10:55663015 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4626T>C (p.Tyr1542=) single nucleotide variant not provided [RCV000977277] Chr10:53810601 [GRCh38]
Chr10:55570361 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4080G>C (p.Val1360=) single nucleotide variant not provided [RCV000945194] Chr10:53831437 [GRCh38]
Chr10:55591197 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4772G>A (p.Arg1591Lys) single nucleotide variant Inborn genetic diseases [RCV002548323]|Usher syndrome type 1F [RCV001277671]|not provided [RCV000967758] Chr10:53822954 [GRCh38]
Chr10:55582714 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.1306-4110C>T single nucleotide variant not provided [RCV000942605] Chr10:54189378 [GRCh38]
Chr10:55949138 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1195A>C (p.Ser399Arg) single nucleotide variant Usher syndrome type 1F [RCV001832137]|not provided [RCV000937218] Chr10:54195793 [GRCh38]
Chr10:55955553 [GRCh37]
Chr10:10q21.1		 benign|likely benign|conflicting interpretations of pathogenicity
NM_001384140.1(PCDH15):c.1605C>T (p.Asp535=) single nucleotide variant not provided [RCV000979801] Chr10:54153279 [GRCh38]
Chr10:55913039 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.882A>G (p.Glu294=) single nucleotide variant Usher syndrome type 1F [RCV001275403]|not provided [RCV000922102] Chr10:54236926 [GRCh38]
Chr10:55996686 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.4560T>C (p.Asp1520=) single nucleotide variant not provided [RCV000978617] Chr10:53823166 [GRCh38]
Chr10:55582926 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4260C>T (p.Pro1420=) single nucleotide variant Usher syndrome type 1 [RCV001102955]|Usher syndrome type 1F [RCV001272408]|not provided [RCV000942067] Chr10:53827500 [GRCh38]
Chr10:55587260 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4308G>T (p.Pro1436=) single nucleotide variant Usher syndrome type 1F [RCV001827082]|not provided [RCV000977657] Chr10:53827452 [GRCh38]
Chr10:55587212 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1809T>C (p.Ile603=) single nucleotide variant not provided [RCV000977213] Chr10:54132983 [GRCh38]
Chr10:55892743 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4254A>G (p.Ala1418=) single nucleotide variant not provided [RCV000979952] Chr10:53827506 [GRCh38]
Chr10:55587266 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4611A>T (p.Ser1537=) single nucleotide variant not provided [RCV000943807] Chr10:53823115 [GRCh38]
Chr10:55582875 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4203-7C>T single nucleotide variant not provided [RCV000978792] Chr10:53828580 [GRCh38]
Chr10:55588340 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2691G>A (p.Glu897=) single nucleotide variant not provided [RCV000980117] Chr10:54020252 [GRCh38]
Chr10:55780012 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5557A>T (p.Met1853Leu) single nucleotide variant not provided [RCV000932457] Chr10:53822169 [GRCh38]
Chr10:55581929 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5406G>T (p.Thr1802=) single nucleotide variant Usher syndrome type 1F [RCV001832251]|not provided [RCV000977649] Chr10:53822320 [GRCh38]
Chr10:55582080 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5004C>T (p.His1668=) single nucleotide variant not provided [RCV000938819] Chr10:53822722 [GRCh38]
Chr10:55582482 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2752-8T>C single nucleotide variant not provided [RCV000980236] Chr10:53995773 [GRCh38]
Chr10:55755533 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.92-13796_92-13795insC insertion not specified [RCV000780577] Chr10:54541672..54541673 [GRCh38]
Chr10:56301432..56301433 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3012G>C (p.Leu1004Phe) single nucleotide variant not provided [RCV003314809] Chr10:53959842 [GRCh38]
Chr10:55719602 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5254_5280del (p.Pro1752_Pro1760del) deletion Usher syndrome type 1F [RCV000768425]|not provided [RCV001248285] Chr10:53822446..53822472 [GRCh38]
Chr10:55582206..55582232 [GRCh37]
Chr10:10q21.1		 likely pathogenic|likely benign|uncertain significance
GRCh37/hg19 10q21.1-21.2(chr10:55589950-63990649)x1 copy number loss not provided [RCV001006325] Chr10:55589950..63990649 [GRCh37]
Chr10:10q21.1-21.2		 pathogenic
NM_001384140.1(PCDH15):c.2400T>C (p.His800=) single nucleotide variant not provided [RCV000841015] Chr10:54023018 [GRCh38]
Chr10:55782778 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2208G>A (p.Val736=) single nucleotide variant not provided [RCV000841323] Chr10:54066769 [GRCh38]
Chr10:55826529 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3951C>T (p.Thr1317=) single nucleotide variant Usher syndrome type 1F [RCV001272410]|not provided [RCV000922871]|not specified [RCV000825809] Chr10:53840352 [GRCh38]
Chr10:55600112 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5642G>T (p.Gly1881Val) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002487870]|Inborn genetic diseases [RCV003353068]|Usher syndrome type 1F [RCV001825687]|not provided [RCV001585772]|not specified [RCV000826015] Chr10:53822084 [GRCh38]
Chr10:55581844 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4203-151C>A single nucleotide variant Usher syndrome type 1F [RCV001533687]|not provided [RCV000829558] Chr10:53828724 [GRCh38]
Chr10:55588484 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.877-94C>T single nucleotide variant not provided [RCV000834831] Chr10:54237025 [GRCh38]
Chr10:55996785 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.985+175T>A single nucleotide variant not provided [RCV000838452] Chr10:54236648 [GRCh38]
Chr10:55996408 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.705+133T>C single nucleotide variant not provided [RCV000838453] Chr10:54329463 [GRCh38]
Chr10:56089223 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.705+190G>A single nucleotide variant not provided [RCV000838454] Chr10:54329406 [GRCh38]
Chr10:56089166 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.705+225T>C single nucleotide variant not provided [RCV000838455] Chr10:54329371 [GRCh38]
Chr10:56089131 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1591-214A>C single nucleotide variant not provided [RCV000838456] Chr10:54153507 [GRCh38]
Chr10:55913267 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1784+179G>A single nucleotide variant not provided [RCV000838457] Chr10:54152921 [GRCh38]
Chr10:55912681 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1590+239T>C single nucleotide variant not provided [RCV000838459] Chr10:54183205 [GRCh38]
Chr10:55942965 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1917+233G>A single nucleotide variant not provided [RCV000838460] Chr10:54132642 [GRCh38]
Chr10:55892402 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.2221-189T>A single nucleotide variant not provided [RCV000838464] Chr10:54023386 [GRCh38]
Chr10:55783146 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.2751+192G>T single nucleotide variant not provided [RCV000838465] Chr10:54020000 [GRCh38]
Chr10:55779760 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.2868+172G>A single nucleotide variant not provided [RCV000838466] Chr10:53995477 [GRCh38]
Chr10:55755237 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.2869-193dup duplication not provided [RCV000838467] Chr10:53962084..53962085 [GRCh38]
Chr10:55721844..55721845 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.2752-75C>G single nucleotide variant Usher syndrome type 1F [RCV001533756]|not provided [RCV000838468] Chr10:53995840 [GRCh38]
Chr10:55755600 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.2869-109T>C single nucleotide variant Usher syndrome type 1F [RCV001533754]|not provided [RCV000838469] Chr10:53962001 [GRCh38]
Chr10:55721761 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3123-244A>C single nucleotide variant not provided [RCV000838470] Chr10:53941219 [GRCh38]
Chr10:55700979 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3123-238A>G single nucleotide variant not provided [RCV000838471] Chr10:53941213 [GRCh38]
Chr10:55700973 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4211+188C>T single nucleotide variant not provided [RCV000838476] Chr10:53828377 [GRCh38]
Chr10:55588137 [GRCh37]
Chr10:10q21.1		 benign
NM_033056.4(PCDH15):c.5547G>A (p.Thr1849=) single nucleotide variant Usher syndrome type 1F [RCV001272396]|not provided [RCV000976405] Chr10:53822179 [GRCh38]
Chr10:55581939 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.4846A>G (p.Thr1616Ala) single nucleotide variant Usher syndrome type 1F [RCV001830837]|not provided [RCV001347012]|not specified [RCV000825425] Chr10:53822880 [GRCh38]
Chr10:55582640 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.11:g.54369306A>G single nucleotide variant not provided [RCV000829536] Chr10:56129066 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1098+107G>A single nucleotide variant not provided [RCV000829539] Chr10:54213829 [GRCh38]
Chr10:55973589 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3502-6G>A single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002489251]|Usher syndrome type 1F [RCV001273386]|not provided [RCV000936505] Chr10:53866863 [GRCh38]
Chr10:55626623 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.91+289G>A single nucleotide variant not provided [RCV000826708] Chr10:54663883 [GRCh38]
Chr10:56423643 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.705+288C>G single nucleotide variant not provided [RCV000826711] Chr10:54329308 [GRCh38]
Chr10:56089068 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3010-343T>C single nucleotide variant not provided [RCV000826729] Chr10:53960187 [GRCh38]
Chr10:55719947 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3010-342T>C single nucleotide variant not provided [RCV000826730] Chr10:53960186 [GRCh38]
Chr10:55719946 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1209T>G (p.Tyr403Ter) single nucleotide variant PCDH15-related disorder [RCV004735805]|Usher syndrome type 1F [RCV002536992]|not provided [RCV000795013] Chr10:54195779 [GRCh38]
Chr10:55955539 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.4367+88A>G single nucleotide variant Usher syndrome type 1F [RCV001533686]|not provided [RCV000835225] Chr10:53827305 [GRCh38]
Chr10:55587065 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.2868+69G>A single nucleotide variant Usher syndrome type 1F [RCV001533755]|not provided [RCV000835334] Chr10:53995580 [GRCh38]
Chr10:55755340 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.2868+8G>T single nucleotide variant not provided [RCV000827563] Chr10:53995641 [GRCh38]
Chr10:55755401 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2751+9T>C single nucleotide variant Usher syndrome type 1F [RCV001832223]|not provided [RCV000975584] Chr10:54020183 [GRCh38]
Chr10:55779943 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.986-208_986-205del deletion not provided [RCV000838458] Chr10:54214253..54214256 [GRCh38]
Chr10:55974013..55974016 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3374-72A>G single nucleotide variant Usher syndrome type 1F [RCV001533693]|not provided [RCV000833705] Chr10:53903442 [GRCh38]
Chr10:55663202 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3374-68T>G single nucleotide variant Usher syndrome type 1F [RCV001533692]|not provided [RCV000833706] Chr10:53903438 [GRCh38]
Chr10:55663198 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3717+35T>C single nucleotide variant Usher syndrome type 1F [RCV001533691]|not provided [RCV000833707] Chr10:53866607 [GRCh38]
Chr10:55626367 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1591-68G>A single nucleotide variant Usher syndrome type 1F [RCV001533758]|not provided [RCV000838462] Chr10:54153361 [GRCh38]
Chr10:55913121 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.2091+141T>C single nucleotide variant not provided [RCV000838463] Chr10:54079190 [GRCh38]
Chr10:55838950 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4202+225C>T single nucleotide variant not provided [RCV000838477] Chr10:53831090 [GRCh38]
Chr10:55590850 [GRCh37]
Chr10:10q21.1		 benign
NM_033056.4(PCDH15):c.5338C>T (p.Pro1780Ser) single nucleotide variant Usher syndrome type 1F [RCV001825680]|not specified [RCV000825427] Chr10:53822388 [GRCh38]
Chr10:55582148 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.462C>T (p.Ala154=) single nucleotide variant not provided [RCV001441143]|not specified [RCV000825810] Chr10:54369132 [GRCh38]
Chr10:56128892 [GRCh37]
Chr10:10q21.1		 likely benign
GRCh37/hg19 10q21.1(chr10:54276542-58024820)x1 copy number loss not provided [RCV000848495] Chr10:54276542..58024820 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh37/hg19 10q21.1(chr10:55468897-55645953)x1 copy number loss not provided [RCV000848528] Chr10:55468897..55645953 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.366del (p.Asn122fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003473520]|not provided [RCV000823168] Chr10:54369228 [GRCh38]
Chr10:56128988 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.595-252G>A single nucleotide variant not provided [RCV000826710] Chr10:54329958 [GRCh38]
Chr10:56089718 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3123-333A>G single nucleotide variant not provided [RCV000826731] Chr10:53941308 [GRCh38]
Chr10:55701068 [GRCh37]
Chr10:10q21.1		 benign
GRCh37/hg19 10q21.1(chr10:54976143-55915352)x1 copy number loss not provided [RCV000848909] Chr10:54976143..55915352 [GRCh37]
Chr10:10q21.1		 pathogenic
GRCh37/hg19 10q21.1(chr10:55938132-56040206)x1 copy number loss not provided [RCV000849295] Chr10:55938132..56040206 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3984-170_3984-168del microsatellite not provided [RCV000838474] Chr10:53831701..53831703 [GRCh38]
Chr10:55591461..55591463 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4367+119T>C single nucleotide variant Usher syndrome type 1F [RCV001533685]|not provided [RCV000829559] Chr10:53827274 [GRCh38]
Chr10:55587034 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4368-3131A>C single nucleotide variant not specified [RCV000784930] Chr10:53823361 [GRCh38]
Chr10:55583121 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1167del (p.Asn389fs) deletion Usher syndrome [RCV000826125]|not provided [RCV003542315] Chr10:54195821 [GRCh38]
Chr10:55955581 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.1863T>G (p.Tyr621Ter) single nucleotide variant Usher syndrome type 1F [RCV000988362]|not provided [RCV002549707] Chr10:54132929 [GRCh38]
Chr10:55892689 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2000C>T (p.Thr667Met) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002479330]|Inborn genetic diseases [RCV004031712]|Usher syndrome type 1F [RCV001274798]|not provided [RCV001054370] Chr10:54079422 [GRCh38]
Chr10:55839182 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.877-70G>A single nucleotide variant not provided [RCV000829537] Chr10:54237001 [GRCh38]
Chr10:55996761 [GRCh37]
Chr10:10q21.1		 benign
NC_000010.11:g.53959892C>T single nucleotide variant not provided [RCV000829541] Chr10:55719652 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4203-162T>C single nucleotide variant Usher syndrome type 1F [RCV001533688]|not provided [RCV000829542] Chr10:53828735 [GRCh38]
Chr10:55588495 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1712T>C (p.Val571Ala) single nucleotide variant Inborn genetic diseases [RCV002553781]|Usher syndrome type 1F [RCV001832497]|not provided [RCV001054785] Chr10:54153172 [GRCh38]
Chr10:55912932 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.602A>G (p.Asn201Ser) single nucleotide variant Usher syndrome type 1F [RCV001827350]|not provided [RCV001054955] Chr10:54329699 [GRCh38]
Chr10:56089459 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3711T>C (p.Asp1237=) single nucleotide variant Usher syndrome type 1F [RCV001273383]|not provided [RCV000978276] Chr10:53866648 [GRCh38]
Chr10:55626408 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.876+271A>G single nucleotide variant not provided [RCV000833192] Chr10:54317000 [GRCh38]
Chr10:56076760 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.321A>C (p.Pro107=) single nucleotide variant Usher syndrome type 1F [RCV001275405]|not provided [RCV000978631] Chr10:54369273 [GRCh38]
Chr10:56129033 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4343_4344del (p.Leu1447_Tyr1448insTer) deletion not specified [RCV000825426] Chr10:53827416..53827417 [GRCh38]
Chr10:55587176..55587177 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.169G>A (p.Val57Met) single nucleotide variant not specified [RCV000826012] Chr10:54378931 [GRCh38]
Chr10:56138691 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.706-21G>T single nucleotide variant not provided [RCV000844364] Chr10:54317462 [GRCh38]
Chr10:56077222 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4671+1067G>A single nucleotide variant not provided [RCV000942193] Chr10:53809489 [GRCh38]
Chr10:55569249 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3946del (p.Gln1316fs) deletion not provided [RCV000794642] Chr10:53840357 [GRCh38]
Chr10:55600117 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.986-259A>T single nucleotide variant not provided [RCV000826728] Chr10:54214307 [GRCh38]
Chr10:55974067 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.986-81C>T single nucleotide variant Usher syndrome type 1F [RCV001533761]|not provided [RCV000829538] Chr10:54214129 [GRCh38]
Chr10:55973889 [GRCh37]
Chr10:10q21.1		 benign
NC_000010.11:g.54020155G>A single nucleotide variant not provided [RCV000829540] Chr10:55779915 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3718-154A>G single nucleotide variant not provided [RCV000838472] Chr10:53857417 [GRCh38]
Chr10:55617177 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3502-133C>T single nucleotide variant not provided [RCV000838473] Chr10:53866990 [GRCh38]
Chr10:55626750 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.595-101G>A single nucleotide variant not provided [RCV000838484] Chr10:54329807 [GRCh38]
Chr10:56089567 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1611C>T (p.Asp537=) single nucleotide variant not provided [RCV000940508] Chr10:54153273 [GRCh38]
Chr10:55913033 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3669T>C (p.Ile1223=) single nucleotide variant not provided [RCV000976699] Chr10:53866690 [GRCh38]
Chr10:55626450 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1912C>T (p.Leu638=) single nucleotide variant Usher syndrome type 1F [RCV001826992]|not provided [RCV000941544] Chr10:54132880 [GRCh38]
Chr10:55892640 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1524C>G (p.Thr508=) single nucleotide variant not provided [RCV000898087] Chr10:54183510 [GRCh38]
Chr10:55943270 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1917+98C>A single nucleotide variant not provided [RCV000839187] Chr10:54132777 [GRCh38]
Chr10:55892537 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4202+129_4202+132del microsatellite not provided [RCV000838475] Chr10:53831183..53831186 [GRCh38]
Chr10:55590943..55590946 [GRCh37]
Chr10:10q21.1		 benign
NC_000010.11:g.54020149G>C single nucleotide variant not provided [RCV000835831] Chr10:55779909 [GRCh37]
Chr10:10q21.1		 benign
NM_033056.4(PCDH15):c.5849_5852del (p.Ser1950fs) deletion Usher syndrome type 1F [RCV001827380]|not provided [RCV001060374] Chr10:53821874..53821877 [GRCh38]
Chr10:55581634..55581637 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4933C>T (p.Leu1645=) single nucleotide variant Usher syndrome type 1F [RCV001832061]|not provided [RCV000914199] Chr10:53822793 [GRCh38]
Chr10:55582553 [GRCh37]
Chr10:10q21.1		 likely benign
GRCh37/hg19 10q21.1(chr10:55942657-56054330)x1 copy number loss not provided [RCV000849853] Chr10:55942657..56054330 [GRCh37]
Chr10:10q21.1		 pathogenic
GRCh37/hg19 10q21.1(chr10:55824016-56468477)x1 copy number loss not provided [RCV000849552] Chr10:55824016..56468477 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.42G>T (p.Gly14=) single nucleotide variant not provided [RCV001055601] Chr10:54664221 [GRCh38]
Chr10:56423981 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4303C>T (p.Pro1435Ser) single nucleotide variant Usher syndrome type 1F [RCV001835331]|not provided [RCV001248289] Chr10:53827457 [GRCh38]
Chr10:55587217 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4127C>T (p.Ala1376Val) single nucleotide variant Inborn genetic diseases [RCV004035280]|Usher syndrome type 1F [RCV001835334]|not provided [RCV001248418] Chr10:53831390 [GRCh38]
Chr10:55591150 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4064G>A (p.Arg1355Gln) single nucleotide variant Usher syndrome type 1F [RCV001834055]|not provided [RCV001236594] Chr10:53831453 [GRCh38]
Chr10:55591213 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.355C>T (p.Gln119Ter) single nucleotide variant not provided [RCV001209140] Chr10:54369239 [GRCh38]
Chr10:56128999 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3673A>G (p.Thr1225Ala) single nucleotide variant Inborn genetic diseases [RCV004034667]|Usher syndrome type 1F [RCV001828963]|not provided [RCV001240938] Chr10:53866686 [GRCh38]
Chr10:55626446 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4810A>G (p.Arg1604Gly) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002484337]|Inborn genetic diseases [RCV004034731]|Usher syndrome type 1F [RCV001829000]|not provided [RCV001242765] Chr10:53822916 [GRCh38]
Chr10:55582676 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1517C>T (p.Thr506Met) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002484306]|Inborn genetic diseases [RCV003263878]|Usher syndrome type 1F [RCV001828916]|not provided [RCV001239321] Chr10:54183517 [GRCh38]
Chr10:55943277 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1450T>C (p.Phe484Leu) single nucleotide variant Usher syndrome type 1F [RCV001835144]|not provided [RCV001242904] Chr10:54183584 [GRCh38]
Chr10:55943344 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5416C>T (p.Pro1806Ser) single nucleotide variant Usher syndrome type 1F [RCV001833959]|not provided [RCV001226954] Chr10:53822310 [GRCh38]
Chr10:55582070 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5287_5301del (p.Ala1763_Pro1767del) deletion Usher syndrome type 1F [RCV001835160]|not provided [RCV001243194] Chr10:53822425..53822439 [GRCh38]
Chr10:55582185..55582199 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.17A>G (p.Tyr6Cys) single nucleotide variant not provided [RCV001241457] Chr10:54664246 [GRCh38]
Chr10:56424006 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3984-2A>T single nucleotide variant not provided [RCV001238071] Chr10:53831535 [GRCh38]
Chr10:55591295 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.824G>A (p.Arg275His) single nucleotide variant Usher syndrome type 1F [RCV001829031]|not provided [RCV001243451] Chr10:54317323 [GRCh38]
Chr10:56077083 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.401G>A (p.Arg134Gln) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003473823]|Usher syndrome type 1F [RCV002568567]|not provided [RCV001243483] Chr10:54369193 [GRCh38]
Chr10:56128953 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|conflicting interpretations of pathogenicity|uncertain significance|no classifications from unflagged records
NM_001384140.1(PCDH15):c.925C>A (p.Gln309Lys) single nucleotide variant Usher syndrome type 1F [RCV001828825]|not provided [RCV001228519] Chr10:54236883 [GRCh38]
Chr10:55996643 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.907C>T (p.Pro303Ser) single nucleotide variant Usher syndrome type 1F [RCV001828954]|not provided [RCV001240542] Chr10:54236901 [GRCh38]
Chr10:55996661 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4319C>T (p.Pro1440Leu) single nucleotide variant Inborn genetic diseases [RCV004034662]|Usher syndrome type 1F [RCV001834130]|not provided [RCV001240798] Chr10:53827441 [GRCh38]
Chr10:55587201 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5408C>T (p.Ser1803Phe) single nucleotide variant Inborn genetic diseases [RCV003259153]|Usher syndrome type 1F [RCV001833847]|not provided [RCV001210183] Chr10:53822318 [GRCh38]
Chr10:55582078 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5701A>G (p.Ser1901Gly) single nucleotide variant Usher syndrome type 1F [RCV001834139]|not provided [RCV001241073] Chr10:53822025 [GRCh38]
Chr10:55581785 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1385A>G (p.Tyr462Cys) single nucleotide variant Usher syndrome type 1F [RCV001835092]|not provided [RCV001241144] Chr10:54185189 [GRCh38]
Chr10:55944949 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3592G>A (p.Glu1198Lys) single nucleotide variant Usher syndrome type 1F [RCV001828797]|not provided [RCV001225618] Chr10:53866767 [GRCh38]
Chr10:55626527 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4672-1689G>A single nucleotide variant Inborn genetic diseases [RCV003346351]|not specified [RCV001195252] Chr10:53808819 [GRCh38]
Chr10:55568579 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.5045A>G (p.Asn1682Ser) single nucleotide variant Usher syndrome type 1D [RCV001198039] Chr10:53806757 [GRCh38]
Chr10:55566517 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.662A>G (p.Asn221Ser) single nucleotide variant Usher syndrome type 1F [RCV001830002]|not provided [RCV001247068] Chr10:54329639 [GRCh38]
Chr10:56089399 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5755T>A (p.Cys1919Ser) single nucleotide variant Usher syndrome type 1F [RCV001277664]|not provided [RCV001230621] Chr10:53821971 [GRCh38]
Chr10:55581731 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.319-5T>G single nucleotide variant not provided [RCV001226254] Chr10:54369280 [GRCh38]
Chr10:56129040 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2645_2646del (p.Asp881_Tyr882insTer) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003473534]|Usher syndrome type 1F [RCV000988361]|not provided [RCV001388718] Chr10:54020297..54020298 [GRCh38]
Chr10:55780057..55780058 [GRCh37]
Chr10:10q21.1		 pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.3791_3792del (p.Ile1264fs) deletion not provided [RCV001210968] Chr10:53857189..53857190 [GRCh38]
Chr10:55616949..55616950 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2148_2155del (p.Phe717fs) deletion Usher syndrome type 1D [RCV001198733] Chr10:54066822..54066829 [GRCh38]
Chr10:55826582..55826589 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.5573_5576dup (p.Lys1859delinsAsnTer) duplication Usher syndrome type 1D [RCV001197248]|Usher syndrome type 1F [RCV001833765]|not provided [RCV001242143] Chr10:53822149..53822150 [GRCh38]
Chr10:55581909..55581910 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.1244C>T (p.Ser415Leu) single nucleotide variant Usher syndrome type 1F [RCV001828827]|not provided [RCV001228666] Chr10:54195744 [GRCh38]
Chr10:55955504 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.92-528C>T single nucleotide variant Usher syndrome type 1D [RCV001199961]|Usher syndrome type 1F [RCV002560269] Chr10:54528405 [GRCh38]
Chr10:56288165 [GRCh37]
Chr10:10q21.1		 pathogenic|uncertain significance
NM_001384140.1(PCDH15):c.3313C>A (p.Leu1105Ile) single nucleotide variant Usher syndrome type 1 [RCV001108251] Chr10:53938875 [GRCh38]
Chr10:55698635 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4385A>G (p.His1462Arg) single nucleotide variant Usher syndrome type 1 [RCV001102953]|not provided [RCV002558029] Chr10:53823341 [GRCh38]
Chr10:55583101 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4368-1028C>A single nucleotide variant Usher syndrome type 1 [RCV001105838] Chr10:53821258 [GRCh38]
Chr10:55581018 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2723G>A (p.Gly908Asp) single nucleotide variant Usher syndrome type 1 [RCV001103053] Chr10:54020220 [GRCh38]
Chr10:55779980 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1808T>C (p.Ile603Thr) single nucleotide variant Usher syndrome type 1 [RCV001106123]|not provided [RCV002556084] Chr10:54132984 [GRCh38]
Chr10:55892744 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1780C>A (p.Arg594=) single nucleotide variant Usher syndrome type 1 [RCV001106124]|not provided [RCV002069749] Chr10:54153104 [GRCh38]
Chr10:55912864 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.8G>A (p.Arg3Gln) single nucleotide variant Inborn genetic diseases [RCV002558034]|Usher syndrome type 1 [RCV001103249]|Usher syndrome type 1F [RCV001828551]|not provided [RCV001340599] Chr10:54664255 [GRCh38]
Chr10:56424015 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.3937A>C (p.Ile1313Leu) single nucleotide variant not provided [RCV003104863] Chr10:53840366 [GRCh38]
Chr10:55600126 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.157+41373T>C single nucleotide variant not specified [RCV003230831] Chr10:54486439 [GRCh38]
Chr10:56246199 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.55T>A (p.Ser19Thr) single nucleotide variant not provided [RCV003104655] Chr10:54664208 [GRCh38]
Chr10:56423968 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4211+73_4211+81dup duplication not provided [RCV001568776] Chr10:53828483..53828484 [GRCh38]
Chr10:55588243..55588244 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.877-167C>T single nucleotide variant not provided [RCV001572179] Chr10:54237098 [GRCh38]
Chr10:55996858 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3122+114G>T single nucleotide variant not provided [RCV001565769] Chr10:53959618 [GRCh38]
Chr10:55719378 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4672-1444_4672-1441dup duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV002488384]|not provided [RCV001566082] Chr10:53808570..53808571 [GRCh38]
Chr10:55568330..55568331 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1998-45A>G single nucleotide variant not provided [RCV001570202] Chr10:54079469 [GRCh38]
Chr10:55839229 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.92-178G>C single nucleotide variant not provided [RCV001574482] Chr10:54528055 [GRCh38]
Chr10:56287815 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2093C>T (p.Thr698Ile) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001578653]|Usher syndrome type 1F [RCV001578695]|not provided [RCV001866082] Chr10:54066884 [GRCh38]
Chr10:55826644 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4367+2444T>C single nucleotide variant not provided [RCV001575492] Chr10:53824949 [GRCh38]
Chr10:55584709 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1305+268A>C single nucleotide variant not provided [RCV001641511] Chr10:54195415 [GRCh38]
Chr10:55955175 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3233-37A>G single nucleotide variant not provided [RCV001575080] Chr10:53938992 [GRCh38]
Chr10:55698752 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4368-3402CAAAAA[3] microsatellite not provided [RCV001559978] Chr10:53823620..53823621 [GRCh38]
Chr10:55583380..55583381 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3984-82A>G single nucleotide variant not provided [RCV001675043] Chr10:53831615 [GRCh38]
Chr10:55591375 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1997+27dup duplication not provided [RCV001575997] Chr10:54089950..54089951 [GRCh38]
Chr10:55849710..55849711 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.474+153A>G single nucleotide variant not provided [RCV001554896] Chr10:54368967 [GRCh38]
Chr10:56128727 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4211+119T>C single nucleotide variant not provided [RCV001560260] Chr10:53828446 [GRCh38]
Chr10:55588206 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1997+41C>G single nucleotide variant not provided [RCV001576171] Chr10:54089943 [GRCh38]
Chr10:55849703 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.705+93C>T single nucleotide variant Usher syndrome type 1F [RCV001533762]|not provided [RCV001713111] Chr10:54329503 [GRCh38]
Chr10:56089263 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3122+186G>A single nucleotide variant not provided [RCV001725275] Chr10:53959546 [GRCh38]
Chr10:55719306 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4367+2313A>G single nucleotide variant not provided [RCV001591468] Chr10:53825080 [GRCh38]
Chr10:55584840 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4368-3342_4368-3335dup duplication not provided [RCV001568865] Chr10:53823564..53823565 [GRCh38]
Chr10:55583324..55583325 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4368-3396_4368-3391del microsatellite not provided [RCV001555820] Chr10:53823621..53823626 [GRCh38]
Chr10:55583381..55583386 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.985+227A>G single nucleotide variant not provided [RCV001598856] Chr10:54236596 [GRCh38]
Chr10:55996356 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1306-3777A>G single nucleotide variant not provided [RCV001690940] Chr10:54189045 [GRCh38]
Chr10:55948805 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3010-49C>T single nucleotide variant not provided [RCV001556901] Chr10:53959893 [GRCh38]
Chr10:55719653 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.877-332T>C single nucleotide variant not provided [RCV001562143] Chr10:54237263 [GRCh38]
Chr10:55997023 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1784+128C>T single nucleotide variant not provided [RCV001717649] Chr10:54152972 [GRCh38]
Chr10:55912732 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1306-203T>C single nucleotide variant not provided [RCV001682520] Chr10:54185471 [GRCh38]
Chr10:55945231 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.475-343G>A single nucleotide variant not provided [RCV001648813] Chr10:54346827 [GRCh38]
Chr10:56106587 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4367+2367G>A single nucleotide variant not provided [RCV001551108] Chr10:53825026 [GRCh38]
Chr10:55584786 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4671+747G>T single nucleotide variant not provided [RCV001620043] Chr10:53809809 [GRCh38]
Chr10:55569569 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.319-161A>T single nucleotide variant not provided [RCV001594088] Chr10:54369436 [GRCh38]
Chr10:56129196 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2091+229C>T single nucleotide variant not provided [RCV001687441] Chr10:54079102 [GRCh38]
Chr10:55838862 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.157+75G>A single nucleotide variant not provided [RCV001674502] Chr10:54527737 [GRCh38]
Chr10:56287497 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1306-4005G>A single nucleotide variant not provided [RCV001594205] Chr10:54189273 [GRCh38]
Chr10:55949033 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3806+143C>T single nucleotide variant not provided [RCV001564600] Chr10:53857032 [GRCh38]
Chr10:55616792 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4672-26_4672-23dup duplication not provided [RCV001544892] Chr10:53807152..53807153 [GRCh38]
Chr10:55566912..55566913 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4552G>A (p.Asp1518Asn) single nucleotide variant Usher syndrome type 1F [RCV001827477]|not provided [RCV001563225] Chr10:53823174 [GRCh38]
Chr10:55582934 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1917+13GT[14] microsatellite not provided [RCV001718494] Chr10:54132840..54132841 [GRCh38]
Chr10:55892600..55892601 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4672-294dup duplication not provided [RCV001582197] Chr10:53807417..53807418 [GRCh38]
Chr10:55567177..55567178 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.876+361A>C single nucleotide variant not provided [RCV001718285] Chr10:54316910 [GRCh38]
Chr10:56076670 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1997+132T>G single nucleotide variant not provided [RCV001654747] Chr10:54089852 [GRCh38]
Chr10:55849612 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3717+174AT[13] microsatellite not provided [RCV001609669] Chr10:53866446..53866447 [GRCh38]
Chr10:55626206..55626207 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4367+2552T>A single nucleotide variant not provided [RCV001667614] Chr10:53824841 [GRCh38]
Chr10:55584601 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.2751+184C>T single nucleotide variant not provided [RCV001644366] Chr10:54020008 [GRCh38]
Chr10:55779768 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4562+235C>T single nucleotide variant not provided [RCV001552613] Chr10:53811314 [GRCh38]
Chr10:55571074 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.706-266T>C single nucleotide variant not provided [RCV001665869] Chr10:54317707 [GRCh38]
Chr10:56077467 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3009+289A>G single nucleotide variant not provided [RCV001677351] Chr10:53961463 [GRCh38]
Chr10:55721223 [GRCh37]
Chr10:10q21.1		 benign
NM_033056.4(PCDH15):c.5674C>T (p.Leu1892Phe) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001578788]|Usher syndrome type 1F [RCV001578789] Chr10:53822052 [GRCh38]
Chr10:55581812 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2082G>A (p.Arg694=) single nucleotide variant Usher syndrome type 1F [RCV001273400]|not provided [RCV000944369] Chr10:54079340 [GRCh38]
Chr10:55839100 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.5862A>G (p.Ser1954=) single nucleotide variant not provided [RCV000929665] Chr10:53821864 [GRCh38]
Chr10:55581624 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4485A>G (p.Ser1495=) single nucleotide variant Usher syndrome type 1F [RCV001825786]|not provided [RCV000885351] Chr10:53823241 [GRCh38]
Chr10:55583001 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5223T>G (p.Ser1741=) single nucleotide variant not provided [RCV000931626] Chr10:53822503 [GRCh38]
Chr10:55582263 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1306-4122G>A single nucleotide variant not provided [RCV000909078] Chr10:54189390 [GRCh38]
Chr10:55949150 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2527-7A>G single nucleotide variant not provided [RCV000909901] Chr10:54020423 [GRCh38]
Chr10:55780183 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4671+1440C>T single nucleotide variant Inborn genetic diseases [RCV003169303]|not provided [RCV000917475] Chr10:53809116 [GRCh38]
Chr10:55568876 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.1185T>C (p.Phe395=) single nucleotide variant Usher syndrome type 1F [RCV001276784]|not provided [RCV000930962] Chr10:54195803 [GRCh38]
Chr10:55955563 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4589G>A (p.Arg1530His) single nucleotide variant not provided [RCV000953628] Chr10:53810638 [GRCh38]
Chr10:55570398 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1494A>G (p.Gln498=) single nucleotide variant Usher syndrome type 1F [RCV001279002]|not provided [RCV000931717] Chr10:54183540 [GRCh38]
Chr10:55943300 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.3933T>C (p.Tyr1311=) single nucleotide variant not provided [RCV000932519] Chr10:53840370 [GRCh38]
Chr10:55600130 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.945G>A (p.Pro315=) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001578791]|Usher syndrome type 1F [RCV001578792]|not provided [RCV000941373] Chr10:54236863 [GRCh38]
Chr10:55996623 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.198T>C (p.Ala66=) single nucleotide variant Usher syndrome type 1F [RCV001825827]|not provided [RCV000907884] Chr10:54378902 [GRCh38]
Chr10:56138662 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4671+1192C>T single nucleotide variant not provided [RCV000931742] Chr10:53809364 [GRCh38]
Chr10:55569124 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4329A>G (p.Pro1443=) single nucleotide variant not provided [RCV000977404] Chr10:53827431 [GRCh38]
Chr10:55587191 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2706T>C (p.Tyr902=) single nucleotide variant not provided [RCV000923127] Chr10:54020237 [GRCh38]
Chr10:55779997 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1306-4116G>A single nucleotide variant not provided [RCV000932595] Chr10:54189384 [GRCh38]
Chr10:55949144 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1785-6C>A single nucleotide variant not provided [RCV000910060] Chr10:54133013 [GRCh38]
Chr10:55892773 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4671+1643G>A single nucleotide variant Inborn genetic diseases [RCV004659251]|not provided [RCV000888250] Chr10:53808913 [GRCh38]
Chr10:55568673 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.3840T>C (p.Pro1280=) single nucleotide variant not provided [RCV000975588] Chr10:53840463 [GRCh38]
Chr10:55600223 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.139G>A (p.Asp47Asn) single nucleotide variant Aganglionic megacolon [RCV000984704] Chr10:54527830 [GRCh38]
Chr10:56287590 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2979T>C (p.Asn993=) single nucleotide variant not provided [RCV000975883] Chr10:53961782 [GRCh38]
Chr10:55721542 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4326G>T (p.Pro1442=) single nucleotide variant not provided [RCV000978772] Chr10:53827434 [GRCh38]
Chr10:55587194 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5283T>G (p.Ala1761=) single nucleotide variant not provided [RCV000941560] Chr10:53822443 [GRCh38]
Chr10:55582203 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4965T>G (p.Ser1655=) single nucleotide variant not provided [RCV000928635] Chr10:53822761 [GRCh38]
Chr10:55582521 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1377T>C (p.Ile459=) single nucleotide variant Usher syndrome type 1F [RCV001275400]|not provided [RCV000931328] Chr10:54185197 [GRCh38]
Chr10:55944957 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.3753T>C (p.Ile1251=) single nucleotide variant Usher syndrome type 1F [RCV001278202]|not provided [RCV000982492] Chr10:53857228 [GRCh38]
Chr10:55616988 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.2202C>T (p.Ala734=) single nucleotide variant Usher syndrome type 1F [RCV001273397]|not provided [RCV000895972]|not specified [RCV004017759] Chr10:54066775 [GRCh38]
Chr10:55826535 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.3042T>C (p.Pro1014=) single nucleotide variant not provided [RCV000930797] Chr10:53959812 [GRCh38]
Chr10:55719572 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2550A>C (p.Ala850=) single nucleotide variant Usher syndrome type 1F [RCV001273394]|not provided [RCV000930799] Chr10:54020393 [GRCh38]
Chr10:55780153 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.945G>T (p.Pro315=) single nucleotide variant not provided [RCV000944213] Chr10:54236863 [GRCh38]
Chr10:55996623 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.567T>A (p.Tyr189Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003473713]|not provided [RCV001092482] Chr10:54346392 [GRCh38]
Chr10:56106152 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_033056.4(PCDH15):c.5270C>T (p.Ser1757Phe) single nucleotide variant not provided [RCV001225825] Chr10:53822456 [GRCh38]
Chr10:55582216 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.805G>A (p.Val269Ile) single nucleotide variant not provided [RCV001244230] Chr10:54317342 [GRCh38]
Chr10:56077102 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1075C>T (p.Gln359Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002290658]|not provided [RCV001244263] Chr10:54213959 [GRCh38]
Chr10:55973719 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.1812A>C (p.Glu604Asp) single nucleotide variant Usher syndrome type 1F [RCV001278999]|not provided [RCV001218862] Chr10:54132980 [GRCh38]
Chr10:55892740 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1836C>A (p.Ser612Arg) single nucleotide variant Inborn genetic diseases [RCV004034792]|Usher syndrome type 1F [RCV001835206]|not provided [RCV001244549] Chr10:54132956 [GRCh38]
Chr10:55892716 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_033056.4(PCDH15):c.4774C>T (p.Pro1592Ser) single nucleotide variant Usher syndrome type 1F [RCV001835210]|not provided [RCV001244555] Chr10:53822952 [GRCh38]
Chr10:55582712 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2168G>T (p.Arg723Ile) single nucleotide variant not provided [RCV001247690] Chr10:54066809 [GRCh38]
Chr10:55826569 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3814G>C (p.Asp1272His) single nucleotide variant Usher syndrome type 1F [RCV001834052]|not provided [RCV001236234] Chr10:53840489 [GRCh38]
Chr10:55600249 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5066TCA[3] (p.Ile1690dup) microsatellite Usher syndrome type 1F [RCV001829009]|not provided [RCV001243037] Chr10:53822654..53822655 [GRCh38]
Chr10:55582414..55582415 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5708T>C (p.Ile1903Thr) single nucleotide variant Usher syndrome type 1F [RCV001835153]|not provided [RCV001243060] Chr10:53822018 [GRCh38]
Chr10:55581778 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.536T>C (p.Ile179Thr) single nucleotide variant not provided [RCV001230389] Chr10:54346423 [GRCh38]
Chr10:56106183 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2522T>C (p.Ile841Thr) single nucleotide variant Usher syndrome type 1F [RCV001830024]|not provided [RCV001247880] Chr10:54022896 [GRCh38]
Chr10:55782656 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4604_4608dup (p.Ser1537fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV002491787]|Usher syndrome type 1D [RCV003989652]|not provided [RCV001239625] Chr10:53823117..53823118 [GRCh38]
Chr10:55582877..55582878 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.4308GCC[8] (p.Pro1441_Pro1443dup) microsatellite Usher syndrome type 1F [RCV001829021]|not provided [RCV001243320] Chr10:53827437..53827438 [GRCh38]
Chr10:55587197..55587198 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5236C>A (p.Pro1746Thr) single nucleotide variant Meniere disease [RCV001797161]|Usher syndrome type 1F [RCV001833909]|not provided [RCV001219769] Chr10:53822490 [GRCh38]
Chr10:55582250 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3974A>G (p.Glu1325Gly) single nucleotide variant not provided [RCV001236797] Chr10:53840329 [GRCh38]
Chr10:55600089 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3932A>G (p.Tyr1311Cys) single nucleotide variant Usher syndrome type 1F [RCV001829027]|not provided [RCV001243383] Chr10:53840371 [GRCh38]
Chr10:55600131 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5343_5351del (p.1780PPS[1]) deletion Usher syndrome type 1F [RCV001829949]|not provided [RCV001245177] Chr10:53822375..53822383 [GRCh38]
Chr10:55582135..55582143 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5404A>G (p.Thr1802Ala) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002499417]|Inborn genetic diseases [RCV004659447]|Usher syndrome type 1F [RCV001835233]|not provided [RCV001245257] Chr10:53822322 [GRCh38]
Chr10:55582082 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4368-1519A>G single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002480478]|Usher syndrome type 1 [RCV001108074]|not provided [RCV004693652] Chr10:53821749 [GRCh38]
Chr10:55581509 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4368-3_4369dup duplication not provided [RCV001230981] Chr10:53823356..53823357 [GRCh38]
Chr10:55583116..55583117 [GRCh37]
Chr10:10q21.1		 pathogenic|conflicting interpretations of pathogenicity|uncertain significance
NM_033056.4(PCDH15):c.5028T>A (p.Thr1676=) single nucleotide variant PCDH15-related disorder [RCV004734081]|Usher syndrome type 1F [RCV001836250]|not provided [RCV001248492] Chr10:53822698 [GRCh38]
Chr10:55582458 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.1709_1719del (p.Gly570fs) deletion not provided [RCV001219992] Chr10:54153165..54153175 [GRCh38]
Chr10:55912925..55912935 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.4797G>C (p.Gln1599His) single nucleotide variant not provided [RCV001208713] Chr10:53822929 [GRCh38]
Chr10:55582689 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1373G>A (p.Gly458Asp) single nucleotide variant Usher syndrome type 1 [RCV001108336] Chr10:54185201 [GRCh38]
Chr10:55944961 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.146A>G (p.Glu49Gly) single nucleotide variant Usher syndrome type 1 [RCV001108430]|Usher syndrome type 1F [RCV001279012]|not provided [RCV002555058] Chr10:54527823 [GRCh38]
Chr10:56287583 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2348A>G (p.Asp783Gly) single nucleotide variant Usher syndrome type 1F [RCV001833883]|not provided [RCV001216819] Chr10:54023070 [GRCh38]
Chr10:55782830 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4203-8C>G single nucleotide variant PCDH15-related disorder [RCV004545034]|Usher syndrome type 1F [RCV001832524]|not provided [RCV001058056] Chr10:53828581 [GRCh38]
Chr10:55588341 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.5510C>T (p.Ser1837Phe) single nucleotide variant Usher syndrome type 1 [RCV001104787]|Usher syndrome type 1F [RCV001833703]|not provided [RCV001223316] Chr10:53822216 [GRCh38]
Chr10:55581976 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.938T>A (p.Ile313Asn) single nucleotide variant not provided [RCV001211726] Chr10:54236870 [GRCh38]
Chr10:55996630 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1439C>T (p.Ser480Leu) single nucleotide variant Usher syndrome type 1F [RCV001833813]|not provided [RCV001206514] Chr10:54185135 [GRCh38]
Chr10:55944895 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5152C>T (p.Pro1718Ser) single nucleotide variant Usher syndrome type 1D [RCV001197249]|not provided [RCV002561052] Chr10:53822574 [GRCh38]
Chr10:55582334 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4486G>A (p.Ala1496Thr) single nucleotide variant Usher syndrome type 1F [RCV001829917]|not provided [RCV001244076] Chr10:53823240 [GRCh38]
Chr10:55583000 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh37/hg19 10q21.1-21.3(chr10:56031210-65660398)x1 copy number loss not provided [RCV001006326] Chr10:56031210..65660398 [GRCh37]
Chr10:10q21.1-21.3		 pathogenic
NM_001384140.1(PCDH15):c.4671+116G>A single nucleotide variant not provided [RCV001561907] Chr10:53810440 [GRCh38]
Chr10:55570200 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5721_5724del (p.Leu1908fs) deletion PCDH15-related disorder [RCV004734225]|Usher syndrome type 1F [RCV001832732]|not provided [RCV001537421] Chr10:53822002..53822005 [GRCh38]
Chr10:55581762..55581765 [GRCh37]
Chr10:10q21.1		 conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.1483G>A (p.Val495Ile) single nucleotide variant PCDH15-related disorder [RCV004734231]|Usher syndrome type 1F [RCV001832748]|not provided [RCV001551154] Chr10:54183551 [GRCh38]
Chr10:55943311 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3374-7C>A single nucleotide variant not provided [RCV002681185] Chr10:53903377 [GRCh38]
Chr10:55663137 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2092-154T>C single nucleotide variant not provided [RCV001562442] Chr10:54067039 [GRCh38]
Chr10:55826799 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2347del (p.Asp783fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003474009]|not provided [RCV001562602] Chr10:54023071 [GRCh38]
Chr10:55782831 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3768T>C (p.Pro1256=) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001578641]|Usher syndrome type 1F [RCV001578642] Chr10:53857213 [GRCh38]
Chr10:55616973 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.902C>T (p.Thr301Met) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001578649]|Usher syndrome type 1F [RCV001578650]|not provided [RCV001810099] Chr10:54236906 [GRCh38]
Chr10:55996666 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3035G>C (p.Gly1012Ala) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001578698]|Usher syndrome type 1F [RCV001578699] Chr10:53959819 [GRCh38]
Chr10:55719579 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3374-134G>A single nucleotide variant not provided [RCV001677026] Chr10:53903504 [GRCh38]
Chr10:55663264 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4803C>T (p.Gly1601=) single nucleotide variant PCDH15-related disorder [RCV004536179]|not provided [RCV001557608] Chr10:53806999 [GRCh38]
Chr10:55566759 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.3717+39A>T single nucleotide variant not provided [RCV001548584] Chr10:53866603 [GRCh38]
Chr10:55626363 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3009+294C>T single nucleotide variant not provided [RCV001719238] Chr10:53961458 [GRCh38]
Chr10:55721218 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1099-282G>T single nucleotide variant not provided [RCV001719242] Chr10:54196171 [GRCh38]
Chr10:55955931 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4671+753T>A single nucleotide variant not provided [RCV001719266] Chr10:53809803 [GRCh38]
Chr10:55569563 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3656A>G (p.Lys1219Arg) single nucleotide variant Usher syndrome type 1F [RCV001832752]|not provided [RCV001552066] Chr10:53866703 [GRCh38]
Chr10:55626463 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4367+2439_4367+2440del deletion not provided [RCV001558283] Chr10:53824953..53824954 [GRCh38]
Chr10:55584713..55584714 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1441-76T>C single nucleotide variant not provided [RCV001593683] Chr10:54183669 [GRCh38]
Chr10:55943429 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2752-300C>A single nucleotide variant not provided [RCV001558842] Chr10:53996065 [GRCh38]
Chr10:55755825 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1651G>A (p.Gly551Arg) single nucleotide variant Usher syndrome type 1F [RCV001827470]|not provided [RCV001558993] Chr10:54153233 [GRCh38]
Chr10:55912993 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1917+246A>C single nucleotide variant not provided [RCV001655963] Chr10:54132629 [GRCh38]
Chr10:55892389 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4203-283T>A single nucleotide variant not provided [RCV001559400] Chr10:53828856 [GRCh38]
Chr10:55588616 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2527-34G>A single nucleotide variant not provided [RCV001593998] Chr10:54020450 [GRCh38]
Chr10:55780210 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2752-230C>A single nucleotide variant not provided [RCV001553133] Chr10:53995995 [GRCh38]
Chr10:55755755 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1449A>C (p.Ala483=) single nucleotide variant not provided [RCV001549898] Chr10:54183585 [GRCh38]
Chr10:55943345 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2091+70A>G single nucleotide variant not provided [RCV001568670] Chr10:54079261 [GRCh38]
Chr10:55839021 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.157+301G>A single nucleotide variant not provided [RCV001594165] Chr10:54527511 [GRCh38]
Chr10:56287271 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1997+23C>T single nucleotide variant not provided [RCV001576268] Chr10:54089961 [GRCh38]
Chr10:55849721 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2751+314G>C single nucleotide variant not provided [RCV001565973] Chr10:54019878 [GRCh38]
Chr10:55779638 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.92-131T>A single nucleotide variant not provided [RCV001556059] Chr10:54528008 [GRCh38]
Chr10:56287768 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.92-483A>G single nucleotide variant not provided [RCV001561463] Chr10:54528360 [GRCh38]
Chr10:56288120 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1306-4237del deletion not provided [RCV001718374] Chr10:54189505 [GRCh38]
Chr10:55949265 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1997+169A>G single nucleotide variant not provided [RCV001636493] Chr10:54089815 [GRCh38]
Chr10:55849575 [GRCh37]
Chr10:10q21.1		 benign
NM_033056.4(PCDH15):c.5850T>A (p.Ser1950Arg) single nucleotide variant not provided [RCV003106659] Chr10:53821876 [GRCh38]
Chr10:55581636 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3074T>C (p.Leu1025Pro) single nucleotide variant Usher syndrome type 1F [RCV001836096]|not provided [RCV001055055] Chr10:53959780 [GRCh38]
Chr10:55719540 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh37/hg19 10q21.1(chr10:54920534-55615937)x3 copy number gain not provided [RCV001006324] Chr10:54920534..55615937 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1736dup (p.Tyr579Ter) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003473554]|not provided [RCV001008048] Chr10:54153147..54153148 [GRCh38]
Chr10:55912907..55912908 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.3806+90del deletion not provided [RCV001656727] Chr10:53857085 [GRCh38]
Chr10:55616845 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1590+317T>G single nucleotide variant not provided [RCV001713617] Chr10:54183127 [GRCh38]
Chr10:55942887 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4671+749A>C single nucleotide variant not provided [RCV001597398] Chr10:53809807 [GRCh38]
Chr10:55569567 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4671+16T>G single nucleotide variant not provided [RCV001688744] Chr10:53810540 [GRCh38]
Chr10:55570300 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.2221-34G>A single nucleotide variant not provided [RCV001619045] Chr10:54023231 [GRCh38]
Chr10:55782991 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4672-1439G>A single nucleotide variant not provided [RCV001619622] Chr10:53808569 [GRCh38]
Chr10:55568329 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.876+412G>C single nucleotide variant not provided [RCV001717496] Chr10:54316859 [GRCh38]
Chr10:56076619 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3501+209A>T single nucleotide variant not provided [RCV001689078] Chr10:53903034 [GRCh38]
Chr10:55662794 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.876+134G>A single nucleotide variant not provided [RCV001595982] Chr10:54317137 [GRCh38]
Chr10:56076897 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.876+115T>C single nucleotide variant not provided [RCV001596117] Chr10:54317156 [GRCh38]
Chr10:56076916 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2527-260CT[9] microsatellite not provided [RCV001719247] Chr10:54020660..54020661 [GRCh38]
Chr10:55780420..55780421 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1784+168A>G single nucleotide variant not provided [RCV001652648] Chr10:54152932 [GRCh38]
Chr10:55912692 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.2527-177C>G single nucleotide variant not provided [RCV001617403] Chr10:54020593 [GRCh38]
Chr10:55780353 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.877-317G>C single nucleotide variant not provided [RCV001719271] Chr10:54237248 [GRCh38]
Chr10:55997008 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3718-31A>G single nucleotide variant not provided [RCV001620571] Chr10:53857294 [GRCh38]
Chr10:55617054 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1441-320G>T single nucleotide variant not provided [RCV001689051] Chr10:54183913 [GRCh38]
Chr10:55943673 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.92-444C>T single nucleotide variant not provided [RCV001676931] Chr10:54528321 [GRCh38]
Chr10:56288081 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4202+125G>A single nucleotide variant not provided [RCV001620756] Chr10:53831190 [GRCh38]
Chr10:55590950 [GRCh37]
Chr10:10q21.1		 benign
NM_033056.4(PCDH15):c.4717C>G (p.Leu1573Val) single nucleotide variant not provided [RCV001700826] Chr10:53823009 [GRCh38]
Chr10:55582769 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4368-1169A>G single nucleotide variant Usher syndrome type 1 [RCV001108073] Chr10:53821399 [GRCh38]
Chr10:55581159 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.526G>A (p.Ala176Thr) single nucleotide variant Usher syndrome type 1 [RCV001108428]|Usher syndrome type 1F [RCV001279011] Chr10:54346433 [GRCh38]
Chr10:56106193 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.986-11A>G single nucleotide variant Usher syndrome type 1 [RCV001105071]|not provided [RCV002069734] Chr10:54214059 [GRCh38]
Chr10:55973819 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.2731A>G (p.Thr911Ala) single nucleotide variant Usher syndrome type 1F [RCV001274794]|not provided [RCV001068276] Chr10:54020212 [GRCh38]
Chr10:55779972 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.952G>C (p.Asp318His) single nucleotide variant Hearing impairment [RCV001375308]|Usher syndrome type 1 [RCV001105072]|not provided [RCV002558048] Chr10:54236856 [GRCh38]
Chr10:55996616 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.833G>A (p.Arg278His) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002483762]|Usher syndrome type 1 [RCV001106210]|Usher syndrome type 1F [RCV002529805]|not provided [RCV001860486]|not specified [RCV002265826] Chr10:54317314 [GRCh38]
Chr10:56077074 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4919G>A (p.Arg1640Lys) single nucleotide variant Usher syndrome type 1F [RCV001274782]|not provided [RCV001054825] Chr10:53822807 [GRCh38]
Chr10:55582567 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4616A>T (p.Asn1539Ile) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002497480]|not provided [RCV001070437] Chr10:53823110 [GRCh38]
Chr10:55582870 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4368-1118T>C single nucleotide variant Usher syndrome type 1 [RCV001105839] Chr10:53821348 [GRCh38]
Chr10:55581108 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3555A>G (p.Ile1185Met) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002482189]|Usher syndrome type 1 [RCV001106030]|not provided [RCV002558063] Chr10:53866804 [GRCh38]
Chr10:55626564 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4928_4945dup (p.Glu1643_Glu1648dup) duplication Usher syndrome type 1F [RCV001272400]|not provided [RCV001055555] Chr10:53822780..53822781 [GRCh38]
Chr10:55582540..55582541 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1757C>T (p.Ala586Val) single nucleotide variant Usher syndrome type 1 [RCV001106125] Chr10:54153127 [GRCh38]
Chr10:55912887 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1179A>G (p.Pro393=) single nucleotide variant Usher syndrome type 1 [RCV001103158]|not provided [RCV002069718] Chr10:54195809 [GRCh38]
Chr10:55955569 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.5257_5271del (p.Ile1753_Ser1757del) deletion Usher syndrome type 1F [RCV001833627]|not provided [RCV001064223] Chr10:53822455..53822469 [GRCh38]
Chr10:55582215..55582229 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.1440+11T>G single nucleotide variant Usher syndrome type 1 [RCV001108335] Chr10:54185123 [GRCh38]
Chr10:55944883 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3373+213G>A single nucleotide variant not provided [RCV001691929] Chr10:53938602 [GRCh38]
Chr10:55698362 [GRCh37]
Chr10:10q21.1		 benign
NM_033056.4(PCDH15):c.4389del (p.Gln1464fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV001580755] Chr10:53823337 [GRCh38]
Chr10:55583097 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.876+56T>G single nucleotide variant not provided [RCV001609689] Chr10:54317215 [GRCh38]
Chr10:56076975 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1411A>G (p.Arg471Gly) single nucleotide variant Usher syndrome type 1F [RCV001836466]|not provided [RCV001588708] Chr10:54185163 [GRCh38]
Chr10:55944923 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5839C>T (p.Gln1947Ter) single nucleotide variant Usher syndrome type 1F [RCV001827158]|not provided [RCV002068791]|not specified [RCV001002367] Chr10:53821887 [GRCh38]
Chr10:55581647 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.3501+207G>A single nucleotide variant not provided [RCV001695518] Chr10:53903036 [GRCh38]
Chr10:55662796 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4671+62G>A single nucleotide variant not provided [RCV001589578] Chr10:53810494 [GRCh38]
Chr10:55570254 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1441-2A>C single nucleotide variant Usher syndrome type 1F [RCV001827443]|not provided [RCV001067733] Chr10:54183595 [GRCh38]
Chr10:55943355 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4367+2122del deletion not provided [RCV001669358] Chr10:53825271 [GRCh38]
Chr10:55585031 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.706-112A>C single nucleotide variant not provided [RCV001713236] Chr10:54317553 [GRCh38]
Chr10:56077313 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1306-21C>T single nucleotide variant not provided [RCV001584590] Chr10:54185289 [GRCh38]
Chr10:55945049 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.594+232A>G single nucleotide variant Usher syndrome type 1F [RCV001533581]|not provided [RCV001712977] Chr10:54346133 [GRCh38]
Chr10:56105893 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.92-52T>G single nucleotide variant Usher syndrome type 1F [RCV001533583]|not provided [RCV001673138] Chr10:54527929 [GRCh38]
Chr10:56287689 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.2220+47T>C single nucleotide variant Usher syndrome type 1F [RCV001533757]|not provided [RCV001673144] Chr10:54066710 [GRCh38]
Chr10:55826470 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4978dup (p.Ser1660fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV002488467]|not provided [RCV001699723] Chr10:53806823..53806824 [GRCh38]
Chr10:55566583..55566584 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4368-3396C>G single nucleotide variant not provided [RCV001611260] Chr10:53823626 [GRCh38]
Chr10:55583386 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1997+244C>T single nucleotide variant not provided [RCV001694558] Chr10:54089740 [GRCh38]
Chr10:55849500 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3717+174AT[12] microsatellite not provided [RCV001714240] Chr10:53866446..53866447 [GRCh38]
Chr10:55626206..55626207 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1590+314G>A single nucleotide variant not provided [RCV001671703] Chr10:54183130 [GRCh38]
Chr10:55942890 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4203-146G>A single nucleotide variant not provided [RCV001714353] Chr10:53828719 [GRCh38]
Chr10:55588479 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.2220+298T>C single nucleotide variant not provided [RCV001568024] Chr10:54066459 [GRCh38]
Chr10:55826219 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4367+2070_4367+2073dup duplication not provided [RCV001547039] Chr10:53825319..53825320 [GRCh38]
Chr10:55585079..55585080 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3501+230G>C single nucleotide variant not provided [RCV001690965] Chr10:53903013 [GRCh38]
Chr10:55662773 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4367+2544_4367+2547dup duplication not provided [RCV001567074] Chr10:53824845..53824846 [GRCh38]
Chr10:55584605..55584606 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5339C>G (p.Pro1780Arg) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001578700]|Usher syndrome type 1F [RCV001578701] Chr10:53822387 [GRCh38]
Chr10:55582147 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2868+2T>C single nucleotide variant not provided [RCV001066590] Chr10:53995647 [GRCh38]
Chr10:55755407 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3101G>A (p.Arg1034His) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001580532]|Non-Syndromic Hereditary Hearing Impairment [RCV001034599]|Usher syndrome type 1F [RCV001580531]|not provided [RCV001861672]|not specified [RCV002271546] Chr10:53959753 [GRCh38]
Chr10:55719513 [GRCh37]
Chr10:10q21.1		 likely pathogenic|uncertain significance
NM_033056.4(PCDH15):c.4449G>A (p.Met1483Ile) single nucleotide variant not provided [RCV001235613] Chr10:53823277 [GRCh38]
Chr10:55583037 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4402G>A (p.Gly1468Arg) single nucleotide variant Usher syndrome type 1F [RCV001832396]|not provided [RCV001039289] Chr10:53823324 [GRCh38]
Chr10:55583084 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1570C>A (p.Pro524Thr) single nucleotide variant not provided [RCV001047809] Chr10:54183464 [GRCh38]
Chr10:55943224 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1762A>G (p.Asn588Asp) single nucleotide variant Usher syndrome type 1F [RCV001827388]|not provided [RCV001061217] Chr10:54153122 [GRCh38]
Chr10:55912882 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5816A>T (p.Asn1939Ile) single nucleotide variant Usher syndrome type 1F [RCV001833809]|not provided [RCV001206117] Chr10:53821910 [GRCh38]
Chr10:55581670 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.11:g.(?_53821848)_(53831543_?)del deletion not provided [RCV001033577] Chr10:55581608..55591303 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3328G>A (p.Asp1110Asn) single nucleotide variant Usher syndrome type 1F [RCV001274792]|not provided [RCV001048313] Chr10:53938860 [GRCh38]
Chr10:55698620 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2793C>G (p.Tyr931Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003473741]|not provided [RCV001203694] Chr10:53995724 [GRCh38]
Chr10:55755484 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.14T>G (p.Phe5Cys) single nucleotide variant not provided [RCV001203834] Chr10:54664249 [GRCh38]
Chr10:56424009 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5650A>G (p.Arg1884Gly) single nucleotide variant Usher syndrome type 1D [RCV001198038] Chr10:53822076 [GRCh38]
Chr10:55581836 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.832C>T (p.Arg278Cys) single nucleotide variant not provided [RCV001048546] Chr10:54317315 [GRCh38]
Chr10:56077075 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5659A>T (p.Lys1887Ter) single nucleotide variant not provided [RCV001169844] Chr10:53822067 [GRCh38]
Chr10:55581827 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3206A>G (p.Tyr1069Cys) single nucleotide variant Usher syndrome type 1F [RCV001832465]|not provided [RCV001050033] Chr10:53940892 [GRCh38]
Chr10:55700652 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4048C>T (p.Arg1350Cys) single nucleotide variant Inborn genetic diseases [RCV003160279]|Usher syndrome type 1F [RCV001274789]|not provided [RCV001041969] Chr10:53831469 [GRCh38]
Chr10:55591229 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4548_4551dup (p.Asp1518delinsIleTer) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV002479312]|not provided [RCV001050605] Chr10:53823174..53823175 [GRCh38]
Chr10:55582934..55582935 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_033056.4(PCDH15):c.5824G>A (p.Glu1942Lys) single nucleotide variant Usher syndrome type 1 [RCV001102863]|not provided [RCV002555001] Chr10:53821902 [GRCh38]
Chr10:55581662 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2685G>C (p.Leu895=) single nucleotide variant Usher syndrome type 1 [RCV001103054]|not provided [RCV001469878] Chr10:54020258 [GRCh38]
Chr10:55780018 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.298G>A (p.Gly100Arg) single nucleotide variant Usher syndrome type 1F [RCV001275406]|not provided [RCV001071208]|not specified [RCV003490061] Chr10:54378802 [GRCh38]
Chr10:56138562 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1306-1G>C single nucleotide variant not provided [RCV001203092] Chr10:54185269 [GRCh38]
Chr10:55945029 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.5155A>G (p.Ile1719Val) single nucleotide variant not provided [RCV001035043] Chr10:53822571 [GRCh38]
Chr10:55582331 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.11:g.(?_54664162)_(54664272_?)del deletion not provided [RCV001031311] Chr10:56423922..56424032 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.1343_1350del (p.Tyr448fs) deletion not provided [RCV001045022] Chr10:54185224..54185231 [GRCh38]
Chr10:55944984..55944991 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3963_3964insA (p.Asp1322fs) insertion not provided [RCV001045058] Chr10:53840339..53840340 [GRCh38]
Chr10:55600099..55600100 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.1280T>C (p.Val427Ala) single nucleotide variant Hearing impairment [RCV001375060]|Usher syndrome type 1F [RCV001828653]|not provided [RCV001206180] Chr10:54195708 [GRCh38]
Chr10:55955468 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2572del (p.Ser858fs) deletion not provided [RCV001236442] Chr10:54020371 [GRCh38]
Chr10:55780131 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.11:g.(?_54183434)_(54189394_?)del deletion not provided [RCV001032440] Chr10:55943194..55949154 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NC_000010.11:g.(?_53938805)_(54664272_?)del deletion not provided [RCV001032601] Chr10:55698565..56424032 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3475dup (p.Met1159fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003473760]|Usher syndrome type 1F [RCV002562390]|not provided [RCV001213218] Chr10:53903268..53903269 [GRCh38]
Chr10:55663028..55663029 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.1007G>A (p.Arg336Gln) single nucleotide variant Usher syndrome type 1F [RCV001830036]|not provided [RCV001248275] Chr10:54214027 [GRCh38]
Chr10:55973787 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.11:g.(?_54378772)_(54378952_?)del deletion not provided [RCV001033033] Chr10:56138532..56138712 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.619C>T (p.Pro207Ser) single nucleotide variant not provided [RCV001231634] Chr10:54329682 [GRCh38]
Chr10:56089442 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5389C>T (p.Pro1797Ser) single nucleotide variant Usher syndrome type 1F [RCV001833755]|not provided [RCV002560192]|not specified [RCV001195249] Chr10:53822337 [GRCh38]
Chr10:55582097 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2891G>A (p.Arg964Lys) single nucleotide variant Inborn genetic diseases [RCV004030974]|Usher syndrome type 1F [RCV001832375]|not provided [RCV001036262] Chr10:53961870 [GRCh38]
Chr10:55721630 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4368-1535T>C single nucleotide variant Usher syndrome type 1 [RCV001102861]|not provided [RCV004693599] Chr10:53821765 [GRCh38]
Chr10:55581525 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4368-1555C>T single nucleotide variant Usher syndrome type 1 [RCV001102862] Chr10:53821785 [GRCh38]
Chr10:55581545 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5044G>A (p.Glu1682Lys) single nucleotide variant Usher syndrome type 1F [RCV001272398]|not provided [RCV001037665]|not specified [RCV001195201] Chr10:53822682 [GRCh38]
Chr10:55582442 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.2220+1G>A single nucleotide variant not provided [RCV001038291] Chr10:54066756 [GRCh38]
Chr10:55826516 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3029A>G (p.Asp1010Gly) single nucleotide variant Usher syndrome type 1F [RCV002570376]|not provided [RCV001248284] Chr10:53959825 [GRCh38]
Chr10:55719585 [GRCh37]
Chr10:10q21.1		 likely pathogenic|uncertain significance
NM_001384140.1(PCDH15):c.1643T>G (p.Ile548Ser) single nucleotide variant Usher syndrome type 1 [RCV001108334] Chr10:54153241 [GRCh38]
Chr10:55913001 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.400C>A (p.Arg134=) single nucleotide variant Usher syndrome type 1 [RCV001108429]|not provided [RCV002069768] Chr10:54369194 [GRCh38]
Chr10:56128954 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4202+3A>G single nucleotide variant not provided [RCV001202728] Chr10:53831312 [GRCh38]
Chr10:55591072 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2868+6T>C single nucleotide variant not provided [RCV001204353] Chr10:53995643 [GRCh38]
Chr10:55755403 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4319C>G (p.Pro1440Arg) single nucleotide variant not provided [RCV001204434] Chr10:53827441 [GRCh38]
Chr10:55587201 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4275A>C (p.Ala1425=) single nucleotide variant Usher syndrome type 1 [RCV001102954]|not provided [RCV001424952] Chr10:53827485 [GRCh38]
Chr10:55587245 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4840A>G (p.Thr1614Ala) single nucleotide variant Usher syndrome type 1D [RCV001196445] Chr10:53806962 [GRCh38]
Chr10:55566722 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3501+1G>A single nucleotide variant Retinal dystrophy [RCV001074213] Chr10:53903242 [GRCh38]
Chr10:55663002 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3373+1G>A single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003473740]|not provided [RCV001203268] Chr10:53938814 [GRCh38]
Chr10:55698574 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.712G>A (p.Ala238Thr) single nucleotide variant not provided [RCV001233817] Chr10:54317435 [GRCh38]
Chr10:56077195 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2564G>A (p.Arg855Gln) single nucleotide variant Usher syndrome type 1F [RCV001827413]|not provided [RCV001064295] Chr10:54020379 [GRCh38]
Chr10:55780139 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1180T>C (p.Tyr394His) single nucleotide variant Usher syndrome type 1F [RCV001827248]|not provided [RCV001041283] Chr10:54195808 [GRCh38]
Chr10:55955568 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3122+1G>A single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003473762]|Usher syndrome type 1F [RCV001836156]|not provided [RCV001214300] Chr10:53959731 [GRCh38]
Chr10:55719491 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.2191G>T (p.Glu731Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003473712]|not provided [RCV001092480] Chr10:54066786 [GRCh38]
Chr10:55826546 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.2214A>C (p.Gln738His) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002482094]|Usher syndrome type 1F [RCV001833637]|not provided [RCV001065749] Chr10:54066763 [GRCh38]
Chr10:55826523 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.11:g.(?_54066757)_(54090063_?)dup duplication not provided [RCV001033154] Chr10:55826517..55849823 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.595-2A>C single nucleotide variant not provided [RCV001215992] Chr10:54329708 [GRCh38]
Chr10:56089468 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1997C>T (p.Thr666Ile) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV004689991]|Usher syndrome type 1 [RCV001104969]|not provided [RCV002292605] Chr10:54089984 [GRCh38]
Chr10:55849744 [GRCh37]
Chr10:10q21.1		 likely pathogenic|uncertain significance
NM_033056.4(PCDH15):c.5371CCT[1] (p.Pro1792_Pro1793del) microsatellite Autosomal recessive nonsyndromic hearing loss 23 [RCV002503305]|not provided [RCV001813855] Chr10:53822347..53822352 [GRCh38]
Chr10:55582107..55582112 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.157+198A>C single nucleotide variant not provided [RCV001663204] Chr10:54527614 [GRCh38]
Chr10:56287374 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1603G>T (p.Asp535Tyr) single nucleotide variant not provided [RCV001324512] Chr10:54153281 [GRCh38]
Chr10:55913041 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3404A>G (p.Gln1135Arg) single nucleotide variant Inborn genetic diseases [RCV002542890]|Usher syndrome type 1F [RCV001278206] Chr10:53903340 [GRCh38]
Chr10:55663100 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3012G>A (p.Leu1004=) single nucleotide variant Usher syndrome type 1F [RCV001278209]|not provided [RCV001404842] Chr10:53959842 [GRCh38]
Chr10:55719602 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.3100C>T (p.Arg1034Cys) single nucleotide variant Usher syndrome type 1F [RCV001835531]|not provided [RCV001312657] Chr10:53959754 [GRCh38]
Chr10:55719514 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2696T>G (p.Phe899Cys) single nucleotide variant not provided [RCV001348708] Chr10:54020247 [GRCh38]
Chr10:55780007 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.10:g.(?_55826517)_(55849823_?)dup duplication not provided [RCV001301322] Chr10:55826517..55849823 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3760A>C (p.Asn1254His) single nucleotide variant not provided [RCV001319185] Chr10:53857221 [GRCh38]
Chr10:55616981 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2868+4A>T single nucleotide variant not provided [RCV001341413] Chr10:53995645 [GRCh38]
Chr10:55755405 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5572A>G (p.Ile1858Val) single nucleotide variant not provided [RCV001307806] Chr10:53822154 [GRCh38]
Chr10:55581914 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3154G>C (p.Gly1052Arg) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002499552]|not provided [RCV001299312] Chr10:53940944 [GRCh38]
Chr10:55700704 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.574C>T (p.Gln192Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001283795]|Usher syndrome type 1D [RCV003992488] Chr10:54346385 [GRCh38]
Chr10:56106145 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.5287G>C (p.Ala1763Pro) single nucleotide variant not provided [RCV001305689] Chr10:53822439 [GRCh38]
Chr10:55582199 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.814C>G (p.Pro272Ala) single nucleotide variant not provided [RCV001299262] Chr10:54317333 [GRCh38]
Chr10:56077093 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4368-2793dup duplication Deafness, autosomal recessive 23 [RCV001334392] Chr10:53823019..53823020 [GRCh38]
Chr10:55582779..55582780 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3667_3668del (p.Ile1223fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV001328030] Chr10:53866691..53866692 [GRCh38]
Chr10:55626451..55626452 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_55581274)_55581984del deletion not provided [RCV001315134]   uncertain significance
NM_001384140.1(PCDH15):c.2673T>G (p.Ser891Arg) single nucleotide variant Usher syndrome type 1F [RCV001825966]|not provided [RCV001350645] Chr10:54020270 [GRCh38]
Chr10:55780030 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5420C>A (p.Thr1807Lys) single nucleotide variant not provided [RCV001318692] Chr10:53822306 [GRCh38]
Chr10:55582066 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3757del (p.Ser1253fs) deletion not provided [RCV001310923] Chr10:53857224 [GRCh38]
Chr10:55616984 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.4581C>T (p.Pro1527=) single nucleotide variant not provided [RCV001396919] Chr10:53823145 [GRCh38]
Chr10:55582905 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4368-3150_4368-3132dup duplication not provided [RCV001397674] Chr10:53823361..53823362 [GRCh38]
Chr10:55583121..55583122 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5727C>T (p.Arg1909=) single nucleotide variant not provided [RCV001391939] Chr10:53821999 [GRCh38]
Chr10:55581759 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4523_4526dup (p.Ala1510fs) duplication not provided [RCV001382467] Chr10:53823199..53823200 [GRCh38]
Chr10:55582959..55582960 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.5335C>T (p.Pro1779Ser) single nucleotide variant Usher syndrome type 1F [RCV001831285]|not provided [RCV001369011] Chr10:53822391 [GRCh38]
Chr10:55582151 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3627C>T (p.Leu1209=) single nucleotide variant not provided [RCV001413244] Chr10:53866732 [GRCh38]
Chr10:55626492 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4265C>G (p.Ala1422Gly) single nucleotide variant Usher syndrome type 1F [RCV001278198] Chr10:53827495 [GRCh38]
Chr10:55587255 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3987T>G (p.Phe1329Leu) single nucleotide variant Usher syndrome type 1F [RCV001278200] Chr10:53831530 [GRCh38]
Chr10:55591290 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.876+1G>C single nucleotide variant Usher syndrome type 1F [RCV001787319] Chr10:54317270 [GRCh38]
Chr10:56077030 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3966T>C (p.Asp1322=) single nucleotide variant not provided [RCV001422344] Chr10:53840337 [GRCh38]
Chr10:55600097 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5275_5286del (p.Pro1759_Pro1762del) deletion Usher syndrome type 1F [RCV001830301]|not provided [RCV001316612] Chr10:53822440..53822451 [GRCh38]
Chr10:55582200..55582211 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.1268C>T (p.Pro423Leu) single nucleotide variant Usher syndrome type 1F [RCV001279005] Chr10:54195720 [GRCh38]
Chr10:55955480 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5853A>G (p.Gln1951=) single nucleotide variant not provided [RCV001415036] Chr10:53821873 [GRCh38]
Chr10:55581633 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2850T>C (p.Ala950=) single nucleotide variant not provided [RCV001415052] Chr10:53995667 [GRCh38]
Chr10:55755427 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5077_5079del (p.Pro1693del) deletion Usher syndrome type 1F [RCV001830220]|not provided [RCV001305828] Chr10:53822647..53822649 [GRCh38]
Chr10:55582407..55582409 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2386G>A (p.Val796Ile) single nucleotide variant PCDH15-related disorder [RCV004734110]|Usher syndrome type 1F [RCV001835505]|not provided [RCV001307730] Chr10:54023032 [GRCh38]
Chr10:55782792 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2441A>G (p.Asp814Gly) single nucleotide variant Usher syndrome type 1F [RCV001835397]|not provided [RCV001296364] Chr10:54022977 [GRCh38]
Chr10:55782737 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.922G>T (p.Asp308Tyr) single nucleotide variant not provided [RCV001307921] Chr10:54236886 [GRCh38]
Chr10:55996646 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.183G>T (p.Leu61=) single nucleotide variant not provided [RCV001433278] Chr10:54378917 [GRCh38]
Chr10:56138677 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3657G>A (p.Lys1219=) single nucleotide variant not provided [RCV001433316] Chr10:53866702 [GRCh38]
Chr10:55626462 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2376A>G (p.Thr792=) single nucleotide variant not provided [RCV001433923] Chr10:54023042 [GRCh38]
Chr10:55782802 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1076A>T (p.Gln359Leu) single nucleotide variant not provided [RCV001369674] Chr10:54213958 [GRCh38]
Chr10:55973718 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5253T>C (p.Pro1751=) single nucleotide variant not provided [RCV001396848] Chr10:53822473 [GRCh38]
Chr10:55582233 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3353A>G (p.Asn1118Ser) single nucleotide variant not provided [RCV001371434] Chr10:53938835 [GRCh38]
Chr10:55698595 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5711A>G (p.Glu1904Gly) single nucleotide variant Usher syndrome type 1F [RCV001825954]|not provided [RCV001349837] Chr10:53822015 [GRCh38]
Chr10:55581775 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1845C>T (p.Arg615=) single nucleotide variant not provided [RCV001422682] Chr10:54132947 [GRCh38]
Chr10:55892707 [GRCh37]
Chr10:10q21.1		 likely benign
NC_000010.10:g.(?_56077031)_(56106244_?)del deletion not provided [RCV001382982] Chr10:56077031..56106244 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.4368-3139TTTC[3] microsatellite not provided [RCV001396418] Chr10:53823361..53823362 [GRCh38]
Chr10:55583121..55583122 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2751+8C>T single nucleotide variant Usher syndrome type 1F [RCV001836277]|not provided [RCV001306448] Chr10:54020184 [GRCh38]
Chr10:55779944 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.386T>G (p.Ile129Ser) single nucleotide variant Hearing impairment [RCV001375132] Chr10:54369208 [GRCh38]
Chr10:56128968 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4728_4736dup (p.Val1578_Ser1579insArgSerVal) duplication Usher syndrome type 1F [RCV001831117]|not provided [RCV001345745] Chr10:53822989..53822990 [GRCh38]
Chr10:55582749..55582750 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2128G>A (p.Val710Ile) single nucleotide variant Usher syndrome type 1F [RCV001831196]|not provided [RCV001360186] Chr10:54066849 [GRCh38]
Chr10:55826609 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4671+1064G>T single nucleotide variant not provided [RCV001355111] Chr10:53809492 [GRCh38]
Chr10:55569252 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1931A>C (p.Glu644Ala) single nucleotide variant not provided [RCV001300059] Chr10:54090050 [GRCh38]
Chr10:55849810 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1067A>T (p.Asp356Val) single nucleotide variant not provided [RCV001346629] Chr10:54213967 [GRCh38]
Chr10:55973727 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1771C>G (p.Pro591Ala) single nucleotide variant not provided [RCV001371311] Chr10:54153113 [GRCh38]
Chr10:55912873 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4308GCC[4] (p.Pro1443del) microsatellite Usher syndrome type 1F [RCV001831203]|not provided [RCV001360529] Chr10:53827438..53827440 [GRCh38]
Chr10:55587198..55587200 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4330G>C (p.Gly1444Arg) single nucleotide variant Usher syndrome type 1F [RCV001831118]|not provided [RCV001345865] Chr10:53827430 [GRCh38]
Chr10:55587190 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4367T>C (p.Ile1456Thr) single nucleotide variant Usher syndrome type 1F [RCV001830086]|not provided [RCV001812926] Chr10:53827393 [GRCh38]
Chr10:55587153 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4279C>T (p.Pro1427Ser) single nucleotide variant Usher syndrome type 1F [RCV001826088]|not provided [RCV001370361] Chr10:53827481 [GRCh38]
Chr10:55587241 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3821A>G (p.Tyr1274Cys) single nucleotide variant Usher syndrome type 1F [RCV001831083]|not provided [RCV001342327] Chr10:53840482 [GRCh38]
Chr10:55600242 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1730G>A (p.Arg577Gln) single nucleotide variant Usher syndrome type 1F [RCV001825921]|not provided [RCV001346008] Chr10:54153154 [GRCh38]
Chr10:55912914 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5597C>G (p.Ser1866Ter) single nucleotide variant Usher syndrome type 1F [RCV001277667]|not provided [RCV002069408] Chr10:53822129 [GRCh38]
Chr10:55581889 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.4898_4901dup (p.Glu1635fs) duplication Usher syndrome type 1F [RCV001277670]|not provided [RCV002069409] Chr10:53822824..53822825 [GRCh38]
Chr10:55582584..55582585 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.5683T>C (p.Ser1895Pro) single nucleotide variant Usher syndrome type 1F [RCV001836337]|not provided [RCV001345037] Chr10:53822043 [GRCh38]
Chr10:55581803 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3319G>C (p.Val1107Leu) single nucleotide variant Deafness, autosomal recessive 23 [RCV001330198] Chr10:53938869 [GRCh38]
Chr10:55698629 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.5339C>A (p.Pro1780His) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001330200] Chr10:53822387 [GRCh38]
Chr10:55582147 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2636G>A (p.Ser879Asn) single nucleotide variant Usher syndrome type 1F [RCV001831166]|not provided [RCV001351170] Chr10:54020307 [GRCh38]
Chr10:55780067 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.49C>A (p.Leu17Met) single nucleotide variant not provided [RCV001351194] Chr10:54664214 [GRCh38]
Chr10:56423974 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5669_5671del (p.Ala1890del) deletion Usher syndrome type 1F [RCV001277665]|not provided [RCV002537760] Chr10:53822055..53822057 [GRCh38]
Chr10:55581815..55581817 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.5599A>G (p.Thr1867Ala) single nucleotide variant Usher syndrome type 1F [RCV001277666]|not provided [RCV001880233] Chr10:53822127 [GRCh38]
Chr10:55581887 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4318C>G (p.Pro1440Ala) single nucleotide variant Usher syndrome type 1F [RCV001278196] Chr10:53827442 [GRCh38]
Chr10:55587202 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3813G>C (p.Leu1271Phe) single nucleotide variant Usher syndrome type 1F [RCV001278201]|not provided [RCV002541675] Chr10:53840490 [GRCh38]
Chr10:55600250 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2713A>G (p.Met905Val) single nucleotide variant PCDH15-related disorder [RCV004538554]|Usher syndrome type 1F [RCV001278212]|not provided [RCV001306162] Chr10:54020230 [GRCh38]
Chr10:55779990 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1799C>G (p.Thr600Ser) single nucleotide variant Usher syndrome type 1F [RCV001279000] Chr10:54132993 [GRCh38]
Chr10:55892753 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1327C>G (p.Leu443Val) single nucleotide variant Inborn genetic diseases [RCV004649552]|Usher syndrome type 1F [RCV001279003]|not provided [RCV001871550] Chr10:54185247 [GRCh38]
Chr10:55945007 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1140T>C (p.Gly380=) single nucleotide variant Usher syndrome type 1F [RCV001279007]|not provided [RCV001489012] Chr10:54195848 [GRCh38]
Chr10:55955608 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.705T>C (p.Asn235=) single nucleotide variant Usher syndrome type 1F [RCV001279010]|not provided [RCV001871551] Chr10:54329596 [GRCh38]
Chr10:56089356 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.998A>C (p.Asp333Ala) single nucleotide variant not provided [RCV001310050] Chr10:54214036 [GRCh38]
Chr10:55973796 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1882G>A (p.Ala628Thr) single nucleotide variant not provided [RCV001342737] Chr10:54132910 [GRCh38]
Chr10:55892670 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.200G>A (p.Gly67Glu) single nucleotide variant Inborn genetic diseases [RCV004656498]|Usher syndrome type 1F [RCV001835450]|not provided [RCV001302225] Chr10:54378900 [GRCh38]
Chr10:56138660 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5656G>A (p.Val1886Ile) single nucleotide variant not provided [RCV001319386] Chr10:53822070 [GRCh38]
Chr10:55581830 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.215C>A (p.Thr72Asn) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002476659]|not provided [RCV001363569] Chr10:54378885 [GRCh38]
Chr10:56138645 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1099G>T (p.Ala367Ser) single nucleotide variant Usher syndrome type 1F [RCV001830411]|not provided [RCV001339265] Chr10:54195889 [GRCh38]
Chr10:55955649 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1522A>G (p.Thr508Ala) single nucleotide variant Usher syndrome type 1F [RCV001830163]|not provided [RCV001299500] Chr10:54183512 [GRCh38]
Chr10:55943272 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2978A>G (p.Asn993Ser) single nucleotide variant Usher syndrome type 1F [RCV001835609]|not provided [RCV001320985] Chr10:53961783 [GRCh38]
Chr10:55721543 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5272_5280del (p.Pro1758_Pro1760del) deletion Usher syndrome type 1F [RCV001825891]|not provided [RCV001343043] Chr10:53822446..53822454 [GRCh38]
Chr10:55582206..55582214 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.206C>T (p.Pro69Leu) single nucleotide variant not provided [RCV001370696] Chr10:54378894 [GRCh38]
Chr10:56138654 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1849C>T (p.Pro617Ser) single nucleotide variant not provided [RCV001345524] Chr10:54132943 [GRCh38]
Chr10:55892703 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2751+14A>G single nucleotide variant not provided [RCV001363794] Chr10:54020178 [GRCh38]
Chr10:55779938 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4192A>C (p.Ser1398Arg) single nucleotide variant Usher syndrome type 1F [RCV001831249]|not provided [RCV001364413] Chr10:53831325 [GRCh38]
Chr10:55591085 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5717dup (p.Asn1906fs) duplication Usher syndrome type 1F [RCV001830178]|not provided [RCV001301125] Chr10:53822008..53822009 [GRCh38]
Chr10:55581768..55581769 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.5690C>G (p.Ala1897Gly) single nucleotide variant Usher syndrome type 1F [RCV001831163]|not provided [RCV001350788] Chr10:53822036 [GRCh38]
Chr10:55581796 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.757G>A (p.Val253Met) single nucleotide variant not provided [RCV001307257] Chr10:54317390 [GRCh38]
Chr10:56077150 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2868+5G>A single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002476424]|Usher syndrome type 1F [RCV001835512]|not provided [RCV001308843] Chr10:53995644 [GRCh38]
Chr10:55755404 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1970C>T (p.Pro657Leu) single nucleotide variant Usher syndrome type 1F [RCV001830161]|not provided [RCV001299390] Chr10:54090011 [GRCh38]
Chr10:55849771 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.284T>A (p.Phe95Tyr) single nucleotide variant not provided [RCV001326817] Chr10:54378816 [GRCh38]
Chr10:56138576 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5757C>A (p.Cys1919Ter) single nucleotide variant not provided [RCV001359162] Chr10:53821969 [GRCh38]
Chr10:55581729 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4368-1737del deletion Deafness, autosomal recessive 23 [RCV001330201] Chr10:53821967 [GRCh38]
Chr10:55581727 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2067A>G (p.Thr689=) single nucleotide variant not provided [RCV001394624] Chr10:54079355 [GRCh38]
Chr10:55839115 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5380A>C (p.Thr1794Pro) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002486026]|Usher syndrome type 1F [RCV001277668]|not provided [RCV002537761] Chr10:53822346 [GRCh38]
Chr10:55582106 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5178C>T (p.Thr1726=) single nucleotide variant Usher syndrome type 1F [RCV001277669]|not provided [RCV001396239] Chr10:53822548 [GRCh38]
Chr10:55582308 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4671+1256del deletion not specified [RCV001449715] Chr10:53809300 [GRCh38]
Chr10:55569060 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3579A>C (p.Glu1193Asp) single nucleotide variant not specified [RCV001449716] Chr10:53866780 [GRCh38]
Chr10:55626540 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3225T>C (p.Asn1075=) single nucleotide variant Usher syndrome type 1F [RCV001278208]|not provided [RCV001427506] Chr10:53940873 [GRCh38]
Chr10:55700633 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.2981T>A (p.Leu994His) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002504395]|Usher syndrome type 1F [RCV001278210] Chr10:53961780 [GRCh38]
Chr10:55721540 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2751+7G>T single nucleotide variant Usher syndrome type 1F [RCV001278211] Chr10:54020185 [GRCh38]
Chr10:55779945 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1998-21GTTT[2] microsatellite Usher syndrome type 1F [RCV001278215]|not provided [RCV001408266] Chr10:54079434..54079437 [GRCh38]
Chr10:55839194..55839197 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.1978G>C (p.Val660Leu) single nucleotide variant Usher syndrome type 1F [RCV001278216]|not provided [RCV001880252] Chr10:54090003 [GRCh38]
Chr10:55849763 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1697_1699del (p.Thr566del) deletion Usher syndrome type 1F [RCV001279001] Chr10:54153185..54153187 [GRCh38]
Chr10:55912945..55912947 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1003C>G (p.Pro335Ala) single nucleotide variant Usher syndrome type 1F [RCV001279008] Chr10:54214031 [GRCh38]
Chr10:55973791 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3119A>G (p.Tyr1040Cys) single nucleotide variant not provided [RCV001316110] Chr10:53959735 [GRCh38]
Chr10:55719495 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3767C>T (p.Pro1256Leu) single nucleotide variant not provided [RCV001326917] Chr10:53857214 [GRCh38]
Chr10:55616974 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3317G>T (p.Arg1106Leu) single nucleotide variant not provided [RCV001338681] Chr10:53938871 [GRCh38]
Chr10:55698631 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4941_4944del (p.Ile1647fs) deletion not provided [RCV001371576] Chr10:53822782..53822785 [GRCh38]
Chr10:55582542..55582545 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.2833A>G (p.Ile945Val) single nucleotide variant not provided [RCV001367415] Chr10:53995684 [GRCh38]
Chr10:55755444 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5007C>T (p.Phe1669=) single nucleotide variant not provided [RCV001412762] Chr10:53822719 [GRCh38]
Chr10:55582479 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5115T>C (p.Pro1705=) single nucleotide variant not provided [RCV001395141] Chr10:53822611 [GRCh38]
Chr10:55582371 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4654T>C (p.Phe1552Leu) single nucleotide variant Usher syndrome type 1F [RCV001825945]|not provided [RCV001348211] Chr10:53823072 [GRCh38]
Chr10:55582832 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2178T>G (p.Ser726=) single nucleotide variant not provided [RCV001421386] Chr10:54066799 [GRCh38]
Chr10:55826559 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2817A>C (p.Ala939=) single nucleotide variant not provided [RCV001421390] Chr10:53995700 [GRCh38]
Chr10:55755460 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3374-7C>T single nucleotide variant not provided [RCV001395804]|not specified [RCV003120600] Chr10:53903377 [GRCh38]
Chr10:55663137 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.250T>C (p.Trp84Arg) single nucleotide variant Inborn genetic diseases [RCV002541859]|not provided [RCV001298317] Chr10:54378850 [GRCh38]
Chr10:56138610 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5210C>T (p.Pro1737Leu) single nucleotide variant Usher syndrome type 1F [RCV001831212]|not provided [RCV001361047] Chr10:53822516 [GRCh38]
Chr10:55582276 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3963C>A (p.Ile1321=) single nucleotide variant not provided [RCV001414263] Chr10:53840340 [GRCh38]
Chr10:55600100 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2810C>T (p.Pro937Leu) single nucleotide variant Usher syndrome type 1F [RCV001836261]|not provided [RCV001298492] Chr10:53995707 [GRCh38]
Chr10:55755467 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3501+7G>A single nucleotide variant not provided [RCV001395065] Chr10:53903236 [GRCh38]
Chr10:55662996 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1228G>T (p.Val410Leu) single nucleotide variant Usher syndrome type 1F [RCV001830289]|not provided [RCV001315189] Chr10:54195760 [GRCh38]
Chr10:55955520 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1755A>G (p.Ala585=) single nucleotide variant not provided [RCV001412912] Chr10:54153129 [GRCh38]
Chr10:55912889 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3797A>C (p.Asp1266Ala) single nucleotide variant Usher syndrome type 1F [RCV001836373]|not provided [RCV001369566] Chr10:53857184 [GRCh38]
Chr10:55616944 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2987A>G (p.Glu996Gly) single nucleotide variant Usher syndrome type 1F [RCV001825984]|not provided [RCV001358841] Chr10:53961774 [GRCh38]
Chr10:55721534 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4583T>C (p.Leu1528Pro) single nucleotide variant not provided [RCV001365588] Chr10:53823143 [GRCh38]
Chr10:55582903 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.30T>C (p.Cys10=) single nucleotide variant not provided [RCV001413826] Chr10:54664233 [GRCh38]
Chr10:56423993 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5195A>C (p.Glu1732Ala) single nucleotide variant Inborn genetic diseases [RCV004034163]|not provided [RCV001308245] Chr10:53822531 [GRCh38]
Chr10:55582291 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2540A>G (p.Asp847Gly) single nucleotide variant not provided [RCV001313705] Chr10:54020403 [GRCh38]
Chr10:55780163 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4712A>C (p.Glu1571Ala) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002504582]|not provided [RCV001358215] Chr10:53807090 [GRCh38]
Chr10:55566850 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5179G>A (p.Glu1727Lys) single nucleotide variant Inborn genetic diseases [RCV003246840]|Usher syndrome type 1F [RCV001830128]|not provided [RCV001295725] Chr10:53822547 [GRCh38]
Chr10:55582307 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.4656T>C (p.Phe1552=) single nucleotide variant not provided [RCV001492131] Chr10:53823070 [GRCh38]
Chr10:55582830 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.595-4G>T single nucleotide variant not provided [RCV001495150] Chr10:54329710 [GRCh38]
Chr10:56089470 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4399A>C (p.Arg1467=) single nucleotide variant not provided [RCV001457509] Chr10:53823327 [GRCh38]
Chr10:55583087 [GRCh37]
Chr10:10q21.1		 likely benign
NC_000010.11:g.53831308TACT[3] microsatellite not provided [RCV001457563] Chr10:53831307..53831308 [GRCh38]
Chr10:55591067..55591068 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2527-4A>T single nucleotide variant not provided [RCV001505552] Chr10:54020420 [GRCh38]
Chr10:55780180 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1099-19C>G single nucleotide variant not provided [RCV001464108] Chr10:54195908 [GRCh38]
Chr10:55955668 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1272A>G (p.Leu424=) single nucleotide variant not provided [RCV001456844] Chr10:54195716 [GRCh38]
Chr10:55955476 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2526+9del deletion not provided [RCV001450555] Chr10:54022883 [GRCh38]
Chr10:55782643 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1368G>A (p.Gln456=) single nucleotide variant not provided [RCV001427671] Chr10:54185206 [GRCh38]
Chr10:55944966 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4869T>C (p.Asn1623=) single nucleotide variant not provided [RCV001424597] Chr10:53822857 [GRCh38]
Chr10:55582617 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2346G>A (p.Arg782=) single nucleotide variant not provided [RCV001435548] Chr10:54023072 [GRCh38]
Chr10:55782832 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2679T>G (p.Thr893=) single nucleotide variant not provided [RCV001464256] Chr10:54020264 [GRCh38]
Chr10:55780024 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.957G>A (p.Arg319=) single nucleotide variant not provided [RCV001469953] Chr10:54236851 [GRCh38]
Chr10:55996611 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4202+8T>A single nucleotide variant not provided [RCV001465215] Chr10:53831307 [GRCh38]
Chr10:55591067 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1784+9T>C single nucleotide variant not provided [RCV001420073] Chr10:54153091 [GRCh38]
Chr10:55912851 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.186C>T (p.Ile62=) single nucleotide variant not provided [RCV001420091] Chr10:54378914 [GRCh38]
Chr10:56138674 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3810C>A (p.Ile1270=) single nucleotide variant not provided [RCV001427950] Chr10:53840493 [GRCh38]
Chr10:55600253 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3010-7T>C single nucleotide variant PCDH15-related disorder [RCV004533823]|not provided [RCV001473397] Chr10:53959851 [GRCh38]
Chr10:55719611 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2769T>A (p.Pro923=) single nucleotide variant not provided [RCV001473400] Chr10:53995748 [GRCh38]
Chr10:55755508 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5217C>T (p.Asn1739=) single nucleotide variant not provided [RCV001492414] Chr10:53822509 [GRCh38]
Chr10:55582269 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1032A>G (p.Thr344=) single nucleotide variant not provided [RCV001475251] Chr10:54214002 [GRCh38]
Chr10:55973762 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.783G>A (p.Leu261=) single nucleotide variant not provided [RCV001454963] Chr10:54317364 [GRCh38]
Chr10:56077124 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2091+8T>C single nucleotide variant not provided [RCV001458483] Chr10:54079323 [GRCh38]
Chr10:55839083 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4409_4413del (p.Asn1470fs) deletion not provided [RCV001380478] Chr10:53823313..53823317 [GRCh38]
Chr10:55583073..55583077 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_033056.4(PCDH15):c.4533_4554dup (p.Glu1519delinsLysIleHisIleSerIleTer) duplication not provided [RCV001389852] Chr10:53823171..53823172 [GRCh38]
Chr10:55582931..55582932 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.1918-8C>T single nucleotide variant not provided [RCV001417185] Chr10:54090071 [GRCh38]
Chr10:55849831 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.642A>C (p.Ile214=) single nucleotide variant not provided [RCV001457561] Chr10:54329659 [GRCh38]
Chr10:56089419 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.429C>T (p.Asn143=) single nucleotide variant not provided [RCV001484390] Chr10:54369165 [GRCh38]
Chr10:56128925 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1137C>T (p.Ala379=) single nucleotide variant not provided [RCV001470379] Chr10:54195851 [GRCh38]
Chr10:55955611 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4203G>A (p.Gln1401=) single nucleotide variant not provided [RCV001473854] Chr10:53828573 [GRCh38]
Chr10:55588333 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1506A>G (p.Ala502=) single nucleotide variant not provided [RCV001473860] Chr10:54183528 [GRCh38]
Chr10:55943288 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.195T>A (p.Thr65=) single nucleotide variant not provided [RCV001475353] Chr10:54378905 [GRCh38]
Chr10:56138665 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2221-9A>T single nucleotide variant not provided [RCV001455362] Chr10:54023206 [GRCh38]
Chr10:55782966 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4989C>T (p.Cys1663=) single nucleotide variant not provided [RCV001496494] Chr10:53822737 [GRCh38]
Chr10:55582497 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5112G>A (p.Arg1704=) single nucleotide variant not provided [RCV001458978] Chr10:53822614 [GRCh38]
Chr10:55582374 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4369_4372dup (p.Phe1458fs) duplication not provided [RCV001380660] Chr10:53823353..53823354 [GRCh38]
Chr10:55583113..55583114 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.477C>T (p.Leu159=) single nucleotide variant not provided [RCV001471179] Chr10:54346482 [GRCh38]
Chr10:56106242 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3186C>T (p.Ala1062=) single nucleotide variant not provided [RCV001465945] Chr10:53940912 [GRCh38]
Chr10:55700672 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2460C>T (p.Thr820=) single nucleotide variant not provided [RCV001503491] Chr10:54022958 [GRCh38]
Chr10:55782718 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.877-4del deletion not provided [RCV001428389] Chr10:54236935 [GRCh38]
Chr10:55996695 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4719G>T (p.Leu1573=) single nucleotide variant not provided [RCV001405385] Chr10:53823007 [GRCh38]
Chr10:55582767 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4020C>T (p.Asp1340=) single nucleotide variant not provided [RCV001461958] Chr10:53831497 [GRCh38]
Chr10:55591257 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.726T>C (p.Asn242=) single nucleotide variant not provided [RCV001461960] Chr10:54317421 [GRCh38]
Chr10:56077181 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2407C>T (p.Leu803=) single nucleotide variant not provided [RCV001484981] Chr10:54023011 [GRCh38]
Chr10:55782771 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2934T>C (p.Ile978=) single nucleotide variant not provided [RCV001471326] Chr10:53961827 [GRCh38]
Chr10:55721587 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4203-6A>T single nucleotide variant not provided [RCV001452294] Chr10:53828579 [GRCh38]
Chr10:55588339 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3233-4C>A single nucleotide variant not provided [RCV001455809] Chr10:53938959 [GRCh38]
Chr10:55698719 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2250T>A (p.Gly750=) single nucleotide variant not provided [RCV001400426] Chr10:54023168 [GRCh38]
Chr10:55782928 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3087T>C (p.Pro1029=) single nucleotide variant not provided [RCV001431158] Chr10:53959767 [GRCh38]
Chr10:55719527 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5592_5605dup (p.Thr1869fs) duplication not provided [RCV001454821] Chr10:53822120..53822121 [GRCh38]
Chr10:55581880..55581881 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3684T>C (p.Tyr1228=) single nucleotide variant not provided [RCV001455356] Chr10:53866675 [GRCh38]
Chr10:55626435 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.405A>C (p.Ile135=) single nucleotide variant not provided [RCV001483620] Chr10:54369189 [GRCh38]
Chr10:56128949 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.873T>C (p.Thr291=) single nucleotide variant not provided [RCV001462401] Chr10:54317274 [GRCh38]
Chr10:56077034 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5472T>C (p.Ser1824=) single nucleotide variant not provided [RCV001468183] Chr10:53822254 [GRCh38]
Chr10:55582014 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5424A>G (p.Pro1808=) single nucleotide variant not provided [RCV001471827] Chr10:53822302 [GRCh38]
Chr10:55582062 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3309T>C (p.Tyr1103=) single nucleotide variant not provided [RCV001471842] Chr10:53938879 [GRCh38]
Chr10:55698639 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1785-5T>C single nucleotide variant not provided [RCV001492870] Chr10:54133012 [GRCh38]
Chr10:55892772 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.411G>A (p.Val137=) single nucleotide variant not provided [RCV001437096] Chr10:54369183 [GRCh38]
Chr10:56128943 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2088_2089insA (p.Gly697fs) insertion not provided [RCV001390696] Chr10:54079333..54079334 [GRCh38]
Chr10:55839093..55839094 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2513T>C (p.Ile838Thr) single nucleotide variant not provided [RCV001521203] Chr10:54022905 [GRCh38]
Chr10:55782665 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3894T>C (p.Phe1298=) single nucleotide variant not provided [RCV001472071] Chr10:53840409 [GRCh38]
Chr10:55600169 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1230G>C (p.Val410=) single nucleotide variant not provided [RCV001475786] Chr10:54195758 [GRCh38]
Chr10:55955518 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4908A>G (p.Lys1636=) single nucleotide variant not provided [RCV001492974] Chr10:53822818 [GRCh38]
Chr10:55582578 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4047A>T (p.Gly1349=) single nucleotide variant not provided [RCV001486923] Chr10:53831470 [GRCh38]
Chr10:55591230 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.816A>G (p.Pro272=) single nucleotide variant not provided [RCV001406097] Chr10:54317331 [GRCh38]
Chr10:56077091 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4308G>A (p.Pro1436=) single nucleotide variant not provided [RCV001468325] Chr10:53827452 [GRCh38]
Chr10:55587212 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1086T>C (p.Asp362=) single nucleotide variant not provided [RCV001472081] Chr10:54213948 [GRCh38]
Chr10:55973708 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.948A>G (p.Pro316=) single nucleotide variant not provided [RCV001472085] Chr10:54236860 [GRCh38]
Chr10:55996620 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3045G>A (p.Val1015=) single nucleotide variant not provided [RCV001492992] Chr10:53959809 [GRCh38]
Chr10:55719569 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4368-3136C>G single nucleotide variant not provided [RCV001470314] Chr10:53823366 [GRCh38]
Chr10:55583126 [GRCh37]
Chr10:10q21.1		 likely benign
NC_000010.10:g.(?_55912850)_(55935851_?)dup duplication not provided [RCV001379369] Chr10:55912850..55935851 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NC_000010.10:g.(?_55849734)_(55996701_?)dup duplication not provided [RCV001379370] Chr10:55849734..55996701 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4102G>T (p.Glu1368Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003474000]|Usher syndrome type 1F [RCV002551578]|not provided [RCV001390835] Chr10:53831415 [GRCh38]
Chr10:55591175 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.1338T>C (p.Asn446=) single nucleotide variant not provided [RCV001500792] Chr10:54185236 [GRCh38]
Chr10:55944996 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5748A>G (p.Gln1916=) single nucleotide variant not provided [RCV001483601] Chr10:53821978 [GRCh38]
Chr10:55581738 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2527-4A>G single nucleotide variant not provided [RCV001498265] Chr10:54020420 [GRCh38]
Chr10:55780180 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5823C>T (p.Val1941=) single nucleotide variant not provided [RCV001501459] Chr10:53821903 [GRCh38]
Chr10:55581663 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1440+8G>A single nucleotide variant not provided [RCV001484457] Chr10:54185126 [GRCh38]
Chr10:55944886 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4893A>G (p.Ala1631=) single nucleotide variant not provided [RCV001403894] Chr10:53822833 [GRCh38]
Chr10:55582593 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2124A>G (p.Thr708=) single nucleotide variant not provided [RCV001406213] Chr10:54066853 [GRCh38]
Chr10:55826613 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4699_4715dup (p.Leu1573fs) duplication not provided [RCV001390979] Chr10:53823010..53823011 [GRCh38]
Chr10:55582770..55582771 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.5604G>A (p.Thr1868=) single nucleotide variant not provided [RCV001442784] Chr10:53822122 [GRCh38]
Chr10:55581882 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4202+10C>T single nucleotide variant not provided [RCV001442821] Chr10:53831305 [GRCh38]
Chr10:55591065 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1725C>A (p.Val575=) single nucleotide variant not provided [RCV001416012] Chr10:54153159 [GRCh38]
Chr10:55912919 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.158-8G>T single nucleotide variant not provided [RCV001456293] Chr10:54378950 [GRCh38]
Chr10:56138710 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3528T>C (p.Tyr1176=) single nucleotide variant not provided [RCV001503893] Chr10:53866831 [GRCh38]
Chr10:55626591 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1099-19C>A single nucleotide variant not provided [RCV001460947] Chr10:54195908 [GRCh38]
Chr10:55955668 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4968C>T (p.Leu1656=) single nucleotide variant not provided [RCV001464160] Chr10:53822758 [GRCh38]
Chr10:55582518 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3228A>G (p.Glu1076=) single nucleotide variant not provided [RCV001505018] Chr10:53940870 [GRCh38]
Chr10:55700630 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3405G>A (p.Gln1135=) single nucleotide variant not provided [RCV001488160] Chr10:53903339 [GRCh38]
Chr10:55663099 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4716G>A (p.Arg1572=) single nucleotide variant not provided [RCV001403921] Chr10:53823010 [GRCh38]
Chr10:55582770 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.348G>T (p.Val116=) single nucleotide variant not provided [RCV001472590] Chr10:54369246 [GRCh38]
Chr10:56129006 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.678T>G (p.Thr226=) single nucleotide variant not provided [RCV001491985] Chr10:54329623 [GRCh38]
Chr10:56089383 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3285G>T (p.Leu1095=) single nucleotide variant not provided [RCV001491988] Chr10:53938903 [GRCh38]
Chr10:55698663 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1306-8T>G single nucleotide variant not provided [RCV001478440] Chr10:54185276 [GRCh38]
Chr10:55945036 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3983+8C>A single nucleotide variant not provided [RCV001424096] Chr10:53840312 [GRCh38]
Chr10:55600072 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3990G>A (p.Leu1330=) single nucleotide variant not provided [RCV001437979] Chr10:53831527 [GRCh38]
Chr10:55591287 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3483T>C (p.Thr1161=) single nucleotide variant not provided [RCV001460091] Chr10:53903261 [GRCh38]
Chr10:55663021 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3708C>T (p.Ala1236=) single nucleotide variant not provided [RCV001493643] Chr10:53866651 [GRCh38]
Chr10:55626411 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3123-182T>C single nucleotide variant not provided [RCV001538825] Chr10:53941157 [GRCh38]
Chr10:55700917 [GRCh37]
Chr10:10q21.1		 benign
NM_033056.4(PCDH15):c.4983A>G (p.Ser1661=) single nucleotide variant not provided [RCV001438361] Chr10:53822743 [GRCh38]
Chr10:55582503 [GRCh37]
Chr10:10q21.1		 likely benign
NC_000010.10:g.(?_55849724)_(55849843_?)del deletion not provided [RCV001388042] Chr10:55849724..55849843 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_55849744)_(55955649_?)del deletion not provided [RCV001388043] Chr10:55849744..55955649 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.4299A>G (p.Ala1433=) single nucleotide variant not provided [RCV001429918] Chr10:53827461 [GRCh38]
Chr10:55587221 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1734T>A (p.Thr578=) single nucleotide variant not provided [RCV001443316] Chr10:54153150 [GRCh38]
Chr10:55912910 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1773T>C (p.Pro591=) single nucleotide variant not provided [RCV001445839] Chr10:54153111 [GRCh38]
Chr10:55912871 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4497C>T (p.Asp1499=) single nucleotide variant not provided [RCV001448482] Chr10:53823229 [GRCh38]
Chr10:55582989 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4248G>A (p.Gln1416=) single nucleotide variant not provided [RCV001441006] Chr10:53827512 [GRCh38]
Chr10:55587272 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4062C>T (p.Ile1354=) single nucleotide variant not provided [RCV001411989] Chr10:53831455 [GRCh38]
Chr10:55591215 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.60_61del (p.Leu20_Phe21insTer) microsatellite Autosomal recessive nonsyndromic hearing loss 23 [RCV003475311]|Usher syndrome type 1F [RCV002250982]|not provided [RCV003679083] Chr10:54664202..54664203 [GRCh38]
Chr10:56423962..56423963 [GRCh37]
Chr10:10q21.1		 pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.3297C>T (p.Thr1099=) single nucleotide variant Usher syndrome type 1D [RCV003988869]|not provided [RCV001394187] Chr10:53938891 [GRCh38]
Chr10:55698651 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.831C>T (p.Cys277=) single nucleotide variant not provided [RCV001394204] Chr10:54317316 [GRCh38]
Chr10:56077076 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.609C>T (p.Thr203=) single nucleotide variant not provided [RCV001426242] Chr10:54329692 [GRCh38]
Chr10:56089452 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5772A>T (p.Thr1924=) single nucleotide variant not provided [RCV001404468] Chr10:53821954 [GRCh38]
Chr10:55581714 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4158C>G (p.Leu1386=) single nucleotide variant not provided [RCV001443747] Chr10:53831359 [GRCh38]
Chr10:55591119 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2382A>G (p.Gly794=) single nucleotide variant not provided [RCV001443797] Chr10:54023036 [GRCh38]
Chr10:55782796 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3888T>C (p.Asp1296=) single nucleotide variant Usher syndrome type 1F [RCV001832575]|not provided [RCV001446410] Chr10:53840415 [GRCh38]
Chr10:55600175 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2649G>A (p.Glu883=) single nucleotide variant not provided [RCV001394277] Chr10:54020294 [GRCh38]
Chr10:55780054 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4911G>A (p.Glu1637=) single nucleotide variant not provided [RCV001409520] Chr10:53822815 [GRCh38]
Chr10:55582575 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3672A>G (p.Ala1224=) single nucleotide variant not provided [RCV001420074] Chr10:53866687 [GRCh38]
Chr10:55626447 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1401del (p.Gln467fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003473978]|Usher syndrome type 1F [RCV002307742]|not provided [RCV001387390] Chr10:54185173 [GRCh38]
Chr10:55944933 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.4368-3147T>C single nucleotide variant not provided [RCV001446398] Chr10:53823377 [GRCh38]
Chr10:55583137 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.84dup (p.Asp29Ter) duplication not provided [RCV001389893] Chr10:54664178..54664179 [GRCh38]
Chr10:56423938..56423939 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2550A>T (p.Ala850=) single nucleotide variant not provided [RCV001417154] Chr10:54020393 [GRCh38]
Chr10:55780153 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3502-4C>T single nucleotide variant not provided [RCV001439741] Chr10:53866861 [GRCh38]
Chr10:55626621 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2321del (p.Ala774fs) deletion not provided [RCV001388314] Chr10:54023097 [GRCh38]
Chr10:55782857 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.4503A>T (p.Ser1501=) single nucleotide variant not provided [RCV001446475] Chr10:53823223 [GRCh38]
Chr10:55582983 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3718-10C>T single nucleotide variant not provided [RCV001446579] Chr10:53857273 [GRCh38]
Chr10:55617033 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3374-4C>G single nucleotide variant not provided [RCV001449049] Chr10:53903374 [GRCh38]
Chr10:55663134 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5223T>A (p.Ser1741=) single nucleotide variant not provided [RCV001449065] Chr10:53822503 [GRCh38]
Chr10:55582263 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3501+20T>C single nucleotide variant not provided [RCV001449083] Chr10:53903223 [GRCh38]
Chr10:55662983 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4332T>C (p.Gly1444=) single nucleotide variant not provided [RCV001400266] Chr10:53827428 [GRCh38]
Chr10:55587188 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1359C>T (p.Thr453=) single nucleotide variant not provided [RCV001397787] Chr10:54185215 [GRCh38]
Chr10:55944975 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.318+10T>C single nucleotide variant not provided [RCV001444127] Chr10:54378772 [GRCh38]
Chr10:56138532 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4212-20C>T single nucleotide variant not provided [RCV001444128] Chr10:53827568 [GRCh38]
Chr10:55587328 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4263G>T (p.Ala1421=) single nucleotide variant not provided [RCV001446685] Chr10:53827497 [GRCh38]
Chr10:55587257 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2961A>G (p.Arg987=) single nucleotide variant not provided [RCV001410100] Chr10:53961800 [GRCh38]
Chr10:55721560 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3717+1G>C single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003473929]|not provided [RCV001380844] Chr10:53866641 [GRCh38]
Chr10:55626401 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.2896A>C (p.Arg966=) single nucleotide variant not provided [RCV001399592] Chr10:53961865 [GRCh38]
Chr10:55721625 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4431A>G (p.Lys1477=) single nucleotide variant not provided [RCV001444260] Chr10:53823295 [GRCh38]
Chr10:55583055 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.300A>C (p.Gly100=) single nucleotide variant not provided [RCV001407662] Chr10:54378800 [GRCh38]
Chr10:56138560 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.92-8C>T single nucleotide variant not provided [RCV001407678] Chr10:54527885 [GRCh38]
Chr10:56287645 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1416A>G (p.Glu472=) single nucleotide variant not provided [RCV001446807] Chr10:54185158 [GRCh38]
Chr10:55944918 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1347C>T (p.Thr449=) single nucleotide variant not provided [RCV001428560] Chr10:54185227 [GRCh38]
Chr10:55944987 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4240C>T (p.Arg1414Ter) single nucleotide variant not provided [RCV001381528] Chr10:53827520 [GRCh38]
Chr10:55587280 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3453A>T (p.Gly1151=) single nucleotide variant not provided [RCV001405300] Chr10:53903291 [GRCh38]
Chr10:55663051 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4251C>G (p.Ala1417=) single nucleotide variant not provided [RCV001405749] Chr10:53827509 [GRCh38]
Chr10:55587269 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.714C>G (p.Ala238=) single nucleotide variant not provided [RCV001444678] Chr10:54317433 [GRCh38]
Chr10:56077193 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3741T>C (p.Asp1247=) single nucleotide variant not provided [RCV001415984] Chr10:53857240 [GRCh38]
Chr10:55617000 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4050C>T (p.Arg1350=) single nucleotide variant not provided [RCV001408008] Chr10:53831467 [GRCh38]
Chr10:55591227 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4899G>A (p.Leu1633=) single nucleotide variant not provided [RCV001447178] Chr10:53822827 [GRCh38]
Chr10:55582587 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1725C>T (p.Val575=) single nucleotide variant not provided [RCV001447188] Chr10:54153159 [GRCh38]
Chr10:55912919 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4350A>G (p.Glu1450=) single nucleotide variant not provided [RCV001434220] Chr10:53827410 [GRCh38]
Chr10:55587170 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1692T>C (p.Leu564=) single nucleotide variant not provided [RCV001392953] Chr10:54153192 [GRCh38]
Chr10:55912952 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.92-8C>G single nucleotide variant not provided [RCV001434279] Chr10:54527885 [GRCh38]
Chr10:56287645 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5589A>G (p.Thr1863=) single nucleotide variant Usher syndrome type 1F [RCV001831476]|not provided [RCV001423463] Chr10:53822137 [GRCh38]
Chr10:55581897 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4599_4600dup (p.Ser1534fs) duplication not provided [RCV001388195] Chr10:53823125..53823126 [GRCh38]
Chr10:55582885..55582886 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3207C>T (p.Tyr1069=) single nucleotide variant not provided [RCV001408357] Chr10:53940891 [GRCh38]
Chr10:55700651 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1917+8C>A single nucleotide variant not provided [RCV001434799] Chr10:54132867 [GRCh38]
Chr10:55892627 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1998-5A>T single nucleotide variant not provided [RCV001440222] Chr10:54079429 [GRCh38]
Chr10:55839189 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4341C>T (p.Leu1447=) single nucleotide variant not provided [RCV001447295] Chr10:53827419 [GRCh38]
Chr10:55587179 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3129T>A (p.Pro1043=) single nucleotide variant not provided [RCV001410717] Chr10:53940969 [GRCh38]
Chr10:55700729 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.903G>A (p.Thr301=) single nucleotide variant not provided [RCV001423483] Chr10:54236905 [GRCh38]
Chr10:55996665 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4233G>A (p.Lys1411=) single nucleotide variant not provided [RCV001444964] Chr10:53827527 [GRCh38]
Chr10:55587287 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1785-10T>C single nucleotide variant not provided [RCV001445073] Chr10:54133017 [GRCh38]
Chr10:55892777 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3297C>A (p.Thr1099=) single nucleotide variant not provided [RCV001447575] Chr10:53938891 [GRCh38]
Chr10:55698651 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.985+1G>C single nucleotide variant not provided [RCV001377101] Chr10:54236822 [GRCh38]
Chr10:55996582 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.2826T>C (p.Gly942=) single nucleotide variant not provided [RCV001437893] Chr10:53995691 [GRCh38]
Chr10:55755451 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1521A>G (p.Pro507=) single nucleotide variant not provided [RCV001427132] Chr10:54183513 [GRCh38]
Chr10:55943273 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2221-17_2221-10del microsatellite not provided [RCV001423671] Chr10:54023207..54023214 [GRCh38]
Chr10:55782967..55782974 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.705+10C>T single nucleotide variant not provided [RCV001406204] Chr10:54329586 [GRCh38]
Chr10:56089346 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4872A>T (p.Pro1624=) single nucleotide variant not provided [RCV001447723] Chr10:53822854 [GRCh38]
Chr10:55582614 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5151A>C (p.Thr1717=) single nucleotide variant not provided [RCV001447733] Chr10:53822575 [GRCh38]
Chr10:55582335 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3233-147del deletion not provided [RCV001534747] Chr10:53939102 [GRCh38]
Chr10:55698862 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1170T>C (p.Asn390=) single nucleotide variant not provided [RCV001424107] Chr10:54195818 [GRCh38]
Chr10:55955578 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5124_5136del (p.Leu1708fs) deletion not provided [RCV001424122] Chr10:53822590..53822602 [GRCh38]
Chr10:55582350..55582362 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.877-12dup duplication not provided [RCV001425761] Chr10:54236934..54236935 [GRCh38]
Chr10:55996694..55996695 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1695C>T (p.Ile565=) single nucleotide variant not provided [RCV001440537] Chr10:54153189 [GRCh38]
Chr10:55912949 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4251C>T (p.Ala1417=) single nucleotide variant not provided [RCV001416275] Chr10:53827509 [GRCh38]
Chr10:55587269 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2658A>C (p.Pro886=) single nucleotide variant not provided [RCV001445455] Chr10:54020285 [GRCh38]
Chr10:55780045 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.-28-242C>T single nucleotide variant not provided [RCV001535007] Chr10:54664532 [GRCh38]
Chr10:56424292 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4685_4688dup (p.Arg1564fs) microsatellite not provided [RCV001384295] Chr10:53823037..53823038 [GRCh38]
Chr10:55582797..55582798 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.4734C>T (p.Val1578=) single nucleotide variant not provided [RCV001400378] Chr10:53822992 [GRCh38]
Chr10:55582752 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.27A>G (p.Thr9=) single nucleotide variant not provided [RCV001428416] Chr10:54664236 [GRCh38]
Chr10:56423996 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3579A>G (p.Glu1193=) single nucleotide variant not provided [RCV001442818] Chr10:53866780 [GRCh38]
Chr10:55626540 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2496G>A (p.Leu832=) single nucleotide variant not provided [RCV001408834] Chr10:54022922 [GRCh38]
Chr10:55782682 [GRCh37]
Chr10:10q21.1		 likely benign
NC_000010.11:g.53840315CTTA[3] microsatellite not provided [RCV001398728] Chr10:53840313..53840314 [GRCh38]
Chr10:55600073..55600074 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4202+117C>T single nucleotide variant not provided [RCV001535378] Chr10:53831198 [GRCh38]
Chr10:55590958 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3983+9T>C single nucleotide variant not provided [RCV001400413] Chr10:53840311 [GRCh38]
Chr10:55600071 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.985+10T>G single nucleotide variant not provided [RCV001425898] Chr10:54236813 [GRCh38]
Chr10:55996573 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1836C>T (p.Ser612=) single nucleotide variant not provided [RCV001402917] Chr10:54132956 [GRCh38]
Chr10:55892716 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4836T>C (p.Thr1612=) single nucleotide variant not provided [RCV001432059] Chr10:53822890 [GRCh38]
Chr10:55582650 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2550A>G (p.Ala850=) single nucleotide variant not provided [RCV001408925] Chr10:54020393 [GRCh38]
Chr10:55780153 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1440+2T>C single nucleotide variant Usher syndrome type 1F [RCV002550243]|not provided [RCV001377586] Chr10:54185132 [GRCh38]
Chr10:55944892 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4083C>A (p.Thr1361=) single nucleotide variant not provided [RCV001424558] Chr10:53831434 [GRCh38]
Chr10:55591194 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1998-8G>T single nucleotide variant not provided [RCV001427504] Chr10:54079432 [GRCh38]
Chr10:55839192 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1545T>C (p.Asp515=) single nucleotide variant not provided [RCV001443207] Chr10:54183489 [GRCh38]
Chr10:55943249 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2869-243A>G single nucleotide variant not provided [RCV001572429] Chr10:53962135 [GRCh38]
Chr10:55721895 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2892G>A (p.Arg964=) single nucleotide variant not provided [RCV001435304] Chr10:53961869 [GRCh38]
Chr10:55721629 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5379_5381del (p.Thr1794del) deletion not provided [RCV001425948] Chr10:53822345..53822347 [GRCh38]
Chr10:55582105..55582107 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3010-16T>A single nucleotide variant not provided [RCV001402961] Chr10:53959860 [GRCh38]
Chr10:55719620 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1596T>C (p.Thr532=) single nucleotide variant not provided [RCV001406566] Chr10:54153288 [GRCh38]
Chr10:55913048 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4202+9del deletion not provided [RCV001416851] Chr10:53831306 [GRCh38]
Chr10:55591066 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4509G>A (p.Lys1503=) single nucleotide variant not provided [RCV001445925] Chr10:53823217 [GRCh38]
Chr10:55582977 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5169T>C (p.Pro1723=) single nucleotide variant not provided [RCV001445999] Chr10:53822557 [GRCh38]
Chr10:55582317 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1305+200G>T single nucleotide variant not provided [RCV001583687] Chr10:54195483 [GRCh38]
Chr10:55955243 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3117A>G (p.Glu1039=) single nucleotide variant not provided [RCV001482069] Chr10:53959737 [GRCh38]
Chr10:55719497 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4290A>C (p.Ala1430=) single nucleotide variant not provided [RCV001450473] Chr10:53827470 [GRCh38]
Chr10:55587230 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4029G>A (p.Pro1343=) single nucleotide variant not provided [RCV001461480] Chr10:53831488 [GRCh38]
Chr10:55591248 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5358C>T (p.Ile1786=) single nucleotide variant not provided [RCV001457156] Chr10:53822368 [GRCh38]
Chr10:55582128 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3666T>G (p.Val1222=) single nucleotide variant not provided [RCV001465023] Chr10:53866693 [GRCh38]
Chr10:55626453 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4524G>A (p.Lys1508=) single nucleotide variant Usher syndrome type 1F [RCV001826278]|not provided [RCV001454374] Chr10:53823202 [GRCh38]
Chr10:55582962 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3123-5T>C single nucleotide variant not provided [RCV001454412] Chr10:53940980 [GRCh38]
Chr10:55700740 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3882T>C (p.His1294=) single nucleotide variant not provided [RCV001454423] Chr10:53840421 [GRCh38]
Chr10:55600181 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.675G>A (p.Lys225=) single nucleotide variant not provided [RCV001450916] Chr10:54329626 [GRCh38]
Chr10:56089386 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2292T>C (p.Arg764=) single nucleotide variant not provided [RCV001461989] Chr10:54023126 [GRCh38]
Chr10:55782886 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.282T>G (p.Leu94=) single nucleotide variant not provided [RCV001465181] Chr10:54378818 [GRCh38]
Chr10:56138578 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.706-31A>G single nucleotide variant not provided [RCV001653102] Chr10:54317472 [GRCh38]
Chr10:56077232 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3502-19T>C single nucleotide variant not provided [RCV001509715] Chr10:53866876 [GRCh38]
Chr10:55626636 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.4077A>G (p.Ala1359=) single nucleotide variant not provided [RCV001486185] Chr10:53831440 [GRCh38]
Chr10:55591200 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.92-165G>A single nucleotide variant not provided [RCV001725693] Chr10:54528042 [GRCh38]
Chr10:56287802 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4211+318T>C single nucleotide variant not provided [RCV001681812] Chr10:53828247 [GRCh38]
Chr10:55588007 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3983+232C>T single nucleotide variant not provided [RCV001684219] Chr10:53840088 [GRCh38]
Chr10:55599848 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4367+1986del deletion not provided [RCV001619491] Chr10:53825407 [GRCh38]
Chr10:55585167 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3267C>T (p.Ile1089=) single nucleotide variant not provided [RCV001502592] Chr10:53938921 [GRCh38]
Chr10:55698681 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3502-22_3502-21dup duplication not provided [RCV001510177] Chr10:53866870..53866871 [GRCh38]
Chr10:55626630..55626631 [GRCh37]
Chr10:10q21.1		 benign
NM_033056.4(PCDH15):c.5145A>G (p.Arg1715=) single nucleotide variant not provided [RCV001496434] Chr10:53822581 [GRCh38]
Chr10:55582341 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3374-9G>C single nucleotide variant not provided [RCV001465539] Chr10:53903379 [GRCh38]
Chr10:55663139 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1758G>T (p.Ala586=) single nucleotide variant not provided [RCV001491243] Chr10:54153126 [GRCh38]
Chr10:55912886 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2622A>G (p.Leu874=) single nucleotide variant not provided [RCV001502674] Chr10:54020321 [GRCh38]
Chr10:55780081 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4212-92del deletion not provided [RCV001687054] Chr10:53827640 [GRCh38]
Chr10:55587400 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1602C>T (p.Val534=) single nucleotide variant not provided [RCV001479738] Chr10:54153282 [GRCh38]
Chr10:55913042 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4110A>G (p.Leu1370=) single nucleotide variant not provided [RCV001503380] Chr10:53831407 [GRCh38]
Chr10:55591167 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1306-4362C>A single nucleotide variant not provided [RCV001655148] Chr10:54189630 [GRCh38]
Chr10:55949390 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1857G>C (p.Leu619=) single nucleotide variant not provided [RCV001476300] Chr10:54132935 [GRCh38]
Chr10:55892695 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3633T>C (p.His1211=) single nucleotide variant not provided [RCV001496817] Chr10:53866726 [GRCh38]
Chr10:55626486 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1518G>T (p.Thr506=) single nucleotide variant not provided [RCV001496861] Chr10:54183516 [GRCh38]
Chr10:55943276 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.81G>A (p.Gln27=) single nucleotide variant not provided [RCV001499950] Chr10:54664182 [GRCh38]
Chr10:56423942 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2091+212C>T single nucleotide variant not provided [RCV001590762] Chr10:54079119 [GRCh38]
Chr10:55838879 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2997A>G (p.Thr999=) single nucleotide variant not provided [RCV001466070] Chr10:53961764 [GRCh38]
Chr10:55721524 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4422A>G (p.Glu1474=) single nucleotide variant not provided [RCV001455858] Chr10:53823304 [GRCh38]
Chr10:55583064 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4413A>T (p.Ser1471=) single nucleotide variant not provided [RCV001503824] Chr10:53823313 [GRCh38]
Chr10:55583073 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4290A>T (p.Ala1430=) single nucleotide variant not provided [RCV001497235] Chr10:53827470 [GRCh38]
Chr10:55587230 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5394T>G (p.Leu1798=) single nucleotide variant not provided [RCV001452646] Chr10:53822332 [GRCh38]
Chr10:55582092 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1449A>T (p.Ala483=) single nucleotide variant not provided [RCV001487346] Chr10:54183585 [GRCh38]
Chr10:55943345 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4251C>A (p.Ala1417=) single nucleotide variant not provided [RCV001456090] Chr10:53827509 [GRCh38]
Chr10:55587269 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4167T>C (p.Ile1389=) single nucleotide variant not provided [RCV001480654] Chr10:53831350 [GRCh38]
Chr10:55591110 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2869-6_2869-2del microsatellite not provided [RCV001487818] Chr10:53961894..53961898 [GRCh38]
Chr10:55721654..55721658 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.475-299G>A single nucleotide variant not provided [RCV001716594] Chr10:54346783 [GRCh38]
Chr10:56106543 [GRCh37]
Chr10:10q21.1		 benign
NM_033056.4(PCDH15):c.4872A>G (p.Pro1624=) single nucleotide variant not provided [RCV001484110] Chr10:53822854 [GRCh38]
Chr10:55582614 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3983+140_3983+141insAAC insertion not provided [RCV001609588] Chr10:53840179..53840180 [GRCh38]
Chr10:55599939..55599940 [GRCh37]
Chr10:10q21.1		 benign
NM_033056.4(PCDH15):c.5865G>C (p.Leu1955=) single nucleotide variant not provided [RCV001453214] Chr10:53821861 [GRCh38]
Chr10:55581621 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3414T>C (p.Asn1138=) single nucleotide variant not provided [RCV001480785] Chr10:53903330 [GRCh38]
Chr10:55663090 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3717+174AT[14] microsatellite not provided [RCV001588266] Chr10:53866446..53866447 [GRCh38]
Chr10:55626206..55626207 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1917+13GT[13] microsatellite not provided [RCV001716063] Chr10:54132840..54132841 [GRCh38]
Chr10:55892600..55892601 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.877-64G>A single nucleotide variant not provided [RCV001687265] Chr10:54236995 [GRCh38]
Chr10:55996755 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.2544T>C (p.Leu848=) single nucleotide variant not provided [RCV001478048] Chr10:54020399 [GRCh38]
Chr10:55780159 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1560A>G (p.Thr520=) single nucleotide variant not provided [RCV001471382] Chr10:54183474 [GRCh38]
Chr10:55943234 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5856T>G (p.Ser1952=) single nucleotide variant not provided [RCV001456553] Chr10:53821870 [GRCh38]
Chr10:55581630 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2391C>T (p.His797=) single nucleotide variant not provided [RCV001485292] Chr10:54023027 [GRCh38]
Chr10:55782787 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3678C>T (p.Asp1226=) single nucleotide variant not provided [RCV001488893] Chr10:53866681 [GRCh38]
Chr10:55626441 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1918-165C>T single nucleotide variant not provided [RCV001692589] Chr10:54090228 [GRCh38]
Chr10:55849988 [GRCh37]
Chr10:10q21.1		 benign
NM_033056.4(PCDH15):c.4974A>T (p.Ser1658=) single nucleotide variant not provided [RCV001464152] Chr10:53822752 [GRCh38]
Chr10:55582512 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1918-6C>T single nucleotide variant Usher syndrome type 1F [RCV001826337]|not provided [RCV001498501] Chr10:54090069 [GRCh38]
Chr10:55849829 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1746G>C (p.Thr582=) single nucleotide variant not provided [RCV001478345] Chr10:54153138 [GRCh38]
Chr10:55912898 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3717+174AT[10] microsatellite not provided [RCV001692692] Chr10:53866447..53866448 [GRCh38]
Chr10:55626207..55626208 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.92-13T>C single nucleotide variant not provided [RCV001590646] Chr10:54527890 [GRCh38]
Chr10:56287650 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3984-7A>T single nucleotide variant not provided [RCV001394166] Chr10:53831540 [GRCh38]
Chr10:55591300 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3717+1G>T single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003473966]|Usher syndrome type 1D [RCV001810507]|Usher syndrome type 1F [RCV002551549]|not provided [RCV001386495] Chr10:53866641 [GRCh38]
Chr10:55626401 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.4212-4C>T single nucleotide variant not provided [RCV001399518] Chr10:53827552 [GRCh38]
Chr10:55587312 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.789A>G (p.Pro263=) single nucleotide variant not provided [RCV001467008] Chr10:54317358 [GRCh38]
Chr10:56077118 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2091+7A>G single nucleotide variant not provided [RCV001467010] Chr10:54079324 [GRCh38]
Chr10:55839084 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4617T>C (p.Asn1539=) single nucleotide variant not provided [RCV001469563] Chr10:53823109 [GRCh38]
Chr10:55582869 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5655C>T (p.His1885=) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001578643]|Usher syndrome type 1F [RCV001578644]|not provided [RCV001469897] Chr10:53822071 [GRCh38]
Chr10:55581831 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.4494A>G (p.Val1498=) single nucleotide variant not provided [RCV001419168] Chr10:53823232 [GRCh38]
Chr10:55582992 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5043G>A (p.Val1681=) single nucleotide variant not provided [RCV001485865] Chr10:53822683 [GRCh38]
Chr10:55582443 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5406G>A (p.Thr1802=) single nucleotide variant not provided [RCV001473408] Chr10:53822320 [GRCh38]
Chr10:55582080 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1479C>A (p.Val493=) single nucleotide variant not provided [RCV001497797] Chr10:54183555 [GRCh38]
Chr10:55943315 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4314G>T (p.Pro1438=) single nucleotide variant not provided [RCV001455336] Chr10:53827446 [GRCh38]
Chr10:55587206 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.822T>G (p.Thr274=) single nucleotide variant not provided [RCV001503037] Chr10:54317325 [GRCh38]
Chr10:56077085 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.363C>T (p.Ile121=) single nucleotide variant not provided [RCV001506495] Chr10:54369231 [GRCh38]
Chr10:56128991 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3324A>G (p.Gln1108=) single nucleotide variant not provided [RCV001473518] Chr10:53938864 [GRCh38]
Chr10:55698624 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2056C>T (p.Leu686=) single nucleotide variant not provided [RCV001460992] Chr10:54079366 [GRCh38]
Chr10:55839126 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3822T>C (p.Tyr1274=) single nucleotide variant not provided [RCV001503209] Chr10:53840481 [GRCh38]
Chr10:55600241 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.876+10C>T single nucleotide variant not provided [RCV001468697] Chr10:54317261 [GRCh38]
Chr10:56077021 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2032A>C (p.Arg678=) single nucleotide variant not provided [RCV001470834] Chr10:54079390 [GRCh38]
Chr10:55839150 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.933G>C (p.Arg311=) single nucleotide variant not provided [RCV001473853] Chr10:54236875 [GRCh38]
Chr10:55996635 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.318+9dup duplication not provided [RCV001497238] Chr10:54378765..54378766 [GRCh38]
Chr10:56138525..56138526 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2046T>C (p.Asp682=) single nucleotide variant not provided [RCV001501924] Chr10:54079376 [GRCh38]
Chr10:55839136 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2316C>T (p.Tyr772=) single nucleotide variant not provided [RCV001502424] Chr10:54023102 [GRCh38]
Chr10:55782862 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4305C>T (p.Pro1435=) single nucleotide variant not provided [RCV001467419] Chr10:53827455 [GRCh38]
Chr10:55587215 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.297C>T (p.Thr99=) single nucleotide variant not provided [RCV001506966] Chr10:54378803 [GRCh38]
Chr10:56138563 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1425A>G (p.Gln475=) single nucleotide variant not provided [RCV001440117] Chr10:54185149 [GRCh38]
Chr10:55944909 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1518G>A (p.Thr506=) single nucleotide variant not provided [RCV001496268] Chr10:54183516 [GRCh38]
Chr10:55943276 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.978C>T (p.Ile326=) single nucleotide variant not provided [RCV001453489] Chr10:54236830 [GRCh38]
Chr10:55996590 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1304_1305delinsCC (p.Asp435Ala) indel not provided [RCV001498257] Chr10:54195683..54195684 [GRCh38]
Chr10:55955443..55955444 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1797C>T (p.Cys599=) single nucleotide variant not provided [RCV001464576] Chr10:54132995 [GRCh38]
Chr10:55892755 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2118G>A (p.Val706=) single nucleotide variant not provided [RCV001488561] Chr10:54066859 [GRCh38]
Chr10:55826619 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1557T>C (p.Tyr519=) single nucleotide variant not provided [RCV001488569] Chr10:54183477 [GRCh38]
Chr10:55943237 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1116T>G (p.Gly372=) single nucleotide variant not provided [RCV001478863] Chr10:54195872 [GRCh38]
Chr10:55955632 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1462C>T (p.Gln488Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003473937]|not provided [RCV001381711] Chr10:54183572 [GRCh38]
Chr10:55943332 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.4211+9A>G single nucleotide variant not provided [RCV001429473] Chr10:53828556 [GRCh38]
Chr10:55588316 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4212-4C>A single nucleotide variant not provided [RCV001403987] Chr10:53827552 [GRCh38]
Chr10:55587312 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1152A>G (p.Glu384=) single nucleotide variant not provided [RCV001425351] Chr10:54195836 [GRCh38]
Chr10:55955596 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5091C>T (p.Ser1697=) single nucleotide variant not provided [RCV001496815] Chr10:53822635 [GRCh38]
Chr10:55582395 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4410C>T (p.Asn1470=) single nucleotide variant not provided [RCV001497862] Chr10:53823316 [GRCh38]
Chr10:55583076 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.318+9T>C single nucleotide variant not provided [RCV001453164] Chr10:54378773 [GRCh38]
Chr10:56138533 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1314C>T (p.Asp438=) single nucleotide variant not provided [RCV001478373] Chr10:54185260 [GRCh38]
Chr10:55945020 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.706-9_706-8delinsGT indel not provided [RCV001415529] Chr10:54317449..54317450 [GRCh38]
Chr10:56077209..56077210 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4548A>G (p.Leu1516=) single nucleotide variant not provided [RCV001392989] Chr10:53823178 [GRCh38]
Chr10:55582938 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4211+7A>G single nucleotide variant not provided [RCV001417607] Chr10:53828558 [GRCh38]
Chr10:55588318 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3501+2T>C single nucleotide variant Usher syndrome type 1F [RCV002550241]|not provided [RCV001376752] Chr10:53903241 [GRCh38]
Chr10:55663001 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.1026T>G (p.Pro342=) single nucleotide variant not provided [RCV001393216] Chr10:54214008 [GRCh38]
Chr10:55973768 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1977_1978del (p.Arg659fs) microsatellite Autosomal recessive nonsyndromic hearing loss 23 [RCV003473947]|not provided [RCV001383714] Chr10:54090003..54090004 [GRCh38]
Chr10:55849763..55849764 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.3729C>G (p.Val1243=) single nucleotide variant not provided [RCV001476750] Chr10:53857252 [GRCh38]
Chr10:55617012 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2823G>A (p.Lys941=) single nucleotide variant not provided [RCV001453516] Chr10:53995694 [GRCh38]
Chr10:55755454 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2805G>T (p.Val935=) single nucleotide variant not provided [RCV001461872] Chr10:53995712 [GRCh38]
Chr10:55755472 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4650C>T (p.Asp1550=) single nucleotide variant not provided [RCV001499443] Chr10:53823076 [GRCh38]
Chr10:55582836 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2616A>G (p.Gly872=) single nucleotide variant not provided [RCV001432409] Chr10:54020327 [GRCh38]
Chr10:55780087 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.595-9T>A single nucleotide variant not provided [RCV001406780] Chr10:54329715 [GRCh38]
Chr10:56089475 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.475-14dup duplication not provided [RCV001511052] Chr10:54346492..54346493 [GRCh38]
Chr10:56106252..56106253 [GRCh37]
Chr10:10q21.1		 benign
NM_033056.4(PCDH15):c.5280T>G (p.Pro1760=) single nucleotide variant not provided [RCV001463233] Chr10:53822446 [GRCh38]
Chr10:55582206 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4671+1624G>A single nucleotide variant not provided [RCV001483447] Chr10:53808932 [GRCh38]
Chr10:55568692 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1344C>T (p.Tyr448=) single nucleotide variant not provided [RCV001434709] Chr10:54185230 [GRCh38]
Chr10:55944990 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4380C>T (p.Leu1460=) single nucleotide variant not provided [RCV001420025] Chr10:53823346 [GRCh38]
Chr10:55583106 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2700T>C (p.Asp900=) single nucleotide variant not provided [RCV001398229] Chr10:54020243 [GRCh38]
Chr10:55780003 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4980T>C (p.Ser1660=) single nucleotide variant not provided [RCV001417726] Chr10:53822746 [GRCh38]
Chr10:55582506 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3411A>G (p.Glu1137=) single nucleotide variant not provided [RCV001417752] Chr10:53903333 [GRCh38]
Chr10:55663093 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.985+6dup duplication not provided [RCV001463364] Chr10:54236816..54236817 [GRCh38]
Chr10:55996576..55996577 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2004G>A (p.Gly668=) single nucleotide variant not provided [RCV001393423] Chr10:54079418 [GRCh38]
Chr10:55839178 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3096C>A (p.Ile1032=) single nucleotide variant not provided [RCV001503907] Chr10:53959758 [GRCh38]
Chr10:55719518 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3984-1G>T single nucleotide variant not provided [RCV001377186] Chr10:53831534 [GRCh38]
Chr10:55591294 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.2013C>T (p.Thr671=) single nucleotide variant not provided [RCV001427674] Chr10:54079409 [GRCh38]
Chr10:55839169 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3306C>T (p.Ser1102=) single nucleotide variant not provided [RCV001432929] Chr10:53938882 [GRCh38]
Chr10:55698642 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3806+7del deletion not provided [RCV001466488] Chr10:53857168 [GRCh38]
Chr10:55616928 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5076T>C (p.Ser1692=) single nucleotide variant not provided [RCV001435171] Chr10:53822650 [GRCh38]
Chr10:55582410 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3010-15T>G single nucleotide variant not provided [RCV001418199] Chr10:53959859 [GRCh38]
Chr10:55719619 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4255T>C (p.Leu1419=) single nucleotide variant not provided [RCV001494122] Chr10:53827505 [GRCh38]
Chr10:55587265 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5580C>T (p.Ser1860=) single nucleotide variant not provided [RCV001483932] Chr10:53822146 [GRCh38]
Chr10:55581906 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2223A>T (p.Ala741=) single nucleotide variant not provided [RCV001505601] Chr10:54023195 [GRCh38]
Chr10:55782955 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4128dup (p.Leu1378fs) duplication not provided [RCV001386493] Chr10:53831388..53831389 [GRCh38]
Chr10:55591148..55591149 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.1899T>C (p.Ala633=) single nucleotide variant not provided [RCV001437092] Chr10:54132893 [GRCh38]
Chr10:55892653 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3654C>T (p.Phe1218=) single nucleotide variant not provided [RCV001441411] Chr10:53866705 [GRCh38]
Chr10:55626465 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.318+8A>G single nucleotide variant not provided [RCV001398995] Chr10:54378774 [GRCh38]
Chr10:56138534 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4644A>G (p.Glu1548=) single nucleotide variant Inborn genetic diseases [RCV003365419]|PCDH15-related disorder [RCV004540466]|not provided [RCV001504143] Chr10:53810583 [GRCh38]
Chr10:55570343 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3374-6C>T single nucleotide variant not provided [RCV001419118] Chr10:53903376 [GRCh38]
Chr10:55663136 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2091+1G>A single nucleotide variant not provided [RCV001379246] Chr10:54079330 [GRCh38]
Chr10:55839090 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.4731A>G (p.Ser1577=) single nucleotide variant not provided [RCV001430831] Chr10:53822995 [GRCh38]
Chr10:55582755 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3333C>A (p.Ser1111=) single nucleotide variant not provided [RCV001466871] Chr10:53938855 [GRCh38]
Chr10:55698615 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5220C>A (p.Ile1740=) single nucleotide variant not provided [RCV001468238] Chr10:53822506 [GRCh38]
Chr10:55582266 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1353C>G (p.Val451=) single nucleotide variant not provided [RCV001468306] Chr10:54185221 [GRCh38]
Chr10:55944981 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3600T>G (p.Tyr1200Ter) single nucleotide variant not provided [RCV001386332] Chr10:53866759 [GRCh38]
Chr10:55626519 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.4437A>G (p.Gln1479=) single nucleotide variant not provided [RCV001439044] Chr10:53823289 [GRCh38]
Chr10:55583049 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.836C>T (p.Pro279Leu) single nucleotide variant not provided [RCV001756835] Chr10:54317311 [GRCh38]
Chr10:56077071 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4982C>A (p.Ser1661Ter) single nucleotide variant not specified [RCV002238668] Chr10:53822744 [GRCh38]
Chr10:55582504 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.10:g.(55849824_55892634)_(55943354_55944893)del deletion Usher syndrome type 1F [RCV002238669] Chr10:55892634..55943354 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.2404A>G (p.Thr802Ala) single nucleotide variant not provided [RCV001758116] Chr10:54023014 [GRCh38]
Chr10:55782774 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2568A>T (p.Ile856=) single nucleotide variant not provided [RCV002104344] Chr10:54020375 [GRCh38]
Chr10:55780135 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3476T>C (p.Met1159Thr) single nucleotide variant not provided [RCV001760992] Chr10:53903268 [GRCh38]
Chr10:55663028 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2336G>T (p.Arg779Ile) single nucleotide variant not provided [RCV001770638] Chr10:54023082 [GRCh38]
Chr10:55782842 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4303C>A (p.Pro1435Thr) single nucleotide variant not provided [RCV001765885] Chr10:53827457 [GRCh38]
Chr10:55587217 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.16T>A (p.Tyr6Asn) single nucleotide variant not provided [RCV001769052] Chr10:54664247 [GRCh38]
Chr10:56424007 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1834A>C (p.Ser612Arg) single nucleotide variant not provided [RCV001774406] Chr10:54132958 [GRCh38]
Chr10:55892718 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4632del (p.Arg1545fs) deletion not provided [RCV001782576] Chr10:53823094 [GRCh38]
Chr10:55582854 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.174C>A (p.Asp58Glu) single nucleotide variant not provided [RCV001758505] Chr10:54378926 [GRCh38]
Chr10:56138686 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4955_4959dup (p.Leu1654fs) duplication not provided [RCV001770819] Chr10:53806842..53806843 [GRCh38]
Chr10:55566602..55566603 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1190T>A (p.Met397Lys) single nucleotide variant not provided [RCV001756748] Chr10:54195798 [GRCh38]
Chr10:55955558 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3861G>T (p.Glu1287Asp) single nucleotide variant not provided [RCV001797339] Chr10:53840442 [GRCh38]
Chr10:55600202 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4672-1712_4672-1710del microsatellite Usher syndrome type 1D [RCV001733544] Chr10:53808840..53808842 [GRCh38]
Chr10:55568600..55568602 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4301C>T (p.Ala1434Val) single nucleotide variant not provided [RCV001776638] Chr10:53827459 [GRCh38]
Chr10:55587219 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3917G>A (p.Cys1306Tyr) single nucleotide variant not provided [RCV001758214] Chr10:53840386 [GRCh38]
Chr10:55600146 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.157+41381G>C single nucleotide variant not specified [RCV001779501] Chr10:54486431 [GRCh38]
Chr10:56246191 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.417C>G (p.Asp139Glu) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001809325] Chr10:54369177 [GRCh38]
Chr10:56128937 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.5353_5355del (p.Ser1785del) deletion not provided [RCV001806593] Chr10:53822371..53822373 [GRCh38]
Chr10:55582131..55582133 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1136C>T (p.Ala379Val) single nucleotide variant not provided [RCV001907606] Chr10:54195852 [GRCh38]
Chr10:55955612 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4208_4209del (p.Lys1403fs) deletion Ear malformation [RCV001814510] Chr10:53828567..53828568 [GRCh38]
Chr10:55588327..55588328 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3101G>T (p.Arg1034Leu) single nucleotide variant Inborn genetic diseases [RCV003247029]|not provided [RCV001806574] Chr10:53959753 [GRCh38]
Chr10:55719513 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5753T>C (p.Met1918Thr) single nucleotide variant not provided [RCV002001690] Chr10:53821973 [GRCh38]
Chr10:55581733 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.318+4A>C single nucleotide variant not provided [RCV002025215] Chr10:54378778 [GRCh38]
Chr10:56138538 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5866T>G (p.Ter1956Glu) single nucleotide variant not provided [RCV001864110] Chr10:53821860 [GRCh38]
Chr10:55581620 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1987C>T (p.Leu663Phe) single nucleotide variant not provided [RCV002009218] Chr10:54089994 [GRCh38]
Chr10:55849754 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5429T>G (p.Leu1810Arg) single nucleotide variant not provided [RCV002024785] Chr10:53822297 [GRCh38]
Chr10:55582057 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4096A>G (p.Arg1366Gly) single nucleotide variant not provided [RCV001896397] Chr10:53831421 [GRCh38]
Chr10:55591181 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4555G>A (p.Glu1519Lys) single nucleotide variant not provided [RCV001913754] Chr10:53823171 [GRCh38]
Chr10:55582931 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3495_3496del (p.Arg1165fs) microsatellite Usher syndrome type 1F [RCV001825103] Chr10:53903248..53903249 [GRCh38]
Chr10:55663008..55663009 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1627G>A (p.Glu543Lys) single nucleotide variant not provided [RCV001896784] Chr10:54153257 [GRCh38]
Chr10:55913017 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4616_4647dup (p.Asp1550delinsIleGlnThrPheHisArgGluGlnIleLeuTer) duplication not provided [RCV001864582] Chr10:53823078..53823079 [GRCh38]
Chr10:55582838..55582839 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3497T>A (p.Val1166Glu) single nucleotide variant not provided [RCV001988834] Chr10:53903247 [GRCh38]
Chr10:55663007 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3134T>C (p.Val1045Ala) single nucleotide variant not provided [RCV001911709] Chr10:53940964 [GRCh38]
Chr10:55700724 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5586G>A (p.Met1862Ile) single nucleotide variant not provided [RCV001969226] Chr10:53822140 [GRCh38]
Chr10:55581900 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4072G>C (p.Glu1358Gln) single nucleotide variant not provided [RCV001929016] Chr10:53831445 [GRCh38]
Chr10:55591205 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4934T>C (p.Leu1645Pro) single nucleotide variant not provided [RCV002008611] Chr10:53822792 [GRCh38]
Chr10:55582552 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5697G>A (p.Met1899Ile) single nucleotide variant not provided [RCV002001494] Chr10:53822029 [GRCh38]
Chr10:55581789 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4905G>T (p.Glu1635Asp) single nucleotide variant not provided [RCV001910565] Chr10:53822821 [GRCh38]
Chr10:55582581 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3536T>C (p.Met1179Thr) single nucleotide variant not provided [RCV001987312] Chr10:53866823 [GRCh38]
Chr10:55626583 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1835G>C (p.Ser612Thr) single nucleotide variant not provided [RCV001988521] Chr10:54132957 [GRCh38]
Chr10:55892717 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4197C>G (p.Tyr1399Ter) single nucleotide variant not provided [RCV001987242] Chr10:53831320 [GRCh38]
Chr10:55591080 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2843_2847dup (p.Ala950fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV002052080] Chr10:53995669..53995670 [GRCh38]
Chr10:55755429..55755430 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.4349_4352dup (p.Gly1452fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV004571496]|not provided [RCV001914524] Chr10:53827407..53827408 [GRCh38]
Chr10:55587167..55587168 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.4193G>A (p.Ser1398Asn) single nucleotide variant not provided [RCV002008991] Chr10:53831324 [GRCh38]
Chr10:55591084 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2410A>T (p.Thr804Ser) single nucleotide variant not provided [RCV001915271] Chr10:54023008 [GRCh38]
Chr10:55782768 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4201C>G (p.Gln1401Glu) single nucleotide variant not provided [RCV001971476] Chr10:53831316 [GRCh38]
Chr10:55591076 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4840A>C (p.Ile1614Leu) single nucleotide variant not provided [RCV002009141] Chr10:53822886 [GRCh38]
Chr10:55582646 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1208A>G (p.Tyr403Cys) single nucleotide variant not provided [RCV001896641] Chr10:54195780 [GRCh38]
Chr10:55955540 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4827T>C (p.Asn1609=) single nucleotide variant not provided [RCV001949367] Chr10:53822899 [GRCh38]
Chr10:55582659 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2212C>T (p.Gln738Ter) single nucleotide variant not provided [RCV001984688] Chr10:54066765 [GRCh38]
Chr10:55826525 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2449C>T (p.Pro817Ser) single nucleotide variant not provided [RCV001984691] Chr10:54022969 [GRCh38]
Chr10:55782729 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3963C>G (p.Ile1321Met) single nucleotide variant not provided [RCV001896172] Chr10:53840340 [GRCh38]
Chr10:55600100 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1590+1G>A single nucleotide variant not provided [RCV001986788] Chr10:54183443 [GRCh38]
Chr10:55943203 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4349A>C (p.Glu1450Ala) single nucleotide variant not provided [RCV001912340] Chr10:53827411 [GRCh38]
Chr10:55587171 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5759C>G (p.Pro1920Arg) single nucleotide variant not provided [RCV001964944] Chr10:53821967 [GRCh38]
Chr10:55581727 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5709A>G (p.Ile1903Met) single nucleotide variant not provided [RCV001891111] Chr10:53822017 [GRCh38]
Chr10:55581777 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4666A>G (p.Ile1556Val) single nucleotide variant not provided [RCV001983299] Chr10:53823060 [GRCh38]
Chr10:55582820 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4280C>A (p.Pro1427Gln) single nucleotide variant not provided [RCV002003950] Chr10:53827480 [GRCh38]
Chr10:55587240 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4835C>G (p.Thr1612Ser) single nucleotide variant not provided [RCV001969174] Chr10:53822891 [GRCh38]
Chr10:55582651 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1099-10T>A single nucleotide variant not provided [RCV002020474] Chr10:54195899 [GRCh38]
Chr10:55955659 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4360A>C (p.Ser1454Arg) single nucleotide variant not provided [RCV002039603] Chr10:53827400 [GRCh38]
Chr10:55587160 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.10:g.(?_56423912)_(56424022_?)dup duplication not provided [RCV001982811] Chr10:56423912..56424022 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.290A>G (p.Asn97Ser) single nucleotide variant not provided [RCV002022451] Chr10:54378810 [GRCh38]
Chr10:56138570 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1034C>T (p.Ala345Val) single nucleotide variant not provided [RCV002020882] Chr10:54214000 [GRCh38]
Chr10:55973760 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3341T>G (p.Val1114Gly) single nucleotide variant Inborn genetic diseases [RCV002552977]|not provided [RCV001908310] Chr10:53938847 [GRCh38]
Chr10:55698607 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.2267del (p.Leu756fs) deletion not provided [RCV001910603] Chr10:54023151 [GRCh38]
Chr10:55782911 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2798G>A (p.Gly933Glu) single nucleotide variant not provided [RCV001893192] Chr10:53995719 [GRCh38]
Chr10:55755479 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.423_430dup (p.Ser144fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003475107]|Usher syndrome type 1F [RCV001844738]|not provided [RCV002543332] Chr10:54369163..54369164 [GRCh38]
Chr10:56128923..56128924 [GRCh37]
Chr10:10q21.1		 pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.1305+2T>A single nucleotide variant not provided [RCV002021200] Chr10:54195681 [GRCh38]
Chr10:55955441 [GRCh37]
Chr10:10q21.1		 likely pathogenic
GRCh37/hg19 10q11.23-21.1(chr10:52752503-57406199) copy number gain not specified [RCV002052870] Chr10:52752503..57406199 [GRCh37]
Chr10:10q11.23-21.1		 uncertain significance
NM_033056.4(PCDH15):c.5072G>C (p.Ser1691Thr) single nucleotide variant not provided [RCV001984527] Chr10:53822654 [GRCh38]
Chr10:55582414 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2573G>A (p.Ser858Asn) single nucleotide variant not provided [RCV001982834] Chr10:54020370 [GRCh38]
Chr10:55780130 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh37/hg19 10q21.1(chr10:56362064-56762641)x1 copy number loss not provided [RCV001833037] Chr10:56362064..56762641 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.10:g.(?_55955423)_(55955669_?)dup duplication not provided [RCV002004811] Chr10:55955423..55955669 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.10:g.(?_55892625)_(55892777_?)del deletion not provided [RCV001947006] Chr10:55892625..55892777 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2210G>C (p.Gly737Ala) single nucleotide variant not provided [RCV002003696] Chr10:54066767 [GRCh38]
Chr10:55826527 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3688A>T (p.Lys1230Ter) single nucleotide variant not provided [RCV002007173] Chr10:53866671 [GRCh38]
Chr10:55626431 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.4739T>C (p.Leu1580Ser) single nucleotide variant not provided [RCV002024660] Chr10:53822987 [GRCh38]
Chr10:55582747 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5473A>G (p.Ile1825Val) single nucleotide variant not provided [RCV002041826] Chr10:53822253 [GRCh38]
Chr10:55582013 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh37/hg19 10q21.1(chr10:55199169-56857578) copy number gain not specified [RCV002052872] Chr10:55199169..56857578 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh37/hg19 10q21.1(chr10:56173058-57499910)x1 copy number loss not provided [RCV001834470] Chr10:56173058..57499910 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5761T>G (p.Ser1921Ala) single nucleotide variant not provided [RCV002007940] Chr10:53821965 [GRCh38]
Chr10:55581725 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2491A>T (p.Asn831Tyr) single nucleotide variant not provided [RCV001983711] Chr10:54022927 [GRCh38]
Chr10:55782687 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh37/hg19 10q21.1(chr10:55584785-55776189)x1 copy number loss not provided [RCV001827890] Chr10:55584785..55776189 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4307C>T (p.Pro1436Leu) single nucleotide variant not provided [RCV001970277] Chr10:53827453 [GRCh38]
Chr10:55587213 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2764T>A (p.Tyr922Asn) single nucleotide variant not provided [RCV001908633] Chr10:53995753 [GRCh38]
Chr10:55755513 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4487C>T (p.Ala1496Val) single nucleotide variant not provided [RCV001970305] Chr10:53823239 [GRCh38]
Chr10:55582999 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.11:g.53995649_54022892del deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV001822909] Chr10:53995649..54022892 [GRCh38]
Chr10:10q21.1		 likely pathogenic
NC_000010.10:g.(55913054_55943203)_(55996692_56077030)del deletion Usher syndrome type 1F [RCV001844737] Chr10:55943203..55996692 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4253C>T (p.Ala1418Val) single nucleotide variant not provided [RCV001893604] Chr10:53827507 [GRCh38]
Chr10:55587267 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.754_755insAA (p.Thr252fs) insertion Autosomal recessive nonsyndromic hearing loss 23 [RCV001823254] Chr10:54317392..54317393 [GRCh38]
Chr10:56077152..56077153 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NC_000010.10:g.(?_55616915)_(55626637_?)del deletion not provided [RCV001949320] Chr10:55616915..55626637 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.4318C>T (p.Pro1440Ser) single nucleotide variant not provided [RCV002021784] Chr10:53827442 [GRCh38]
Chr10:55587202 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4644dup (p.Val1549fs) duplication not provided [RCV002007429] Chr10:53823081..53823082 [GRCh38]
Chr10:55582841..55582842 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.4403_4418dup (p.Ser1473_Glu1474insLysTer) duplication not provided [RCV002007437] Chr10:53823307..53823308 [GRCh38]
Chr10:55583067..55583068 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2259C>G (p.His753Gln) single nucleotide variant not provided [RCV001913562] Chr10:54023159 [GRCh38]
Chr10:55782919 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5623C>A (p.Pro1875Thr) single nucleotide variant not provided [RCV001890652] Chr10:53822103 [GRCh38]
Chr10:55581863 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2756del (p.Met919fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV001822910] Chr10:53995761 [GRCh38]
Chr10:55755521 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.5194G>A (p.Glu1732Lys) single nucleotide variant not provided [RCV001912035] Chr10:53822532 [GRCh38]
Chr10:55582292 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1855C>A (p.Leu619Met) single nucleotide variant Inborn genetic diseases [RCV004042431]|not provided [RCV001986040] Chr10:54132937 [GRCh38]
Chr10:55892697 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2039G>A (p.Ser680Asn) single nucleotide variant not provided [RCV001894850] Chr10:54079383 [GRCh38]
Chr10:55839143 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1784+1_1784+12del deletion not provided [RCV001986329] Chr10:54153088..54153099 [GRCh38]
Chr10:55912848..55912859 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1655C>T (p.Ala552Val) single nucleotide variant not provided [RCV002041869] Chr10:54153229 [GRCh38]
Chr10:55912989 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.639T>G (p.Asn213Lys) single nucleotide variant not provided [RCV001968166] Chr10:54329662 [GRCh38]
Chr10:56089422 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.368A>G (p.Lys123Arg) single nucleotide variant not provided [RCV001926658] Chr10:54369226 [GRCh38]
Chr10:56128986 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5618C>G (p.Thr1873Arg) single nucleotide variant not provided [RCV001912830] Chr10:53822108 [GRCh38]
Chr10:55581868 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.261G>A (p.Met87Ile) single nucleotide variant not provided [RCV002001858] Chr10:54378839 [GRCh38]
Chr10:56138599 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1305+2T>G single nucleotide variant not provided [RCV002022949] Chr10:54195681 [GRCh38]
Chr10:55955441 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NC_000010.10:g.(?_55566339)_(56288162_?)del deletion not provided [RCV001964850] Chr10:55566339..56288162 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.4970C>T (p.Ser1657Phe) single nucleotide variant not provided [RCV002040219] Chr10:53822756 [GRCh38]
Chr10:55582516 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.841A>G (p.Thr281Ala) single nucleotide variant Usher syndrome type 1F [RCV002545252]|not specified [RCV001844739] Chr10:54317306 [GRCh38]
Chr10:56077066 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.10:g.(?_55616925)_(55782967_?)del deletion not provided [RCV001948253] Chr10:55616925..55782967 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3484T>G (p.Ser1162Ala) single nucleotide variant not provided [RCV002041159] Chr10:53903260 [GRCh38]
Chr10:55663020 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.10:g.(?_55996563)_(56089486_?)del deletion not provided [RCV001964855] Chr10:55996563..56089486 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.566A>G (p.Tyr189Cys) single nucleotide variant Inborn genetic diseases [RCV002562170]|not provided [RCV001965256] Chr10:54346393 [GRCh38]
Chr10:56106153 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2029_2044del (p.Asp677fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV004571629]|not provided [RCV001926640] Chr10:54079378..54079393 [GRCh38]
Chr10:55839138..55839153 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.317A>T (p.Asp106Val) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV001823253] Chr10:54378783 [GRCh38]
Chr10:56138543 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3731A>G (p.Asn1244Ser) single nucleotide variant not provided [RCV001961327] Chr10:53857250 [GRCh38]
Chr10:55617010 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.680G>T (p.Arg227Leu) single nucleotide variant not provided [RCV001923781] Chr10:54329621 [GRCh38]
Chr10:56089381 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2127T>A (p.Asp709Glu) single nucleotide variant not provided [RCV001955792] Chr10:54066850 [GRCh38]
Chr10:55826610 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.562G>C (p.Glu188Gln) single nucleotide variant not provided [RCV001944522] Chr10:54346397 [GRCh38]
Chr10:56106157 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2526+2T>C single nucleotide variant not provided [RCV002028343] Chr10:54022890 [GRCh38]
Chr10:55782650 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4090A>G (p.Lys1364Glu) single nucleotide variant not provided [RCV001941329] Chr10:53831427 [GRCh38]
Chr10:55591187 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2904T>A (p.Asp968Glu) single nucleotide variant not provided [RCV002000454] Chr10:53961857 [GRCh38]
Chr10:55721617 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2002G>A (p.Gly668Arg) single nucleotide variant not provided [RCV001887781] Chr10:54079420 [GRCh38]
Chr10:55839180 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2462A>G (p.Asn821Ser) single nucleotide variant not provided [RCV002001304] Chr10:54022956 [GRCh38]
Chr10:55782716 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5204C>T (p.Ala1735Val) single nucleotide variant Inborn genetic diseases [RCV004039078]|not provided [RCV001886670] Chr10:53822522 [GRCh38]
Chr10:55582282 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2264G>T (p.Ser755Ile) single nucleotide variant not provided [RCV002031321] Chr10:54023154 [GRCh38]
Chr10:55782914 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2333A>G (p.Asn778Ser) single nucleotide variant not provided [RCV001978821] Chr10:54023085 [GRCh38]
Chr10:55782845 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4429A>C (p.Lys1477Gln) single nucleotide variant not provided [RCV001961991] Chr10:53823297 [GRCh38]
Chr10:55583057 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.488G>T (p.Gly163Val) single nucleotide variant Inborn genetic diseases [RCV004043174]|not provided [RCV001941434] Chr10:54346471 [GRCh38]
Chr10:56106231 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1399C>T (p.Gln467Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002479590]|not provided [RCV001963061] Chr10:54185175 [GRCh38]
Chr10:55944935 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.2134G>A (p.Asp712Asn) single nucleotide variant not provided [RCV001864792] Chr10:54066843 [GRCh38]
Chr10:55826603 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1343A>G (p.Tyr448Cys) single nucleotide variant not provided [RCV001915720] Chr10:54185231 [GRCh38]
Chr10:55944991 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2365G>C (p.Val789Leu) single nucleotide variant not provided [RCV001917130] Chr10:54023053 [GRCh38]
Chr10:55782813 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.10:g.(?_55581618)_(55663150_?)del deletion not provided [RCV001956408] Chr10:55581618..55663150 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_55566329)_(55583128_?)del deletion not provided [RCV001963077] Chr10:55566329..55583128 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.264T>G (p.Asp88Glu) single nucleotide variant not provided [RCV001887855] Chr10:54378836 [GRCh38]
Chr10:56138596 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2647G>A (p.Glu883Lys) single nucleotide variant not provided [RCV002001355] Chr10:54020296 [GRCh38]
Chr10:55780056 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5695A>G (p.Met1899Val) single nucleotide variant not provided [RCV001979204] Chr10:53822031 [GRCh38]
Chr10:55581791 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3647C>A (p.Ser1216Tyr) single nucleotide variant not provided [RCV001918496] Chr10:53866712 [GRCh38]
Chr10:55626472 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.960_967del (p.Gly321fs) deletion not provided [RCV002037890] Chr10:54236841..54236848 [GRCh38]
Chr10:55996601..55996608 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_55755389)_(55892787_?)dup duplication not provided [RCV002037350] Chr10:55755389..55892787 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NC_000010.10:g.(?_55616915)_(55626637_?)dup duplication not provided [RCV002037358] Chr10:55616915..55626637 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.2768C>A (p.Pro923His) single nucleotide variant not provided [RCV002028975] Chr10:53995749 [GRCh38]
Chr10:55755509 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4976A>G (p.Asp1659Gly) single nucleotide variant not provided [RCV001870000]|not specified [RCV002282617] Chr10:53822750 [GRCh38]
Chr10:55582510 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2630T>A (p.Leu877Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003475222]|not provided [RCV001942135] Chr10:54020313 [GRCh38]
Chr10:55780073 [GRCh37]
Chr10:10q21.1		 pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.1917+12G>A single nucleotide variant not provided [RCV002012569] Chr10:54132863 [GRCh38]
Chr10:55892623 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.4274del (p.Ala1425fs) deletion not provided [RCV002000189] Chr10:53827486 [GRCh38]
Chr10:55587246 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.4292C>T (p.Pro1431Leu) single nucleotide variant not provided [RCV001881490] Chr10:53827468 [GRCh38]
Chr10:55587228 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1108G>A (p.Asp370Asn) single nucleotide variant not provided [RCV001962789] Chr10:54195880 [GRCh38]
Chr10:55955640 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1382G>A (p.Arg461His) single nucleotide variant not provided [RCV001943742] Chr10:54185192 [GRCh38]
Chr10:55944952 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2651del (p.Ala884fs) deletion not provided [RCV001887216] Chr10:54020292 [GRCh38]
Chr10:55780052 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.561dup (p.Glu188fs) duplication not provided [RCV001901538] Chr10:54346397..54346398 [GRCh38]
Chr10:56106157..56106158 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3865A>G (p.Ile1289Val) single nucleotide variant not provided [RCV001878897] Chr10:53840438 [GRCh38]
Chr10:55600198 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.787C>T (p.Pro263Ser) single nucleotide variant not provided [RCV001976589] Chr10:54317360 [GRCh38]
Chr10:56077120 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5798A>G (p.Asn1933Ser) single nucleotide variant not provided [RCV001992247] Chr10:53821928 [GRCh38]
Chr10:55581688 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4762G>A (p.Val1588Ile) single nucleotide variant not provided [RCV001870551] Chr10:53822964 [GRCh38]
Chr10:55582724 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1487A>G (p.Asn496Ser) single nucleotide variant not provided [RCV001993741] Chr10:54183547 [GRCh38]
Chr10:55943307 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3789del (p.Lys1263_Ile1264insTer) deletion not provided [RCV001916600] Chr10:53857192 [GRCh38]
Chr10:55616952 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3010-1G>C single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003475302]|not provided [RCV002031530] Chr10:53959845 [GRCh38]
Chr10:55719605 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_033056.4(PCDH15):c.5196A>T (p.Glu1732Asp) single nucleotide variant not provided [RCV002048213] Chr10:53822530 [GRCh38]
Chr10:55582290 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4203-1G>A single nucleotide variant not provided [RCV002050834] Chr10:53828574 [GRCh38]
Chr10:55588334 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3122+1G>T single nucleotide variant Usher syndrome type 1F [RCV002571248]|not provided [RCV001972905] Chr10:53959731 [GRCh38]
Chr10:55719491 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.859C>A (p.Pro287Thr) single nucleotide variant not provided [RCV001902553] Chr10:54317288 [GRCh38]
Chr10:56077048 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1081T>C (p.Phe361Leu) single nucleotide variant not provided [RCV001881654] Chr10:54213953 [GRCh38]
Chr10:55973713 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4775C>T (p.Pro1592Leu) single nucleotide variant not provided [RCV001921842] Chr10:53822951 [GRCh38]
Chr10:55582711 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.91+1G>A single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003475288]|not provided [RCV002016937] Chr10:54664171 [GRCh38]
Chr10:56423931 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1855C>G (p.Leu619Val) single nucleotide variant not provided [RCV002029857] Chr10:54132937 [GRCh38]
Chr10:55892697 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2059A>C (p.Ile687Leu) single nucleotide variant not provided [RCV002048310] Chr10:54079363 [GRCh38]
Chr10:55839123 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1357_1358del (p.Thr453fs) deletion not provided [RCV001898269] Chr10:54185216..54185217 [GRCh38]
Chr10:55944976..55944977 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.5799C>G (p.Asn1933Lys) single nucleotide variant not provided [RCV001992891] Chr10:53821927 [GRCh38]
Chr10:55581687 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.640A>G (p.Ile214Val) single nucleotide variant not provided [RCV001920836] Chr10:54329661 [GRCh38]
Chr10:56089421 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.319-3C>T single nucleotide variant not provided [RCV002011979] Chr10:54369278 [GRCh38]
Chr10:56129038 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2932A>G (p.Ile978Val) single nucleotide variant not provided [RCV002049677] Chr10:53961829 [GRCh38]
Chr10:55721589 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4596_4600dup (p.Ser1534delinsThrTer) duplication not provided [RCV001994593] Chr10:53823125..53823126 [GRCh38]
Chr10:55582885..55582886 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_55912850)_(56138712_?)del deletion not provided [RCV001953517] Chr10:55912850..56138712 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2868+5del deletion not provided [RCV002027509] Chr10:53995644 [GRCh38]
Chr10:55755404 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.996_999del (p.Glu332fs) deletion not provided [RCV001898455] Chr10:54214035..54214038 [GRCh38]
Chr10:55973795..55973798 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.617_618del (p.Ile206fs) deletion not provided [RCV001881890] Chr10:54329683..54329684 [GRCh38]
Chr10:56089443..56089444 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.4394A>G (p.Gln1465Arg) single nucleotide variant not provided [RCV002009794] Chr10:53823332 [GRCh38]
Chr10:55583092 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.319C>T (p.Pro107Ser) single nucleotide variant not provided [RCV001878302] Chr10:54369275 [GRCh38]
Chr10:56129035 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3161T>C (p.Met1054Thr) single nucleotide variant not provided [RCV001881324] Chr10:53940937 [GRCh38]
Chr10:55700697 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.182T>G (p.Leu61Arg) single nucleotide variant not provided [RCV001897339] Chr10:54378918 [GRCh38]
Chr10:56138678 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5826G>A (p.Glu1942=) single nucleotide variant not provided [RCV001934447] Chr10:53821900 [GRCh38]
Chr10:55581660 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.1306-3A>G single nucleotide variant not provided [RCV001919908] Chr10:54185271 [GRCh38]
Chr10:55945031 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5683T>G (p.Ser1895Ala) single nucleotide variant not provided [RCV002009929] Chr10:53822043 [GRCh38]
Chr10:55581803 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1529del (p.Pro510fs) deletion Usher syndrome type 1F [RCV002568520]|not provided [RCV001994809] Chr10:54183505 [GRCh38]
Chr10:55943265 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2200G>A (p.Ala734Thr) single nucleotide variant not provided [RCV001875675] Chr10:54066777 [GRCh38]
Chr10:55826537 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.935A>G (p.Asn312Ser) single nucleotide variant not provided [RCV001877239] Chr10:54236873 [GRCh38]
Chr10:55996633 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1527C>A (p.Phe509Leu) single nucleotide variant not provided [RCV001901569] Chr10:54183507 [GRCh38]
Chr10:55943267 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2240G>T (p.Gly747Val) single nucleotide variant not provided [RCV001990774] Chr10:54023178 [GRCh38]
Chr10:55782938 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.675G>C (p.Lys225Asn) single nucleotide variant Inborn genetic diseases [RCV003164135]|not provided [RCV001900051] Chr10:54329626 [GRCh38]
Chr10:56089386 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1313del (p.Asp438fs) deletion not provided [RCV001878435] Chr10:54185261 [GRCh38]
Chr10:55945021 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.1074C>G (p.His358Gln) single nucleotide variant not provided [RCV001956882] Chr10:54213960 [GRCh38]
Chr10:55973720 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5527A>G (p.Ile1843Val) single nucleotide variant not provided [RCV001957495] Chr10:53822199 [GRCh38]
Chr10:55581959 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1609G>A (p.Asp537Asn) single nucleotide variant not provided [RCV001992215] Chr10:54153275 [GRCh38]
Chr10:55913035 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1831C>T (p.Gln611Ter) single nucleotide variant not provided [RCV001903651] Chr10:54132961 [GRCh38]
Chr10:55892721 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.596C>A (p.Thr199Lys) single nucleotide variant not provided [RCV002016208] Chr10:54329705 [GRCh38]
Chr10:56089465 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3496G>A (p.Val1166Met) single nucleotide variant not provided [RCV001937817] Chr10:53903248 [GRCh38]
Chr10:55663008 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.641T>C (p.Ile214Thr) single nucleotide variant not provided [RCV001998175] Chr10:54329660 [GRCh38]
Chr10:56089420 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3441del (p.Lys1147fs) deletion not provided [RCV001897843] Chr10:53903303 [GRCh38]
Chr10:55663063 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.4403G>A (p.Gly1468Glu) single nucleotide variant not provided [RCV001953062] Chr10:53823323 [GRCh38]
Chr10:55583083 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.10:g.(?_55755389)_(55755545_?)dup duplication not provided [RCV001958491] Chr10:55755389..55755545 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3179C>T (p.Ala1060Val) single nucleotide variant not provided [RCV001925084] Chr10:53940919 [GRCh38]
Chr10:55700679 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3275A>G (p.Asn1092Ser) single nucleotide variant not provided [RCV001954366] Chr10:53938913 [GRCh38]
Chr10:55698673 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1684A>G (p.Thr562Ala) single nucleotide variant not provided [RCV001901822] Chr10:54153200 [GRCh38]
Chr10:55912960 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.596C>T (p.Thr199Ile) single nucleotide variant not provided [RCV001881336] Chr10:54329705 [GRCh38]
Chr10:56089465 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4024C>T (p.Gln1342Ter) single nucleotide variant not provided [RCV001937096] Chr10:53831493 [GRCh38]
Chr10:55591253 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3878G>A (p.Arg1293Gln) single nucleotide variant not provided [RCV001903880] Chr10:53840425 [GRCh38]
Chr10:55600185 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4203-9C>A single nucleotide variant not provided [RCV001979518] Chr10:53828582 [GRCh38]
Chr10:55588342 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1021C>T (p.His341Tyr) single nucleotide variant not provided [RCV001924615] Chr10:54214013 [GRCh38]
Chr10:55973773 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3542A>G (p.Tyr1181Cys) single nucleotide variant not provided [RCV001940347] Chr10:53866817 [GRCh38]
Chr10:55626577 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5725C>T (p.Arg1909Cys) single nucleotide variant not provided [RCV002036772] Chr10:53822001 [GRCh38]
Chr10:55581761 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2510C>T (p.Thr837Ile) single nucleotide variant not provided [RCV001957914] Chr10:54022908 [GRCh38]
Chr10:55782668 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3981_3982insTTTTTTTTTTTTTTTTTTTTNNNNNNNNNNAGGTATATCTCCCAATGCTATCCCTCCCCCCTCCCCCGACCCCACCACAGTCCCCAGAAATGAGCTTTTT (p.Lys1328delinsPhePhePhePhePhePheXaaXaaXaaXaaArgTyrIleSerGlnCysTyrProSerProLeuProArgProHisHisSerProGlnLysTer) microsatellite not provided [RCV001926238] Chr10:53840321..53840322 [GRCh38]
Chr10:55600081..55600082 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.5762C>T (p.Ser1921Leu) single nucleotide variant not provided [RCV001866357] Chr10:53821964 [GRCh38]
Chr10:55581724 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.319-11C>T single nucleotide variant not provided [RCV001899542] Chr10:54369286 [GRCh38]
Chr10:56129046 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5675T>A (p.Leu1892His) single nucleotide variant not provided [RCV001899604] Chr10:53822051 [GRCh38]
Chr10:55581811 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4246C>A (p.Gln1416Lys) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002484418]|Usher syndrome type 1F [RCV002555420]|not provided [RCV001915713] Chr10:53827514 [GRCh38]
Chr10:55587274 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2102C>A (p.Ala701Asp) single nucleotide variant not provided [RCV001937427] Chr10:54066875 [GRCh38]
Chr10:55826635 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2188G>A (p.Glu730Lys) single nucleotide variant not provided [RCV001884667] Chr10:54066789 [GRCh38]
Chr10:55826549 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4406_4409dup (p.Asn1470delinsLysTer) duplication not provided [RCV001953684] Chr10:53823316..53823317 [GRCh38]
Chr10:55583076..55583077 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.1379C>T (p.Thr460Ile) single nucleotide variant not provided [RCV002050038] Chr10:54185195 [GRCh38]
Chr10:55944955 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.10:g.(?_55581608)_(55626627_?)del deletion not provided [RCV001950963] Chr10:55581608..55626627 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.5249C>T (p.Pro1750Leu) single nucleotide variant not provided [RCV001884106] Chr10:53822477 [GRCh38]
Chr10:55582237 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3718-3C>T single nucleotide variant not provided [RCV002009742] Chr10:53857266 [GRCh38]
Chr10:55617026 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3717C>A (p.Leu1239=) single nucleotide variant not provided [RCV001989232] Chr10:53866642 [GRCh38]
Chr10:55626402 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.10:g.(?_55581618)_(56424022_?)del deletion not provided [RCV001958853] Chr10:55581618..56424022 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2156del (p.Pro719fs) deletion not provided [RCV001904960] Chr10:54066821 [GRCh38]
Chr10:55826581 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.451A>G (p.Ser151Gly) single nucleotide variant not provided [RCV001885524] Chr10:54369143 [GRCh38]
Chr10:56128903 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4212-1G>A single nucleotide variant not provided [RCV001978211] Chr10:53827549 [GRCh38]
Chr10:55587309 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1615G>A (p.Gly539Arg) single nucleotide variant not provided [RCV001932071] Chr10:54153269 [GRCh38]
Chr10:55913029 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5620G>A (p.Asp1874Asn) single nucleotide variant not provided [RCV002012581] Chr10:53822106 [GRCh38]
Chr10:55581866 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4111G>A (p.Gly1371Arg) single nucleotide variant not provided [RCV001903445] Chr10:53831406 [GRCh38]
Chr10:55591166 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4368-2238_4368-2227del deletion not provided [RCV001907367] Chr10:53822457..53822468 [GRCh38]
Chr10:55582217..55582228 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1306-1G>T single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003475299]|not provided [RCV002046475] Chr10:54185269 [GRCh38]
Chr10:55945029 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.1489A>G (p.Ile497Val) single nucleotide variant not provided [RCV002012680] Chr10:54183545 [GRCh38]
Chr10:55943305 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.10:g.(?_55616925)_(55996701_?)del deletion not provided [RCV001958990] Chr10:55616925..55996701 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2029_2044dup (p.Asp682delinsGlyGlnGlyLysHisTer) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003475252]|not provided [RCV001975106] Chr10:54079377..54079378 [GRCh38]
Chr10:55839137..55839138 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.3433C>T (p.Gln1145Ter) single nucleotide variant Usher syndrome type 1F [RCV002548051]|not provided [RCV001932211] Chr10:53903311 [GRCh38]
Chr10:55663071 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.344T>C (p.Val115Ala) single nucleotide variant not provided [RCV002047901] Chr10:54369250 [GRCh38]
Chr10:56129010 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5549C>T (p.Thr1850Ile) single nucleotide variant not provided [RCV001957469] Chr10:53822177 [GRCh38]
Chr10:55581937 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1913_1917+8del deletion not provided [RCV001990713] Chr10:54132867..54132879 [GRCh38]
Chr10:55892627..55892639 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.5312T>G (p.Ile1771Ser) single nucleotide variant not provided [RCV001903590] Chr10:53822414 [GRCh38]
Chr10:55582174 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.158-9G>A single nucleotide variant not provided [RCV001995496] Chr10:54378951 [GRCh38]
Chr10:56138711 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1843C>A (p.Arg615Ser) single nucleotide variant not provided [RCV002046641] Chr10:54132949 [GRCh38]
Chr10:55892709 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.10:g.(?_55973686)_(55973818_?)del deletion not provided [RCV001958985] Chr10:55973686..55973818 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3448A>G (p.Ile1150Val) single nucleotide variant not provided [RCV001997112] Chr10:53903296 [GRCh38]
Chr10:55663056 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.10:g.(?_55755399)_(56138712_?)del deletion not provided [RCV001953518] Chr10:55755399..56138712 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3001A>G (p.Ile1001Val) single nucleotide variant not provided [RCV001904653] Chr10:53961760 [GRCh38]
Chr10:55721520 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3425dup (p.Val1143fs) duplication not provided [RCV001981401] Chr10:53903318..53903319 [GRCh38]
Chr10:55663078..55663079 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3937A>G (p.Ile1313Val) single nucleotide variant not provided [RCV002034954] Chr10:53840366 [GRCh38]
Chr10:55600126 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2450C>T (p.Pro817Leu) single nucleotide variant not provided [RCV001925104] Chr10:54022968 [GRCh38]
Chr10:55782728 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3048G>A (p.Met1016Ile) single nucleotide variant not provided [RCV001981765] Chr10:53959806 [GRCh38]
Chr10:55719566 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5068A>T (p.Ile1690Phe) single nucleotide variant not provided [RCV001938733] Chr10:53822658 [GRCh38]
Chr10:55582418 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3983+3_3983+6del microsatellite not provided [RCV001959486] Chr10:53840314..53840317 [GRCh38]
Chr10:55600074..55600077 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2786_2787delinsAC (p.Arg929His) indel not provided [RCV002036007] Chr10:53995730..53995731 [GRCh38]
Chr10:55755490..55755491 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4944A>C (p.Glu1648Asp) single nucleotide variant not provided [RCV001883596] Chr10:53822782 [GRCh38]
Chr10:55582542 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4920G>T (p.Arg1640Ser) single nucleotide variant not provided [RCV001884819] Chr10:53822806 [GRCh38]
Chr10:55582566 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1175del (p.Ser392fs) deletion not provided [RCV001939622] Chr10:54195813 [GRCh38]
Chr10:55955573 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.1709G>C (p.Gly570Ala) single nucleotide variant not provided [RCV002035877] Chr10:54153175 [GRCh38]
Chr10:55912935 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1942A>G (p.Ile648Val) single nucleotide variant not provided [RCV001926007] Chr10:54090039 [GRCh38]
Chr10:55849799 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4360A>G (p.Ser1454Gly) single nucleotide variant not provided [RCV001988909] Chr10:53827400 [GRCh38]
Chr10:55587160 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1034C>A (p.Ala345Glu) single nucleotide variant not provided [RCV001901523] Chr10:54214000 [GRCh38]
Chr10:55973760 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4557G>C (p.Glu1519Asp) single nucleotide variant not provided [RCV002019336] Chr10:53823169 [GRCh38]
Chr10:55582929 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.323C>T (p.Pro108Leu) single nucleotide variant not provided [RCV001905656] Chr10:54369271 [GRCh38]
Chr10:56129031 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4411_4412dup (p.Val1472fs) duplication not provided [RCV001950882] Chr10:53823313..53823314 [GRCh38]
Chr10:55583073..55583074 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2969C>A (p.Thr990Lys) single nucleotide variant not provided [RCV001916777] Chr10:53961792 [GRCh38]
Chr10:55721552 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4198A>G (p.Arg1400Gly) single nucleotide variant Inborn genetic diseases [RCV002561479]|not provided [RCV001952821] Chr10:53831319 [GRCh38]
Chr10:55591079 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.176A>G (p.Asn59Ser) single nucleotide variant not provided [RCV001921131] Chr10:54378924 [GRCh38]
Chr10:56138684 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5294T>A (p.Leu1765His) single nucleotide variant not provided [RCV001897058] Chr10:53822432 [GRCh38]
Chr10:55582192 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5108C>T (p.Ser1703Leu) single nucleotide variant not provided [RCV002029730] Chr10:53822618 [GRCh38]
Chr10:55582378 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.527C>T (p.Ala176Val) single nucleotide variant not provided [RCV001920365] Chr10:54346432 [GRCh38]
Chr10:56106192 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.10:g.(?_55943194)_(55996701_?)del deletion not provided [RCV002049867] Chr10:55943194..55996701 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.2389C>T (p.His797Tyr) single nucleotide variant not provided [RCV001934258] Chr10:54023029 [GRCh38]
Chr10:55782789 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2728G>A (p.Ala910Thr) single nucleotide variant not provided [RCV002049116] Chr10:54020215 [GRCh38]
Chr10:55779975 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1231G>A (p.Gly411Arg) single nucleotide variant not provided [RCV001992092] Chr10:54195757 [GRCh38]
Chr10:55955517 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.790A>T (p.Met264Leu) single nucleotide variant not provided [RCV001958314] Chr10:54317357 [GRCh38]
Chr10:56077117 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2179G>C (p.Val727Leu) single nucleotide variant not provided [RCV001915968] Chr10:54066798 [GRCh38]
Chr10:55826558 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2358A>C (p.Glu786Asp) single nucleotide variant not provided [RCV002048111] Chr10:54023060 [GRCh38]
Chr10:55782820 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3562A>G (p.Ile1188Val) single nucleotide variant not provided [RCV001875604] Chr10:53866797 [GRCh38]
Chr10:55626557 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4343A>C (p.Tyr1448Ser) single nucleotide variant not provided [RCV001989411]|not specified [RCV002271713] Chr10:53827417 [GRCh38]
Chr10:55587177 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1469G>C (p.Ser490Thr) single nucleotide variant not provided [RCV001877654] Chr10:54183565 [GRCh38]
Chr10:55943325 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.524G>A (p.Gly175Glu) single nucleotide variant not provided [RCV002029291] Chr10:54346435 [GRCh38]
Chr10:56106195 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1559C>T (p.Thr520Ile) single nucleotide variant not provided [RCV001933533] Chr10:54183475 [GRCh38]
Chr10:55943235 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4591G>T (p.Glu1531Ter) single nucleotide variant not provided [RCV001993179] Chr10:53823135 [GRCh38]
Chr10:55582895 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2125_2126insC (p.Asp709fs) insertion not provided [RCV001957166] Chr10:54066851..54066852 [GRCh38]
Chr10:55826611..55826612 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2615G>A (p.Gly872Glu) single nucleotide variant not provided [RCV001937741] Chr10:54020328 [GRCh38]
Chr10:55780088 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5269T>C (p.Ser1757Pro) single nucleotide variant not provided [RCV001866607] Chr10:53822457 [GRCh38]
Chr10:55582217 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4566_4569dup (p.Ala1524fs) duplication not provided [RCV001993120] Chr10:53823156..53823157 [GRCh38]
Chr10:55582916..55582917 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2919_2923del (p.Tyr974fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003475153]|not provided [RCV001932838] Chr10:53961838..53961842 [GRCh38]
Chr10:55721598..55721602 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.4306C>T (p.Pro1436Ser) single nucleotide variant not provided [RCV001867694] Chr10:53827454 [GRCh38]
Chr10:55587214 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.905C>G (p.Pro302Arg) single nucleotide variant not provided [RCV002033910] Chr10:54236903 [GRCh38]
Chr10:55996663 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.144A>G (p.Glu48=) single nucleotide variant not provided [RCV002167733] Chr10:54527825 [GRCh38]
Chr10:56287585 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5523_5526dup (p.Ile1843fs) duplication not provided [RCV002188539] Chr10:53822199..53822200 [GRCh38]
Chr10:55581959..55581960 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.475-9del deletion not provided [RCV002108637] Chr10:54346493 [GRCh38]
Chr10:56106253 [GRCh37]
Chr10:10q21.1		 benign
NM_033056.4(PCDH15):c.4689G>C (p.Leu1563=) single nucleotide variant not provided [RCV002071498] Chr10:53823037 [GRCh38]
Chr10:55582797 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4211+11T>A single nucleotide variant not provided [RCV002167761] Chr10:53828554 [GRCh38]
Chr10:55588314 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2133T>C (p.Asn711=) single nucleotide variant not provided [RCV002192267] Chr10:54066844 [GRCh38]
Chr10:55826604 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.721C>T (p.Leu241=) single nucleotide variant not provided [RCV002148460] Chr10:54317426 [GRCh38]
Chr10:56077186 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.73T>C (p.Leu25=) single nucleotide variant not provided [RCV002085770] Chr10:54664190 [GRCh38]
Chr10:56423950 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5257_5274del (p.Ile1753_Pro1758del) deletion not provided [RCV002207385] Chr10:53822452..53822469 [GRCh38]
Chr10:55582212..55582229 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4701A>G (p.Arg1567=) single nucleotide variant not provided [RCV002167848] Chr10:53823025 [GRCh38]
Chr10:55582785 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4539C>T (p.Phe1513=) single nucleotide variant not provided [RCV002075715] Chr10:53823187 [GRCh38]
Chr10:55582947 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4203-7del deletion not provided [RCV002166431] Chr10:53828580 [GRCh38]
Chr10:55588340 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4368-3138T>G single nucleotide variant not provided [RCV002130263] Chr10:53823368 [GRCh38]
Chr10:55583128 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4278G>T (p.Val1426=) single nucleotide variant not provided [RCV002168760] Chr10:53827482 [GRCh38]
Chr10:55587242 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5767_5781del (p.Val1923_Glu1927del) deletion not provided [RCV002191274] Chr10:53821945..53821959 [GRCh38]
Chr10:55581705..55581719 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4592_4627dup (p.Ser1543Ter) duplication not provided [RCV002224272] Chr10:53823098..53823099 [GRCh38]
Chr10:55582858..55582859 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.986-7C>T single nucleotide variant not provided [RCV002147001] Chr10:54214055 [GRCh38]
Chr10:55973815 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2562C>T (p.Tyr854=) single nucleotide variant not provided [RCV002170065] Chr10:54020381 [GRCh38]
Chr10:55780141 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.876+13_876+14del deletion not provided [RCV002146020] Chr10:54317257..54317258 [GRCh38]
Chr10:56077017..56077018 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.432A>T (p.Ser144=) single nucleotide variant not provided [RCV002091220] Chr10:54369162 [GRCh38]
Chr10:56128922 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4203-4del deletion not provided [RCV002190995] Chr10:53828577 [GRCh38]
Chr10:55588337 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5517G>A (p.Glu1839=) single nucleotide variant not provided [RCV002087615] Chr10:53822209 [GRCh38]
Chr10:55581969 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3069G>A (p.Lys1023=) single nucleotide variant not provided [RCV002107725] Chr10:53959785 [GRCh38]
Chr10:55719545 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2847T>C (p.Tyr949=) single nucleotide variant not provided [RCV002072532] Chr10:53995670 [GRCh38]
Chr10:55755430 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5281_5283del (p.Ala1761del) deletion not provided [RCV002167030] Chr10:53822443..53822445 [GRCh38]
Chr10:55582203..55582205 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3807-7T>C single nucleotide variant not provided [RCV002091064] Chr10:53840503 [GRCh38]
Chr10:55600263 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4202+19T>A single nucleotide variant not provided [RCV002089329] Chr10:53831296 [GRCh38]
Chr10:55591056 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3630C>T (p.Phe1210=) single nucleotide variant not provided [RCV002168934] Chr10:53866729 [GRCh38]
Chr10:55626489 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3122+17G>A single nucleotide variant not provided [RCV002111215] Chr10:53959715 [GRCh38]
Chr10:55719475 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5516_5517del (p.Glu1839fs) microsatellite PCDH15-related disorder [RCV004734435]|not provided [RCV002104724] Chr10:53822209..53822210 [GRCh38]
Chr10:55581969..55581970 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.3333C>G (p.Ser1111=) single nucleotide variant not provided [RCV002167102] Chr10:53938855 [GRCh38]
Chr10:55698615 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5100_5101dup (p.Ser1701fs) duplication not provided [RCV002129260]|not specified [RCV002282697] Chr10:53822624..53822625 [GRCh38]
Chr10:55582384..55582385 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.3502-14T>C single nucleotide variant not provided [RCV002169618] Chr10:53866871 [GRCh38]
Chr10:55626631 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.158-9G>C single nucleotide variant not provided [RCV002189877] Chr10:54378951 [GRCh38]
Chr10:56138711 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4014T>C (p.Asn1338=) single nucleotide variant not provided [RCV002189923] Chr10:53831503 [GRCh38]
Chr10:55591263 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.393T>C (p.His131=) single nucleotide variant not provided [RCV002146215] Chr10:54369201 [GRCh38]
Chr10:56128961 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3806+19T>C single nucleotide variant not provided [RCV002091517] Chr10:53857156 [GRCh38]
Chr10:55616916 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2736C>A (p.Val912=) single nucleotide variant not provided [RCV002205343] Chr10:54020207 [GRCh38]
Chr10:55779967 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5052_5055dup (p.Glu1686fs) duplication not provided [RCV002224693] Chr10:53822670..53822671 [GRCh38]
Chr10:55582430..55582431 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3321C>G (p.Val1107=) single nucleotide variant not provided [RCV002170445] Chr10:53938867 [GRCh38]
Chr10:55698627 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4202+15A>G single nucleotide variant not provided [RCV002107019] Chr10:53831300 [GRCh38]
Chr10:55591060 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1099-11_1099-10del deletion not provided [RCV002206577] Chr10:54195899..54195900 [GRCh38]
Chr10:55955659..55955660 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3373+13_3373+22del deletion not provided [RCV002205427] Chr10:53938793..53938802 [GRCh38]
Chr10:55698553..55698562 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1917+12_1917+13dup duplication not provided [RCV002130250] Chr10:54132861..54132862 [GRCh38]
Chr10:55892621..55892622 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4533A>G (p.Arg1511=) single nucleotide variant not provided [RCV002085773] Chr10:53823193 [GRCh38]
Chr10:55582953 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3807-10del deletion not provided [RCV002185794] Chr10:53840506 [GRCh38]
Chr10:55600266 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4203-10T>C single nucleotide variant not provided [RCV002088936] Chr10:53828583 [GRCh38]
Chr10:55588343 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5415C>T (p.Pro1805=) single nucleotide variant not provided [RCV002089146] Chr10:53822311 [GRCh38]
Chr10:55582071 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3159C>G (p.Thr1053=) single nucleotide variant not provided [RCV002207547] Chr10:53940939 [GRCh38]
Chr10:55700699 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2754T>C (p.Asp918=) single nucleotide variant not provided [RCV002086979] Chr10:53995763 [GRCh38]
Chr10:55755523 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3252C>T (p.Asn1084=) single nucleotide variant not provided [RCV002088149] Chr10:53938936 [GRCh38]
Chr10:55698696 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1099-18T>C single nucleotide variant not provided [RCV002207683] Chr10:54195907 [GRCh38]
Chr10:55955667 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4323T>G (p.Pro1441=) single nucleotide variant not provided [RCV002186651] Chr10:53827437 [GRCh38]
Chr10:55587197 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1770T>A (p.Pro590=) single nucleotide variant not provided [RCV002207870] Chr10:54153114 [GRCh38]
Chr10:55912874 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5706_5709dup (p.Glu1904fs) duplication not provided [RCV002127613] Chr10:53822016..53822017 [GRCh38]
Chr10:55581776..55581777 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3736C>T (p.Leu1246=) single nucleotide variant not provided [RCV002207777] Chr10:53857245 [GRCh38]
Chr10:55617005 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5490T>C (p.Pro1830=) single nucleotide variant not provided [RCV002106722] Chr10:53822236 [GRCh38]
Chr10:55581996 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.319-7A>T single nucleotide variant not provided [RCV002148275] Chr10:54369282 [GRCh38]
Chr10:56129042 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5323del (p.Ser1775fs) deletion not provided [RCV002207922] Chr10:53822403 [GRCh38]
Chr10:55582163 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5619A>C (p.Thr1873=) single nucleotide variant not provided [RCV002089604] Chr10:53822107 [GRCh38]
Chr10:55581867 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3010-12T>C single nucleotide variant not provided [RCV002107955] Chr10:53959856 [GRCh38]
Chr10:55719616 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2859A>T (p.Ala953=) single nucleotide variant not provided [RCV002092021] Chr10:53995658 [GRCh38]
Chr10:55755418 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1918-15G>A single nucleotide variant not provided [RCV002210471] Chr10:54090078 [GRCh38]
Chr10:55849838 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.157+3_157+6del deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV002223342] Chr10:54527806..54527809 [GRCh38]
Chr10:56287566..56287569 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1647T>C (p.Leu549=) single nucleotide variant not provided [RCV002164887] Chr10:54153237 [GRCh38]
Chr10:55912997 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4945G>T (p.Gly1649Ter) single nucleotide variant not provided [RCV002210124] Chr10:53822781 [GRCh38]
Chr10:55582541 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2869-13_2869-11del microsatellite not provided [RCV002130252] Chr10:53961903..53961905 [GRCh38]
Chr10:55721663..55721665 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4281G>A (p.Pro1427=) single nucleotide variant not provided [RCV002186424] Chr10:53827479 [GRCh38]
Chr10:55587239 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1746G>T (p.Thr582=) single nucleotide variant not provided [RCV002107393] Chr10:54153138 [GRCh38]
Chr10:55912898 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5388del (p.Pro1797fs) deletion not provided [RCV002166481] Chr10:53822338 [GRCh38]
Chr10:55582098 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4335G>C (p.Ala1445=) single nucleotide variant not provided [RCV002148135] Chr10:53827425 [GRCh38]
Chr10:55587185 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.319-15A>G single nucleotide variant not provided [RCV002129980] Chr10:54369290 [GRCh38]
Chr10:56129050 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.324G>A (p.Pro108=) single nucleotide variant not provided [RCV002079618] Chr10:54369270 [GRCh38]
Chr10:56129030 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4464T>C (p.Asn1488=) single nucleotide variant not provided [RCV002151315] Chr10:53823262 [GRCh38]
Chr10:55583022 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2514C>T (p.Ile838=) single nucleotide variant not provided [RCV002174276] Chr10:54022904 [GRCh38]
Chr10:55782664 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1784+10A>G single nucleotide variant not provided [RCV002096757] Chr10:54153090 [GRCh38]
Chr10:55912850 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4851_4854dup (p.Arg1619fs) microsatellite not provided [RCV002215455] Chr10:53822871..53822872 [GRCh38]
Chr10:55582631..55582632 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4461C>T (p.Ser1487=) single nucleotide variant not provided [RCV002096838] Chr10:53823265 [GRCh38]
Chr10:55583025 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5271T>C (p.Ser1757=) single nucleotide variant not provided [RCV002077987] Chr10:53822455 [GRCh38]
Chr10:55582215 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5469T>G (p.Pro1823=) single nucleotide variant not provided [RCV002151543] Chr10:53822257 [GRCh38]
Chr10:55582017 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5717del (p.Asn1906fs) deletion not provided [RCV002213110] Chr10:53822009 [GRCh38]
Chr10:55581769 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1306-13T>C single nucleotide variant not provided [RCV002093792] Chr10:54185281 [GRCh38]
Chr10:55945041 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.351G>A (p.Gln117=) single nucleotide variant not provided [RCV002076823] Chr10:54369243 [GRCh38]
Chr10:56129003 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3502-14_3502-13insTC insertion not provided [RCV002133071] Chr10:53866870..53866871 [GRCh38]
Chr10:55626630..55626631 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3010-18T>C single nucleotide variant not provided [RCV002097573] Chr10:53959862 [GRCh38]
Chr10:55719622 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4203-12T>C single nucleotide variant not provided [RCV002215009] Chr10:53828585 [GRCh38]
Chr10:55588345 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2844T>A (p.Val948=) single nucleotide variant not provided [RCV002135191] Chr10:53995673 [GRCh38]
Chr10:55755433 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1218A>G (p.Glu406=) single nucleotide variant not provided [RCV002192961] Chr10:54195770 [GRCh38]
Chr10:55955530 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3483T>A (p.Thr1161=) single nucleotide variant not provided [RCV002089845] Chr10:53903261 [GRCh38]
Chr10:55663021 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2058G>A (p.Leu686=) single nucleotide variant not provided [RCV002169494] Chr10:54079364 [GRCh38]
Chr10:55839124 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4367+4_4367+7dup duplication not provided [RCV002132988] Chr10:53827385..53827386 [GRCh38]
Chr10:55587145..55587146 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4975_4976del (p.Asp1659fs) deletion not provided [RCV002195797] Chr10:53822750..53822751 [GRCh38]
Chr10:55582510..55582511 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1737C>T (p.Tyr579=) single nucleotide variant not provided [RCV002080427] Chr10:54153147 [GRCh38]
Chr10:55912907 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.319-18G>C single nucleotide variant not provided [RCV002171437] Chr10:54369293 [GRCh38]
Chr10:56129053 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1701C>T (p.Ile567=) single nucleotide variant not provided [RCV002088459] Chr10:54153183 [GRCh38]
Chr10:55912943 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1590+10C>T single nucleotide variant not provided [RCV002212863] Chr10:54183434 [GRCh38]
Chr10:55943194 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4211+12T>G single nucleotide variant not provided [RCV002215741] Chr10:53828553 [GRCh38]
Chr10:55588313 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.931C>A (p.Arg311=) single nucleotide variant not provided [RCV002080511] Chr10:54236877 [GRCh38]
Chr10:55996637 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2199T>C (p.Asn733=) single nucleotide variant not provided [RCV002212511] Chr10:54066778 [GRCh38]
Chr10:55826538 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3123-16T>A single nucleotide variant not provided [RCV002145188] Chr10:53940991 [GRCh38]
Chr10:55700751 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1095T>C (p.Ile365=) single nucleotide variant not provided [RCV002196479] Chr10:54213939 [GRCh38]
Chr10:55973699 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5332del (p.Cys1778fs) deletion not provided [RCV002080821] Chr10:53822394 [GRCh38]
Chr10:55582154 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5333del (p.Cys1778fs) deletion not provided [RCV002108545] Chr10:53822393 [GRCh38]
Chr10:55582153 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2092-7C>T single nucleotide variant not provided [RCV002078926] Chr10:54066892 [GRCh38]
Chr10:55826652 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3927T>C (p.Thr1309=) single nucleotide variant not provided [RCV002210873] Chr10:53840376 [GRCh38]
Chr10:55600136 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2091+17dup duplication not provided [RCV002133697] Chr10:54079313..54079314 [GRCh38]
Chr10:55839073..55839074 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4335G>A (p.Ala1445=) single nucleotide variant not provided [RCV002081093] Chr10:53827425 [GRCh38]
Chr10:55587185 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3963C>T (p.Ile1321=) single nucleotide variant not provided [RCV002212141] Chr10:53840340 [GRCh38]
Chr10:55600100 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4275A>T (p.Ala1425=) single nucleotide variant not provided [RCV002170618] Chr10:53827485 [GRCh38]
Chr10:55587245 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5595A>G (p.Leu1865=) single nucleotide variant not provided [RCV002114631] Chr10:53822131 [GRCh38]
Chr10:55581891 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4895_4923del (p.Asn1632fs) deletion not provided [RCV002175151] Chr10:53822803..53822831 [GRCh38]
Chr10:55582563..55582591 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5214A>G (p.Pro1738=) single nucleotide variant not provided [RCV002168438] Chr10:53822512 [GRCh38]
Chr10:55582272 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3233-14A>G single nucleotide variant not provided [RCV002173494] Chr10:53938969 [GRCh38]
Chr10:55698729 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.126C>A (p.Thr42=) single nucleotide variant not provided [RCV002215889] Chr10:54527843 [GRCh38]
Chr10:56287603 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4367+11C>T single nucleotide variant not provided [RCV002078084] Chr10:53827382 [GRCh38]
Chr10:55587142 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2361T>C (p.Leu787=) single nucleotide variant not provided [RCV002152213] Chr10:54023057 [GRCh38]
Chr10:55782817 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4368-3135T>C single nucleotide variant not provided [RCV002109294] Chr10:53823365 [GRCh38]
Chr10:55583125 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.318+7G>A single nucleotide variant not provided [RCV002172211] Chr10:54378775 [GRCh38]
Chr10:56138535 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1629G>A (p.Glu543=) single nucleotide variant not provided [RCV002092639] Chr10:54153255 [GRCh38]
Chr10:55913015 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.213C>T (p.Pro71=) single nucleotide variant not provided [RCV002185014] Chr10:54378887 [GRCh38]
Chr10:56138647 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1305+14A>G single nucleotide variant not provided [RCV002188395] Chr10:54195669 [GRCh38]
Chr10:55955429 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4122A>G (p.Glu1374=) single nucleotide variant not provided [RCV002188442] Chr10:53831395 [GRCh38]
Chr10:55591155 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3273G>T (p.Val1091=) single nucleotide variant not provided [RCV002170933] Chr10:53938915 [GRCh38]
Chr10:55698675 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2526+9G>A single nucleotide variant not provided [RCV002095460] Chr10:54022883 [GRCh38]
Chr10:55782643 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5692_5695dup (p.Met1899fs) duplication not provided [RCV002116360] Chr10:53822030..53822031 [GRCh38]
Chr10:55581790..55581791 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1441-20G>A single nucleotide variant not provided [RCV002196623] Chr10:54183613 [GRCh38]
Chr10:55943373 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1650T>C (p.Val550=) single nucleotide variant not provided [RCV002170492] Chr10:54153234 [GRCh38]
Chr10:55912994 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1365A>G (p.Thr455=) single nucleotide variant not provided [RCV002089948] Chr10:54185209 [GRCh38]
Chr10:55944969 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.168G>T (p.Leu56=) single nucleotide variant not provided [RCV002214793] Chr10:54378932 [GRCh38]
Chr10:56138692 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5733T>C (p.Asn1911=) single nucleotide variant not provided [RCV002133839] Chr10:53821993 [GRCh38]
Chr10:55581753 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1239C>T (p.Thr413=) single nucleotide variant not provided [RCV002208440] Chr10:54195749 [GRCh38]
Chr10:55955509 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4632G>A (p.Gln1544=) single nucleotide variant not provided [RCV002194283] Chr10:53823094 [GRCh38]
Chr10:55582854 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4840dup (p.Ile1614fs) duplication not provided [RCV002145044] Chr10:53822885..53822886 [GRCh38]
Chr10:55582645..55582646 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1785-12C>G single nucleotide variant not provided [RCV002153085] Chr10:54133019 [GRCh38]
Chr10:55892779 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5215_5218dup (p.Ile1740fs) duplication not provided [RCV002131070] Chr10:53822507..53822508 [GRCh38]
Chr10:55582267..55582268 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2220+10A>G single nucleotide variant not provided [RCV002126658] Chr10:54066747 [GRCh38]
Chr10:55826507 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.258G>A (p.Leu86=) single nucleotide variant not provided [RCV002093078] Chr10:54378842 [GRCh38]
Chr10:56138602 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.216C>T (p.Thr72=) single nucleotide variant not provided [RCV002171387] Chr10:54378884 [GRCh38]
Chr10:56138644 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3373+8A>T single nucleotide variant not provided [RCV002113629] Chr10:53938807 [GRCh38]
Chr10:55698567 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1713G>A (p.Val571=) single nucleotide variant not provided [RCV002215477] Chr10:54153171 [GRCh38]
Chr10:55912931 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2919T>C (p.Pro973=) single nucleotide variant not provided [RCV002076651] Chr10:53961842 [GRCh38]
Chr10:55721602 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1404A>G (p.Pro468=) single nucleotide variant not provided [RCV002215695] Chr10:54185170 [GRCh38]
Chr10:55944930 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4011C>T (p.Ile1337=) single nucleotide variant not provided [RCV002149797] Chr10:53831506 [GRCh38]
Chr10:55591266 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5118T>A (p.Cys1706Ter) single nucleotide variant not provided [RCV002196851] Chr10:53822608 [GRCh38]
Chr10:55582368 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4836_4837del (p.Gly1613fs) deletion not provided [RCV002215583] Chr10:53822889..53822890 [GRCh38]
Chr10:55582649..55582650 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.819C>T (p.Asn273=) single nucleotide variant not provided [RCV002207230] Chr10:54317328 [GRCh38]
Chr10:56077088 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.333A>C (p.Ile111=) single nucleotide variant not provided [RCV002076696] Chr10:54369261 [GRCh38]
Chr10:56129021 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5241_5247del (p.Pro1748fs) deletion not provided [RCV002150222] Chr10:53822479..53822485 [GRCh38]
Chr10:55582239..55582245 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3010-19A>G single nucleotide variant not provided [RCV002133493] Chr10:53959863 [GRCh38]
Chr10:55719623 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.158-10T>G single nucleotide variant not provided [RCV002171149] Chr10:54378952 [GRCh38]
Chr10:56138712 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.636A>G (p.Gly212=) single nucleotide variant not provided [RCV002212046] Chr10:54329665 [GRCh38]
Chr10:56089425 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.765T>C (p.Val255=) single nucleotide variant not provided [RCV002172030] Chr10:54317382 [GRCh38]
Chr10:56077142 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5847C>T (p.His1949=) single nucleotide variant not provided [RCV002078520] Chr10:53821879 [GRCh38]
Chr10:55581639 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5580C>A (p.Ser1860=) single nucleotide variant not provided [RCV002213595] Chr10:53822146 [GRCh38]
Chr10:55581906 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3501+8G>A single nucleotide variant not provided [RCV002078638] Chr10:53903235 [GRCh38]
Chr10:55662995 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1575G>C (p.Gly525=) single nucleotide variant not provided [RCV002194001] Chr10:54183459 [GRCh38]
Chr10:55943219 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2607A>G (p.Pro869=) single nucleotide variant not provided [RCV002134800] Chr10:54020336 [GRCh38]
Chr10:55780096 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4158C>T (p.Leu1386=) single nucleotide variant not provided [RCV002072552] Chr10:53831359 [GRCh38]
Chr10:55591119 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1317A>G (p.Pro439=) single nucleotide variant not provided [RCV002112344] Chr10:54185257 [GRCh38]
Chr10:55945017 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.319-18G>A single nucleotide variant not provided [RCV002150894] Chr10:54369293 [GRCh38]
Chr10:56129053 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.465A>G (p.Thr155=) single nucleotide variant PCDH15-related disorder [RCV004538780]|not provided [RCV002157483] Chr10:54369129 [GRCh38]
Chr10:56128889 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_033056.4(PCDH15):c.5433A>G (p.Leu1811=) single nucleotide variant not provided [RCV002180769] Chr10:53822293 [GRCh38]
Chr10:55582053 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1099-23TTTTC[2] microsatellite not provided [RCV002099593] Chr10:54195898..54195902 [GRCh38]
Chr10:55955658..55955662 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1458T>A (p.Gly486=) single nucleotide variant not provided [RCV002159544] Chr10:54183576 [GRCh38]
Chr10:55943336 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.912C>T (p.Ile304=) single nucleotide variant not provided [RCV002199808] Chr10:54236896 [GRCh38]
Chr10:55996656 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1182T>C (p.Tyr394=) single nucleotide variant not provided [RCV002201657] Chr10:54195806 [GRCh38]
Chr10:55955566 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.706-21_706-19del microsatellite not provided [RCV002098354] Chr10:54317460..54317462 [GRCh38]
Chr10:56077220..56077222 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5347CCT[1] (p.Pro1784del) microsatellite not provided [RCV002102229] Chr10:53822374..53822376 [GRCh38]
Chr10:55582134..55582136 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4161C>T (p.Cys1387=) single nucleotide variant not provided [RCV002200334] Chr10:53831356 [GRCh38]
Chr10:55591116 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3906T>C (p.Asp1302=) single nucleotide variant not provided [RCV002156396] Chr10:53840397 [GRCh38]
Chr10:55600157 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4968_4971del (p.Ser1657fs) microsatellite not provided [RCV002220940] Chr10:53822755..53822758 [GRCh38]
Chr10:55582515..55582518 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2034G>A (p.Arg678=) single nucleotide variant not provided [RCV002138036] Chr10:54079388 [GRCh38]
Chr10:55839148 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5334TCC[2] (p.Pro1781del) microsatellite not provided [RCV002138037] Chr10:53822384..53822386 [GRCh38]
Chr10:55582144..55582146 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.621C>G (p.Pro207=) single nucleotide variant not provided [RCV002202356] Chr10:54329680 [GRCh38]
Chr10:56089440 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5719dup (p.Tyr1907fs) duplication not provided [RCV002118313] Chr10:53822006..53822007 [GRCh38]
Chr10:55581766..55581767 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5039del (p.Thr1680fs) deletion not provided [RCV002217402] Chr10:53822687 [GRCh38]
Chr10:55582447 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2922C>T (p.Tyr974=) single nucleotide variant not provided [RCV002202557] Chr10:53961839 [GRCh38]
Chr10:55721599 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5252_5256del (p.Pro1751fs) deletion not provided [RCV002200511] Chr10:53822470..53822474 [GRCh38]
Chr10:55582230..55582234 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.42G>C (p.Gly14=) single nucleotide variant not provided [RCV002082347] Chr10:54664221 [GRCh38]
Chr10:56423981 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.877-5_877-4del deletion not provided [RCV002155027] Chr10:54236935..54236936 [GRCh38]
Chr10:55996695..55996696 [GRCh37]
Chr10:10q21.1		 benign
NC_000010.10:g.(56138703_56287571)_(56287638_56423931)dup duplication not specified [RCV002222950] Chr10:56287571..56287638 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5257_5260dup (p.Ser1754fs) duplication not provided [RCV002182062] Chr10:53822465..53822466 [GRCh38]
Chr10:55582225..55582226 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5253_5266del (p.Pro1752fs) deletion not specified [RCV002222963] Chr10:53822460..53822473 [GRCh38]
Chr10:55582220..55582233 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1146C>T (p.His382=) single nucleotide variant not provided [RCV002199002] Chr10:54195842 [GRCh38]
Chr10:55955602 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3825T>G (p.Val1275=) single nucleotide variant not provided [RCV002120901] Chr10:53840478 [GRCh38]
Chr10:55600238 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5598A>G (p.Ser1866=) single nucleotide variant not provided [RCV002118943] Chr10:53822128 [GRCh38]
Chr10:55581888 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1306-20G>A single nucleotide variant not provided [RCV002203157] Chr10:54185288 [GRCh38]
Chr10:55945048 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2869-19A>G single nucleotide variant not provided [RCV002159861] Chr10:53961911 [GRCh38]
Chr10:55721671 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4866C>T (p.Ser1622=) single nucleotide variant not provided [RCV002098040] Chr10:53822860 [GRCh38]
Chr10:55582620 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3084T>C (p.His1028=) single nucleotide variant not provided [RCV002141298] Chr10:53959770 [GRCh38]
Chr10:55719530 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.157+9G>T single nucleotide variant not provided [RCV002198350] Chr10:54527803 [GRCh38]
Chr10:56287563 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4797G>A (p.Gln1599=) single nucleotide variant not provided [RCV002175910] Chr10:53822929 [GRCh38]
Chr10:55582689 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1515C>T (p.Asn505=) single nucleotide variant not provided [RCV002081782] Chr10:54183519 [GRCh38]
Chr10:55943279 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3374-19A>G single nucleotide variant not provided [RCV002141682] Chr10:53903389 [GRCh38]
Chr10:55663149 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5016C>T (p.Ser1672=) single nucleotide variant not provided [RCV002163704] Chr10:53822710 [GRCh38]
Chr10:55582470 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1590+20A>C single nucleotide variant not provided [RCV002118258] Chr10:54183424 [GRCh38]
Chr10:55943184 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1441-1G>T single nucleotide variant Usher syndrome type 1D [RCV002250176] Chr10:54183594 [GRCh38]
Chr10:55943354 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.1731G>A (p.Arg577=) single nucleotide variant not provided [RCV002156712] Chr10:54153153 [GRCh38]
Chr10:55912913 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5310C>T (p.Asp1770=) single nucleotide variant not provided [RCV002181993] Chr10:53822416 [GRCh38]
Chr10:55582176 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.921T>C (p.Ile307=) single nucleotide variant not provided [RCV002118449] Chr10:54236887 [GRCh38]
Chr10:55996647 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1326C>T (p.His442=) single nucleotide variant not provided [RCV002178064] Chr10:54185248 [GRCh38]
Chr10:55945008 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2247T>C (p.Asn749=) single nucleotide variant not provided [RCV002084223] Chr10:54023171 [GRCh38]
Chr10:55782931 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4202+13G>C single nucleotide variant not provided [RCV002140048] Chr10:53831302 [GRCh38]
Chr10:55591062 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2838A>G (p.Thr946=) single nucleotide variant not provided [RCV002204615] Chr10:53995679 [GRCh38]
Chr10:55755439 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3723C>T (p.Ser1241=) single nucleotide variant not provided [RCV002120546] Chr10:53857258 [GRCh38]
Chr10:55617018 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3111G>A (p.Gln1037=) single nucleotide variant not provided [RCV002156946] Chr10:53959743 [GRCh38]
Chr10:55719503 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.606C>T (p.Asp202=) single nucleotide variant not provided [RCV002164288] Chr10:54329695 [GRCh38]
Chr10:56089455 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2271T>G (p.Gly757=) single nucleotide variant not provided [RCV002176422] Chr10:54023147 [GRCh38]
Chr10:55782907 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5227del (p.Ser1743fs) deletion not provided [RCV002155326] Chr10:53822499 [GRCh38]
Chr10:55582259 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2457C>T (p.Phe819=) single nucleotide variant not provided [RCV002099212] Chr10:54022961 [GRCh38]
Chr10:55782721 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5155_5158dup (p.Cys1720fs) duplication not provided [RCV002082811] Chr10:53822567..53822568 [GRCh38]
Chr10:55582327..55582328 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1518G>C (p.Thr506=) single nucleotide variant not provided [RCV002178833] Chr10:54183516 [GRCh38]
Chr10:55943276 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4143C>T (p.Ala1381=) single nucleotide variant not provided [RCV002119196] Chr10:53831374 [GRCh38]
Chr10:55591134 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.628T>C (p.Leu210=) single nucleotide variant not provided [RCV002135371] Chr10:54329673 [GRCh38]
Chr10:56089433 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4845T>C (p.Cys1615=) single nucleotide variant not provided [RCV002202871] Chr10:53822881 [GRCh38]
Chr10:55582641 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3983+13dup duplication not provided [RCV002121492] Chr10:53840306..53840307 [GRCh38]
Chr10:55600066..55600067 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3374-18T>A single nucleotide variant not provided [RCV002180760] Chr10:53903388 [GRCh38]
Chr10:55663148 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.789A>C (p.Pro263=) single nucleotide variant not provided [RCV002177433] Chr10:54317358 [GRCh38]
Chr10:56077118 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1918-20A>G single nucleotide variant not provided [RCV002201786] Chr10:54090083 [GRCh38]
Chr10:55849843 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2751+11G>A single nucleotide variant not provided [RCV002137766] Chr10:54020181 [GRCh38]
Chr10:55779941 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1591-10dup duplication not provided [RCV002121698] Chr10:54153302..54153303 [GRCh38]
Chr10:55913062..55913063 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.475-7del deletion not provided [RCV002159541] Chr10:54346491 [GRCh38]
Chr10:56106251 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5704C>T (p.Gln1902Ter) single nucleotide variant not provided [RCV002140877] Chr10:53822022 [GRCh38]
Chr10:55581782 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3666T>C (p.Val1222=) single nucleotide variant not provided [RCV002135926] Chr10:53866693 [GRCh38]
Chr10:55626453 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5257_5268del (p.Ile1753_Pro1756del) deletion not provided [RCV002083800] Chr10:53822458..53822469 [GRCh38]
Chr10:55582218..55582229 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.108G>A (p.Arg36=) single nucleotide variant not provided [RCV002203462] Chr10:54527861 [GRCh38]
Chr10:56287621 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5230_5294dup (p.Ala1766fs) duplication not provided [RCV002140975] Chr10:53822431..53822432 [GRCh38]
Chr10:55582191..55582192 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1473G>A (p.Glu491=) single nucleotide variant not provided [RCV002182989] Chr10:54183561 [GRCh38]
Chr10:55943321 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1683A>G (p.Thr561=) single nucleotide variant not provided [RCV002217123] Chr10:54153201 [GRCh38]
Chr10:55912961 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4119A>T (p.Thr1373=) single nucleotide variant not provided [RCV002221026] Chr10:53831398 [GRCh38]
Chr10:55591158 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.684C>T (p.Tyr228=) single nucleotide variant not provided [RCV002141328] Chr10:54329617 [GRCh38]
Chr10:56089377 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5367T>G (p.Pro1789=) single nucleotide variant not provided [RCV002198802] Chr10:53822359 [GRCh38]
Chr10:55582119 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5451T>C (p.Pro1817=) single nucleotide variant not provided [RCV002084288] Chr10:53822275 [GRCh38]
Chr10:55582035 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3591G>A (p.Val1197=) single nucleotide variant not provided [RCV002200796] Chr10:53866768 [GRCh38]
Chr10:55626528 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.153G>T (p.Arg51=) single nucleotide variant not provided [RCV002102679] Chr10:54527816 [GRCh38]
Chr10:56287576 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4761A>G (p.Lys1587=) single nucleotide variant not provided [RCV002123681] Chr10:53822965 [GRCh38]
Chr10:55582725 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.987G>C (p.Gly329=) single nucleotide variant not provided [RCV002180069] Chr10:54214047 [GRCh38]
Chr10:55973807 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5382A>G (p.Thr1794=) single nucleotide variant not provided [RCV002162276] Chr10:53822344 [GRCh38]
Chr10:55582104 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1533A>G (p.Glu511=) single nucleotide variant not provided [RCV002199168] Chr10:54183501 [GRCh38]
Chr10:55943261 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3042T>A (p.Pro1014=) single nucleotide variant not provided [RCV002118981] Chr10:53959812 [GRCh38]
Chr10:55719572 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5514A>G (p.Thr1838=) single nucleotide variant not provided [RCV002119084] Chr10:53822212 [GRCh38]
Chr10:55581972 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3549C>G (p.Leu1183=) single nucleotide variant not provided [RCV002201270] Chr10:53866810 [GRCh38]
Chr10:55626570 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5223T>C (p.Ser1741=) single nucleotide variant not provided [RCV002103485] Chr10:53822503 [GRCh38]
Chr10:55582263 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.706-10T>C single nucleotide variant not provided [RCV002199660] Chr10:54317451 [GRCh38]
Chr10:56077211 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2664A>G (p.Gln888=) single nucleotide variant not provided [RCV002138992] Chr10:54020279 [GRCh38]
Chr10:55780039 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5832T>C (p.Thr1944=) single nucleotide variant not provided [RCV002216447] Chr10:53821894 [GRCh38]
Chr10:55581654 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4254A>C (p.Ala1418=) single nucleotide variant not provided [RCV002153971] Chr10:53827506 [GRCh38]
Chr10:55587266 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4977C>T (p.Asp1659=) single nucleotide variant not provided [RCV002216515] Chr10:53822749 [GRCh38]
Chr10:55582509 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1482C>T (p.Ile494=) single nucleotide variant not provided [RCV002119463] Chr10:54183552 [GRCh38]
Chr10:55943312 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4302G>A (p.Ala1434=) single nucleotide variant not provided [RCV002121770] Chr10:53827458 [GRCh38]
Chr10:55587218 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2221-15dup duplication not provided [RCV002081456] Chr10:54023211..54023212 [GRCh38]
Chr10:55782971..55782972 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.877-8T>C single nucleotide variant not provided [RCV002181144] Chr10:54236939 [GRCh38]
Chr10:55996699 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3339A>G (p.Glu1113=) single nucleotide variant not provided [RCV002203670] Chr10:53938849 [GRCh38]
Chr10:55698609 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5281_5292del (p.Ala1761_Pro1764del) deletion not provided [RCV002120059] Chr10:53822434..53822445 [GRCh38]
Chr10:55582194..55582205 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4971T>A (p.Ser1657=) single nucleotide variant not provided [RCV002176040] Chr10:53822755 [GRCh38]
Chr10:55582515 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2529C>A (p.Ala843=) single nucleotide variant not provided [RCV002183606] Chr10:54020414 [GRCh38]
Chr10:55780174 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5618_5637dup (p.Lys1880fs) duplication not provided [RCV002202303] Chr10:53822088..53822089 [GRCh38]
Chr10:55581848..55581849 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3621T>G (p.Ala1207=) single nucleotide variant not provided [RCV002123630] Chr10:53866738 [GRCh38]
Chr10:55626498 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2751+10A>G single nucleotide variant not provided [RCV002143797] Chr10:54020182 [GRCh38]
Chr10:55779942 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1953C>T (p.Ala651=) single nucleotide variant not provided [RCV002183949] Chr10:54090028 [GRCh38]
Chr10:55849788 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2286T>C (p.Leu762=) single nucleotide variant not provided [RCV002118459] Chr10:54023132 [GRCh38]
Chr10:55782892 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2685G>T (p.Leu895=) single nucleotide variant not provided [RCV002098847] Chr10:54020258 [GRCh38]
Chr10:55780018 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5269_5274del (p.Ser1757_Pro1758del) deletion not provided [RCV002219430] Chr10:53822452..53822457 [GRCh38]
Chr10:55582212..55582217 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4923del (p.Gly1642fs) deletion not provided [RCV002141880] Chr10:53822803 [GRCh38]
Chr10:55582563 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.92-7T>C single nucleotide variant not provided [RCV002201072] Chr10:54527884 [GRCh38]
Chr10:56287644 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1785-6C>G single nucleotide variant not provided [RCV002184232] Chr10:54133013 [GRCh38]
Chr10:55892773 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4368-3138T>C single nucleotide variant not provided [RCV002160808] Chr10:53823368 [GRCh38]
Chr10:55583128 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4647A>T (p.Val1549=) single nucleotide variant not provided [RCV002199257] Chr10:53823079 [GRCh38]
Chr10:55582839 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4878T>G (p.Leu1626=) single nucleotide variant not provided [RCV002219927] Chr10:53822848 [GRCh38]
Chr10:55582608 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3456T>G (p.Gly1152=) single nucleotide variant not provided [RCV002180356] Chr10:53903288 [GRCh38]
Chr10:55663048 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2751+9dup duplication not provided [RCV002182320] Chr10:54020182..54020183 [GRCh38]
Chr10:55779942..55779943 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4203-19C>T single nucleotide variant not provided [RCV002121170] Chr10:53828592 [GRCh38]
Chr10:55588352 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2064C>T (p.Ile688=) single nucleotide variant not provided [RCV002159240] Chr10:54079358 [GRCh38]
Chr10:55839118 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4560T>A (p.Asp1520Glu) single nucleotide variant not provided [RCV003110524] Chr10:53823166 [GRCh38]
Chr10:55582926 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1509T>G (p.Asn503Lys) single nucleotide variant not provided [RCV003110291] Chr10:54183525 [GRCh38]
Chr10:55943285 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3551T>C (p.Ile1184Thr) single nucleotide variant not provided [RCV003118022] Chr10:53866808 [GRCh38]
Chr10:55626568 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5141G>A (p.Arg1714Lys) single nucleotide variant not provided [RCV003111863] Chr10:53822585 [GRCh38]
Chr10:55582345 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.985+12A>C single nucleotide variant not provided [RCV003111866] Chr10:54236811 [GRCh38]
Chr10:55996571 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.823C>T (p.Arg275Cys) single nucleotide variant not provided [RCV003118225] Chr10:54317324 [GRCh38]
Chr10:56077084 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3807-12_3807-9del microsatellite not provided [RCV003115991] Chr10:53840505..53840508 [GRCh38]
Chr10:55600265..55600268 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.284T>C (p.Phe95Ser) single nucleotide variant not provided [RCV003118294] Chr10:54378816 [GRCh38]
Chr10:56138576 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.481C>G (p.Pro161Ala) single nucleotide variant not provided [RCV003116061] Chr10:54346478 [GRCh38]
Chr10:56106238 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2069C>T (p.Ala690Val) single nucleotide variant not provided [RCV003118176] Chr10:54079353 [GRCh38]
Chr10:55839113 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5245CCT[2] (p.Pro1751_Pro1752del) microsatellite not provided [RCV003118053] Chr10:53822470..53822475 [GRCh38]
Chr10:55582230..55582235 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.71G>C (p.Cys24Ser) single nucleotide variant not provided [RCV003112155] Chr10:54664192 [GRCh38]
Chr10:56423952 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5084A>C (p.Glu1695Ala) single nucleotide variant not provided [RCV003115626] Chr10:53822642 [GRCh38]
Chr10:55582402 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3718-16T>G single nucleotide variant not provided [RCV003115649] Chr10:53857279 [GRCh38]
Chr10:55617039 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3875G>A (p.Arg1292His) single nucleotide variant not provided [RCV003117928] Chr10:53840428 [GRCh38]
Chr10:55600188 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.10:g.(?_55955423)_(55955669_?)del deletion not provided [RCV003122930] Chr10:55955423..55955669 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.10:g.(?_55698555)_(55698735_?)del deletion not provided [RCV003122931] Chr10:55698555..55698735 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.10:g.(?_56287562)_(56288172_?)del deletion not provided [RCV003122932] Chr10:56287562..56288172 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_55588305)_(55588353_?)del deletion not provided [RCV003122933] Chr10:55588305..55588353 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NC_000010.10:g.(?_56106115)_(56106254_?)del deletion not provided [RCV003122934] Chr10:56106115..56106254 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_55826507)_(56424032_?)del deletion not provided [RCV003122935] Chr10:55826507..56424032 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_55755399)_(56424032_?)del deletion not provided [RCV003122936] Chr10:55755399..56424032 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_55698565)_(55700745_?)del deletion not provided [RCV003122937] Chr10:55698565..55700745 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_55826507)_(56106254_?)del deletion not provided [RCV003122938] Chr10:55826507..56106254 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_55581618)_(56424022_?)dup duplication not provided [RCV003122939] Chr10:55581618..56424022 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.10:g.(?_55662993)_(55663140_?)dup duplication not provided [RCV003122940] Chr10:55662993..55663140 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NC_000010.10:g.(?_56077021)_(56138712_?)dup duplication not provided [RCV003122941] Chr10:56077021..56138712 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NC_000010.10:g.(?_55892683)_(55893842_?)del deletion not provided [RCV003122942] Chr10:55892683..55893842 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NC_000010.10:g.(?_55849734)_(55849833_?)del deletion not provided [RCV003122943] Chr10:55849734..55849833 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_55912840)_(55913073_?)dup duplication not provided [RCV003122944] Chr10:55912840..55913073 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.4466C>G (p.Thr1489Ser) single nucleotide variant not provided [RCV003118507] Chr10:53823260 [GRCh38]
Chr10:55583020 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4203-5_4203-2dup duplication not provided [RCV003121360] Chr10:53828574..53828575 [GRCh38]
Chr10:55588334..55588335 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4847C>T (p.Thr1616Ile) single nucleotide variant not provided [RCV003121368] Chr10:53822879 [GRCh38]
Chr10:55582639 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.301A>G (p.Arg101Gly) single nucleotide variant not provided [RCV003121448] Chr10:54378799 [GRCh38]
Chr10:56138559 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.372A>G (p.Lys124=) single nucleotide variant not provided [RCV003129293] Chr10:54369222 [GRCh38]
Chr10:56128982 [GRCh37]
Chr10:10q21.1		 conflicting interpretations of pathogenicity|uncertain significance
NM_001384140.1(PCDH15):c.2869G>A (p.Gly957Arg) single nucleotide variant not provided [RCV003151997] Chr10:53961892 [GRCh38]
Chr10:55721652 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.152G>A (p.Arg51Gln) single nucleotide variant not provided [RCV002275452] Chr10:54527817 [GRCh38]
Chr10:56287577 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4768A>G (p.Asn1590Asp) single nucleotide variant not specified [RCV002266139] Chr10:53822958 [GRCh38]
Chr10:55582718 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.657G>T (p.Arg219Ser) single nucleotide variant not provided [RCV002286023] Chr10:54329644 [GRCh38]
Chr10:56089404 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4672-8_4672-4del microsatellite PCDH15-related disorder [RCV004534031]|not provided [RCV002276359] Chr10:53807134..53807138 [GRCh38]
Chr10:55566894..55566898 [GRCh37]
Chr10:10q21.1		 benign|likely benign
NM_001384140.1(PCDH15):c.4308GCC[3] (p.Pro1442_Pro1443del) microsatellite not provided [RCV002280449] Chr10:53827438..53827443 [GRCh38]
Chr10:55587198..55587203 [GRCh37]
Chr10:10q21.1		 likely benign|conflicting interpretations of pathogenicity
NM_001384140.1(PCDH15):c.946C>G (p.Pro316Ala) single nucleotide variant not provided [RCV002293670] Chr10:54236862 [GRCh38]
Chr10:55996622 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2436T>G (p.Ile812Met) single nucleotide variant not provided [RCV002273583] Chr10:54022982 [GRCh38]
Chr10:55782742 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4671+1393G>C single nucleotide variant Usher syndrome type 1F [RCV002281542] Chr10:53809163 [GRCh38]
Chr10:55568923 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1235C>G (p.Ala412Gly) single nucleotide variant Inborn genetic diseases [RCV003256590] Chr10:54195753 [GRCh38]
Chr10:55955513 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.458A>G (p.Tyr153Cys) single nucleotide variant not provided [RCV003129329] Chr10:54369136 [GRCh38]
Chr10:56128896 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001354404.2(PCDH15):c.-156+225495_-156+225533del deletion Schizophrenia [RCV002463504] Chr10:55402092..55402130 [GRCh38]
Chr10:57161852..57161890 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2552del (p.Asn851fs) deletion not provided [RCV003012234] Chr10:54020391 [GRCh38]
Chr10:55780151 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.4085G>T (p.Ser1362Ile) single nucleotide variant Inborn genetic diseases [RCV004067562]|not provided [RCV002467276] Chr10:53831432 [GRCh38]
Chr10:55591192 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4586A>G (p.Tyr1529Cys) single nucleotide variant Inborn genetic diseases [RCV003287874] Chr10:53823140 [GRCh38]
Chr10:55582900 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1037A>G (p.Glu346Gly) single nucleotide variant not provided [RCV003129077] Chr10:54213997 [GRCh38]
Chr10:55973757 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.475-2A>G single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002468759]|not provided [RCV003574976] Chr10:54346486 [GRCh38]
Chr10:56106246 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4015A>T (p.Lys1339Ter) single nucleotide variant Usher syndrome type 1D [RCV002306497] Chr10:53831502 [GRCh38]
Chr10:55591262 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3910_3911del (p.Thr1304fs) microsatellite Usher syndrome type 1D [RCV002306702] Chr10:53840392..53840393 [GRCh38]
Chr10:55600152..55600153 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.838_839delinsG (p.Leu280fs) indel Usher syndrome type 1D [RCV002307248] Chr10:54317308..54317309 [GRCh38]
Chr10:56077068..56077069 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.4542_4567dup (p.Ser1523delinsAsnPheTyrLeuMetArgMetThrTer) duplication PCDH15-related disorder [RCV004735068] Chr10:53823158..53823159 [GRCh38]
Chr10:55582918..55582919 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2809C>G (p.Pro937Ala) single nucleotide variant not provided [RCV002304468] Chr10:53995708 [GRCh38]
Chr10:55755468 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3112G>T (p.Glu1038Ter) single nucleotide variant Usher syndrome type 1D [RCV002307868] Chr10:53959742 [GRCh38]
Chr10:55719502 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.2118_2119insA (p.Val707fs) insertion Usher syndrome type 1D [RCV002308320] Chr10:54066858..54066859 [GRCh38]
Chr10:55826618..55826619 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NC_000010.10:g.(55663131_55698574)_(55945029_55955442)dup duplication Usher syndrome type 1F [RCV002308568] Chr10:55698574..55945029 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3144dup (p.Ala1049fs) duplication Usher syndrome type 1D [RCV002307276] Chr10:53940953..53940954 [GRCh38]
Chr10:55700713..55700714 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1322_1323insGTCTCTA (p.His442fs) insertion Usher syndrome type 1D [RCV002307345] Chr10:54185251..54185252 [GRCh38]
Chr10:55945011..55945012 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1102_1103del (p.Glu368fs) deletion Usher syndrome type 1D [RCV002308051] Chr10:54195885..54195886 [GRCh38]
Chr10:55955645..55955646 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.355del (p.Gln119fs) deletion Usher syndrome type 1D [RCV002309325] Chr10:54369239 [GRCh38]
Chr10:56128999 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1231G>T (p.Gly411Ter) single nucleotide variant Usher syndrome type 1D [RCV002309449] Chr10:54195757 [GRCh38]
Chr10:55955517 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.2208_2211del (p.Gly737fs) deletion Usher syndrome type 1D [RCV002309270] Chr10:54066766..54066769 [GRCh38]
Chr10:55826526..55826529 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4034_4035del (p.Tyr1345fs) deletion Usher syndrome type 1D [RCV002308293] Chr10:53831482..53831483 [GRCh38]
Chr10:55591242..55591243 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1423C>T (p.Gln475Ter) single nucleotide variant Usher syndrome type 1D [RCV002309418] Chr10:54185151 [GRCh38]
Chr10:55944911 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1073_1074del (p.His358fs) deletion Usher syndrome type 1D [RCV002308428] Chr10:54213960..54213961 [GRCh38]
Chr10:55973720..55973721 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1316del (p.Pro439fs) deletion Usher syndrome type 1D [RCV002310299] Chr10:54185258 [GRCh38]
Chr10:55945018 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3462_3463del (p.Glu1155fs) deletion Usher syndrome type 1D [RCV002310360] Chr10:53903281..53903282 [GRCh38]
Chr10:55663041..55663042 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3613A>T (p.Lys1205Ter) single nucleotide variant Usher syndrome type 1D [RCV002307948] Chr10:53866746 [GRCh38]
Chr10:55626506 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.811dup (p.Val271fs) duplication Usher syndrome type 1D [RCV002310166] Chr10:54317335..54317336 [GRCh38]
Chr10:56077095..56077096 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1105C>T (p.Gln369Ter) single nucleotide variant Usher syndrome type 1D [RCV002310358] Chr10:54195883 [GRCh38]
Chr10:55955643 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3488del (p.Val1163fs) deletion Usher syndrome type 1D [RCV002309894] Chr10:53903256 [GRCh38]
Chr10:55663016 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.2097_2098insG (p.Thr700fs) insertion Usher syndrome type 1D [RCV002310204] Chr10:54066879..54066880 [GRCh38]
Chr10:55826639..55826640 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.738_739insT (p.Thr247fs) insertion Usher syndrome type 1D [RCV002308425] Chr10:54317408..54317409 [GRCh38]
Chr10:56077168..56077169 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.2205del (p.Phe735fs) deletion Usher syndrome type 1D [RCV002306742] Chr10:54066772 [GRCh38]
Chr10:55826532 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.4902del (p.Glu1635fs) deletion not provided [RCV003560938]|not specified [RCV002308539] Chr10:53822824 [GRCh38]
Chr10:55582584 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.2119G>A (p.Val707Met) single nucleotide variant not provided [RCV002306170] Chr10:54066858 [GRCh38]
Chr10:55826618 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3788del (p.Lys1263fs) deletion Usher syndrome type 1D [RCV002310540] Chr10:53857193 [GRCh38]
Chr10:55616953 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.2714T>G (p.Met905Arg) single nucleotide variant not provided [RCV002296053] Chr10:54020229 [GRCh38]
Chr10:55779989 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3745C>T (p.Gln1249Ter) single nucleotide variant Usher syndrome type 1D [RCV002306621] Chr10:53857236 [GRCh38]
Chr10:55616996 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.2215G>C (p.Val739Leu) single nucleotide variant not provided [RCV002296490] Chr10:54066762 [GRCh38]
Chr10:55826522 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2952_2953delinsC (p.Ser985fs) indel Usher syndrome type 1D [RCV002307292] Chr10:53961808..53961809 [GRCh38]
Chr10:55721568..55721569 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1515dup (p.Thr506fs) duplication Usher syndrome type 1D [RCV002307187] Chr10:54183518..54183519 [GRCh38]
Chr10:55943278..55943279 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.2898_2899del (p.Arg966fs) microsatellite Usher syndrome type 1D [RCV002307936] Chr10:53961862..53961863 [GRCh38]
Chr10:55721622..55721623 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1495_1496insA (p.Val499fs) insertion Usher syndrome type 1D [RCV002309114] Chr10:54183538..54183539 [GRCh38]
Chr10:55943298..55943299 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4098_4099dup (p.Gly1367fs) microsatellite Usher syndrome type 1D [RCV002306698] Chr10:53831417..53831418 [GRCh38]
Chr10:55591177..55591178 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1568G>C (p.Arg523Thr) single nucleotide variant not provided [RCV002302640] Chr10:54183466 [GRCh38]
Chr10:55943226 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4204T>G (p.Phe1402Val) single nucleotide variant not provided [RCV002295533] Chr10:53828572 [GRCh38]
Chr10:55588332 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.251G>A (p.Trp84Ter) single nucleotide variant Usher syndrome type 1D [RCV002306927]|not provided [RCV003099158] Chr10:54378849 [GRCh38]
Chr10:56138609 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.2518_2519del (p.Gln840fs) deletion Usher syndrome type 1D [RCV002309377] Chr10:54022899..54022900 [GRCh38]
Chr10:55782659..55782660 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.2036A>G (p.Glu679Gly) single nucleotide variant not provided [RCV002296660] Chr10:54079386 [GRCh38]
Chr10:55839146 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.60_63del (p.Phe21fs) deletion Usher syndrome type 1D [RCV002309504] Chr10:54664200..54664203 [GRCh38]
Chr10:56423960..56423963 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3907del (p.Tyr1303fs) deletion Usher syndrome type 1D [RCV002309675] Chr10:53840396 [GRCh38]
Chr10:55600156 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1454_1455del (p.Asp485fs) deletion Usher syndrome type 1D [RCV002309696] Chr10:54183579..54183580 [GRCh38]
Chr10:55943339..55943340 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3204_3205del (p.Tyr1069fs) microsatellite Usher syndrome type 1D [RCV002309833] Chr10:53940893..53940894 [GRCh38]
Chr10:55700653..55700654 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.2822del (p.Lys941fs) deletion Usher syndrome type 1D [RCV002310257]|not provided [RCV003546760] Chr10:53995695 [GRCh38]
Chr10:55755455 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.3152_3153insC (p.Lys1051fs) insertion Usher syndrome type 1D [RCV002310101] Chr10:53940945..53940946 [GRCh38]
Chr10:55700705..55700706 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.2176_2188del (p.Ser726fs) deletion Usher syndrome type 1D [RCV002308321] Chr10:54066789..54066801 [GRCh38]
Chr10:55826549..55826561 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3600T>A (p.Tyr1200Ter) single nucleotide variant Usher syndrome type 1D [RCV002310434] Chr10:53866759 [GRCh38]
Chr10:55626519 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.837A>T (p.Pro279=) single nucleotide variant not provided [RCV002861906] Chr10:54317310 [GRCh38]
Chr10:56077070 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3486T>C (p.Ser1162=) single nucleotide variant not provided [RCV003015894] Chr10:53903258 [GRCh38]
Chr10:55663018 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.54_55inv (p.Ser19Ala) inversion not provided [RCV002617002] Chr10:54664208..54664209 [GRCh38]
Chr10:56423968..56423969 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1987C>G (p.Leu663Val) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV002509882] Chr10:54089994 [GRCh38]
Chr10:55849754 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4051A>G (p.Ile1351Val) single nucleotide variant not provided [RCV002511208] Chr10:53831466 [GRCh38]
Chr10:55591226 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3797A>G (p.Asp1266Gly) single nucleotide variant not provided [RCV002511213] Chr10:53857184 [GRCh38]
Chr10:55616944 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5282C>T (p.Ala1761Val) single nucleotide variant Inborn genetic diseases [RCV002901871] Chr10:53822444 [GRCh38]
Chr10:55582204 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3877C>T (p.Arg1293Trp) single nucleotide variant not provided [RCV002751431] Chr10:53840426 [GRCh38]
Chr10:55600186 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.96C>T (p.Cys32=) single nucleotide variant not provided [RCV002816339] Chr10:54527873 [GRCh38]
Chr10:56287633 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3543C>T (p.Tyr1181=) single nucleotide variant not provided [RCV002681721] Chr10:53866816 [GRCh38]
Chr10:55626576 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4341C>A (p.Leu1447=) single nucleotide variant not provided [RCV003015113] Chr10:53827419 [GRCh38]
Chr10:55587179 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1781G>T (p.Arg594Leu) single nucleotide variant not provided [RCV002776384] Chr10:54153103 [GRCh38]
Chr10:55912863 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4367+18G>C single nucleotide variant not provided [RCV002681465] Chr10:53827375 [GRCh38]
Chr10:55587135 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3168T>C (p.Gly1056=) single nucleotide variant not provided [RCV002815548] Chr10:53940930 [GRCh38]
Chr10:55700690 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1950T>C (p.Tyr650=) single nucleotide variant not provided [RCV002685457] Chr10:54090031 [GRCh38]
Chr10:55849791 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4368-2A>G single nucleotide variant not provided [RCV002880669] Chr10:53823360 [GRCh38]
Chr10:55583120 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.594+12C>T single nucleotide variant not provided [RCV002615107] Chr10:54346353 [GRCh38]
Chr10:56106113 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1722A>C (p.Ile574=) single nucleotide variant not provided [RCV002880877] Chr10:54153162 [GRCh38]
Chr10:55912922 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5630G>A (p.Arg1877Lys) single nucleotide variant not provided [RCV002816075] Chr10:53822096 [GRCh38]
Chr10:55581856 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.71G>A (p.Cys24Tyr) single nucleotide variant not provided [RCV002511221] Chr10:54664192 [GRCh38]
Chr10:56423952 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5304T>G (p.Pro1768=) single nucleotide variant not provided [RCV002685467] Chr10:53822422 [GRCh38]
Chr10:55582182 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3162G>A (p.Met1054Ile) single nucleotide variant not provided [RCV002838972] Chr10:53940936 [GRCh38]
Chr10:55700696 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1892T>C (p.Val631Ala) single nucleotide variant not provided [RCV002726447] Chr10:54132900 [GRCh38]
Chr10:55892660 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.459T>C (p.Tyr153=) single nucleotide variant not provided [RCV002995570] Chr10:54369135 [GRCh38]
Chr10:56128895 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5341C>T (p.Pro1781Ser) single nucleotide variant not provided [RCV002617870] Chr10:53822385 [GRCh38]
Chr10:55582145 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4408_4470dup (p.Ile1490_Glu1491insAsnSerValSerGluAspArgLysHisGlnGlnValValMetProPheSerSerAsnThrIle) duplication not provided [RCV002750688] Chr10:53823255..53823256 [GRCh38]
Chr10:55583015..55583016 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4791G>A (p.Leu1597=) single nucleotide variant not provided [RCV002613746] Chr10:53822935 [GRCh38]
Chr10:55582695 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3122+7A>T single nucleotide variant not provided [RCV002774926] Chr10:53959725 [GRCh38]
Chr10:55719485 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4915A>G (p.Ile1639Val) single nucleotide variant not provided [RCV003075982] Chr10:53822811 [GRCh38]
Chr10:55582571 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2547A>G (p.Gly849=) single nucleotide variant not provided [RCV003074896] Chr10:54020396 [GRCh38]
Chr10:55780156 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4618T>A (p.Ser1540Thr) single nucleotide variant not provided [RCV002615531] Chr10:53823108 [GRCh38]
Chr10:55582868 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.610T>A (p.Phe204Ile) single nucleotide variant not provided [RCV003074390] Chr10:54329691 [GRCh38]
Chr10:56089451 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.709C>A (p.Arg237Ser) single nucleotide variant not provided [RCV003075878] Chr10:54317438 [GRCh38]
Chr10:56077198 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.111A>C (p.Gly37=) single nucleotide variant not provided [RCV003034756] Chr10:54527858 [GRCh38]
Chr10:56287618 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4462_4470dup (p.Ile1490_Glu1491insAsnThrIle) duplication not provided [RCV003076781] Chr10:53823255..53823256 [GRCh38]
Chr10:55583015..55583016 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2427T>C (p.Val809=) single nucleotide variant not provided [RCV002881290] Chr10:54022991 [GRCh38]
Chr10:55782751 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1789del (p.Ser597fs) deletion not provided [RCV002820057] Chr10:54133003 [GRCh38]
Chr10:55892763 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.729G>A (p.Glu243=) single nucleotide variant not provided [RCV002866080] Chr10:54317418 [GRCh38]
Chr10:56077178 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5257_5280del (p.Ile1753_Pro1760del) deletion not provided [RCV002756523] Chr10:53822446..53822469 [GRCh38]
Chr10:55582206..55582229 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4671+1535A>T single nucleotide variant Inborn genetic diseases [RCV002688400] Chr10:53809021 [GRCh38]
Chr10:55568781 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4663A>C (p.Lys1555Gln) single nucleotide variant Inborn genetic diseases [RCV002907172] Chr10:53823063 [GRCh38]
Chr10:55582823 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3460T>C (p.Ser1154Pro) single nucleotide variant not provided [RCV002843744] Chr10:53903284 [GRCh38]
Chr10:55663044 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4035T>C (p.Tyr1345=) single nucleotide variant not provided [RCV002636109] Chr10:53831482 [GRCh38]
Chr10:55591242 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.706-8_706-7delinsTT indel not provided [RCV002909066] Chr10:54317448..54317449 [GRCh38]
Chr10:56077208..56077209 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2397T>G (p.Arg799=) single nucleotide variant not provided [RCV002819187] Chr10:54023021 [GRCh38]
Chr10:55782781 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5193T>C (p.Phe1731=) single nucleotide variant not provided [RCV002819307] Chr10:53822533 [GRCh38]
Chr10:55582293 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3123-4G>T single nucleotide variant not provided [RCV002862810] Chr10:53940979 [GRCh38]
Chr10:55700739 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5593C>T (p.Leu1865=) single nucleotide variant not provided [RCV002816198] Chr10:53822133 [GRCh38]
Chr10:55581893 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4047A>G (p.Gly1349=) single nucleotide variant not provided [RCV002862936] Chr10:53831470 [GRCh38]
Chr10:55591230 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4630_4631del (p.Gln1544fs) microsatellite not provided [RCV002862942] Chr10:53823095..53823096 [GRCh38]
Chr10:55582855..55582856 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.4323_4328dup (p.Pro1443_Gly1444insProPro) duplication not provided [RCV003073891]|not specified [RCV003155507] Chr10:53827431..53827432 [GRCh38]
Chr10:55587191..55587192 [GRCh37]
Chr10:10q21.1		 likely benign|uncertain significance
NM_001384140.1(PCDH15):c.3359G>A (p.Arg1120Gln) single nucleotide variant not provided [RCV003073913] Chr10:53938829 [GRCh38]
Chr10:55698589 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.162A>G (p.Thr54=) single nucleotide variant not provided [RCV003074502] Chr10:54378938 [GRCh38]
Chr10:56138698 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3938T>C (p.Ile1313Thr) single nucleotide variant not provided [RCV002972212] Chr10:53840365 [GRCh38]
Chr10:55600125 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3857T>C (p.Val1286Ala) single nucleotide variant not provided [RCV002995284] Chr10:53840446 [GRCh38]
Chr10:55600206 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4408_4468dup (p.Ile1490fs) duplication not provided [RCV002727229] Chr10:53823257..53823258 [GRCh38]
Chr10:55583017..55583018 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.1890G>A (p.Arg630=) single nucleotide variant not provided [RCV002858378] Chr10:54132902 [GRCh38]
Chr10:55892662 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3233-7T>C single nucleotide variant not provided [RCV002861940] Chr10:53938962 [GRCh38]
Chr10:55698722 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2668G>A (p.Ala890Thr) single nucleotide variant not provided [RCV003074144] Chr10:54020275 [GRCh38]
Chr10:55780035 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3061A>G (p.Thr1021Ala) single nucleotide variant not provided [RCV003097465] Chr10:53959793 [GRCh38]
Chr10:55719553 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1968T>C (p.Asp656=) single nucleotide variant not provided [RCV002863278] Chr10:54090013 [GRCh38]
Chr10:55849773 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1735T>G (p.Tyr579Asp) single nucleotide variant not provided [RCV002842143] Chr10:54153149 [GRCh38]
Chr10:55912909 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2451T>C (p.Pro817=) single nucleotide variant not provided [RCV003033140] Chr10:54022967 [GRCh38]
Chr10:55782727 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4523A>C (p.Lys1508Thr) single nucleotide variant not provided [RCV002726833] Chr10:53823203 [GRCh38]
Chr10:55582963 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2130C>T (p.Val710=) single nucleotide variant not provided [RCV002816700] Chr10:54066847 [GRCh38]
Chr10:55826607 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.417C>T (p.Asp139=) single nucleotide variant not provided [RCV002838725] Chr10:54369177 [GRCh38]
Chr10:56128937 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.546A>T (p.Gly182=) single nucleotide variant not provided [RCV002837918] Chr10:54346413 [GRCh38]
Chr10:56106173 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.5017T>A (p.Phe1673Ile) single nucleotide variant Inborn genetic diseases [RCV002732302] Chr10:53806785 [GRCh38]
Chr10:55566545 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1010T>C (p.Phe337Ser) single nucleotide variant Inborn genetic diseases [RCV002906609] Chr10:54214024 [GRCh38]
Chr10:55973784 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.706-2A>G single nucleotide variant not provided [RCV002991434] Chr10:54317443 [GRCh38]
Chr10:56077203 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1284T>G (p.Ala428=) single nucleotide variant not provided [RCV002994027] Chr10:54195704 [GRCh38]
Chr10:55955464 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3718-3C>G single nucleotide variant not provided [RCV003074342] Chr10:53857266 [GRCh38]
Chr10:55617026 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4740A>G (p.Leu1580=) single nucleotide variant not provided [RCV002838030] Chr10:53822986 [GRCh38]
Chr10:55582746 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.555A>G (p.Gly185=) single nucleotide variant not provided [RCV003015010] Chr10:54346404 [GRCh38]
Chr10:56106164 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.626T>C (p.Met209Thr) single nucleotide variant Inborn genetic diseases [RCV003250728]|not provided [RCV003074319] Chr10:54329675 [GRCh38]
Chr10:56089435 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5481C>A (p.Cys1827Ter) single nucleotide variant not provided [RCV002861765] Chr10:53822245 [GRCh38]
Chr10:55582005 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4372_4390dup (p.Gln1464fs) duplication not provided [RCV002991662] Chr10:53823335..53823336 [GRCh38]
Chr10:55583095..55583096 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2273A>T (p.Asn758Ile) single nucleotide variant not provided [RCV003073964] Chr10:54023145 [GRCh38]
Chr10:55782905 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3717+15del deletion not provided [RCV002816459] Chr10:53866627 [GRCh38]
Chr10:55626387 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3029A>T (p.Asp1010Val) single nucleotide variant not provided [RCV002816480] Chr10:53959825 [GRCh38]
Chr10:55719585 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2648A>C (p.Glu883Ala) single nucleotide variant not provided [RCV002686263] Chr10:54020295 [GRCh38]
Chr10:55780055 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4536dup (p.Phe1513fs) duplication not provided [RCV002881925] Chr10:53823189..53823190 [GRCh38]
Chr10:55582949..55582950 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.5138C>G (p.Ser1713Cys) single nucleotide variant not provided [RCV002755275] Chr10:53822588 [GRCh38]
Chr10:55582348 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.732G>A (p.Arg244=) single nucleotide variant not provided [RCV003034360] Chr10:54317415 [GRCh38]
Chr10:56077175 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1710G>T (p.Gly570=) single nucleotide variant not provided [RCV002819766] Chr10:54153174 [GRCh38]
Chr10:55912934 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2187A>G (p.Glu729=) single nucleotide variant not provided [RCV003034742] Chr10:54066790 [GRCh38]
Chr10:55826550 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3753dup (p.Val1252fs) duplication not provided [RCV003017518] Chr10:53857227..53857228 [GRCh38]
Chr10:55616987..55616988 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.877-17C>G single nucleotide variant not provided [RCV002615802] Chr10:54236948 [GRCh38]
Chr10:55996708 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4551T>G (p.Ser1517=) single nucleotide variant not provided [RCV002862715] Chr10:53823175 [GRCh38]
Chr10:55582935 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3730A>G (p.Asn1244Asp) single nucleotide variant not provided [RCV003074539] Chr10:53857251 [GRCh38]
Chr10:55617011 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1917+13G>A single nucleotide variant not provided [RCV002838152] Chr10:54132862 [GRCh38]
Chr10:55892622 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2421C>A (p.Ile807=) single nucleotide variant not provided [RCV002970698] Chr10:54022997 [GRCh38]
Chr10:55782757 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3603A>G (p.Thr1201=) single nucleotide variant not provided [RCV002842910] Chr10:53866756 [GRCh38]
Chr10:55626516 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5702_5705del (p.Ser1901fs) deletion not provided [RCV002618148] Chr10:53822021..53822024 [GRCh38]
Chr10:55581781..55581784 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4550C>T (p.Ser1517Phe) single nucleotide variant not provided [RCV002756437] Chr10:53823176 [GRCh38]
Chr10:55582936 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3102C>T (p.Arg1034=) single nucleotide variant not provided [RCV002908866] Chr10:53959752 [GRCh38]
Chr10:55719512 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2058G>C (p.Leu686=) single nucleotide variant not provided [RCV002862051] Chr10:54079364 [GRCh38]
Chr10:55839124 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2786_2787delinsAG (p.Arg929Gln) indel not provided [RCV002842936] Chr10:53995730..53995731 [GRCh38]
Chr10:55755490..55755491 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5351C>A (p.Pro1784His) single nucleotide variant not provided [RCV003075973] Chr10:53822375 [GRCh38]
Chr10:55582135 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.6T>C (p.Phe2=) single nucleotide variant not provided [RCV002819284] Chr10:54664257 [GRCh38]
Chr10:56424017 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1800T>A (p.Thr600=) single nucleotide variant not provided [RCV002881794] Chr10:54132992 [GRCh38]
Chr10:55892752 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1099-19C>T single nucleotide variant not provided [RCV002731429] Chr10:54195908 [GRCh38]
Chr10:55955668 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4671+1688G>C single nucleotide variant Inborn genetic diseases [RCV002794040] Chr10:53808868 [GRCh38]
Chr10:55568628 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4504C>T (p.Leu1502Phe) single nucleotide variant not provided [RCV003076672] Chr10:53823222 [GRCh38]
Chr10:55582982 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4854_4857dup (p.Gly1620fs) duplication not provided [RCV002705446] Chr10:53822868..53822869 [GRCh38]
Chr10:55582628..55582629 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.91+5G>A single nucleotide variant not provided [RCV002640357] Chr10:54664167 [GRCh38]
Chr10:56423927 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4736G>A (p.Ser1579Asn) single nucleotide variant Inborn genetic diseases [RCV004071760]|not provided [RCV003081492] Chr10:53822990 [GRCh38]
Chr10:55582750 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.866T>C (p.Leu289Ser) single nucleotide variant not provided [RCV003039617] Chr10:54317281 [GRCh38]
Chr10:56077041 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4307C>G (p.Pro1436Arg) single nucleotide variant not provided [RCV002740514] Chr10:53827453 [GRCh38]
Chr10:55587213 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3342G>A (p.Val1114=) single nucleotide variant not provided [RCV002889213] Chr10:53938846 [GRCh38]
Chr10:55698606 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4163G>A (p.Cys1388Tyr) single nucleotide variant not provided [RCV003038335] Chr10:53831354 [GRCh38]
Chr10:55591114 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4467T>C (p.Thr1489=) single nucleotide variant not provided [RCV003077616] Chr10:53823259 [GRCh38]
Chr10:55583019 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5201T>C (p.Phe1734Ser) single nucleotide variant not provided [RCV003022080] Chr10:53822525 [GRCh38]
Chr10:55582285 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.446A>C (p.His149Pro) single nucleotide variant not provided [RCV002780671] Chr10:54369148 [GRCh38]
Chr10:56128908 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1281A>C (p.Val427=) single nucleotide variant not provided [RCV002740139] Chr10:54195707 [GRCh38]
Chr10:55955467 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3756T>C (p.Val1252=) single nucleotide variant not provided [RCV002825361] Chr10:53857225 [GRCh38]
Chr10:55616985 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2064C>A (p.Ile688=) single nucleotide variant not provided [RCV002889510] Chr10:54079358 [GRCh38]
Chr10:55839118 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3875G>C (p.Arg1292Pro) single nucleotide variant not provided [RCV003078949] Chr10:53840428 [GRCh38]
Chr10:55600188 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4085G>C (p.Ser1362Thr) single nucleotide variant not provided [RCV002695783] Chr10:53831432 [GRCh38]
Chr10:55591192 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4032T>C (p.Tyr1344=) single nucleotide variant not provided [RCV002695784] Chr10:53831485 [GRCh38]
Chr10:55591245 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4934T>G (p.Leu1645Arg) single nucleotide variant Inborn genetic diseases [RCV002762879] Chr10:53822792 [GRCh38]
Chr10:55582552 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3122+11C>A single nucleotide variant not provided [RCV002927675] Chr10:53959721 [GRCh38]
Chr10:55719481 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5533G>C (p.Gly1845Arg) single nucleotide variant not provided [RCV003021669] Chr10:53822193 [GRCh38]
Chr10:55581953 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.396A>G (p.Glu132=) single nucleotide variant not provided [RCV003002212] Chr10:54369198 [GRCh38]
Chr10:56128958 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1420C>G (p.Gln474Glu) single nucleotide variant not provided [RCV003020074] Chr10:54185154 [GRCh38]
Chr10:55944914 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.986-8T>C single nucleotide variant not provided [RCV002571851] Chr10:54214056 [GRCh38]
Chr10:55973816 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3418C>T (p.His1140Tyr) single nucleotide variant not provided [RCV003081649] Chr10:53903326 [GRCh38]
Chr10:55663086 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1194del (p.Ser399fs) deletion not provided [RCV002867583] Chr10:54195794 [GRCh38]
Chr10:55955554 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.10C>T (p.Gln4Ter) single nucleotide variant not provided [RCV003037674] Chr10:54664253 [GRCh38]
Chr10:56424013 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3123-4G>A single nucleotide variant not provided [RCV002824181] Chr10:53940979 [GRCh38]
Chr10:55700739 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5835A>G (p.Glu1945=) single nucleotide variant not provided [RCV002949680] Chr10:53821891 [GRCh38]
Chr10:55581651 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1744dup (p.Thr582fs) duplication not provided [RCV003035769] Chr10:54153139..54153140 [GRCh38]
Chr10:55912899..55912900 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.4028C>T (p.Pro1343Leu) single nucleotide variant Inborn genetic diseases [RCV002911865] Chr10:53831489 [GRCh38]
Chr10:55591249 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5699dup (p.Tyr1900Ter) duplication not provided [RCV002866451] Chr10:53822026..53822027 [GRCh38]
Chr10:55581786..55581787 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.268G>A (p.Val90Ile) single nucleotide variant not provided [RCV003100630] Chr10:54378832 [GRCh38]
Chr10:56138592 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.594+9A>G single nucleotide variant not provided [RCV002823751] Chr10:54346356 [GRCh38]
Chr10:56106116 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2526+9dup duplication not provided [RCV002638921] Chr10:54022882..54022883 [GRCh38]
Chr10:55782642..55782643 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.157+12T>G single nucleotide variant not provided [RCV003018330] Chr10:54527800 [GRCh38]
Chr10:56287560 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3486T>G (p.Ser1162=) single nucleotide variant not provided [RCV002569952] Chr10:53903258 [GRCh38]
Chr10:55663018 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1290C>T (p.Asp430=) single nucleotide variant not provided [RCV002735144] Chr10:54195698 [GRCh38]
Chr10:55955458 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.318+1G>A single nucleotide variant not provided [RCV002886585] Chr10:54378781 [GRCh38]
Chr10:56138541 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4671+1104C>A single nucleotide variant Inborn genetic diseases [RCV002911940] Chr10:53809452 [GRCh38]
Chr10:55569212 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5292T>A (p.Pro1764=) single nucleotide variant not provided [RCV002823767] Chr10:53822434 [GRCh38]
Chr10:55582194 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3879G>T (p.Arg1293=) single nucleotide variant not provided [RCV002658881] Chr10:53840424 [GRCh38]
Chr10:55600184 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1997+17T>C single nucleotide variant not provided [RCV002820765] Chr10:54089967 [GRCh38]
Chr10:55849727 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5716A>G (p.Asn1906Asp) single nucleotide variant Inborn genetic diseases [RCV003250821]|not provided [RCV002638209] Chr10:53822010 [GRCh38]
Chr10:55581770 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1471G>A (p.Glu491Lys) single nucleotide variant not provided [RCV002694777] Chr10:54183563 [GRCh38]
Chr10:55943323 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1626G>A (p.Gly542=) single nucleotide variant not provided [RCV002979182] Chr10:54153258 [GRCh38]
Chr10:55913018 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3375C>T (p.Ser1125=) single nucleotide variant not provided [RCV002780541] Chr10:53903369 [GRCh38]
Chr10:55663129 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4211+1G>T single nucleotide variant not provided [RCV002885540] Chr10:53828564 [GRCh38]
Chr10:55588324 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3717+15C>T single nucleotide variant not provided [RCV002736212] Chr10:53866627 [GRCh38]
Chr10:55626387 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1189A>G (p.Met397Val) single nucleotide variant Inborn genetic diseases [RCV002910688] Chr10:54195799 [GRCh38]
Chr10:55955559 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.389A>G (p.Tyr130Cys) single nucleotide variant not provided [RCV003019359] Chr10:54369205 [GRCh38]
Chr10:56128965 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.291C>T (p.Asn97=) single nucleotide variant not provided [RCV002621090] Chr10:54378809 [GRCh38]
Chr10:56138569 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3909C>T (p.Tyr1303=) single nucleotide variant not provided [RCV002736341] Chr10:53840394 [GRCh38]
Chr10:55600154 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3983+9T>G single nucleotide variant not provided [RCV002909170] Chr10:53840311 [GRCh38]
Chr10:55600071 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3544del (p.Arg1182fs) deletion not provided [RCV002867525] Chr10:53866815 [GRCh38]
Chr10:55626575 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.576G>A (p.Gln192=) single nucleotide variant not provided [RCV003035714] Chr10:54346383 [GRCh38]
Chr10:56106143 [GRCh37]
Chr10:10q21.1		 likely benign
NC_000010.10:g.(?_55580859)_(55591294_55600079)del deletion Usher syndrome type 1F [RCV002510465] Chr10:55580859..55591294 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.468G>T (p.Val156=) single nucleotide variant not provided [RCV003018603] Chr10:54369126 [GRCh38]
Chr10:56128886 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3738G>C (p.Leu1246=) single nucleotide variant not provided [RCV003036401] Chr10:53857243 [GRCh38]
Chr10:55617003 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3636T>C (p.Asn1212=) single nucleotide variant not provided [RCV002695043] Chr10:53866723 [GRCh38]
Chr10:55626483 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1859T>A (p.Met620Lys) single nucleotide variant not provided [RCV002619084] Chr10:54132933 [GRCh38]
Chr10:55892693 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3576A>G (p.Lys1192=) single nucleotide variant not provided [RCV002948481] Chr10:53866783 [GRCh38]
Chr10:55626543 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2328G>A (p.Lys776=) single nucleotide variant not provided [RCV003035786] Chr10:54023090 [GRCh38]
Chr10:55782850 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2511C>T (p.Thr837=) single nucleotide variant not provided [RCV002868057] Chr10:54022907 [GRCh38]
Chr10:55782667 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.453C>T (p.Ser151=) single nucleotide variant not provided [RCV003054843] Chr10:54369141 [GRCh38]
Chr10:56128901 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1001dup (p.Tyr334Ter) duplication not provided [RCV002867584] Chr10:54214032..54214033 [GRCh38]
Chr10:55973792..55973793 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.5554T>C (p.Leu1852=) single nucleotide variant not provided [RCV003078679] Chr10:53822172 [GRCh38]
Chr10:55581932 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4153A>G (p.Ile1385Val) single nucleotide variant not provided [RCV002571647] Chr10:53831364 [GRCh38]
Chr10:55591124 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1884C>A (p.Ala628=) single nucleotide variant not provided [RCV002867849] Chr10:54132908 [GRCh38]
Chr10:55892668 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1704T>C (p.Ala568=) single nucleotide variant not provided [RCV002848216] Chr10:54153180 [GRCh38]
Chr10:55912940 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2413T>G (p.Leu805Val) single nucleotide variant not provided [RCV002592735] Chr10:54023005 [GRCh38]
Chr10:55782765 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3600T>C (p.Tyr1200=) single nucleotide variant not provided [RCV002590738] Chr10:53866759 [GRCh38]
Chr10:55626519 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1764T>C (p.Asn588=) single nucleotide variant not provided [RCV002847182] Chr10:54153120 [GRCh38]
Chr10:55912880 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3135A>G (p.Val1045=) single nucleotide variant not provided [RCV003054503] Chr10:53940963 [GRCh38]
Chr10:55700723 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5452C>T (p.Leu1818Phe) single nucleotide variant not provided [RCV002820396] Chr10:53822274 [GRCh38]
Chr10:55582034 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5291C>T (p.Pro1764Leu) single nucleotide variant not provided [RCV002636529] Chr10:53822435 [GRCh38]
Chr10:55582195 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5558T>C (p.Met1853Thr) single nucleotide variant not provided [RCV002695291] Chr10:53822168 [GRCh38]
Chr10:55581928 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3232+8G>A single nucleotide variant not provided [RCV003038942] Chr10:53940858 [GRCh38]
Chr10:55700618 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5259_5271dup (p.Pro1758fs) duplication not provided [RCV003036537] Chr10:53822454..53822455 [GRCh38]
Chr10:55582214..55582215 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2007T>C (p.Ile669=) single nucleotide variant not provided [RCV002736646] Chr10:54079415 [GRCh38]
Chr10:55839175 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.985_985+3del deletion not provided [RCV003054923] Chr10:54236820..54236823 [GRCh38]
Chr10:55996580..55996583 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.5049C>T (p.Leu1683=) single nucleotide variant not provided [RCV003038610] Chr10:53822677 [GRCh38]
Chr10:55582437 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5821G>A (p.Val1941Ile) single nucleotide variant not provided [RCV002781261] Chr10:53821905 [GRCh38]
Chr10:55581665 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4211+5G>T single nucleotide variant not provided [RCV002999847] Chr10:53828560 [GRCh38]
Chr10:55588320 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5446A>C (p.Thr1816Pro) single nucleotide variant not provided [RCV002780647] Chr10:53822280 [GRCh38]
Chr10:55582040 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4498G>A (p.Gly1500Arg) single nucleotide variant not provided [RCV003053231] Chr10:53823228 [GRCh38]
Chr10:55582988 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2526+17A>G single nucleotide variant not provided [RCV002781022] Chr10:54022875 [GRCh38]
Chr10:55782635 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1623T>C (p.Asn541=) single nucleotide variant not provided [RCV002620065] Chr10:54153261 [GRCh38]
Chr10:55913021 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4667T>C (p.Ile1556Thr) single nucleotide variant not provided [RCV002761395] Chr10:53823059 [GRCh38]
Chr10:55582819 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.804T>A (p.Cys268Ter) single nucleotide variant not provided [RCV002824461] Chr10:54317343 [GRCh38]
Chr10:56077103 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.4592G>A (p.Arg1531His) single nucleotide variant Inborn genetic diseases [RCV002781967] Chr10:53810635 [GRCh38]
Chr10:55570395 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4147ATC[2] (p.Ile1385del) microsatellite not provided [RCV002796069] Chr10:53831362..53831364 [GRCh38]
Chr10:55591122..55591124 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3471A>G (p.Ala1157=) single nucleotide variant not provided [RCV003018727] Chr10:53903273 [GRCh38]
Chr10:55663033 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4662C>G (p.Pro1554=) single nucleotide variant not provided [RCV002824318] Chr10:53823064 [GRCh38]
Chr10:55582824 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5636C>A (p.Pro1879Gln) single nucleotide variant not provided [RCV002780540] Chr10:53822090 [GRCh38]
Chr10:55581850 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4782C>T (p.Ile1594=) single nucleotide variant not provided [RCV002796583] Chr10:53822944 [GRCh38]
Chr10:55582704 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5411G>T (p.Gly1804Val) single nucleotide variant not provided [RCV002886229] Chr10:53822315 [GRCh38]
Chr10:55582075 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1047C>G (p.Leu349=) single nucleotide variant not provided [RCV002847883] Chr10:54213987 [GRCh38]
Chr10:55973747 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2092-482_2092del deletion not provided [RCV002870702] Chr10:54066885..54067367 [GRCh38]
Chr10:55826645..55827127 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1656T>A (p.Ala552=) single nucleotide variant not provided [RCV002820728] Chr10:54153228 [GRCh38]
Chr10:55912988 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1406T>C (p.Val469Ala) single nucleotide variant not provided [RCV002638554] Chr10:54185168 [GRCh38]
Chr10:55944928 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1441-9C>T single nucleotide variant not provided [RCV002976416] Chr10:54183602 [GRCh38]
Chr10:55943362 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4079T>C (p.Val1360Ala) single nucleotide variant not provided [RCV003078800] Chr10:53831438 [GRCh38]
Chr10:55591198 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4290A>G (p.Ala1430=) single nucleotide variant not provided [RCV002846859] Chr10:53827470 [GRCh38]
Chr10:55587230 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4367+6T>C single nucleotide variant not provided [RCV003038284] Chr10:53827387 [GRCh38]
Chr10:55587147 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5854T>C (p.Ser1952Pro) single nucleotide variant not provided [RCV003078550] Chr10:53821872 [GRCh38]
Chr10:55581632 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1099-15T>C single nucleotide variant not provided [RCV002795238] Chr10:54195904 [GRCh38]
Chr10:55955664 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2088T>C (p.Asp696=) single nucleotide variant not provided [RCV003005197] Chr10:54079334 [GRCh38]
Chr10:55839094 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2031C>T (p.Asp677=) single nucleotide variant not provided [RCV003007517] Chr10:54079391 [GRCh38]
Chr10:55839151 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5206C>T (p.His1736Tyr) single nucleotide variant Inborn genetic diseases [RCV003059109]|not provided [RCV003059110] Chr10:53822520 [GRCh38]
Chr10:55582280 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2687dup (p.Glu897fs) duplication not provided [RCV003026060] Chr10:54020255..54020256 [GRCh38]
Chr10:55780015..55780016 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.1571C>G (p.Pro524Arg) single nucleotide variant Inborn genetic diseases [RCV003358091]|not provided [RCV003084707] Chr10:54183463 [GRCh38]
Chr10:55943223 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2741T>C (p.Val914Ala) single nucleotide variant not provided [RCV002666956] Chr10:54020202 [GRCh38]
Chr10:55779962 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4489_4508dup (p.Lys1503delinsAsnMetTer) duplication not provided [RCV002791555] Chr10:53823217..53823218 [GRCh38]
Chr10:55582977..55582978 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.4211+9_4211+11dup duplication not provided [RCV002663452] Chr10:53828553..53828554 [GRCh38]
Chr10:55588313..55588314 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4588C>T (p.Arg1530Cys) single nucleotide variant Inborn genetic diseases [RCV003003842] Chr10:53810639 [GRCh38]
Chr10:55570399 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2291G>A (p.Arg764His) single nucleotide variant Inborn genetic diseases [RCV003083174]|not provided [RCV003071628] Chr10:54023127 [GRCh38]
Chr10:55782887 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4415del (p.Val1472fs) deletion not provided [RCV002830107] Chr10:53823311 [GRCh38]
Chr10:55583071 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.1099-5T>G single nucleotide variant not provided [RCV003059758] Chr10:54195894 [GRCh38]
Chr10:55955654 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1541A>G (p.Tyr514Cys) single nucleotide variant not provided [RCV003058719] Chr10:54183493 [GRCh38]
Chr10:55943253 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4830A>G (p.Glu1610=) single nucleotide variant not provided [RCV002851573] Chr10:53822896 [GRCh38]
Chr10:55582656 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2943G>A (p.Val981=) single nucleotide variant not provided [RCV002805457] Chr10:53961818 [GRCh38]
Chr10:55721578 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4733_4736del (p.Val1578fs) microsatellite not provided [RCV002766324] Chr10:53822990..53822993 [GRCh38]
Chr10:55582750..55582753 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3761dup (p.Asn1254fs) duplication Usher syndrome type 1F [RCV002789950]|not provided [RCV003720761] Chr10:53857219..53857220 [GRCh38]
Chr10:55616979..55616980 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.1461A>G (p.Val487=) single nucleotide variant not provided [RCV002667772] Chr10:54183573 [GRCh38]
Chr10:55943333 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4552G>T (p.Asp1518Tyr) single nucleotide variant not provided [RCV002954348] Chr10:53823174 [GRCh38]
Chr10:55582934 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1068C>T (p.Asp356=) single nucleotide variant not provided [RCV003007312] Chr10:54213966 [GRCh38]
Chr10:55973726 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3099A>G (p.Pro1033=) single nucleotide variant not provided [RCV003043597] Chr10:53959755 [GRCh38]
Chr10:55719515 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.657G>A (p.Arg219=) single nucleotide variant not provided [RCV003043695] Chr10:54329644 [GRCh38]
Chr10:56089404 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4812G>A (p.Arg1604=) single nucleotide variant not provided [RCV002853262] Chr10:53822914 [GRCh38]
Chr10:55582674 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5649C>T (p.Leu1883=) single nucleotide variant not provided [RCV002765885] Chr10:53822077 [GRCh38]
Chr10:55581837 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1369A>G (p.Thr457Ala) single nucleotide variant Inborn genetic diseases [RCV002915987] Chr10:54185205 [GRCh38]
Chr10:55944965 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.158-4G>T single nucleotide variant not provided [RCV002853329] Chr10:54378946 [GRCh38]
Chr10:56138706 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5764del (p.Glu1922fs) deletion not provided [RCV002933125] Chr10:53821962 [GRCh38]
Chr10:55581722 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.522T>C (p.Asn174=) single nucleotide variant not provided [RCV003040736] Chr10:54346437 [GRCh38]
Chr10:56106197 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.810T>C (p.Leu270=) single nucleotide variant not provided [RCV003039780] Chr10:54317337 [GRCh38]
Chr10:56077097 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2526+10A>G single nucleotide variant not provided [RCV002876515] Chr10:54022882 [GRCh38]
Chr10:55782642 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4074G>A (p.Glu1358=) single nucleotide variant not provided [RCV002932635] Chr10:53831443 [GRCh38]
Chr10:55591203 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2913G>A (p.Gln971=) single nucleotide variant not provided [RCV002805604] Chr10:53961848 [GRCh38]
Chr10:55721608 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5714A>G (p.Lys1905Arg) single nucleotide variant not provided [RCV002623429] Chr10:53822012 [GRCh38]
Chr10:55581772 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.181C>T (p.Leu61=) single nucleotide variant not provided [RCV003022733] Chr10:54378919 [GRCh38]
Chr10:56138679 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5282_5308del (p.Ala1761_Pro1769del) deletion not provided [RCV002954019] Chr10:53822418..53822444 [GRCh38]
Chr10:55582178..55582204 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1103A>G (p.Glu368Gly) single nucleotide variant not provided [RCV003022507] Chr10:54195885 [GRCh38]
Chr10:55955645 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.382A>G (p.Ile128Val) single nucleotide variant not provided [RCV002575021] Chr10:54369212 [GRCh38]
Chr10:56128972 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2595dup (p.Ala866fs) duplication not provided [RCV002928418] Chr10:54020347..54020348 [GRCh38]
Chr10:55780107..55780108 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.4037G>C (p.Gly1346Ala) single nucleotide variant not provided [RCV002825772] Chr10:53831480 [GRCh38]
Chr10:55591240 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5006T>A (p.Phe1669Tyr) single nucleotide variant Inborn genetic diseases [RCV002850090] Chr10:53822720 [GRCh38]
Chr10:55582480 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1895G>C (p.Gly632Ala) single nucleotide variant not provided [RCV003056057] Chr10:54132897 [GRCh38]
Chr10:55892657 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5075C>T (p.Ser1692Phe) single nucleotide variant not provided [RCV002663961] Chr10:53822651 [GRCh38]
Chr10:55582411 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.877-11T>C single nucleotide variant not provided [RCV003083153] Chr10:54236942 [GRCh38]
Chr10:55996702 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5326_5327del (p.Leu1776fs) microsatellite not provided [RCV003006491] Chr10:53822399..53822400 [GRCh38]
Chr10:55582159..55582160 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.75G>C (p.Leu25Phe) single nucleotide variant not provided [RCV002623756] Chr10:54664188 [GRCh38]
Chr10:56423948 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5094_5137dup (p.Ser1713fs) duplication not provided [RCV003022857] Chr10:53822588..53822589 [GRCh38]
Chr10:55582348..55582349 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4703A>G (p.Glu1568Gly) single nucleotide variant not provided [RCV002741457] Chr10:53823023 [GRCh38]
Chr10:55582783 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.29G>A (p.Cys10Tyr) single nucleotide variant not provided [RCV002664363] Chr10:54664234 [GRCh38]
Chr10:56423994 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4188G>A (p.Leu1396=) single nucleotide variant not provided [RCV002852707] Chr10:53831329 [GRCh38]
Chr10:55591089 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1999A>G (p.Thr667Ala) single nucleotide variant not provided [RCV002625304] Chr10:54079423 [GRCh38]
Chr10:55839183 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.595A>G (p.Thr199Ala) single nucleotide variant not provided [RCV002625660] Chr10:54329706 [GRCh38]
Chr10:56089466 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3232+1G>A single nucleotide variant Usher syndrome type 1F [RCV002789951]|not provided [RCV003720762] Chr10:53940865 [GRCh38]
Chr10:55700625 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.985G>A (p.Gly329Arg) single nucleotide variant Usher syndrome type 1F [RCV002789955] Chr10:54236823 [GRCh38]
Chr10:55996583 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.440T>G (p.Phe147Cys) single nucleotide variant Usher syndrome type 1F [RCV002789956] Chr10:54369154 [GRCh38]
Chr10:56128914 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.865T>C (p.Leu289=) single nucleotide variant not provided [RCV002572702] Chr10:54317282 [GRCh38]
Chr10:56077042 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1098+13A>T single nucleotide variant not provided [RCV003083218] Chr10:54213923 [GRCh38]
Chr10:55973683 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4043G>C (p.Gly1348Ala) single nucleotide variant Inborn genetic diseases [RCV002893364] Chr10:53831474 [GRCh38]
Chr10:55591234 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1499T>A (p.Met500Lys) single nucleotide variant not provided [RCV002917920] Chr10:54183535 [GRCh38]
Chr10:55943295 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2868+2T>A single nucleotide variant not provided [RCV003039976] Chr10:53995647 [GRCh38]
Chr10:55755407 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.39A>T (p.Ser13=) single nucleotide variant not provided [RCV002871677] Chr10:54664224 [GRCh38]
Chr10:56423984 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5505T>G (p.Phe1835Leu) single nucleotide variant Inborn genetic diseases [RCV002954545] Chr10:53822221 [GRCh38]
Chr10:55581981 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3852C>G (p.Val1284=) single nucleotide variant not provided [RCV002663283] Chr10:53840451 [GRCh38]
Chr10:55600211 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1468A>G (p.Ser490Gly) single nucleotide variant Inborn genetic diseases [RCV002873065] Chr10:54183566 [GRCh38]
Chr10:55943326 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2927C>A (p.Ala976Asp) single nucleotide variant not provided [RCV002805535] Chr10:53961834 [GRCh38]
Chr10:55721594 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5715_5718del (p.Lys1905fs) deletion not provided [RCV003023317] Chr10:53822008..53822011 [GRCh38]
Chr10:55581768..55581771 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2060T>C (p.Ile687Thr) single nucleotide variant Inborn genetic diseases [RCV002763183] Chr10:54079362 [GRCh38]
Chr10:55839122 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5849G>C (p.Ser1950Thr) single nucleotide variant not provided [RCV003022566] Chr10:53821877 [GRCh38]
Chr10:55581637 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3694C>T (p.Leu1232=) single nucleotide variant not provided [RCV002876303] Chr10:53866665 [GRCh38]
Chr10:55626425 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.859C>T (p.Pro287Ser) single nucleotide variant not provided [RCV002667879] Chr10:54317288 [GRCh38]
Chr10:56077048 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3601A>T (p.Thr1201Ser) single nucleotide variant not provided [RCV002890643] Chr10:53866758 [GRCh38]
Chr10:55626518 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.318+17del deletion not provided [RCV002828288] Chr10:54378765 [GRCh38]
Chr10:56138525 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5207_5249dup (p.Pro1751fs) duplication not provided [RCV002853096] Chr10:53822476..53822477 [GRCh38]
Chr10:55582236..55582237 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5843C>G (p.Ser1948Cys) single nucleotide variant not provided [RCV003022626] Chr10:53821883 [GRCh38]
Chr10:55581643 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4310C>T (p.Pro1437Leu) single nucleotide variant Usher syndrome type 1F [RCV002789948] Chr10:53827450 [GRCh38]
Chr10:55587210 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2754dup (p.Met919fs) duplication Usher syndrome type 1F [RCV002789952] Chr10:53995762..53995763 [GRCh38]
Chr10:55755522..55755523 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.428A>G (p.Asn143Ser) single nucleotide variant not provided [RCV003042348] Chr10:54369166 [GRCh38]
Chr10:56128926 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1306-2A>G single nucleotide variant not provided [RCV002766917] Chr10:54185270 [GRCh38]
Chr10:55945030 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.2232T>C (p.Pro744=) single nucleotide variant not provided [RCV003042649] Chr10:54023186 [GRCh38]
Chr10:55782946 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5245CCT[5] (p.Pro1752_Ile1753insPro) microsatellite not provided [RCV002627137] Chr10:53822469..53822470 [GRCh38]
Chr10:55582229..55582230 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2723G>C (p.Gly908Ala) single nucleotide variant not provided [RCV003083575] Chr10:54020220 [GRCh38]
Chr10:55779980 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3196A>C (p.Ser1066Arg) single nucleotide variant not provided [RCV002829077] Chr10:53940902 [GRCh38]
Chr10:55700662 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2918C>T (p.Pro973Leu) single nucleotide variant Inborn genetic diseases [RCV003060380]|not provided [RCV003058575] Chr10:53961843 [GRCh38]
Chr10:55721603 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3502-10C>A single nucleotide variant not provided [RCV003042958] Chr10:53866867 [GRCh38]
Chr10:55626627 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2025A>T (p.Ala675=) single nucleotide variant not provided [RCV002791267] Chr10:54079397 [GRCh38]
Chr10:55839157 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4293A>C (p.Pro1431=) single nucleotide variant not provided [RCV002663725] Chr10:53827467 [GRCh38]
Chr10:55587227 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4302G>T (p.Ala1434=) single nucleotide variant not provided [RCV003023666] Chr10:53827458 [GRCh38]
Chr10:55587218 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.192G>A (p.Gly64=) single nucleotide variant not provided [RCV002852373] Chr10:54378908 [GRCh38]
Chr10:56138668 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3685G>A (p.Gly1229Arg) single nucleotide variant Inborn genetic diseases [RCV002803750] Chr10:53866674 [GRCh38]
Chr10:55626434 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4907_4910dup (p.Glu1638fs) duplication not provided [RCV002745601] Chr10:53822815..53822816 [GRCh38]
Chr10:55582575..55582576 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.416A>T (p.Asp139Val) single nucleotide variant not provided [RCV002828404] Chr10:54369178 [GRCh38]
Chr10:56128938 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.951A>C (p.Ser317=) single nucleotide variant not provided [RCV002894206] Chr10:54236857 [GRCh38]
Chr10:55996617 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.274C>G (p.Gln92Glu) single nucleotide variant Inborn genetic diseases [RCV002645116] Chr10:54378826 [GRCh38]
Chr10:56138586 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3814G>T (p.Asp1272Tyr) single nucleotide variant not provided [RCV002825773] Chr10:53840489 [GRCh38]
Chr10:55600249 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1997+12del deletion not provided [RCV002624935] Chr10:54089972 [GRCh38]
Chr10:55849732 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1625G>C (p.Gly542Ala) single nucleotide variant not provided [RCV002765566] Chr10:54153259 [GRCh38]
Chr10:55913019 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3806+7G>A single nucleotide variant not provided [RCV003040903] Chr10:53857168 [GRCh38]
Chr10:55616928 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.809T>C (p.Leu270Pro) single nucleotide variant not provided [RCV002765655] Chr10:54317338 [GRCh38]
Chr10:56077098 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4536A>G (p.Lys1512=) single nucleotide variant not provided [RCV002872375] Chr10:53823190 [GRCh38]
Chr10:55582950 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.734G>T (p.Arg245Leu) single nucleotide variant not provided [RCV002594168] Chr10:54317413 [GRCh38]
Chr10:56077173 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4672-1672C>T single nucleotide variant not provided [RCV003056607] Chr10:53808802 [GRCh38]
Chr10:55568562 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2477dup (p.Leu827fs) duplication not provided [RCV002894451] Chr10:54022940..54022941 [GRCh38]
Chr10:55782700..55782701 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.5710G>C (p.Glu1904Gln) single nucleotide variant not provided [RCV002917800] Chr10:53822016 [GRCh38]
Chr10:55581776 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1998-13G>C single nucleotide variant not provided [RCV003085279] Chr10:54079437 [GRCh38]
Chr10:55839197 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5323T>C (p.Ser1775Pro) single nucleotide variant not provided [RCV002790255] Chr10:53822403 [GRCh38]
Chr10:55582163 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4212-11_4212-7dup duplication not provided [RCV002852889] Chr10:53827554..53827555 [GRCh38]
Chr10:55587314..55587315 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1784+1G>T single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003475524]|Usher syndrome type 1F [RCV002789953] Chr10:54153099 [GRCh38]
Chr10:55912859 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.4314G>C (p.Pro1438=) single nucleotide variant not provided [RCV002876005] Chr10:53827446 [GRCh38]
Chr10:55587206 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.158-8G>C single nucleotide variant not provided [RCV002711405] Chr10:54378950 [GRCh38]
Chr10:56138710 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4946del (p.Gly1649fs) deletion not provided [RCV002575152] Chr10:53822780 [GRCh38]
Chr10:55582540 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4281G>C (p.Pro1427=) single nucleotide variant not provided [RCV002982457] Chr10:53827479 [GRCh38]
Chr10:55587239 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1255A>C (p.Asn419His) single nucleotide variant not provided [RCV003083303] Chr10:54195733 [GRCh38]
Chr10:55955493 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4280C>T (p.Pro1427Leu) single nucleotide variant not provided [RCV003058926] Chr10:53827480 [GRCh38]
Chr10:55587240 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3586G>A (p.Val1196Ile) single nucleotide variant not provided [RCV002741026] Chr10:53866773 [GRCh38]
Chr10:55626533 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.308T>C (p.Leu103Pro) single nucleotide variant not provided [RCV002805320] Chr10:54378792 [GRCh38]
Chr10:56138552 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.474+20C>A single nucleotide variant not provided [RCV003007750] Chr10:54369100 [GRCh38]
Chr10:56128860 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4323_4328del (p.Pro1442_Pro1443del) deletion Usher syndrome type 1F [RCV003062259]|not provided [RCV003058249] Chr10:53827432..53827437 [GRCh38]
Chr10:55587192..55587197 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.682T>C (p.Tyr228His) single nucleotide variant Inborn genetic diseases [RCV002812750] Chr10:54329619 [GRCh38]
Chr10:56089379 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3597A>G (p.Thr1199=) single nucleotide variant not provided [RCV002721100] Chr10:53866762 [GRCh38]
Chr10:55626522 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3846C>T (p.Ala1282=) single nucleotide variant not provided [RCV003030704] Chr10:53840457 [GRCh38]
Chr10:55600217 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2220+18A>G single nucleotide variant not provided [RCV002632977] Chr10:54066739 [GRCh38]
Chr10:55826499 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4905G>C (p.Glu1635Asp) single nucleotide variant not provided [RCV003091400] Chr10:53822821 [GRCh38]
Chr10:55582581 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1671C>T (p.Ile557=) single nucleotide variant not provided [RCV003045572] Chr10:54153213 [GRCh38]
Chr10:55912973 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.409G>T (p.Val137Leu) single nucleotide variant not provided [RCV002580221] Chr10:54369185 [GRCh38]
Chr10:56128945 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2799G>A (p.Gly933=) single nucleotide variant not provided [RCV002720152] Chr10:53995718 [GRCh38]
Chr10:55755478 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1274G>T (p.Arg425Ile) single nucleotide variant Inborn genetic diseases [RCV004070427]|not provided [RCV003060783] Chr10:54195714 [GRCh38]
Chr10:55955474 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3281C>T (p.Pro1094Leu) single nucleotide variant Inborn genetic diseases [RCV002647735]|not provided [RCV002647734] Chr10:53938907 [GRCh38]
Chr10:55698667 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4738_4816del (p.Leu1580fs) deletion not provided [RCV003029833] Chr10:53822910..53822988 [GRCh38]
Chr10:55582670..55582748 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5432T>C (p.Leu1811Pro) single nucleotide variant Inborn genetic diseases [RCV002634324]|not provided [RCV002651383] Chr10:53822294 [GRCh38]
Chr10:55582054 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1794C>A (p.Ile598=) single nucleotide variant not provided [RCV002720626] Chr10:54132998 [GRCh38]
Chr10:55892758 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4212-7del deletion not provided [RCV002933810] Chr10:53827555 [GRCh38]
Chr10:55587315 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4059G>A (p.Glu1353=) single nucleotide variant not provided [RCV003045770] Chr10:53831458 [GRCh38]
Chr10:55591218 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3516T>C (p.Asp1172=) single nucleotide variant not provided [RCV002833197] Chr10:53866843 [GRCh38]
Chr10:55626603 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2082G>C (p.Arg694Ser) single nucleotide variant not provided [RCV003065443] Chr10:54079340 [GRCh38]
Chr10:55839100 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5483C>T (p.Pro1828Leu) single nucleotide variant not provided [RCV002581909] Chr10:53822243 [GRCh38]
Chr10:55582003 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2617G>A (p.Glu873Lys) single nucleotide variant not provided [RCV003088326] Chr10:54020326 [GRCh38]
Chr10:55780086 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3350C>T (p.Ala1117Val) single nucleotide variant not provided [RCV003091165] Chr10:53938838 [GRCh38]
Chr10:55698598 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3069G>C (p.Lys1023Asn) single nucleotide variant not provided [RCV003026296] Chr10:53959785 [GRCh38]
Chr10:55719545 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.324G>C (p.Pro108=) single nucleotide variant not provided [RCV002857639] Chr10:54369270 [GRCh38]
Chr10:56129030 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1938C>T (p.Asp646=) single nucleotide variant not provided [RCV003064183] Chr10:54090043 [GRCh38]
Chr10:55849803 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1145A>G (p.His382Arg) single nucleotide variant not provided [RCV003091540] Chr10:54195843 [GRCh38]
Chr10:55955603 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4513_4571del (p.Asn1505fs) deletion not provided [RCV002899630] Chr10:53823155..53823213 [GRCh38]
Chr10:55582915..55582973 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.4679G>C (p.Ser1560Thr) single nucleotide variant not provided [RCV002933567] Chr10:53823047 [GRCh38]
Chr10:55582807 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.980T>A (p.Leu327His) single nucleotide variant not provided [RCV002579992] Chr10:54236828 [GRCh38]
Chr10:55996588 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1306-6del deletion not provided [RCV002857788] Chr10:54185274 [GRCh38]
Chr10:55945034 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1686A>G (p.Thr562=) single nucleotide variant not provided [RCV003031209] Chr10:54153198 [GRCh38]
Chr10:55912958 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1134T>G (p.Phe378Leu) single nucleotide variant not provided [RCV003063705] Chr10:54195854 [GRCh38]
Chr10:55955614 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.2100T>C (p.Thr700=) single nucleotide variant not provided [RCV003045883] Chr10:54066877 [GRCh38]
Chr10:55826637 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2091+7A>C single nucleotide variant not provided [RCV003044706] Chr10:54079324 [GRCh38]
Chr10:55839084 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1381C>T (p.Arg461Cys) single nucleotide variant not provided [RCV003087053] Chr10:54185193 [GRCh38]
Chr10:55944953 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5086T>G (p.Cys1696Gly) single nucleotide variant not provided [RCV003062086] Chr10:53822640 [GRCh38]
Chr10:55582400 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3606del (p.Ile1204fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003475449]|not provided [RCV002877600] Chr10:53866753 [GRCh38]
Chr10:55626513 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.3085C>A (p.Pro1029Thr) single nucleotide variant not provided [RCV002577671] Chr10:53959769 [GRCh38]
Chr10:55719529 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1711G>A (p.Val571Met) single nucleotide variant not provided [RCV002627635] Chr10:54153173 [GRCh38]
Chr10:55912933 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.876+9A>T single nucleotide variant not provided [RCV002810107] Chr10:54317262 [GRCh38]
Chr10:56077022 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2604T>A (p.His868Gln) single nucleotide variant not provided [RCV003061152] Chr10:54020339 [GRCh38]
Chr10:55780099 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5827G>A (p.Gly1943Arg) single nucleotide variant not provided [RCV003089421] Chr10:53821899 [GRCh38]
Chr10:55581659 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4367+10C>T single nucleotide variant not provided [RCV002833376] Chr10:53827383 [GRCh38]
Chr10:55587143 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.710G>A (p.Arg237His) single nucleotide variant not provided [RCV003086737] Chr10:54317437 [GRCh38]
Chr10:56077197 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3251del (p.Asn1084fs) deletion not provided [RCV002791827] Chr10:53938937 [GRCh38]
Chr10:55698697 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2092-8del deletion not provided [RCV002646028] Chr10:54066893 [GRCh38]
Chr10:55826653 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.875C>T (p.Pro292Leu) single nucleotide variant Inborn genetic diseases [RCV003348995]|not provided [RCV003060406] Chr10:54317272 [GRCh38]
Chr10:56077032 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3668T>G (p.Ile1223Ser) single nucleotide variant not provided [RCV002671388] Chr10:53866691 [GRCh38]
Chr10:55626451 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3317G>C (p.Arg1106Pro) single nucleotide variant Inborn genetic diseases [RCV004065873]|not provided [RCV002630781] Chr10:53938871 [GRCh38]
Chr10:55698631 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4554T>C (p.Asp1518=) single nucleotide variant not provided [RCV002717103] Chr10:53823172 [GRCh38]
Chr10:55582932 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.42G>A (p.Gly14=) single nucleotide variant not provided [RCV002937183] Chr10:54664221 [GRCh38]
Chr10:56423981 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5326C>T (p.Leu1776Phe) single nucleotide variant not provided [RCV003060430] Chr10:53822400 [GRCh38]
Chr10:55582160 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5463A>G (p.Pro1821=) single nucleotide variant not provided [RCV002895662] Chr10:53822263 [GRCh38]
Chr10:55582023 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3691G>C (p.Gly1231Arg) single nucleotide variant not provided [RCV002598974] Chr10:53866668 [GRCh38]
Chr10:55626428 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.239A>G (p.Asn80Ser) single nucleotide variant not provided [RCV002937494] Chr10:54378861 [GRCh38]
Chr10:56138621 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5405C>T (p.Thr1802Met) single nucleotide variant not provided [RCV003063144] Chr10:53822321 [GRCh38]
Chr10:55582081 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2903A>G (p.Asp968Gly) single nucleotide variant not provided [RCV003044200] Chr10:53961858 [GRCh38]
Chr10:55721618 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.999T>C (p.Asp333=) single nucleotide variant not provided [RCV002792104] Chr10:54214035 [GRCh38]
Chr10:55973795 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.846T>C (p.Tyr282=) single nucleotide variant not provided [RCV002899060] Chr10:54317301 [GRCh38]
Chr10:56077061 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.475-14T>C single nucleotide variant not provided [RCV002805941] Chr10:54346498 [GRCh38]
Chr10:56106258 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2930G>A (p.Ser977Asn) single nucleotide variant not provided [RCV003060457] Chr10:53961831 [GRCh38]
Chr10:55721591 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5574T>C (p.Ile1858=) single nucleotide variant not provided [RCV003009022] Chr10:53822152 [GRCh38]
Chr10:55581912 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2132A>G (p.Asn711Ser) single nucleotide variant not provided [RCV003060822] Chr10:54066845 [GRCh38]
Chr10:55826605 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3806+13G>A single nucleotide variant not provided [RCV002629850] Chr10:53857162 [GRCh38]
Chr10:55616922 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2624C>T (p.Ser875Leu) single nucleotide variant PCDH15-related disorder [RCV004536602]|Usher syndrome type 1F [RCV003086311]|not provided [RCV003092480]|not specified [RCV003230768] Chr10:54020319 [GRCh38]
Chr10:55780079 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2829A>T (p.Thr943=) single nucleotide variant not provided [RCV003087338] Chr10:53995688 [GRCh38]
Chr10:55755448 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.758T>C (p.Val253Ala) single nucleotide variant not provided [RCV002832838] Chr10:54317389 [GRCh38]
Chr10:56077149 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1730G>T (p.Arg577Leu) single nucleotide variant not provided [RCV003063373] Chr10:54153154 [GRCh38]
Chr10:55912914 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1204G>A (p.Gly402Ser) single nucleotide variant not provided [RCV002581123] Chr10:54195784 [GRCh38]
Chr10:55955544 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3928G>C (p.Val1310Leu) single nucleotide variant not provided [RCV002627947] Chr10:53840375 [GRCh38]
Chr10:55600135 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4935G>T (p.Leu1645=) single nucleotide variant not provided [RCV002857640] Chr10:53822791 [GRCh38]
Chr10:55582551 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4398_4414del (p.Arg1467fs) deletion not provided [RCV003029817] Chr10:53823312..53823328 [GRCh38]
Chr10:55583072..55583088 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.5338C>A (p.Pro1780Thr) single nucleotide variant not provided [RCV002580572] Chr10:53822388 [GRCh38]
Chr10:55582148 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2048G>A (p.Arg683His) single nucleotide variant Inborn genetic diseases [RCV002878276] Chr10:54079374 [GRCh38]
Chr10:55839134 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.157+7G>A single nucleotide variant not provided [RCV002961957] Chr10:54527805 [GRCh38]
Chr10:56287565 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4289_4319del (p.Ala1430fs) deletion not provided [RCV002833767] Chr10:53827441..53827471 [GRCh38]
Chr10:55587201..55587231 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.340A>G (p.Ile114Val) single nucleotide variant not provided [RCV002720347] Chr10:54369254 [GRCh38]
Chr10:56129014 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2685G>A (p.Leu895=) single nucleotide variant not provided [RCV003061119] Chr10:54020258 [GRCh38]
Chr10:55780018 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2869-17T>G single nucleotide variant not provided [RCV003047559] Chr10:53961909 [GRCh38]
Chr10:55721669 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1542T>C (p.Tyr514=) single nucleotide variant not provided [RCV002631510] Chr10:54183492 [GRCh38]
Chr10:55943252 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3778G>C (p.Val1260Leu) single nucleotide variant not provided [RCV002601618] Chr10:53857203 [GRCh38]
Chr10:55616963 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1614A>G (p.Glu538=) single nucleotide variant not provided [RCV003031083] Chr10:54153270 [GRCh38]
Chr10:55913030 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.649A>G (p.Arg217Gly) single nucleotide variant not provided [RCV002631531] Chr10:54329652 [GRCh38]
Chr10:56089412 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2468C>T (p.Thr823Ile) single nucleotide variant not provided [RCV002580632] Chr10:54022950 [GRCh38]
Chr10:55782710 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1744A>G (p.Thr582Ala) single nucleotide variant not provided [RCV003065000] Chr10:54153140 [GRCh38]
Chr10:55912900 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.595-8A>T single nucleotide variant not provided [RCV002810081] Chr10:54329714 [GRCh38]
Chr10:56089474 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2889G>A (p.Val963=) single nucleotide variant not provided [RCV002834291] Chr10:53961872 [GRCh38]
Chr10:55721632 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.669A>C (p.Glu223Asp) single nucleotide variant not provided [RCV002631844] Chr10:54329632 [GRCh38]
Chr10:56089392 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1099-10dup duplication not provided [RCV003062677] Chr10:54195898..54195899 [GRCh38]
Chr10:55955658..55955659 [GRCh37]
Chr10:10q21.1		 benign
NM_033056.4(PCDH15):c.5454T>C (p.Leu1818=) single nucleotide variant not provided [RCV002877593] Chr10:53822272 [GRCh38]
Chr10:55582032 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1008A>G (p.Arg336=) single nucleotide variant not provided [RCV003044923] Chr10:54214026 [GRCh38]
Chr10:55973786 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.63T>C (p.Phe21=) single nucleotide variant not provided [RCV002770555] Chr10:54664200 [GRCh38]
Chr10:56423960 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3306C>G (p.Ser1102Arg) single nucleotide variant not provided [RCV002717199] Chr10:53938882 [GRCh38]
Chr10:55698642 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.157+9G>A single nucleotide variant not provided [RCV003029709] Chr10:54527803 [GRCh38]
Chr10:56287563 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.695T>C (p.Ile232Thr) single nucleotide variant Inborn genetic diseases [RCV002579374]|not provided [RCV002579375] Chr10:54329606 [GRCh38]
Chr10:56089366 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4383C>G (p.Tyr1461Ter) single nucleotide variant not provided [RCV002806933] Chr10:53823343 [GRCh38]
Chr10:55583103 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.5806_5809dup (p.Leu1937Ter) duplication not provided [RCV002921969] Chr10:53821916..53821917 [GRCh38]
Chr10:55581676..55581677 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5553C>T (p.Asn1851=) single nucleotide variant not provided [RCV002857169] Chr10:53822173 [GRCh38]
Chr10:55581933 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3622A>G (p.Met1208Val) single nucleotide variant not provided [RCV002647039] Chr10:53866737 [GRCh38]
Chr10:55626497 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1056A>G (p.Pro352=) single nucleotide variant not provided [RCV002833039] Chr10:54213978 [GRCh38]
Chr10:55973738 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.319-7A>G single nucleotide variant not provided [RCV003045565] Chr10:54369282 [GRCh38]
Chr10:56129042 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3308A>G (p.Tyr1103Cys) single nucleotide variant not provided [RCV003090940] Chr10:53938880 [GRCh38]
Chr10:55698640 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5064T>C (p.Asn1688=) single nucleotide variant not provided [RCV003027051] Chr10:53822662 [GRCh38]
Chr10:55582422 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4978T>C (p.Ser1660Pro) single nucleotide variant not provided [RCV003048979] Chr10:53822748 [GRCh38]
Chr10:55582508 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.372A>T (p.Lys124Asn) single nucleotide variant not provided [RCV002629756] Chr10:54369222 [GRCh38]
Chr10:56128982 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5183G>T (p.Arg1728Ile) single nucleotide variant not provided [RCV002632748] Chr10:53822543 [GRCh38]
Chr10:55582303 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3123-12C>T single nucleotide variant not provided [RCV002833098] Chr10:53940987 [GRCh38]
Chr10:55700747 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2106A>G (p.Thr702=) single nucleotide variant not provided [RCV003009611] Chr10:54066871 [GRCh38]
Chr10:55826631 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4368-3_4373dup duplication not provided [RCV002810453] Chr10:53823352..53823353 [GRCh38]
Chr10:55583112..55583113 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3258A>G (p.Thr1086=) single nucleotide variant not provided [RCV002857347] Chr10:53938930 [GRCh38]
Chr10:55698690 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4213C>T (p.Arg1405Cys) single nucleotide variant not provided [RCV002770065] Chr10:53827547 [GRCh38]
Chr10:55587307 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1745C>A (p.Thr582Lys) single nucleotide variant Inborn genetic diseases [RCV004066698]|not provided [RCV002646554] Chr10:54153139 [GRCh38]
Chr10:55912899 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.180G>A (p.Met60Ile) single nucleotide variant Usher syndrome type 1F [RCV002810020]|not provided [RCV004593208] Chr10:54378920 [GRCh38]
Chr10:56138680 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1440G>A (p.Ser480=) single nucleotide variant not provided [RCV003091895] Chr10:54185134 [GRCh38]
Chr10:55944894 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2451_2452delinsAA (p.Val818Met) indel not provided [RCV003090087] Chr10:54022966..54022967 [GRCh38]
Chr10:55782726..55782727 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.373G>A (p.Val125Met) single nucleotide variant not provided [RCV002602490] Chr10:54369221 [GRCh38]
Chr10:56128981 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.925C>G (p.Gln309Glu) single nucleotide variant not provided [RCV003027098] Chr10:54236883 [GRCh38]
Chr10:55996643 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3738G>T (p.Leu1246=) single nucleotide variant not provided [RCV003010291] Chr10:53857243 [GRCh38]
Chr10:55617003 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3494G>T (p.Arg1165Ile) single nucleotide variant not provided [RCV002899374] Chr10:53903250 [GRCh38]
Chr10:55663010 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1689G>A (p.Gly563=) single nucleotide variant not provided [RCV002675692] Chr10:54153195 [GRCh38]
Chr10:55912955 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3660_3666del (p.Phe1220fs) microsatellite not provided [RCV002938736] Chr10:53866693..53866699 [GRCh38]
Chr10:55626453..55626459 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3691G>A (p.Gly1231Arg) single nucleotide variant not provided [RCV003060431] Chr10:53866668 [GRCh38]
Chr10:55626428 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1863_1864dup (p.Ser622fs) microsatellite Autosomal recessive nonsyndromic hearing loss 23 [RCV003475489]|Usher syndrome type 1F [RCV003062261]|not provided [RCV003062260] Chr10:54132927..54132928 [GRCh38]
Chr10:55892687..55892688 [GRCh37]
Chr10:10q21.1		 pathogenic|no classifications from unflagged records
NM_033056.4(PCDH15):c.5159G>T (p.Cys1720Phe) single nucleotide variant not provided [RCV003090206] Chr10:53822567 [GRCh38]
Chr10:55582327 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.873T>G (p.Thr291=) single nucleotide variant not provided [RCV002671461] Chr10:54317274 [GRCh38]
Chr10:56077034 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2793C>T (p.Tyr931=) single nucleotide variant not provided [RCV002600387] Chr10:53995724 [GRCh38]
Chr10:55755484 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5771C>T (p.Thr1924Ile) single nucleotide variant not provided [RCV002600782] Chr10:53821955 [GRCh38]
Chr10:55581715 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1837C>T (p.Pro613Ser) single nucleotide variant not provided [RCV003091194] Chr10:54132955 [GRCh38]
Chr10:55892715 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4325C>T (p.Pro1442Leu) single nucleotide variant not provided [RCV002598861] Chr10:53827435 [GRCh38]
Chr10:55587195 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1664A>C (p.Asp555Ala) single nucleotide variant not provided [RCV003090693] Chr10:54153220 [GRCh38]
Chr10:55912980 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1546G>A (p.Val516Met) single nucleotide variant not provided [RCV002576998] Chr10:54183488 [GRCh38]
Chr10:55943248 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5125C>T (p.His1709Tyr) single nucleotide variant Inborn genetic diseases [RCV003087956]|not provided [RCV003087957] Chr10:53822601 [GRCh38]
Chr10:55582361 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4964C>G (p.Ser1655Cys) single nucleotide variant not provided [RCV002933622] Chr10:53822762 [GRCh38]
Chr10:55582522 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4223A>G (p.Glu1408Gly) single nucleotide variant not provided [RCV002598600] Chr10:53827537 [GRCh38]
Chr10:55587297 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4680T>C (p.Ser1560=) single nucleotide variant not provided [RCV002583078] Chr10:53823046 [GRCh38]
Chr10:55582806 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3766C>T (p.Pro1256Ser) single nucleotide variant not provided [RCV003068502] Chr10:53857215 [GRCh38]
Chr10:55616975 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.908C>A (p.Pro303Gln) single nucleotide variant not provided [RCV002605135] Chr10:54236900 [GRCh38]
Chr10:55996660 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3124C>A (p.Pro1042Thr) single nucleotide variant not provided [RCV003067231] Chr10:53940974 [GRCh38]
Chr10:55700734 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2450C>G (p.Pro817Arg) single nucleotide variant not provided [RCV002943336] Chr10:54022968 [GRCh38]
Chr10:55782728 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.475-18A>T single nucleotide variant not provided [RCV003050730] Chr10:54346502 [GRCh38]
Chr10:56106262 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.2814T>C (p.Asp938=) single nucleotide variant not provided [RCV002725752] Chr10:53995703 [GRCh38]
Chr10:55755463 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3606G>T (p.Gly1202=) single nucleotide variant not provided [RCV002584744] Chr10:53866753 [GRCh38]
Chr10:55626513 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4995C>G (p.Pro1665=) single nucleotide variant not provided [RCV003092378] Chr10:53822731 [GRCh38]
Chr10:55582491 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1338T>A (p.Asn446Lys) single nucleotide variant not provided [RCV003051619] Chr10:54185236 [GRCh38]
Chr10:55944996 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4125G>C (p.Gly1375=) single nucleotide variant not provided [RCV002722119] Chr10:53831392 [GRCh38]
Chr10:55591152 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5584A>G (p.Met1862Val) single nucleotide variant not provided [RCV002658390] Chr10:53822142 [GRCh38]
Chr10:55581902 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3374-17C>T single nucleotide variant not provided [RCV003068563] Chr10:53903387 [GRCh38]
Chr10:55663147 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4844G>A (p.Cys1615Tyr) single nucleotide variant not provided [RCV003068565] Chr10:53822882 [GRCh38]
Chr10:55582642 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.541G>A (p.Asp181Asn) single nucleotide variant Inborn genetic diseases [RCV003358004]|not provided [RCV002815120] Chr10:54346418 [GRCh38]
Chr10:56106178 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4671+1552A>G single nucleotide variant not provided [RCV002943219] Chr10:53809004 [GRCh38]
Chr10:55568764 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1302A>C (p.Glu434Asp) single nucleotide variant not provided [RCV003052038] Chr10:54195686 [GRCh38]
Chr10:55955446 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5053T>C (p.Ser1685Pro) single nucleotide variant Inborn genetic diseases [RCV004073380]|not provided [RCV002584894] Chr10:53822673 [GRCh38]
Chr10:55582433 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.618T>A (p.Ile206=) single nucleotide variant not provided [RCV002603603] Chr10:54329683 [GRCh38]
Chr10:56089443 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3123-5T>G single nucleotide variant not provided [RCV002653926] Chr10:53940980 [GRCh38]
Chr10:55700740 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1561_1580delinsTAAAAGTGTTCCTGTTTCTCCACATCCTCTCCAGCACCTGTTGTTTCCTGACTTTTTAATGATTGCCATTCTAACTGGTGTGAGATGGTATCTCATTGTGGTTTTGTCATGGCCATCAGAGAAATGCAAATCAAAACATA (p.Asp521_Ser527delinsTer) indel not provided [RCV003049662] Chr10:54183454..54183473 [GRCh38]
Chr10:55943214..55943233 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.1784+18C>A single nucleotide variant not provided [RCV003066907] Chr10:54153082 [GRCh38]
Chr10:55912842 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3122+16C>T single nucleotide variant not provided [RCV003050840] Chr10:53959716 [GRCh38]
Chr10:55719476 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1958A>G (p.Glu653Gly) single nucleotide variant not provided [RCV002584777] Chr10:54090023 [GRCh38]
Chr10:55849783 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5831C>A (p.Thr1944Asn) single nucleotide variant not provided [RCV002609210] Chr10:53821895 [GRCh38]
Chr10:55581655 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1752A>G (p.Gln584=) single nucleotide variant not provided [RCV003066319] Chr10:54153132 [GRCh38]
Chr10:55912892 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.548C>A (p.Pro183Gln) single nucleotide variant not provided [RCV003050949] Chr10:54346411 [GRCh38]
Chr10:56106171 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4689G>T (p.Leu1563=) single nucleotide variant not provided [RCV003052349] Chr10:53823037 [GRCh38]
Chr10:55582797 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.850G>A (p.Ala284Thr) single nucleotide variant not provided [RCV002588972] Chr10:54317297 [GRCh38]
Chr10:56077057 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5297C>T (p.Ala1766Val) single nucleotide variant not provided [RCV002609547] Chr10:53822429 [GRCh38]
Chr10:55582189 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3018G>C (p.Val1006=) single nucleotide variant not provided [RCV002725440] Chr10:53959836 [GRCh38]
Chr10:55719596 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1519C>G (p.Pro507Ala) single nucleotide variant not provided [RCV002587738] Chr10:54183515 [GRCh38]
Chr10:55943275 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4212-18A>G single nucleotide variant not provided [RCV003071776] Chr10:53827566 [GRCh38]
Chr10:55587326 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5680_5693dup (p.Asn1898delinsLysAsnGlnTer) duplication not provided [RCV003073035] Chr10:53822032..53822033 [GRCh38]
Chr10:55581792..55581793 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.876G>A (p.Pro292=) single nucleotide variant not provided [RCV003067270] Chr10:54317271 [GRCh38]
Chr10:56077031 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4693G>A (p.Gly1565Ser) single nucleotide variant Inborn genetic diseases [RCV004654156]|not provided [RCV002607787] Chr10:53823033 [GRCh38]
Chr10:55582793 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1805A>G (p.Tyr602Cys) single nucleotide variant Inborn genetic diseases [RCV004066672]|not provided [RCV002653224] Chr10:54132987 [GRCh38]
Chr10:55892747 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3554T>C (p.Ile1185Thr) single nucleotide variant not provided [RCV002584551] Chr10:53866805 [GRCh38]
Chr10:55626565 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2875C>T (p.Pro959Ser) single nucleotide variant not provided [RCV002606915] Chr10:53961886 [GRCh38]
Chr10:55721646 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1698C>T (p.Thr566=) single nucleotide variant not provided [RCV003070900] Chr10:54153186 [GRCh38]
Chr10:55912946 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3444C>A (p.Phe1148Leu) single nucleotide variant not provided [RCV002602967] Chr10:53903300 [GRCh38]
Chr10:55663060 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3590T>G (p.Val1197Gly) single nucleotide variant not provided [RCV003049696] Chr10:53866769 [GRCh38]
Chr10:55626529 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.168G>A (p.Leu56=) single nucleotide variant not provided [RCV003066330] Chr10:54378932 [GRCh38]
Chr10:56138692 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4203G>T (p.Gln1401His) single nucleotide variant not provided [RCV003093770] Chr10:53828573 [GRCh38]
Chr10:55588333 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5741_5743dup (p.Glu1914_Leu1915insGln) duplication not provided [RCV002611123] Chr10:53821982..53821983 [GRCh38]
Chr10:55581742..55581743 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3509_3520del (p.Asp1170_Thr1173del) deletion not provided [RCV002611124] Chr10:53866839..53866850 [GRCh38]
Chr10:55626599..55626610 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2201C>T (p.Ala734Val) single nucleotide variant not provided [RCV003067857] Chr10:54066776 [GRCh38]
Chr10:55826536 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1644C>T (p.Ile548=) single nucleotide variant not provided [RCV003052457] Chr10:54153240 [GRCh38]
Chr10:55913000 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3590_3591dup (p.Glu1198fs) duplication not provided [RCV002814687] Chr10:53866767..53866768 [GRCh38]
Chr10:55626527..55626528 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3392A>G (p.Tyr1131Cys) single nucleotide variant not provided [RCV003069428] Chr10:53903352 [GRCh38]
Chr10:55663112 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5599A>T (p.Thr1867Ser) single nucleotide variant not provided [RCV002680781] Chr10:53822127 [GRCh38]
Chr10:55581887 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2580A>T (p.Glu860Asp) single nucleotide variant not provided [RCV002680887] Chr10:54020363 [GRCh38]
Chr10:55780123 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.838C>G (p.Leu280Val) single nucleotide variant not provided [RCV003070027] Chr10:54317309 [GRCh38]
Chr10:56077069 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2458A>G (p.Thr820Ala) single nucleotide variant not provided [RCV002611856] Chr10:54022960 [GRCh38]
Chr10:55782720 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3709G>A (p.Asp1237Asn) single nucleotide variant PCDH15-related disorder [RCV004736262]|not provided [RCV003093261] Chr10:53866650 [GRCh38]
Chr10:55626410 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1887G>A (p.Met629Ile) single nucleotide variant not provided [RCV003067215] Chr10:54132905 [GRCh38]
Chr10:55892665 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1928G>A (p.Arg643Gln) single nucleotide variant not provided [RCV003068708] Chr10:54090053 [GRCh38]
Chr10:55849813 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2972G>A (p.Arg991Gln) single nucleotide variant not provided [RCV002606633] Chr10:53961789 [GRCh38]
Chr10:55721549 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.985+16C>T single nucleotide variant not provided [RCV002589899] Chr10:54236807 [GRCh38]
Chr10:55996567 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1635A>G (p.Thr545=) single nucleotide variant not provided [RCV003071004] Chr10:54153249 [GRCh38]
Chr10:55913009 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.461C>A (p.Ala154Asp) single nucleotide variant not provided [RCV003073275] Chr10:54369133 [GRCh38]
Chr10:56128893 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4671+1349_4671+1353dup duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003155579] Chr10:53809202..53809203 [GRCh38]
Chr10:55568962..55568963 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.1178C>T (p.Pro393Leu) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003155593] Chr10:54195810 [GRCh38]
Chr10:55955570 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.4898T>G (p.Leu1633Trp) single nucleotide variant Inborn genetic diseases [RCV003277484] Chr10:53822828 [GRCh38]
Chr10:55582588 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4042G>A (p.Gly1348Arg) single nucleotide variant Inborn genetic diseases [RCV003212992] Chr10:53831475 [GRCh38]
Chr10:55591235 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1612G>A (p.Glu538Lys) single nucleotide variant not provided [RCV003134763] Chr10:54153272 [GRCh38]
Chr10:55913032 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3818G>A (p.Arg1273His) single nucleotide variant not provided [RCV003134764] Chr10:53840485 [GRCh38]
Chr10:55600245 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5054C>G (p.Ser1685Ter) single nucleotide variant not provided [RCV003135600] Chr10:53822672 [GRCh38]
Chr10:55582432 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1615G>C (p.Gly539Arg) single nucleotide variant Inborn genetic diseases [RCV003210330] Chr10:54153269 [GRCh38]
Chr10:55913029 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2135A>T (p.Asp712Val) single nucleotide variant not provided [RCV003227442] Chr10:54066842 [GRCh38]
Chr10:55826602 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4649A>G (p.Glu1550Gly) single nucleotide variant Inborn genetic diseases [RCV003220872] Chr10:53810578 [GRCh38]
Chr10:55570338 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3671C>T (p.Ala1224Val) single nucleotide variant not provided [RCV003228538] Chr10:53866688 [GRCh38]
Chr10:55626448 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4777_4801dup (p.Gln1601fs) duplication not specified [RCV003324249] Chr10:53822924..53822925 [GRCh38]
Chr10:55582684..55582685 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4671+1458A>T single nucleotide variant Inborn genetic diseases [RCV003286541] Chr10:53809098 [GRCh38]
Chr10:55568858 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1163A>G (p.Glu388Gly) single nucleotide variant Inborn genetic diseases [RCV003261709] Chr10:54195825 [GRCh38]
Chr10:55955585 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh37/hg19 10p13-q26.3(chr10:12829206-135427143) copy number loss Distal 10q deletion syndrome [RCV003319583] Chr10:12829206..135427143 [GRCh37]
Chr10:10p13-q26.3		 pathogenic
GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143) copy number gain Distal trisomy 10q [RCV003319593] Chr10:11138692..135427143 [GRCh37]
Chr10:10p14-q26.3		 pathogenic
NM_033056.4(PCDH15):c.4586A>T (p.Tyr1529Phe) single nucleotide variant Inborn genetic diseases [RCV003345962] Chr10:53823140 [GRCh38]
Chr10:55582900 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4045G>A (p.Gly1349Arg) single nucleotide variant Inborn genetic diseases [RCV003383195] Chr10:53831472 [GRCh38]
Chr10:55591232 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5750C>G (p.Thr1917Ser) single nucleotide variant Inborn genetic diseases [RCV003350839] Chr10:53821976 [GRCh38]
Chr10:55581736 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.218T>C (p.Ile73Thr) single nucleotide variant Inborn genetic diseases [RCV003372502] Chr10:54378882 [GRCh38]
Chr10:56138642 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1101T>C (p.Ala367=) single nucleotide variant not provided [RCV003686260] Chr10:54195887 [GRCh38]
Chr10:55955647 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2782A>T (p.Lys928Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003476666] Chr10:53995735 [GRCh38]
Chr10:55755495 [GRCh37]
Chr10:10q21.1		 pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.42del (p.Ile15fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003476669] Chr10:54664221 [GRCh38]
Chr10:56423981 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.3612del (p.Thr1206fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003476676] Chr10:53866747 [GRCh38]
Chr10:55626507 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.3981dup (p.Lys1328Ter) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003476685] Chr10:53840321..53840322 [GRCh38]
Chr10:55600081..55600082 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.3009+1G>C single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003476687] Chr10:53961751 [GRCh38]
Chr10:55721511 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.2092-2A>G single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003476691] Chr10:54066887 [GRCh38]
Chr10:55826647 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.3984-2A>C single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003476697] Chr10:53831535 [GRCh38]
Chr10:55591295 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.3751del (p.Ile1251fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003476709] Chr10:53857230 [GRCh38]
Chr10:55616990 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.4209A>G (p.Lys1403=) single nucleotide variant not provided [RCV003826710] Chr10:53828567 [GRCh38]
Chr10:55588327 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.876+2T>C single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003476694] Chr10:54317269 [GRCh38]
Chr10:56077029 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.4367+2dup duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003476698] Chr10:53827390..53827391 [GRCh38]
Chr10:55587150..55587151 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.3300_3319dup (p.Val1107fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003476708] Chr10:53938868..53938869 [GRCh38]
Chr10:55698628..55698629 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.1224C>T (p.Ala408=) single nucleotide variant not provided [RCV003571479] Chr10:54195764 [GRCh38]
Chr10:55955524 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2220+8G>T single nucleotide variant not provided [RCV003873456] Chr10:54066749 [GRCh38]
Chr10:55826509 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2163G>C (p.Leu721=) single nucleotide variant not provided [RCV003571522] Chr10:54066814 [GRCh38]
Chr10:55826574 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.876+15A>C single nucleotide variant not provided [RCV003571549] Chr10:54317256 [GRCh38]
Chr10:56077016 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4920G>A (p.Arg1640=) single nucleotide variant not provided [RCV003569912] Chr10:53822806 [GRCh38]
Chr10:55582566 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.57T>G (p.Ser19=) single nucleotide variant not provided [RCV003570756] Chr10:54664206 [GRCh38]
Chr10:56423966 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3122+11C>T single nucleotide variant not provided [RCV003543235] Chr10:53959721 [GRCh38]
Chr10:55719481 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2232T>G (p.Pro744=) single nucleotide variant not provided [RCV003569985] Chr10:54023186 [GRCh38]
Chr10:55782946 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5349_5365del (p.Pro1784fs) deletion not provided [RCV003570020] Chr10:53822361..53822377 [GRCh38]
Chr10:55582121..55582137 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.877-18_877-15del deletion not provided [RCV003571796] Chr10:54236946..54236949 [GRCh38]
Chr10:55996706..55996709 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2031del (p.Asp677fs) deletion not provided [RCV003570536] Chr10:54079391 [GRCh38]
Chr10:55839151 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.5673_5697dup (p.Tyr1900delinsThrTer) duplication not provided [RCV003570518] Chr10:53822028..53822029 [GRCh38]
Chr10:55581788..55581789 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3502-15_3502-14insC insertion not provided [RCV003570587] Chr10:53866871..53866872 [GRCh38]
Chr10:55626631..55626632 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1287G>A (p.Leu429=) single nucleotide variant not provided [RCV003571510] Chr10:54195701 [GRCh38]
Chr10:55955461 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3122+16C>G single nucleotide variant not provided [RCV003874707] Chr10:53959716 [GRCh38]
Chr10:55719476 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1917+14T>G single nucleotide variant not provided [RCV003874028] Chr10:54132861 [GRCh38]
Chr10:55892621 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5009C>A (p.Ser1670Ter) single nucleotide variant not provided [RCV003570513] Chr10:53822717 [GRCh38]
Chr10:55582477 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.319-20A>T single nucleotide variant not provided [RCV003874382] Chr10:54369295 [GRCh38]
Chr10:56129055 [GRCh37]
Chr10:10q21.1		 likely benign
GRCh37/hg19 10q11.23-22.1(chr10:51735638-70791246)x1 copy number loss not provided [RCV003483092] Chr10:51735638..70791246 [GRCh37]
Chr10:10q11.23-22.1		 pathogenic
NM_001384140.1(PCDH15):c.2502T>G (p.Ala834=) single nucleotide variant not provided [RCV003568933] Chr10:54022916 [GRCh38]
Chr10:55782676 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4901_4902insGAGGCAATCCATTGCTTACAACTGA (p.Thr1634_Glu1635insArgGlnSerIleAlaTyrAsnTer) insertion not provided [RCV003569112] Chr10:53822824..53822825 [GRCh38]
Chr10:55582584..55582585 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2526+9G>C single nucleotide variant not provided [RCV003570614] Chr10:54022883 [GRCh38]
Chr10:55782643 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5532A>C (p.Thr1844=) single nucleotide variant not provided [RCV003570911] Chr10:53822194 [GRCh38]
Chr10:55581954 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1098+18C>T single nucleotide variant not provided [RCV003543614] Chr10:54213918 [GRCh38]
Chr10:55973678 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4368-3146A>G single nucleotide variant not provided [RCV003874399] Chr10:53823376 [GRCh38]
Chr10:55583136 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3717+1del deletion not provided [RCV003543079] Chr10:53866641 [GRCh38]
Chr10:55626401 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1306-11T>C single nucleotide variant not provided [RCV003568957] Chr10:54185279 [GRCh38]
Chr10:55945039 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2825_2828dup (p.Pro944fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003476664] Chr10:53995688..53995689 [GRCh38]
Chr10:55755448..55755449 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.1299del (p.Ile433fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003476679] Chr10:54195689 [GRCh38]
Chr10:55955449 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.2151del (p.Phe717fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003476680]|not provided [RCV003553963] Chr10:54066826 [GRCh38]
Chr10:55826586 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.1917+1G>A single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003476683]|not provided [RCV003669433] Chr10:54132874 [GRCh38]
Chr10:55892634 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.1778_1784dup (p.Asn596fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003476684] Chr10:54153099..54153100 [GRCh38]
Chr10:55912859..55912860 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.3499A>T (p.Lys1167Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003476670] Chr10:53903245 [GRCh38]
Chr10:55663005 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.2544del (p.Gly849fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003476674] Chr10:54020399 [GRCh38]
Chr10:55780159 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.4367+2251G>A single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003476690] Chr10:53825142 [GRCh38]
Chr10:55584902 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.915dup (p.Ala306fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003476695] Chr10:54236892..54236893 [GRCh38]
Chr10:55996652..55996653 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1430dup (p.Tyr477Ter) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003476704] Chr10:54185143..54185144 [GRCh38]
Chr10:55944903..55944904 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.457dup (p.Tyr153fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003476710] Chr10:54369136..54369137 [GRCh38]
Chr10:56128896..56128897 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.2662C>T (p.Gln888Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003476668] Chr10:54020281 [GRCh38]
Chr10:55780041 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.1728del (p.Arg577fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003476671]|not provided [RCV003549102] Chr10:54153156 [GRCh38]
Chr10:55912916 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.2356G>T (p.Glu786Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003476692] Chr10:54023062 [GRCh38]
Chr10:55782822 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.3982dup (p.Phe1329fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003476667] Chr10:53840319..53840320 [GRCh38]
Chr10:55600079..55600080 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.4126del (p.Ala1376fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003476701] Chr10:53831391 [GRCh38]
Chr10:55591151 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.3373+2T>C single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003476705] Chr10:53938813 [GRCh38]
Chr10:55698573 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.2388dup (p.His797fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003476707] Chr10:54023029..54023030 [GRCh38]
Chr10:55782789..55782790 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_033056.4(PCDH15):c.5023C>G (p.Pro1675Ala) single nucleotide variant PCDH15-related disorder [RCV004527950] Chr10:53822703 [GRCh38]
Chr10:55582463 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh37/hg19 10q11.21-24.2(chr10:42709645-100834951)x3 copy number gain not provided [RCV003484798] Chr10:42709645..100834951 [GRCh37]
Chr10:10q11.21-24.2		 pathogenic
NM_001384140.1(PCDH15):c.2507C>G (p.Thr836Ser) single nucleotide variant not provided [RCV003481969] Chr10:54022911 [GRCh38]
Chr10:55782671 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.821C>G (p.Thr274Ser) single nucleotide variant not provided [RCV003481970] Chr10:54317326 [GRCh38]
Chr10:56077086 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1841del (p.Pro614fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003476663] Chr10:54132951 [GRCh38]
Chr10:55892711 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.2107del (p.Thr702_Val703insTer) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003476673]|not provided [RCV003720921] Chr10:54066870 [GRCh38]
Chr10:55826630 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.4094dup (p.Arg1366fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003476675] Chr10:53831422..53831423 [GRCh38]
Chr10:55591182..55591183 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.3989del (p.Leu1330fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003476700] Chr10:53831528 [GRCh38]
Chr10:55591288 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.371_372delinsT (p.Lys124fs) indel Autosomal recessive nonsyndromic hearing loss 23 [RCV003476703] Chr10:54369222..54369223 [GRCh38]
Chr10:56128982..56128983 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.1738del (p.Ala580fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003476711] Chr10:54153146 [GRCh38]
Chr10:55912906 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.705+5G>A single nucleotide variant Usher syndrome [RCV003389536] Chr10:54329591 [GRCh38]
Chr10:56089351 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1797C>A (p.Cys599Ter) single nucleotide variant Usher syndrome [RCV003389546] Chr10:54132995 [GRCh38]
Chr10:55892755 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.4851_4854del (p.Asn1617fs) microsatellite PCDH15-related disorder [RCV004527835] Chr10:53822872..53822875 [GRCh38]
Chr10:55582632..55582635 [GRCh37]
Chr10:10q21.1		 likely pathogenic|uncertain significance
NM_001384140.1(PCDH15):c.3781dup (p.Glu1261fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV004573156]|not provided [RCV003690727] Chr10:53857199..53857200 [GRCh38]
Chr10:55616959..55616960 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.3009+1G>T single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003476665] Chr10:53961751 [GRCh38]
Chr10:55721511 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.1431C>A (p.Tyr477Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003476672] Chr10:54185143 [GRCh38]
Chr10:55944903 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.1717_1729del (p.Met573fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003476677] Chr10:54153155..54153167 [GRCh38]
Chr10:55912915..55912927 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.2718_2719insGG (p.Pro907fs) insertion Autosomal recessive nonsyndromic hearing loss 23 [RCV003476681] Chr10:54020224..54020225 [GRCh38]
Chr10:55779984..55779985 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.1737C>A (p.Tyr579Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003476682] Chr10:54153147 [GRCh38]
Chr10:55912907 [GRCh37]
Chr10:10q21.1		 pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.4223_4226dup (p.Cys1409Ter) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003476693] Chr10:53827533..53827534 [GRCh38]
Chr10:55587293..55587294 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.1013dup (p.His339fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003476702] Chr10:54214020..54214021 [GRCh38]
Chr10:55973780..55973781 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.17dup (p.Tyr6Ter) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV003476678]|not provided [RCV003708811] Chr10:54664245..54664246 [GRCh38]
Chr10:56424005..56424006 [GRCh37]
Chr10:10q21.1		 pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.1591-2A>C single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003476686] Chr10:54153295 [GRCh38]
Chr10:55913055 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.2922C>G (p.Tyr974Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003476688] Chr10:53961839 [GRCh38]
Chr10:55721599 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.1738_1739del (p.Ala580fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV003476689] Chr10:54153145..54153146 [GRCh38]
Chr10:55912905..55912906 [GRCh37]
Chr10:10q21.1		 likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.3037G>T (p.Glu1013Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV003476696]|not provided [RCV003679223] Chr10:53959817 [GRCh38]
Chr10:55719577 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic|no classifications from unflagged records
NM_001384140.1(PCDH15):c.1022A>G (p.His341Arg) single nucleotide variant PCDH15-related disorder [RCV004529699] Chr10:54214012 [GRCh38]
Chr10:55973772 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5546C>T (p.Thr1849Met) single nucleotide variant not provided [RCV003441211] Chr10:53822180 [GRCh38]
Chr10:55581940 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5747A>G (p.Gln1916Arg) single nucleotide variant not provided [RCV003441255] Chr10:53821979 [GRCh38]
Chr10:55581739 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5671G>A (p.Glu1891Lys) single nucleotide variant Usher syndrome [RCV003389530] Chr10:53822055 [GRCh38]
Chr10:55581815 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.4633A>G (p.Arg1545Gly) single nucleotide variant PCDH15-related disorder [RCV004527880] Chr10:53823093 [GRCh38]
Chr10:55582853 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4671+1657C>T single nucleotide variant not provided [RCV003417395] Chr10:53808899 [GRCh38]
Chr10:55568659 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5861C>G (p.Ser1954Ter) single nucleotide variant Usher syndrome [RCV003389537] Chr10:53821865 [GRCh38]
Chr10:55581625 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.22_23delinsC (p.Trp8fs) indel PCDH15-related disorder [RCV004527864] Chr10:54664240..54664241 [GRCh38]
Chr10:56424000..56424001 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4367+19A>G single nucleotide variant not provided [RCV003686822] Chr10:53827374 [GRCh38]
Chr10:55587134 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2307G>A (p.Gly769=) single nucleotide variant not provided [RCV003714444] Chr10:54023111 [GRCh38]
Chr10:55782871 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3717+8G>T single nucleotide variant not provided [RCV003573715] Chr10:53866634 [GRCh38]
Chr10:55626394 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1306-14del deletion not provided [RCV003828068] Chr10:54185282 [GRCh38]
Chr10:55945042 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5865G>A (p.Leu1955=) single nucleotide variant not provided [RCV003695209] Chr10:53821861 [GRCh38]
Chr10:55581621 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5021T>A (p.Leu1674Ter) single nucleotide variant not provided [RCV003831435] Chr10:53822705 [GRCh38]
Chr10:55582465 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.474+9C>A single nucleotide variant not provided [RCV003579196] Chr10:54369111 [GRCh38]
Chr10:56128871 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1392C>T (p.Thr464=) single nucleotide variant not provided [RCV003573771] Chr10:54185182 [GRCh38]
Chr10:55944942 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1576del (p.Asp526fs) deletion not provided [RCV003694528] Chr10:54183458 [GRCh38]
Chr10:55943218 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3745del (p.Gln1249fs) deletion not provided [RCV003578369] Chr10:53857236 [GRCh38]
Chr10:55616996 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3373+11C>T single nucleotide variant not provided [RCV003740082] Chr10:53938804 [GRCh38]
Chr10:55698564 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4211+4_4211+7dup duplication not provided [RCV003695701] Chr10:53828557..53828558 [GRCh38]
Chr10:55588317..55588318 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4203-18T>G single nucleotide variant not provided [RCV003849001] Chr10:53828591 [GRCh38]
Chr10:55588351 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1275A>G (p.Arg425=) single nucleotide variant not provided [RCV003687265] Chr10:54195713 [GRCh38]
Chr10:55955473 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2694C>A (p.Ala898=) single nucleotide variant not provided [RCV003574144] Chr10:54020249 [GRCh38]
Chr10:55780009 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2895T>A (p.Tyr965Ter) single nucleotide variant not provided [RCV003694696] Chr10:53961866 [GRCh38]
Chr10:55721626 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3009+13T>C single nucleotide variant not provided [RCV003691164] Chr10:53961739 [GRCh38]
Chr10:55721499 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4211+15del deletion not provided [RCV003579110] Chr10:53828550 [GRCh38]
Chr10:55588310 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2877T>G (p.Pro959=) single nucleotide variant not provided [RCV003696372] Chr10:53961884 [GRCh38]
Chr10:55721644 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.986-10T>C single nucleotide variant not provided [RCV003849176] Chr10:54214058 [GRCh38]
Chr10:55973818 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.92-19G>A single nucleotide variant not provided [RCV003573011] Chr10:54527896 [GRCh38]
Chr10:56287656 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3233-13T>G single nucleotide variant not provided [RCV003739304] Chr10:53938968 [GRCh38]
Chr10:55698728 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.475-2A>C single nucleotide variant not provided [RCV003716364] Chr10:54346486 [GRCh38]
Chr10:56106246 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.738C>A (p.Thr246=) single nucleotide variant not provided [RCV003574618] Chr10:54317409 [GRCh38]
Chr10:56077169 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2403A>G (p.Ser801=) single nucleotide variant not provided [RCV003547776] Chr10:54023015 [GRCh38]
Chr10:55782775 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5823C>G (p.Val1941=) single nucleotide variant not provided [RCV003696554] Chr10:53821903 [GRCh38]
Chr10:55581663 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3373+16T>G single nucleotide variant not provided [RCV003714103] Chr10:53938799 [GRCh38]
Chr10:55698559 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1917+19_1917+20insGTGTGTGGGTGT microsatellite not provided [RCV003545260] Chr10:54132855..54132856 [GRCh38]
Chr10:55892615..55892616 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1147A>G (p.Ile383Val) single nucleotide variant not provided [RCV003828830] Chr10:54195841 [GRCh38]
Chr10:55955601 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.2058G>T (p.Leu686=) single nucleotide variant not provided [RCV003579459] Chr10:54079364 [GRCh38]
Chr10:55839124 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1047C>A (p.Leu349=) single nucleotide variant not provided [RCV003579577] Chr10:54213987 [GRCh38]
Chr10:55973747 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1440+14G>C single nucleotide variant not provided [RCV003687906] Chr10:54185120 [GRCh38]
Chr10:55944880 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2526+15G>A single nucleotide variant not provided [RCV003740394] Chr10:54022877 [GRCh38]
Chr10:55782637 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1306-9T>C single nucleotide variant not provided [RCV003576922] Chr10:54185277 [GRCh38]
Chr10:55945037 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1387_1396del (p.Leu463fs) deletion not provided [RCV003576348] Chr10:54185178..54185187 [GRCh38]
Chr10:55944938..55944947 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.92-18G>A single nucleotide variant not provided [RCV003738790] Chr10:54527895 [GRCh38]
Chr10:56287655 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1997+14G>T single nucleotide variant not provided [RCV003661122] Chr10:54089970 [GRCh38]
Chr10:55849730 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2752-6T>C single nucleotide variant not provided [RCV003574307] Chr10:53995771 [GRCh38]
Chr10:55755531 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3060C>T (p.Ala1020=) single nucleotide variant not provided [RCV003694880] Chr10:53959794 [GRCh38]
Chr10:55719554 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4596_4599dup (p.Ser1534fs) duplication not provided [RCV003578240] Chr10:53823126..53823127 [GRCh38]
Chr10:55582886..55582887 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.1215G>A (p.Leu405=) single nucleotide variant not provided [RCV003687370] Chr10:54195773 [GRCh38]
Chr10:55955533 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4311G>T (p.Pro1437=) single nucleotide variant not provided [RCV003713715] Chr10:53827449 [GRCh38]
Chr10:55587209 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4367+18del deletion not provided [RCV003574337] Chr10:53827375 [GRCh38]
Chr10:55587135 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2638T>C (p.Leu880=) single nucleotide variant not provided [RCV003578274] Chr10:54020305 [GRCh38]
Chr10:55780065 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3315T>C (p.Leu1105=) single nucleotide variant not provided [RCV003694331] Chr10:53938873 [GRCh38]
Chr10:55698633 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5325_5332del (p.Leu1776fs) deletion not provided [RCV003714402] Chr10:53822394..53822401 [GRCh38]
Chr10:55582154..55582161 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1441-17T>G single nucleotide variant not provided [RCV003544298] Chr10:54183610 [GRCh38]
Chr10:55943370 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2869-13A>C single nucleotide variant not provided [RCV003881161] Chr10:53961905 [GRCh38]
Chr10:55721665 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1918-1G>A single nucleotide variant not provided [RCV003695460] Chr10:54090064 [GRCh38]
Chr10:55849824 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.319-4G>T single nucleotide variant not provided [RCV003546406] Chr10:54369279 [GRCh38]
Chr10:56129039 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2278A>G (p.Asn760Asp) single nucleotide variant not provided [RCV003488190] Chr10:54023140 [GRCh38]
Chr10:55782900 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.435C>T (p.Pro145=) single nucleotide variant not provided [RCV003713982] Chr10:54369159 [GRCh38]
Chr10:56128919 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3806+1G>T single nucleotide variant not provided [RCV003686994] Chr10:53857174 [GRCh38]
Chr10:55616934 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.474+12T>C single nucleotide variant not provided [RCV003660086] Chr10:54369108 [GRCh38]
Chr10:56128868 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1957_1960del (p.Glu653fs) deletion not provided [RCV003547857] Chr10:54090021..54090024 [GRCh38]
Chr10:55849781..55849784 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.1006C>A (p.Arg336=) single nucleotide variant not provided [RCV003695074] Chr10:54214028 [GRCh38]
Chr10:55973788 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5716_5718del (p.Asn1906del) deletion not provided [RCV003573202] Chr10:53822008..53822010 [GRCh38]
Chr10:55581768..55581770 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1470T>C (p.Ser490=) single nucleotide variant not provided [RCV003575464] Chr10:54183564 [GRCh38]
Chr10:55943324 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1440+17T>C single nucleotide variant not provided [RCV003739154] Chr10:54185117 [GRCh38]
Chr10:55944877 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2184G>T (p.Val728=) single nucleotide variant not provided [RCV003578489] Chr10:54066793 [GRCh38]
Chr10:55826553 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3726G>A (p.Val1242=) single nucleotide variant not provided [RCV003712789] Chr10:53857255 [GRCh38]
Chr10:55617015 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5061T>C (p.Pro1687=) single nucleotide variant not provided [RCV003577934] Chr10:53822665 [GRCh38]
Chr10:55582425 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.876+14T>C single nucleotide variant not provided [RCV003714914] Chr10:54317257 [GRCh38]
Chr10:56077017 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4482_4506dup (p.Lys1503delinsValSerSerCysArgArgIleThrTer) duplication not provided [RCV003689486] Chr10:53823219..53823220 [GRCh38]
Chr10:55582979..55582980 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.318+16del deletion not provided [RCV003882311] Chr10:54378766 [GRCh38]
Chr10:56138526 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.4119A>G (p.Thr1373=) single nucleotide variant not provided [RCV003712928] Chr10:53831398 [GRCh38]
Chr10:55591158 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3010-8T>G single nucleotide variant not provided [RCV003830068] Chr10:53959852 [GRCh38]
Chr10:55719612 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1917+11T>G single nucleotide variant not provided [RCV003577087] Chr10:54132864 [GRCh38]
Chr10:55892624 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4836T>G (p.Thr1612=) single nucleotide variant not provided [RCV003693494] Chr10:53822890 [GRCh38]
Chr10:55582650 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.472G>T (p.Glu158Ter) single nucleotide variant not provided [RCV003572369] Chr10:54369122 [GRCh38]
Chr10:56128882 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.4029G>T (p.Pro1343=) single nucleotide variant not provided [RCV003663410] Chr10:53831488 [GRCh38]
Chr10:55591248 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5307_5342del (p.Asp1770_Pro1781del) deletion not provided [RCV003577950] Chr10:53822384..53822419 [GRCh38]
Chr10:55582144..55582179 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3973G>T (p.Glu1325Ter) single nucleotide variant not provided [RCV003692379] Chr10:53840330 [GRCh38]
Chr10:55600090 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.5257_5286del (p.Ile1753_Pro1762del) deletion not provided [RCV003713392] Chr10:53822440..53822469 [GRCh38]
Chr10:55582200..55582229 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1617G>A (p.Gly539=) single nucleotide variant not provided [RCV003687918] Chr10:54153267 [GRCh38]
Chr10:55913027 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2160T>A (p.Tyr720Ter) single nucleotide variant not provided [RCV003695887] Chr10:54066817 [GRCh38]
Chr10:55826577 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2904T>C (p.Asp968=) single nucleotide variant not provided [RCV003690892] Chr10:53961857 [GRCh38]
Chr10:55721617 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2394T>C (p.Pro798=) single nucleotide variant not provided [RCV003690585] Chr10:54023024 [GRCh38]
Chr10:55782784 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3788dup (p.Ile1264fs) duplication not provided [RCV003686807] Chr10:53857192..53857193 [GRCh38]
Chr10:55616952..55616953 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3983+8C>T single nucleotide variant not provided [RCV003695278] Chr10:53840312 [GRCh38]
Chr10:55600072 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3777A>T (p.Leu1259=) single nucleotide variant not provided [RCV003695944] Chr10:53857204 [GRCh38]
Chr10:55616964 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3721del (p.Ser1241fs) deletion not provided [RCV003696157] Chr10:53857260 [GRCh38]
Chr10:55617020 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3232+13_3232+14del deletion not provided [RCV003691254] Chr10:53940852..53940853 [GRCh38]
Chr10:55700612..55700613 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3984-5T>C single nucleotide variant not provided [RCV003544344] Chr10:53831538 [GRCh38]
Chr10:55591298 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1717del (p.Glu572_Met573insTer) deletion not provided [RCV003688180] Chr10:54153167 [GRCh38]
Chr10:55912927 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3807-14T>G single nucleotide variant not provided [RCV003877642] Chr10:53840510 [GRCh38]
Chr10:55600270 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3120T>G (p.Tyr1040Ter) single nucleotide variant not provided [RCV003576503] Chr10:53959734 [GRCh38]
Chr10:55719494 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.91+15A>G single nucleotide variant not provided [RCV003578167] Chr10:54664157 [GRCh38]
Chr10:56423917 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.705+19T>C single nucleotide variant not provided [RCV003576493] Chr10:54329577 [GRCh38]
Chr10:56089337 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1591-11T>C single nucleotide variant not provided [RCV003694677] Chr10:54153304 [GRCh38]
Chr10:55913064 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3009+19T>A single nucleotide variant not provided [RCV003739295] Chr10:53961733 [GRCh38]
Chr10:55721493 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1353C>A (p.Val451=) single nucleotide variant not provided [RCV003696230] Chr10:54185221 [GRCh38]
Chr10:55944981 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3374-18T>C single nucleotide variant not provided [RCV003662865] Chr10:53903388 [GRCh38]
Chr10:55663148 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4202+18G>A single nucleotide variant not provided [RCV003692890] Chr10:53831297 [GRCh38]
Chr10:55591057 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2910A>G (p.Val970=) single nucleotide variant not provided [RCV003713243] Chr10:53961851 [GRCh38]
Chr10:55721611 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1441-8T>C single nucleotide variant not provided [RCV003692631] Chr10:54183601 [GRCh38]
Chr10:55943361 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1441-11T>C single nucleotide variant not provided [RCV003692632] Chr10:54183604 [GRCh38]
Chr10:55943364 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1306-11T>G single nucleotide variant not provided [RCV003828006] Chr10:54185279 [GRCh38]
Chr10:55945039 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3316C>A (p.Arg1106=) single nucleotide variant not provided [RCV003691666] Chr10:53938872 [GRCh38]
Chr10:55698632 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3256del (p.Thr1086fs) deletion not provided [RCV003544241] Chr10:53938932 [GRCh38]
Chr10:55698692 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.158-15T>C single nucleotide variant not provided [RCV003547188] Chr10:54378957 [GRCh38]
Chr10:56138717 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3912C>G (p.Thr1304=) single nucleotide variant not provided [RCV003828548] Chr10:53840391 [GRCh38]
Chr10:55600151 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3374-8T>C single nucleotide variant not provided [RCV003693701] Chr10:53903378 [GRCh38]
Chr10:55663138 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.895A>G (p.Ile299Val) single nucleotide variant not specified [RCV003489592] Chr10:54236913 [GRCh38]
Chr10:55996673 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2532A>G (p.Lys844=) single nucleotide variant not provided [RCV003574542] Chr10:54020411 [GRCh38]
Chr10:55780171 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2091+14C>T single nucleotide variant not provided [RCV003880123] Chr10:54079317 [GRCh38]
Chr10:55839077 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2220+19T>C single nucleotide variant not provided [RCV003661871] Chr10:54066738 [GRCh38]
Chr10:55826498 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.706-20T>C single nucleotide variant not provided [RCV003879843] Chr10:54317461 [GRCh38]
Chr10:56077221 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3597A>C (p.Thr1199=) single nucleotide variant not provided [RCV003692373] Chr10:53866762 [GRCh38]
Chr10:55626522 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.91+15A>T single nucleotide variant not provided [RCV003692746] Chr10:54664157 [GRCh38]
Chr10:56423917 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3009+19T>C single nucleotide variant not provided [RCV003876825] Chr10:53961733 [GRCh38]
Chr10:55721493 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4729_4736del (p.Ser1577fs) microsatellite not provided [RCV003687267] Chr10:53822990..53822997 [GRCh38]
Chr10:55582750..55582757 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2527-13C>T single nucleotide variant not provided [RCV003688365] Chr10:54020429 [GRCh38]
Chr10:55780189 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2712A>G (p.Thr904=) single nucleotide variant not provided [RCV003661955] Chr10:54020231 [GRCh38]
Chr10:55779991 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3232+18T>C single nucleotide variant not provided [RCV003576291] Chr10:53940848 [GRCh38]
Chr10:55700608 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1665C>T (p.Asp555=) single nucleotide variant not provided [RCV003660443] Chr10:54153219 [GRCh38]
Chr10:55912979 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4344T>C (p.Tyr1448=) single nucleotide variant not provided [RCV003544865] Chr10:53827416 [GRCh38]
Chr10:55587176 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.158-9G>T single nucleotide variant not provided [RCV003574018] Chr10:54378951 [GRCh38]
Chr10:56138711 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1099-16T>C single nucleotide variant not provided [RCV003878740] Chr10:54195905 [GRCh38]
Chr10:55955665 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4182G>T (p.Val1394=) single nucleotide variant not provided [RCV003826199] Chr10:53831335 [GRCh38]
Chr10:55591095 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4559del (p.Asp1520fs) deletion not provided [RCV003687804] Chr10:53823167 [GRCh38]
Chr10:55582927 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.4416C>T (p.Val1472=) single nucleotide variant not provided [RCV003687786] Chr10:53823310 [GRCh38]
Chr10:55583070 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1002C>T (p.Tyr334=) single nucleotide variant not provided [RCV003575719] Chr10:54214032 [GRCh38]
Chr10:55973792 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2751+18C>T single nucleotide variant not provided [RCV003686618] Chr10:54020174 [GRCh38]
Chr10:55779934 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2334C>T (p.Asn778=) single nucleotide variant not provided [RCV003714271] Chr10:54023084 [GRCh38]
Chr10:55782844 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.909A>T (p.Pro303=) single nucleotide variant not provided [RCV003714234] Chr10:54236899 [GRCh38]
Chr10:55996659 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.444G>A (p.Lys148=) single nucleotide variant not provided [RCV003662477] Chr10:54369150 [GRCh38]
Chr10:56128910 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3010-15T>C single nucleotide variant not provided [RCV003689478] Chr10:53959859 [GRCh38]
Chr10:55719619 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1441-13T>C single nucleotide variant not provided [RCV003880018] Chr10:54183606 [GRCh38]
Chr10:55943366 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.594+19G>A single nucleotide variant not provided [RCV003543937] Chr10:54346346 [GRCh38]
Chr10:56106106 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1785-8C>T single nucleotide variant not provided [RCV003572271] Chr10:54133015 [GRCh38]
Chr10:55892775 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1099-20del deletion not provided [RCV003572290] Chr10:54195909 [GRCh38]
Chr10:55955669 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.3233-16G>A single nucleotide variant not provided [RCV003572428] Chr10:53938971 [GRCh38]
Chr10:55698731 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1785-8C>A single nucleotide variant not provided [RCV003573772] Chr10:54133015 [GRCh38]
Chr10:55892775 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3009+20A>G single nucleotide variant not provided [RCV003698560] Chr10:53961732 [GRCh38]
Chr10:55721492 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1866C>T (p.Ser622=) single nucleotide variant not provided [RCV003549913] Chr10:54132926 [GRCh38]
Chr10:55892686 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.723G>C (p.Leu241=) single nucleotide variant not provided [RCV003716779] Chr10:54317424 [GRCh38]
Chr10:56077184 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3864C>T (p.Ser1288=) single nucleotide variant not provided [RCV003696906] Chr10:53840439 [GRCh38]
Chr10:55600199 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.117A>T (p.Pro39=) single nucleotide variant not provided [RCV003833050] Chr10:54527852 [GRCh38]
Chr10:56287612 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4367+15C>G single nucleotide variant not provided [RCV003698017] Chr10:53827378 [GRCh38]
Chr10:55587138 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1918-20A>T single nucleotide variant not provided [RCV003665602] Chr10:54090083 [GRCh38]
Chr10:55849843 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5757C>T (p.Cys1919=) single nucleotide variant not provided [RCV003697087] Chr10:53821969 [GRCh38]
Chr10:55581729 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.92A>T (p.Asp31Val) single nucleotide variant not provided [RCV003579815] Chr10:54527877 [GRCh38]
Chr10:56287637 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4212-17T>C single nucleotide variant not provided [RCV003664571] Chr10:53827565 [GRCh38]
Chr10:55587325 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4887A>G (p.Glu1629=) single nucleotide variant not provided [RCV003549209] Chr10:53822839 [GRCh38]
Chr10:55582599 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.391del (p.His131fs) deletion not provided [RCV003549162] Chr10:54369203 [GRCh38]
Chr10:56128963 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.876+17C>G single nucleotide variant not provided [RCV003697063] Chr10:54317254 [GRCh38]
Chr10:56077014 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1725C>G (p.Val575=) single nucleotide variant not provided [RCV003850811] Chr10:54153159 [GRCh38]
Chr10:55912919 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3233-11T>G single nucleotide variant not provided [RCV003810655] Chr10:53938966 [GRCh38]
Chr10:55698726 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3960C>A (p.Ala1320=) single nucleotide variant not provided [RCV003664975] Chr10:53840343 [GRCh38]
Chr10:55600103 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3918T>A (p.Cys1306Ter) single nucleotide variant not provided [RCV003697452] Chr10:53840385 [GRCh38]
Chr10:55600145 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.5827G>T (p.Gly1943Ter) single nucleotide variant not provided [RCV003580382] Chr10:53821899 [GRCh38]
Chr10:55581659 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3373+19A>G single nucleotide variant not provided [RCV003548726] Chr10:53938796 [GRCh38]
Chr10:55698556 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.378C>G (p.Gly126=) single nucleotide variant not provided [RCV003673588] Chr10:54369216 [GRCh38]
Chr10:56128976 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1917+7T>A single nucleotide variant not provided [RCV003702508] Chr10:54132868 [GRCh38]
Chr10:55892628 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5079T>C (p.Pro1693=) single nucleotide variant not provided [RCV003673268] Chr10:53822647 [GRCh38]
Chr10:55582407 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.158-13C>T single nucleotide variant not provided [RCV003670145] Chr10:54378955 [GRCh38]
Chr10:56138715 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001354404.2(PCDH15):c.-156+27658C>T single nucleotide variant not specified [RCV004510132] Chr10:55599967 [GRCh38]
Chr10:57359727 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3364C>T (p.Pro1122Ser) single nucleotide variant not provided [RCV003668190] Chr10:53938824 [GRCh38]
Chr10:55698584 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5814C>T (p.Asn1938=) single nucleotide variant not provided [RCV003699384] Chr10:53821912 [GRCh38]
Chr10:55581672 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1281A>G (p.Val427=) single nucleotide variant not provided [RCV003703529] Chr10:54195707 [GRCh38]
Chr10:55955467 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.381T>A (p.Thr127=) single nucleotide variant not provided [RCV003840463] Chr10:54369213 [GRCh38]
Chr10:56128973 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5046del (p.Glu1682fs) deletion not provided [RCV003723429] Chr10:53822680 [GRCh38]
Chr10:55582440 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4365A>G (p.Ser1455=) single nucleotide variant not provided [RCV003700322] Chr10:53827395 [GRCh38]
Chr10:55587155 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.876+12C>T single nucleotide variant not provided [RCV003559962] Chr10:54317259 [GRCh38]
Chr10:56077019 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.741C>T (p.Thr247=) single nucleotide variant not provided [RCV003580711] Chr10:54317406 [GRCh38]
Chr10:56077166 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4293A>G (p.Pro1431=) single nucleotide variant not provided [RCV003562119] Chr10:53827467 [GRCh38]
Chr10:55587227 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3718-19C>T single nucleotide variant not provided [RCV003659065] Chr10:53857282 [GRCh38]
Chr10:55617042 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5859T>C (p.Thr1953=) single nucleotide variant not provided [RCV003548620] Chr10:53821867 [GRCh38]
Chr10:55581627 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1998-5A>G single nucleotide variant not provided [RCV003699486] Chr10:54079429 [GRCh38]
Chr10:55839189 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5516_5519del (p.Glu1839fs) deletion not provided [RCV003699517] Chr10:53822207..53822210 [GRCh38]
Chr10:55581967..55581970 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.126C>T (p.Thr42=) single nucleotide variant not provided [RCV003665081] Chr10:54527843 [GRCh38]
Chr10:56287603 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1768C>G (p.Pro590Ala) single nucleotide variant not provided [RCV003856371] Chr10:54153116 [GRCh38]
Chr10:55912876 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2781T>C (p.Ser927=) single nucleotide variant not provided [RCV003562140] Chr10:53995736 [GRCh38]
Chr10:55755496 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.876+17C>A single nucleotide variant not provided [RCV003560201] Chr10:54317254 [GRCh38]
Chr10:56077014 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1593C>T (p.Leu531=) single nucleotide variant not provided [RCV003851622] Chr10:54153291 [GRCh38]
Chr10:55913051 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1440+13T>G single nucleotide variant not provided [RCV003703107] Chr10:54185121 [GRCh38]
Chr10:55944881 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1441-10C>T single nucleotide variant not provided [RCV003833118] Chr10:54183603 [GRCh38]
Chr10:55943363 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2527-16C>G single nucleotide variant not provided [RCV003580426] Chr10:54020432 [GRCh38]
Chr10:55780192 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4410_4413dup (p.Val1472fs) duplication not provided [RCV003856824] Chr10:53823312..53823313 [GRCh38]
Chr10:55583072..55583073 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3374-2A>G single nucleotide variant not provided [RCV003557506] Chr10:53903372 [GRCh38]
Chr10:55663132 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.2752-15A>G single nucleotide variant not provided [RCV003548743] Chr10:53995780 [GRCh38]
Chr10:55755540 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3502-10C>T single nucleotide variant not provided [RCV003725759] Chr10:53866867 [GRCh38]
Chr10:55626627 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.985+19T>G single nucleotide variant not provided [RCV003674331] Chr10:54236804 [GRCh38]
Chr10:55996564 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1305+11T>C single nucleotide variant not provided [RCV003855585] Chr10:54195672 [GRCh38]
Chr10:55955432 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1098+7T>C single nucleotide variant not provided [RCV003725714] Chr10:54213929 [GRCh38]
Chr10:55973689 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4367+15C>T single nucleotide variant not provided [RCV003702722] Chr10:53827378 [GRCh38]
Chr10:55587138 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3122+13G>T single nucleotide variant not provided [RCV003557957] Chr10:53959719 [GRCh38]
Chr10:55719479 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5148_5149del (p.Glu1716fs) microsatellite not provided [RCV003668372] Chr10:53822577..53822578 [GRCh38]
Chr10:55582337..55582338 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.319-15A>C single nucleotide variant not provided [RCV003855535] Chr10:54369290 [GRCh38]
Chr10:56129050 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5340T>A (p.Pro1780=) single nucleotide variant not provided [RCV003669884] Chr10:53822386 [GRCh38]
Chr10:55582146 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3373+14C>A single nucleotide variant not provided [RCV003673840] Chr10:53938801 [GRCh38]
Chr10:55698561 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1201C>T (p.Gln401Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV004574181]|not provided [RCV003672441] Chr10:54195787 [GRCh38]
Chr10:55955547 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.1784+14G>C single nucleotide variant not provided [RCV003855476] Chr10:54153086 [GRCh38]
Chr10:55912846 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2221-16T>A single nucleotide variant not provided [RCV003674244] Chr10:54023213 [GRCh38]
Chr10:55782973 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1917+11T>C single nucleotide variant not provided [RCV003816356] Chr10:54132864 [GRCh38]
Chr10:55892624 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5272_5355del (p.Pro1758_Ser1785del) deletion not provided [RCV003674073] Chr10:53822371..53822454 [GRCh38]
Chr10:55582131..55582214 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.475-16T>C single nucleotide variant not provided [RCV003668789] Chr10:54346500 [GRCh38]
Chr10:56106260 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3373+14C>T single nucleotide variant not provided [RCV003580000] Chr10:53938801 [GRCh38]
Chr10:55698561 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5263CCT[1] (p.Pro1756del) microsatellite not provided [RCV003667898] Chr10:53822458..53822460 [GRCh38]
Chr10:55582218..55582220 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2117T>C (p.Val706Ala) single nucleotide variant not provided [RCV003671890] Chr10:54066860 [GRCh38]
Chr10:55826620 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.877-16T>C single nucleotide variant not provided [RCV003816464] Chr10:54236947 [GRCh38]
Chr10:55996707 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.120A>G (p.Pro40=) single nucleotide variant not provided [RCV003558297] Chr10:54527849 [GRCh38]
Chr10:56287609 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1785-14C>T single nucleotide variant not provided [RCV003849960] Chr10:54133021 [GRCh38]
Chr10:55892781 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3806+20T>C single nucleotide variant not provided [RCV003667702] Chr10:53857155 [GRCh38]
Chr10:55616915 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3570G>A (p.Glu1190=) single nucleotide variant not provided [RCV003559599] Chr10:53866789 [GRCh38]
Chr10:55626549 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.582T>C (p.Asn194=) single nucleotide variant not provided [RCV003700417] Chr10:54346377 [GRCh38]
Chr10:56106137 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4368-3141_4368-3139del microsatellite not provided [RCV003671980] Chr10:53823369..53823371 [GRCh38]
Chr10:55583129..55583131 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3373+12T>G single nucleotide variant not provided [RCV003672670] Chr10:53938803 [GRCh38]
Chr10:55698563 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2924del (p.Pro975fs) deletion not provided [RCV003557773] Chr10:53961837 [GRCh38]
Chr10:55721597 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.475-9T>A single nucleotide variant not provided [RCV003673682] Chr10:54346493 [GRCh38]
Chr10:56106253 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1590+12C>T single nucleotide variant not provided [RCV003717902] Chr10:54183432 [GRCh38]
Chr10:55943192 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.876+12C>G single nucleotide variant not provided [RCV003834892] Chr10:54317259 [GRCh38]
Chr10:56077019 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3984-18A>G single nucleotide variant not provided [RCV003838210] Chr10:53831551 [GRCh38]
Chr10:55591311 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.876+17C>T single nucleotide variant not provided [RCV003669806] Chr10:54317254 [GRCh38]
Chr10:56077014 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5033C>G (p.Ser1678Ter) single nucleotide variant not provided [RCV003849421] Chr10:53822693 [GRCh38]
Chr10:55582453 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1590+8C>G single nucleotide variant not provided [RCV003726209] Chr10:54183436 [GRCh38]
Chr10:55943196 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4203-7C>A single nucleotide variant not provided [RCV003670239] Chr10:53828580 [GRCh38]
Chr10:55588340 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4437_4452dup (p.Phe1485fs) duplication not provided [RCV003701795] Chr10:53823273..53823274 [GRCh38]
Chr10:55583033..55583034 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.1551T>C (p.Tyr517=) single nucleotide variant not provided [RCV003666079] Chr10:54183483 [GRCh38]
Chr10:55943243 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.594+12C>G single nucleotide variant not provided [RCV003701401] Chr10:54346353 [GRCh38]
Chr10:56106113 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.672T>C (p.Asp224=) single nucleotide variant not provided [RCV003701847] Chr10:54329629 [GRCh38]
Chr10:56089389 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.813G>C (p.Val271=) single nucleotide variant not provided [RCV003855117] Chr10:54317334 [GRCh38]
Chr10:56077094 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1998-15T>C single nucleotide variant not provided [RCV003832999] Chr10:54079439 [GRCh38]
Chr10:55839199 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3233-18T>C single nucleotide variant not provided [RCV003724293] Chr10:53938973 [GRCh38]
Chr10:55698733 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.708C>T (p.Asp236=) single nucleotide variant not provided [RCV003835494] Chr10:54317439 [GRCh38]
Chr10:56077199 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4305C>G (p.Pro1435=) single nucleotide variant not provided [RCV003666551] Chr10:53827455 [GRCh38]
Chr10:55587215 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2527-19A>G single nucleotide variant not provided [RCV003724108] Chr10:54020435 [GRCh38]
Chr10:55780195 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4284T>C (p.Ala1428=) single nucleotide variant not provided [RCV003702458] Chr10:53827476 [GRCh38]
Chr10:55587236 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1305+3_1305+6dup duplication not provided [RCV003837300] Chr10:54195676..54195677 [GRCh38]
Chr10:55955436..55955437 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5092T>C (p.Leu1698=) single nucleotide variant not provided [RCV003699291] Chr10:53822634 [GRCh38]
Chr10:55582394 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3806+16T>C single nucleotide variant not provided [RCV003836153] Chr10:53857159 [GRCh38]
Chr10:55616919 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4965T>C (p.Ser1655=) single nucleotide variant not provided [RCV003580694] Chr10:53822761 [GRCh38]
Chr10:55582521 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5020_5042dup (p.Glu1682fs) duplication not provided [RCV003697441] Chr10:53822683..53822684 [GRCh38]
Chr10:55582443..55582444 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1926T>A (p.Asp642Glu) single nucleotide variant not provided [RCV003700853] Chr10:54090055 [GRCh38]
Chr10:55849815 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4201C>T (p.Gln1401Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV004574132]|not provided [RCV003580271] Chr10:53831316 [GRCh38]
Chr10:55591076 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_001384140.1(PCDH15):c.567T>C (p.Tyr189=) single nucleotide variant not provided [RCV003816624] Chr10:54346392 [GRCh38]
Chr10:56106152 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1591-19T>C single nucleotide variant not provided [RCV003816629] Chr10:54153312 [GRCh38]
Chr10:55913072 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2221-5A>G single nucleotide variant not provided [RCV003659582] Chr10:54023202 [GRCh38]
Chr10:55782962 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4897_4909dup (p.Glu1637fs) duplication not provided [RCV003580928] Chr10:53822816..53822817 [GRCh38]
Chr10:55582576..55582577 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3753T>A (p.Ile1251=) single nucleotide variant not provided [RCV003566364] Chr10:53857228 [GRCh38]
Chr10:55616988 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5160T>C (p.Cys1720=) single nucleotide variant not provided [RCV003542093] Chr10:53822566 [GRCh38]
Chr10:55582326 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.110del (p.Gly37fs) deletion not provided [RCV003552284] Chr10:54527859 [GRCh38]
Chr10:56287619 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.4191C>G (p.Val1397=) single nucleotide variant not provided [RCV003552286] Chr10:53831326 [GRCh38]
Chr10:55591086 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2556G>A (p.Val852=) single nucleotide variant not provided [RCV003708409] Chr10:54020387 [GRCh38]
Chr10:55780147 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4367+12G>T single nucleotide variant not provided [RCV003731235] Chr10:53827381 [GRCh38]
Chr10:55587141 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4382_4385dup (p.His1462fs) duplication not provided [RCV003729844] Chr10:53823340..53823341 [GRCh38]
Chr10:55583100..55583101 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3502-18T>G single nucleotide variant not provided [RCV003678166] Chr10:53866875 [GRCh38]
Chr10:55626635 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3718-11T>C single nucleotide variant not provided [RCV003730765] Chr10:53857274 [GRCh38]
Chr10:55617034 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3167del (p.Gly1056fs) deletion not provided [RCV003567008] Chr10:53940931 [GRCh38]
Chr10:55700691 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.573T>C (p.Ile191=) single nucleotide variant not provided [RCV003567014] Chr10:54346386 [GRCh38]
Chr10:56106146 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1087T>C (p.Leu363=) single nucleotide variant not provided [RCV003677252] Chr10:54213947 [GRCh38]
Chr10:55973707 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4367+12G>A single nucleotide variant not provided [RCV003562672] Chr10:53827381 [GRCh38]
Chr10:55587141 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4367+10C>A single nucleotide variant not provided [RCV003680139] Chr10:53827383 [GRCh38]
Chr10:55587143 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3221_3222del (p.Gly1074fs) deletion not provided [RCV003567924] Chr10:53940876..53940877 [GRCh38]
Chr10:55700636..55700637 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.4296G>A (p.Val1432=) single nucleotide variant not provided [RCV003681962] Chr10:53827464 [GRCh38]
Chr10:55587224 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5715A>G (p.Lys1905=) single nucleotide variant not provided [RCV003683473] Chr10:53822011 [GRCh38]
Chr10:55581771 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.519C>T (p.Asp173=) single nucleotide variant not provided [RCV003704018] Chr10:54346440 [GRCh38]
Chr10:56106200 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.186C>A (p.Ile62=) single nucleotide variant not provided [RCV003563655] Chr10:54378914 [GRCh38]
Chr10:56138674 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2092-12T>G single nucleotide variant not provided [RCV003858492] Chr10:54066897 [GRCh38]
Chr10:55826657 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2526+20T>A single nucleotide variant not provided [RCV003565072] Chr10:54022872 [GRCh38]
Chr10:55782632 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2217A>G (p.Val739=) single nucleotide variant not provided [RCV003858775] Chr10:54066760 [GRCh38]
Chr10:55826520 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3980T>A (p.Phe1327Tyr) single nucleotide variant not provided [RCV003858038] Chr10:53840323 [GRCh38]
Chr10:55600083 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1784+18C>G single nucleotide variant not provided [RCV003822240] Chr10:54153082 [GRCh38]
Chr10:55912842 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5220del (p.Ser1741fs) deletion not provided [RCV003566080] Chr10:53822506 [GRCh38]
Chr10:55582266 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3270T>G (p.Tyr1090Ter) single nucleotide variant not provided [RCV003678834] Chr10:53938918 [GRCh38]
Chr10:55698678 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.1784+16A>T single nucleotide variant not provided [RCV003675605] Chr10:54153084 [GRCh38]
Chr10:55912844 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2298A>G (p.Thr766=) single nucleotide variant not provided [RCV003682148] Chr10:54023120 [GRCh38]
Chr10:55782880 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4954C>T (p.Gln1652Ter) single nucleotide variant not provided [RCV003707918] Chr10:53822772 [GRCh38]
Chr10:55582532 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2751+13G>T single nucleotide variant not provided [RCV003846831] Chr10:54020179 [GRCh38]
Chr10:55779939 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.319-10T>C single nucleotide variant not provided [RCV003680392] Chr10:54369285 [GRCh38]
Chr10:56129045 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3502-11C>A single nucleotide variant not provided [RCV003732429] Chr10:53866868 [GRCh38]
Chr10:55626628 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.158-14T>C single nucleotide variant not provided [RCV003732430] Chr10:54378956 [GRCh38]
Chr10:56138716 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4238del (p.Ala1413fs) deletion not provided [RCV003704381] Chr10:53827522 [GRCh38]
Chr10:55587282 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.4278G>A (p.Val1426=) single nucleotide variant not provided [RCV003563063] Chr10:53827482 [GRCh38]
Chr10:55587242 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5138_5139del (p.Leu1712_Ser1713insTer) microsatellite not provided [RCV003564265] Chr10:53822587..53822588 [GRCh38]
Chr10:55582347..55582348 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2256G>A (p.Val752=) single nucleotide variant not provided [RCV003859681] Chr10:54023162 [GRCh38]
Chr10:55782922 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3507T>C (p.Thr1169=) single nucleotide variant not provided [RCV003562802] Chr10:53866852 [GRCh38]
Chr10:55626612 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3207C>A (p.Tyr1069Ter) single nucleotide variant not provided [RCV003552825] Chr10:53940891 [GRCh38]
Chr10:55700651 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.4587T>C (p.Tyr1529=) single nucleotide variant not provided [RCV003566591] Chr10:53823139 [GRCh38]
Chr10:55582899 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1998-4del deletion not provided [RCV003551069] Chr10:54079428 [GRCh38]
Chr10:55839188 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.475-4T>G single nucleotide variant not provided [RCV003709022] Chr10:54346488 [GRCh38]
Chr10:56106248 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.877-15T>A single nucleotide variant not provided [RCV003709860] Chr10:54236946 [GRCh38]
Chr10:55996706 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4546_4565dup (p.Leu1522fs) duplication not provided [RCV003711476] Chr10:53823160..53823161 [GRCh38]
Chr10:55582920..55582921 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.3234T>C (p.Asp1078=) single nucleotide variant not provided [RCV003707530] Chr10:53938954 [GRCh38]
Chr10:55698714 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.711T>C (p.Arg237=) single nucleotide variant not provided [RCV003555690] Chr10:54317436 [GRCh38]
Chr10:56077196 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1773T>G (p.Pro591=) single nucleotide variant not provided [RCV003706177] Chr10:54153111 [GRCh38]
Chr10:55912871 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5622C>T (p.Asp1874=) single nucleotide variant not provided [RCV003566108] Chr10:53822104 [GRCh38]
Chr10:55581864 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4599A>C (p.Ile1533=) single nucleotide variant not provided [RCV003566129] Chr10:53823127 [GRCh38]
Chr10:55582887 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2527-14_2527-12del microsatellite not provided [RCV003555723] Chr10:54020428..54020430 [GRCh38]
Chr10:55780188..55780190 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1440+14G>A single nucleotide variant not provided [RCV003679330] Chr10:54185120 [GRCh38]
Chr10:55944880 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3502-15_3502-14del deletion not provided [RCV003712165] Chr10:53866871..53866872 [GRCh38]
Chr10:55626631..55626632 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.468G>A (p.Val156=) single nucleotide variant not provided [RCV003563549] Chr10:54369126 [GRCh38]
Chr10:56128886 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5601A>G (p.Thr1867=) single nucleotide variant not provided [RCV003843343] Chr10:53822125 [GRCh38]
Chr10:55581885 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5136C>T (p.Leu1712=) single nucleotide variant not provided [RCV003551623] Chr10:53822590 [GRCh38]
Chr10:55582350 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3210C>A (p.Ser1070=) single nucleotide variant not provided [RCV003552763] Chr10:53940888 [GRCh38]
Chr10:55700648 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.706-20T>G single nucleotide variant not provided [RCV003711831] Chr10:54317461 [GRCh38]
Chr10:56077221 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.975del (p.Ile326fs) deletion not provided [RCV003706454] Chr10:54236833 [GRCh38]
Chr10:55996593 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.1729C>A (p.Arg577=) single nucleotide variant not provided [RCV003705693] Chr10:54153155 [GRCh38]
Chr10:55912915 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2226A>G (p.Thr742=) single nucleotide variant not provided [RCV003682643] Chr10:54023192 [GRCh38]
Chr10:55782952 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2985T>C (p.Asn995=) single nucleotide variant not provided [RCV003840657] Chr10:53961776 [GRCh38]
Chr10:55721536 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.240T>C (p.Asn80=) single nucleotide variant not provided [RCV003563212] Chr10:54378860 [GRCh38]
Chr10:56138620 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.595-13T>G single nucleotide variant not provided [RCV003734767] Chr10:54329719 [GRCh38]
Chr10:56089479 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.474+20C>G single nucleotide variant not provided [RCV003707705] Chr10:54369100 [GRCh38]
Chr10:56128860 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1591-14A>C single nucleotide variant not provided [RCV003674519] Chr10:54153307 [GRCh38]
Chr10:55913067 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2617G>T (p.Glu873Ter) single nucleotide variant not provided [RCV003551699] Chr10:54020326 [GRCh38]
Chr10:55780086 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.4159T>C (p.Cys1387Arg) single nucleotide variant not provided [RCV003557504] Chr10:53831358 [GRCh38]
Chr10:55591118 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3964del (p.Asp1322fs) deletion not provided [RCV003557505] Chr10:53840339 [GRCh38]
Chr10:55600099 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.75G>A (p.Leu25=) single nucleotide variant not provided [RCV003550371] Chr10:54664188 [GRCh38]
Chr10:56423948 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3924G>A (p.Leu1308=) single nucleotide variant not provided [RCV003563535] Chr10:53840379 [GRCh38]
Chr10:55600139 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.876+14T>G single nucleotide variant not provided [RCV003675998] Chr10:54317257 [GRCh38]
Chr10:56077017 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.12G>A (p.Gln4=) single nucleotide variant not provided [RCV003721091] Chr10:54664251 [GRCh38]
Chr10:56424011 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.47T>C (p.Ile16Thr) single nucleotide variant not provided [RCV003557532] Chr10:54664216 [GRCh38]
Chr10:56423976 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.1539C>T (p.Ser513=) single nucleotide variant not provided [RCV003818657] Chr10:54183495 [GRCh38]
Chr10:55943255 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1306-14A>T single nucleotide variant not provided [RCV003705435] Chr10:54185282 [GRCh38]
Chr10:55945042 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4368-3155_4368-3147del deletion not provided [RCV003552623] Chr10:53823377..53823385 [GRCh38]
Chr10:55583137..55583145 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2043T>C (p.Thr681=) single nucleotide variant not provided [RCV003552683] Chr10:54079379 [GRCh38]
Chr10:55839139 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1784+13A>G single nucleotide variant not provided [RCV003719597] Chr10:54153087 [GRCh38]
Chr10:55912847 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4821T>C (p.Ala1607=) single nucleotide variant not provided [RCV003562826] Chr10:53822905 [GRCh38]
Chr10:55582665 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.877-21CT[2] microsatellite not provided [RCV003871905] Chr10:54236947..54236948 [GRCh38]
Chr10:55996707..55996708 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1441-12C>G single nucleotide variant not provided [RCV003736301] Chr10:54183605 [GRCh38]
Chr10:55943365 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2869-5T>C single nucleotide variant not provided [RCV003685416] Chr10:53961897 [GRCh38]
Chr10:55721657 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2752-20C>T single nucleotide variant not provided [RCV003872114] Chr10:53995785 [GRCh38]
Chr10:55755545 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1639G>T (p.Glu547Ter) single nucleotide variant not provided [RCV003683827] Chr10:54153245 [GRCh38]
Chr10:55913005 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.2869-13A>G single nucleotide variant not provided [RCV003685070] Chr10:53961905 [GRCh38]
Chr10:55721665 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1998-21GTTT[4] microsatellite not provided [RCV003870416] Chr10:54079433..54079434 [GRCh38]
Chr10:55839193..55839194 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3233-13T>C single nucleotide variant not provided [RCV003719661] Chr10:53938968 [GRCh38]
Chr10:55698728 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5247del (p.Pro1750fs) deletion not provided [RCV003681907] Chr10:53822479 [GRCh38]
Chr10:55582239 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1758G>A (p.Ala586=) single nucleotide variant not provided [RCV003684885] Chr10:54153126 [GRCh38]
Chr10:55912886 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.157+20T>C single nucleotide variant not provided [RCV003685895] Chr10:54527792 [GRCh38]
Chr10:56287552 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4700_4728dup (p.Ser1577fs) duplication not provided [RCV003685950] Chr10:53822997..53822998 [GRCh38]
Chr10:55582757..55582758 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.4386T>C (p.His1462=) single nucleotide variant not provided [RCV003685980] Chr10:53823340 [GRCh38]
Chr10:55583100 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.705+19_705+29del deletion not provided [RCV003675538] Chr10:54329567..54329577 [GRCh38]
Chr10:56089327..56089337 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.877-15dup duplication not provided [RCV003704778] Chr10:54236945..54236946 [GRCh38]
Chr10:55996705..55996706 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5225_5345dup (p.Ser1782_Pro1783insPheCysLeuSerProSerProSerSerSerTyrPheSerSerPheSerSerSerCysSerCysSerSerCysSerSerSerTer) duplication not provided [RCV003564621] Chr10:53822380..53822381 [GRCh38]
Chr10:55582140..55582141 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.876+16T>C single nucleotide variant not provided [RCV003729362] Chr10:54317255 [GRCh38]
Chr10:56077015 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5616_5619dup (p.Asp1874fs) duplication not provided [RCV003551690] Chr10:53822106..53822107 [GRCh38]
Chr10:55581866..55581867 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.297C>A (p.Thr99=) single nucleotide variant not provided [RCV003711527] Chr10:54378803 [GRCh38]
Chr10:56138563 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.594+20C>T single nucleotide variant not provided [RCV003719814] Chr10:54346345 [GRCh38]
Chr10:56106105 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3502-17T>C single nucleotide variant not provided [RCV003719257] Chr10:53866874 [GRCh38]
Chr10:55626634 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4806C>A (p.Gly1602=) single nucleotide variant not provided [RCV003721507] Chr10:53822920 [GRCh38]
Chr10:55582680 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3780G>A (p.Val1260=) single nucleotide variant not provided [RCV003709801] Chr10:53857201 [GRCh38]
Chr10:55616961 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3075T>C (p.Leu1025=) single nucleotide variant not provided [RCV003684168] Chr10:53959779 [GRCh38]
Chr10:55719539 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.303A>G (p.Arg101=) single nucleotide variant not provided [RCV003737431] Chr10:54378797 [GRCh38]
Chr10:56138557 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3010-14del deletion not provided [RCV003869695] Chr10:53959858 [GRCh38]
Chr10:55719618 [GRCh37]
Chr10:10q21.1		 benign
NM_001384140.1(PCDH15):c.123T>C (p.Ala41=) single nucleotide variant not provided [RCV003674773] Chr10:54527846 [GRCh38]
Chr10:56287606 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3009+16C>T single nucleotide variant not provided [RCV003738618] Chr10:53961736 [GRCh38]
Chr10:55721496 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5673_5676dup (p.Glu1893delinsThrTer) duplication not provided [RCV003868625] Chr10:53822049..53822050 [GRCh38]
Chr10:55581809..55581810 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3334C>T (p.Leu1112=) single nucleotide variant not provided [RCV003723212] Chr10:53938854 [GRCh38]
Chr10:55698614 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5460A>G (p.Pro1820=) single nucleotide variant not provided [RCV003542958] Chr10:53822266 [GRCh38]
Chr10:55582026 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.973dup (p.Ser325fs) duplication not provided [RCV003706689] Chr10:54236834..54236835 [GRCh38]
Chr10:55996594..55996595 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.4140G>C (p.Leu1380=) single nucleotide variant not provided [RCV003684345] Chr10:53831377 [GRCh38]
Chr10:55591137 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5691T>C (p.Ala1897=) single nucleotide variant not provided [RCV003565206] Chr10:53822035 [GRCh38]
Chr10:55581795 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.877-20T>C single nucleotide variant not provided [RCV003853697] Chr10:54236951 [GRCh38]
Chr10:55996711 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.474+17T>C single nucleotide variant not provided [RCV003864214] Chr10:54369103 [GRCh38]
Chr10:56128863 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.985+12A>G single nucleotide variant not provided [RCV003727491] Chr10:54236811 [GRCh38]
Chr10:55996571 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.693A>T (p.Ile231=) single nucleotide variant not provided [RCV003563944] Chr10:54329608 [GRCh38]
Chr10:56089368 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2220+16A>G single nucleotide variant not provided [RCV003707005] Chr10:54066741 [GRCh38]
Chr10:55826501 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2319A>T (p.Thr773=) single nucleotide variant not provided [RCV003683299] Chr10:54023099 [GRCh38]
Chr10:55782859 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4368-3146A>T single nucleotide variant not provided [RCV003869030] Chr10:53823376 [GRCh38]
Chr10:55583136 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.699A>G (p.Gln233=) single nucleotide variant not provided [RCV003866827] Chr10:54329602 [GRCh38]
Chr10:56089362 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.738C>T (p.Thr246=) single nucleotide variant not provided [RCV003737821] Chr10:54317409 [GRCh38]
Chr10:56077169 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5355_5371del (p.Ile1786fs) deletion not provided [RCV003708968] Chr10:53822355..53822371 [GRCh38]
Chr10:55582115..55582131 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1785-22_1785-20del microsatellite not provided [RCV003564142] Chr10:54133027..54133029 [GRCh38]
Chr10:55892787..55892789 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2752-13T>A single nucleotide variant not provided [RCV003541977] Chr10:53995778 [GRCh38]
Chr10:55755538 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.408G>C (p.Val136=) single nucleotide variant not provided [RCV003563223] Chr10:54369186 [GRCh38]
Chr10:56128946 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1074C>T (p.His358=) single nucleotide variant not provided [RCV003564285] Chr10:54213960 [GRCh38]
Chr10:55973720 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.595-15C>G single nucleotide variant not provided [RCV003731898] Chr10:54329721 [GRCh38]
Chr10:56089481 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3807-18A>G single nucleotide variant not provided [RCV003568762] Chr10:53840514 [GRCh38]
Chr10:55600274 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4212-12A>G single nucleotide variant not provided [RCV003563191] Chr10:53827560 [GRCh38]
Chr10:55587320 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1998-13G>T single nucleotide variant not provided [RCV003555610] Chr10:54079437 [GRCh38]
Chr10:55839197 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1428T>G (p.Thr476=) single nucleotide variant not provided [RCV003563380] Chr10:54185146 [GRCh38]
Chr10:55944906 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4686T>G (p.Ser1562=) single nucleotide variant not provided [RCV003682435] Chr10:53823040 [GRCh38]
Chr10:55582800 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5798dup (p.Asn1933fs) duplication not provided [RCV003679531] Chr10:53821927..53821928 [GRCh38]
Chr10:55581687..55581688 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3219A>T (p.Ser1073=) single nucleotide variant not provided [RCV003552770] Chr10:53940879 [GRCh38]
Chr10:55700639 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1099-14C>T single nucleotide variant not provided [RCV003726786] Chr10:54195903 [GRCh38]
Chr10:55955663 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1918-15G>C single nucleotide variant not provided [RCV003703830] Chr10:54090078 [GRCh38]
Chr10:55849838 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5379T>C (p.Pro1793=) single nucleotide variant not provided [RCV003542253] Chr10:53822347 [GRCh38]
Chr10:55582107 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4419A>G (p.Ser1473=) single nucleotide variant not provided [RCV003704790] Chr10:53823307 [GRCh38]
Chr10:55583067 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4721G>A (p.Trp1574Ter) single nucleotide variant not provided [RCV003682749] Chr10:53823005 [GRCh38]
Chr10:55582765 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.91+16G>T single nucleotide variant not provided [RCV003840584] Chr10:54664156 [GRCh38]
Chr10:56423916 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1422G>A (p.Gln474=) single nucleotide variant not provided [RCV003710470] Chr10:54185152 [GRCh38]
Chr10:55944912 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1059A>G (p.Val353=) single nucleotide variant not provided [RCV003842930] Chr10:54213975 [GRCh38]
Chr10:55973735 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4203-14G>C single nucleotide variant not provided [RCV003551631] Chr10:53828587 [GRCh38]
Chr10:55588347 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1446A>T (p.Thr482=) single nucleotide variant not provided [RCV003542956] Chr10:54183588 [GRCh38]
Chr10:55943348 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1998-1G>A single nucleotide variant not provided [RCV003824091] Chr10:54079425 [GRCh38]
Chr10:55839185 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.158-1G>T single nucleotide variant not provided [RCV003681347] Chr10:54378943 [GRCh38]
Chr10:56138703 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1630dup (p.Ile544fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV004574276]|not provided [RCV003681415] Chr10:54153253..54153254 [GRCh38]
Chr10:55913013..55913014 [GRCh37]
Chr10:10q21.1		 pathogenic|likely pathogenic
NM_033056.4(PCDH15):c.4929_4932dup (p.Leu1645fs) duplication not provided [RCV003563752] Chr10:53822793..53822794 [GRCh38]
Chr10:55582553..55582554 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2752-13T>C single nucleotide variant not provided [RCV003729673] Chr10:53995778 [GRCh38]
Chr10:55755538 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2092-15G>A single nucleotide variant not provided [RCV003735854] Chr10:54066900 [GRCh38]
Chr10:55826660 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3718-17G>A single nucleotide variant not provided [RCV003682936] Chr10:53857280 [GRCh38]
Chr10:55617040 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2142T>C (p.Ala714=) single nucleotide variant not provided [RCV003566074] Chr10:54066835 [GRCh38]
Chr10:55826595 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2221-16T>C single nucleotide variant not provided [RCV003564901] Chr10:54023213 [GRCh38]
Chr10:55782973 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1591-16T>C single nucleotide variant not provided [RCV003678391] Chr10:54153309 [GRCh38]
Chr10:55913069 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.840C>T (p.Leu280=) single nucleotide variant not provided [RCV003707657] Chr10:54317307 [GRCh38]
Chr10:56077067 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3501+15G>T single nucleotide variant not provided [RCV003822899] Chr10:53903228 [GRCh38]
Chr10:55662988 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.877-19C>A single nucleotide variant not provided [RCV003681623] Chr10:54236950 [GRCh38]
Chr10:55996710 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3501+16T>A single nucleotide variant not provided [RCV003676078] Chr10:53903227 [GRCh38]
Chr10:55662987 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1917+9C>T single nucleotide variant not provided [RCV003565069] Chr10:54132866 [GRCh38]
Chr10:55892626 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5133A>G (p.Ser1711=) single nucleotide variant not provided [RCV003681636] Chr10:53822593 [GRCh38]
Chr10:55582353 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3502-6G>T single nucleotide variant not provided [RCV003734235] Chr10:53866863 [GRCh38]
Chr10:55626623 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.319-16A>G single nucleotide variant not provided [RCV003731109] Chr10:54369291 [GRCh38]
Chr10:56129051 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3502-9T>A single nucleotide variant not provided [RCV003568369] Chr10:53866866 [GRCh38]
Chr10:55626626 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5577G>A (p.Lys1859=) single nucleotide variant not provided [RCV003704398] Chr10:53822149 [GRCh38]
Chr10:55581909 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.3358C>A (p.Arg1120=) single nucleotide variant not provided [RCV003704374] Chr10:53938830 [GRCh38]
Chr10:55698590 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2760T>C (p.Asn920=) single nucleotide variant not provided [RCV003550700] Chr10:53995757 [GRCh38]
Chr10:55755517 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2868+17_2868+20del deletion not provided [RCV003683289] Chr10:53995629..53995632 [GRCh38]
Chr10:55755389..55755392 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.1908A>G (p.Leu636=) single nucleotide variant not provided [RCV003681798] Chr10:54132884 [GRCh38]
Chr10:55892644 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2527-20T>C single nucleotide variant not provided [RCV003866535] Chr10:54020436 [GRCh38]
Chr10:55780196 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.4462_4468dup (p.Ile1490fs) duplication not provided [RCV003708945] Chr10:53823257..53823258 [GRCh38]
Chr10:55583017..55583018 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.1050G>A (p.Leu350=) single nucleotide variant not provided [RCV003680547] Chr10:54213984 [GRCh38]
Chr10:55973744 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4671+1564del deletion Usher syndrome type 1D [RCV003992138] Chr10:53808992 [GRCh38]
Chr10:55568752 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.280C>T (p.Leu94Phe) single nucleotide variant not provided [RCV003887115] Chr10:54378820 [GRCh38]
Chr10:56138580 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.423T>G (p.Asn141Lys) single nucleotide variant Usher syndrome type 1D [RCV003992139] Chr10:54369171 [GRCh38]
Chr10:56128931 [GRCh37]
Chr10:10q21.1		 uncertain significance
GRCh37/hg19 10q21.1(chr10:54790789-56488063)x1 copy number loss not specified [RCV003986855] Chr10:54790789..56488063 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.594+10T>G single nucleotide variant PCDH15-related disorder [RCV004544117] Chr10:54346355 [GRCh38]
Chr10:56106115 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4260C>A (p.Pro1420=) single nucleotide variant not provided [RCV003885093] Chr10:53827500 [GRCh38]
Chr10:55587260 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4672-1601G>T single nucleotide variant PCDH15-related disorder [RCV004531896] Chr10:53808731 [GRCh38]
Chr10:55568491 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.5052G>A (p.Ala1684=) single nucleotide variant PCDH15-related disorder [RCV004542477] Chr10:53806750 [GRCh38]
Chr10:55566510 [GRCh37]
Chr10:10q21.1		 likely benign
GRCh37/hg19 10q21.1(chr10:54459920-56080457)x1 copy number loss not specified [RCV003986854] Chr10:54459920..56080457 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.282T>C (p.Leu94=) single nucleotide variant not specified [RCV004018144] Chr10:54378818 [GRCh38]
Chr10:56138578 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.407T>C (p.Val136Ala) single nucleotide variant not specified [RCV004586317] Chr10:54369187 [GRCh38]
Chr10:56128947 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.211C>A (p.Pro71Thr) single nucleotide variant Inborn genetic diseases [RCV004505020] Chr10:54378889 [GRCh38]
Chr10:56138649 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2813A>G (p.Asp938Gly) single nucleotide variant Inborn genetic diseases [RCV004505021] Chr10:53995704 [GRCh38]
Chr10:55755464 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4671+1031A>G single nucleotide variant Inborn genetic diseases [RCV004505026] Chr10:53809525 [GRCh38]
Chr10:55569285 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4835C>T (p.Thr1612Ile) single nucleotide variant Inborn genetic diseases [RCV004505028] Chr10:53822891 [GRCh38]
Chr10:55582651 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4949C>T (p.Thr1650Ile) single nucleotide variant Inborn genetic diseases [RCV004505029] Chr10:53822777 [GRCh38]
Chr10:55582537 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3670G>T (p.Ala1224Ser) single nucleotide variant not provided [RCV004590758] Chr10:53866689 [GRCh38]
Chr10:55626449 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3106A>G (p.Thr1036Ala) single nucleotide variant Inborn genetic diseases [RCV004505023] Chr10:53959748 [GRCh38]
Chr10:55719508 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2091+1dup duplication Usher syndrome type 1F [RCV004585123] Chr10:54079329..54079330 [GRCh38]
Chr10:55839089..55839090 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.4671+1640C>T single nucleotide variant Inborn genetic diseases [RCV004505030] Chr10:53808916 [GRCh38]
Chr10:55568676 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2693C>A (p.Ala898Asp) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV004555528]|not provided [RCV004697347] Chr10:54020250 [GRCh38]
Chr10:55780010 [GRCh37]
Chr10:10q21.1		 pathogenic|uncertain significance
NM_001384140.1(PCDH15):c.2897G>A (p.Arg966Lys) single nucleotide variant Inborn genetic diseases [RCV004505022] Chr10:53961864 [GRCh38]
Chr10:55721624 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3314T>G (p.Leu1105Arg) single nucleotide variant Inborn genetic diseases [RCV004505024] Chr10:53938874 [GRCh38]
Chr10:55698634 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.4715G>A (p.Arg1572Lys) single nucleotide variant Inborn genetic diseases [RCV004505027] Chr10:53823011 [GRCh38]
Chr10:55582771 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4672-1669T>C single nucleotide variant Inborn genetic diseases [RCV004505031] Chr10:53808799 [GRCh38]
Chr10:55568559 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4672-1582G>T single nucleotide variant Inborn genetic diseases [RCV004505032] Chr10:53808712 [GRCh38]
Chr10:55568472 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5622C>A (p.Asp1874Glu) single nucleotide variant Inborn genetic diseases [RCV004505034] Chr10:53822104 [GRCh38]
Chr10:55581864 [GRCh37]
Chr10:10q21.1		 uncertain significance
NC_000010.10:g.(?_55581618)_(55583138_?)del deletion not provided [RCV004581784] Chr10:55581618..55583138 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_56077011)_(56424022_?)del deletion not provided [RCV004581789] Chr10:56077011..56424022 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_55581618)_(55755545_?)del deletion not provided [RCV004581790] Chr10:55581618..55755545 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_55698555)_(55782977_?)dup duplication not provided [RCV004581800] Chr10:55698555..55782977 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NC_000010.10:g.(?_55587133)_(56138722_?)dup duplication not provided [RCV004581801] Chr10:55587133..56138722 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3123-1G>C single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV004574465] Chr10:53940976 [GRCh38]
Chr10:55700736 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.1997+1G>C single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV004574467] Chr10:54089983 [GRCh38]
Chr10:55849743 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NC_000010.10:g.(?_55912840)_(55913073_?)del deletion not provided [RCV004581781] Chr10:55912840..55913073 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_56423912)_(56424022_?)del deletion not provided [RCV004581783] Chr10:56423912..56424022 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_56138522)_(56138722_?)del deletion not provided [RCV004581785] Chr10:56138522..56138722 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_55755389)_(55913073_?)del deletion not provided [RCV004581786] Chr10:55755389..55913073 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_55826497)_(55892787_?)del deletion not provided [RCV004581787] Chr10:55826497..55892787 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_55662983)_(55849843_?)del deletion not provided [RCV004581788] Chr10:55662983..55849843 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_55912840)_(56287657_?)del deletion not provided [RCV004581791] Chr10:55912840..56287657 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_55581618)_(55591313_?)del deletion not provided [RCV004581792] Chr10:55581618..55591313 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_55782632)_(56138722_?)del deletion not provided [RCV004581795] Chr10:55782632..56138722 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_56106115)_(56138712_?)del deletion not provided [RCV004581796] Chr10:56106115..56138712 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_56077011)_(56106264_?)del deletion not provided [RCV004581797] Chr10:56077011..56106264 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_55581618)_(56077221_?)del deletion not provided [RCV004581798] Chr10:55581618..56077221 [GRCh37]
Chr10:10q21.1		 pathogenic
NC_000010.10:g.(?_55826497)_(55996711_?)del deletion not provided [RCV004581799] Chr10:55826497..55996711 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_033056.4(PCDH15):c.4954C>G (p.Gln1652Glu) single nucleotide variant Inborn genetic diseases [RCV004664285] Chr10:53822772 [GRCh38]
Chr10:55582532 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4672-1694T>A single nucleotide variant Inborn genetic diseases [RCV004664287] Chr10:53808824 [GRCh38]
Chr10:55568584 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.571del (p.Ile191fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV004574471] Chr10:54346388 [GRCh38]
Chr10:56106148 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.127_130del (p.Ile43fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV004574469] Chr10:54527839..54527842 [GRCh38]
Chr10:56287599..56287602 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4809_4827dup (p.Ser1610fs) duplication Usher syndrome type 1F [RCV004585124] Chr10:53806974..53806975 [GRCh38]
Chr10:55566734..55566735 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.4671+1295G>A single nucleotide variant Inborn genetic diseases [RCV004664288] Chr10:53809261 [GRCh38]
Chr10:55569021 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.1956del (p.Ile652fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV004574464] Chr10:54090025 [GRCh38]
Chr10:55849785 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.810dup (p.Val271fs) duplication Autosomal recessive nonsyndromic hearing loss 23 [RCV004574468] Chr10:54317336..54317337 [GRCh38]
Chr10:56077096..56077097 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4620G>A (p.Glu1540=) single nucleotide variant Inborn genetic diseases [RCV004653053] Chr10:53810607 [GRCh38]
Chr10:55570367 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.4210G>T (p.Val1404Leu) single nucleotide variant Inborn genetic diseases [RCV004653055] Chr10:53828566 [GRCh38]
Chr10:55588326 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.715C>T (p.Gln239Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV004574466] Chr10:54317432 [GRCh38]
Chr10:56077192 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.268del (p.Val90fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV004574470] Chr10:54378832 [GRCh38]
Chr10:56138592 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3179del (p.Ala1060fs) deletion Autosomal recessive nonsyndromic hearing loss 23 [RCV004574472] Chr10:53940919 [GRCh38]
Chr10:55700679 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.3946C>T (p.Gln1316Ter) single nucleotide variant Autosomal recessive nonsyndromic hearing loss 23 [RCV004574473] Chr10:53840357 [GRCh38]
Chr10:55600117 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_001384140.1(PCDH15):c.4671+1574A>T single nucleotide variant Inborn genetic diseases [RCV004664284] Chr10:53808982 [GRCh38]
Chr10:55568742 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2380G>A (p.Gly794Arg) single nucleotide variant Inborn genetic diseases [RCV004664286] Chr10:54023038 [GRCh38]
Chr10:55782798 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.92-24483A>G single nucleotide variant Hearing impairment [RCV004698620] Chr10:54552360 [GRCh38]
Chr10:56312120 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2127dup (p.Val710fs) duplication Usher syndrome type 1F [RCV004698411] Chr10:54066849..54066850 [GRCh38]
Chr10:55826609..55826610 [GRCh37]
Chr10:10q21.1		 pathogenic
NM_001384140.1(PCDH15):c.4671+1644A>G single nucleotide variant not provided [RCV004599040] Chr10:53808912 [GRCh38]
Chr10:55568672 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.5160_5163dup (p.Asp1722Ter) duplication Usher syndrome type 1D [RCV004576157] Chr10:53806638..53806639 [GRCh38]
Chr10:55566398..55566399 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.4937_4940dup (p.Glu1648fs) duplication Usher syndrome type 1D [RCV004576158] Chr10:53822785..53822786 [GRCh38]
Chr10:55582545..55582546 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.5576_5577insTAAT (p.Lys1859fs) insertion Usher syndrome type 1D [RCV004576159] Chr10:53822149..53822150 [GRCh38]
Chr10:55581909..55581910 [GRCh37]
Chr10:10q21.1		 likely pathogenic
NM_033056.4(PCDH15):c.4792C>A (p.Gln1598Lys) single nucleotide variant not provided [RCV004701999] Chr10:53822934 [GRCh38]
Chr10:55582694 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4765C>T (p.Arg1589Cys) single nucleotide variant PCDH15-related disorder [RCV004736462] Chr10:53807037 [GRCh38]
Chr10:55566797 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.460G>A (p.Ala154Thr) single nucleotide variant not provided [RCV004722264] Chr10:54369134 [GRCh38]
Chr10:56128894 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.5041_5044dup (p.Asn1682fs) duplication PCDH15-related disorder [RCV004735435] Chr10:53806757..53806758 [GRCh38]
Chr10:55566517..55566518 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.3043G>A (p.Val1015Met) single nucleotide variant not provided [RCV004727446] Chr10:53959811 [GRCh38]
Chr10:55719571 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2868+21A>G single nucleotide variant PCDH15-related disorder [RCV004735054] Chr10:53995628 [GRCh38]
Chr10:55755388 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.2650G>A (p.Ala884Thr) single nucleotide variant not provided [RCV004723744] Chr10:54020293 [GRCh38]
Chr10:55780053 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.4672-10_4672-7dup duplication PCDH15-related disorder [RCV004735197] Chr10:53807136..53807137 [GRCh38]
Chr10:55566896..55566897 [GRCh37]
Chr10:10q21.1		 likely benign
NM_033056.4(PCDH15):c.5278C>G (p.Pro1760Ala) single nucleotide variant not provided [RCV004729326] Chr10:53822448 [GRCh38]
Chr10:55582208 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5281GCTCCT[3] (p.Pro1764_Leu1765insAlaPro) microsatellite not provided [RCV004774824] Chr10:53822433..53822434 [GRCh38]
Chr10:55582193..55582194 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_033056.4(PCDH15):c.5585T>C (p.Met1862Thr) single nucleotide variant not provided [RCV004726086] Chr10:53822141 [GRCh38]
Chr10:55581901 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.2722G>A (p.Gly908Ser) single nucleotide variant not provided [RCV004763780]   uncertain significance
NM_001384140.1(PCDH15):c.1844G>A (p.Arg615His) single nucleotide variant not provided [RCV004763003]   uncertain significance
NM_001384140.1(PCDH15):c.3463G>A (p.Glu1155Lys) single nucleotide variant not provided [RCV004766206] Chr10:53903281 [GRCh38]
Chr10:55663041 [GRCh37]
Chr10:10q21.1		 uncertain significance
NM_001384140.1(PCDH15):c.733C>A (p.Arg245=) single nucleotide variant not specified [RCV004702899] Chr10:54317414 [GRCh38]
Chr10:56077174 [GRCh37]
Chr10:10q21.1		 likely benign
NM_001384140.1(PCDH15):c.262G>A (p.Asp88Asn) single nucleotide variant not provided [RCV004771850] Chr10:54378838 [GRCh38]
Chr10:56138598 [GRCh37]
Chr10:10q21.1		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:10735
Count of miRNA genes:1373
Interacting mature miRNAs:1806
Transcripts:ENST00000320301, ENST00000361849, ENST00000373955, ENST00000373956, ENST00000373957, ENST00000373965, ENST00000395430, ENST00000395432, ENST00000395433, ENST00000395438, ENST00000395440, ENST00000395442, ENST00000395445, ENST00000395446, ENST00000409834, ENST00000414367, ENST00000414778, ENST00000437009, ENST00000448885, ENST00000458638, ENST00000463095, ENST00000476074, ENST00000495484
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
406932289GWAS581265_Hsmoking initiation QTL GWAS581265 (human)4e-14smoking initiation105541464155414642Human
407027783GWAS676759_Hbody weight QTL GWAS676759 (human)0.000005body mass (VT:0001259)body weight (CMO:0000012)105503120955031210Human
407283777GWAS932753_Hshort-term memory QTL GWAS932753 (human)0.000008short-term memory105411710054117101Human
406934345GWAS583321_Heducational attainment QTL GWAS583321 (human)2e-11educational attainment105407898054078981Human
406999242GWAS648218_Hadolescent idiopathic scoliosis QTL GWAS648218 (human)0.0000003adolescent idiopathic scoliosis105473440354734404Human
406947019GWAS595995_Hirritable bowel syndrome QTL GWAS595995 (human)0.000005irritable bowel syndrome105419585054195851Human
407325005GWAS973981_Hrisk-taking behaviour QTL GWAS973981 (human)7e-10risk-taking behaviour105494083754940838Human
406994894GWAS643870_Hsmoking cessation QTL GWAS643870 (human)1e-09smoking cessation105493047454930475Human
406958668GWAS607644_Hcarotid artery intima media thickness QTL GWAS607644 (human)7e-09carotid artery intima media thickness105486084854860849Human
407195594GWAS844570_Hunipolar depression, information processing speed, cognitive function measurement QTL GWAS844570 (human)1e-10unipolar depression, information processing speed, cognitive function measurement105453895354538954Human
406989267GWAS638243_Hage at menarche, spine bone mineral density QTL GWAS638243 (human)6e-08hip bone mineral density, age at menarchebone mineral density (CMO:0001226)105445799254457993Human
407211860GWAS860836_Hvelopharyngeal dysfunction QTL GWAS860836 (human)0.000003velopharyngeal dysfunction105458753354587534Human
407051473GWAS700449_Hphenylalanine measurement QTL GWAS700449 (human)0.000002phenylalanine measurement105438133154381332Human
407003344GWAS652320_Hchronotype measurement QTL GWAS652320 (human)4e-08chronotype measurement105493957854939579Human
407284821GWAS933797_Hinsomnia QTL GWAS933797 (human)9e-10insomnia105542046955420470Human
406985174GWAS634150_Hmagnesium measurement, trait in response to platinum QTL GWAS634150 (human)0.000008magnesium measurement, trait in response to platinumserum magnesium level (CMO:0000541)105493923654939237Human
407380188GWAS1029164_Hacute myeloid leukemia QTL GWAS1029164 (human)4e-40acute myeloid leukemia105542371755423718Human
407190736GWAS839712_Hcolor vision disorder QTL GWAS839712 (human)0.000006color vision disorder105440162854401629Human
407380189GWAS1029165_Hacute myeloid leukemia QTL GWAS1029165 (human)8e-27acute myeloid leukemia105542371755423718Human
407010010GWAS658986_Hlifestyle measurement QTL GWAS658986 (human)6e-09lifestyle measurement105490067754900678Human
407051866GWAS700842_Hlung disease severity measurement QTL GWAS700842 (human)0.000006lung integrity trait (VT:0010906)105449596454495965Human
407018971GWAS667947_Hchronotype measurement QTL GWAS667947 (human)4e-08chronotype measurement105493446254934463Human
407184988GWAS833964_Hexecutive function measurement QTL GWAS833964 (human)6e-08executive function measurement105531748755317488Human
407316318GWAS965294_Hceramide measurement QTL GWAS965294 (human)0.0000004ceramide measurement105548540055485401Human
406976731GWAS625707_Htrait in response to ethanol QTL GWAS625707 (human)0.000007trait in response to ethanol105483310554833106Human
407199967GWAS848943_Hattention deficit hyperactivity disorder, substance abuse, antisocial behaviour measurement QTL GWAS848943 (human)1e-13attention deficit hyperactivity disorder, substance abuse, antisocial behaviour measurement105488018054880181Human
407064920GWAS713896_HHOMA-B QTL GWAS713896 (human)0.0000002HOMA-BHomeostatic Model Assessment of Beta cell function (CMO:0003211)105427953454279535Human
407182425GWAS831401_HStuttering QTL GWAS831401 (human)0.0000005Stuttering105462719854627199Human
406953567GWAS602543_HPituitary Gland Adenoma QTL GWAS602543 (human)7e-10Pituitary Gland Adenoma105501726455017265Human
407160155GWAS809131_Hfaecalibacterium seropositivity QTL GWAS809131 (human)5e-08faecalibacterium seropositivity105460173954601740Human
407362663GWAS1011639_Hrisky sexual behaviour measurement QTL GWAS1011639 (human)2e-09risky sexual behaviour measurement105487221854872219Human
406929250GWAS578226_Hserum metabolite measurement QTL GWAS578226 (human)1e-10serum metabolite measurement105425589654255897Human
407195360GWAS844336_Hunipolar depression, information processing speed, cognitive function measurement QTL GWAS844336 (human)8e-09unipolar depression, information processing speed, cognitive function measurement105453895354538954Human
407199968GWAS848944_Hattention deficit hyperactivity disorder, substance abuse, antisocial behaviour measurement QTL GWAS848944 (human)2e-09attention deficit hyperactivity disorder, substance abuse, antisocial behaviour measurement105542574955425750Human
406954342GWAS603318_Hsleep duration QTL GWAS603318 (human)0.0000004sleep duration105481119454811195Human
406922473GWAS571449_Htriglyceride measurement QTL GWAS571449 (human)5e-08triglyceride measurementblood triglyceride level (CMO:0000118)105488018054880181Human
406919019GWAS567995_Hbody mass index QTL GWAS567995 (human)9e-08body mass indexbody mass index (BMI) (CMO:0000105)105403525054035251Human
407146350GWAS795326_Hairway responsiveness measurement QTL GWAS795326 (human)6e-08airway responsiveness measurementrespiratory system measurement (CMO:0000094)105415394054153941Human
407250678GWAS899654_Hword reading QTL GWAS899654 (human)0.000001word reading105459599254595993Human
407118452GWAS767428_Hsmoking status measurement QTL GWAS767428 (human)7e-09smoking status measurement105493841454938415Human
407110390GWAS759366_Hprotein measurement QTL GWAS759366 (human)2e-08protein measurement105431598554315986Human
406919027GWAS568003_Hsmoking behavior QTL GWAS568003 (human)8e-09smoking behavior105494083754940838Human
407282034GWAS931010_Hshort-term memory QTL GWAS931010 (human)0.000007short-term memory105411888554118886Human
407315067GWAS964043_Hschizophrenia QTL GWAS964043 (human)0.000002schizophrenia105403948054039481Human
406932221GWAS581197_Hsmoking initiation QTL GWAS581197 (human)1e-28smoking initiation105493999254939993Human
406931837GWAS580813_Hbody mass index QTL GWAS580813 (human)6e-08body mass indexbody mass index (BMI) (CMO:0000105)105523484355234844Human
406932220GWAS581196_Hsmoking initiation QTL GWAS581196 (human)2e-09smoking initiation105489287054892871Human
407097603GWAS746579_HEpstein-Barr virus infection QTL GWAS746579 (human)0.000002Epstein-Barr virus infection105380674753806748Human
406957826GWAS606802_Hresponse to xenobiotic stimulus QTL GWAS606802 (human)0.0000008response to xenobiotic stimulus105508922555089226Human
407354500GWAS1003476_Hsmoking status measurement QTL GWAS1003476 (human)2e-08smoking status measurement105542574955425750Human
407126913GWAS775889_Hforced expiratory volume QTL GWAS775889 (human)0.000001forced expiratory volumeforced expiratory volume (CMO:0000254)105463154354631544Human
407186563GWAS835539_HX-11423--O-sulfo-L-tyrosine measurement QTL GWAS835539 (human)0.000005X-11423--O-sulfo-L-tyrosine measurement105423199354231994Human
406902534GWAS551510_Hlip morphology measurement QTL GWAS551510 (human)0.000002lip morphology measurement105446199054461991Human
406921997GWAS570973_Hsmoking initiation QTL GWAS570973 (human)4e-24smoking initiation105493999254939993Human
406921998GWAS570974_Hsmoking initiation QTL GWAS570974 (human)5e-13smoking initiation105542046955420470Human
407061267GWAS710243_Hchemotherapy-induced alopecia QTL GWAS710243 (human)0.0000003chemotherapy-induced alopecia105444453154444532Human
407198745GWAS847721_Hlipid measurement QTL GWAS847721 (human)0.000006lipid measurementblood lipid measurement (CMO:0000050)105441404054414041Human
406920350GWAS569326_Hrisk-taking behaviour QTL GWAS569326 (human)4e-09risk-taking behaviour105488990854889909Human
407270822GWAS919798_Hinsomnia measurement QTL GWAS919798 (human)1e-08insomnia measurement105541771055417711Human
407165223GWAS814199_HFEV/FVC ratio, response to bronchodilator QTL GWAS814199 (human)0.000003FEV/FVC ratio, response to bronchodilatorforced expiratory volume to forced vital capacity ratio (CMO:0000241)105413731154137312Human
406897316GWAS546292_Hopioid dependence QTL GWAS546292 (human)0.000002opioid dependence105445046754450468Human
407157409GWAS806385_Hattempted suicide QTL GWAS806385 (human)0.000001attempted suicide105508958455089585Human
406946343GWAS595319_Hpyruvate measurement QTL GWAS595319 (human)5e-09pyruvate measurementblood pyruvate level (CMO:0002422)105396779753967798Human
407276717GWAS925693_Hbody height QTL GWAS925693 (human)6e-11body height (VT:0001253)body height (CMO:0000106)105412464854124649Human
406929327GWAS578303_Hserum metabolite measurement QTL GWAS578303 (human)7e-10serum metabolite measurement105425589654255897Human
407051181GWAS700157_Hphenylalanine measurement QTL GWAS700157 (human)0.000002phenylalanine measurement105427869254278693Human
406905774GWAS554750_HS-6-hydroxywarfarin measurement QTL GWAS554750 (human)0.000006S-6-hydroxywarfarin measurement105500889155008892Human
407079475GWAS728451_Hgut microbiome measurement QTL GWAS728451 (human)3e-08gut microbiome measurement105446599354465994Human
407118389GWAS767365_Hsmoking status measurement QTL GWAS767365 (human)4e-12smoking status measurement105494050854940509Human
406929333GWAS578309_Hserum metabolite measurement QTL GWAS578309 (human)4e-10serum metabolite measurement105425589654255897Human
407249331GWAS898307_Hcomplement factor H-related protein 3 measurement QTL GWAS898307 (human)0.000005complement factor H-related protein 3 measurement105394136053941361Human
407131057GWAS780033_Hschizophrenia QTL GWAS780033 (human)0.000002schizophrenia105402542854025429Human
407167922GWAS816898_HParkinson's disease symptom measurement QTL GWAS816898 (human)0.000008Parkinson's disease symptom measurement105466164054661641Human
406951479GWAS600455_Hextraversion QTL GWAS600455 (human)5e-10extraversion105490160254901603Human
406888762GWAS537738_HBMI-adjusted hip circumference QTL GWAS537738 (human)0.000002BMI-adjusted hip circumferencehip circumference (CMO:0000014)105494847054948471Human
407200699GWAS849675_Hschizophrenia QTL GWAS849675 (human)2e-08schizophrenia105402338654023387Human
406932287GWAS581263_Hsmoking initiation QTL GWAS581263 (human)1e-13smoking initiation105541087855410879Human
407014461GWAS663437_Hreading QTL GWAS663437 (human)0.000009reading105459599254595993Human
406932286GWAS581262_Hsmoking initiation QTL GWAS581262 (human)1e-28smoking initiation105494129954941300Human

Markers in Region
D10S546  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371056,094,398 - 56,094,551UniSTSGRCh37
Build 361055,764,404 - 55,764,557RGDNCBI36
Celera1049,357,262 - 49,357,411RGD
Cytogenetic Map10q21.1UniSTS
HuRef1050,078,000 - 50,078,149UniSTS
Marshfield Genetic Map1075.57UniSTS
Marshfield Genetic Map1075.57RGD
Genethon Genetic Map1078.4UniSTS
TNG Radiation Hybrid Map1025149.0UniSTS
deCODE Assembly Map1073.25UniSTS
GeneMap99-GB4 RH Map10336.52UniSTS
Whitehead-RH Map10406.3UniSTS
Whitehead-YAC Contig Map10 UniSTS
NCBI RH Map10661.7UniSTS
RH78831  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,593,939 - 55,594,066UniSTSGRCh37
Build 361055,263,945 - 55,264,072RGDNCBI36
Celera1048,856,906 - 48,857,033RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,575,536 - 49,575,663UniSTS
GeneMap99-GB4 RH Map10342.27UniSTS
RH79971  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,631,457 - 55,631,667UniSTSGRCh37
Build 361055,301,463 - 55,301,673RGDNCBI36
Celera1048,894,435 - 48,894,648RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,613,047 - 49,613,257UniSTS
G42342  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,593,900 - 55,594,038UniSTSGRCh37
Build 361055,263,906 - 55,264,044RGDNCBI36
Celera1048,856,867 - 48,857,005RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,575,497 - 49,575,635UniSTS
RH120854  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371056,433,917 - 56,434,218UniSTSGRCh37
Build 361056,103,923 - 56,104,224RGDNCBI36
Celera1049,697,071 - 49,697,372RGD
Cytogenetic Map10q21.1UniSTS
HuRef1050,418,001 - 50,418,302UniSTS
RH120548  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,913,730 - 55,914,079UniSTSGRCh37
Build 361055,583,736 - 55,584,085RGDNCBI36
Celera1049,176,678 - 49,177,027RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,896,827 - 49,897,176UniSTS
TNG Radiation Hybrid Map1025212.0UniSTS
RH122852  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,646,629 - 55,646,921UniSTSGRCh37
Build 361055,316,635 - 55,316,927RGDNCBI36
Celera1048,909,593 - 48,909,885RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,628,217 - 49,628,509UniSTS
G62732  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,985,020 - 55,985,314UniSTSGRCh37
Build 361055,655,026 - 55,655,320RGDNCBI36
Celera1049,247,961 - 49,248,255RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,968,214 - 49,968,508UniSTS
TNG Radiation Hybrid Map1025193.0UniSTS
GDB:676462  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,951,604 - 55,952,020UniSTSGRCh37
Build 361055,621,610 - 55,622,026RGDNCBI36
Celera1049,214,548 - 49,214,964RGD
HuRef1049,934,784 - 49,935,200UniSTS
G66781  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371056,008,013 - 56,008,305UniSTSGRCh37
Build 361055,678,019 - 55,678,311RGDNCBI36
Celera1049,270,950 - 49,271,242RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,991,211 - 49,991,503UniSTS
SHGC-151080  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371056,414,989 - 56,415,175UniSTSGRCh37
Build 361056,084,995 - 56,085,181RGDNCBI36
Celera1049,678,144 - 49,678,342RGD
Cytogenetic Map10q21.1UniSTS
HuRef1050,399,087 - 50,399,271UniSTS
TNG Radiation Hybrid Map13184.0UniSTS
TNG Radiation Hybrid Map1025065.0UniSTS
stSG72239  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,802,118 - 55,802,237UniSTSGRCh37
Build 361055,472,124 - 55,472,243RGDNCBI36
Celera1049,065,027 - 49,065,146RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,783,545 - 49,783,664UniSTS
G65575  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,593,666 - 55,594,062UniSTSGRCh37
Build 361055,263,672 - 55,264,068RGDNCBI36
Celera1048,856,633 - 48,857,029RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,575,263 - 49,575,659UniSTS
NEF3_219  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371056,360,295 - 56,360,933UniSTSGRCh37
GRCh37824,775,971 - 24,776,603UniSTSGRCh37
Build 36824,831,876 - 24,832,508RGDNCBI36
Celera1049,623,439 - 49,624,077UniSTS
Celera823,739,382 - 23,740,014RGD
HuRef1050,344,320 - 50,344,958UniSTS
HuRef823,320,675 - 23,321,307UniSTS
PCDH15_1881  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,580,950 - 55,581,811UniSTSGRCh37
Build 361055,250,956 - 55,251,817RGDNCBI36
Celera1048,843,919 - 48,844,780RGD
HuRef1049,562,551 - 49,563,412UniSTS
ECD00042  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,892,648 - 55,893,598UniSTSGRCh37
Build 361055,562,654 - 55,563,604RGDNCBI36
Celera1049,155,552 - 49,156,502RGD
Cytogenetic Map10q21.1UniSTS
ECD00203  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,947,608 - 55,948,531UniSTSGRCh37
Build 361055,617,614 - 55,618,537RGDNCBI36
Celera1049,210,552 - 49,211,475RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,930,791 - 49,931,714UniSTS
ECD00386  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,646,395 - 55,647,304UniSTSGRCh37
Build 361055,316,401 - 55,317,310RGDNCBI36
Celera1048,909,359 - 48,910,268RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,627,983 - 49,628,892UniSTS
ECD00387  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,756,557 - 55,757,466UniSTSGRCh37
Build 361055,426,563 - 55,427,472RGDNCBI36
Celera1049,019,445 - 49,020,354RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,737,976 - 49,738,885UniSTS
ECD00650  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,757,553 - 55,758,448UniSTSGRCh37
Build 361055,427,559 - 55,428,454RGDNCBI36
Celera1049,020,441 - 49,021,336RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,738,972 - 49,739,867UniSTS
ECD00962  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,681,636 - 55,682,518UniSTSGRCh37
Build 361055,351,642 - 55,352,524RGDNCBI36
Celera1048,944,528 - 48,945,410RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,663,132 - 49,664,014UniSTS
ECD01074  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,566,353 - 55,567,231UniSTSGRCh37
Build 361055,236,359 - 55,237,237RGDNCBI36
Celera1048,829,322 - 48,830,200RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,547,956 - 49,548,834UniSTS
ECD01093  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,954,959 - 55,955,836UniSTSGRCh37
Build 361055,624,965 - 55,625,842RGDNCBI36
Celera1049,217,909 - 49,218,786RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,938,144 - 49,939,021UniSTS
ECD01413  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,580,205 - 55,581,070UniSTSGRCh37
Build 361055,250,211 - 55,251,076RGDNCBI36
Celera1048,843,174 - 48,844,039RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,561,806 - 49,562,671UniSTS
ECD01510  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,599,270 - 55,600,132UniSTSGRCh37
Build 361055,269,276 - 55,270,138RGDNCBI36
Celera1048,862,236 - 48,863,097RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,580,861 - 49,581,723UniSTS
ECD01744  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,788,775 - 55,789,629UniSTSGRCh37
Build 361055,458,781 - 55,459,635RGDNCBI36
Celera1049,051,674 - 49,052,528RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,770,190 - 49,771,044UniSTS
ECD01797  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,967,201 - 55,968,053UniSTSGRCh37
Build 361055,637,207 - 55,638,059RGDNCBI36
Cytogenetic Map10q21.1UniSTS
ECD01902  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,578,388 - 55,579,236UniSTSGRCh37
Build 361055,248,394 - 55,249,242RGDNCBI36
Celera1048,841,357 - 48,842,205RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,559,989 - 49,560,837UniSTS
ECD01958  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,581,084 - 55,581,930UniSTSGRCh37
Build 361055,251,090 - 55,251,936RGDNCBI36
Celera1048,844,053 - 48,844,899RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,562,685 - 49,563,531UniSTS
ECD01981  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,605,837 - 55,606,682UniSTSGRCh37
Build 361055,275,843 - 55,276,688RGDNCBI36
Celera1048,868,802 - 48,869,647RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,587,428 - 49,588,273UniSTS
ECD01982  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,789,700 - 55,790,545UniSTSGRCh37
Build 361055,459,706 - 55,460,551RGDNCBI36
Celera1049,052,599 - 49,053,443RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,771,115 - 49,771,960UniSTS
ECD02116  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,925,590 - 55,926,430UniSTSGRCh37
Build 361055,595,596 - 55,596,436RGDNCBI36
Celera1049,188,533 - 49,189,373RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,908,685 - 49,909,525UniSTS
ECD02167  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,768,408 - 55,769,246UniSTSGRCh37
Build 361055,438,414 - 55,439,252RGDNCBI36
Celera1049,031,303 - 49,032,140RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,749,820 - 49,750,657UniSTS
ECD02168  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,826,873 - 55,827,711UniSTSGRCh37
Build 361055,496,879 - 55,497,717RGDNCBI36
Celera1049,089,781 - 49,090,619RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,808,305 - 49,809,143UniSTS
ECD02602  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,794,098 - 55,794,921UniSTSGRCh37
Build 361055,464,104 - 55,464,927RGDNCBI36
Celera1049,056,995 - 49,057,830RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,775,513 - 49,776,348UniSTS
ECD02634  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,839,896 - 55,840,718UniSTSGRCh37
Build 361055,509,902 - 55,510,724RGDNCBI36
Celera1049,102,804 - 49,103,626RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,821,327 - 49,822,149UniSTS
ECD02635  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,965,430 - 55,966,252UniSTSGRCh37
Build 361055,635,436 - 55,636,258RGDNCBI36
Celera1049,228,384 - 49,229,206RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,948,634 - 49,949,456UniSTS
ECD02662  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,600,158 - 55,600,979UniSTSGRCh37
Build 361055,270,164 - 55,270,985RGDNCBI36
Celera1048,863,123 - 48,863,944RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,581,749 - 49,582,570UniSTS
ECD02690  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,579,272 - 55,580,092UniSTSGRCh37
Build 361055,249,278 - 55,250,098RGDNCBI36
Celera1048,842,241 - 48,843,061RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,560,873 - 49,561,693UniSTS
ECD02708  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,722,158 - 55,722,977UniSTSGRCh37
Build 361055,392,164 - 55,392,983RGDNCBI36
Celera1048,985,046 - 48,985,865RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,703,649 - 49,704,468UniSTS
ECD02833  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,793,211 - 55,794,026UniSTSGRCh37
Build 361055,463,217 - 55,464,032RGDNCBI36
Celera1049,056,108 - 49,056,923RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,774,626 - 49,775,441UniSTS
ECD02931  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,706,966 - 55,707,777UniSTSGRCh37
Build 361055,376,972 - 55,377,783RGDNCBI36
Celera1048,969,849 - 48,970,660RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,688,452 - 49,689,263UniSTS
ECD02992  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,767,584 - 55,768,393UniSTSGRCh37
Build 361055,437,590 - 55,438,399RGDNCBI36
Celera1049,030,479 - 49,031,288RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,748,996 - 49,749,805UniSTS
ECD03077  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,766,665 - 55,767,471UniSTSGRCh37
Build 361055,436,671 - 55,437,477RGDNCBI36
Celera1049,029,560 - 49,030,366RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,748,077 - 49,748,883UniSTS
ECD03102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,872,580 - 55,873,385UniSTSGRCh37
Build 361055,542,586 - 55,543,391RGDNCBI36
Celera1049,135,481 - 49,136,286RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,854,010 - 49,854,815UniSTS
ECD03130  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,576,402 - 55,577,206UniSTSGRCh37
Build 361055,246,408 - 55,247,212RGDNCBI36
Celera1048,839,371 - 48,840,175RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,558,003 - 49,558,807UniSTS
ECD03223  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,790,899 - 55,791,700UniSTSGRCh37
Build 361055,460,905 - 55,461,706RGDNCBI36
Celera1049,053,797 - 49,054,597RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,772,314 - 49,773,115UniSTS
ECD03288  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,803,471 - 55,804,270UniSTSGRCh37
Build 361055,473,477 - 55,474,276RGDNCBI36
Celera1049,066,380 - 49,067,179RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,784,898 - 49,785,697UniSTS
ECD03289  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,964,378 - 55,965,177UniSTSGRCh37
Build 361055,634,384 - 55,635,183RGDNCBI36
Celera1049,227,332 - 49,228,131RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,947,582 - 49,948,381UniSTS
ECD03329  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,664,290 - 55,665,088UniSTSGRCh37
Build 361055,334,296 - 55,335,094RGDNCBI36
Celera1048,927,207 - 48,928,005RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,645,814 - 49,646,610UniSTS
ECD03384  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,753,237 - 55,754,033UniSTSGRCh37
Build 361055,423,243 - 55,424,039RGDNCBI36
Celera1049,016,125 - 49,016,921RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,734,654 - 49,735,450UniSTS
ECD03454  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,687,798 - 55,688,592UniSTSGRCh37
Build 361055,357,804 - 55,358,598RGDNCBI36
Celera1048,950,694 - 48,951,488RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,669,298 - 49,670,092UniSTS
ECD03505  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,752,238 - 55,753,030UniSTSGRCh37
Build 361055,422,244 - 55,423,036RGDNCBI36
Celera1049,015,126 - 49,015,918RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,733,655 - 49,734,447UniSTS
ECD03506  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,804,365 - 55,805,157UniSTSGRCh37
Build 361055,474,371 - 55,475,163RGDNCBI36
Celera1049,067,274 - 49,068,066RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,785,792 - 49,786,584UniSTS
ECD03537  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,890,184 - 55,890,975UniSTSGRCh37
Build 361055,560,190 - 55,560,981RGDNCBI36
Celera1049,153,086 - 49,153,877RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,871,617 - 49,872,408UniSTS
ECD03589  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,765,841 - 55,766,630UniSTSGRCh37
Build 361055,435,847 - 55,436,636RGDNCBI36
Celera1049,028,736 - 49,029,525RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,747,253 - 49,748,042UniSTS
ECD03615  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,654,867 - 55,655,655UniSTSGRCh37
Build 361055,324,873 - 55,325,661RGDNCBI36
Celera1048,917,783 - 48,918,571RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,636,799 - 49,637,587UniSTS
ECD03646  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,945,747 - 55,946,534UniSTSGRCh37
Build 361055,615,753 - 55,616,540RGDNCBI36
Celera1049,208,691 - 49,209,478RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,928,930 - 49,929,717UniSTS
ECD03647  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,966,286 - 55,967,073UniSTSGRCh37
Build 361055,636,292 - 55,637,079RGDNCBI36
Celera1049,229,240 - 49,230,024RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,949,490 - 49,950,274UniSTS
ECD03785  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,569,607 - 55,570,390UniSTSGRCh37
Build 361055,239,613 - 55,240,396RGDNCBI36
Celera1048,832,576 - 48,833,359RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,551,205 - 49,551,988UniSTS
ECD03786  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,713,876 - 55,714,659UniSTSGRCh37
Build 361055,383,882 - 55,384,665RGDNCBI36
Celera1048,976,759 - 48,977,542RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,695,362 - 49,696,145UniSTS
ECD04053  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,838,227 - 55,839,002UniSTSGRCh37
Build 361055,508,233 - 55,509,008RGDNCBI36
Celera1049,101,135 - 49,101,910RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,819,658 - 49,820,433UniSTS
ECD04192  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,858,166 - 55,858,937UniSTSGRCh37
Build 361055,528,172 - 55,528,943RGDNCBI36
Celera1049,121,072 - 49,121,843RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,839,596 - 49,840,367UniSTS
ECD04314  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,663,491 - 55,664,258UniSTSGRCh37
Build 361055,333,497 - 55,334,264RGDNCBI36
Celera1048,926,407 - 48,927,175RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,645,013 - 49,645,782UniSTS
ECD04660  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,939,601 - 55,940,358UniSTSGRCh37
Build 361055,609,607 - 55,610,364RGDNCBI36
Celera1049,202,545 - 49,203,302RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,922,780 - 49,923,537UniSTS
ECD04788  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,577,543 - 55,578,296UniSTSGRCh37
Build 361055,247,549 - 55,248,302RGDNCBI36
Celera1048,840,512 - 48,841,265RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,559,144 - 49,559,897UniSTS
ECD05039  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,662,705 - 55,663,451UniSTSGRCh37
Build 361055,332,711 - 55,333,457RGDNCBI36
Celera1048,925,620 - 48,926,367RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,644,227 - 49,644,973UniSTS
ECD05113  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,582,269 - 55,583,013UniSTSGRCh37
Build 361055,252,275 - 55,253,019RGDNCBI36
Celera1048,845,238 - 48,845,982RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,563,870 - 49,564,614UniSTS
ECD05114  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,798,997 - 55,799,741UniSTSGRCh37
Build 361055,469,003 - 55,469,747RGDNCBI36
Celera1049,061,906 - 49,062,650RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,780,424 - 49,781,168UniSTS
ECD05115  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,906,846 - 55,907,590UniSTSGRCh37
Build 361055,576,852 - 55,577,596RGDNCBI36
Celera1049,169,794 - 49,170,538RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,889,943 - 49,890,687UniSTS
ECD05150  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,822,028 - 55,822,771UniSTSGRCh37
Build 361055,492,034 - 55,492,777RGDNCBI36
Celera1049,084,937 - 49,085,679RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,803,461 - 49,804,203UniSTS
ECD05215  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,625,386 - 55,626,127UniSTSGRCh37
Build 361055,295,392 - 55,296,133RGDNCBI36
Celera1048,888,356 - 48,889,097RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,606,961 - 49,607,705UniSTS
ECD05249  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,696,441 - 55,697,181UniSTSGRCh37
Build 361055,366,447 - 55,367,187RGDNCBI36
Celera1048,959,335 - 48,960,075RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,677,939 - 49,678,679UniSTS
ECD05294  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,744,844 - 55,745,583UniSTSGRCh37
Build 361055,414,850 - 55,415,589RGDNCBI36
Celera1049,007,732 - 49,008,471RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,726,248 - 49,726,987UniSTS
ECD05359  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,779,563 - 55,780,300UniSTSGRCh37
Build 361055,449,569 - 55,450,306RGDNCBI36
Celera1049,042,464 - 49,043,201RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,760,981 - 49,761,718UniSTS
ECD05656  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,635,192 - 55,635,921UniSTSGRCh37
Build 361055,305,198 - 55,305,927RGDNCBI36
Celera1048,898,177 - 48,898,906RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,616,788 - 49,617,517UniSTS
ECD05657  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,940,369 - 55,941,098UniSTSGRCh37
Build 361055,610,375 - 55,611,104RGDNCBI36
Celera1049,203,313 - 49,204,042RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,923,548 - 49,924,277UniSTS
ECD05813  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,833,183 - 55,833,908UniSTSGRCh37
Build 361055,503,189 - 55,503,914RGDNCBI36
Celera1049,096,091 - 49,096,816RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,814,615 - 49,815,340UniSTS
ECD05845  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,839,103 - 55,839,827UniSTSGRCh37
Build 361055,509,109 - 55,509,833RGDNCBI36
Celera1049,102,011 - 49,102,735RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,820,534 - 49,821,258UniSTS
ECD05942  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,845,060 - 55,845,781UniSTSGRCh37
Build 361055,515,066 - 55,515,787RGDNCBI36
Celera1049,107,968 - 49,108,689RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,826,493 - 49,827,214UniSTS
ECD06017  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,645,230 - 55,645,949UniSTSGRCh37
Build 361055,315,236 - 55,315,955RGDNCBI36
Celera1048,908,197 - 48,908,916RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,626,821 - 49,627,540UniSTS
ECD06091  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,826,016 - 55,826,733UniSTSGRCh37
Build 361055,496,022 - 55,496,739RGDNCBI36
Celera1049,088,924 - 49,089,641RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,807,448 - 49,808,165UniSTS
ECD06092  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,908,418 - 55,909,135UniSTSGRCh37
Build 361055,578,424 - 55,579,141RGDNCBI36
Celera1049,171,366 - 49,172,083RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,891,515 - 49,892,232UniSTS
ECD06172  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,891,833 - 55,892,548UniSTSGRCh37
Build 361055,561,839 - 55,562,554RGDNCBI36
Celera1049,154,735 - 49,155,450RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,873,266 - 49,873,981UniSTS
ECD06173  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,923,363 - 55,924,078UniSTSGRCh37
Build 361055,593,369 - 55,594,084RGDNCBI36
Celera1049,186,306 - 49,187,021RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,906,458 - 49,907,173UniSTS
ECD06312  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,698,209 - 55,698,920UniSTSGRCh37
Build 361055,368,215 - 55,368,926RGDNCBI36
Celera1048,961,103 - 48,961,814RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,679,707 - 49,680,418UniSTS
ECD06394  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,658,955 - 55,659,664UniSTSGRCh37
Build 361055,328,961 - 55,329,670RGDNCBI36
Celera1048,921,871 - 48,922,580RGD
Cytogenetic Map10q21.1UniSTS
ECD06466  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,717,552 - 55,718,259UniSTSGRCh37
Build 361055,387,558 - 55,388,265RGDNCBI36
Celera1048,980,440 - 48,981,147RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,699,043 - 49,699,750UniSTS
ECD06624  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,666,423 - 55,667,126UniSTSGRCh37
Build 361055,336,429 - 55,337,132RGDNCBI36
Celera1048,929,340 - 48,930,042RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,647,945 - 49,648,647UniSTS
ECD06625  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,946,769 - 55,947,472UniSTSGRCh37
Build 361055,616,775 - 55,617,478RGDNCBI36
Celera1049,209,713 - 49,210,416RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,929,952 - 49,930,655UniSTS
ECD06738  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,825,306 - 55,826,006UniSTSGRCh37
Build 361055,495,312 - 55,496,012RGDNCBI36
Celera1049,088,214 - 49,088,914RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,806,738 - 49,807,438UniSTS
ECD06796  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,743,039 - 55,743,737UniSTSGRCh37
Build 361055,413,045 - 55,413,743RGDNCBI36
Celera1049,005,927 - 49,006,625RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,724,441 - 49,725,139UniSTS
ECD06868  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,685,331 - 55,686,027UniSTSGRCh37
Build 361055,355,337 - 55,356,033RGDNCBI36
Celera1048,948,223 - 48,948,919RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,666,827 - 49,667,523UniSTS
ECD07024  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,715,018 - 55,715,710UniSTSGRCh37
Build 361055,385,024 - 55,385,716RGDNCBI36
Celera1048,977,901 - 48,978,593RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,696,504 - 49,697,196UniSTS
ECD07061  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,612,063 - 55,612,754UniSTSGRCh37
Build 361055,282,069 - 55,282,760RGDNCBI36
Celera1048,875,027 - 48,875,718RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,593,632 - 49,594,323UniSTS
ECD07613  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,674,635 - 55,675,311UniSTSGRCh37
Build 361055,344,641 - 55,345,317RGDNCBI36
Celera1048,937,548 - 48,938,224RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,656,153 - 49,656,829UniSTS
ECD07614  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,697,383 - 55,698,059UniSTSGRCh37
Build 361055,367,389 - 55,368,065RGDNCBI36
Celera1048,960,277 - 48,960,953RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,678,881 - 49,679,557UniSTS
ECD07647  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,969,430 - 55,970,105UniSTSGRCh37
Build 361055,639,436 - 55,640,111RGDNCBI36
Celera1049,232,372 - 49,233,047RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,952,617 - 49,953,292UniSTS
ECD07832  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,590,860 - 55,591,530UniSTSGRCh37
Build 361055,260,866 - 55,261,536RGDNCBI36
Celera1048,853,827 - 48,854,497RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,572,461 - 49,573,131UniSTS
ECD07939  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,968,626 - 55,969,293UniSTSGRCh37
Build 361055,638,632 - 55,639,299RGDNCBI36
Celera1049,231,568 - 49,232,235RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,951,813 - 49,952,480UniSTS
ECD08022  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,962,676 - 55,963,341UniSTSGRCh37
Build 361055,632,682 - 55,633,347RGDNCBI36
Celera1049,225,631 - 49,226,296RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,945,881 - 49,946,546UniSTS
ECD08061  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,831,053 - 55,831,717UniSTSGRCh37
Build 361055,501,059 - 55,501,723RGDNCBI36
Celera1049,093,961 - 49,094,625RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,812,485 - 49,813,149UniSTS
ECD08062  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,924,871 - 55,925,535UniSTSGRCh37
Build 361055,594,877 - 55,595,541RGDNCBI36
Celera1049,187,814 - 49,188,478RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,907,966 - 49,908,630UniSTS
ECD08137  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,667,150 - 55,667,812UniSTSGRCh37
Build 361055,337,156 - 55,337,818RGDNCBI36
Celera1048,930,066 - 48,930,728RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,648,671 - 49,649,333UniSTS
ECD08170  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,686,964 - 55,687,625UniSTSGRCh37
Build 361055,356,970 - 55,357,631RGDNCBI36
Celera1048,949,860 - 48,950,521RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,668,464 - 49,669,125UniSTS
ECD08469  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,573,753 - 55,574,406UniSTSGRCh37
Build 361055,243,759 - 55,244,412RGDNCBI36
Celera1048,836,722 - 48,837,375RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,555,351 - 49,556,004UniSTS
ECD08538  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,846,226 - 55,846,877UniSTSGRCh37
Build 361055,516,232 - 55,516,883RGDNCBI36
Celera1049,109,134 - 49,109,785RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,827,659 - 49,828,310UniSTS
ECD08539  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,959,377 - 55,960,028UniSTSGRCh37
Build 361055,629,383 - 55,630,034RGDNCBI36
Celera1049,222,333 - 49,222,984RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,942,582 - 49,943,233UniSTS
ECD08587  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,563,895 - 55,564,545UniSTSGRCh37
Build 361055,233,901 - 55,234,551RGDNCBI36
Celera1048,826,864 - 48,827,514RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,545,494 - 49,546,144UniSTS
ECD08752  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,782,674 - 55,783,320UniSTSGRCh37
Build 361055,452,680 - 55,453,326RGDNCBI36
Celera1049,045,574 - 49,046,220RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,764,091 - 49,764,737UniSTS
ECD08814  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,815,225 - 55,815,869UniSTSGRCh37
Build 361055,485,231 - 55,485,875RGDNCBI36
Celera1049,078,135 - 49,078,779RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,796,652 - 49,797,298UniSTS
ECD08855  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,583,040 - 55,583,683UniSTSGRCh37
Build 361055,253,046 - 55,253,689RGDNCBI36
Celera1048,846,009 - 48,846,652RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,564,641 - 49,565,284UniSTS
ECD08893  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,586,146 - 55,586,788UniSTSGRCh37
Build 361055,256,152 - 55,256,794RGDNCBI36
Celera1048,849,114 - 48,849,756RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,567,748 - 49,568,390UniSTS
ECD09115  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,668,143 - 55,668,779UniSTSGRCh37
Build 361055,338,149 - 55,338,785RGDNCBI36
Celera1048,931,059 - 48,931,695RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,649,664 - 49,650,300UniSTS
ECD09202  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,591,665 - 55,592,299UniSTSGRCh37
Build 361055,261,671 - 55,262,305RGDNCBI36
Celera1048,854,632 - 48,855,266RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,573,266 - 49,573,900UniSTS
ECD09431  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,563,247 - 55,563,875UniSTSGRCh37
Build 361055,233,253 - 55,233,881RGDNCBI36
Celera1048,826,216 - 48,826,844RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,544,846 - 49,545,474UniSTS
ECD09552  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,748,971 - 55,749,596UniSTSGRCh37
Build 361055,418,977 - 55,419,602RGDNCBI36
Celera1049,011,859 - 49,012,484RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,730,375 - 49,731,000UniSTS
ECD09596  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,661,888 - 55,662,512UniSTSGRCh37
Build 361055,331,894 - 55,332,518RGDNCBI36
Celera1048,924,803 - 48,925,427RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,643,410 - 49,644,034UniSTS
ECD09597  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,747,971 - 55,748,595UniSTSGRCh37
Build 361055,417,977 - 55,418,601RGDNCBI36
Celera1049,010,859 - 49,011,483RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,729,375 - 49,729,999UniSTS
ECD09635  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,778,774 - 55,779,397UniSTSGRCh37
Build 361055,448,780 - 55,449,403RGDNCBI36
Celera1049,041,675 - 49,042,298RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,760,192 - 49,760,815UniSTS
ECD09668  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,592,547 - 55,593,169UniSTSGRCh37
Build 361055,262,553 - 55,263,175RGDNCBI36
Celera1048,855,514 - 48,856,136RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,574,148 - 49,574,770UniSTS
ECD09669  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,720,721 - 55,721,343UniSTSGRCh37
Build 361055,390,727 - 55,391,349RGDNCBI36
Celera1048,983,609 - 48,984,231RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,702,211 - 49,702,833UniSTS
ECD09756  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,571,296 - 55,571,916UniSTSGRCh37
Build 361055,241,302 - 55,241,922RGDNCBI36
Celera1048,834,265 - 48,834,885RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,552,894 - 49,553,514UniSTS
ECD09757  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,575,539 - 55,576,159UniSTSGRCh37
Build 361055,245,545 - 55,246,165RGDNCBI36
Celera1048,838,508 - 48,839,128RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,557,140 - 49,557,760UniSTS
ECD09926  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,849,416 - 55,850,031UniSTSGRCh37
Build 361055,519,422 - 55,520,037RGDNCBI36
Celera1049,112,324 - 49,112,939RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,830,849 - 49,831,464UniSTS
ECD10028  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,870,922 - 55,871,534UniSTSGRCh37
Build 361055,540,928 - 55,541,540RGDNCBI36
Celera1049,133,823 - 49,134,435RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,852,352 - 49,852,964UniSTS
ECD10209  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,719,936 - 55,720,543UniSTSGRCh37
Build 361055,389,942 - 55,390,549RGDNCBI36
Cytogenetic Map10q21.1UniSTS
ECD10365  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,643,874 - 55,644,477UniSTSGRCh37
Build 361055,313,880 - 55,314,483RGDNCBI36
Celera1048,906,841 - 48,907,444RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,625,465 - 49,626,068UniSTS
ECD10442  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,607,808 - 55,608,409UniSTSGRCh37
Build 361055,277,814 - 55,278,415RGDNCBI36
Celera1048,870,773 - 48,871,374RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,589,399 - 49,590,000UniSTS
ECD10538  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,840,859 - 55,841,457UniSTSGRCh37
Build 361055,510,865 - 55,511,463RGDNCBI36
Celera1049,103,767 - 49,104,365RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,822,290 - 49,822,892UniSTS
ECD10634  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,688,686 - 55,689,281UniSTSGRCh37
Build 361055,358,692 - 55,359,287RGDNCBI36
Celera1048,951,582 - 48,952,177RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,670,186 - 49,670,781UniSTS
ECD10699  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,680,914 - 55,681,507UniSTSGRCh37
Build 361055,350,920 - 55,351,513RGDNCBI36
Celera1048,943,805 - 48,944,399RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,662,409 - 49,663,003UniSTS
ECD10734  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,913,336 - 55,913,928UniSTSGRCh37
Build 361055,583,342 - 55,583,934RGDNCBI36
Celera1049,176,284 - 49,176,876RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,896,433 - 49,897,025UniSTS
ECD10735  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,914,056 - 55,914,648UniSTSGRCh37
Build 361055,584,062 - 55,584,654RGDNCBI36
Celera1049,177,004 - 49,177,596RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,897,153 - 49,897,745UniSTS
ECD10768  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,584,692 - 55,585,283UniSTSGRCh37
Build 361055,254,698 - 55,255,289RGDNCBI36
Celera1048,847,660 - 48,848,251RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,566,292 - 49,566,881UniSTS
ECD10867  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,593,914 - 55,594,502UniSTSGRCh37
Build 361055,263,920 - 55,264,508RGDNCBI36
Celera1048,856,881 - 48,857,470RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,575,511 - 49,576,101UniSTS
ECD10903  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,937,837 - 55,938,424UniSTSGRCh37
Build 361055,607,843 - 55,608,430RGDNCBI36
Celera1049,200,781 - 49,201,368RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,921,016 - 49,921,603UniSTS
ECD10940  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,583,949 - 55,584,535UniSTSGRCh37
Build 361055,253,955 - 55,254,541RGDNCBI36
Celera1048,846,917 - 48,847,503RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,565,549 - 49,566,135UniSTS
ECD10967  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,568,792 - 55,569,377UniSTSGRCh37
Build 361055,238,798 - 55,239,383RGDNCBI36
Celera1048,831,761 - 48,832,346RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,550,390 - 49,550,975UniSTS
ECD10968  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,848,816 - 55,849,401UniSTSGRCh37
Build 361055,518,822 - 55,519,407RGDNCBI36
Celera1049,111,724 - 49,112,309RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,830,249 - 49,830,834UniSTS
ECD11040  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,912,551 - 55,913,134UniSTSGRCh37
Build 361055,582,557 - 55,583,140RGDNCBI36
Celera1049,175,499 - 49,176,082RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,895,648 - 49,896,231UniSTS
ECD11077  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,850,754 - 55,851,336UniSTSGRCh37
Build 361055,520,760 - 55,521,342RGDNCBI36
Celera1049,113,662 - 49,114,244RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,832,186 - 49,832,768UniSTS
ECD11109  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,963,425 - 55,964,006UniSTSGRCh37
Build 361055,633,431 - 55,634,012RGDNCBI36
Celera1049,226,380 - 49,226,961RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,946,630 - 49,947,211UniSTS
ECD11147  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,924,157 - 55,924,737UniSTSGRCh37
Build 361055,594,163 - 55,594,743RGDNCBI36
Celera1049,187,100 - 49,187,680RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,907,252 - 49,907,832UniSTS
ECD11148  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,949,059 - 55,949,639UniSTSGRCh37
Build 361055,619,065 - 55,619,645RGDNCBI36
Celera1049,212,003 - 49,212,583RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,932,242 - 49,932,822UniSTS
ECD11355  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,784,332 - 55,784,906UniSTSGRCh37
Build 361055,454,338 - 55,454,912RGDNCBI36
Celera1049,047,232 - 49,047,806RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,765,747 - 49,766,321UniSTS
ECD11356  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,820,504 - 55,821,078UniSTSGRCh37
Build 361055,490,510 - 55,491,084RGDNCBI36
Celera1049,083,414 - 49,083,988RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,801,933 - 49,802,507UniSTS
ECD11443  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,952,927 - 55,953,498UniSTSGRCh37
Build 361055,622,933 - 55,623,504RGDNCBI36
Celera1049,215,871 - 49,216,442RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,936,107 - 49,936,678UniSTS
ECD11505  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,665,690 - 55,666,259UniSTSGRCh37
Build 361055,335,696 - 55,336,265RGDNCBI36
Celera1048,928,607 - 48,929,176RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,647,212 - 49,647,781UniSTS
ECD11506  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,870,202 - 55,870,771UniSTSGRCh37
Build 361055,540,208 - 55,540,777RGDNCBI36
Celera1049,133,103 - 49,133,672RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,851,632 - 49,852,201UniSTS
ECD11755  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,589,135 - 55,589,697UniSTSGRCh37
Build 361055,259,141 - 55,259,703RGDNCBI36
Celera1048,852,102 - 48,852,664RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,570,736 - 49,571,298UniSTS
ECD11858  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,866,683 - 55,867,242UniSTSGRCh37
Build 361055,536,689 - 55,537,248RGDNCBI36
Celera1049,129,583 - 49,130,142RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,848,113 - 49,848,672UniSTS
ECD11920  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,778,069 - 55,778,626UniSTSGRCh37
Build 361055,448,075 - 55,448,632RGDNCBI36
Celera1049,040,970 - 49,041,527RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,759,487 - 49,760,044UniSTS
ECD11921  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,891,245 - 55,891,802UniSTSGRCh37
Build 361055,561,251 - 55,561,808RGDNCBI36
Celera1049,154,147 - 49,154,704RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,872,678 - 49,873,235UniSTS
ECD12021  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,590,228 - 55,590,782UniSTSGRCh37
Build 361055,260,234 - 55,260,788RGDNCBI36
Celera1048,853,195 - 48,853,749RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,571,829 - 49,572,383UniSTS
ECD12070  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,867,304 - 55,867,857UniSTSGRCh37
Build 361055,537,310 - 55,537,863RGDNCBI36
Celera1049,130,204 - 49,130,757RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,848,734 - 49,849,287UniSTS
ECD12106  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,606,975 - 55,607,527UniSTSGRCh37
Build 361055,276,981 - 55,277,533RGDNCBI36
Celera1048,869,940 - 48,870,492RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,588,566 - 49,589,118UniSTS
ECD12144  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,633,862 - 55,634,413UniSTSGRCh37
Build 361055,303,868 - 55,304,419RGDNCBI36
Celera1048,896,843 - 48,897,394RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,615,453 - 49,616,004UniSTS
ECD12246  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,636,838 - 55,637,386UniSTSGRCh37
Build 361055,306,844 - 55,307,392RGDNCBI36
Celera1048,899,825 - 48,900,373RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,618,436 - 49,618,990UniSTS
ECD12282  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,943,625 - 55,944,172UniSTSGRCh37
Build 361055,613,631 - 55,614,178RGDNCBI36
Celera1049,206,569 - 49,207,116RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,926,807 - 49,927,355UniSTS
ECD12332  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,905,303 - 55,905,849UniSTSGRCh37
Build 361055,575,309 - 55,575,855RGDNCBI36
Celera1049,168,207 - 49,168,753RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,888,372 - 49,888,918UniSTS
ECD12393  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,627,367 - 55,627,911UniSTSGRCh37
Build 361055,297,373 - 55,297,917RGDNCBI36
Celera1048,890,337 - 48,890,881RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,608,947 - 49,609,491UniSTS
ECD12394  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,904,665 - 55,905,209UniSTSGRCh37
Build 361055,574,671 - 55,575,215RGDNCBI36
Celera1049,167,569 - 49,168,113RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,887,734 - 49,888,278UniSTS
ECD12421  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,676,634 - 55,677,177UniSTSGRCh37
Build 361055,346,640 - 55,347,183RGDNCBI36
Celera1048,939,551 - 48,940,093RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,658,156 - 49,658,698UniSTS
ECD12422  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,971,661 - 55,972,204UniSTSGRCh37
Build 361055,641,667 - 55,642,210RGDNCBI36
Celera1049,234,603 - 49,235,146RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,954,848 - 49,955,391UniSTS
ECD12462  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,564,713 - 55,565,255UniSTSGRCh37
Build 361055,234,719 - 55,235,261RGDNCBI36
Celera1048,827,682 - 48,828,224RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,546,312 - 49,546,854UniSTS
ECD12498  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,568,114 - 55,568,655UniSTSGRCh37
Build 361055,238,120 - 55,238,661RGDNCBI36
Celera1048,831,083 - 48,831,624RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,549,712 - 49,550,253UniSTS
ECD12499  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,740,567 - 55,741,108UniSTSGRCh37
Build 361055,410,573 - 55,411,114RGDNCBI36
Celera1049,003,455 - 49,003,996RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,721,969 - 49,722,510UniSTS
ECD12686  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,832,329 - 55,832,865UniSTSGRCh37
Build 361055,502,335 - 55,502,871RGDNCBI36
Celera1049,095,237 - 49,095,773RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,813,761 - 49,814,297UniSTS
ECD12727  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,644,491 - 55,645,026UniSTSGRCh37
Build 361055,314,497 - 55,315,032RGDNCBI36
Celera1048,907,458 - 48,907,993RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,626,082 - 49,626,617UniSTS
ECD12767  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,747,425 - 55,747,959UniSTSGRCh37
Build 361055,417,431 - 55,417,965RGDNCBI36
Celera1049,010,313 - 49,010,847RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,728,829 - 49,729,363UniSTS
ECD12860  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,689,317 - 55,689,849UniSTSGRCh37
Build 361055,359,323 - 55,359,855RGDNCBI36
Celera1048,952,213 - 48,952,745RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,670,817 - 49,671,349UniSTS
ECD12861  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,921,831 - 55,922,363UniSTSGRCh37
Build 361055,591,837 - 55,592,369RGDNCBI36
Celera1049,184,774 - 49,185,306RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,904,926 - 49,905,458UniSTS
ECD12937  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,650,234 - 55,650,764UniSTSGRCh37
Build 361055,320,240 - 55,320,770RGDNCBI36
Celera1048,913,193 - 48,913,723RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,631,868 - 49,632,398UniSTS
ECD12976  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,973,574 - 55,974,103UniSTSGRCh37
Build 361055,643,580 - 55,644,109RGDNCBI36
Celera1049,236,515 - 49,237,044RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,956,761 - 49,957,290UniSTS
ECD13004  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,922,401 - 55,922,929UniSTSGRCh37
Build 361055,592,407 - 55,592,935RGDNCBI36
Celera1049,185,344 - 49,185,872RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,905,496 - 49,906,024UniSTS
ECD13076  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,888,314 - 55,888,840UniSTSGRCh37
Build 361055,558,320 - 55,558,846RGDNCBI36
Celera1049,151,216 - 49,151,742RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,869,747 - 49,870,273UniSTS
ECD13115  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,814,593 - 55,815,118UniSTSGRCh37
Build 361055,484,599 - 55,485,124RGDNCBI36
Celera1049,077,503 - 49,078,028RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,796,020 - 49,796,545UniSTS
ECD13116  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,887,073 - 55,887,598UniSTSGRCh37
Build 361055,557,079 - 55,557,604RGDNCBI36
Celera1049,149,975 - 49,150,500RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,868,506 - 49,869,031UniSTS
ECD13351  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,699,537 - 55,700,056UniSTSGRCh37
Build 361055,369,543 - 55,370,062RGDNCBI36
Celera1048,962,431 - 48,962,950RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,681,035 - 49,681,554UniSTS
ECD13352  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,906,087 - 55,906,606UniSTSGRCh37
Build 361055,576,093 - 55,576,612RGDNCBI36
Celera1049,168,991 - 49,169,511RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,889,156 - 49,889,675UniSTS
ECD13392  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,637,398 - 55,637,916UniSTSGRCh37
Build 361055,307,404 - 55,307,922RGDNCBI36
Celera1048,900,385 - 48,900,903RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,619,002 - 49,619,520UniSTS
ECD13430  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,716,654 - 55,717,171UniSTSGRCh37
Build 361055,386,660 - 55,387,177RGDNCBI36
Celera1048,979,537 - 48,980,054RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,698,140 - 49,698,657UniSTS
ECD13509  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,886,503 - 55,887,018UniSTSGRCh37
Build 361055,556,509 - 55,557,024RGDNCBI36
Celera1049,149,405 - 49,149,920RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,867,936 - 49,868,451UniSTS
ECD13589  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,567,475 - 55,567,988UniSTSGRCh37
Build 361055,237,481 - 55,237,994RGDNCBI36
Celera1048,830,444 - 48,830,957RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,549,073 - 49,549,586UniSTS
ECD13638  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,887,738 - 55,888,250UniSTSGRCh37
Build 361055,557,744 - 55,558,256RGDNCBI36
Celera1049,150,640 - 49,151,152RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,869,171 - 49,869,683UniSTS
ECD13675  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,783,754 - 55,784,265UniSTSGRCh37
Build 361055,453,760 - 55,454,271RGDNCBI36
Celera1049,046,654 - 49,047,165RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,765,169 - 49,765,680UniSTS
ECD13749  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,896,080 - 55,896,589UniSTSGRCh37
Build 361055,566,086 - 55,566,595RGDNCBI36
Celera1049,158,984 - 49,159,493RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,879,150 - 49,879,659UniSTS
ECD14037  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,755,555 - 55,756,057UniSTSGRCh37
Build 361055,425,561 - 55,426,063RGDNCBI36
Celera1049,018,443 - 49,018,945RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,736,972 - 49,737,476UniSTS
ECD14038  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,813,012 - 55,813,514UniSTSGRCh37
Build 361055,483,018 - 55,483,520RGDNCBI36
Celera1049,075,922 - 49,076,424RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,794,439 - 49,794,941UniSTS
ECD14069  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,650,881 - 55,651,382UniSTSGRCh37
Build 361055,320,887 - 55,321,388RGDNCBI36
Celera1048,913,841 - 48,914,343RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,632,516 - 49,633,018UniSTS
ECD14070  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,884,279 - 55,884,780UniSTSGRCh37
Build 361055,554,285 - 55,554,786RGDNCBI36
Celera1049,147,180 - 49,147,681RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,865,711 - 49,866,212UniSTS
ECD14110  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,896,633 - 55,897,133UniSTSGRCh37
Build 361055,566,639 - 55,567,139RGDNCBI36
Celera1049,159,537 - 49,160,037RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,879,703 - 49,880,203UniSTS
ECD14249  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,700,245 - 55,700,742UniSTSGRCh37
Build 361055,370,251 - 55,370,748RGDNCBI36
Celera1048,963,139 - 48,963,636RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,681,743 - 49,682,240UniSTS
ECD14281  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,630,288 - 55,630,784UniSTSGRCh37
Build 361055,300,294 - 55,300,790RGDNCBI36
Celera1048,893,258 - 48,893,754RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,611,868 - 49,612,364UniSTS
ECD14282  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,640,238 - 55,640,734UniSTSGRCh37
Build 361055,310,244 - 55,310,740RGDNCBI36
Celera1048,903,224 - 48,903,719RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,621,848 - 49,622,343UniSTS
ECD14380  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,587,294 - 55,587,788UniSTSGRCh37
Build 361055,257,300 - 55,257,794RGDNCBI36
Celera1048,850,262 - 48,850,756RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,568,896 - 49,569,390UniSTS
ECD14573  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,626,363 - 55,626,853UniSTSGRCh37
Build 361055,296,369 - 55,296,859RGDNCBI36
Celera1048,889,333 - 48,889,823RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,607,943 - 49,608,433UniSTS
ECD14574  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,857,451 - 55,857,941UniSTSGRCh37
Build 361055,527,457 - 55,527,947RGDNCBI36
Celera1049,120,359 - 49,120,849RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,838,883 - 49,839,373UniSTS
ECD14608  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,570,475 - 55,570,964UniSTSGRCh37
Build 361055,240,481 - 55,240,970RGDNCBI36
Celera1048,833,444 - 48,833,933RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,552,073 - 49,552,562UniSTS
ECD14609  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,884,840 - 55,885,329UniSTSGRCh37
Build 361055,554,846 - 55,555,335RGDNCBI36
Celera1049,147,741 - 49,148,230RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,866,272 - 49,866,761UniSTS
ECD14700  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,594,562 - 55,595,049UniSTSGRCh37
Build 361055,264,568 - 55,265,055RGDNCBI36
Celera1048,857,530 - 48,858,017RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,576,161 - 49,576,648UniSTS
ECD14701  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,733,236 - 55,733,723UniSTSGRCh37
Build 361055,403,242 - 55,403,729RGDNCBI36
Celera1048,996,124 - 48,996,611RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,714,642 - 49,715,129UniSTS
ECD14736  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,588,049 - 55,588,535UniSTSGRCh37
Build 361055,258,055 - 55,258,541RGDNCBI36
Celera1048,851,016 - 48,851,502RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,569,650 - 49,570,136UniSTS
ECD14737  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,708,795 - 55,709,281UniSTSGRCh37
Build 361055,378,801 - 55,379,287RGDNCBI36
Celera1048,971,678 - 48,972,164RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,690,281 - 49,690,767UniSTS
ECD14738  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,802,661 - 55,803,147UniSTSGRCh37
Build 361055,472,667 - 55,473,153RGDNCBI36
Celera1049,065,570 - 49,066,056RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,784,088 - 49,784,574UniSTS
ECD14922  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,641,267 - 55,641,749UniSTSGRCh37
Build 361055,311,273 - 55,311,755RGDNCBI36
Celera1048,904,252 - 48,904,734RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,622,876 - 49,623,358UniSTS
ECD14923  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,679,463 - 55,679,945UniSTSGRCh37
Build 361055,349,469 - 55,349,951RGDNCBI36
Cytogenetic Map10q21.1UniSTS
ECD14959  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,971,151 - 55,971,632UniSTSGRCh37
Build 361055,641,157 - 55,641,638RGDNCBI36
Celera1049,234,093 - 49,234,574RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,954,338 - 49,954,819UniSTS
ECD14994  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,638,827 - 55,639,307UniSTSGRCh37
Build 361055,308,833 - 55,309,313RGDNCBI36
Celera1048,901,814 - 48,902,293RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,620,438 - 49,620,917UniSTS
ECD15033  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,680,359 - 55,680,838UniSTSGRCh37
Build 361055,350,365 - 55,350,844RGDNCBI36
Celera1048,943,250 - 48,943,729RGD
Cytogenetic Map10q21.1UniSTS
ECD15034  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,936,098 - 55,936,577UniSTSGRCh37
Build 361055,606,104 - 55,606,583RGDNCBI36
Celera1049,199,041 - 49,199,520RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,919,276 - 49,919,755UniSTS
ECD15123  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,958,553 - 55,959,030UniSTSGRCh37
Build 361055,628,559 - 55,629,036RGDNCBI36
Celera1049,221,503 - 49,221,980RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,941,746 - 49,942,223UniSTS
ECD15257  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,806,649 - 55,807,123UniSTSGRCh37
Build 361055,476,655 - 55,477,129RGDNCBI36
Celera1049,069,559 - 49,070,033RGD
Cytogenetic Map10q21.1UniSTS
ECD15294  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,800,348 - 55,800,821UniSTSGRCh37
Build 361055,470,354 - 55,470,827RGDNCBI36
Celera1049,063,257 - 49,063,730RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,781,775 - 49,782,248UniSTS
ECD15316  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,716,081 - 55,716,553UniSTSGRCh37
Build 361055,386,087 - 55,386,559RGDNCBI36
Celera1048,978,964 - 48,979,436RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,697,567 - 49,698,039UniSTS
ECD15317  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,961,496 - 55,961,968UniSTSGRCh37
Build 361055,631,502 - 55,631,974RGDNCBI36
Celera1049,224,452 - 49,224,922RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,944,702 - 49,945,172UniSTS
ECD15361  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,562,666 - 55,563,137UniSTSGRCh37
Build 361055,232,672 - 55,233,143RGDNCBI36
Celera1048,825,635 - 48,826,106RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,544,265 - 49,544,736UniSTS
ECD15401  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,565,258 - 55,565,728UniSTSGRCh37
Build 361055,235,264 - 55,235,734RGDNCBI36
Celera1048,828,227 - 48,828,697RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,546,857 - 49,547,327UniSTS
ECD15435  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,800,869 - 55,801,338UniSTSGRCh37
GRCh371055,800,352 - 55,801,338UniSTSGRCh37
Build 361055,470,875 - 55,471,344RGDNCBI36
Celera1049,063,261 - 49,064,247UniSTS
Celera1049,063,778 - 49,064,247RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,782,296 - 49,782,765UniSTS
HuRef1049,781,779 - 49,782,765UniSTS
ECD15579  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,836,361 - 55,836,827UniSTSGRCh37
Build 361055,506,367 - 55,506,833RGDNCBI36
Celera1049,099,269 - 49,099,735RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,817,792 - 49,818,258UniSTS
ECD15633  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,601,101 - 55,601,566UniSTSGRCh37
Build 361055,271,107 - 55,271,572RGDNCBI36
Celera1048,864,066 - 48,864,531RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,582,692 - 49,583,157UniSTS
ECD15707  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,915,572 - 55,916,035UniSTSGRCh37
Build 361055,585,578 - 55,586,041RGDNCBI36
Celera1049,178,520 - 49,178,983RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,898,669 - 49,899,132UniSTS
ECD15750  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,797,585 - 55,798,047UniSTSGRCh37
Build 361055,467,591 - 55,468,053RGDNCBI36
Celera1049,060,494 - 49,060,956RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,779,012 - 49,779,474UniSTS
ECD15988  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,691,997 - 55,692,453UniSTSGRCh37
Build 361055,362,003 - 55,362,459RGDNCBI36
Celera1048,954,891 - 48,955,347RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,673,495 - 49,673,951UniSTS
ECD16057  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,944,920 - 55,945,374UniSTSGRCh37
Build 361055,614,926 - 55,615,380RGDNCBI36
Celera1049,207,864 - 49,208,318RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,928,103 - 49,928,557UniSTS
ECD16084  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,642,991 - 55,643,444UniSTSGRCh37
Build 361055,312,997 - 55,313,450RGDNCBI36
Celera1048,905,958 - 48,906,411RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,624,581 - 49,625,034UniSTS
ECD16085  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,831,845 - 55,832,298UniSTSGRCh37
Build 361055,501,851 - 55,502,304RGDNCBI36
Celera1049,094,753 - 49,095,206RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,813,277 - 49,813,730UniSTS
ECD16447  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,852,870 - 55,853,309UniSTSGRCh37
Build 361055,522,876 - 55,523,315RGDNCBI36
Celera1049,115,778 - 49,116,217RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,834,302 - 49,834,741UniSTS
ECD16613  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,855,300 - 55,855,732UniSTSGRCh37
Build 361055,525,306 - 55,525,738RGDNCBI36
Celera1049,118,208 - 49,118,640RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,836,732 - 49,837,164UniSTS
ECD16637  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,819,694 - 55,820,125UniSTSGRCh37
Build 361055,489,700 - 55,490,131RGDNCBI36
Celera1049,082,604 - 49,083,035RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,801,123 - 49,801,554UniSTS
ECD16662  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,690,734 - 55,691,164UniSTSGRCh37
Build 361055,360,740 - 55,361,170RGDNCBI36
Celera1048,953,628 - 48,954,058RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,672,232 - 49,672,662UniSTS
ECD16698  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,777,607 - 55,778,035UniSTSGRCh37
Build 361055,447,613 - 55,448,041RGDNCBI36
Celera1049,040,508 - 49,040,936RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,759,025 - 49,759,453UniSTS
ECD16779  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,652,649 - 55,653,074UniSTSGRCh37
Build 361055,322,655 - 55,323,080RGDNCBI36
Celera1048,915,565 - 48,915,990RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,634,581 - 49,635,006UniSTS
ECD16780  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,704,313 - 55,704,738UniSTSGRCh37
Build 361055,374,319 - 55,374,744RGDNCBI36
Celera1048,967,207 - 48,967,632RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,685,810 - 49,686,235UniSTS
ECD16854  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,791,865 - 55,792,287UniSTSGRCh37
Build 361055,461,871 - 55,462,293RGDNCBI36
Celera1049,054,762 - 49,055,184RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,773,280 - 49,773,702UniSTS
ECD16855  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,852,167 - 55,852,589UniSTSGRCh37
Build 361055,522,173 - 55,522,595RGDNCBI36
Celera1049,115,075 - 49,115,497RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,833,599 - 49,834,021UniSTS
ECD16928  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,754,333 - 55,754,752UniSTSGRCh37
Build 361055,424,339 - 55,424,758RGDNCBI36
Celera1049,017,221 - 49,017,640RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,735,750 - 49,736,169UniSTS
ECD17178  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,758,845 - 55,759,254UniSTSGRCh37
Build 361055,428,851 - 55,429,260RGDNCBI36
Celera1049,021,732 - 49,022,141RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,740,262 - 49,740,671UniSTS
ECD17179  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,854,575 - 55,854,984UniSTSGRCh37
Build 361055,524,581 - 55,524,990RGDNCBI36
Celera1049,117,483 - 49,117,892RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,836,007 - 49,836,416UniSTS
ECD17180  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,935,507 - 55,935,916UniSTSGRCh37
Build 361055,605,513 - 55,605,922RGDNCBI36
Celera1049,198,450 - 49,198,859RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,918,685 - 49,919,094UniSTS
ECD17253  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,932,847 - 55,933,253UniSTSGRCh37
Build 361055,602,853 - 55,603,259RGDNCBI36
Celera1049,195,790 - 49,196,196RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,916,025 - 49,916,431UniSTS
ECD17273  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,691,576 - 55,691,981UniSTSGRCh37
Build 361055,361,582 - 55,361,987RGDNCBI36
Celera1048,954,470 - 48,954,875RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,673,074 - 49,673,479UniSTS
ECD17295  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,813,994 - 55,814,398UniSTSGRCh37
Build 361055,484,000 - 55,484,404RGDNCBI36
Celera1049,076,904 - 49,077,308RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,795,421 - 49,795,825UniSTS
ECD17376  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,895,061 - 55,895,461UniSTSGRCh37
Build 361055,565,067 - 55,565,467RGDNCBI36
Celera1049,157,965 - 49,158,365RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,878,131 - 49,878,531UniSTS
ECD17429  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,615,092 - 55,615,490UniSTSGRCh37
Build 361055,285,098 - 55,285,496RGDNCBI36
Celera1048,878,056 - 48,878,454RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,596,661 - 49,597,059UniSTS
ECD17430  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,708,048 - 55,708,446UniSTSGRCh37
Build 361055,378,054 - 55,378,452RGDNCBI36
Celera1048,970,931 - 48,971,329RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,689,534 - 49,689,932UniSTS
ECD17480  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,608,853 - 55,609,249UniSTSGRCh37
Build 361055,278,859 - 55,279,255RGDNCBI36
Celera1048,871,818 - 48,872,214RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,590,444 - 49,590,840UniSTS
ECD17481  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,616,969 - 55,617,365UniSTSGRCh37
Build 361055,286,975 - 55,287,371RGDNCBI36
Celera1048,879,939 - 48,880,335RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,598,544 - 49,598,940UniSTS
ECD17620  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,611,611 - 55,612,001UniSTSGRCh37
Build 361055,281,617 - 55,282,007RGDNCBI36
Celera1048,874,575 - 48,874,965RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,593,180 - 49,593,570UniSTS
ECD17681  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,957,846 - 55,958,233UniSTSGRCh37
Build 361055,627,852 - 55,628,239RGDNCBI36
Celera1049,220,796 - 49,221,183RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,941,031 - 49,941,418UniSTS
ECD17749  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,911,622 - 55,912,007UniSTSGRCh37
Build 361055,581,628 - 55,582,013RGDNCBI36
Celera1049,174,570 - 49,174,955RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,894,719 - 49,895,104UniSTS
ECD17835  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,828,642 - 55,829,024UniSTSGRCh37
Build 361055,498,648 - 55,499,030RGDNCBI36
Celera1049,091,550 - 49,091,932RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,810,074 - 49,810,456UniSTS
ECD17909  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,618,810 - 55,619,189UniSTSGRCh37
Build 361055,288,816 - 55,289,195RGDNCBI36
Celera1048,881,780 - 48,882,159RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,600,385 - 49,600,764UniSTS
ECD17910  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,724,308 - 55,724,687UniSTSGRCh37
Build 361055,394,314 - 55,394,693RGDNCBI36
Celera1048,987,199 - 48,987,578RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,705,802 - 49,706,181UniSTS
ECD17963  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,943,213 - 55,943,590UniSTSGRCh37
Build 361055,613,219 - 55,613,596RGDNCBI36
Celera1049,206,157 - 49,206,534RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,926,395 - 49,926,772UniSTS
ECD18030  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,565,820 - 55,566,195UniSTSGRCh37
Build 361055,235,826 - 55,236,201RGDNCBI36
Celera1048,828,789 - 48,829,164RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,547,423 - 49,547,798UniSTS
ECD18056  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,609,755 - 55,610,129UniSTSGRCh37
Build 361055,279,761 - 55,280,135RGDNCBI36
Celera1048,872,719 - 48,873,093RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,591,344 - 49,591,718UniSTS
ECD18086  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,983,419 - 55,983,792UniSTSGRCh37
Build 361055,653,425 - 55,653,798RGDNCBI36
Celera1049,246,360 - 49,246,733RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,966,613 - 49,966,986UniSTS
ECD18208  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,915,068 - 55,915,436UniSTSGRCh37
Build 361055,585,074 - 55,585,442RGDNCBI36
Celera1049,178,016 - 49,178,384RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,898,165 - 49,898,533UniSTS
ECD18431  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,652,089 - 55,652,448UniSTSGRCh37
Build 361055,322,095 - 55,322,454RGDNCBI36
Celera1048,915,005 - 48,915,364RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,634,021 - 49,634,380UniSTS
ECD18471  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,744,259 - 55,744,617UniSTSGRCh37
Build 361055,414,265 - 55,414,623RGDNCBI36
Celera1049,007,147 - 49,007,505RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,725,663 - 49,726,021UniSTS
ECD18472  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,798,427 - 55,798,785UniSTSGRCh37
Build 361055,468,433 - 55,468,791RGDNCBI36
Celera1049,061,336 - 49,061,694RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,779,854 - 49,780,212UniSTS
ECD18473  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,949,806 - 55,950,164UniSTSGRCh37
Build 361055,619,812 - 55,620,170RGDNCBI36
Celera1049,212,750 - 49,213,108RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,932,985 - 49,933,343UniSTS
ECD18523  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,710,142 - 55,710,498UniSTSGRCh37
Build 361055,380,148 - 55,380,504RGDNCBI36
Celera1048,973,025 - 48,973,381RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,691,628 - 49,691,984UniSTS
ECD18564  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,755,113 - 55,755,467UniSTSGRCh37
Build 361055,425,119 - 55,425,473RGDNCBI36
Celera1049,018,001 - 49,018,355RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,736,530 - 49,736,884UniSTS
ECD18565  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,866,095 - 55,866,449UniSTSGRCh37
Build 361055,536,101 - 55,536,455RGDNCBI36
Celera1049,128,995 - 49,129,349RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,847,525 - 49,847,879UniSTS
ECD18591  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,628,876 - 55,629,229UniSTSGRCh37
Build 361055,298,882 - 55,299,235RGDNCBI36
Celera1048,891,846 - 48,892,199RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,610,456 - 49,610,809UniSTS
ECD18622  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,725,182 - 55,725,534UniSTSGRCh37
Build 361055,395,188 - 55,395,540RGDNCBI36
Celera1048,988,071 - 48,988,423RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,706,674 - 49,707,026UniSTS
ECD18731  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,942,355 - 55,942,703UniSTSGRCh37
Build 361055,612,361 - 55,612,709RGDNCBI36
Celera1049,205,299 - 49,205,647RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,925,536 - 49,925,884UniSTS
ECD18811  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,970,551 - 55,970,896UniSTSGRCh37
Build 361055,640,557 - 55,640,902RGDNCBI36
Celera1049,233,493 - 49,233,838RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,953,738 - 49,954,083UniSTS
ECD18847  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,973,214 - 55,973,558UniSTSGRCh37
Build 361055,643,220 - 55,643,564RGDNCBI36
Celera1049,236,155 - 49,236,499RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,956,401 - 49,956,745UniSTS
ECD18875  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,598,074 - 55,598,417UniSTSGRCh37
Build 361055,268,080 - 55,268,423RGDNCBI36
Celera1048,861,040 - 48,861,382RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,579,665 - 49,580,007UniSTS
ECD18906  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,711,040 - 55,711,382UniSTSGRCh37
Build 361055,381,046 - 55,381,388RGDNCBI36
Celera1048,973,923 - 48,974,265RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,692,526 - 49,692,868UniSTS
ECD18948  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,586,850 - 55,587,190UniSTSGRCh37
Build 361055,256,856 - 55,257,196RGDNCBI36
Celera1048,849,818 - 48,850,158RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,568,452 - 49,568,792UniSTS
ECD18965  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,859,345 - 55,859,684UniSTSGRCh37
Build 361055,529,351 - 55,529,690RGDNCBI36
Celera1049,122,251 - 49,122,590RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,840,781 - 49,841,120UniSTS
ECD19168  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,844,393 - 55,844,724UniSTSGRCh37
Build 361055,514,399 - 55,514,730RGDNCBI36
Celera1049,107,301 - 49,107,632RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,825,826 - 49,826,157UniSTS
ECD19191  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,719,375 - 55,719,705UniSTSGRCh37
Build 361055,389,381 - 55,389,711RGDNCBI36
Celera1048,982,263 - 48,982,593RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,700,865 - 49,701,195UniSTS
ECD19192  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,780,716 - 55,781,046UniSTSGRCh37
Build 361055,450,722 - 55,451,052RGDNCBI36
Celera1049,043,617 - 49,043,947RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,762,134 - 49,762,464UniSTS
ECD19310  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,588,652 - 55,588,977UniSTSGRCh37
Build 361055,258,658 - 55,258,983RGDNCBI36
Celera1048,851,619 - 48,851,944RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,570,253 - 49,570,578UniSTS
ECD19311  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,631,774 - 55,632,099UniSTSGRCh37
Build 361055,301,780 - 55,302,105RGDNCBI36
Celera1048,894,755 - 48,895,080RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,613,364 - 49,613,689UniSTS
ECD19312  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,749,726 - 55,750,051UniSTSGRCh37
Build 361055,419,732 - 55,420,057RGDNCBI36
Celera1049,012,614 - 49,012,939RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,731,130 - 49,731,455UniSTS
ECD19335  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,602,463 - 55,602,787UniSTSGRCh37
Build 361055,272,469 - 55,272,793RGDNCBI36
Celera1048,865,428 - 48,865,752RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,584,054 - 49,584,378UniSTS
ECD19336  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,739,271 - 55,739,595UniSTSGRCh37
Build 361055,409,277 - 55,409,601RGDNCBI36
Celera1049,002,158 - 49,002,482RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,720,673 - 49,720,997UniSTS
ECD19372  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,654,163 - 55,654,486UniSTSGRCh37
Build 361055,324,169 - 55,324,492RGDNCBI36
Celera1048,917,079 - 48,917,402RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,636,095 - 49,636,418UniSTS
ECD19373  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,837,170 - 55,837,493UniSTSGRCh37
Build 361055,507,176 - 55,507,499RGDNCBI36
Celera1049,100,078 - 49,100,401RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,818,601 - 49,818,924UniSTS
ECD19432  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,709,505 - 55,709,826UniSTSGRCh37
Build 361055,379,511 - 55,379,832RGDNCBI36
Celera1048,972,388 - 48,972,709RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,690,991 - 49,691,312UniSTS
ECD19486  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,829,210 - 55,829,529UniSTSGRCh37
Build 361055,499,216 - 55,499,535RGDNCBI36
Celera1049,092,118 - 49,092,437RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,810,642 - 49,810,961UniSTS
ECD19687  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,821,130 - 55,821,442UniSTSGRCh37
Build 361055,491,136 - 55,491,448RGDNCBI36
Celera1049,084,040 - 49,084,352RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,802,559 - 49,802,871UniSTS
ECD19716  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,919,305 - 55,919,616UniSTSGRCh37
Build 361055,589,311 - 55,589,622RGDNCBI36
Celera1049,182,253 - 49,182,564RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,902,405 - 49,902,716UniSTS
ECD19769  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,639,837 - 55,640,146UniSTSGRCh37
Build 361055,309,843 - 55,310,152RGDNCBI36
Celera1048,902,823 - 48,903,132RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,621,447 - 49,621,756UniSTS
ECD19770  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,725,696 - 55,726,005UniSTSGRCh37
Build 361055,395,702 - 55,396,011RGDNCBI36
Celera1048,988,585 - 48,988,894RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,707,189 - 49,707,410UniSTS
ECD19877  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,934,601 - 55,934,906UniSTSGRCh37
Build 361055,604,607 - 55,604,912RGDNCBI36
Celera1049,197,544 - 49,197,849RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,917,779 - 49,918,084UniSTS
ECD19930  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,827,785 - 55,828,088UniSTSGRCh37
Build 361055,497,791 - 55,498,094RGDNCBI36
Celera1049,090,693 - 49,090,996RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,809,217 - 49,809,520UniSTS
ECD19978  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,620,700 - 55,621,001UniSTSGRCh37
Build 361055,290,706 - 55,291,007RGDNCBI36
Celera1048,883,670 - 48,883,971RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,602,275 - 49,602,576UniSTS
ECD20086  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,619,405 - 55,619,702UniSTSGRCh37
Build 361055,289,411 - 55,289,708RGDNCBI36
Celera1048,882,375 - 48,882,672RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,600,980 - 49,601,277UniSTS
ECD20111  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,952,057 - 55,952,353UniSTSGRCh37
Build 361055,622,063 - 55,622,359RGDNCBI36
Celera1049,215,001 - 49,215,297RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,935,237 - 49,935,533UniSTS
ECD20132  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,742,630 - 55,742,925UniSTSGRCh37
Build 361055,412,636 - 55,412,931RGDNCBI36
Celera1049,005,518 - 49,005,813RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,724,032 - 49,724,327UniSTS
ECD20152  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,889,653 - 55,889,947UniSTSGRCh37
Build 361055,559,659 - 55,559,953RGDNCBI36
Celera1049,152,555 - 49,152,849RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,871,086 - 49,871,380UniSTS
ECD20258  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,703,317 - 55,703,607UniSTSGRCh37
Build 361055,373,323 - 55,373,613RGDNCBI36
Celera1048,966,211 - 48,966,501RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,684,814 - 49,685,104UniSTS
ECD20279  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,782,025 - 55,782,314UniSTSGRCh37
Build 361055,452,031 - 55,452,320RGDNCBI36
Celera1049,044,926 - 49,045,214RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,763,443 - 49,763,731UniSTS
ECD20338  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,721,682 - 55,721,969UniSTSGRCh37
Build 361055,391,688 - 55,391,975RGDNCBI36
Celera1048,984,570 - 48,984,857RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,703,172 - 49,703,460UniSTS
ECD20498  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,853,529 - 55,853,810UniSTSGRCh37
Build 361055,523,535 - 55,523,816RGDNCBI36
Celera1049,116,437 - 49,116,718RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,834,961 - 49,835,242UniSTS
ECD20524  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,781,601 - 55,781,881UniSTSGRCh37
Build 361055,451,607 - 55,451,887RGDNCBI36
Celera1049,044,502 - 49,044,782RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,763,019 - 49,763,299UniSTS
ECD20592  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,933,725 - 55,934,003UniSTSGRCh37
Build 361055,603,731 - 55,604,009RGDNCBI36
Celera1049,196,668 - 49,196,946RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,916,903 - 49,917,181UniSTS
ECD20764  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,952,447 - 55,952,719UniSTSGRCh37
Build 361055,622,453 - 55,622,725RGDNCBI36
Celera1049,215,391 - 49,215,663RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,935,627 - 49,935,899UniSTS
ECD20864  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,682,981 - 55,683,249UniSTSGRCh37
Build 361055,352,987 - 55,353,255RGDNCBI36
Celera1048,945,873 - 48,946,141RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,664,477 - 49,664,745UniSTS
ECD20865  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,918,273 - 55,918,541UniSTSGRCh37
Build 361055,588,279 - 55,588,547RGDNCBI36
Celera1049,181,221 - 49,181,489RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,901,370 - 49,901,638UniSTS
ECD21015  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,823,040 - 55,823,303UniSTSGRCh37
Build 361055,493,046 - 55,493,309RGDNCBI36
Celera1049,085,948 - 49,086,211RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,804,472 - 49,804,735UniSTS
ECD21053  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,678,192 - 55,678,454UniSTSGRCh37
Build 361055,348,198 - 55,348,460RGDNCBI36
Celera1048,941,108 - 48,941,370RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,659,713 - 49,659,975UniSTS
ECD21054  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,885,495 - 55,885,757UniSTSGRCh37
Build 361055,555,501 - 55,555,763RGDNCBI36
Celera1049,148,396 - 49,148,658RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,866,927 - 49,867,189UniSTS
ECD21145  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,676,158 - 55,676,417UniSTSGRCh37
Build 361055,346,164 - 55,346,423RGDNCBI36
Celera1048,939,071 - 48,939,334RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,657,676 - 49,657,939UniSTS
ECD21146  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,954,532 - 55,954,791UniSTSGRCh37
Build 361055,624,538 - 55,624,797RGDNCBI36
Celera1049,217,482 - 49,217,741RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,937,717 - 49,937,976UniSTS
ECD21147  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,977,029 - 55,977,288UniSTSGRCh37
Build 361055,647,035 - 55,647,294RGDNCBI36
Celera1049,239,970 - 49,240,229RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,960,219 - 49,960,478UniSTS
ECD21321  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,636,438 - 55,636,690UniSTSGRCh37
Build 361055,306,444 - 55,306,696RGDNCBI36
Celera1048,899,425 - 48,899,677RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,618,036 - 49,618,288UniSTS
ECD21353  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,860,496 - 55,860,747UniSTSGRCh37
Build 361055,530,502 - 55,530,753RGDNCBI36
Celera1049,123,402 - 49,123,653RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,841,932 - 49,842,183UniSTS
ECD21491  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,713,046 - 55,713,293UniSTSGRCh37
Build 361055,383,052 - 55,383,299RGDNCBI36
Celera1048,975,929 - 48,976,176RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,694,532 - 49,694,779UniSTS
ECD21711  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,861,105 - 55,861,346UniSTSGRCh37
Build 361055,531,111 - 55,531,352RGDNCBI36
Celera1049,124,011 - 49,124,252RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,842,541 - 49,842,782UniSTS
ECD21802  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,701,690 - 55,701,928UniSTSGRCh37
Build 361055,371,696 - 55,371,934RGDNCBI36
Celera1048,964,584 - 48,964,822RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,683,188 - 49,683,426UniSTS
ECD21884  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,956,816 - 55,957,051UniSTSGRCh37
Build 361055,626,822 - 55,627,057RGDNCBI36
Celera1049,219,766 - 49,220,001RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,940,001 - 49,940,236UniSTS
ECD21925  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,597,265 - 55,597,499UniSTSGRCh37
Build 361055,267,271 - 55,267,505RGDNCBI36
Celera1048,860,233 - 48,860,467RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,578,864 - 49,579,098UniSTS
ECD22082  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,686,622 - 55,686,851UniSTSGRCh37
Build 361055,356,628 - 55,356,857RGDNCBI36
Celera1048,949,514 - 48,949,743RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,668,118 - 49,668,347UniSTS
ECD22198  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,646,121 - 55,646,346UniSTSGRCh37
Build 361055,316,127 - 55,316,352RGDNCBI36
Celera1048,909,088 - 48,909,313RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,627,712 - 49,627,937UniSTS
ECD22199  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,869,773 - 55,869,998UniSTSGRCh37
Build 361055,539,779 - 55,540,004RGDNCBI36
Celera1049,132,673 - 49,132,898RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,851,203 - 49,851,428UniSTS
ECD22310  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,642,457 - 55,642,679UniSTSGRCh37
Build 361055,312,463 - 55,312,685RGDNCBI36
Celera1048,905,422 - 48,905,644RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,624,045 - 49,624,267UniSTS
ECD22446  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,721,435 - 55,721,653UniSTSGRCh37
Build 361055,391,441 - 55,391,659RGDNCBI36
Celera1048,984,323 - 48,984,541RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,702,925 - 49,703,143UniSTS
ECD22471  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,574,755 - 55,574,972UniSTSGRCh37
Build 361055,244,761 - 55,244,978RGDNCBI36
Celera1048,837,724 - 48,837,941RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,556,356 - 49,556,573UniSTS
ECD22505  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,819,073 - 55,819,289UniSTSGRCh37
Build 361055,489,079 - 55,489,295RGDNCBI36
Celera1049,081,983 - 49,082,199RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,800,502 - 49,800,718UniSTS
ECD22859  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,703,697 - 55,703,902UniSTSGRCh37
Build 361055,373,703 - 55,373,908RGDNCBI36
Celera1048,966,591 - 48,966,796RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,685,194 - 49,685,399UniSTS
ECD22860  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,829,745 - 55,829,950UniSTSGRCh37
Build 361055,499,751 - 55,499,956RGDNCBI36
Celera1049,092,653 - 49,092,858RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,811,177 - 49,811,382UniSTS
ECD22861  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,873,991 - 55,874,196UniSTSGRCh37
Build 361055,543,997 - 55,544,202RGDNCBI36
Celera1049,136,892 - 49,137,097RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,855,421 - 49,855,626UniSTS
ECD22946  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,658,200 - 55,658,402UniSTSGRCh37
Build 361055,328,206 - 55,328,408RGDNCBI36
Celera1048,921,115 - 48,921,317RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,640,125 - 49,640,327UniSTS
ECD23040  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,762,441 - 55,762,640UniSTSGRCh37
Build 361055,432,447 - 55,432,646RGDNCBI36
Celera1049,025,324 - 49,025,523RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,743,854 - 49,744,053UniSTS
ECD23088  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,872,289 - 55,872,487UniSTSGRCh37
Build 361055,542,295 - 55,542,493RGDNCBI36
Celera1049,135,190 - 49,135,388RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,853,719 - 49,853,917UniSTS
ECD23203  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,638,337 - 55,638,532UniSTSGRCh37
Build 361055,308,343 - 55,308,538RGDNCBI36
Celera1048,901,324 - 48,901,519RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,619,948 - 49,620,143UniSTS
ECD23413  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,740,147 - 55,740,336UniSTSGRCh37
Build 361055,410,153 - 55,410,342RGDNCBI36
Celera1049,003,035 - 49,003,224RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,721,550 - 49,721,738UniSTS
ECD23538  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,647,799 - 55,647,984UniSTSGRCh37
Build 361055,317,805 - 55,317,990RGDNCBI36
Celera1048,910,763 - 48,910,948RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,629,387 - 49,629,572UniSTS
ECD23623  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,895,746 - 55,895,928UniSTSGRCh37
Build 361055,565,752 - 55,565,934RGDNCBI36
Celera1049,158,650 - 49,158,832RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,878,816 - 49,878,998UniSTS
ECD23681  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,786,159 - 55,786,339UniSTSGRCh37
Build 361055,456,165 - 55,456,345RGDNCBI36
Celera1049,049,059 - 49,049,239RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,767,574 - 49,767,754UniSTS
ECD23701  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,618,408 - 55,618,587UniSTSGRCh37
Build 361055,288,414 - 55,288,593RGDNCBI36
Celera1048,881,378 - 48,881,557RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,599,983 - 49,600,162UniSTS
ECD23798  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,948,689 - 55,948,864UniSTSGRCh37
Build 361055,618,695 - 55,618,870RGDNCBI36
Celera1049,211,633 - 49,211,808RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,931,872 - 49,932,047UniSTS
ECD24114  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,956,221 - 55,956,380UniSTSGRCh37
Build 361055,626,227 - 55,626,386RGDNCBI36
Celera1049,219,171 - 49,219,330RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,939,406 - 49,939,565UniSTS
ECD24145  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,736,291 - 55,736,448UniSTSGRCh37
Build 361055,406,297 - 55,406,454RGDNCBI36
Celera1048,999,179 - 48,999,336RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,717,693 - 49,717,850UniSTS
ECD24202  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,656,879 - 55,657,031UniSTSGRCh37
Build 361055,326,885 - 55,327,037RGDNCBI36
Celera1048,919,795 - 48,919,947RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,638,811 - 49,638,964UniSTS
ECD24252  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,573,001 - 55,573,149UniSTSGRCh37
Build 361055,243,007 - 55,243,155RGDNCBI36
Celera1048,835,970 - 48,836,118RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,554,599 - 49,554,747UniSTS
ECD24367  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,632,208 - 55,632,345UniSTSGRCh37
Build 361055,302,214 - 55,302,351RGDNCBI36
Celera1048,895,189 - 48,895,326RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,613,798 - 49,613,935UniSTS
ECD24423  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,937,430 - 55,937,559UniSTSGRCh37
Build 361055,607,436 - 55,607,565RGDNCBI36
Celera1049,200,374 - 49,200,503RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,920,609 - 49,920,738UniSTS
ECD24430  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,665,479 - 55,665,607UniSTSGRCh37
Build 361055,335,485 - 55,335,613RGDNCBI36
Celera1048,928,396 - 48,928,524RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,647,001 - 49,647,129UniSTS
ECD24481  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,756,311 - 55,756,429UniSTSGRCh37
Build 361055,426,317 - 55,426,435RGDNCBI36
Celera1049,019,199 - 49,019,317RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,737,730 - 49,737,848UniSTS
FB23G7  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,758,517 - 55,758,674UniSTSGRCh37
Build 361055,428,523 - 55,428,680RGDNCBI36
Celera1049,021,405 - 49,021,562RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,739,936 - 49,740,093UniSTS
GeneMap99-GB4 RH Map10333.45UniSTS
Whitehead-RH Map10403.9UniSTS
SHGC-36014  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,594,073 - 55,594,172UniSTSGRCh37
Build 361055,264,079 - 55,264,178RGDNCBI36
Celera1048,857,040 - 48,857,139RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,575,670 - 49,575,769UniSTS
Stanford-G3 RH Map102488.0UniSTS
NCBI RH Map10650.8UniSTS
GeneMap99-G3 RH Map102464.0UniSTS
SHGC-53843  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371056,011,202 - 56,011,325UniSTSGRCh37
Build 361055,681,208 - 55,681,331RGDNCBI36
Celera1049,274,139 - 49,274,262RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,994,400 - 49,994,523UniSTS
TNG Radiation Hybrid Map1025185.0UniSTS
ECD24521  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,679,085 - 55,679,192UniSTSGRCh37
Build 361055,349,091 - 55,349,198RGDNCBI36
Celera1048,941,976 - 48,942,083RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,660,580 - 49,660,687UniSTS
REN6710  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,562,081 - 55,562,319UniSTSGRCh37
Build 361055,232,087 - 55,232,325RGDNCBI36
Celera1048,825,050 - 48,825,288RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,543,680 - 49,543,918UniSTS
REN6711  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,562,292 - 55,562,521UniSTSGRCh37
Build 361055,232,298 - 55,232,527RGDNCBI36
Celera1048,825,261 - 48,825,490RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,543,891 - 49,544,120UniSTS
REN6712  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,562,498 - 55,562,745UniSTSGRCh37
Build 361055,232,504 - 55,232,751RGDNCBI36
Celera1048,825,467 - 48,825,714RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,544,097 - 49,544,344UniSTS
REN6713  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,562,743 - 55,562,988UniSTSGRCh37
Build 361055,232,749 - 55,232,994RGDNCBI36
Celera1048,825,712 - 48,825,957RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,544,342 - 49,544,587UniSTS
REN6714  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,562,964 - 55,563,222UniSTSGRCh37
Build 361055,232,970 - 55,233,228RGDNCBI36
Celera1048,825,933 - 48,826,191RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,544,563 - 49,544,821UniSTS
REN6715  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,563,199 - 55,563,449UniSTSGRCh37
Build 361055,233,205 - 55,233,455RGDNCBI36
Celera1048,826,168 - 48,826,418RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,544,798 - 49,545,048UniSTS
REN6716  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,563,436 - 55,563,661UniSTSGRCh37
Build 361055,233,442 - 55,233,667RGDNCBI36
Celera1048,826,405 - 48,826,630RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,545,035 - 49,545,260UniSTS
REN6717  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,563,633 - 55,563,876UniSTSGRCh37
Build 361055,233,639 - 55,233,882RGDNCBI36
Celera1048,826,602 - 48,826,845RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,545,232 - 49,545,475UniSTS
REN6718  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,563,851 - 55,564,109UniSTSGRCh37
Build 361055,233,857 - 55,234,115RGDNCBI36
Celera1048,826,820 - 48,827,078RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,545,450 - 49,545,708UniSTS
REN6719  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,564,095 - 55,564,346UniSTSGRCh37
Build 361055,234,101 - 55,234,352RGDNCBI36
Celera1048,827,064 - 48,827,315RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,545,694 - 49,545,945UniSTS
REN6720  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,564,323 - 55,564,578UniSTSGRCh37
Build 361055,234,329 - 55,234,584RGDNCBI36
Celera1048,827,292 - 48,827,547RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,545,922 - 49,546,177UniSTS
REN6721  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,564,555 - 55,564,808UniSTSGRCh37
Build 361055,234,561 - 55,234,814RGDNCBI36
Celera1048,827,524 - 48,827,777RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,546,154 - 49,546,407UniSTS
REN6722  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,564,780 - 55,565,021UniSTSGRCh37
Build 361055,234,786 - 55,235,027RGDNCBI36
Celera1048,827,749 - 48,827,990RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,546,379 - 49,546,620UniSTS
REN6723  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,565,012 - 55,565,272UniSTSGRCh37
Build 361055,235,018 - 55,235,278RGDNCBI36
Celera1048,827,981 - 48,828,241RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,546,611 - 49,546,871UniSTS
REN6724  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,565,249 - 55,565,499UniSTSGRCh37
Build 361055,235,255 - 55,235,505RGDNCBI36
Celera1048,828,218 - 48,828,468RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,546,848 - 49,547,098UniSTS
REN6725  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,565,476 - 55,565,727UniSTSGRCh37
Build 361055,235,482 - 55,235,733RGDNCBI36
Celera1048,828,445 - 48,828,696RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,547,075 - 49,547,326UniSTS
REN6726  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,565,704 - 55,565,953UniSTSGRCh37
Build 361055,235,710 - 55,235,959RGDNCBI36
Celera1048,828,673 - 48,828,922RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,547,303 - 49,547,556UniSTS
REN6727  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,565,939 - 55,566,197UniSTSGRCh37
Build 361055,235,945 - 55,236,203RGDNCBI36
Celera1048,828,908 - 48,829,166RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,547,542 - 49,547,800UniSTS
REN6728  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,566,173 - 55,566,416UniSTSGRCh37
Build 361055,236,179 - 55,236,422RGDNCBI36
Celera1048,829,142 - 48,829,385RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,547,776 - 49,548,019UniSTS
REN6729  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,566,393 - 55,566,638UniSTSGRCh37
Build 361055,236,399 - 55,236,644RGDNCBI36
Celera1048,829,362 - 48,829,607RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,547,996 - 49,548,241UniSTS
REN6730  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,566,615 - 55,566,858UniSTSGRCh37
Build 361055,236,621 - 55,236,864RGDNCBI36
Celera1048,829,584 - 48,829,827RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,548,218 - 49,548,461UniSTS
REN6731  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,566,826 - 55,567,073UniSTSGRCh37
Build 361055,236,832 - 55,237,079RGDNCBI36
Celera1048,829,795 - 48,830,042RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,548,429 - 49,548,676UniSTS
REN6732  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,567,054 - 55,567,305UniSTSGRCh37
Build 361055,237,060 - 55,237,311RGDNCBI36
Celera1048,830,023 - 48,830,274RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,548,657 - 49,548,908UniSTS
REN6733  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,567,284 - 55,567,552UniSTSGRCh37
Build 361055,237,290 - 55,237,558RGDNCBI36
Celera1048,830,253 - 48,830,521RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,548,887 - 49,549,150UniSTS
REN6734  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,567,534 - 55,567,771UniSTSGRCh37
Build 361055,237,540 - 55,237,777RGDNCBI36
Celera1048,830,503 - 48,830,740RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,549,132 - 49,549,369UniSTS
REN6735  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,567,739 - 55,567,992UniSTSGRCh37
Build 361055,237,745 - 55,237,998RGDNCBI36
Celera1048,830,708 - 48,830,961RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,549,337 - 49,549,590UniSTS
REN6736  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,567,985 - 55,568,230UniSTSGRCh37
Build 361055,237,991 - 55,238,236RGDNCBI36
Celera1048,830,954 - 48,831,199RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,549,583 - 49,549,828UniSTS
REN6737  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,568,215 - 55,568,464UniSTSGRCh37
Build 361055,238,221 - 55,238,470RGDNCBI36
Celera1048,831,184 - 48,831,433RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,549,813 - 49,550,062UniSTS
REN6738  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,568,453 - 55,568,695UniSTSGRCh37
Build 361055,238,459 - 55,238,701RGDNCBI36
Celera1048,831,422 - 48,831,664RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,550,051 - 49,550,293UniSTS
REN6739  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,568,674 - 55,568,920UniSTSGRCh37
Build 361055,238,680 - 55,238,926RGDNCBI36
Celera1048,831,643 - 48,831,889RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,550,272 - 49,550,518UniSTS
REN6740  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,568,908 - 55,569,135UniSTSGRCh37
Build 361055,238,914 - 55,239,141RGDNCBI36
Celera1048,831,877 - 48,832,104RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,550,506 - 49,550,733UniSTS
REN6741  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,569,112 - 55,569,351UniSTSGRCh37
Build 361055,239,118 - 55,239,357RGDNCBI36
Celera1048,832,081 - 48,832,320RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,550,710 - 49,550,949UniSTS
REN6742  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,569,325 - 55,569,571UniSTSGRCh37
Build 361055,239,331 - 55,239,577RGDNCBI36
Celera1048,832,294 - 48,832,540RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,550,923 - 49,551,169UniSTS
REN6743  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,569,553 - 55,569,787UniSTSGRCh37
Build 361055,239,559 - 55,239,793RGDNCBI36
Celera1048,832,522 - 48,832,756RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,551,151 - 49,551,385UniSTS
REN6744  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,569,763 - 55,569,998UniSTSGRCh37
Build 361055,239,769 - 55,240,004RGDNCBI36
Celera1048,832,732 - 48,832,967RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,551,361 - 49,551,596UniSTS
REN6745  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,569,986 - 55,570,252UniSTSGRCh37
Build 361055,239,992 - 55,240,258RGDNCBI36
Celera1048,832,955 - 48,833,221RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,551,584 - 49,551,850UniSTS
REN6746  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,570,245 - 55,570,505UniSTSGRCh37
Build 361055,240,251 - 55,240,511RGDNCBI36
Celera1048,833,214 - 48,833,474RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,551,843 - 49,552,103UniSTS
REN6747  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,570,481 - 55,570,731UniSTSGRCh37
Build 361055,240,487 - 55,240,737RGDNCBI36
Celera1048,833,450 - 48,833,700RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,552,079 - 49,552,329UniSTS
REN6748  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,570,718 - 55,570,966UniSTSGRCh37
Build 361055,240,724 - 55,240,972RGDNCBI36
Celera1048,833,687 - 48,833,935RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,552,316 - 49,552,564UniSTS
REN6749  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,570,903 - 55,571,127UniSTSGRCh37
Build 361055,240,909 - 55,241,133RGDNCBI36
Celera1048,833,872 - 48,834,096RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,552,501 - 49,552,725UniSTS
REN6750  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,571,087 - 55,571,349UniSTSGRCh37
Build 361055,241,093 - 55,241,355RGDNCBI36
Celera1048,834,056 - 48,834,318RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,552,685 - 49,552,947UniSTS
REN6751  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,571,358 - 55,571,594UniSTSGRCh37
Build 361055,241,364 - 55,241,600RGDNCBI36
Celera1048,834,327 - 48,834,563RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,552,956 - 49,553,192UniSTS
REN6752  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,571,572 - 55,571,825UniSTSGRCh37
Build 361055,241,578 - 55,241,831RGDNCBI36
Celera1048,834,541 - 48,834,794RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,553,170 - 49,553,423UniSTS
REN6753  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,571,808 - 55,572,061UniSTSGRCh37
Build 361055,241,814 - 55,242,067RGDNCBI36
Celera1048,834,777 - 48,835,030RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,553,406 - 49,553,659UniSTS
REN6754  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,572,206 - 55,572,462UniSTSGRCh37
Build 361055,242,212 - 55,242,468RGDNCBI36
Celera1048,835,175 - 48,835,431RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,553,804 - 49,554,060UniSTS
REN6755  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,572,443 - 55,572,694UniSTSGRCh37
Build 361055,242,449 - 55,242,700RGDNCBI36
Celera1048,835,412 - 48,835,663RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,554,041 - 49,554,292UniSTS
REN6756  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,572,670 - 55,572,910UniSTSGRCh37
Build 361055,242,676 - 55,242,916RGDNCBI36
Celera1048,835,639 - 48,835,879RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,554,268 - 49,554,508UniSTS
REN6757  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,572,825 - 55,573,080UniSTSGRCh37
Build 361055,242,831 - 55,243,086RGDNCBI36
Celera1048,835,794 - 48,836,049RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,554,423 - 49,554,678UniSTS
REN6758  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,573,067 - 55,573,297UniSTSGRCh37
Build 361055,243,073 - 55,243,303RGDNCBI36
Celera1048,836,036 - 48,836,266RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,554,665 - 49,554,895UniSTS
REN6759  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,573,258 - 55,573,512UniSTSGRCh37
Build 361055,243,264 - 55,243,518RGDNCBI36
Celera1048,836,227 - 48,836,481RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,554,856 - 49,555,110UniSTS
REN6760  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,573,465 - 55,573,723UniSTSGRCh37
Build 361055,243,471 - 55,243,729RGDNCBI36
Celera1048,836,434 - 48,836,692RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,555,063 - 49,555,321UniSTS
REN6761  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,573,703 - 55,573,976UniSTSGRCh37
Build 361055,243,709 - 55,243,982RGDNCBI36
Celera1048,836,672 - 48,836,945RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,555,301 - 49,555,574UniSTS
REN6762  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,573,951 - 55,574,199UniSTSGRCh37
Build 361055,243,957 - 55,244,205RGDNCBI36
Celera1048,836,920 - 48,837,168RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,555,549 - 49,555,797UniSTS
REN6763  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,574,173 - 55,574,419UniSTSGRCh37
Build 361055,244,179 - 55,244,425RGDNCBI36
Celera1048,837,142 - 48,837,388RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,555,771 - 49,556,017UniSTS
REN6764  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,574,274 - 55,574,529UniSTSGRCh37
Build 361055,244,280 - 55,244,535RGDNCBI36
Celera1048,837,243 - 48,837,498RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,555,872 - 49,556,127UniSTS
REN6765  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,574,502 - 55,574,762UniSTSGRCh37
Build 361055,244,508 - 55,244,768RGDNCBI36
Celera1048,837,471 - 48,837,731RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,556,100 - 49,556,363UniSTS
REN6766  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,574,739 - 55,574,980UniSTSGRCh37
Build 361055,244,745 - 55,244,986RGDNCBI36
Celera1048,837,708 - 48,837,949RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,556,340 - 49,556,581UniSTS
REN6767  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,574,954 - 55,575,205UniSTSGRCh37
Build 361055,244,960 - 55,245,211RGDNCBI36
Celera1048,837,923 - 48,838,174RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,556,555 - 49,556,806UniSTS
REN6768  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,575,204 - 55,575,446UniSTSGRCh37
Build 361055,245,210 - 55,245,452RGDNCBI36
Celera1048,838,173 - 48,838,415RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,556,805 - 49,557,047UniSTS
REN6769  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,575,415 - 55,575,682UniSTSGRCh37
Build 361055,245,421 - 55,245,688RGDNCBI36
Celera1048,838,384 - 48,838,651RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,557,016 - 49,557,283UniSTS
REN6770  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,575,653 - 55,575,906UniSTSGRCh37
Build 361055,245,659 - 55,245,912RGDNCBI36
Celera1048,838,622 - 48,838,875RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,557,254 - 49,557,507UniSTS
REN6771  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,575,879 - 55,576,103UniSTSGRCh37
Build 361055,245,885 - 55,246,109RGDNCBI36
Celera1048,838,848 - 48,839,072RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,557,480 - 49,557,704UniSTS
REN6772  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,576,086 - 55,576,341UniSTSGRCh37
Build 361055,246,092 - 55,246,347RGDNCBI36
Celera1048,839,055 - 48,839,310RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,557,687 - 49,557,942UniSTS
REN6773  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,576,318 - 55,576,570UniSTSGRCh37
Build 361055,246,324 - 55,246,576RGDNCBI36
Celera1048,839,287 - 48,839,539RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,557,919 - 49,558,171UniSTS
REN6774  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,576,549 - 55,576,792UniSTSGRCh37
Build 361055,246,555 - 55,246,798RGDNCBI36
Celera1048,839,518 - 48,839,761RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,558,150 - 49,558,393UniSTS
REN6775  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,576,770 - 55,577,026UniSTSGRCh37
Build 361055,246,776 - 55,247,032RGDNCBI36
Celera1048,839,739 - 48,839,995RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,558,371 - 49,558,627UniSTS
REN6776  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,576,984 - 55,577,210UniSTSGRCh37
Build 361055,246,990 - 55,247,216RGDNCBI36
Celera1048,839,953 - 48,840,179RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,558,585 - 49,558,811UniSTS
REN6777  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,577,465 - 55,577,715UniSTSGRCh37
Build 361055,247,471 - 55,247,721RGDNCBI36
Celera1048,840,434 - 48,840,684RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,559,066 - 49,559,316UniSTS
REN6778  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,577,687 - 55,577,929UniSTSGRCh37
Build 361055,247,693 - 55,247,935RGDNCBI36
Celera1048,840,656 - 48,840,898RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,559,288 - 49,559,530UniSTS
REN6779  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,577,818 - 55,578,044UniSTSGRCh37
Build 361055,247,824 - 55,248,050RGDNCBI36
Celera1048,840,787 - 48,841,013RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,559,419 - 49,559,645UniSTS
REN6780  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,578,000 - 55,578,249UniSTSGRCh37
Build 361055,248,006 - 55,248,255RGDNCBI36
Celera1048,840,969 - 48,841,218RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,559,601 - 49,559,850UniSTS
REN6781  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,578,221 - 55,578,455UniSTSGRCh37
Build 361055,248,227 - 55,248,461RGDNCBI36
Celera1048,841,190 - 48,841,424RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,559,822 - 49,560,056UniSTS
REN6782  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,578,424 - 55,578,681UniSTSGRCh37
Build 361055,248,430 - 55,248,687RGDNCBI36
Celera1048,841,393 - 48,841,650RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,560,025 - 49,560,282UniSTS
REN6783  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,578,663 - 55,578,887UniSTSGRCh37
Build 361055,248,669 - 55,248,893RGDNCBI36
Celera1048,841,632 - 48,841,856RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,560,264 - 49,560,488UniSTS
REN6784  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,578,856 - 55,579,120UniSTSGRCh37
Build 361055,248,862 - 55,249,126RGDNCBI36
Celera1048,841,825 - 48,842,089RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,560,457 - 49,560,721UniSTS
REN6785  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,579,042 - 55,579,290UniSTSGRCh37
Build 361055,249,048 - 55,249,296RGDNCBI36
Celera1048,842,011 - 48,842,259RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,560,643 - 49,560,891UniSTS
REN6786  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,579,268 - 55,579,514UniSTSGRCh37
Build 361055,249,274 - 55,249,520RGDNCBI36
Celera1048,842,237 - 48,842,483RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,560,869 - 49,561,115UniSTS
REN6787  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,579,493 - 55,579,761UniSTSGRCh37
Build 361055,249,499 - 55,249,767RGDNCBI36
Celera1048,842,462 - 48,842,730RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,561,094 - 49,561,362UniSTS
REN6788  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,579,738 - 55,579,970UniSTSGRCh37
Build 361055,249,744 - 55,249,976RGDNCBI36
Celera1048,842,707 - 48,842,939RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,561,339 - 49,561,571UniSTS
REN6789  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,579,962 - 55,580,210UniSTSGRCh37
Build 361055,249,968 - 55,250,216RGDNCBI36
Celera1048,842,931 - 48,843,179RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,561,563 - 49,561,811UniSTS
REN6790  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,580,173 - 55,580,425UniSTSGRCh37
Build 361055,250,179 - 55,250,431RGDNCBI36
Celera1048,843,142 - 48,843,394RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,561,774 - 49,562,026UniSTS
REN6791  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,580,404 - 55,580,652UniSTSGRCh37
Build 361055,250,410 - 55,250,658RGDNCBI36
Celera1048,843,373 - 48,843,621RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,562,005 - 49,562,253UniSTS
REN6792  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,580,627 - 55,580,857UniSTSGRCh37
Build 361055,250,633 - 55,250,863RGDNCBI36
Celera1048,843,596 - 48,843,826RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,562,228 - 49,562,458UniSTS
REN6793  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,580,842 - 55,581,086UniSTSGRCh37
Build 361055,250,848 - 55,251,092RGDNCBI36
Celera1048,843,811 - 48,844,055RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,562,443 - 49,562,687UniSTS
REN6794  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,581,077 - 55,581,335UniSTSGRCh37
Build 361055,251,083 - 55,251,341RGDNCBI36
Celera1048,844,046 - 48,844,304RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,562,678 - 49,562,936UniSTS
REN6795  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,581,330 - 55,581,595UniSTSGRCh37
Build 361055,251,336 - 55,251,601RGDNCBI36
Celera1048,844,299 - 48,844,564RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,562,931 - 49,563,196UniSTS
REN6796  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,581,590 - 55,581,846UniSTSGRCh37
Build 361055,251,596 - 55,251,852RGDNCBI36
Celera1048,844,559 - 48,844,815RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,563,191 - 49,563,447UniSTS
REN6797  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,581,845 - 55,582,069UniSTSGRCh37
Build 361055,251,851 - 55,252,075RGDNCBI36
Celera1048,844,814 - 48,845,038RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,563,446 - 49,563,670UniSTS
REN6798  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,582,045 - 55,582,295UniSTSGRCh37
Build 361055,252,051 - 55,252,301RGDNCBI36
Celera1048,845,014 - 48,845,264RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,563,646 - 49,563,896UniSTS
REN6799  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,582,274 - 55,582,515UniSTSGRCh37
Build 361055,252,280 - 55,252,521RGDNCBI36
Celera1048,845,243 - 48,845,484RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,563,875 - 49,564,116UniSTS
REN6800  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,582,492 - 55,582,735UniSTSGRCh37
Build 361055,252,498 - 55,252,741RGDNCBI36
Celera1048,845,461 - 48,845,704RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,564,093 - 49,564,336UniSTS
REN6801  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,582,691 - 55,582,924UniSTSGRCh37
Build 361055,252,697 - 55,252,930RGDNCBI36
Celera1048,845,660 - 48,845,893RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,564,292 - 49,564,525UniSTS
REN6802  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,582,914 - 55,583,169UniSTSGRCh37
Build 361055,252,920 - 55,253,175RGDNCBI36
Celera1048,845,883 - 48,846,138RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,564,515 - 49,564,770UniSTS
REN6803  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,583,085 - 55,583,339UniSTSGRCh37
Build 361055,253,091 - 55,253,345RGDNCBI36
Celera1048,846,054 - 48,846,308RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,564,686 - 49,564,940UniSTS
REN6804  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,583,311 - 55,583,575UniSTSGRCh37
Build 361055,253,317 - 55,253,581RGDNCBI36
Celera1048,846,280 - 48,846,544RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,564,912 - 49,565,176UniSTS
REN6805  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,583,561 - 55,583,790UniSTSGRCh37
Build 361055,253,567 - 55,253,796RGDNCBI36
Celera1048,846,530 - 48,846,759RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,565,162 - 49,565,391UniSTS
REN6806  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,583,761 - 55,584,023UniSTSGRCh37
Build 361055,253,767 - 55,254,029RGDNCBI36
Celera1048,846,730 - 48,846,991RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,565,362 - 49,565,623UniSTS
REN6807  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,584,017 - 55,584,278UniSTSGRCh37
Build 361055,254,023 - 55,254,284RGDNCBI36
Celera1048,846,985 - 48,847,246RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,565,617 - 49,565,878UniSTS
REN6808  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,584,269 - 55,584,520UniSTSGRCh37
Build 361055,254,275 - 55,254,526RGDNCBI36
Celera1048,847,237 - 48,847,488RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,565,869 - 49,566,120UniSTS
REN6809  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,584,516 - 55,584,765UniSTSGRCh37
Build 361055,254,522 - 55,254,771RGDNCBI36
Celera1048,847,484 - 48,847,733RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,566,116 - 49,566,365UniSTS
REN6810  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,584,741 - 55,585,004UniSTSGRCh37
Build 361055,254,747 - 55,255,010RGDNCBI36
Celera1048,847,709 - 48,847,972RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,566,341 - 49,566,604UniSTS
REN6811  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,584,993 - 55,585,261UniSTSGRCh37
Build 361055,254,999 - 55,255,267RGDNCBI36
Celera1048,847,961 - 48,848,229RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,566,593 - 49,566,859UniSTS
REN6812  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,585,168 - 55,585,392UniSTSGRCh37
Build 361055,255,174 - 55,255,398RGDNCBI36
Celera1048,848,136 - 48,848,360RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,566,766 - 49,566,990UniSTS
REN6813  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,585,612 - 55,585,847UniSTSGRCh37
Build 361055,255,618 - 55,255,853RGDNCBI36
Celera1048,848,580 - 48,848,815RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,567,210 - 49,567,445UniSTS
REN6814  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,585,778 - 55,586,014UniSTSGRCh37
Build 361055,255,784 - 55,256,020RGDNCBI36
Celera1048,848,746 - 48,848,982RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,567,376 - 49,567,616UniSTS
REN6815  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,585,990 - 55,586,234UniSTSGRCh37
Build 361055,255,996 - 55,256,240RGDNCBI36
Celera1048,848,958 - 48,849,202RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,567,592 - 49,567,836UniSTS
REN6816  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,586,195 - 55,586,420UniSTSGRCh37
Build 361055,256,201 - 55,256,426RGDNCBI36
Celera1048,849,163 - 48,849,388RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,567,797 - 49,568,022UniSTS
REN6817  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,586,368 - 55,586,592UniSTSGRCh37
Build 361055,256,374 - 55,256,598RGDNCBI36
Celera1048,849,336 - 48,849,560RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,567,970 - 49,568,194UniSTS
REN6818  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,586,530 - 55,586,778UniSTSGRCh37
Build 361055,256,536 - 55,256,784RGDNCBI36
Celera1048,849,498 - 48,849,746RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,568,132 - 49,568,380UniSTS
REN6819  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,586,764 - 55,587,029UniSTSGRCh37
Build 361055,256,770 - 55,257,035RGDNCBI36
Celera1048,849,732 - 48,849,997RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,568,366 - 49,568,631UniSTS
REN6820  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,586,953 - 55,587,189UniSTSGRCh37
Build 361055,256,959 - 55,257,195RGDNCBI36
Celera1048,849,921 - 48,850,157RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,568,555 - 49,568,791UniSTS
REN6821  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,587,154 - 55,587,415UniSTSGRCh37
Build 361055,257,160 - 55,257,421RGDNCBI36
Celera1048,850,122 - 48,850,383RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,568,756 - 49,569,017UniSTS
REN6822  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,587,394 - 55,587,630UniSTSGRCh37
Build 361055,257,400 - 55,257,636RGDNCBI36
Celera1048,850,362 - 48,850,598RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,568,996 - 49,569,232UniSTS
REN6823  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,587,523 - 55,587,764UniSTSGRCh37
Build 361055,257,529 - 55,257,770RGDNCBI36
Celera1048,850,491 - 48,850,732RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,569,125 - 49,569,366UniSTS
REN6824  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,587,767 - 55,588,033UniSTSGRCh37
Build 361055,257,773 - 55,258,039RGDNCBI36
Celera1048,850,735 - 48,851,000RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,569,369 - 49,569,634UniSTS
REN6825  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,588,006 - 55,588,248UniSTSGRCh37
Build 361055,258,012 - 55,258,254RGDNCBI36
Celera1048,850,973 - 48,851,215RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,569,607 - 49,569,849UniSTS
REN6826  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,588,238 - 55,588,506UniSTSGRCh37
Build 361055,258,244 - 55,258,512RGDNCBI36
Celera1048,851,205 - 48,851,473RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,569,839 - 49,570,107UniSTS
REN6827  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,588,481 - 55,588,734UniSTSGRCh37
Build 361055,258,487 - 55,258,740RGDNCBI36
Celera1048,851,448 - 48,851,701RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,570,082 - 49,570,335UniSTS
REN6828  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,588,711 - 55,588,970UniSTSGRCh37
Build 361055,258,717 - 55,258,976RGDNCBI36
Celera1048,851,678 - 48,851,937RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,570,312 - 49,570,571UniSTS
REN6829  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,588,939 - 55,589,180UniSTSGRCh37
Build 361055,258,945 - 55,259,186RGDNCBI36
Celera1048,851,906 - 48,852,147RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,570,540 - 49,570,781UniSTS
REN6830  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,589,160 - 55,589,402UniSTSGRCh37
Build 361055,259,166 - 55,259,408RGDNCBI36
Celera1048,852,127 - 48,852,369RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,570,761 - 49,571,003UniSTS
REN6831  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,589,379 - 55,589,610UniSTSGRCh37
Build 361055,259,385 - 55,259,616RGDNCBI36
Celera1048,852,346 - 48,852,577RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,570,980 - 49,571,211UniSTS
REN6832  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,589,540 - 55,589,789UniSTSGRCh37
Build 361055,259,546 - 55,259,795RGDNCBI36
Celera1048,852,507 - 48,852,756RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,571,141 - 49,571,390UniSTS
REN6833  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,589,739 - 55,589,987UniSTSGRCh37
Build 361055,259,745 - 55,259,993RGDNCBI36
Celera1048,852,706 - 48,852,954RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,571,340 - 49,571,588UniSTS
REN6834  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,590,110 - 55,590,336UniSTSGRCh37
Build 361055,260,116 - 55,260,342RGDNCBI36
Celera1048,853,077 - 48,853,303RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,571,711 - 49,571,937UniSTS
REN6835  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,590,330 - 55,590,572UniSTSGRCh37
Build 361055,260,336 - 55,260,578RGDNCBI36
Celera1048,853,297 - 48,853,539RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,571,931 - 49,572,173UniSTS
REN6836  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,590,547 - 55,590,790UniSTSGRCh37
Build 361055,260,553 - 55,260,796RGDNCBI36
Celera1048,853,514 - 48,853,757RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,572,148 - 49,572,391UniSTS
REN6837  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,590,767 - 55,591,021UniSTSGRCh37
Build 361055,260,773 - 55,261,027RGDNCBI36
Celera1048,853,734 - 48,853,988RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,572,368 - 49,572,622UniSTS
REN6838  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,591,011 - 55,591,258UniSTSGRCh37
Build 361055,261,017 - 55,261,264RGDNCBI36
Celera1048,853,978 - 48,854,225RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,572,612 - 49,572,859UniSTS
REN6839  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,591,238 - 55,591,472UniSTSGRCh37
Build 361055,261,244 - 55,261,478RGDNCBI36
Celera1048,854,205 - 48,854,439RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,572,839 - 49,573,073UniSTS
REN6840  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,591,445 - 55,591,684UniSTSGRCh37
Build 361055,261,451 - 55,261,690RGDNCBI36
Celera1048,854,412 - 48,854,651RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,573,046 - 49,573,285UniSTS
REN6841  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,591,661 - 55,591,914UniSTSGRCh37
Build 361055,261,667 - 55,261,920RGDNCBI36
Celera1048,854,628 - 48,854,881RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,573,262 - 49,573,515UniSTS
REN6842  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,591,882 - 55,592,147UniSTSGRCh37
Build 361055,261,888 - 55,262,153RGDNCBI36
Celera1048,854,849 - 48,855,114RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,573,483 - 49,573,748UniSTS
REN6843  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,592,024 - 55,592,285UniSTSGRCh37
Build 361055,262,030 - 55,262,291RGDNCBI36
Celera1048,854,991 - 48,855,252RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,573,625 - 49,573,886UniSTS
REN6844  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,592,276 - 55,592,503UniSTSGRCh37
Build 361055,262,282 - 55,262,509RGDNCBI36
Celera1048,855,243 - 48,855,470RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,573,877 - 49,574,104UniSTS
REN6845  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,592,443 - 55,592,681UniSTSGRCh37
Build 361055,262,449 - 55,262,687RGDNCBI36
Celera1048,855,410 - 48,855,648RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,574,044 - 49,574,282UniSTS
REN6846  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,592,664 - 55,592,904UniSTSGRCh37
Build 361055,262,670 - 55,262,910RGDNCBI36
Celera1048,855,631 - 48,855,871RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,574,265 - 49,574,505UniSTS
REN6847  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,592,881 - 55,593,127UniSTSGRCh37
Build 361055,262,887 - 55,263,133RGDNCBI36
Celera1048,855,848 - 48,856,094RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,574,482 - 49,574,728UniSTS
REN6848  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,593,098 - 55,593,322UniSTSGRCh37
Build 361055,263,104 - 55,263,328RGDNCBI36
Celera1048,856,065 - 48,856,289RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,574,699 - 49,574,923UniSTS
REN6849  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,593,296 - 55,593,540UniSTSGRCh37
Build 361055,263,302 - 55,263,546RGDNCBI36
Celera1048,856,263 - 48,856,507RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,574,897 - 49,575,137UniSTS
REN6850  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,593,394 - 55,593,659UniSTSGRCh37
Build 361055,263,400 - 55,263,665RGDNCBI36
Celera1048,856,361 - 48,856,626RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,574,991 - 49,575,256UniSTS
REN6851  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,593,639 - 55,593,888UniSTSGRCh37
Build 361055,263,645 - 55,263,894RGDNCBI36
Celera1048,856,606 - 48,856,855RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,575,236 - 49,575,485UniSTS
REN6852  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,593,856 - 55,594,108UniSTSGRCh37
Build 361055,263,862 - 55,264,114RGDNCBI36
Celera1048,856,823 - 48,857,075RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,575,453 - 49,575,705UniSTS
REN6853  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,594,085 - 55,594,355UniSTSGRCh37
Build 361055,264,091 - 55,264,361RGDNCBI36
Celera1048,857,052 - 48,857,323RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,575,682 - 49,575,954UniSTS
REN6854  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,594,336 - 55,594,575UniSTSGRCh37
Build 361055,264,342 - 55,264,581RGDNCBI36
Celera1048,857,304 - 48,857,543RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,575,935 - 49,576,174UniSTS
REN6855  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,594,505 - 55,594,748UniSTSGRCh37
Build 361055,264,511 - 55,264,754RGDNCBI36
Celera1048,857,473 - 48,857,716RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,576,104 - 49,576,347UniSTS
REN6856  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,594,724 - 55,594,969UniSTSGRCh37
Build 361055,264,730 - 55,264,975RGDNCBI36
Celera1048,857,692 - 48,857,937RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,576,323 - 49,576,568UniSTS
REN6857  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,594,960 - 55,595,205UniSTSGRCh37
Build 361055,264,966 - 55,265,211RGDNCBI36
Celera1048,857,928 - 48,858,173RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,576,559 - 49,576,804UniSTS
REN6858  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,595,171 - 55,595,395UniSTSGRCh37
Build 361055,265,177 - 55,265,401RGDNCBI36
Celera1048,858,139 - 48,858,363RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,576,770 - 49,576,994UniSTS
REN6859  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,595,372 - 55,595,616UniSTSGRCh37
Build 361055,265,378 - 55,265,622RGDNCBI36
Celera1048,858,340 - 48,858,584RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,576,971 - 49,577,215UniSTS
REN6860  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,595,593 - 55,595,849UniSTSGRCh37
Build 361055,265,599 - 55,265,855RGDNCBI36
Celera1048,858,561 - 48,858,817RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,577,192 - 49,577,448UniSTS
REN6861  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,595,816 - 55,596,061UniSTSGRCh37
Build 361055,265,822 - 55,266,067RGDNCBI36
Celera1048,858,784 - 48,859,029RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,577,415 - 49,577,660UniSTS
REN6862  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,596,045 - 55,596,273UniSTSGRCh37
Build 361055,266,051 - 55,266,279RGDNCBI36
Celera1048,859,013 - 48,859,241RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,577,644 - 49,577,872UniSTS
REN6863  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,596,250 - 55,596,501UniSTSGRCh37
Build 361055,266,256 - 55,266,507RGDNCBI36
Celera1048,859,218 - 48,859,469RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,577,849 - 49,578,100UniSTS
REN6864  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,596,476 - 55,596,700UniSTSGRCh37
Build 361055,266,482 - 55,266,706RGDNCBI36
Celera1048,859,444 - 48,859,668RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,578,075 - 49,578,299UniSTS
REN6865  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,596,653 - 55,596,897UniSTSGRCh37
Build 361055,266,659 - 55,266,903RGDNCBI36
Celera1048,859,621 - 48,859,865RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,578,252 - 49,578,496UniSTS
REN6866  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,596,874 - 55,597,132UniSTSGRCh37
Build 361055,266,880 - 55,267,138RGDNCBI36
Celera1048,859,842 - 48,860,100RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,578,473 - 49,578,731UniSTS
REN6867  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,597,100 - 55,597,347UniSTSGRCh37
Build 361055,267,106 - 55,267,353RGDNCBI36
Celera1048,860,068 - 48,860,315RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,578,699 - 49,578,946UniSTS
REN6868  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,597,260 - 55,597,516UniSTSGRCh37
Build 361055,267,266 - 55,267,522RGDNCBI36
Celera1048,860,228 - 48,860,484RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,578,859 - 49,579,115UniSTS
REN6869  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,597,483 - 55,597,707UniSTSGRCh37
Build 361055,267,489 - 55,267,713RGDNCBI36
Celera1048,860,451 - 48,860,675RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,579,082 - 49,579,306UniSTS
REN6870  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,597,580 - 55,597,821UniSTSGRCh37
Build 361055,267,586 - 55,267,827RGDNCBI36
Celera1048,860,548 - 48,860,787RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,579,179 - 49,579,412UniSTS
REN6871  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,598,076 - 55,598,305UniSTSGRCh37
Build 361055,268,082 - 55,268,311RGDNCBI36
Celera1048,861,042 - 48,861,270RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,579,667 - 49,579,895UniSTS
REN6872  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,598,222 - 55,598,447UniSTSGRCh37
Build 361055,268,228 - 55,268,453RGDNCBI36
Celera1048,861,187 - 48,861,412RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,579,812 - 49,580,037UniSTS
REN6873  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,598,421 - 55,598,654UniSTSGRCh37
Build 361055,268,427 - 55,268,660RGDNCBI36
Celera1048,861,386 - 48,861,619RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,580,011 - 49,580,244UniSTS
REN6874  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,599,055 - 55,599,287UniSTSGRCh37
Build 361055,269,061 - 55,269,293RGDNCBI36
Celera1048,862,021 - 48,862,253RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,580,646 - 49,580,878UniSTS
REN6875  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,599,268 - 55,599,514UniSTSGRCh37
Build 361055,269,274 - 55,269,520RGDNCBI36
Celera1048,862,234 - 48,862,479RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,580,859 - 49,581,105UniSTS
REN6876  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,599,491 - 55,599,731UniSTSGRCh37
Build 361055,269,497 - 55,269,737RGDNCBI36
Celera1048,862,456 - 48,862,696RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,581,082 - 49,581,322UniSTS
REN6877  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,599,706 - 55,599,964UniSTSGRCh37
Build 361055,269,712 - 55,269,970RGDNCBI36
Celera1048,862,671 - 48,862,929RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,581,297 - 49,581,555UniSTS
REN6878  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,599,963 - 55,600,221UniSTSGRCh37
Build 361055,269,969 - 55,270,227RGDNCBI36
Celera1048,862,928 - 48,863,186RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,581,554 - 49,581,812UniSTS
REN6879  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,600,195 - 55,600,443UniSTSGRCh37
Build 361055,270,201 - 55,270,449RGDNCBI36
Celera1048,863,160 - 48,863,408RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,581,786 - 49,582,034UniSTS
REN6880  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,600,426 - 55,600,659UniSTSGRCh37
Build 361055,270,432 - 55,270,665RGDNCBI36
Celera1048,863,391 - 48,863,624RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,582,017 - 49,582,250UniSTS
REN6881  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,600,592 - 55,600,832UniSTSGRCh37
Build 361055,270,598 - 55,270,838RGDNCBI36
Celera1048,863,557 - 48,863,797RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,582,183 - 49,582,423UniSTS
REN6882  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,600,763 - 55,600,987UniSTSGRCh37
Build 361055,270,769 - 55,270,993RGDNCBI36
Celera1048,863,728 - 48,863,952RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,582,354 - 49,582,578UniSTS
REN6883  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,600,958 - 55,601,221UniSTSGRCh37
Build 361055,270,964 - 55,271,227RGDNCBI36
Celera1048,863,923 - 48,864,186RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,582,549 - 49,582,812UniSTS
REN6884  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,601,212 - 55,601,468UniSTSGRCh37
Build 361055,271,218 - 55,271,474RGDNCBI36
Celera1048,864,177 - 48,864,433RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,582,803 - 49,583,059UniSTS
REN6885  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,601,443 - 55,601,709UniSTSGRCh37
Build 361055,271,449 - 55,271,715RGDNCBI36
Celera1048,864,408 - 48,864,674RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,583,034 - 49,583,300UniSTS
REN6886  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,601,686 - 55,601,939UniSTSGRCh37
Build 361055,271,692 - 55,271,945RGDNCBI36
Celera1048,864,651 - 48,864,904RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,583,277 - 49,583,530UniSTS
REN6887  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,601,924 - 55,602,149UniSTSGRCh37
Build 361055,271,930 - 55,272,155RGDNCBI36
Celera1048,864,889 - 48,865,114RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,583,515 - 49,583,740UniSTS
REN6888  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,602,126 - 55,602,380UniSTSGRCh37
Build 361055,272,132 - 55,272,386RGDNCBI36
Celera1048,865,091 - 48,865,345RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,583,717 - 49,583,971UniSTS
REN6889  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,602,353 - 55,602,612UniSTSGRCh37
Build 361055,272,359 - 55,272,618RGDNCBI36
Celera1048,865,318 - 48,865,577RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,583,944 - 49,584,203UniSTS
REN6890  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,602,599 - 55,602,864UniSTSGRCh37
Build 361055,272,605 - 55,272,870RGDNCBI36
Celera1048,865,564 - 48,865,829RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,584,190 - 49,584,455UniSTS
REN6891  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,602,824 - 55,603,072UniSTSGRCh37
Build 361055,272,830 - 55,273,078RGDNCBI36
Celera1048,865,789 - 48,866,037RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,584,415 - 49,584,663UniSTS
REN6892  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,603,039 - 55,603,280UniSTSGRCh37
Build 361055,273,045 - 55,273,286RGDNCBI36
Celera1048,866,004 - 48,866,245RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,584,630 - 49,584,871UniSTS
REN6893  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,603,233 - 55,603,457UniSTSGRCh37
Build 361055,273,239 - 55,273,463RGDNCBI36
Celera1048,866,198 - 48,866,422RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,584,824 - 49,585,048UniSTS
REN6894  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,603,435 - 55,603,660UniSTSGRCh37
Build 361055,273,441 - 55,273,666RGDNCBI36
Celera1048,866,400 - 48,866,625RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,585,026 - 49,585,251UniSTS
REN6895  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,603,653 - 55,603,904UniSTSGRCh37
Build 361055,273,659 - 55,273,910RGDNCBI36
Celera1048,866,618 - 48,866,869RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,585,244 - 49,585,495UniSTS
REN6896  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,603,885 - 55,604,122UniSTSGRCh37
Build 361055,273,891 - 55,274,128RGDNCBI36
Celera1048,866,850 - 48,867,087RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,585,476 - 49,585,713UniSTS
REN6897  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,604,095 - 55,604,356UniSTSGRCh37
Build 361055,274,101 - 55,274,362RGDNCBI36
Celera1048,867,060 - 48,867,321RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,585,686 - 49,585,947UniSTS
REN6898  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,604,333 - 55,604,577UniSTSGRCh37
Build 361055,274,339 - 55,274,583RGDNCBI36
Celera1048,867,298 - 48,867,542RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,585,924 - 49,586,168UniSTS
REN6899  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,604,576 - 55,604,839UniSTSGRCh37
Build 361055,274,582 - 55,274,845RGDNCBI36
Celera1048,867,541 - 48,867,804RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,586,167 - 49,586,430UniSTS
REN6900  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,604,811 - 55,605,036UniSTSGRCh37
Build 361055,274,817 - 55,275,042RGDNCBI36
Celera1048,867,776 - 48,868,001RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,586,402 - 49,586,627UniSTS
REN6901  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,605,008 - 55,605,255UniSTSGRCh37
Build 361055,275,014 - 55,275,261RGDNCBI36
Celera1048,867,973 - 48,868,220RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,586,599 - 49,586,846UniSTS
REN6902  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,605,245 - 55,605,499UniSTSGRCh37
Build 361055,275,251 - 55,275,505RGDNCBI36
Celera1048,868,210 - 48,868,464RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,586,836 - 49,587,090UniSTS
REN6903  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,605,479 - 55,605,742UniSTSGRCh37
Build 361055,275,485 - 55,275,748RGDNCBI36
Celera1048,868,444 - 48,868,707RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,587,070 - 49,587,333UniSTS
REN6904  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,605,717 - 55,605,970UniSTSGRCh37
Build 361055,275,723 - 55,275,976RGDNCBI36
Celera1048,868,682 - 48,868,935RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,587,308 - 49,587,561UniSTS
REN6905  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,605,889 - 55,606,136UniSTSGRCh37
Build 361055,275,895 - 55,276,142RGDNCBI36
Celera1048,868,854 - 48,869,101RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,587,480 - 49,587,727UniSTS
REN6906  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,606,088 - 55,606,352UniSTSGRCh37
Build 361055,276,094 - 55,276,358RGDNCBI36
Celera1048,869,053 - 48,869,317RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,587,679 - 49,587,943UniSTS
REN6907  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,606,343 - 55,606,614UniSTSGRCh37
Build 361055,276,349 - 55,276,620RGDNCBI36
Celera1048,869,308 - 48,869,579RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,587,934 - 49,588,205UniSTS
REN6908  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,606,611 - 55,606,866UniSTSGRCh37
Build 361055,276,617 - 55,276,872RGDNCBI36
Celera1048,869,576 - 48,869,831RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,588,202 - 49,588,457UniSTS
REN6909  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,606,845 - 55,607,091UniSTSGRCh37
Build 361055,276,851 - 55,277,097RGDNCBI36
Celera1048,869,810 - 48,870,056RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,588,436 - 49,588,682UniSTS
REN6910  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,607,068 - 55,607,314UniSTSGRCh37
Build 361055,277,074 - 55,277,320RGDNCBI36
Celera1048,870,033 - 48,870,279RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,588,659 - 49,588,905UniSTS
REN6911  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,607,263 - 55,607,518UniSTSGRCh37
Build 361055,277,269 - 55,277,524RGDNCBI36
Celera1048,870,228 - 48,870,483RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,588,854 - 49,589,109UniSTS
REN6912  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,607,493 - 55,607,763UniSTSGRCh37
Build 361055,277,499 - 55,277,769RGDNCBI36
Celera1048,870,458 - 48,870,728RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,589,084 - 49,589,354UniSTS
REN6913  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,607,746 - 55,607,996UniSTSGRCh37
Build 361055,277,752 - 55,278,002RGDNCBI36
Celera1048,870,711 - 48,870,961RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,589,337 - 49,589,587UniSTS
REN6914  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,607,978 - 55,608,229UniSTSGRCh37
Build 361055,277,984 - 55,278,235RGDNCBI36
Celera1048,870,943 - 48,871,194RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,589,569 - 49,589,820UniSTS
REN6915  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,608,211 - 55,608,470UniSTSGRCh37
Build 361055,278,217 - 55,278,476RGDNCBI36
Celera1048,871,176 - 48,871,435RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,589,802 - 49,590,061UniSTS
REN6916  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,608,373 - 55,608,617UniSTSGRCh37
Build 361055,278,379 - 55,278,623RGDNCBI36
Celera1048,871,338 - 48,871,582RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,589,964 - 49,590,208UniSTS
REN6917  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,608,575 - 55,608,829UniSTSGRCh37
Build 361055,278,581 - 55,278,835RGDNCBI36
Celera1048,871,540 - 48,871,794RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,590,166 - 49,590,420UniSTS
REN6918  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,608,805 - 55,609,034UniSTSGRCh37
Build 361055,278,811 - 55,279,040RGDNCBI36
Celera1048,871,770 - 48,871,999RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,590,396 - 49,590,625UniSTS
REN6919  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,609,008 - 55,609,259UniSTSGRCh37
Build 361055,279,014 - 55,279,265RGDNCBI36
Celera1048,871,973 - 48,872,224RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,590,599 - 49,590,850UniSTS
REN6920  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,609,209 - 55,609,437UniSTSGRCh37
Build 361055,279,215 - 55,279,443RGDNCBI36
Celera1048,872,174 - 48,872,402RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,590,800 - 49,591,028UniSTS
REN6921  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,609,593 - 55,609,832UniSTSGRCh37
Build 361055,279,599 - 55,279,838RGDNCBI36
Celera1048,872,558 - 48,872,796RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,591,184 - 49,591,421UniSTS
REN6922  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,609,812 - 55,610,070UniSTSGRCh37
Build 361055,279,818 - 55,280,076RGDNCBI36
Celera1048,872,776 - 48,873,034RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,591,401 - 49,591,659UniSTS
REN6923  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,610,057 - 55,610,299UniSTSGRCh37
Build 361055,280,063 - 55,280,305RGDNCBI36
Celera1048,873,021 - 48,873,263RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,591,646 - 49,591,888UniSTS
REN6924  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,610,295 - 55,610,540UniSTSGRCh37
Build 361055,280,301 - 55,280,546RGDNCBI36
Celera1048,873,259 - 48,873,504RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,591,884 - 49,592,129UniSTS
REN6925  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,610,519 - 55,610,770UniSTSGRCh37
Build 361055,280,525 - 55,280,776RGDNCBI36
Celera1048,873,483 - 48,873,734RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,592,108 - 49,592,359UniSTS
REN6926  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,610,753 - 55,611,000UniSTSGRCh37
Build 361055,280,759 - 55,281,006RGDNCBI36
Celera1048,873,717 - 48,873,964RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,592,342 - 49,592,589UniSTS
REN6927  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,610,983 - 55,611,255UniSTSGRCh37
Build 361055,280,989 - 55,281,261RGDNCBI36
Celera1048,873,947 - 48,874,219RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,592,572 - 49,592,844UniSTS
REN6928  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,611,196 - 55,611,420UniSTSGRCh37
Build 361055,281,202 - 55,281,426RGDNCBI36
Celera1048,874,160 - 48,874,384RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,592,785 - 49,593,009UniSTS
REN6929  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,611,403 - 55,611,669UniSTSGRCh37
Build 361055,281,409 - 55,281,675RGDNCBI36
Celera1048,874,367 - 48,874,633RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,592,992 - 49,593,238UniSTS
REN6930  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,611,646 - 55,611,916UniSTSGRCh37
Build 361055,281,652 - 55,281,922RGDNCBI36
Celera1048,874,610 - 48,874,880RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,593,215 - 49,593,485UniSTS
REN6931  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,611,907 - 55,612,157UniSTSGRCh37
Build 361055,281,913 - 55,282,163RGDNCBI36
Celera1048,874,871 - 48,875,121RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,593,476 - 49,593,726UniSTS
REN6932  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,612,146 - 55,612,371UniSTSGRCh37
Build 361055,282,152 - 55,282,377RGDNCBI36
Celera1048,875,110 - 48,875,335RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,593,715 - 49,593,940UniSTS
REN6933  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,612,340 - 55,612,582UniSTSGRCh37
Build 361055,282,346 - 55,282,588RGDNCBI36
Celera1048,875,304 - 48,875,546RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,593,909 - 49,594,151UniSTS
REN6934  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,612,573 - 55,612,797UniSTSGRCh37
Build 361055,282,579 - 55,282,803RGDNCBI36
Celera1048,875,537 - 48,875,761RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,594,142 - 49,594,366UniSTS
REN6935  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,612,724 - 55,612,948UniSTSGRCh37
Build 361055,282,730 - 55,282,954RGDNCBI36
Celera1048,875,688 - 48,875,912RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,594,293 - 49,594,517UniSTS
REN6936  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,612,914 - 55,613,163UniSTSGRCh37
Build 361055,282,920 - 55,283,169RGDNCBI36
Celera1048,875,878 - 48,876,127RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,594,483 - 49,594,732UniSTS
REN6937  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,613,073 - 55,613,297UniSTSGRCh37
Build 361055,283,079 - 55,283,303RGDNCBI36
Celera1048,876,037 - 48,876,261RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,594,642 - 49,594,866UniSTS
REN6938  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,613,204 - 55,613,453UniSTSGRCh37
Build 361055,283,210 - 55,283,459RGDNCBI36
Celera1048,876,168 - 48,876,417RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,594,773 - 49,595,022UniSTS
REN6939  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,613,428 - 55,613,680UniSTSGRCh37
Build 361055,283,434 - 55,283,686RGDNCBI36
Celera1048,876,392 - 48,876,644RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,594,997 - 49,595,249UniSTS
REN6940  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,613,671 - 55,613,906UniSTSGRCh37
Build 361055,283,677 - 55,283,912RGDNCBI36
Celera1048,876,635 - 48,876,870RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,595,240 - 49,595,475UniSTS
REN6941  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,613,875 - 55,614,101UniSTSGRCh37
Build 361055,283,881 - 55,284,107RGDNCBI36
Celera1048,876,839 - 48,877,065RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,595,444 - 49,595,670UniSTS
REN6942  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,614,084 - 55,614,341UniSTSGRCh37
Build 361055,284,090 - 55,284,347RGDNCBI36
Celera1048,877,048 - 48,877,305RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,595,653 - 49,595,910UniSTS
REN6943  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,614,299 - 55,614,523UniSTSGRCh37
Build 361055,284,305 - 55,284,529RGDNCBI36
Celera1048,877,263 - 48,877,487RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,595,868 - 49,596,092UniSTS
REN6944  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,614,479 - 55,614,703UniSTSGRCh37
Build 361055,284,485 - 55,284,709RGDNCBI36
Celera1048,877,443 - 48,877,667RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,596,048 - 49,596,272UniSTS
REN6945  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,614,675 - 55,614,928UniSTSGRCh37
Build 361055,284,681 - 55,284,934RGDNCBI36
Celera1048,877,639 - 48,877,892RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,596,244 - 49,596,497UniSTS
REN6946  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,614,901 - 55,615,160UniSTSGRCh37
Build 361055,284,907 - 55,285,166RGDNCBI36
Celera1048,877,865 - 48,878,124RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,596,470 - 49,596,729UniSTS
REN6947  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,615,136 - 55,615,366UniSTSGRCh37
Build 361055,285,142 - 55,285,372RGDNCBI36
Celera1048,878,100 - 48,878,330RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,596,705 - 49,596,935UniSTS
REN6948  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,615,337 - 55,615,566UniSTSGRCh37
Build 361055,285,343 - 55,285,572RGDNCBI36
Celera1048,878,301 - 48,878,530RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,596,906 - 49,597,135UniSTS
REN6949  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,615,529 - 55,615,762UniSTSGRCh37
Build 361055,285,535 - 55,285,768RGDNCBI36
Celera1048,878,493 - 48,878,732RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,597,098 - 49,597,337UniSTS
REN6950  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,615,737 - 55,615,961UniSTSGRCh37
Build 361055,285,743 - 55,285,967RGDNCBI36
Celera1048,878,707 - 48,878,931RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,597,312 - 49,597,536UniSTS
REN6951  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,615,953 - 55,616,206UniSTSGRCh37
Build 361055,285,959 - 55,286,212RGDNCBI36
Celera1048,878,923 - 48,879,176RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,597,528 - 49,597,781UniSTS
REN6952  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,616,183 - 55,616,422UniSTSGRCh37
Build 361055,286,189 - 55,286,428RGDNCBI36
Celera1048,879,153 - 48,879,392RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,597,758 - 49,597,997UniSTS
REN6953  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,616,408 - 55,616,675UniSTSGRCh37
Build 361055,286,414 - 55,286,681RGDNCBI36
Celera1048,879,378 - 48,879,645RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,597,983 - 49,598,250UniSTS
REN6954  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,616,589 - 55,616,815UniSTSGRCh37
Build 361055,286,595 - 55,286,821RGDNCBI36
Celera1048,879,559 - 48,879,785RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,598,164 - 49,598,390UniSTS
REN6955  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,616,792 - 55,617,034UniSTSGRCh37
Build 361055,286,798 - 55,287,040RGDNCBI36
Celera1048,879,762 - 48,880,004RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,598,367 - 49,598,609UniSTS
REN6956  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,617,013 - 55,617,240UniSTSGRCh37
Build 361055,287,019 - 55,287,246RGDNCBI36
Celera1048,879,983 - 48,880,210RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,598,588 - 49,598,815UniSTS
REN6957  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,617,208 - 55,617,461UniSTSGRCh37
Build 361055,287,214 - 55,287,467RGDNCBI36
Celera1048,880,178 - 48,880,431RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,598,783 - 49,599,036UniSTS
REN6958  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,617,342 - 55,617,596UniSTSGRCh37
Build 361055,287,348 - 55,287,602RGDNCBI36
Celera1048,880,312 - 48,880,566RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,598,917 - 49,599,171UniSTS
REN6959  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,617,571 - 55,617,834UniSTSGRCh37
Build 361055,287,577 - 55,287,840RGDNCBI36
Celera1048,880,541 - 48,880,804RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,599,146 - 49,599,409UniSTS
REN6960  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,617,833 - 55,618,103UniSTSGRCh37
Build 361055,287,839 - 55,288,109RGDNCBI36
Celera1048,880,803 - 48,881,073RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,599,408 - 49,599,678UniSTS
REN6961  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,618,057 - 55,618,281UniSTSGRCh37
Build 361055,288,063 - 55,288,287RGDNCBI36
Celera1048,881,027 - 48,881,251RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,599,632 - 49,599,856UniSTS
REN6962  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,618,251 - 55,618,495UniSTSGRCh37
Build 361055,288,257 - 55,288,501RGDNCBI36
Celera1048,881,221 - 48,881,465RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,599,826 - 49,600,070UniSTS
REN6963  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,618,415 - 55,618,645UniSTSGRCh37
Build 361055,288,421 - 55,288,651RGDNCBI36
Celera1048,881,385 - 48,881,615RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,599,990 - 49,600,220UniSTS
REN6964  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,618,616 - 55,618,879UniSTSGRCh37
Build 361055,288,622 - 55,288,885RGDNCBI36
Celera1048,881,586 - 48,881,849RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,600,191 - 49,600,454UniSTS
REN6965  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,618,856 - 55,619,100UniSTSGRCh37
Build 361055,288,862 - 55,289,106RGDNCBI36
Celera1048,881,826 - 48,882,070RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,600,431 - 49,600,675UniSTS
REN6966  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,619,077 - 55,619,333UniSTSGRCh37
Build 361055,289,083 - 55,289,339RGDNCBI36
Celera1048,882,047 - 48,882,303RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,600,652 - 49,600,908UniSTS
REN6967  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,619,312 - 55,619,550UniSTSGRCh37
Build 361055,289,318 - 55,289,556RGDNCBI36
Celera1048,882,282 - 48,882,520RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,600,887 - 49,601,125UniSTS
REN6968  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,619,526 - 55,619,775UniSTSGRCh37
Build 361055,289,532 - 55,289,781RGDNCBI36
Celera1048,882,496 - 48,882,745RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,601,101 - 49,601,350UniSTS
REN6969  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,619,753 - 55,620,024UniSTSGRCh37
Build 361055,289,759 - 55,290,030RGDNCBI36
Celera1048,882,723 - 48,882,994RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,601,328 - 49,601,599UniSTS
REN6970  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,620,001 - 55,620,241UniSTSGRCh37
Build 361055,290,007 - 55,290,247RGDNCBI36
Celera1048,882,971 - 48,883,211RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,601,576 - 49,601,816UniSTS
REN6971  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,620,200 - 55,620,454UniSTSGRCh37
Build 361055,290,206 - 55,290,460RGDNCBI36
Celera1048,883,170 - 48,883,424RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,601,775 - 49,602,029UniSTS
REN6972  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,620,514 - 55,620,740UniSTSGRCh37
Build 361055,290,520 - 55,290,746RGDNCBI36
Celera1048,883,484 - 48,883,710RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,602,089 - 49,602,315UniSTS
REN6973  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,620,708 - 55,620,975UniSTSGRCh37
Build 361055,290,714 - 55,290,981RGDNCBI36
Celera1048,883,678 - 48,883,945RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,602,283 - 49,602,550UniSTS
REN6974  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,620,941 - 55,621,172UniSTSGRCh37
Build 361055,290,947 - 55,291,178RGDNCBI36
Celera1048,883,911 - 48,884,142RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,602,516 - 49,602,747UniSTS
REN6975  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,621,143 - 55,621,371UniSTSGRCh37
Build 361055,291,149 - 55,291,377RGDNCBI36
Celera1048,884,113 - 48,884,341RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,602,718 - 49,602,946UniSTS
REN6976  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,621,340 - 55,621,584UniSTSGRCh37
Build 361055,291,346 - 55,291,590RGDNCBI36
Celera1048,884,310 - 48,884,554RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,602,915 - 49,603,159UniSTS
REN6977  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,621,533 - 55,621,777UniSTSGRCh37
Build 361055,291,539 - 55,291,783RGDNCBI36
Celera1048,884,503 - 48,884,747RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,603,108 - 49,603,352UniSTS
REN6978  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,621,642 - 55,621,879UniSTSGRCh37
Build 361055,291,648 - 55,291,885RGDNCBI36
Celera1048,884,612 - 48,884,849RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,603,217 - 49,603,454UniSTS
REN6980  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,622,081 - 55,622,319UniSTSGRCh37
Build 361055,292,087 - 55,292,325RGDNCBI36
Celera1048,885,051 - 48,885,289RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,603,656 - 49,603,894UniSTS
REN6981  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,622,296 - 55,622,538UniSTSGRCh37
Build 361055,292,302 - 55,292,544RGDNCBI36
Celera1048,885,266 - 48,885,508RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,603,871 - 49,604,113UniSTS
REN6982  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,622,515 - 55,622,756UniSTSGRCh37
Build 361055,292,521 - 55,292,762RGDNCBI36
Celera1048,885,485 - 48,885,726RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,604,090 - 49,604,331UniSTS
REN6983  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,622,735 - 55,622,985UniSTSGRCh37
Build 361055,292,741 - 55,292,991RGDNCBI36
Celera1048,885,705 - 48,885,955RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,604,310 - 49,604,560UniSTS
REN6984  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,622,975 - 55,623,214UniSTSGRCh37
Build 361055,292,981 - 55,293,220RGDNCBI36
Celera1048,885,945 - 48,886,184RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,604,550 - 49,604,789UniSTS
REN6985  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,623,193 - 55,623,420UniSTSGRCh37
Build 361055,293,199 - 55,293,426RGDNCBI36
Celera1048,886,163 - 48,886,390RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,604,768 - 49,604,995UniSTS
REN6986  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,623,383 - 55,623,642UniSTSGRCh37
Build 361055,293,389 - 55,293,648RGDNCBI36
Celera1048,886,353 - 48,886,612RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,604,958 - 49,605,217UniSTS
REN6987  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,623,617 - 55,623,866UniSTSGRCh37
Build 361055,293,623 - 55,293,872RGDNCBI36
Celera1048,886,587 - 48,886,836RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,605,192 - 49,605,441UniSTS
REN6988  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,623,842 - 55,624,081UniSTSGRCh37
Build 361055,293,848 - 55,294,087RGDNCBI36
Celera1048,886,812 - 48,887,051RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,605,417 - 49,605,656UniSTS
REN6989  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,624,062 - 55,624,309UniSTSGRCh37
Build 361055,294,068 - 55,294,315RGDNCBI36
Celera1048,887,032 - 48,887,279RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,605,637 - 49,605,884UniSTS
REN6990  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,624,287 - 55,624,543UniSTSGRCh37
Build 361055,294,293 - 55,294,549RGDNCBI36
Celera1048,887,257 - 48,887,513RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,605,862 - 49,606,118UniSTS
REN6991  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,624,516 - 55,624,754UniSTSGRCh37
Build 361055,294,522 - 55,294,760RGDNCBI36
Celera1048,887,486 - 48,887,724RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,606,091 - 49,606,329UniSTS
REN6992  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,624,731 - 55,624,983UniSTSGRCh37
Build 361055,294,737 - 55,294,989RGDNCBI36
Celera1048,887,701 - 48,887,953RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,606,306 - 49,606,558UniSTS
REN6993  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,624,963 - 55,625,224UniSTSGRCh37
Build 361055,294,969 - 55,295,230RGDNCBI36
Celera1048,887,933 - 48,888,194RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,606,538 - 49,606,799UniSTS
REN6994  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,625,202 - 55,625,455UniSTSGRCh37
Build 361055,295,208 - 55,295,461RGDNCBI36
Celera1048,888,172 - 48,888,425RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,606,777 - 49,607,030UniSTS
REN6995  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,625,438 - 55,625,693UniSTSGRCh37
Build 361055,295,444 - 55,295,699RGDNCBI36
Celera1048,888,408 - 48,888,663RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,607,013 - 49,607,271UniSTS
REN6996  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,625,681 - 55,625,910UniSTSGRCh37
Build 361055,295,687 - 55,295,916RGDNCBI36
Celera1048,888,651 - 48,888,880RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,607,259 - 49,607,488UniSTS
REN6997  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,625,879 - 55,626,129UniSTSGRCh37
Build 361055,295,885 - 55,296,135RGDNCBI36
Celera1048,888,849 - 48,889,099RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,607,457 - 49,607,707UniSTS
REN6998  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,626,106 - 55,626,357UniSTSGRCh37
Build 361055,296,112 - 55,296,363RGDNCBI36
Celera1048,889,076 - 48,889,327RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,607,684 - 49,607,937UniSTS
REN6999  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,626,334 - 55,626,564UniSTSGRCh37
Build 361055,296,340 - 55,296,570RGDNCBI36
Celera1048,889,304 - 48,889,534RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,607,914 - 49,608,144UniSTS
REN7000  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,626,541 - 55,626,806UniSTSGRCh37
Build 361055,296,547 - 55,296,812RGDNCBI36
Celera1048,889,511 - 48,889,776RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,608,121 - 49,608,386UniSTS
REN7001  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,626,783 - 55,627,023UniSTSGRCh37
Build 361055,296,789 - 55,297,029RGDNCBI36
Celera1048,889,753 - 48,889,993RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,608,363 - 49,608,603UniSTS
REN7002  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,626,984 - 55,627,208UniSTSGRCh37
Build 361055,296,990 - 55,297,214RGDNCBI36
Celera1048,889,954 - 48,890,178RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,608,564 - 49,608,788UniSTS
REN7003  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,627,196 - 55,627,444UniSTSGRCh37
Build 361055,297,202 - 55,297,450RGDNCBI36
Celera1048,890,166 - 48,890,414RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,608,776 - 49,609,024UniSTS
REN7004  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,627,395 - 55,627,664UniSTSGRCh37
Build 361055,297,401 - 55,297,670RGDNCBI36
Celera1048,890,365 - 48,890,634RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,608,975 - 49,609,244UniSTS
REN7005  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,627,654 - 55,627,911UniSTSGRCh37
Build 361055,297,660 - 55,297,917RGDNCBI36
Celera1048,890,624 - 48,890,881RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,609,234 - 49,609,491UniSTS
REN7006  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,627,884 - 55,628,131UniSTSGRCh37
Build 361055,297,890 - 55,298,137RGDNCBI36
Celera1048,890,854 - 48,891,101RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,609,464 - 49,609,711UniSTS
REN7007  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,628,061 - 55,628,311UniSTSGRCh37
Build 361055,298,067 - 55,298,317RGDNCBI36
Celera1048,891,031 - 48,891,281RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,609,641 - 49,609,891UniSTS
REN7008  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,628,288 - 55,628,556UniSTSGRCh37
Build 361055,298,294 - 55,298,562RGDNCBI36
Celera1048,891,258 - 48,891,526RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,609,868 - 49,610,136UniSTS
REN7009  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,628,552 - 55,628,812UniSTSGRCh37
Build 361055,298,558 - 55,298,818RGDNCBI36
Celera1048,891,522 - 48,891,782RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,610,132 - 49,610,392UniSTS
REN7010  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,628,788 - 55,629,018UniSTSGRCh37
Build 361055,298,794 - 55,299,024RGDNCBI36
Celera1048,891,758 - 48,891,988RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,610,368 - 49,610,598UniSTS
REN7011  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,628,989 - 55,629,230UniSTSGRCh37
Build 361055,298,995 - 55,299,236RGDNCBI36
Celera1048,891,959 - 48,892,200RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,610,569 - 49,610,810UniSTS
REN7012  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,629,198 - 55,629,425UniSTSGRCh37
Build 361055,299,204 - 55,299,431RGDNCBI36
Celera1048,892,168 - 48,892,395RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,610,778 - 49,611,005UniSTS
REN7013  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,629,388 - 55,629,624UniSTSGRCh37
Build 361055,299,394 - 55,299,630RGDNCBI36
Celera1048,892,358 - 48,892,594RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,610,968 - 49,611,204UniSTS
REN7014  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,629,608 - 55,629,835UniSTSGRCh37
Build 361055,299,614 - 55,299,841RGDNCBI36
Celera1048,892,578 - 48,892,805RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,611,188 - 49,611,415UniSTS
REN7015  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,629,812 - 55,630,045UniSTSGRCh37
Build 361055,299,818 - 55,300,051RGDNCBI36
Celera1048,892,782 - 48,893,015RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,611,392 - 49,611,625UniSTS
REN7016  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,630,025 - 55,630,296UniSTSGRCh37
Build 361055,300,031 - 55,300,302RGDNCBI36
Celera1048,892,995 - 48,893,266RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,611,605 - 49,611,876UniSTS
REN7017  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,630,284 - 55,630,525UniSTSGRCh37
Build 361055,300,290 - 55,300,531RGDNCBI36
Celera1048,893,254 - 48,893,495RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,611,864 - 49,612,105UniSTS
REN7018  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,630,503 - 55,630,768UniSTSGRCh37
Build 361055,300,509 - 55,300,774RGDNCBI36
Celera1048,893,473 - 48,893,738RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,612,083 - 49,612,348UniSTS
REN7019  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,630,594 - 55,630,819UniSTSGRCh37
Build 361055,300,600 - 55,300,825RGDNCBI36
Celera1048,893,564 - 48,893,789RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,612,174 - 49,612,399UniSTS
REN7020  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,631,104 - 55,631,331UniSTSGRCh37
Build 361055,301,110 - 55,301,337RGDNCBI36
Celera1048,894,074 - 48,894,309RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,612,684 - 49,612,921UniSTS
REN7021  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,631,643 - 55,631,877UniSTSGRCh37
Build 361055,301,649 - 55,301,883RGDNCBI36
Celera1048,894,624 - 48,894,858RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,613,233 - 49,613,467UniSTS
REN7022  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,631,854 - 55,632,101UniSTSGRCh37
Build 361055,301,860 - 55,302,107RGDNCBI36
Celera1048,894,835 - 48,895,082RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,613,444 - 49,613,691UniSTS
REN7023  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,632,078 - 55,632,330UniSTSGRCh37
Build 361055,302,084 - 55,302,336RGDNCBI36
Celera1048,895,059 - 48,895,311RGD
Cytogenetic Map10q21.1UniSTS
REN7024  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,632,321 - 55,632,568UniSTSGRCh37
Build 361055,302,327 - 55,302,574RGDNCBI36
Celera1048,895,302 - 48,895,549RGD
Cytogenetic Map10q21.1UniSTS
REN7025  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,632,545 - 55,632,793UniSTSGRCh37
Build 361055,302,551 - 55,302,799RGDNCBI36
Celera1048,895,526 - 48,895,774RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,614,136 - 49,614,384UniSTS
REN7026  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,632,767 - 55,633,019UniSTSGRCh37
Build 361055,302,773 - 55,303,025RGDNCBI36
Celera1048,895,748 - 48,896,000RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,614,358 - 49,614,610UniSTS
REN7027  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,632,997 - 55,633,227UniSTSGRCh37
Build 361055,303,003 - 55,303,233RGDNCBI36
Celera1048,895,978 - 48,896,208RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,614,588 - 49,614,818UniSTS
REN7028  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,633,203 - 55,633,467UniSTSGRCh37
Build 361055,303,209 - 55,303,473RGDNCBI36
Celera1048,896,184 - 48,896,448RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,614,794 - 49,615,058UniSTS
REN7029  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,633,429 - 55,633,677UniSTSGRCh37
Build 361055,303,435 - 55,303,683RGDNCBI36
Celera1048,896,410 - 48,896,658RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,615,020 - 49,615,268UniSTS
REN7030  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,633,654 - 55,633,890UniSTSGRCh37
Build 361055,303,660 - 55,303,896RGDNCBI36
Celera1048,896,635 - 48,896,871RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,615,245 - 49,615,481UniSTS
REN7031  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,633,864 - 55,634,113UniSTSGRCh37
Build 361055,303,870 - 55,304,119RGDNCBI36
Celera1048,896,845 - 48,897,094RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,615,455 - 49,615,704UniSTS
REN7032  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,634,071 - 55,634,297UniSTSGRCh37
Build 361055,304,077 - 55,304,303RGDNCBI36
Celera1048,897,052 - 48,897,278RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,615,662 - 49,615,888UniSTS
REN7033  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,634,261 - 55,634,487UniSTSGRCh37
Build 361055,304,267 - 55,304,493RGDNCBI36
Celera1048,897,242 - 48,897,468RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,615,852 - 49,616,078UniSTS
REN7034  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,634,460 - 55,634,715UniSTSGRCh37
Build 361055,304,466 - 55,304,721RGDNCBI36
Celera1048,897,441 - 48,897,696RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,616,051 - 49,616,307UniSTS
REN7035  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,634,689 - 55,634,949UniSTSGRCh37
Build 361055,304,695 - 55,304,955RGDNCBI36
Celera1048,897,670 - 48,897,930RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,616,281 - 49,616,541UniSTS
REN7036  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,634,945 - 55,635,214UniSTSGRCh37
Build 361055,304,951 - 55,305,220RGDNCBI36
Celera1048,897,926 - 48,898,199RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,616,537 - 49,616,810UniSTS
REN7037  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,635,138 - 55,635,362UniSTSGRCh37
Build 361055,305,144 - 55,305,368RGDNCBI36
Celera1048,898,123 - 48,898,347RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,616,734 - 49,616,958UniSTS
REN7038  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,635,323 - 55,635,593UniSTSGRCh37
Build 361055,305,329 - 55,305,599RGDNCBI36
Celera1048,898,308 - 48,898,578RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,616,919 - 49,617,189UniSTS
REN7039  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,635,571 - 55,635,798UniSTSGRCh37
Build 361055,305,577 - 55,305,804RGDNCBI36
Celera1048,898,556 - 48,898,783RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,617,167 - 49,617,394UniSTS
REN7040  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,635,705 - 55,635,929UniSTSGRCh37
Build 361055,305,711 - 55,305,935RGDNCBI36
Celera1048,898,690 - 48,898,914RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,617,301 - 49,617,525UniSTS
REN7041  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,635,895 - 55,636,146UniSTSGRCh37
Build 361055,305,901 - 55,306,152RGDNCBI36
Celera1048,898,880 - 48,899,134RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,617,491 - 49,617,745UniSTS
REN7042  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,636,239 - 55,636,487UniSTSGRCh37
Build 361055,306,245 - 55,306,493RGDNCBI36
Celera1048,899,227 - 48,899,474RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,617,838 - 49,618,085UniSTS
REN7043  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,636,441 - 55,636,691UniSTSGRCh37
Build 361055,306,447 - 55,306,697RGDNCBI36
Celera1048,899,428 - 48,899,678RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,618,039 - 49,618,289UniSTS
REN7044  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,636,687 - 55,636,911UniSTSGRCh37
Build 361055,306,693 - 55,306,917RGDNCBI36
Celera1048,899,674 - 48,899,898RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,618,285 - 49,618,509UniSTS
REN7045  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,636,870 - 55,637,131UniSTSGRCh37
Build 361055,306,876 - 55,307,137RGDNCBI36
Celera1048,899,857 - 48,900,118RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,618,468 - 49,618,729UniSTS
REN7046  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,637,114 - 55,637,371UniSTSGRCh37
Build 361055,307,120 - 55,307,377RGDNCBI36
Celera1048,900,101 - 48,900,358RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,618,712 - 49,618,975UniSTS
REN7047  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,637,348 - 55,637,589UniSTSGRCh37
Build 361055,307,354 - 55,307,595RGDNCBI36
Celera1048,900,335 - 48,900,576RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,618,952 - 49,619,193UniSTS
REN7048  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,637,563 - 55,637,823UniSTSGRCh37
Build 361055,307,569 - 55,307,829RGDNCBI36
Celera1048,900,550 - 48,900,810RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,619,167 - 49,619,427UniSTS
REN7049  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,637,707 - 55,637,957UniSTSGRCh37
Build 361055,307,713 - 55,307,963RGDNCBI36
Celera1048,900,694 - 48,900,944RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,619,311 - 49,619,561UniSTS
REN7050  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,637,823 - 55,638,049UniSTSGRCh37
Build 361055,307,829 - 55,308,055RGDNCBI36
Celera1048,900,810 - 48,901,036RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,619,427 - 49,619,649UniSTS
REN7051  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,638,152 - 55,638,376UniSTSGRCh37
Build 361055,308,158 - 55,308,382RGDNCBI36
Celera1048,901,139 - 48,901,363RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,619,759 - 49,619,987UniSTS
REN7052  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,638,339 - 55,638,602UniSTSGRCh37
Build 361055,308,345 - 55,308,608RGDNCBI36
Celera1048,901,326 - 48,901,589RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,619,950 - 49,620,213UniSTS
REN7053  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,638,576 - 55,638,800UniSTSGRCh37
Build 361055,308,582 - 55,308,806RGDNCBI36
Celera1048,901,563 - 48,901,787RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,620,187 - 49,620,411UniSTS
REN7054  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,638,773 - 55,639,040UniSTSGRCh37
Build 361055,308,779 - 55,309,046RGDNCBI36
Celera1048,901,760 - 48,902,026RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,620,384 - 49,620,650UniSTS
REN7055  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,639,023 - 55,639,295UniSTSGRCh37
Build 361055,309,029 - 55,309,301RGDNCBI36
Celera1048,902,009 - 48,902,281RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,620,633 - 49,620,905UniSTS
REN7056  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,639,279 - 55,639,507UniSTSGRCh37
Build 361055,309,285 - 55,309,513RGDNCBI36
Celera1048,902,265 - 48,902,493RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,620,889 - 49,621,117UniSTS
REN7057  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,639,478 - 55,639,702UniSTSGRCh37
Build 361055,309,484 - 55,309,708RGDNCBI36
Celera1048,902,464 - 48,902,688RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,621,088 - 49,621,312UniSTS
REN7058  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,639,629 - 55,639,859UniSTSGRCh37
GRCh371055,639,582 - 55,639,859UniSTSGRCh37
Build 361055,309,588 - 55,309,865RGDNCBI36
Celera1048,902,568 - 48,902,845RGD
Celera1048,902,615 - 48,902,845UniSTS
Cytogenetic Map10q21.1UniSTS
HuRef1049,621,192 - 49,621,469UniSTS
HuRef1049,621,239 - 49,621,469UniSTS
REN7059  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,639,835 - 55,640,084UniSTSGRCh37
Build 361055,309,841 - 55,310,090RGDNCBI36
Celera1048,902,821 - 48,903,070RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,621,445 - 49,621,694UniSTS
REN7060  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,640,060 - 55,640,300UniSTSGRCh37
Build 361055,310,066 - 55,310,306RGDNCBI36
Celera1048,903,046 - 48,903,286RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,621,670 - 49,621,910UniSTS
REN7061  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,640,294 - 55,640,531UniSTSGRCh37
Build 361055,310,300 - 55,310,537RGDNCBI36
Celera1048,903,280 - 48,903,516RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,621,904 - 49,622,140UniSTS
REN7062  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,640,472 - 55,640,719UniSTSGRCh37
Build 361055,310,478 - 55,310,725RGDNCBI36
Celera1048,903,457 - 48,903,704RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,622,081 - 49,622,328UniSTS
REN7063  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,640,703 - 55,640,933UniSTSGRCh37
Build 361055,310,709 - 55,310,939RGDNCBI36
Celera1048,903,688 - 48,903,919RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,622,312 - 49,622,543UniSTS
REN7064  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,640,907 - 55,641,144UniSTSGRCh37
Build 361055,310,913 - 55,311,150RGDNCBI36
Cytogenetic Map10q21.1UniSTS
REN7065  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,641,106 - 55,641,360UniSTSGRCh37
Build 361055,311,112 - 55,311,366RGDNCBI36
Celera1048,904,091 - 48,904,345RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,622,715 - 49,622,969UniSTS
REN7066  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,641,336 - 55,641,589UniSTSGRCh37
Build 361055,311,342 - 55,311,595RGDNCBI36
Celera1048,904,321 - 48,904,574RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,622,945 - 49,623,198UniSTS
REN7067  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,641,504 - 55,641,753UniSTSGRCh37
Build 361055,311,510 - 55,311,759RGDNCBI36
Celera1048,904,489 - 48,904,738RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,623,113 - 49,623,362UniSTS
REN7068  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,641,730 - 55,641,983UniSTSGRCh37
Build 361055,311,736 - 55,311,989RGDNCBI36
Celera1048,904,715 - 48,904,948RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,623,339 - 49,623,572UniSTS
REN7070  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,642,029 - 55,642,269UniSTSGRCh37
Build 361055,312,035 - 55,312,275RGDNCBI36
Celera1048,904,994 - 48,905,234RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,623,618 - 49,623,857UniSTS
REN7071  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,642,453 - 55,642,677UniSTSGRCh37
Build 361055,312,459 - 55,312,683RGDNCBI36
Celera1048,905,418 - 48,905,642RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,624,041 - 49,624,265UniSTS
REN7072  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,642,539 - 55,642,782UniSTSGRCh37
Build 361055,312,545 - 55,312,788RGDNCBI36
Celera1048,905,504 - 48,905,747RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,624,127 - 49,624,370UniSTS
REN7073  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,642,749 - 55,643,010UniSTSGRCh37
Build 361055,312,755 - 55,313,016RGDNCBI36
Celera1048,905,714 - 48,905,977RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,624,337 - 49,624,600UniSTS
REN7074  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,643,009 - 55,643,258UniSTSGRCh37
Build 361055,313,015 - 55,313,264RGDNCBI36
Celera1048,905,976 - 48,906,225RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,624,599 - 49,624,848UniSTS
REN7075  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,643,226 - 55,643,450UniSTSGRCh37
Build 361055,313,232 - 55,313,456RGDNCBI36
Celera1048,906,193 - 48,906,417RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,624,816 - 49,625,040UniSTS
REN7076  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,643,795 - 55,644,027UniSTSGRCh37
Build 361055,313,801 - 55,314,033RGDNCBI36
Celera1048,906,762 - 48,906,994RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,625,386 - 49,625,618UniSTS
REN7077  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,644,010 - 55,644,239UniSTSGRCh37
Build 361055,314,016 - 55,314,245RGDNCBI36
Celera1048,906,977 - 48,907,206RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,625,601 - 49,625,830UniSTS
REN7078  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,644,195 - 55,644,442UniSTSGRCh37
Build 361055,314,201 - 55,314,448RGDNCBI36
Celera1048,907,162 - 48,907,409RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,625,786 - 49,626,033UniSTS
REN7079  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,644,435 - 55,644,673UniSTSGRCh37
Build 361055,314,441 - 55,314,679RGDNCBI36
Celera1048,907,402 - 48,907,640RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,626,026 - 49,626,264UniSTS
REN7080  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,644,639 - 55,644,896UniSTSGRCh37
Build 361055,314,645 - 55,314,902RGDNCBI36
Celera1048,907,606 - 48,907,863RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,626,230 - 49,626,487UniSTS
REN7081  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,644,861 - 55,645,126UniSTSGRCh37
Build 361055,314,867 - 55,315,132RGDNCBI36
Celera1048,907,828 - 48,908,093RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,626,452 - 49,626,717UniSTS
REN7082  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,645,109 - 55,645,340UniSTSGRCh37
Build 361055,315,115 - 55,315,346RGDNCBI36
Celera1048,908,076 - 48,908,307RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,626,700 - 49,626,931UniSTS
REN7083  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,645,316 - 55,645,547UniSTSGRCh37
Build 361055,315,322 - 55,315,553RGDNCBI36
Celera1048,908,283 - 48,908,514RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,626,907 - 49,627,138UniSTS
REN7084  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,645,517 - 55,645,777UniSTSGRCh37
Build 361055,315,523 - 55,315,783RGDNCBI36
Celera1048,908,484 - 48,908,744RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,627,108 - 49,627,368UniSTS
REN7085  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,645,756 - 55,645,982UniSTSGRCh37
Build 361055,315,762 - 55,315,988RGDNCBI36
Celera1048,908,723 - 48,908,949RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,627,347 - 49,627,573UniSTS
REN7086  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,645,963 - 55,646,226UniSTSGRCh37
Build 361055,315,969 - 55,316,232RGDNCBI36
Celera1048,908,930 - 48,909,193RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,627,554 - 49,627,817UniSTS
REN7087  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,646,214 - 55,646,470UniSTSGRCh37
Build 361055,316,220 - 55,316,476RGDNCBI36
Celera1048,909,181 - 48,909,434RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,627,805 - 49,628,058UniSTS
REN7088  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,646,455 - 55,646,689UniSTSGRCh37
Build 361055,316,461 - 55,316,695RGDNCBI36
Celera1048,909,419 - 48,909,653RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,628,043 - 49,628,277UniSTS
REN7089  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,646,680 - 55,646,924UniSTSGRCh37
Build 361055,316,686 - 55,316,930RGDNCBI36
Celera1048,909,644 - 48,909,888RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,628,268 - 49,628,512UniSTS
REN7090  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,646,898 - 55,647,151UniSTSGRCh37
Build 361055,316,904 - 55,317,157RGDNCBI36
Celera1048,909,862 - 48,910,115RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,628,486 - 49,628,739UniSTS
REN7091  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,647,130 - 55,647,374UniSTSGRCh37
Build 361055,317,136 - 55,317,380RGDNCBI36
Celera1048,910,094 - 48,910,338RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,628,718 - 49,628,962UniSTS
REN7092  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,647,706 - 55,647,937UniSTSGRCh37
Build 361055,317,712 - 55,317,943RGDNCBI36
Celera1048,910,670 - 48,910,901RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,629,294 - 49,629,525UniSTS
REN7093  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,647,912 - 55,648,155UniSTSGRCh37
Build 361055,317,918 - 55,318,161RGDNCBI36
Celera1048,910,876 - 48,911,119RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,629,500 - 49,629,773UniSTS
REN7094  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,648,135 - 55,648,387UniSTSGRCh37
Build 361055,318,141 - 55,318,393RGDNCBI36
Celera1048,911,099 - 48,911,351RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,629,753 - 49,630,002UniSTS
REN7095  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,648,364 - 55,648,625UniSTSGRCh37
Build 361055,318,370 - 55,318,631RGDNCBI36
Celera1048,911,328 - 48,911,584RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,629,979 - 49,630,259UniSTS
REN7096  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,648,606 - 55,648,831UniSTSGRCh37
Build 361055,318,612 - 55,318,837RGDNCBI36
Celera1048,911,565 - 48,911,790RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,630,240 - 49,630,465UniSTS
REN7097  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,648,806 - 55,649,057UniSTSGRCh37
Build 361055,318,812 - 55,319,063RGDNCBI36
Celera1048,911,765 - 48,912,016RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,630,440 - 49,630,691UniSTS
REN7098  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,649,033 - 55,649,283UniSTSGRCh37
Build 361055,319,039 - 55,319,289RGDNCBI36
Celera1048,911,992 - 48,912,242RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,630,667 - 49,630,917UniSTS
REN7099  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,649,248 - 55,649,502UniSTSGRCh37
Build 361055,319,254 - 55,319,508RGDNCBI36
Celera1048,912,207 - 48,912,461RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,630,882 - 49,631,136UniSTS
REN7100  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,649,478 - 55,649,736UniSTSGRCh37
Build 361055,319,484 - 55,319,742RGDNCBI36
Celera1048,912,437 - 48,912,695RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,631,112 - 49,631,370UniSTS
REN7101  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,649,684 - 55,649,918UniSTSGRCh37
Build 361055,319,690 - 55,319,924RGDNCBI36
Celera1048,912,643 - 48,912,877RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,631,318 - 49,631,552UniSTS
REN7102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,650,138 - 55,650,369UniSTSGRCh37
Build 361055,320,144 - 55,320,375RGDNCBI36
Celera1048,913,097 - 48,913,328RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,631,772 - 49,632,003UniSTS
REN7103  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,650,344 - 55,650,603UniSTSGRCh37
Build 361055,320,350 - 55,320,609RGDNCBI36
Celera1048,913,303 - 48,913,562RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,631,978 - 49,632,237UniSTS
REN7104  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,650,569 - 55,650,793UniSTSGRCh37
Build 361055,320,575 - 55,320,799RGDNCBI36
Celera1048,913,528 - 48,913,752RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,632,203 - 49,632,427UniSTS
REN7105  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,650,726 - 55,650,993UniSTSGRCh37
Build 361055,320,732 - 55,320,999RGDNCBI36
Celera1048,913,685 - 48,913,954RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,632,360 - 49,632,629UniSTS
REN7106  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,650,970 - 55,651,226UniSTSGRCh37
Build 361055,320,976 - 55,321,232RGDNCBI36
Celera1048,913,931 - 48,914,187RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,632,606 - 49,632,862UniSTS
REN7107  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,651,185 - 55,651,439UniSTSGRCh37
Build 361055,321,191 - 55,321,445RGDNCBI36
Celera1048,914,146 - 48,914,400RGD
Cytogenetic Map10q21.1UniSTS
REN7108  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,651,368 - 55,651,613UniSTSGRCh37
Build 361055,321,374 - 55,321,619RGDNCBI36
Cytogenetic Map10q21.1UniSTS
REN7109  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,651,493 - 55,651,738UniSTSGRCh37
Build 361055,321,499 - 55,321,744RGDNCBI36
Cytogenetic Map10q21.1UniSTS
REN7110  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,651,855 - 55,652,107UniSTSGRCh37
Build 361055,321,861 - 55,322,113RGDNCBI36
Celera1048,914,771 - 48,915,023RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,633,787 - 49,634,039UniSTS
REN7111  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,652,086 - 55,652,322UniSTSGRCh37
Build 361055,322,092 - 55,322,328RGDNCBI36
Celera1048,915,002 - 48,915,238RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,634,018 - 49,634,254UniSTS
REN7112  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,652,293 - 55,652,524UniSTSGRCh37
Build 361055,322,299 - 55,322,530RGDNCBI36
Celera1048,915,209 - 48,915,440RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,634,225 - 49,634,456UniSTS
REN7113  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,652,424 - 55,652,669UniSTSGRCh37
Build 361055,322,430 - 55,322,675RGDNCBI36
Celera1048,915,340 - 48,915,585RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,634,356 - 49,634,601UniSTS
REN7114  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,652,645 - 55,652,869UniSTSGRCh37
Build 361055,322,651 - 55,322,875RGDNCBI36
Celera1048,915,561 - 48,915,785RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,634,577 - 49,634,801UniSTS
REN7115  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,652,846 - 55,653,099UniSTSGRCh37
Build 361055,322,852 - 55,323,105RGDNCBI36
Celera1048,915,762 - 48,916,015RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,634,778 - 49,635,031UniSTS
REN7116  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,653,071 - 55,653,313UniSTSGRCh37
Build 361055,323,077 - 55,323,319RGDNCBI36
Celera1048,915,987 - 48,916,229RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,635,003 - 49,635,245UniSTS
REN7117  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,653,165 - 55,653,406UniSTSGRCh37
Build 361055,323,171 - 55,323,412RGDNCBI36
Celera1048,916,081 - 48,916,322RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,635,097 - 49,635,338UniSTS
REN7118  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,653,470 - 55,653,697UniSTSGRCh37
Build 361055,323,476 - 55,323,703RGDNCBI36
Celera1048,916,386 - 48,916,613RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,635,402 - 49,635,629UniSTS
REN7119  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,653,676 - 55,653,913UniSTSGRCh37
Build 361055,323,682 - 55,323,919RGDNCBI36
Celera1048,916,592 - 48,916,829RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,635,608 - 49,635,845UniSTS
REN7120  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,653,893 - 55,654,132UniSTSGRCh37
Build 361055,323,899 - 55,324,138RGDNCBI36
Celera1048,916,809 - 48,917,048RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,635,825 - 49,636,064UniSTS
REN7121  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,654,109 - 55,654,348UniSTSGRCh37
Build 361055,324,115 - 55,324,354RGDNCBI36
Celera1048,917,025 - 48,917,264RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,636,041 - 49,636,280UniSTS
REN7122  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,654,347 - 55,654,607UniSTSGRCh37
Build 361055,324,353 - 55,324,613RGDNCBI36
Celera1048,917,263 - 48,917,523RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,636,279 - 49,636,539UniSTS
REN7123  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,654,584 - 55,654,833UniSTSGRCh37
Build 361055,324,590 - 55,324,839RGDNCBI36
Celera1048,917,500 - 48,917,749RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,636,516 - 49,636,765UniSTS
REN7124  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,654,779 - 55,655,032UniSTSGRCh37
Build 361055,324,785 - 55,325,038RGDNCBI36
Celera1048,917,695 - 48,917,948RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,636,711 - 49,636,964UniSTS
REN7125  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,655,003 - 55,655,261UniSTSGRCh37
Build 361055,325,009 - 55,325,267RGDNCBI36
Celera1048,917,919 - 48,918,177RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,636,935 - 49,637,193UniSTS
REN7126  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,655,094 - 55,655,348UniSTSGRCh37
Build 361055,325,100 - 55,325,354RGDNCBI36
Celera1048,918,010 - 48,918,264RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,637,026 - 49,637,280UniSTS
REN7127  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,655,325 - 55,655,574UniSTSGRCh37
Build 361055,325,331 - 55,325,580RGDNCBI36
Celera1048,918,241 - 48,918,490RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,637,257 - 49,637,506UniSTS
REN7128  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,655,547 - 55,655,790UniSTSGRCh37
Build 361055,325,553 - 55,325,796RGDNCBI36
Celera1048,918,463 - 48,918,706RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,637,479 - 49,637,722UniSTS
REN7129  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,655,775 - 55,656,021UniSTSGRCh37
Build 361055,325,781 - 55,326,027RGDNCBI36
Celera1048,918,691 - 48,918,937RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,637,707 - 49,637,953UniSTS
REN7130  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,656,000 - 55,656,256UniSTSGRCh37
Build 361055,326,006 - 55,326,262RGDNCBI36
Celera1048,918,916 - 48,919,172RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,637,932 - 49,638,188UniSTS
REN7131  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,656,243 - 55,656,478UniSTSGRCh37
Build 361055,326,249 - 55,326,484RGDNCBI36
Celera1048,919,159 - 48,919,394RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,638,175 - 49,638,410UniSTS
REN7132  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,656,442 - 55,656,666UniSTSGRCh37
Build 361055,326,448 - 55,326,672RGDNCBI36
Celera1048,919,358 - 48,919,582RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,638,374 - 49,638,598UniSTS
REN7133  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,656,640 - 55,656,894UniSTSGRCh37
Build 361055,326,646 - 55,326,900RGDNCBI36
Celera1048,919,556 - 48,919,810RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,638,572 - 49,638,826UniSTS
REN7134  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,656,893 - 55,657,132UniSTSGRCh37
Build 361055,326,899 - 55,327,138RGDNCBI36
Celera1048,919,809 - 48,920,048RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,638,825 - 49,639,065UniSTS
REN7135  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,657,128 - 55,657,381UniSTSGRCh37
Build 361055,327,134 - 55,327,387RGDNCBI36
Celera1048,920,044 - 48,920,297RGD
Cytogenetic Map10q21.1UniSTS
REN7136  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,657,371 - 55,657,600UniSTSGRCh37
Build 361055,327,377 - 55,327,606RGDNCBI36
Celera1048,920,287 - 48,920,516RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,639,302 - 49,639,531UniSTS
REN7137  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,657,404 - 55,657,651UniSTSGRCh37
Build 361055,327,410 - 55,327,657RGDNCBI36
Celera1048,920,320 - 48,920,567RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,639,335 - 49,639,582UniSTS
REN7138  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,658,071 - 55,658,295UniSTSGRCh37
Build 361055,328,077 - 55,328,301RGDNCBI36
Celera1048,920,986 - 48,921,210RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,639,996 - 49,640,220UniSTS
REN7139  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,658,285 - 55,658,534UniSTSGRCh37
Build 361055,328,291 - 55,328,540RGDNCBI36
Celera1048,921,200 - 48,921,449RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,640,210 - 49,640,459UniSTS
REN7140  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,658,508 - 55,658,745UniSTSGRCh37
Build 361055,328,514 - 55,328,751RGDNCBI36
Celera1048,921,423 - 48,921,660RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,640,433 - 49,640,670UniSTS
REN7141  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,658,719 - 55,658,953UniSTSGRCh37
Build 361055,328,725 - 55,328,959RGDNCBI36
Celera1048,921,634 - 48,921,869RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,640,644 - 49,640,879UniSTS
REN7142  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,658,930 - 55,659,195UniSTSGRCh37
Build 361055,328,936 - 55,329,201RGDNCBI36
Celera1048,921,846 - 48,922,111RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,640,856 - 49,641,121UniSTS
REN7143  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,659,173 - 55,659,441UniSTSGRCh37
Build 361055,329,179 - 55,329,447RGDNCBI36
Celera1048,922,089 - 48,922,357RGD
Cytogenetic Map10q21.1UniSTS
REN7144  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,659,418 - 55,659,665UniSTSGRCh37
Build 361055,329,424 - 55,329,671RGDNCBI36
Celera1048,922,334 - 48,922,581RGD
Cytogenetic Map10q21.1UniSTS
REN7145  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,659,662 - 55,659,916UniSTSGRCh37
Build 361055,329,668 - 55,329,922RGDNCBI36
Celera1048,922,578 - 48,922,832RGD
Cytogenetic Map10q21.1UniSTS
REN7146  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,659,894 - 55,660,135UniSTSGRCh37
Build 361055,329,900 - 55,330,141RGDNCBI36
Celera1048,922,810 - 48,923,049RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,641,420 - 49,641,657UniSTS
REN7147  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,660,108 - 55,660,364UniSTSGRCh37
Build 361055,330,114 - 55,330,370RGDNCBI36
Celera1048,923,022 - 48,923,278RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,641,630 - 49,641,886UniSTS
REN7148  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,660,359 - 55,660,607UniSTSGRCh37
Build 361055,330,365 - 55,330,613RGDNCBI36
Celera1048,923,273 - 48,923,521RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,641,881 - 49,642,129UniSTS
REN7149  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,660,584 - 55,660,836UniSTSGRCh37
Build 361055,330,590 - 55,330,842RGDNCBI36
Celera1048,923,498 - 48,923,750RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,642,106 - 49,642,358UniSTS
REN7150  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,660,818 - 55,661,070UniSTSGRCh37
Build 361055,330,824 - 55,331,076RGDNCBI36
Celera1048,923,732 - 48,923,985RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,642,340 - 49,642,592UniSTS
REN7151  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,661,066 - 55,661,308UniSTSGRCh37
Build 361055,331,072 - 55,331,314RGDNCBI36
Celera1048,923,981 - 48,924,223RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,642,588 - 49,642,830UniSTS
REN7152  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,661,285 - 55,661,538UniSTSGRCh37
Build 361055,331,291 - 55,331,544RGDNCBI36
Celera1048,924,200 - 48,924,453RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,642,807 - 49,643,060UniSTS
REN7153  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,661,515 - 55,661,766UniSTSGRCh37
Build 361055,331,521 - 55,331,772RGDNCBI36
Celera1048,924,430 - 48,924,681RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,643,037 - 49,643,288UniSTS
REN7154  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,661,743 - 55,661,997UniSTSGRCh37
Build 361055,331,749 - 55,332,003RGDNCBI36
Celera1048,924,658 - 48,924,912RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,643,265 - 49,643,519UniSTS
REN7155  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,661,963 - 55,662,196UniSTSGRCh37
Build 361055,331,969 - 55,332,202RGDNCBI36
Celera1048,924,878 - 48,925,111RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,643,485 - 49,643,718UniSTS
REN7156  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,662,061 - 55,662,289UniSTSGRCh37
Build 361055,332,067 - 55,332,295RGDNCBI36
Celera1048,924,976 - 48,925,204RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,643,583 - 49,643,811UniSTS
REN7157  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,662,250 - 55,662,512UniSTSGRCh37
Build 361055,332,256 - 55,332,518RGDNCBI36
Celera1048,925,165 - 48,925,427RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,643,772 - 49,644,034UniSTS
REN7158  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,662,489 - 55,662,736UniSTSGRCh37
Build 361055,332,495 - 55,332,742RGDNCBI36
Celera1048,925,404 - 48,925,651RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,644,011 - 49,644,258UniSTS
REN7159  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,662,705 - 55,662,966UniSTSGRCh37
Build 361055,332,711 - 55,332,972RGDNCBI36
Celera1048,925,620 - 48,925,881RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,644,227 - 49,644,488UniSTS
REN7160  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,662,933 - 55,663,178UniSTSGRCh37
Build 361055,332,939 - 55,333,184RGDNCBI36
Celera1048,925,848 - 48,926,094RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,644,455 - 49,644,700UniSTS
REN7161  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,663,116 - 55,663,371UniSTSGRCh37
Build 361055,333,122 - 55,333,377RGDNCBI36
Celera1048,926,032 - 48,926,287RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,644,638 - 49,644,893UniSTS
REN7162  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,663,345 - 55,663,574UniSTSGRCh37
Build 361055,333,351 - 55,333,580RGDNCBI36
Celera1048,926,261 - 48,926,490RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,644,867 - 49,645,096UniSTS
REN7163  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,663,473 - 55,663,727UniSTSGRCh37
Build 361055,333,479 - 55,333,733RGDNCBI36
Celera1048,926,389 - 48,926,643RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,644,995 - 49,645,249UniSTS
REN7164  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,663,707 - 55,663,956UniSTSGRCh37
Build 361055,333,713 - 55,333,962RGDNCBI36
Celera1048,926,623 - 48,926,872RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,645,229 - 49,645,478UniSTS
REN7165  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,663,932 - 55,664,160UniSTSGRCh37
Build 361055,333,938 - 55,334,166RGDNCBI36
Celera1048,926,848 - 48,927,076RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,645,454 - 49,645,682UniSTS
REN7166  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,664,153 - 55,664,409UniSTSGRCh37
Build 361055,334,159 - 55,334,415RGDNCBI36
Celera1048,927,069 - 48,927,326RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,645,675 - 49,645,933UniSTS
REN7167  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,664,397 - 55,664,642UniSTSGRCh37
Build 361055,334,403 - 55,334,648RGDNCBI36
Celera1048,927,314 - 48,927,559RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,645,921 - 49,646,166UniSTS
REN7168  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,664,619 - 55,664,873UniSTSGRCh37
Build 361055,334,625 - 55,334,879RGDNCBI36
Celera1048,927,536 - 48,927,790RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,646,143 - 49,646,395UniSTS
REN7169  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,664,853 - 55,665,084UniSTSGRCh37
Build 361055,334,859 - 55,335,090RGDNCBI36
Celera1048,927,770 - 48,928,001RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,646,375 - 49,646,606UniSTS
REN7170  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,665,057 - 55,665,313UniSTSGRCh37
Build 361055,335,063 - 55,335,319RGDNCBI36
Celera1048,927,974 - 48,928,230RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,646,579 - 49,646,835UniSTS
REN7171  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,665,293 - 55,665,550UniSTSGRCh37
Build 361055,335,299 - 55,335,556RGDNCBI36
Celera1048,928,210 - 48,928,467RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,646,815 - 49,647,072UniSTS
REN7172  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,665,546 - 55,665,790UniSTSGRCh37
Build 361055,335,552 - 55,335,796RGDNCBI36
Celera1048,928,463 - 48,928,707RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,647,068 - 49,647,312UniSTS
REN7173  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,665,692 - 55,665,953UniSTSGRCh37
Build 361055,335,698 - 55,335,959RGDNCBI36
Celera1048,928,609 - 48,928,870RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,647,214 - 49,647,475UniSTS
REN7174  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,665,925 - 55,666,149UniSTSGRCh37
Build 361055,335,931 - 55,336,155RGDNCBI36
Celera1048,928,842 - 48,929,066RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,647,447 - 49,647,671UniSTS
REN7175  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,666,026 - 55,666,275UniSTSGRCh37
Build 361055,336,032 - 55,336,281RGDNCBI36
Celera1048,928,943 - 48,929,192RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,647,548 - 49,647,797UniSTS
REN7176  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,666,216 - 55,666,444UniSTSGRCh37
Build 361055,336,222 - 55,336,450RGDNCBI36
Celera1048,929,133 - 48,929,361RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,647,738 - 49,647,966UniSTS
REN7177  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,666,419 - 55,666,660UniSTSGRCh37
Build 361055,336,425 - 55,336,666RGDNCBI36
Celera1048,929,336 - 48,929,576RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,647,941 - 49,648,181UniSTS
REN7178  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,666,638 - 55,666,893UniSTSGRCh37
Build 361055,336,644 - 55,336,899RGDNCBI36
Celera1048,929,554 - 48,929,809RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,648,159 - 49,648,414UniSTS
REN7179  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,666,870 - 55,667,126UniSTSGRCh37
Build 361055,336,876 - 55,337,132RGDNCBI36
Celera1048,929,786 - 48,930,042RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,648,391 - 49,648,647UniSTS
REN7180  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,667,104 - 55,667,328UniSTSGRCh37
Build 361055,337,110 - 55,337,334RGDNCBI36
Celera1048,930,020 - 48,930,244RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,648,625 - 49,648,849UniSTS
REN7181  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,667,323 - 55,667,571UniSTSGRCh37
Build 361055,337,329 - 55,337,577RGDNCBI36
Celera1048,930,239 - 48,930,487RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,648,844 - 49,649,092UniSTS
REN7182  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,667,543 - 55,667,807UniSTSGRCh37
Build 361055,337,549 - 55,337,813RGDNCBI36
Celera1048,930,459 - 48,930,723RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,649,064 - 49,649,328UniSTS
REN7183  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,667,787 - 55,668,021UniSTSGRCh37
Build 361055,337,793 - 55,338,027RGDNCBI36
Celera1048,930,703 - 48,930,937RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,649,308 - 49,649,542UniSTS
REN7184  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,667,996 - 55,668,225UniSTSGRCh37
Build 361055,338,002 - 55,338,231RGDNCBI36
Celera1048,930,912 - 48,931,141RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,649,517 - 49,649,746UniSTS
REN7185  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,668,213 - 55,668,437UniSTSGRCh37
Build 361055,338,219 - 55,338,443RGDNCBI36
Celera1048,931,129 - 48,931,353RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,649,734 - 49,649,958UniSTS
REN7186  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,668,403 - 55,668,661UniSTSGRCh37
Build 361055,338,409 - 55,338,667RGDNCBI36
Celera1048,931,319 - 48,931,577RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,649,924 - 49,650,182UniSTS
REN7187  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,668,646 - 55,668,908UniSTSGRCh37
Build 361055,338,652 - 55,338,914RGDNCBI36
Celera1048,931,562 - 48,931,824RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,650,167 - 49,650,429UniSTS
REN7188  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,668,906 - 55,669,143UniSTSGRCh37
Build 361055,338,912 - 55,339,149RGDNCBI36
Celera1048,931,822 - 48,932,059RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,650,427 - 49,650,664UniSTS
REN7189  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,668,950 - 55,669,200UniSTSGRCh37
Build 361055,338,956 - 55,339,206RGDNCBI36
Celera1048,931,866 - 48,932,116RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,650,471 - 49,650,721UniSTS
REN7190  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,669,174 - 55,669,415UniSTSGRCh37
Build 361055,339,180 - 55,339,421RGDNCBI36
Celera1048,932,090 - 48,932,331RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,650,695 - 49,650,936UniSTS
REN7191  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,669,383 - 55,669,631UniSTSGRCh37
Build 361055,339,389 - 55,339,637RGDNCBI36
Celera1048,932,299 - 48,932,547RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,650,904 - 49,651,152UniSTS
REN7192  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,669,594 - 55,669,822UniSTSGRCh37
Build 361055,339,600 - 55,339,828RGDNCBI36
Celera1048,932,510 - 48,932,738RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,651,115 - 49,651,343UniSTS
REN7193  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,669,796 - 55,670,040UniSTSGRCh37
Build 361055,339,802 - 55,340,046RGDNCBI36
Celera1048,932,712 - 48,932,956RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,651,317 - 49,651,561UniSTS
REN7194  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,669,877 - 55,670,133UniSTSGRCh37
Build 361055,339,883 - 55,340,139RGDNCBI36
Celera1048,932,793 - 48,933,049RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,651,398 - 49,651,654UniSTS
REN7195  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,670,163 - 55,670,406UniSTSGRCh37
Build 361055,340,169 - 55,340,412RGDNCBI36
Celera1048,933,079 - 48,933,322RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,651,684 - 49,651,927UniSTS
REN7196  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,670,383 - 55,670,626UniSTSGRCh37
Build 361055,340,389 - 55,340,632RGDNCBI36
Celera1048,933,299 - 48,933,542RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,651,904 - 49,652,147UniSTS
REN7197  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,670,606 - 55,670,855UniSTSGRCh37
Build 361055,340,612 - 55,340,861RGDNCBI36
Celera1048,933,522 - 48,933,771RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,652,127 - 49,652,376UniSTS
REN7198  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,671,335 - 55,671,597UniSTSGRCh37
Build 361055,341,341 - 55,341,603RGDNCBI36
Celera1048,934,251 - 48,934,513RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,652,856 - 49,653,118UniSTS
REN7199  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,671,804 - 55,672,068UniSTSGRCh37
Build 361055,341,810 - 55,342,074RGDNCBI36
Celera1048,934,720 - 48,934,984RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,653,325 - 49,653,589UniSTS
REN7200  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,672,658 - 55,672,896UniSTSGRCh37
Build 361055,342,664 - 55,342,902RGDNCBI36
Celera1048,935,574 - 48,935,812RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,654,179 - 49,654,417UniSTS
REN7201  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,672,724 - 55,672,949UniSTSGRCh37
Build 361055,342,730 - 55,342,955RGDNCBI36
Celera1048,935,640 - 48,935,865RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,654,245 - 49,654,470UniSTS
REN7202  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,674,602 - 55,674,826UniSTSGRCh37
Build 361055,344,608 - 55,344,832RGDNCBI36
Celera1048,937,515 - 48,937,739RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,656,120 - 49,656,344UniSTS
REN7203  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,674,791 - 55,675,057UniSTSGRCh37
Build 361055,344,797 - 55,345,063RGDNCBI36
Celera1048,937,704 - 48,937,970RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,656,309 - 49,656,575UniSTS
REN7204  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,675,046 - 55,675,316UniSTSGRCh37
Build 361055,345,052 - 55,345,322RGDNCBI36
Celera1048,937,959 - 48,938,229RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,656,564 - 49,656,834UniSTS
REN7205  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,675,546 - 55,675,779UniSTSGRCh37
Build 361055,345,552 - 55,345,785RGDNCBI36
Celera1048,938,459 - 48,938,692RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,657,064 - 49,657,297UniSTS
REN7206  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,675,743 - 55,675,982UniSTSGRCh37
Build 361055,345,749 - 55,345,988RGDNCBI36
Celera1048,938,656 - 48,938,895RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,657,261 - 49,657,500UniSTS
REN7207  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,675,963 - 55,676,214UniSTSGRCh37
Build 361055,345,969 - 55,346,220RGDNCBI36
Celera1048,938,876 - 48,939,127RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,657,481 - 49,657,732UniSTS
REN7208  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,676,204 - 55,676,453UniSTSGRCh37
Build 361055,346,210 - 55,346,459RGDNCBI36
Celera1048,939,117 - 48,939,370RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,657,722 - 49,657,975UniSTS
REN7209  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,676,427 - 55,676,672UniSTSGRCh37
Build 361055,346,433 - 55,346,678RGDNCBI36
Celera1048,939,344 - 48,939,589RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,657,949 - 49,658,194UniSTS
REN7210  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,676,652 - 55,676,901UniSTSGRCh37
Build 361055,346,658 - 55,346,907RGDNCBI36
Celera1048,939,569 - 48,939,817RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,658,174 - 49,658,422UniSTS
REN7211  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,676,863 - 55,677,087UniSTSGRCh37
Build 361055,346,869 - 55,347,093RGDNCBI36
Celera1048,939,779 - 48,940,003RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,658,384 - 49,658,608UniSTS
REN7212  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,677,062 - 55,677,311UniSTSGRCh37
Build 361055,347,068 - 55,347,317RGDNCBI36
Celera1048,939,978 - 48,940,227RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,658,583 - 49,658,832UniSTS
REN7213  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,677,288 - 55,677,538UniSTSGRCh37
Build 361055,347,294 - 55,347,544RGDNCBI36
Celera1048,940,204 - 48,940,454RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,658,809 - 49,659,059UniSTS
REN7214  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,677,473 - 55,677,727UniSTSGRCh37
Build 361055,347,479 - 55,347,733RGDNCBI36
Celera1048,940,389 - 48,940,643RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,658,994 - 49,659,248UniSTS
REN7215  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,677,707 - 55,677,949UniSTSGRCh37
Build 361055,347,713 - 55,347,955RGDNCBI36
Celera1048,940,623 - 48,940,865RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,659,228 - 49,659,470UniSTS
REN7216  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,677,935 - 55,678,200UniSTSGRCh37
Build 361055,347,941 - 55,348,206RGDNCBI36
Cytogenetic Map10q21.1UniSTS
REN7217  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,678,191 - 55,678,447UniSTSGRCh37
Build 361055,348,197 - 55,348,453RGDNCBI36
Celera1048,941,107 - 48,941,363RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,659,712 - 49,659,968UniSTS
REN7218  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,678,438 - 55,678,682UniSTSGRCh37
Build 361055,348,444 - 55,348,688RGDNCBI36
Celera1048,941,354 - 48,941,573RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,659,959 - 49,660,177UniSTS
REN7219  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,678,678 - 55,678,932UniSTSGRCh37
Build 361055,348,684 - 55,348,938RGDNCBI36
Celera1048,941,569 - 48,941,823RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,660,173 - 49,660,427UniSTS
REN7220  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,678,919 - 55,679,163UniSTSGRCh37
Build 361055,348,925 - 55,349,169RGDNCBI36
Celera1048,941,810 - 48,942,054RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,660,414 - 49,660,658UniSTS
REN7221  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,679,143 - 55,679,391UniSTSGRCh37
Build 361055,349,149 - 55,349,397RGDNCBI36
Celera1048,942,034 - 48,942,282RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,660,638 - 49,660,886UniSTS
REN7222  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,679,366 - 55,679,598UniSTSGRCh37
Build 361055,349,372 - 55,349,604RGDNCBI36
Celera1048,942,257 - 48,942,489RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,660,861 - 49,661,093UniSTS
REN7223  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,679,578 - 55,679,833UniSTSGRCh37
Build 361055,349,584 - 55,349,839RGDNCBI36
Celera1048,942,469 - 48,942,724RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,661,073 - 49,661,328UniSTS
REN7224  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,679,822 - 55,680,083UniSTSGRCh37
Build 361055,349,828 - 55,350,089RGDNCBI36
Celera1048,942,713 - 48,942,974RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,661,317 - 49,661,578UniSTS
REN7225  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,680,019 - 55,680,244UniSTSGRCh37
Build 361055,350,025 - 55,350,250RGDNCBI36
Celera1048,942,910 - 48,943,135RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,661,514 - 49,661,739UniSTS
REN7226  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,680,220 - 55,680,476UniSTSGRCh37
Build 361055,350,226 - 55,350,482RGDNCBI36
Celera1048,943,111 - 48,943,367RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,661,715 - 49,661,971UniSTS
REN7227  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,680,437 - 55,680,662UniSTSGRCh37
Build 361055,350,443 - 55,350,668RGDNCBI36
Celera1048,943,328 - 48,943,553RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,661,932 - 49,662,157UniSTS
REN7228  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,680,635 - 55,680,880UniSTSGRCh37
Build 361055,350,641 - 55,350,886RGDNCBI36
Celera1048,943,526 - 48,943,771RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,662,130 - 49,662,375UniSTS
REN7229  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,680,873 - 55,681,124UniSTSGRCh37
Build 361055,350,879 - 55,351,130RGDNCBI36
Celera1048,943,764 - 48,944,015RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,662,368 - 49,662,619UniSTS
REN7230  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,681,113 - 55,681,362UniSTSGRCh37
Build 361055,351,119 - 55,351,368RGDNCBI36
Celera1048,944,004 - 48,944,254RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,662,608 - 49,662,858UniSTS
REN7231  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,681,346 - 55,681,599UniSTSGRCh37
Build 361055,351,352 - 55,351,605RGDNCBI36
Celera1048,944,238 - 48,944,491RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,662,842 - 49,663,095UniSTS
REN7232  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,681,578 - 55,681,833UniSTSGRCh37
Build 361055,351,584 - 55,351,839RGDNCBI36
Celera1048,944,470 - 48,944,725RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,663,074 - 49,663,329UniSTS
REN7233  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,681,804 - 55,682,050UniSTSGRCh37
Build 361055,351,810 - 55,352,056RGDNCBI36
Celera1048,944,696 - 48,944,942RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,663,300 - 49,663,546UniSTS
REN7234  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,682,033 - 55,682,273UniSTSGRCh37
Build 361055,352,039 - 55,352,279RGDNCBI36
Celera1048,944,925 - 48,945,165RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,663,529 - 49,663,769UniSTS
REN7235  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,682,261 - 55,682,518UniSTSGRCh37
Build 361055,352,267 - 55,352,524RGDNCBI36
Celera1048,945,153 - 48,945,410RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,663,757 - 49,664,014UniSTS
REN7236  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,682,341 - 55,682,581UniSTSGRCh37
Build 361055,352,347 - 55,352,587RGDNCBI36
Celera1048,945,233 - 48,945,473RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,663,837 - 49,664,077UniSTS
REN7237  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,682,864 - 55,683,091UniSTSGRCh37
Build 361055,352,870 - 55,353,097RGDNCBI36
Celera1048,945,756 - 48,945,983RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,664,360 - 49,664,587UniSTS
REN7238  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,683,052 - 55,683,282UniSTSGRCh37
Build 361055,353,058 - 55,353,288RGDNCBI36
Celera1048,945,944 - 48,946,174RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,664,548 - 49,664,778UniSTS
REN7239  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,683,261 - 55,683,506UniSTSGRCh37
Build 361055,353,267 - 55,353,512RGDNCBI36
Celera1048,946,153 - 48,946,398RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,664,757 - 49,665,002UniSTS
REN7240  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,683,497 - 55,683,756UniSTSGRCh37
Build 361055,353,503 - 55,353,762RGDNCBI36
Celera1048,946,389 - 48,946,648RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,664,993 - 49,665,252UniSTS
REN7241  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,683,589 - 55,683,820UniSTSGRCh37
Build 361055,353,595 - 55,353,826RGDNCBI36
Celera1048,946,481 - 48,946,712RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,665,085 - 49,665,316UniSTS
REN7242  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,683,798 - 55,684,031UniSTSGRCh37
Build 361055,353,804 - 55,354,037RGDNCBI36
Celera1048,946,690 - 48,946,923RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,665,294 - 49,665,527UniSTS
REN7243  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,684,413 - 55,684,641UniSTSGRCh37
Build 361055,354,419 - 55,354,647RGDNCBI36
Celera1048,947,305 - 48,947,533RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,665,909 - 49,666,137UniSTS
REN7244  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,684,608 - 55,684,842UniSTSGRCh37
Build 361055,354,614 - 55,354,848RGDNCBI36
Celera1048,947,500 - 48,947,734RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,666,104 - 49,666,338UniSTS
REN7245  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,684,818 - 55,685,053UniSTSGRCh37
Build 361055,354,824 - 55,355,059RGDNCBI36
Celera1048,947,710 - 48,947,945RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,666,314 - 49,666,549UniSTS
REN7246  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,685,045 - 55,685,309UniSTSGRCh37
Build 361055,355,051 - 55,355,315RGDNCBI36
Celera1048,947,937 - 48,948,201RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,666,541 - 49,666,805UniSTS
REN7247  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,685,299 - 55,685,533UniSTSGRCh37
Build 361055,355,305 - 55,355,539RGDNCBI36
Celera1048,948,191 - 48,948,425RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,666,795 - 49,667,029UniSTS
REN7248  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,685,517 - 55,685,761UniSTSGRCh37
Build 361055,355,523 - 55,355,767RGDNCBI36
Celera1048,948,409 - 48,948,653RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,667,013 - 49,667,257UniSTS
REN7249  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,685,738 - 55,685,985UniSTSGRCh37
Build 361055,355,744 - 55,355,991RGDNCBI36
Celera1048,948,630 - 48,948,877RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,667,234 - 49,667,481UniSTS
REN7250  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,685,961 - 55,686,194UniSTSGRCh37
Build 361055,355,967 - 55,356,200RGDNCBI36
Celera1048,948,853 - 48,949,086RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,667,457 - 49,667,690UniSTS
REN7251  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,686,171 - 55,686,412UniSTSGRCh37
Build 361055,356,177 - 55,356,418RGDNCBI36
Celera1048,949,063 - 48,949,304RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,667,667 - 49,667,908UniSTS
REN7252  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,686,392 - 55,686,642UniSTSGRCh37
Build 361055,356,398 - 55,356,648RGDNCBI36
Celera1048,949,284 - 48,949,534RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,667,888 - 49,668,138UniSTS
REN7253  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,686,627 - 55,686,851UniSTSGRCh37
Build 361055,356,633 - 55,356,857RGDNCBI36
Celera1048,949,519 - 48,949,743RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,668,123 - 49,668,347UniSTS
REN7254  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,686,830 - 55,687,072UniSTSGRCh37
Build 361055,356,836 - 55,357,078RGDNCBI36
Celera1048,949,722 - 48,949,968RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,668,326 - 49,668,572UniSTS
REN7255  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,687,064 - 55,687,288UniSTSGRCh37
Build 361055,357,070 - 55,357,294RGDNCBI36
Celera1048,949,960 - 48,950,184RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,668,564 - 49,668,788UniSTS
REN7256  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,687,255 - 55,687,518UniSTSGRCh37
Build 361055,357,261 - 55,357,524RGDNCBI36
Celera1048,950,151 - 48,950,414RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,668,755 - 49,669,018UniSTS
REN7257  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,687,494 - 55,687,723UniSTSGRCh37
Build 361055,357,500 - 55,357,729RGDNCBI36
Celera1048,950,390 - 48,950,619RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,668,994 - 49,669,223UniSTS
REN7258  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,687,698 - 55,687,959UniSTSGRCh37
Build 361055,357,704 - 55,357,965RGDNCBI36
Celera1048,950,594 - 48,950,855RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,669,198 - 49,669,459UniSTS
REN7259  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,687,945 - 55,688,212UniSTSGRCh37
Build 361055,357,951 - 55,358,218RGDNCBI36
Celera1048,950,841 - 48,951,108RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,669,445 - 49,669,712UniSTS
REN7260  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,688,180 - 55,688,442UniSTSGRCh37
Build 361055,358,186 - 55,358,448RGDNCBI36
Celera1048,951,076 - 48,951,338RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,669,680 - 49,669,942UniSTS
REN7261  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,688,427 - 55,688,683UniSTSGRCh37
Build 361055,358,433 - 55,358,689RGDNCBI36
Celera1048,951,323 - 48,951,579RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,669,927 - 49,670,183UniSTS
REN7262  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,688,660 - 55,688,902UniSTSGRCh37
Build 361055,358,666 - 55,358,908RGDNCBI36
Celera1048,951,556 - 48,951,798RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,670,160 - 49,670,402UniSTS
REN7263  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,688,890 - 55,689,135UniSTSGRCh37
Build 361055,358,896 - 55,359,141RGDNCBI36
Celera1048,951,786 - 48,952,031RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,670,390 - 49,670,635UniSTS
REN7264  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,689,026 - 55,689,284UniSTSGRCh37
Build 361055,359,032 - 55,359,290RGDNCBI36
Celera1048,951,922 - 48,952,180RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,670,526 - 49,670,784UniSTS
REN7265  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,689,258 - 55,689,503UniSTSGRCh37
Build 361055,359,264 - 55,359,509RGDNCBI36
Celera1048,952,154 - 48,952,399RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,670,758 - 49,671,003UniSTS
REN7266  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,689,481 - 55,689,720UniSTSGRCh37
Build 361055,359,487 - 55,359,726RGDNCBI36
Celera1048,952,377 - 48,952,616RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,670,981 - 49,671,220UniSTS
REN7267  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,689,695 - 55,689,938UniSTSGRCh37
Build 361055,359,701 - 55,359,944RGDNCBI36
Celera1048,952,591 - 48,952,834RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,671,195 - 49,671,438UniSTS
REN7268  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,689,908 - 55,690,171UniSTSGRCh37
Build 361055,359,914 - 55,360,177RGDNCBI36
Celera1048,952,804 - 48,953,067RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,671,408 - 49,671,671UniSTS
REN7269  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,690,151 - 55,690,397UniSTSGRCh37
Build 361055,360,157 - 55,360,403RGDNCBI36
Celera1048,953,047 - 48,953,291RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,671,651 - 49,671,895UniSTS
REN7270  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,690,372 - 55,690,608UniSTSGRCh37
Build 361055,360,378 - 55,360,614RGDNCBI36
Celera1048,953,266 - 48,953,502RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,671,870 - 49,672,106UniSTS
REN7271  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,690,581 - 55,690,832UniSTSGRCh37
Build 361055,360,587 - 55,360,838RGDNCBI36
Celera1048,953,475 - 48,953,726RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,672,079 - 49,672,330UniSTS
REN7272  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,690,828 - 55,691,083UniSTSGRCh37
Build 361055,360,834 - 55,361,089RGDNCBI36
Celera1048,953,722 - 48,953,977RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,672,326 - 49,672,581UniSTS
REN7273  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,691,077 - 55,691,335UniSTSGRCh37
Build 361055,361,083 - 55,361,341RGDNCBI36
Celera1048,953,971 - 48,954,229RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,672,575 - 49,672,833UniSTS
REN7274  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,691,306 - 55,691,576UniSTSGRCh37
Build 361055,361,312 - 55,361,582RGDNCBI36
Celera1048,954,200 - 48,954,470RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,672,804 - 49,673,074UniSTS
REN7275  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,691,558 - 55,691,782UniSTSGRCh37
Build 361055,361,564 - 55,361,788RGDNCBI36
Celera1048,954,452 - 48,954,676RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,673,056 - 49,673,280UniSTS
REN7276  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,691,740 - 55,691,993UniSTSGRCh37
Build 361055,361,746 - 55,361,999RGDNCBI36
Celera1048,954,634 - 48,954,887RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,673,238 - 49,673,491UniSTS
REN7277  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,691,942 - 55,692,196UniSTSGRCh37
Build 361055,361,948 - 55,362,202RGDNCBI36
Celera1048,954,836 - 48,955,090RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,673,440 - 49,673,694UniSTS
REN7278  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,692,174 - 55,692,403UniSTSGRCh37
Build 361055,362,180 - 55,362,409RGDNCBI36
Celera1048,955,068 - 48,955,297RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,673,672 - 49,673,901UniSTS
REN7279  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,692,383 - 55,692,635UniSTSGRCh37
Build 361055,362,389 - 55,362,641RGDNCBI36
Celera1048,955,277 - 48,955,529RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,673,881 - 49,674,133UniSTS
REN7280  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,692,615 - 55,692,867UniSTSGRCh37
Build 361055,362,621 - 55,362,873RGDNCBI36
Celera1048,955,509 - 48,955,761RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,674,113 - 49,674,365UniSTS
REN7281  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,692,658 - 55,692,882UniSTSGRCh37
Build 361055,362,664 - 55,362,888RGDNCBI36
Celera1048,955,552 - 48,955,776RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,674,156 - 49,674,380UniSTS
REN7282  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,693,892 - 55,694,117UniSTSGRCh37
Build 361055,363,898 - 55,364,123RGDNCBI36
Celera1048,956,786 - 48,957,011RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,675,390 - 49,675,615UniSTS
REN7283  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,693,962 - 55,694,208UniSTSGRCh37
Build 361055,363,968 - 55,364,214RGDNCBI36
Celera1048,956,856 - 48,957,102RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,675,460 - 49,675,706UniSTS
REN7284  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,694,185 - 55,694,438UniSTSGRCh37
Build 361055,364,191 - 55,364,444RGDNCBI36
Celera1048,957,079 - 48,957,332RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,675,683 - 49,675,936UniSTS
REN7285  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,694,436 - 55,694,687UniSTSGRCh37
Build 361055,364,442 - 55,364,693RGDNCBI36
Celera1048,957,330 - 48,957,581RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,675,934 - 49,676,185UniSTS
REN7286  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,694,661 - 55,694,924UniSTSGRCh37
Build 361055,364,667 - 55,364,930RGDNCBI36
Celera1048,957,555 - 48,957,818RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,676,159 - 49,676,422UniSTS
REN7287  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,694,897 - 55,695,150UniSTSGRCh37
Build 361055,364,903 - 55,365,156RGDNCBI36
Celera1048,957,791 - 48,958,044RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,676,395 - 49,676,648UniSTS
REN7288  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,695,128 - 55,695,382UniSTSGRCh37
Build 361055,365,134 - 55,365,388RGDNCBI36
Celera1048,958,022 - 48,958,276RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,676,626 - 49,676,880UniSTS
REN7289  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,695,361 - 55,695,586UniSTSGRCh37
Build 361055,365,367 - 55,365,592RGDNCBI36
Celera1048,958,255 - 48,958,480RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,676,859 - 49,677,084UniSTS
REN7290  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,695,539 - 55,695,792UniSTSGRCh37
Build 361055,365,545 - 55,365,798RGDNCBI36
Celera1048,958,433 - 48,958,686RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,677,037 - 49,677,290UniSTS
REN7291  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,695,774 - 55,695,998UniSTSGRCh37
Build 361055,365,780 - 55,366,004RGDNCBI36
Celera1048,958,668 - 48,958,892RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,677,272 - 49,677,496UniSTS
REN7292  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,695,966 - 55,696,216UniSTSGRCh37
Build 361055,365,972 - 55,366,222RGDNCBI36
Celera1048,958,860 - 48,959,110RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,677,464 - 49,677,714UniSTS
REN7293  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,696,089 - 55,696,314UniSTSGRCh37
Build 361055,366,095 - 55,366,320RGDNCBI36
Celera1048,958,983 - 48,959,208RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,677,587 - 49,677,812UniSTS
REN7294  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,696,244 - 55,696,471UniSTSGRCh37
Build 361055,366,250 - 55,366,477RGDNCBI36
Celera1048,959,138 - 48,959,365RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,677,742 - 49,677,969UniSTS
REN7295  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,696,443 - 55,696,680UniSTSGRCh37
Build 361055,366,449 - 55,366,686RGDNCBI36
Celera1048,959,337 - 48,959,574RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,677,941 - 49,678,178UniSTS
REN7296  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,696,655 - 55,696,893UniSTSGRCh37
Build 361055,366,661 - 55,366,899RGDNCBI36
Celera1048,959,549 - 48,959,787RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,678,153 - 49,678,391UniSTS
REN7297  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,696,876 - 55,697,112UniSTSGRCh37
Build 361055,366,882 - 55,367,118RGDNCBI36
Celera1048,959,770 - 48,960,006RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,678,374 - 49,678,610UniSTS
REN7298  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,697,068 - 55,697,326UniSTSGRCh37
Build 361055,367,074 - 55,367,332RGDNCBI36
Celera1048,959,962 - 48,960,220RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,678,566 - 49,678,824UniSTS
REN7299  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,697,315 - 55,697,560UniSTSGRCh37
Build 361055,367,321 - 55,367,566RGDNCBI36
Celera1048,960,209 - 48,960,454RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,678,813 - 49,679,058UniSTS
REN7300  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,697,535 - 55,697,789UniSTSGRCh37
Build 361055,367,541 - 55,367,795RGDNCBI36
Celera1048,960,429 - 48,960,683RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,679,033 - 49,679,287UniSTS
REN7301  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,697,787 - 55,698,011UniSTSGRCh37
Build 361055,367,793 - 55,368,017RGDNCBI36
Celera1048,960,681 - 48,960,905RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,679,285 - 49,679,509UniSTS
REN7302  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,697,981 - 55,698,234UniSTSGRCh37
Build 361055,367,987 - 55,368,240RGDNCBI36
Celera1048,960,875 - 48,961,128RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,679,479 - 49,679,732UniSTS
REN7303  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,698,201 - 55,698,455UniSTSGRCh37
Build 361055,368,207 - 55,368,461RGDNCBI36
Celera1048,961,095 - 48,961,349RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,679,699 - 49,679,953UniSTS
REN7304  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,698,424 - 55,698,676UniSTSGRCh37
Build 361055,368,430 - 55,368,682RGDNCBI36
Celera1048,961,318 - 48,961,570RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,679,922 - 49,680,174UniSTS
REN7305  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,698,667 - 55,698,921UniSTSGRCh37
Build 361055,368,673 - 55,368,927RGDNCBI36
Celera1048,961,561 - 48,961,815RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,680,165 - 49,680,419UniSTS
REN7306  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,698,872 - 55,699,122UniSTSGRCh37
Build 361055,368,878 - 55,369,128RGDNCBI36
Celera1048,961,766 - 48,962,016RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,680,370 - 49,680,620UniSTS
REN7307  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,699,067 - 55,699,320UniSTSGRCh37
Build 361055,369,073 - 55,369,326RGDNCBI36
Celera1048,961,961 - 48,962,214RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,680,565 - 49,680,818UniSTS
REN7308  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,699,303 - 55,699,576UniSTSGRCh37
Build 361055,369,309 - 55,369,582RGDNCBI36
Celera1048,962,197 - 48,962,470RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,680,801 - 49,681,074UniSTS
REN7309  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,699,566 - 55,699,797UniSTSGRCh37
Build 361055,369,572 - 55,369,803RGDNCBI36
Celera1048,962,460 - 48,962,691RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,681,064 - 49,681,295UniSTS
REN7310  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,699,777 - 55,700,029UniSTSGRCh37
Build 361055,369,783 - 55,370,035RGDNCBI36
Celera1048,962,671 - 48,962,923RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,681,275 - 49,681,527UniSTS
REN7311  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,700,019 - 55,700,264UniSTSGRCh37
Build 361055,370,025 - 55,370,270RGDNCBI36
Celera1048,962,913 - 48,963,158RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,681,517 - 49,681,762UniSTS
REN7312  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,700,241 - 55,700,496UniSTSGRCh37
Build 361055,370,247 - 55,370,502RGDNCBI36
Celera1048,963,135 - 48,963,390RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,681,739 - 49,681,994UniSTS
REN7313  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,700,494 - 55,700,751UniSTSGRCh37
Build 361055,370,500 - 55,370,757RGDNCBI36
Celera1048,963,388 - 48,963,645RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,681,992 - 49,682,249UniSTS
REN7314  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,700,730 - 55,700,981UniSTSGRCh37
Build 361055,370,736 - 55,370,987RGDNCBI36
Celera1048,963,624 - 48,963,875RGD
Cytogenetic Map10q21.1UniSTS
REN7315  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,700,956 - 55,701,212UniSTSGRCh37
Build 361055,370,962 - 55,371,218RGDNCBI36
Celera1048,963,850 - 48,964,106RGD
Cytogenetic Map10q21.1UniSTS
REN7316  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,701,153 - 55,701,392UniSTSGRCh37
Build 361055,371,159 - 55,371,398RGDNCBI36
Celera1048,964,047 - 48,964,286RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,682,651 - 49,682,890UniSTS
REN7317  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,701,354 - 55,701,603UniSTSGRCh37
Build 361055,371,360 - 55,371,609RGDNCBI36
Celera1048,964,248 - 48,964,497RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,682,852 - 49,683,101UniSTS
REN7318  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,701,580 - 55,701,826UniSTSGRCh37
Build 361055,371,586 - 55,371,832RGDNCBI36
Celera1048,964,474 - 48,964,720RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,683,078 - 49,683,324UniSTS
REN7319  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,701,824 - 55,702,081UniSTSGRCh37
Build 361055,371,830 - 55,372,087RGDNCBI36
Celera1048,964,718 - 48,964,974RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,683,322 - 49,683,578UniSTS
REN7320  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,702,055 - 55,702,300UniSTSGRCh37
Build 361055,372,061 - 55,372,306RGDNCBI36
Celera1048,964,948 - 48,965,193RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,683,552 - 49,683,797UniSTS
REN7321  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,702,275 - 55,702,528UniSTSGRCh37
Build 361055,372,281 - 55,372,534RGDNCBI36
Celera1048,965,168 - 48,965,421RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,683,772 - 49,684,025UniSTS
REN7322  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,702,509 - 55,702,774UniSTSGRCh37
Build 361055,372,515 - 55,372,780RGDNCBI36
Celera1048,965,402 - 48,965,667RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,684,006 - 49,684,271UniSTS
REN7323  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,702,747 - 55,702,971UniSTSGRCh37
Build 361055,372,753 - 55,372,977RGDNCBI36
Celera1048,965,640 - 48,965,864RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,684,244 - 49,684,468UniSTS
REN7324  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,702,869 - 55,703,117UniSTSGRCh37
Build 361055,372,875 - 55,373,123RGDNCBI36
Celera1048,965,762 - 48,966,010RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,684,366 - 49,684,614UniSTS
REN7325  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,703,123 - 55,703,357UniSTSGRCh37
Build 361055,373,129 - 55,373,363RGDNCBI36
Celera1048,966,016 - 48,966,251RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,684,620 - 49,684,854UniSTS
REN7326  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,703,337 - 55,703,607UniSTSGRCh37
Build 361055,373,343 - 55,373,613RGDNCBI36
Celera1048,966,231 - 48,966,501RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,684,834 - 49,685,104UniSTS
REN7327  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,703,590 - 55,703,823UniSTSGRCh37
Build 361055,373,596 - 55,373,829RGDNCBI36
Celera1048,966,484 - 48,966,717RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,685,087 - 49,685,320UniSTS
REN7328  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,703,802 - 55,704,055UniSTSGRCh37
Build 361055,373,808 - 55,374,061RGDNCBI36
Celera1048,966,696 - 48,966,949RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,685,299 - 49,685,552UniSTS
REN7329  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,704,033 - 55,704,307UniSTSGRCh37
Build 361055,374,039 - 55,374,313RGDNCBI36
Celera1048,966,927 - 48,967,201RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,685,530 - 49,685,804UniSTS
REN7330  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,704,286 - 55,704,537UniSTSGRCh37
Build 361055,374,292 - 55,374,543RGDNCBI36
Celera1048,967,180 - 48,967,431RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,685,783 - 49,686,034UniSTS
REN7331  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,704,502 - 55,704,751UniSTSGRCh37
Build 361055,374,508 - 55,374,757RGDNCBI36
Celera1048,967,396 - 48,967,645RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,685,999 - 49,686,248UniSTS
REN7332  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,704,733 - 55,704,984UniSTSGRCh37
Build 361055,374,739 - 55,374,990RGDNCBI36
Celera1048,967,627 - 48,967,878RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,686,230 - 49,686,481UniSTS
REN7333  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,704,961 - 55,705,201UniSTSGRCh37
Build 361055,374,967 - 55,375,207RGDNCBI36
Celera1048,967,855 - 48,968,095RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,686,458 - 49,686,698UniSTS
REN7334  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,705,184 - 55,705,457UniSTSGRCh37
Build 361055,375,190 - 55,375,463RGDNCBI36
Celera1048,968,078 - 48,968,336RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,686,681 - 49,686,939UniSTS
REN7335  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,705,328 - 55,705,568UniSTSGRCh37
Build 361055,375,334 - 55,375,574RGDNCBI36
Celera1048,968,207 - 48,968,447RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,686,810 - 49,687,050UniSTS
REN7336  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,705,532 - 55,705,786UniSTSGRCh37
Build 361055,375,538 - 55,375,792RGDNCBI36
Celera1048,968,411 - 48,968,669RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,687,014 - 49,687,272UniSTS
REN7337  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,705,763 - 55,705,995UniSTSGRCh37
Build 361055,375,769 - 55,376,001RGDNCBI36
Celera1048,968,646 - 48,968,878RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,687,249 - 49,687,481UniSTS
REN7338  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,705,972 - 55,706,230UniSTSGRCh37
Build 361055,375,978 - 55,376,236RGDNCBI36
Celera1048,968,855 - 48,969,113RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,687,458 - 49,687,716UniSTS
REN7339  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,706,212 - 55,706,444UniSTSGRCh37
Build 361055,376,218 - 55,376,450RGDNCBI36
Celera1048,969,095 - 48,969,327RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,687,698 - 49,687,930UniSTS
REN7340  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,706,403 - 55,706,639UniSTSGRCh37
Build 361055,376,409 - 55,376,645RGDNCBI36
Celera1048,969,286 - 48,969,522RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,687,889 - 49,688,125UniSTS
REN7341  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,706,620 - 55,706,849UniSTSGRCh37
Build 361055,376,626 - 55,376,855RGDNCBI36
Celera1048,969,503 - 48,969,732RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,688,106 - 49,688,335UniSTS
REN7342  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,706,826 - 55,707,088UniSTSGRCh37
Build 361055,376,832 - 55,377,094RGDNCBI36
Celera1048,969,709 - 48,969,971RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,688,312 - 49,688,574UniSTS
REN7343  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,706,941 - 55,707,187UniSTSGRCh37
Build 361055,376,947 - 55,377,193RGDNCBI36
Celera1048,969,824 - 48,970,070RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,688,427 - 49,688,673UniSTS
REN7344  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,707,151 - 55,707,379UniSTSGRCh37
Build 361055,377,157 - 55,377,385RGDNCBI36
Celera1048,970,034 - 48,970,262RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,688,637 - 49,688,865UniSTS
REN7345  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,707,353 - 55,707,580UniSTSGRCh37
Build 361055,377,359 - 55,377,586RGDNCBI36
Celera1048,970,236 - 48,970,463RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,688,839 - 49,689,066UniSTS
REN7346  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,707,572 - 55,707,823UniSTSGRCh37
Build 361055,377,578 - 55,377,829RGDNCBI36
Celera1048,970,455 - 48,970,706RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,689,058 - 49,689,309UniSTS
REN7347  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,707,815 - 55,708,071UniSTSGRCh37
Build 361055,377,821 - 55,378,077RGDNCBI36
Celera1048,970,698 - 48,970,954RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,689,301 - 49,689,557UniSTS
REN7348  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,708,047 - 55,708,274UniSTSGRCh37
Build 361055,378,053 - 55,378,280RGDNCBI36
Celera1048,970,930 - 48,971,157RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,689,533 - 49,689,760UniSTS
REN7349  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,708,262 - 55,708,511UniSTSGRCh37
Build 361055,378,268 - 55,378,517RGDNCBI36
Celera1048,971,145 - 48,971,394RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,689,748 - 49,689,997UniSTS
REN7350  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,708,503 - 55,708,764UniSTSGRCh37
Build 361055,378,509 - 55,378,770RGDNCBI36
Celera1048,971,386 - 48,971,647RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,689,989 - 49,690,250UniSTS
REN7351  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,708,755 - 55,709,000UniSTSGRCh37
Build 361055,378,761 - 55,379,006RGDNCBI36
Celera1048,971,638 - 48,971,883RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,690,241 - 49,690,486UniSTS
REN7352  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,708,998 - 55,709,222UniSTSGRCh37
Build 361055,379,004 - 55,379,228RGDNCBI36
Celera1048,971,881 - 48,972,105RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,690,484 - 49,690,708UniSTS
REN7353  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,709,197 - 55,709,437UniSTSGRCh37
Build 361055,379,203 - 55,379,443RGDNCBI36
Celera1048,972,080 - 48,972,320RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,690,683 - 49,690,923UniSTS
REN7354  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,709,390 - 55,709,617UniSTSGRCh37
Build 361055,379,396 - 55,379,623RGDNCBI36
Celera1048,972,273 - 48,972,500RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,690,876 - 49,691,103UniSTS
REN7355  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,709,572 - 55,709,829UniSTSGRCh37
Build 361055,379,578 - 55,379,835RGDNCBI36
Celera1048,972,455 - 48,972,712RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,691,058 - 49,691,315UniSTS
REN7356  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,710,073 - 55,710,304UniSTSGRCh37
Build 361055,380,079 - 55,380,310RGDNCBI36
Celera1048,972,956 - 48,973,187RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,691,559 - 49,691,790UniSTS
REN7357  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,710,295 - 55,710,557UniSTSGRCh37
Build 361055,380,301 - 55,380,563RGDNCBI36
Celera1048,973,178 - 48,973,440RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,691,781 - 49,692,043UniSTS
REN7358  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,710,533 - 55,710,785UniSTSGRCh37
Build 361055,380,539 - 55,380,791RGDNCBI36
Celera1048,973,416 - 48,973,668RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,692,019 - 49,692,271UniSTS
REN7359  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,710,783 - 55,711,007UniSTSGRCh37
Build 361055,380,789 - 55,381,013RGDNCBI36
Celera1048,973,666 - 48,973,890RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,692,269 - 49,692,493UniSTS
REN7360  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,710,981 - 55,711,243UniSTSGRCh37
Build 361055,380,987 - 55,381,249RGDNCBI36
Celera1048,973,864 - 48,974,126RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,692,467 - 49,692,729UniSTS
REN7361  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,711,220 - 55,711,466UniSTSGRCh37
Build 361055,381,226 - 55,381,472RGDNCBI36
Celera1048,974,103 - 48,974,349RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,692,706 - 49,692,952UniSTS
REN7362  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,711,436 - 55,711,678UniSTSGRCh37
Build 361055,381,442 - 55,381,684RGDNCBI36
Celera1048,974,319 - 48,974,561RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,692,922 - 49,693,164UniSTS
REN7363  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,711,622 - 55,711,849UniSTSGRCh37
Build 361055,381,628 - 55,381,855RGDNCBI36
Celera1048,974,505 - 48,974,732RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,693,108 - 49,693,335UniSTS
REN7364  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,711,821 - 55,712,085UniSTSGRCh37
Build 361055,381,827 - 55,382,091RGDNCBI36
Celera1048,974,704 - 48,974,968RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,693,307 - 49,693,571UniSTS
REN7365  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,712,062 - 55,712,286UniSTSGRCh37
Build 361055,382,068 - 55,382,292RGDNCBI36
Celera1048,974,945 - 48,975,169RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,693,548 - 49,693,772UniSTS
REN7366  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,712,246 - 55,712,493UniSTSGRCh37
Build 361055,382,252 - 55,382,499RGDNCBI36
Celera1048,975,129 - 48,975,376RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,693,732 - 49,693,979UniSTS
REN7367  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,712,471 - 55,712,731UniSTSGRCh37
Build 361055,382,477 - 55,382,737RGDNCBI36
Celera1048,975,354 - 48,975,614RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,693,957 - 49,694,217UniSTS
REN7368  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,712,708 - 55,712,952UniSTSGRCh37
Build 361055,382,714 - 55,382,958RGDNCBI36
Celera1048,975,591 - 48,975,835RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,694,194 - 49,694,438UniSTS
REN7369  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,712,935 - 55,713,174UniSTSGRCh37
Build 361055,382,941 - 55,383,180RGDNCBI36
Celera1048,975,818 - 48,976,057RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,694,421 - 49,694,660UniSTS
REN7370  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,713,135 - 55,713,360UniSTSGRCh37
Build 361055,383,141 - 55,383,366RGDNCBI36
Celera1048,976,018 - 48,976,243RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,694,621 - 49,694,846UniSTS
REN7371  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,713,331 - 55,713,582UniSTSGRCh37
Build 361055,383,337 - 55,383,588RGDNCBI36
Celera1048,976,214 - 48,976,465RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,694,817 - 49,695,068UniSTS
REN7372  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,713,866 - 55,714,090UniSTSGRCh37
Build 361055,383,872 - 55,384,096RGDNCBI36
Celera1048,976,749 - 48,976,973RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,695,352 - 49,695,576UniSTS
REN7373  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,714,075 - 55,714,332UniSTSGRCh37
Build 361055,384,081 - 55,384,338RGDNCBI36
Celera1048,976,958 - 48,977,215RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,695,561 - 49,695,818UniSTS
REN7374  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,714,309 - 55,714,534UniSTSGRCh37
Build 361055,384,315 - 55,384,540RGDNCBI36
Celera1048,977,192 - 48,977,417RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,695,795 - 49,696,020UniSTS
REN7375  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,714,505 - 55,714,764UniSTSGRCh37
Build 361055,384,511 - 55,384,770RGDNCBI36
Celera1048,977,388 - 48,977,647RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,695,991 - 49,696,250UniSTS
REN7376  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,714,744 - 55,714,982UniSTSGRCh37
Build 361055,384,750 - 55,384,988RGDNCBI36
Celera1048,977,627 - 48,977,865RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,696,230 - 49,696,468UniSTS
REN7377  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,714,964 - 55,715,216UniSTSGRCh37
Build 361055,384,970 - 55,385,222RGDNCBI36
Celera1048,977,847 - 48,978,099RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,696,450 - 49,696,702UniSTS
REN7378  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,715,161 - 55,715,420UniSTSGRCh37
Build 361055,385,167 - 55,385,426RGDNCBI36
Celera1048,978,044 - 48,978,303RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,696,647 - 49,696,906UniSTS
REN7379  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,715,397 - 55,715,647UniSTSGRCh37
Build 361055,385,403 - 55,385,653RGDNCBI36
Celera1048,978,280 - 48,978,530RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,696,883 - 49,697,133UniSTS
REN7380  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,715,635 - 55,715,898UniSTSGRCh37
Build 361055,385,641 - 55,385,904RGDNCBI36
Celera1048,978,518 - 48,978,781RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,697,121 - 49,697,384UniSTS
REN7381  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,715,857 - 55,716,094UniSTSGRCh37
Build 361055,385,863 - 55,386,100RGDNCBI36
Celera1048,978,740 - 48,978,977RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,697,343 - 49,697,580UniSTS
REN7382  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,716,045 - 55,716,278UniSTSGRCh37
Build 361055,386,051 - 55,386,284RGDNCBI36
Celera1048,978,928 - 48,979,161RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,697,531 - 49,697,764UniSTS
REN7383  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,716,257 - 55,716,497UniSTSGRCh37
Build 361055,386,263 - 55,386,503RGDNCBI36
Celera1048,979,140 - 48,979,380RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,697,743 - 49,697,983UniSTS
REN7384  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,716,484 - 55,716,733UniSTSGRCh37
Build 361055,386,490 - 55,386,739RGDNCBI36
Celera1048,979,367 - 48,979,616RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,697,970 - 49,698,219UniSTS
REN7385  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,716,705 - 55,716,964UniSTSGRCh37
Build 361055,386,711 - 55,386,970RGDNCBI36
Celera1048,979,588 - 48,979,847RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,698,191 - 49,698,450UniSTS
REN7386  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,716,931 - 55,717,175UniSTSGRCh37
Build 361055,386,937 - 55,387,181RGDNCBI36
Celera1048,979,814 - 48,980,058RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,698,417 - 49,698,661UniSTS
REN7387  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,717,147 - 55,717,385UniSTSGRCh37
Build 361055,387,153 - 55,387,391RGDNCBI36
Celera1048,980,030 - 48,980,273RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,698,633 - 49,698,876UniSTS
REN7388  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,717,317 - 55,717,584UniSTSGRCh37
Build 361055,387,323 - 55,387,590RGDNCBI36
Celera1048,980,205 - 48,980,472RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,698,808 - 49,699,075UniSTS
REN7389  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,717,565 - 55,717,817UniSTSGRCh37
Build 361055,387,571 - 55,387,823RGDNCBI36
Celera1048,980,453 - 48,980,705RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,699,056 - 49,699,308UniSTS
REN7390  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,717,771 - 55,718,001UniSTSGRCh37
Build 361055,387,777 - 55,388,007RGDNCBI36
Celera1048,980,659 - 48,980,889RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,699,262 - 49,699,492UniSTS
REN7391  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,717,974 - 55,718,228UniSTSGRCh37
Build 361055,387,980 - 55,388,234RGDNCBI36
Celera1048,980,862 - 48,981,116RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,699,465 - 49,699,719UniSTS
REN7392  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,718,227 - 55,718,464UniSTSGRCh37
Build 361055,388,233 - 55,388,470RGDNCBI36
Celera1048,981,115 - 48,981,352RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,699,718 - 49,699,955UniSTS
REN7393  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,718,286 - 55,718,540UniSTSGRCh37
Build 361055,388,292 - 55,388,546RGDNCBI36
Celera1048,981,174 - 48,981,428RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,699,777 - 49,700,031UniSTS
REN7394  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,718,812 - 55,719,068UniSTSGRCh37
Build 361055,388,818 - 55,389,074RGDNCBI36
Celera1048,981,700 - 48,981,956RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,700,302 - 49,700,558UniSTS
REN7395  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,719,058 - 55,719,307UniSTSGRCh37
Build 361055,389,064 - 55,389,313RGDNCBI36
Celera1048,981,946 - 48,982,195RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,700,548 - 49,700,797UniSTS
REN7396  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,719,278 - 55,719,540UniSTSGRCh37
Build 361055,389,284 - 55,389,546RGDNCBI36
Celera1048,982,166 - 48,982,428RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,700,768 - 49,701,030UniSTS
REN7397  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,719,536 - 55,719,766UniSTSGRCh37
Build 361055,389,542 - 55,389,772RGDNCBI36
Celera1048,982,424 - 48,982,654RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,701,026 - 49,701,256UniSTS
REN7398  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,719,753 - 55,719,989UniSTSGRCh37
Build 361055,389,759 - 55,389,995RGDNCBI36
Celera1048,982,641 - 48,982,877RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,701,243 - 49,701,479UniSTS
REN7399  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,719,962 - 55,720,221UniSTSGRCh37
Build 361055,389,968 - 55,390,227RGDNCBI36
Celera1048,982,850 - 48,983,109RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,701,452 - 49,701,711UniSTS
REN7400  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,720,197 - 55,720,467UniSTSGRCh37
Build 361055,390,203 - 55,390,473RGDNCBI36
Celera1048,983,085 - 48,983,355RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,701,687 - 49,701,957UniSTS
REN7401  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,720,461 - 55,720,726UniSTSGRCh37
Build 361055,390,467 - 55,390,732RGDNCBI36
Celera1048,983,349 - 48,983,614RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,701,951 - 49,702,216UniSTS
REN7402  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,720,725 - 55,720,958UniSTSGRCh37
Build 361055,390,731 - 55,390,964RGDNCBI36
Celera1048,983,613 - 48,983,846RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,702,215 - 49,702,448UniSTS
REN7403  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,720,936 - 55,721,199UniSTSGRCh37
Build 361055,390,942 - 55,391,205RGDNCBI36
Celera1048,983,824 - 48,984,087RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,702,426 - 49,702,689UniSTS
REN7404  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,721,072 - 55,721,308UniSTSGRCh37
Build 361055,391,078 - 55,391,314RGDNCBI36
Celera1048,983,960 - 48,984,196RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,702,562 - 49,702,798UniSTS
REN7405  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,721,303 - 55,721,552UniSTSGRCh37
Build 361055,391,309 - 55,391,558RGDNCBI36
Celera1048,984,191 - 48,984,440RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,702,793 - 49,703,042UniSTS
REN7406  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,721,528 - 55,721,791UniSTSGRCh37
Build 361055,391,534 - 55,391,797RGDNCBI36
Celera1048,984,416 - 48,984,679RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,703,018 - 49,703,281UniSTS
REN7407  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,721,784 - 55,722,053UniSTSGRCh37
Build 361055,391,790 - 55,392,059RGDNCBI36
Celera1048,984,672 - 48,984,941RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,703,274 - 49,703,544UniSTS
REN7408  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,722,030 - 55,722,279UniSTSGRCh37
Build 361055,392,036 - 55,392,285RGDNCBI36
Celera1048,984,918 - 48,985,167RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,703,521 - 49,703,770UniSTS
REN7409  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,722,244 - 55,722,486UniSTSGRCh37
Build 361055,392,250 - 55,392,492RGDNCBI36
Celera1048,985,132 - 48,985,374RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,703,735 - 49,703,977UniSTS
REN7410  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,722,463 - 55,722,725UniSTSGRCh37
Build 361055,392,469 - 55,392,731RGDNCBI36
Celera1048,985,351 - 48,985,613RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,703,954 - 49,704,216UniSTS
REN7411  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,722,703 - 55,722,968UniSTSGRCh37
Build 361055,392,709 - 55,392,974RGDNCBI36
Celera1048,985,591 - 48,985,856RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,704,194 - 49,704,459UniSTS
REN7412  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,722,958 - 55,723,211UniSTSGRCh37
Build 361055,392,964 - 55,393,217RGDNCBI36
Celera1048,985,846 - 48,986,099RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,704,449 - 49,704,702UniSTS
REN7413  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,723,188 - 55,723,421UniSTSGRCh37
Build 361055,393,194 - 55,393,427RGDNCBI36
Cytogenetic Map10q21.1UniSTS
REN7414  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,723,398 - 55,723,666UniSTSGRCh37
Build 361055,393,404 - 55,393,672RGDNCBI36
Cytogenetic Map10q21.1UniSTS
REN7415  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,723,658 - 55,723,921UniSTSGRCh37
Build 361055,393,664 - 55,393,927RGDNCBI36
Celera1048,986,549 - 48,986,812RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,705,152 - 49,705,415UniSTS
REN7416  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,723,843 - 55,724,087UniSTSGRCh37
Build 361055,393,849 - 55,394,093RGDNCBI36
Celera1048,986,734 - 48,986,978RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,705,337 - 49,705,581UniSTS
REN7417  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,724,076 - 55,724,331UniSTSGRCh37
Build 361055,394,082 - 55,394,337RGDNCBI36
Celera1048,986,967 - 48,987,222RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,705,570 - 49,705,825UniSTS
REN7418  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,724,303 - 55,724,527UniSTSGRCh37
Build 361055,394,309 - 55,394,533RGDNCBI36
Celera1048,987,194 - 48,987,418RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,705,797 - 49,706,021UniSTS
REN7419  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,724,483 - 55,724,707UniSTSGRCh37
Build 361055,394,489 - 55,394,713RGDNCBI36
Celera1048,987,374 - 48,987,598RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,705,977 - 49,706,201UniSTS
REN7420  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,724,621 - 55,724,865UniSTSGRCh37
Build 361055,394,627 - 55,394,871RGDNCBI36
Celera1048,987,512 - 48,987,754RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,706,115 - 49,706,357UniSTS
REN7421  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,724,776 - 55,725,038UniSTSGRCh37
Build 361055,394,782 - 55,395,044RGDNCBI36
Celera1048,987,667 - 48,987,927RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,706,270 - 49,706,530UniSTS
REN7422  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,725,025 - 55,725,257UniSTSGRCh37
Build 361055,395,031 - 55,395,263RGDNCBI36
Celera1048,987,914 - 48,988,146RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,706,517 - 49,706,749UniSTS
REN7423  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,725,231 - 55,725,488UniSTSGRCh37
Build 361055,395,237 - 55,395,494RGDNCBI36
Celera1048,988,120 - 48,988,377RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,706,723 - 49,706,980UniSTS
REN7424  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,725,466 - 55,725,718UniSTSGRCh37
Build 361055,395,472 - 55,395,724RGDNCBI36
Celera1048,988,355 - 48,988,607RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,706,958 - 49,707,211UniSTS
REN7425  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,725,714 - 55,725,973UniSTSGRCh37
GRCh371055,725,802 - 55,725,973UniSTSGRCh37
Build 361055,395,720 - 55,395,979RGDNCBI36
Celera1048,988,603 - 48,988,862RGD
Celera1048,988,691 - 48,988,862UniSTS
Cytogenetic Map10q21.1UniSTS
HuRef1049,707,207 - 49,707,378UniSTS
REN7426  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,725,942 - 55,726,173UniSTSGRCh37
Build 361055,395,948 - 55,396,179RGDNCBI36
Celera1048,988,831 - 48,989,062RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,707,347 - 49,707,578UniSTS
REN7427  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,726,140 - 55,726,393UniSTSGRCh37
Build 361055,396,146 - 55,396,399RGDNCBI36
Celera1048,989,029 - 48,989,282RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,707,545 - 49,707,798UniSTS
REN7428  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,726,191 - 55,726,422UniSTSGRCh37
Build 361055,396,197 - 55,396,428RGDNCBI36
Celera1048,989,080 - 48,989,311RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,707,596 - 49,707,827UniSTS
REN7429  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,726,683 - 55,726,923UniSTSGRCh37
Build 361055,396,689 - 55,396,929RGDNCBI36
Celera1048,989,572 - 48,989,812RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,708,088 - 49,708,328UniSTS
REN7430  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,726,917 - 55,727,176UniSTSGRCh37
Build 361055,396,923 - 55,397,182RGDNCBI36
Celera1048,989,806 - 48,990,065RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,708,322 - 49,708,581UniSTS
REN7431  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,727,110 - 55,727,346UniSTSGRCh37
Build 361055,397,116 - 55,397,352RGDNCBI36
Celera1048,989,999 - 48,990,235RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,708,515 - 49,708,751UniSTS
REN7432  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,727,323 - 55,727,597UniSTSGRCh37
Build 361055,397,329 - 55,397,603RGDNCBI36
Celera1048,990,212 - 48,990,486RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,708,728 - 49,709,002UniSTS
REN7433  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,727,600 - 55,727,854UniSTSGRCh37
Build 361055,397,606 - 55,397,860RGDNCBI36
Celera1048,990,489 - 48,990,743RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,709,005 - 49,709,259UniSTS
REN7434  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,727,643 - 55,727,913UniSTSGRCh37
Build 361055,397,649 - 55,397,919RGDNCBI36
Celera1048,990,532 - 48,990,802RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,709,048 - 49,709,318UniSTS
REN7435  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,728,104 - 55,728,370UniSTSGRCh37
Build 361055,398,110 - 55,398,376RGDNCBI36
Celera1048,990,993 - 48,991,259RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,709,509 - 49,709,775UniSTS
REN7436  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,731,907 - 55,732,157UniSTSGRCh37
Build 361055,401,913 - 55,402,163RGDNCBI36
Celera1048,994,796 - 48,995,045RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,713,314 - 49,713,563UniSTS
REN7437  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,733,233 - 55,733,457UniSTSGRCh37
Build 361055,403,239 - 55,403,463RGDNCBI36
Celera1048,996,121 - 48,996,345RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,714,639 - 49,714,863UniSTS
REN7438  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,733,368 - 55,733,607UniSTSGRCh37
Build 361055,403,374 - 55,403,613RGDNCBI36
Celera1048,996,256 - 48,996,495RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,714,774 - 49,715,013UniSTS
REN7439  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,733,517 - 55,733,741UniSTSGRCh37
Build 361055,403,523 - 55,403,747RGDNCBI36
Celera1048,996,405 - 48,996,629RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,714,923 - 49,715,147UniSTS
REN7440  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,733,699 - 55,733,933UniSTSGRCh37
Build 361055,403,705 - 55,403,939RGDNCBI36
Celera1048,996,587 - 48,996,821RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,715,105 - 49,715,335UniSTS
REN7441  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,733,881 - 55,734,111UniSTSGRCh37
Build 361055,403,887 - 55,404,117RGDNCBI36
Celera1048,996,769 - 48,996,999RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,715,283 - 49,715,513UniSTS
REN7442  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,734,073 - 55,734,344UniSTSGRCh37
Build 361055,404,079 - 55,404,350RGDNCBI36
Celera1048,996,961 - 48,997,232RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,715,475 - 49,715,746UniSTS
REN7443  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,734,264 - 55,734,501UniSTSGRCh37
Build 361055,404,270 - 55,404,507RGDNCBI36
Celera1048,997,152 - 48,997,389RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,715,666 - 49,715,903UniSTS
REN7444  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,734,492 - 55,734,738UniSTSGRCh37
Build 361055,404,498 - 55,404,744RGDNCBI36
Celera1048,997,380 - 48,997,626RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,715,894 - 49,716,140UniSTS
REN7445  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,734,715 - 55,734,960UniSTSGRCh37
Build 361055,404,721 - 55,404,966RGDNCBI36
Celera1048,997,603 - 48,997,848RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,716,117 - 49,716,362UniSTS
REN7446  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,734,861 - 55,735,099UniSTSGRCh37
Build 361055,404,867 - 55,405,105RGDNCBI36
Celera1048,997,749 - 48,997,987RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,716,263 - 49,716,501UniSTS
REN7447  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,735,070 - 55,735,337UniSTSGRCh37
Build 361055,405,076 - 55,405,343RGDNCBI36
Celera1048,997,958 - 48,998,225RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,716,472 - 49,716,739UniSTS
REN7448  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,735,243 - 55,735,513UniSTSGRCh37
Build 361055,405,249 - 55,405,519RGDNCBI36
Celera1048,998,131 - 48,998,401RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,716,645 - 49,716,915UniSTS
REN7449  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,735,509 - 55,735,742UniSTSGRCh37
Build 361055,405,515 - 55,405,748RGDNCBI36
Celera1048,998,397 - 48,998,630RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,716,911 - 49,717,144UniSTS
REN7450  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,735,712 - 55,735,976UniSTSGRCh37
Build 361055,405,718 - 55,405,982RGDNCBI36
Celera1048,998,600 - 48,998,864RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,717,114 - 49,717,378UniSTS
REN7451  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,735,959 - 55,736,214UniSTSGRCh37
Build 361055,405,965 - 55,406,220RGDNCBI36
Celera1048,998,847 - 48,999,102RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,717,361 - 49,717,616UniSTS
REN7452  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,736,197 - 55,736,446UniSTSGRCh37
Build 361055,406,203 - 55,406,452RGDNCBI36
Celera1048,999,085 - 48,999,334RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,717,599 - 49,717,848UniSTS
REN7453  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,736,423 - 55,736,652UniSTSGRCh37
Build 361055,406,429 - 55,406,658RGDNCBI36
Celera1048,999,311 - 48,999,540RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,717,825 - 49,718,055UniSTS
REN7454  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,736,629 - 55,736,877UniSTSGRCh37
Build 361055,406,635 - 55,406,883RGDNCBI36
Celera1048,999,517 - 48,999,765RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,718,032 - 49,718,280UniSTS
REN7455  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,736,870 - 55,737,122UniSTSGRCh37
Build 361055,406,876 - 55,407,128RGDNCBI36
Celera1048,999,758 - 49,000,010RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,718,273 - 49,718,525UniSTS
REN7456  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,737,034 - 55,737,268UniSTSGRCh37
Build 361055,407,040 - 55,407,274RGDNCBI36
Celera1048,999,922 - 49,000,156RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,718,437 - 49,718,671UniSTS
REN7457  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,737,253 - 55,737,506UniSTSGRCh37
Build 361055,407,259 - 55,407,512RGDNCBI36
Celera1049,000,141 - 49,000,394RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,718,656 - 49,718,909UniSTS
REN7458  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,737,498 - 55,737,757UniSTSGRCh37
Build 361055,407,504 - 55,407,763RGDNCBI36
Celera1049,000,386 - 49,000,645RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,718,901 - 49,719,160UniSTS
REN7459  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,737,734 - 55,737,963UniSTSGRCh37
Build 361055,407,740 - 55,407,969RGDNCBI36
Celera1049,000,622 - 49,000,851RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,719,137 - 49,719,366UniSTS
REN7460  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,737,925 - 55,738,160UniSTSGRCh37
Build 361055,407,931 - 55,408,166RGDNCBI36
Celera1049,000,813 - 49,001,048RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,719,328 - 49,719,563UniSTS
REN7461  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,738,108 - 55,738,364UniSTSGRCh37
Build 361055,408,114 - 55,408,370RGDNCBI36
Celera1049,000,996 - 49,001,252RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,719,511 - 49,719,767UniSTS
REN7462  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,738,335 - 55,738,601UniSTSGRCh37
Build 361055,408,341 - 55,408,607RGDNCBI36
Celera1049,001,223 - 49,001,488RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,719,738 - 49,720,003UniSTS
REN7463  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,738,596 - 55,738,841UniSTSGRCh37
Build 361055,408,602 - 55,408,847RGDNCBI36
Celera1049,001,483 - 49,001,728RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,719,998 - 49,720,243UniSTS
REN7464  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,738,819 - 55,739,066UniSTSGRCh37
Build 361055,408,825 - 55,409,072RGDNCBI36
Celera1049,001,706 - 49,001,953RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,720,221 - 49,720,468UniSTS
REN7465  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,739,042 - 55,739,296UniSTSGRCh37
Build 361055,409,048 - 55,409,302RGDNCBI36
Celera1049,001,929 - 49,002,183RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,720,444 - 49,720,698UniSTS
REN7466  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,739,273 - 55,739,527UniSTSGRCh37
Build 361055,409,279 - 55,409,533RGDNCBI36
Celera1049,002,160 - 49,002,414RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,720,675 - 49,720,929UniSTS
REN7467  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,739,483 - 55,739,707UniSTSGRCh37
Build 361055,409,489 - 55,409,713RGDNCBI36
Celera1049,002,370 - 49,002,594RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,720,885 - 49,721,109UniSTS
REN7468  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,739,680 - 55,739,915UniSTSGRCh37
Build 361055,409,686 - 55,409,921RGDNCBI36
Celera1049,002,567 - 49,002,802RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,721,082 - 49,721,317UniSTS
REN7469  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,740,011 - 55,740,236UniSTSGRCh37
Build 361055,410,017 - 55,410,242RGDNCBI36
Celera1049,002,899 - 49,003,124RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,721,414 - 49,721,638UniSTS
REN7470  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,740,215 - 55,740,444UniSTSGRCh37
Build 361055,410,221 - 55,410,450RGDNCBI36
Celera1049,003,103 - 49,003,332RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,721,617 - 49,721,846UniSTS
REN7471  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,740,407 - 55,740,653UniSTSGRCh37
Build 361055,410,413 - 55,410,659RGDNCBI36
Celera1049,003,295 - 49,003,541RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,721,809 - 49,722,055UniSTS
REN7472  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,740,627 - 55,740,866UniSTSGRCh37
Build 361055,410,633 - 55,410,872RGDNCBI36
Celera1049,003,515 - 49,003,754RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,722,029 - 49,722,268UniSTS
REN7473  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,740,843 - 55,741,071UniSTSGRCh37
Build 361055,410,849 - 55,411,077RGDNCBI36
Celera1049,003,731 - 49,003,959RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,722,245 - 49,722,473UniSTS
REN7474  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,741,007 - 55,741,272UniSTSGRCh37
Build 361055,411,013 - 55,411,278RGDNCBI36
Celera1049,003,895 - 49,004,160RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,722,409 - 49,722,674UniSTS
REN7475  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,742,632 - 55,742,860UniSTSGRCh37
Build 361055,412,638 - 55,412,866RGDNCBI36
Celera1049,005,520 - 49,005,748RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,724,034 - 49,724,262UniSTS
REN7476  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,742,823 - 55,743,066UniSTSGRCh37
Build 361055,412,829 - 55,413,072RGDNCBI36
Celera1049,005,711 - 49,005,954RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,724,225 - 49,724,468UniSTS
REN7477  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,743,065 - 55,743,313UniSTSGRCh37
Build 361055,413,071 - 55,413,319RGDNCBI36
Celera1049,005,953 - 49,006,201RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,724,467 - 49,724,715UniSTS
REN7478  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,743,253 - 55,743,525UniSTSGRCh37
Build 361055,413,259 - 55,413,531RGDNCBI36
Celera1049,006,141 - 49,006,413RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,724,655 - 49,724,927UniSTS
REN7479  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,743,502 - 55,743,767UniSTSGRCh37
Build 361055,413,508 - 55,413,773RGDNCBI36
Celera1049,006,390 - 49,006,655RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,724,904 - 49,725,169UniSTS
REN7480  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,743,733 - 55,743,963UniSTSGRCh37
Build 361055,413,739 - 55,413,969RGDNCBI36
Celera1049,006,621 - 49,006,851RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,725,135 - 49,725,367UniSTS
REN7481  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,744,203 - 55,744,451UniSTSGRCh37
Build 361055,414,209 - 55,414,457RGDNCBI36
Celera1049,007,091 - 49,007,339RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,725,607 - 49,725,855UniSTS
REN7482  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,744,443 - 55,744,697UniSTSGRCh37
Build 361055,414,449 - 55,414,703RGDNCBI36
Celera1049,007,331 - 49,007,585RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,725,847 - 49,726,101UniSTS
REN7483  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,744,658 - 55,744,916UniSTSGRCh37
Build 361055,414,664 - 55,414,922RGDNCBI36
Celera1049,007,546 - 49,007,804RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,726,062 - 49,726,320UniSTS
REN7484  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,744,894 - 55,745,134UniSTSGRCh37
Build 361055,414,900 - 55,415,140RGDNCBI36
Celera1049,007,782 - 49,008,022RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,726,298 - 49,726,538UniSTS
REN7485  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,745,109 - 55,745,364UniSTSGRCh37
Build 361055,415,115 - 55,415,370RGDNCBI36
Celera1049,007,997 - 49,008,252RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,726,513 - 49,726,768UniSTS
REN7486  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,745,357 - 55,745,589UniSTSGRCh37
Build 361055,415,363 - 55,415,595RGDNCBI36
Celera1049,008,245 - 49,008,477RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,726,761 - 49,726,993UniSTS
REN7487  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,745,566 - 55,745,836UniSTSGRCh37
Build 361055,415,572 - 55,415,842RGDNCBI36
Celera1049,008,454 - 49,008,724RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,726,970 - 49,727,240UniSTS
REN7488  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,745,825 - 55,746,064UniSTSGRCh37
Build 361055,415,831 - 55,416,070RGDNCBI36
Celera1049,008,713 - 49,008,952RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,727,229 - 49,727,468UniSTS
REN7489  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,746,041 - 55,746,302UniSTSGRCh37
Build 361055,416,047 - 55,416,308RGDNCBI36
Celera1049,008,929 - 49,009,190RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,727,445 - 49,727,706UniSTS
REN7490  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,746,279 - 55,746,515UniSTSGRCh37
Build 361055,416,285 - 55,416,521RGDNCBI36
Celera1049,009,167 - 49,009,403RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,727,683 - 49,727,919UniSTS
REN7491  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,746,483 - 55,746,743UniSTSGRCh37
Build 361055,416,489 - 55,416,749RGDNCBI36
Celera1049,009,371 - 49,009,631RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,727,887 - 49,728,147UniSTS
REN7492  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,746,634 - 55,746,858UniSTSGRCh37
Build 361055,416,640 - 55,416,864RGDNCBI36
Celera1049,009,522 - 49,009,746RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,728,038 - 49,728,262UniSTS
REN7493  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,746,751 - 55,747,012UniSTSGRCh37
Build 361055,416,757 - 55,417,018RGDNCBI36
Celera1049,009,639 - 49,009,900RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,728,155 - 49,728,416UniSTS
REN7494  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,747,164 - 55,747,397UniSTSGRCh37
Build 361055,417,170 - 55,417,403RGDNCBI36
Celera1049,010,052 - 49,010,285RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,728,568 - 49,728,801UniSTS
REN7495  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,747,392 - 55,747,632UniSTSGRCh37
Build 361055,417,398 - 55,417,638RGDNCBI36
Celera1049,010,280 - 49,010,520RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,728,796 - 49,729,036UniSTS
REN7496  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,747,609 - 55,747,867UniSTSGRCh37
Build 361055,417,615 - 55,417,873RGDNCBI36
Celera1049,010,497 - 49,010,755RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,729,013 - 49,729,271UniSTS
REN7497  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,747,844 - 55,748,087UniSTSGRCh37
Build 361055,417,850 - 55,418,093RGDNCBI36
Celera1049,010,732 - 49,010,975RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,729,248 - 49,729,491UniSTS
REN7498  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,748,078 - 55,748,325UniSTSGRCh37
Build 361055,418,084 - 55,418,331RGDNCBI36
Celera1049,010,966 - 49,011,213RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,729,482 - 49,729,729UniSTS
REN7499  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,748,302 - 55,748,561UniSTSGRCh37
Build 361055,418,308 - 55,418,567RGDNCBI36
Celera1049,011,190 - 49,011,449RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,729,706 - 49,729,965UniSTS
REN7500  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,748,557 - 55,748,802UniSTSGRCh37
Build 361055,418,563 - 55,418,808RGDNCBI36
Celera1049,011,445 - 49,011,690RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,729,961 - 49,730,206UniSTS
REN7501  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,748,733 - 55,748,987UniSTSGRCh37
Build 361055,418,739 - 55,418,993RGDNCBI36
Celera1049,011,621 - 49,011,875RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,730,137 - 49,730,391UniSTS
REN7502  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,748,971 - 55,749,232UniSTSGRCh37
Build 361055,418,977 - 55,419,238RGDNCBI36
Celera1049,011,859 - 49,012,120RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,730,375 - 49,730,636UniSTS
REN7503  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371081,670,657 - 81,670,904UniSTSGRCh37
GRCh371055,749,214 - 55,749,461UniSTSGRCh37
Build 361055,419,220 - 55,419,467RGDNCBI36
Celera1075,661,577 - 75,661,824UniSTS
Celera1049,012,102 - 49,012,349RGD
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map10q21.1UniSTS
HuRef1075,513,458 - 75,513,705UniSTS
HuRef1049,730,618 - 49,730,865UniSTS
REN7504  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371081,670,880 - 81,671,150UniSTSGRCh37
GRCh371055,749,437 - 55,749,707UniSTSGRCh37
Build 361055,419,443 - 55,419,713RGDNCBI36
Celera1075,661,800 - 75,662,070UniSTS
Celera1049,012,325 - 49,012,595RGD
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map10q21.1UniSTS
HuRef1075,513,681 - 75,513,951UniSTS
HuRef1049,730,841 - 49,731,111UniSTS
REN7505  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,749,700 - 55,749,963UniSTSGRCh37
Build 361055,419,706 - 55,419,969RGDNCBI36
Celera1049,012,588 - 49,012,851RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,731,104 - 49,731,367UniSTS
REN7506  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,749,933 - 55,750,157UniSTSGRCh37
Build 361055,419,939 - 55,420,163RGDNCBI36
Celera1049,012,821 - 49,013,045RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,731,337 - 49,731,561UniSTS
REN7507  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,750,132 - 55,750,393UniSTSGRCh37
Build 361055,420,138 - 55,420,399RGDNCBI36
Celera1049,013,020 - 49,013,281RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,731,536 - 49,731,810UniSTS
REN7508  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,750,368 - 55,750,592UniSTSGRCh37
Build 361055,420,374 - 55,420,598RGDNCBI36
Celera1049,013,256 - 49,013,480RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,731,785 - 49,732,009UniSTS
REN7510  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,752,218 - 55,752,445UniSTSGRCh37
Build 361055,422,224 - 55,422,451RGDNCBI36
Celera1049,015,106 - 49,015,333RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,733,635 - 49,733,862UniSTS
REN7511  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,752,444 - 55,752,709UniSTSGRCh37
Build 361055,422,450 - 55,422,715RGDNCBI36
Celera1049,015,332 - 49,015,597RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,733,861 - 49,734,126UniSTS
REN7512  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,752,698 - 55,752,960UniSTSGRCh37
Build 361055,422,704 - 55,422,966RGDNCBI36
Celera1049,015,586 - 49,015,848RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,734,115 - 49,734,377UniSTS
REN7513  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,752,936 - 55,753,187UniSTSGRCh37
Build 361055,422,942 - 55,423,193RGDNCBI36
Celera1049,015,824 - 49,016,075RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,734,353 - 49,734,604UniSTS
REN7514  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,753,139 - 55,753,363UniSTSGRCh37
Build 361055,423,145 - 55,423,369RGDNCBI36
Celera1049,016,027 - 49,016,251RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,734,556 - 49,734,780UniSTS
REN7515  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,753,337 - 55,753,598UniSTSGRCh37
Build 361055,423,343 - 55,423,604RGDNCBI36
Celera1049,016,225 - 49,016,486RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,734,754 - 49,735,015UniSTS
REN7516  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,753,574 - 55,753,807UniSTSGRCh37
Build 361055,423,580 - 55,423,813RGDNCBI36
Celera1049,016,462 - 49,016,695RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,734,991 - 49,735,224UniSTS
REN7517  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,753,783 - 55,754,016UniSTSGRCh37
Build 361055,423,789 - 55,424,022RGDNCBI36
Celera1049,016,671 - 49,016,904RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,735,200 - 49,735,433UniSTS
REN7518  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,753,989 - 55,754,232UniSTSGRCh37
Build 361055,423,995 - 55,424,238RGDNCBI36
Celera1049,016,877 - 49,017,120RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,735,406 - 49,735,649UniSTS
REN7519  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,754,208 - 55,754,471UniSTSGRCh37
Build 361055,424,214 - 55,424,477RGDNCBI36
Celera1049,017,096 - 49,017,359RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,735,625 - 49,735,888UniSTS
REN7520  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,754,401 - 55,754,648UniSTSGRCh37
Build 361055,424,407 - 55,424,654RGDNCBI36
Celera1049,017,289 - 49,017,536RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,735,818 - 49,736,065UniSTS
REN7521  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,754,529 - 55,754,758UniSTSGRCh37
Build 361055,424,535 - 55,424,764RGDNCBI36
Celera1049,017,417 - 49,017,646RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,735,946 - 49,736,175UniSTS
REN7522  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,754,739 - 55,754,987UniSTSGRCh37
Build 361055,424,745 - 55,424,993RGDNCBI36
Celera1049,017,627 - 49,017,875RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,736,156 - 49,736,404UniSTS
REN7523  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,754,894 - 55,755,129UniSTSGRCh37
Build 361055,424,900 - 55,425,135RGDNCBI36
Celera1049,017,782 - 49,018,017RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,736,311 - 49,736,546UniSTS
REN7524  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,755,114 - 55,755,349UniSTSGRCh37
Build 361055,425,120 - 55,425,355RGDNCBI36
Celera1049,018,002 - 49,018,237RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,736,531 - 49,736,766UniSTS
REN7525  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,755,326 - 55,755,575UniSTSGRCh37
Build 361055,425,332 - 55,425,581RGDNCBI36
Celera1049,018,214 - 49,018,463RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,736,743 - 49,736,992UniSTS
REN7526  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,755,552 - 55,755,807UniSTSGRCh37
Build 361055,425,558 - 55,425,813RGDNCBI36
Celera1049,018,440 - 49,018,695RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,736,969 - 49,737,224UniSTS
REN7527  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,755,784 - 55,756,019UniSTSGRCh37
Build 361055,425,790 - 55,426,025RGDNCBI36
Celera1049,018,672 - 49,018,907RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,737,201 - 49,737,438UniSTS
REN7528  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,756,005 - 55,756,261UniSTSGRCh37
Build 361055,426,011 - 55,426,267RGDNCBI36
Celera1049,018,893 - 49,019,149RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,737,424 - 49,737,680UniSTS
REN7529  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,756,209 - 55,756,433UniSTSGRCh37
Build 361055,426,215 - 55,426,439RGDNCBI36
Celera1049,019,097 - 49,019,321RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,737,628 - 49,737,852UniSTS
REN7530  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,756,403 - 55,756,629UniSTSGRCh37
Build 361055,426,409 - 55,426,635RGDNCBI36
Celera1049,019,291 - 49,019,517RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,737,822 - 49,738,048UniSTS
REN7531  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,756,606 - 55,756,842UniSTSGRCh37
Build 361055,426,612 - 55,426,848RGDNCBI36
Celera1049,019,494 - 49,019,730RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,738,025 - 49,738,261UniSTS
REN7532  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,756,820 - 55,757,071UniSTSGRCh37
Build 361055,426,826 - 55,427,077RGDNCBI36
Celera1049,019,708 - 49,019,959RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,738,239 - 49,738,490UniSTS
REN7533  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,757,043 - 55,757,272UniSTSGRCh37
Build 361055,427,049 - 55,427,278RGDNCBI36
Celera1049,019,931 - 49,020,160RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,738,462 - 49,738,691UniSTS
REN7534  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,757,203 - 55,757,470UniSTSGRCh37
Build 361055,427,209 - 55,427,476RGDNCBI36
Celera1049,020,091 - 49,020,358RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,738,622 - 49,738,889UniSTS
REN7535  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,757,443 - 55,757,696UniSTSGRCh37
Build 361055,427,449 - 55,427,702RGDNCBI36
Celera1049,020,331 - 49,020,584RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,738,862 - 49,739,115UniSTS
REN7536  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,757,664 - 55,757,912UniSTSGRCh37
Build 361055,427,670 - 55,427,918RGDNCBI36
Celera1049,020,552 - 49,020,800RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,739,083 - 49,739,331UniSTS
REN7537  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,757,898 - 55,758,153UniSTSGRCh37
Build 361055,427,904 - 55,428,159RGDNCBI36
Celera1049,020,786 - 49,021,041RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,739,317 - 49,739,572UniSTS
REN7538  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,758,130 - 55,758,381UniSTSGRCh37
Build 361055,428,136 - 55,428,387RGDNCBI36
Celera1049,021,018 - 49,021,269RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,739,549 - 49,739,800UniSTS
REN7539  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,758,312 - 55,758,571UniSTSGRCh37
Build 361055,428,318 - 55,428,577RGDNCBI36
Celera1049,021,200 - 49,021,459RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,739,731 - 49,739,990UniSTS
REN7540  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,758,418 - 55,758,675UniSTSGRCh37
Build 361055,428,424 - 55,428,681RGDNCBI36
Celera1049,021,306 - 49,021,563RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,739,837 - 49,740,094UniSTS
REN7541  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,758,711 - 55,758,935UniSTSGRCh37
Build 361055,428,717 - 55,428,941RGDNCBI36
Celera1049,021,599 - 49,021,822RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,740,130 - 49,740,352UniSTS
REN7542  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,758,918 - 55,759,155UniSTSGRCh37
Build 361055,428,924 - 55,429,161RGDNCBI36
Celera1049,021,805 - 49,022,042RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,740,335 - 49,740,572UniSTS
REN7543  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,759,129 - 55,759,381UniSTSGRCh37
Build 361055,429,135 - 55,429,387RGDNCBI36
Celera1049,022,016 - 49,022,268RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,740,546 - 49,740,798UniSTS
REN7544  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,759,371 - 55,759,608UniSTSGRCh37
Build 361055,429,377 - 55,429,614RGDNCBI36
Celera1049,022,258 - 49,022,495RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,740,788 - 49,741,025UniSTS
REN7545  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,759,585 - 55,759,827UniSTSGRCh37
Build 361055,429,591 - 55,429,833RGDNCBI36
Celera1049,022,472 - 49,022,714RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,741,002 - 49,741,244UniSTS
REN7546  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,759,806 - 55,760,070UniSTSGRCh37
Build 361055,429,812 - 55,430,076RGDNCBI36
Celera1049,022,693 - 49,022,957RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,741,223 - 49,741,487UniSTS
REN7547  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,760,067 - 55,760,319UniSTSGRCh37
Build 361055,430,073 - 55,430,325RGDNCBI36
Celera1049,022,954 - 49,023,206RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,741,484 - 49,741,736UniSTS
REN7548  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,760,288 - 55,760,520UniSTSGRCh37
Build 361055,430,294 - 55,430,526RGDNCBI36
Celera1049,023,175 - 49,023,406RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,741,705 - 49,741,936UniSTS
REN7549  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,760,464 - 55,760,697UniSTSGRCh37
Build 361055,430,470 - 55,430,703RGDNCBI36
Celera1049,023,350 - 49,023,583RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,741,880 - 49,742,113UniSTS
REN7550  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,760,609 - 55,760,866UniSTSGRCh37
Build 361055,430,615 - 55,430,872RGDNCBI36
Celera1049,023,495 - 49,023,751RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,742,025 - 49,742,281UniSTS
REN7551  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,760,747 - 55,761,003UniSTSGRCh37
Build 361055,430,753 - 55,431,009RGDNCBI36
Cytogenetic Map10q21.1UniSTS
REN7552  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,760,967 - 55,761,213UniSTSGRCh37
Build 361055,430,973 - 55,431,219RGDNCBI36
Celera1049,023,852 - 49,024,098RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,742,382 - 49,742,628UniSTS
REN7553  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,761,186 - 55,761,446UniSTSGRCh37
Build 361055,431,192 - 55,431,452RGDNCBI36
Celera1049,024,071 - 49,024,331RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,742,601 - 49,742,861UniSTS
REN7554  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,761,425 - 55,761,675UniSTSGRCh37
Build 361055,431,431 - 55,431,681RGDNCBI36
Celera1049,024,310 - 49,024,560RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,742,840 - 49,743,090UniSTS
REN7555  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,761,526 - 55,761,750UniSTSGRCh37
Build 361055,431,532 - 55,431,756RGDNCBI36
Celera1049,024,411 - 49,024,635RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,742,941 - 49,743,165UniSTS
REN7556  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,761,682 - 55,761,947UniSTSGRCh37
Build 361055,431,688 - 55,431,953RGDNCBI36
Celera1049,024,567 - 49,024,830RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,743,097 - 49,743,360UniSTS
REN7557  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,761,935 - 55,762,193UniSTSGRCh37
Build 361055,431,941 - 55,432,199RGDNCBI36
Celera1049,024,818 - 49,025,076RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,743,348 - 49,743,606UniSTS
REN7558  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,762,184 - 55,762,446UniSTSGRCh37
Build 361055,432,190 - 55,432,452RGDNCBI36
Celera1049,025,067 - 49,025,329RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,743,597 - 49,743,859UniSTS
REN7559  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,762,439 - 55,762,670UniSTSGRCh37
Build 361055,432,445 - 55,432,676RGDNCBI36
Celera1049,025,322 - 49,025,553RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,743,852 - 49,744,083UniSTS
REN7560  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,762,573 - 55,762,822UniSTSGRCh37
GRCh37X87,596,377 - 87,596,625UniSTSGRCh37
Build 36X87,483,033 - 87,483,281RGDNCBI36
Celera1049,025,456 - 49,025,705UniSTS
CeleraX87,834,716 - 87,834,964RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,743,986 - 49,744,235UniSTS
HuRefX81,179,582 - 81,179,830UniSTS
REN7561  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,762,813 - 55,763,060UniSTSGRCh37
Build 361055,432,819 - 55,433,066RGDNCBI36
Celera1049,025,696 - 49,025,943RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,744,226 - 49,744,473UniSTS
REN7562  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,763,023 - 55,763,263UniSTSGRCh37
Build 361055,433,029 - 55,433,269RGDNCBI36
Celera1049,025,906 - 49,026,146RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,744,436 - 49,744,676UniSTS
REN7563  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,763,224 - 55,763,448UniSTSGRCh37
Build 361055,433,230 - 55,433,454RGDNCBI36
Celera1049,026,107 - 49,026,331RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,744,637 - 49,744,861UniSTS
REN7564  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,763,392 - 55,763,636UniSTSGRCh37
Build 361055,433,398 - 55,433,642RGDNCBI36
Celera1049,026,275 - 49,026,517RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,744,805 - 49,745,046UniSTS
REN7565  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,763,634 - 55,763,895UniSTSGRCh37
Build 361055,433,640 - 55,433,901RGDNCBI36
Celera1049,026,515 - 49,026,784RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,745,044 - 49,745,313UniSTS
REN7566  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,763,874 - 55,764,101UniSTSGRCh37
Build 361055,433,880 - 55,434,107RGDNCBI36
Celera1049,026,763 - 49,026,990RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,745,292 - 49,745,519UniSTS
REN7567  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,763,966 - 55,764,206UniSTSGRCh37
Build 361055,433,972 - 55,434,212RGDNCBI36
Celera1049,026,855 - 49,027,103RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,745,384 - 49,745,620UniSTS
REN7568  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,764,174 - 55,764,422UniSTSGRCh37
Build 361055,434,180 - 55,434,428RGDNCBI36
Celera1049,027,072 - 49,027,320RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,745,589 - 49,745,837UniSTS
REN7569  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,764,396 - 55,764,658UniSTSGRCh37
Build 361055,434,402 - 55,434,664RGDNCBI36
Celera1049,027,294 - 49,027,555RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,745,811 - 49,746,072UniSTS
REN7570  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,764,600 - 55,764,837UniSTSGRCh37
Build 361055,434,606 - 55,434,843RGDNCBI36
Celera1049,027,498 - 49,027,732RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,746,015 - 49,746,249UniSTS
REN7571  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,764,794 - 55,765,027UniSTSGRCh37
Build 361055,434,800 - 55,435,033RGDNCBI36
Celera1049,027,689 - 49,027,922RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,746,206 - 49,746,439UniSTS
REN7572  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,764,971 - 55,765,225UniSTSGRCh37
Build 361055,434,977 - 55,435,231RGDNCBI36
Celera1049,027,866 - 49,028,120RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,746,383 - 49,746,637UniSTS
REN7573  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,765,200 - 55,765,448UniSTSGRCh37
Build 361055,435,206 - 55,435,454RGDNCBI36
Celera1049,028,095 - 49,028,343RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,746,612 - 49,746,860UniSTS
REN7574  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,765,400 - 55,765,653UniSTSGRCh37
Build 361055,435,406 - 55,435,659RGDNCBI36
Celera1049,028,295 - 49,028,548RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,746,812 - 49,747,065UniSTS
REN7575  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,765,564 - 55,765,817UniSTSGRCh37
Build 361055,435,570 - 55,435,823RGDNCBI36
Celera1049,028,459 - 49,028,712RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,746,976 - 49,747,229UniSTS
REN7576  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,765,794 - 55,766,023UniSTSGRCh37
Build 361055,435,800 - 55,436,029RGDNCBI36
Celera1049,028,689 - 49,028,918RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,747,206 - 49,747,435UniSTS
REN7577  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,765,995 - 55,766,233UniSTSGRCh37
Build 361055,436,001 - 55,436,239RGDNCBI36
Celera1049,028,890 - 49,029,128RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,747,407 - 49,747,645UniSTS
REN7578  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,766,204 - 55,766,450UniSTSGRCh37
Build 361055,436,210 - 55,436,456RGDNCBI36
Celera1049,029,099 - 49,029,345RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,747,616 - 49,747,862UniSTS
REN7579  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,766,425 - 55,766,677UniSTSGRCh37
Build 361055,436,431 - 55,436,683RGDNCBI36
Celera1049,029,320 - 49,029,572RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,747,837 - 49,748,089UniSTS
REN7580  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,766,654 - 55,766,903UniSTSGRCh37
Build 361055,436,660 - 55,436,909RGDNCBI36
Celera1049,029,549 - 49,029,798RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,748,066 - 49,748,315UniSTS
REN7581  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,766,835 - 55,767,059UniSTSGRCh37
Build 361055,436,841 - 55,437,065RGDNCBI36
Celera1049,029,730 - 49,029,954RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,748,247 - 49,748,471UniSTS
REN7582  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,767,330 - 55,767,557UniSTSGRCh37
Build 361055,437,336 - 55,437,563RGDNCBI36
Celera1049,030,225 - 49,030,452RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,748,742 - 49,748,969UniSTS
REN7583  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,767,536 - 55,767,760UniSTSGRCh37
Build 361055,437,542 - 55,437,766RGDNCBI36
Celera1049,030,431 - 49,030,655RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,748,948 - 49,749,172UniSTS
REN7584  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,767,689 - 55,767,916UniSTSGRCh37
Build 361055,437,695 - 55,437,922RGDNCBI36
Celera1049,030,584 - 49,030,811RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,749,101 - 49,749,328UniSTS
REN7585  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,767,894 - 55,768,135UniSTSGRCh37
Build 361055,437,900 - 55,438,141RGDNCBI36
Celera1049,030,789 - 49,031,030RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,749,306 - 49,749,547UniSTS
REN7586  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,768,122 - 55,768,363UniSTSGRCh37
Build 361055,438,128 - 55,438,369RGDNCBI36
Celera1049,031,017 - 49,031,258RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,749,534 - 49,749,775UniSTS
REN7587  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,768,311 - 55,768,570UniSTSGRCh37
Build 361055,438,317 - 55,438,576RGDNCBI36
Celera1049,031,206 - 49,031,464RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,749,723 - 49,749,981UniSTS
REN7588  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,768,554 - 55,768,804UniSTSGRCh37
Build 361055,438,560 - 55,438,810RGDNCBI36
Celera1049,031,448 - 49,031,698RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,749,965 - 49,750,215UniSTS
REN7589  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,768,803 - 55,769,049UniSTSGRCh37
Build 361055,438,809 - 55,439,055RGDNCBI36
Celera1049,031,697 - 49,031,943RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,750,214 - 49,750,460UniSTS
REN7590  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,769,029 - 55,769,272UniSTSGRCh37
Build 361055,439,035 - 55,439,278RGDNCBI36
Celera1049,031,923 - 49,032,166RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,750,440 - 49,750,683UniSTS
REN7591  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,769,271 - 55,769,513UniSTSGRCh37
Build 361055,439,277 - 55,439,519RGDNCBI36
Celera1049,032,165 - 49,032,407RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,750,682 - 49,750,924UniSTS
REN7592  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,769,484 - 55,769,749UniSTSGRCh37
Build 361055,439,490 - 55,439,755RGDNCBI36
Celera1049,032,378 - 49,032,643RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,750,895 - 49,751,160UniSTS
REN7593  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,769,717 - 55,769,975UniSTSGRCh37
Build 361055,439,723 - 55,439,981RGDNCBI36
Celera1049,032,611 - 49,032,869RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,751,128 - 49,751,386UniSTS
REN7594  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,769,949 - 55,770,204UniSTSGRCh37
Build 361055,439,955 - 55,440,210RGDNCBI36
Celera1049,032,843 - 49,033,098RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,751,360 - 49,751,614UniSTS
REN7595  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,770,182 - 55,770,432UniSTSGRCh37
Build 361055,440,188 - 55,440,438RGDNCBI36
Celera1049,033,076 - 49,033,326RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,751,592 - 49,751,842UniSTS
REN7596  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,770,427 - 55,770,690UniSTSGRCh37
Build 361055,440,433 - 55,440,696RGDNCBI36
Celera1049,033,321 - 49,033,584RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,751,837 - 49,752,100UniSTS
REN7597  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,770,689 - 55,770,929UniSTSGRCh37
Build 361055,440,695 - 55,440,935RGDNCBI36
Celera1049,033,583 - 49,033,823RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,752,099 - 49,752,339UniSTS
REN7598  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,770,905 - 55,771,162UniSTSGRCh37
Build 361055,440,911 - 55,441,168RGDNCBI36
Celera1049,033,799 - 49,034,056RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,752,315 - 49,752,572UniSTS
REN7599  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,771,147 - 55,771,399UniSTSGRCh37
Build 361055,441,153 - 55,441,405RGDNCBI36
Celera1049,034,041 - 49,034,293RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,752,557 - 49,752,809UniSTS
REN7600  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,771,373 - 55,771,609UniSTSGRCh37
Build 361055,441,379 - 55,441,615RGDNCBI36
Celera1049,034,267 - 49,034,503RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,752,783 - 49,753,019UniSTS
REN7601  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,771,569 - 55,771,837UniSTSGRCh37
Build 361055,441,575 - 55,441,843RGDNCBI36
Celera1049,034,463 - 49,034,731RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,752,979 - 49,753,247UniSTS
REN7602  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,771,835 - 55,772,080UniSTSGRCh37
Build 361055,441,841 - 55,442,086RGDNCBI36
Celera1049,034,729 - 49,034,974RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,753,245 - 49,753,490UniSTS
REN7603  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,772,057 - 55,772,321UniSTSGRCh37
Build 361055,442,063 - 55,442,327RGDNCBI36
Celera1049,034,951 - 49,035,215RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,753,467 - 49,753,731UniSTS
REN7604  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,772,318 - 55,772,559UniSTSGRCh37
Build 361055,442,324 - 55,442,565RGDNCBI36
Celera1049,035,212 - 49,035,453RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,753,728 - 49,753,969UniSTS
REN7605  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,772,557 - 55,772,816UniSTSGRCh37
Build 361055,442,563 - 55,442,822RGDNCBI36
Celera1049,035,451 - 49,035,710RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,753,967 - 49,754,226UniSTS
REN7606  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,772,802 - 55,773,062UniSTSGRCh37
Build 361055,442,808 - 55,443,068RGDNCBI36
Celera1049,035,696 - 49,035,956RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,754,212 - 49,754,472UniSTS
REN7607  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,773,053 - 55,773,288UniSTSGRCh37
Build 361055,443,059 - 55,443,294RGDNCBI36
Celera1049,035,947 - 49,036,182RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,754,463 - 49,754,698UniSTS
REN7608  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371625,497,652 - 25,497,896UniSTSGRCh37
GRCh371055,773,255 - 55,773,498UniSTSGRCh37
Build 361055,443,261 - 55,443,504RGDNCBI36
Celera1049,036,149 - 49,036,392RGD
Celera1624,276,018 - 24,276,262UniSTS
Cytogenetic Map10q21.1UniSTS
HuRef1623,590,323 - 23,590,567UniSTS
HuRef1049,754,665 - 49,754,908UniSTS
REN7609  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,773,466 - 55,773,695UniSTSGRCh37
Build 361055,443,472 - 55,443,701RGDNCBI36
Celera1049,036,360 - 49,036,589RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,754,876 - 49,755,105UniSTS
REN7610  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,773,685 - 55,773,933UniSTSGRCh37
Build 361055,443,691 - 55,443,939RGDNCBI36
Celera1049,036,579 - 49,036,827RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,755,095 - 49,755,343UniSTS
REN7611  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,773,896 - 55,774,120UniSTSGRCh37
Build 361055,443,902 - 55,444,126RGDNCBI36
Cytogenetic Map10q21.1UniSTS
REN7612  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,773,937 - 55,774,191UniSTSGRCh37
Build 361055,443,943 - 55,444,197RGDNCBI36
Celera1049,036,831 - 49,037,087RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,755,347 - 49,755,604UniSTS
REN7613  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,774,164 - 55,774,406UniSTSGRCh37
Build 361055,444,170 - 55,444,412RGDNCBI36
Celera1049,037,060 - 49,037,302RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,755,577 - 49,755,819UniSTS
REN7614  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,774,383 - 55,774,643UniSTSGRCh37
Build 361055,444,389 - 55,444,649RGDNCBI36
Celera1049,037,279 - 49,037,539RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,755,796 - 49,756,056UniSTS
REN7615  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,774,547 - 55,774,794UniSTSGRCh37
Build 361055,444,553 - 55,444,800RGDNCBI36
Celera1049,037,443 - 49,037,690RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,755,960 - 49,756,207UniSTS
REN7616  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,774,776 - 55,775,020UniSTSGRCh37
Build 361055,444,782 - 55,445,026RGDNCBI36
Celera1049,037,672 - 49,037,917RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,756,189 - 49,756,433UniSTS
REN7617  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,774,989 - 55,775,213UniSTSGRCh37
Build 361055,444,995 - 55,445,219RGDNCBI36
Celera1049,037,886 - 49,038,115RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,756,402 - 49,756,631UniSTS
REN7618  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,775,191 - 55,775,438UniSTSGRCh37
Build 361055,445,197 - 55,445,444RGDNCBI36
Celera1049,038,093 - 49,038,340RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,756,609 - 49,756,856UniSTS
REN7619  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,775,403 - 55,775,645UniSTSGRCh37
Build 361055,445,409 - 55,445,651RGDNCBI36
Celera1049,038,305 - 49,038,547RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,756,821 - 49,757,063UniSTS
REN7620  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,775,623 - 55,775,894UniSTSGRCh37
Build 361055,445,629 - 55,445,900RGDNCBI36
Celera1049,038,525 - 49,038,795RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,757,041 - 49,757,312UniSTS
REN7621  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,775,893 - 55,776,117UniSTSGRCh37
Build 361055,445,899 - 55,446,123RGDNCBI36
Celera1049,038,794 - 49,039,018RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,757,311 - 49,757,535UniSTS
REN7622  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,775,986 - 55,776,249UniSTSGRCh37
Build 361055,445,992 - 55,446,255RGDNCBI36
Celera1049,038,887 - 49,039,150RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,757,404 - 49,757,667UniSTS
REN7623  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,776,217 - 55,776,443UniSTSGRCh37
Build 361055,446,223 - 55,446,449RGDNCBI36
Celera1049,039,118 - 49,039,344RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,757,635 - 49,757,861UniSTS
REN7624  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,776,408 - 55,776,636UniSTSGRCh37
Build 361055,446,414 - 55,446,642RGDNCBI36
Celera1049,039,309 - 49,039,537RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,757,826 - 49,758,054UniSTS
REN7625  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,776,497 - 55,776,727UniSTSGRCh37
Build 361055,446,503 - 55,446,733RGDNCBI36
Celera1049,039,398 - 49,039,628RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,757,915 - 49,758,145UniSTS
REN7626  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,776,686 - 55,776,940UniSTSGRCh37
Build 361055,446,692 - 55,446,946RGDNCBI36
Celera1049,039,587 - 49,039,841RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,758,104 - 49,758,358UniSTS
REN7627  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,777,039 - 55,777,272UniSTSGRCh37
Build 361055,447,045 - 55,447,278RGDNCBI36
Celera1049,039,940 - 49,040,173RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,758,457 - 49,758,690UniSTS
REN7628  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,777,251 - 55,777,493UniSTSGRCh37
Build 361055,447,257 - 55,447,499RGDNCBI36
Celera1049,040,152 - 49,040,394RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,758,669 - 49,758,911UniSTS
REN7629  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,777,385 - 55,777,627UniSTSGRCh37
Build 361055,447,391 - 55,447,633RGDNCBI36
Celera1049,040,286 - 49,040,528RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,758,803 - 49,759,045UniSTS
REN7630  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,777,599 - 55,777,852UniSTSGRCh37
Build 361055,447,605 - 55,447,858RGDNCBI36
Celera1049,040,500 - 49,040,753RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,759,017 - 49,759,270UniSTS
REN7631  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,777,826 - 55,778,089UniSTSGRCh37
Build 361055,447,832 - 55,448,095RGDNCBI36
Celera1049,040,727 - 49,040,990RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,759,244 - 49,759,507UniSTS
REN7632  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,778,067 - 55,778,326UniSTSGRCh37
Build 361055,448,073 - 55,448,332RGDNCBI36
Celera1049,040,968 - 49,041,227RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,759,485 - 49,759,744UniSTS
REN7633  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,778,300 - 55,778,525UniSTSGRCh37
Build 361055,448,306 - 55,448,531RGDNCBI36
Celera1049,041,201 - 49,041,426RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,759,718 - 49,759,943UniSTS
REN7634  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,778,493 - 55,778,763UniSTSGRCh37
Build 361055,448,499 - 55,448,769RGDNCBI36
Celera1049,041,394 - 49,041,664RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,759,911 - 49,760,181UniSTS
REN7635  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,778,732 - 55,778,971UniSTSGRCh37
Build 361055,448,738 - 55,448,977RGDNCBI36
Celera1049,041,633 - 49,041,872RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,760,150 - 49,760,389UniSTS
REN7636  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,778,944 - 55,779,198UniSTSGRCh37
Build 361055,448,950 - 55,449,204RGDNCBI36
Celera1049,041,845 - 49,042,099RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,760,362 - 49,760,616UniSTS
REN7637  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,779,173 - 55,779,408UniSTSGRCh37
Build 361055,449,179 - 55,449,414RGDNCBI36
Celera1049,042,074 - 49,042,309RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,760,591 - 49,760,826UniSTS
REN7638  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,779,385 - 55,779,640UniSTSGRCh37
Build 361055,449,391 - 55,449,646RGDNCBI36
Celera1049,042,286 - 49,042,541RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,760,803 - 49,761,058UniSTS
REN7639  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,779,633 - 55,779,865UniSTSGRCh37
Build 361055,449,639 - 55,449,871RGDNCBI36
Celera1049,042,534 - 49,042,766RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,761,051 - 49,761,283UniSTS
REN7640  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,779,825 - 55,780,061UniSTSGRCh37
Build 361055,449,831 - 55,450,067RGDNCBI36
Celera1049,042,726 - 49,042,962RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,761,243 - 49,761,479UniSTS
REN7641  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,780,038 - 55,780,288UniSTSGRCh37
Build 361055,450,044 - 55,450,294RGDNCBI36
Celera1049,042,939 - 49,043,189RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,761,456 - 49,761,706UniSTS
REN7642  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,780,263 - 55,780,487UniSTSGRCh37
Build 361055,450,269 - 55,450,493RGDNCBI36
Celera1049,043,164 - 49,043,388RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,761,681 - 49,761,905UniSTS
REN7643  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,780,456 - 55,780,711UniSTSGRCh37
Build 361055,450,462 - 55,450,717RGDNCBI36
Celera1049,043,357 - 49,043,612RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,761,874 - 49,762,129UniSTS
REN7644  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,780,684 - 55,780,932UniSTSGRCh37
Build 361055,450,690 - 55,450,938RGDNCBI36
Celera1049,043,585 - 49,043,833RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,762,102 - 49,762,350UniSTS
REN7645  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,780,926 - 55,781,164UniSTSGRCh37
Build 361055,450,932 - 55,451,170RGDNCBI36
Celera1049,043,827 - 49,044,065RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,762,344 - 49,762,582UniSTS
REN7646  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,781,152 - 55,781,401UniSTSGRCh37
Build 361055,451,158 - 55,451,407RGDNCBI36
Celera1049,044,053 - 49,044,302RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,762,570 - 49,762,819UniSTS
REN7647  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,781,384 - 55,781,632UniSTSGRCh37
Build 361055,451,390 - 55,451,638RGDNCBI36
Celera1049,044,285 - 49,044,533RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,762,802 - 49,763,050UniSTS
REN7648  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,781,616 - 55,781,862UniSTSGRCh37
Build 361055,451,622 - 55,451,868RGDNCBI36
Celera1049,044,517 - 49,044,763RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,763,034 - 49,763,280UniSTS
REN7649  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,781,838 - 55,782,100UniSTSGRCh37
Build 361055,451,844 - 55,452,106RGDNCBI36
Celera1049,044,739 - 49,045,001RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,763,256 - 49,763,518UniSTS
REN7650  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,782,092 - 55,782,332UniSTSGRCh37
Build 361055,452,098 - 55,452,338RGDNCBI36
Celera1049,044,992 - 49,045,232RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,763,509 - 49,763,749UniSTS
REN7651  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,782,301 - 55,782,560UniSTSGRCh37
Build 361055,452,307 - 55,452,566RGDNCBI36
Celera1049,045,201 - 49,045,460RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,763,718 - 49,763,977UniSTS
REN7652  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,782,549 - 55,782,787UniSTSGRCh37
Build 361055,452,555 - 55,452,793RGDNCBI36
Celera1049,045,449 - 49,045,687RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,763,966 - 49,764,204UniSTS
REN7653  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,782,771 - 55,783,021UniSTSGRCh37
Build 361055,452,777 - 55,453,027RGDNCBI36
Celera1049,045,671 - 49,045,921RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,764,188 - 49,764,438UniSTS
REN7654  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,782,997 - 55,783,260UniSTSGRCh37
Build 361055,453,003 - 55,453,266RGDNCBI36
Celera1049,045,897 - 49,046,160RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,764,414 - 49,764,677UniSTS
REN7655  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,783,080 - 55,783,323UniSTSGRCh37
Build 361055,453,086 - 55,453,329RGDNCBI36
Celera1049,045,980 - 49,046,223RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,764,497 - 49,764,740UniSTS
REN7656  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,783,293 - 55,783,536UniSTSGRCh37
Build 361055,453,299 - 55,453,542RGDNCBI36
Celera1049,046,193 - 49,046,436RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,764,710 - 49,764,950UniSTS
REN7657  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,783,513 - 55,783,783UniSTSGRCh37
Build 361055,453,519 - 55,453,789RGDNCBI36
Celera1049,046,413 - 49,046,683RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,764,927 - 49,765,198UniSTS
REN7658  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,783,760 - 55,784,022UniSTSGRCh37
Build 361055,453,766 - 55,454,028RGDNCBI36
Celera1049,046,660 - 49,046,922RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,765,175 - 49,765,437UniSTS
REN7659  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,784,003 - 55,784,240UniSTSGRCh37
Build 361055,454,009 - 55,454,246RGDNCBI36
Celera1049,046,903 - 49,047,140RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,765,418 - 49,765,655UniSTS
REN7660  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,784,215 - 55,784,456UniSTSGRCh37
Build 361055,454,221 - 55,454,462RGDNCBI36
Celera1049,047,115 - 49,047,356RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,765,630 - 49,765,871UniSTS
REN7661  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,784,432 - 55,784,690UniSTSGRCh37
Build 361055,454,438 - 55,454,696RGDNCBI36
Celera1049,047,332 - 49,047,590RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,765,847 - 49,766,105UniSTS
REN7662  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,784,663 - 55,784,921UniSTSGRCh37
Build 361055,454,669 - 55,454,927RGDNCBI36
Celera1049,047,563 - 49,047,821RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,766,078 - 49,766,336UniSTS
REN7663  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,784,894 - 55,785,141UniSTSGRCh37
Build 361055,454,900 - 55,455,147RGDNCBI36
Celera1049,047,794 - 49,048,041RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,766,309 - 49,766,556UniSTS
REN7664  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,785,007 - 55,785,251UniSTSGRCh37
Build 361055,455,013 - 55,455,257RGDNCBI36
Celera1049,047,907 - 49,048,151RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,766,422 - 49,766,666UniSTS
REN7665  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,785,550 - 55,785,775UniSTSGRCh37
Build 361055,455,556 - 55,455,781RGDNCBI36
Celera1049,048,450 - 49,048,675RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,766,965 - 49,767,190UniSTS
REN7666  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,785,770 - 55,786,028UniSTSGRCh37
Build 361055,455,776 - 55,456,034RGDNCBI36
Celera1049,048,670 - 49,048,928RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,767,185 - 49,767,443UniSTS
REN7667  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,786,007 - 55,786,232UniSTSGRCh37
Build 361055,456,013 - 55,456,238RGDNCBI36
Celera1049,048,907 - 49,049,132RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,767,422 - 49,767,647UniSTS
REN7668  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,786,204 - 55,786,477UniSTSGRCh37
Build 361055,456,210 - 55,456,483RGDNCBI36
Celera1049,049,104 - 49,049,377RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,767,619 - 49,767,892UniSTS
REN7669  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,786,265 - 55,786,509UniSTSGRCh37
Build 361055,456,271 - 55,456,515RGDNCBI36
Celera1049,049,165 - 49,049,409RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,767,680 - 49,767,924UniSTS
REN7670  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,788,743 - 55,788,967UniSTSGRCh37
Build 361055,458,749 - 55,458,973RGDNCBI36
Celera1049,051,642 - 49,051,866RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,770,158 - 49,770,382UniSTS
REN7671  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,788,952 - 55,789,196UniSTSGRCh37
Build 361055,458,958 - 55,459,202RGDNCBI36
Celera1049,051,851 - 49,052,095RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,770,367 - 49,770,611UniSTS
REN7672  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,789,173 - 55,789,427UniSTSGRCh37
Build 361055,459,179 - 55,459,433RGDNCBI36
Celera1049,052,072 - 49,052,326RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,770,588 - 49,770,842UniSTS
REN7673  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,789,408 - 55,789,659UniSTSGRCh37
Build 361055,459,414 - 55,459,665RGDNCBI36
Celera1049,052,307 - 49,052,558RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,770,823 - 49,771,074UniSTS
REN7674  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,789,654 - 55,789,879UniSTSGRCh37
Build 361055,459,660 - 55,459,885RGDNCBI36
Celera1049,052,553 - 49,052,778RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,771,069 - 49,771,294UniSTS
REN7675  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,789,830 - 55,790,070UniSTSGRCh37
Build 361055,459,836 - 55,460,076RGDNCBI36
Celera1049,052,729 - 49,052,969RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,771,245 - 49,771,485UniSTS
REN7676  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,790,047 - 55,790,293UniSTSGRCh37
Build 361055,460,053 - 55,460,299RGDNCBI36
Celera1049,052,946 - 49,053,191RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,771,462 - 49,771,708UniSTS
REN7677  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,790,289 - 55,790,543UniSTSGRCh37
Build 361055,460,295 - 55,460,549RGDNCBI36
Celera1049,053,187 - 49,053,441RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,771,704 - 49,771,958UniSTS
REN7678  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,790,540 - 55,790,787UniSTSGRCh37
Build 361055,460,546 - 55,460,793RGDNCBI36
Celera1049,053,438 - 49,053,685RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,771,955 - 49,772,202UniSTS
REN7679  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,790,763 - 55,791,003UniSTSGRCh37
Build 361055,460,769 - 55,461,009RGDNCBI36
Celera1049,053,661 - 49,053,901RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,772,178 - 49,772,418UniSTS
REN7680  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,790,978 - 55,791,239UniSTSGRCh37
Build 361055,460,984 - 55,461,245RGDNCBI36
Celera1049,053,876 - 49,054,136RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,772,393 - 49,772,653UniSTS
REN7681  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,791,213 - 55,791,451UniSTSGRCh37
Build 361055,461,219 - 55,461,457RGDNCBI36
Celera1049,054,110 - 49,054,348RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,772,627 - 49,772,866UniSTS
REN7682  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,791,426 - 55,791,691UniSTSGRCh37
Build 361055,461,432 - 55,461,697RGDNCBI36
Celera1049,054,323 - 49,054,588RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,772,841 - 49,773,106UniSTS
REN7683  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,791,688 - 55,791,930UniSTSGRCh37
Build 361055,461,694 - 55,461,936RGDNCBI36
Celera1049,054,585 - 49,054,827RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,773,103 - 49,773,345UniSTS
REN7684  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,791,905 - 55,792,162UniSTSGRCh37
Build 361055,461,911 - 55,462,168RGDNCBI36
Celera1049,054,802 - 49,055,059RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,773,320 - 49,773,577UniSTS
REN7685  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,792,135 - 55,792,362UniSTSGRCh37
Build 361055,462,141 - 55,462,368RGDNCBI36
Celera1049,055,032 - 49,055,259RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,773,550 - 49,773,777UniSTS
REN7686  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,792,285 - 55,792,543UniSTSGRCh37
Build 361055,462,291 - 55,462,549RGDNCBI36
Celera1049,055,182 - 49,055,440RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,773,700 - 49,773,958UniSTS
REN7687  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,792,509 - 55,792,747UniSTSGRCh37
Build 361055,462,515 - 55,462,753RGDNCBI36
Celera1049,055,406 - 49,055,644RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,773,924 - 49,774,162UniSTS
REN7688  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,792,669 - 55,792,899UniSTSGRCh37
Build 361055,462,675 - 55,462,905RGDNCBI36
Celera1049,055,566 - 49,055,796RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,774,084 - 49,774,314UniSTS
REN7689  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,792,838 - 55,793,090UniSTSGRCh37
Build 361055,462,844 - 55,463,096RGDNCBI36
Celera1049,055,735 - 49,055,987RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,774,253 - 49,774,505UniSTS
REN7690  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,793,062 - 55,793,301UniSTSGRCh37
Build 361055,463,068 - 55,463,307RGDNCBI36
Celera1049,055,959 - 49,056,198RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,774,477 - 49,774,716UniSTS
REN7691  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,793,294 - 55,793,528UniSTSGRCh37
Build 361055,463,300 - 55,463,534RGDNCBI36
Celera1049,056,191 - 49,056,425RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,774,709 - 49,774,943UniSTS
REN7692  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,793,497 - 55,793,737UniSTSGRCh37
Build 361055,463,503 - 55,463,743RGDNCBI36
Celera1049,056,394 - 49,056,634RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,774,912 - 49,775,152UniSTS
REN7693  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,793,692 - 55,793,917UniSTSGRCh37
Build 361055,463,698 - 55,463,923RGDNCBI36
Celera1049,056,589 - 49,056,814RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,775,107 - 49,775,332UniSTS
REN7694  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,793,857 - 55,794,120UniSTSGRCh37
Build 361055,463,863 - 55,464,126RGDNCBI36
Celera1049,056,754 - 49,057,017RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,775,272 - 49,775,535UniSTS
REN7695  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,794,095 - 55,794,349UniSTSGRCh37
Build 361055,464,101 - 55,464,355RGDNCBI36
Celera1049,056,992 - 49,057,246RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,775,510 - 49,775,764UniSTS
REN7696  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,794,323 - 55,794,563UniSTSGRCh37
Build 361055,464,329 - 55,464,569RGDNCBI36
Celera1049,057,220 - 49,057,472RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,775,738 - 49,775,990UniSTS
REN7697  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,794,540 - 55,794,789UniSTSGRCh37
Build 361055,464,546 - 55,464,795RGDNCBI36
Celera1049,057,449 - 49,057,698RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,775,967 - 49,776,216UniSTS
REN7698  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,794,768 - 55,795,006UniSTSGRCh37
Build 361055,464,774 - 55,465,012RGDNCBI36
Celera1049,057,677 - 49,057,915RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,776,195 - 49,776,433UniSTS
REN7699  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,794,998 - 55,795,244UniSTSGRCh37
Build 361055,465,004 - 55,465,250RGDNCBI36
Celera1049,057,907 - 49,058,153RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,776,425 - 49,776,671UniSTS
REN7700  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,795,214 - 55,795,461UniSTSGRCh37
Build 361055,465,220 - 55,465,467RGDNCBI36
Celera1049,058,123 - 49,058,370RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,776,641 - 49,776,888UniSTS
REN7701  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,795,455 - 55,795,700UniSTSGRCh37
Build 361055,465,461 - 55,465,706RGDNCBI36
Celera1049,058,364 - 49,058,609RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,776,882 - 49,777,127UniSTS
REN7702  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,795,635 - 55,795,869UniSTSGRCh37
Build 361055,465,641 - 55,465,875RGDNCBI36
Celera1049,058,544 - 49,058,778RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,777,062 - 49,777,296UniSTS
REN7703  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,795,834 - 55,796,093UniSTSGRCh37
Build 361055,465,840 - 55,466,099RGDNCBI36
Celera1049,058,743 - 49,059,002RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,777,261 - 49,777,520UniSTS
REN7704  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,796,083 - 55,796,330UniSTSGRCh37
Build 361055,466,089 - 55,466,336RGDNCBI36
Celera1049,058,992 - 49,059,239RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,777,510 - 49,777,757UniSTS
REN7705  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,796,321 - 55,796,577UniSTSGRCh37
Build 361055,466,327 - 55,466,583RGDNCBI36
Celera1049,059,230 - 49,059,486RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,777,748 - 49,778,004UniSTS
REN7706  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,796,544 - 55,796,787UniSTSGRCh37
Build 361055,466,550 - 55,466,793RGDNCBI36
Celera1049,059,453 - 49,059,696RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,777,971 - 49,778,214UniSTS
REN7707  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,796,763 - 55,797,007UniSTSGRCh37
Build 361055,466,769 - 55,467,013RGDNCBI36
Celera1049,059,672 - 49,059,916RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,778,190 - 49,778,434UniSTS
REN7708  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,796,983 - 55,797,246UniSTSGRCh37
Build 361055,466,989 - 55,467,252RGDNCBI36
Celera1049,059,892 - 49,060,155RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,778,410 - 49,778,673UniSTS
REN7709  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,797,229 - 55,797,455UniSTSGRCh37
Build 361055,467,235 - 55,467,461RGDNCBI36
Celera1049,060,138 - 49,060,364RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,778,656 - 49,778,882UniSTS
REN7710  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,797,433 - 55,797,677UniSTSGRCh37
Build 361055,467,439 - 55,467,683RGDNCBI36
Celera1049,060,342 - 49,060,586RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,778,860 - 49,779,104UniSTS
REN7711  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,797,654 - 55,797,906UniSTSGRCh37
Build 361055,467,660 - 55,467,912RGDNCBI36
Celera1049,060,563 - 49,060,815RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,779,081 - 49,779,333UniSTS
REN7712  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,797,895 - 55,798,132UniSTSGRCh37
Build 361055,467,901 - 55,468,138RGDNCBI36
Celera1049,060,804 - 49,061,041RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,779,322 - 49,779,559UniSTS
REN7713  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,798,123 - 55,798,361UniSTSGRCh37
Build 361055,468,129 - 55,468,367RGDNCBI36
Celera1049,061,032 - 49,061,270RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,779,550 - 49,779,788UniSTS
REN7714  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,798,351 - 55,798,593UniSTSGRCh37
Build 361055,468,357 - 55,468,599RGDNCBI36
Celera1049,061,260 - 49,061,502RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,779,778 - 49,780,020UniSTS
REN7715  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,798,564 - 55,798,789UniSTSGRCh37
Build 361055,468,570 - 55,468,795RGDNCBI36
Celera1049,061,473 - 49,061,698RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,779,991 - 49,780,216UniSTS
REN7716  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,798,765 - 55,799,020UniSTSGRCh37
Build 361055,468,771 - 55,469,026RGDNCBI36
Celera1049,061,674 - 49,061,929RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,780,192 - 49,780,447UniSTS
REN7717  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,798,997 - 55,799,267UniSTSGRCh37
Build 361055,469,003 - 55,469,273RGDNCBI36
Celera1049,061,906 - 49,062,176RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,780,424 - 49,780,694UniSTS
REN7718  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,799,259 - 55,799,515UniSTSGRCh37
Build 361055,469,265 - 55,469,521RGDNCBI36
Celera1049,062,168 - 49,062,424RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,780,686 - 49,780,942UniSTS
REN7719  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,799,497 - 55,799,739UniSTSGRCh37
Build 361055,469,503 - 55,469,745RGDNCBI36
Celera1049,062,406 - 49,062,648RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,780,924 - 49,781,166UniSTS
REN7720  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,799,715 - 55,799,962UniSTSGRCh37
Build 361055,469,721 - 55,469,968RGDNCBI36
Celera1049,062,624 - 49,062,871RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,781,142 - 49,781,389UniSTS
REN7721  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,799,900 - 55,800,125UniSTSGRCh37
Build 361055,469,906 - 55,470,131RGDNCBI36
Celera1049,062,809 - 49,063,034RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,781,327 - 49,781,552UniSTS
REN7722  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,800,113 - 55,800,362UniSTSGRCh37
Build 361055,470,119 - 55,470,368RGDNCBI36
Celera1049,063,022 - 49,063,271RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,781,540 - 49,781,789UniSTS
REN7723  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,800,333 - 55,800,584UniSTSGRCh37
Build 361055,470,339 - 55,470,590RGDNCBI36
Celera1049,063,242 - 49,063,493RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,781,760 - 49,782,011UniSTS
REN7724  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,800,570 - 55,800,821UniSTSGRCh37
Build 361055,470,576 - 55,470,827RGDNCBI36
Celera1049,063,479 - 49,063,730RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,781,997 - 49,782,248UniSTS
REN7725  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,800,803 - 55,801,047UniSTSGRCh37
Build 361055,470,809 - 55,471,053RGDNCBI36
Celera1049,063,712 - 49,063,956RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,782,230 - 49,782,474UniSTS
REN7726  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,800,972 - 55,801,236UniSTSGRCh37
Build 361055,470,978 - 55,471,242RGDNCBI36
Celera1049,063,881 - 49,064,145RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,782,399 - 49,782,663UniSTS
REN7727  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,801,209 - 55,801,437UniSTSGRCh37
Build 361055,471,215 - 55,471,443RGDNCBI36
Celera1049,064,118 - 49,064,346RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,782,636 - 49,782,864UniSTS
REN7728  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,801,348 - 55,801,605UniSTSGRCh37
Build 361055,471,354 - 55,471,611RGDNCBI36
Celera1049,064,257 - 49,064,514RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,782,775 - 49,783,032UniSTS
REN7729  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,801,582 - 55,801,833UniSTSGRCh37
Build 361055,471,588 - 55,471,839RGDNCBI36
Celera1049,064,491 - 49,064,742RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,783,009 - 49,783,260UniSTS
REN7730  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,801,810 - 55,802,052UniSTSGRCh37
Build 361055,471,816 - 55,472,058RGDNCBI36
Celera1049,064,719 - 49,064,961RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,783,237 - 49,783,479UniSTS
REN7731  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,802,029 - 55,802,278UniSTSGRCh37
Build 361055,472,035 - 55,472,284RGDNCBI36
Celera1049,064,938 - 49,065,187RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,783,456 - 49,783,705UniSTS
REN7732  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,802,256 - 55,802,504UniSTSGRCh37
Build 361055,472,262 - 55,472,510RGDNCBI36
Celera1049,065,165 - 49,065,413RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,783,683 - 49,783,931UniSTS
REN7733  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,802,500 - 55,802,741UniSTSGRCh37
Build 361055,472,506 - 55,472,747RGDNCBI36
Celera1049,065,409 - 49,065,650RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,783,927 - 49,784,168UniSTS
REN7734  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,802,707 - 55,802,960UniSTSGRCh37
Build 361055,472,713 - 55,472,966RGDNCBI36
Celera1049,065,616 - 49,065,869RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,784,134 - 49,784,387UniSTS
REN7735  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,802,898 - 55,803,147UniSTSGRCh37
Build 361055,472,904 - 55,473,153RGDNCBI36
Celera1049,065,807 - 49,066,056RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,784,325 - 49,784,574UniSTS
REN7736  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,803,090 - 55,803,354UniSTSGRCh37
Build 361055,473,096 - 55,473,360RGDNCBI36
Celera1049,065,999 - 49,066,263RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,784,517 - 49,784,781UniSTS
REN7737  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,803,329 - 55,803,587UniSTSGRCh37
Build 361055,473,335 - 55,473,593RGDNCBI36
Celera1049,066,238 - 49,066,496RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,784,756 - 49,785,014UniSTS
REN7738  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,803,576 - 55,803,832UniSTSGRCh37
Build 361055,473,582 - 55,473,838RGDNCBI36
Celera1049,066,485 - 49,066,741RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,785,003 - 49,785,259UniSTS
REN7739  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,803,830 - 55,804,084UniSTSGRCh37
Build 361055,473,836 - 55,474,090RGDNCBI36
Celera1049,066,739 - 49,066,993RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,785,257 - 49,785,511UniSTS
REN7740  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,804,061 - 55,804,306UniSTSGRCh37
Build 361055,474,067 - 55,474,312RGDNCBI36
Celera1049,066,970 - 49,067,215RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,785,488 - 49,785,733UniSTS
REN7741  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,804,282 - 55,804,520UniSTSGRCh37
Build 361055,474,288 - 55,474,526RGDNCBI36
Celera1049,067,191 - 49,067,429RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,785,709 - 49,785,947UniSTS
REN7742  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,804,497 - 55,804,747UniSTSGRCh37
Build 361055,474,503 - 55,474,753RGDNCBI36
Celera1049,067,406 - 49,067,656RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,785,924 - 49,786,174UniSTS
REN7743  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,804,742 - 55,804,995UniSTSGRCh37
Build 361055,474,748 - 55,475,001RGDNCBI36
Celera1049,067,651 - 49,067,904RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,786,169 - 49,786,422UniSTS
REN7744  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,804,990 - 55,805,239UniSTSGRCh37
Build 361055,474,996 - 55,475,245RGDNCBI36
Celera1049,067,899 - 49,068,148RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,786,417 - 49,786,666UniSTS
REN7745  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,805,221 - 55,805,453UniSTSGRCh37
Build 361055,475,227 - 55,475,459RGDNCBI36
Celera1049,068,130 - 49,068,362RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,786,648 - 49,786,880UniSTS
REN7746  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,805,430 - 55,805,668UniSTSGRCh37
Build 361055,475,436 - 55,475,674RGDNCBI36
Celera1049,068,339 - 49,068,577RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,786,857 - 49,787,095UniSTS
REN7747  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,805,660 - 55,805,913UniSTSGRCh37
Build 361055,475,666 - 55,475,919RGDNCBI36
Celera1049,068,569 - 49,068,822RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,787,087 - 49,787,340UniSTS
REN7748  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,805,893 - 55,806,148UniSTSGRCh37
Build 361055,475,899 - 55,476,154RGDNCBI36
Celera1049,068,802 - 49,069,057RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,787,320 - 49,787,575UniSTS
REN7749  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,806,122 - 55,806,378UniSTSGRCh37
Build 361055,476,128 - 55,476,384RGDNCBI36
Celera1049,069,031 - 49,069,287RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,787,549 - 49,787,805UniSTS
REN7750  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,806,351 - 55,806,604UniSTSGRCh37
Build 361055,476,357 - 55,476,610RGDNCBI36
Celera1049,069,260 - 49,069,514RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,787,778 - 49,788,031UniSTS
REN7751  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,806,575 - 55,806,799UniSTSGRCh37
Build 361055,476,581 - 55,476,805RGDNCBI36
Celera1049,069,485 - 49,069,709RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,788,002 - 49,788,225UniSTS
REN7752  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,806,787 - 55,807,039UniSTSGRCh37
Build 361055,476,793 - 55,477,045RGDNCBI36
Celera1049,069,697 - 49,069,949RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,788,213 - 49,788,465UniSTS
REN7753  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,807,011 - 55,807,249UniSTSGRCh37
Build 361055,477,017 - 55,477,255RGDNCBI36
Celera1049,069,921 - 49,070,159RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,788,437 - 49,788,675UniSTS
REN7754  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,807,216 - 55,807,444UniSTSGRCh37
Build 361055,477,222 - 55,477,450RGDNCBI36
Celera1049,070,126 - 49,070,354RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,788,642 - 49,788,870UniSTS
REN7755  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,807,423 - 55,807,647UniSTSGRCh37
Build 361055,477,429 - 55,477,653RGDNCBI36
Celera1049,070,333 - 49,070,557RGD
Cytogenetic Map10q21.1UniSTS
HuRef1754,983,572 - 54,983,797UniSTS
HuRef1049,788,849 - 49,789,073UniSTS
REN7756  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,807,603 - 55,807,830UniSTSGRCh37
Build 361055,477,609 - 55,477,836RGDNCBI36
Celera1049,070,513 - 49,070,740RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,789,029 - 49,789,256UniSTS
REN7757  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,807,813 - 55,808,079UniSTSGRCh37
Build 361055,477,819 - 55,478,085RGDNCBI36
Celera1049,070,723 - 49,070,989RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,789,239 - 49,789,505UniSTS
REN7758  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,808,064 - 55,808,315UniSTSGRCh37
Build 361055,478,070 - 55,478,321RGDNCBI36
Celera1049,070,974 - 49,071,225RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,789,490 - 49,789,741UniSTS
REN7759  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,808,290 - 55,808,515UniSTSGRCh37
Build 361055,478,296 - 55,478,521RGDNCBI36
Celera1049,071,200 - 49,071,425RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,789,716 - 49,789,941UniSTS
REN7760  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,808,469 - 55,808,725UniSTSGRCh37
Build 361055,478,475 - 55,478,731RGDNCBI36
Celera1049,071,379 - 49,071,635RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,789,895 - 49,790,151UniSTS
REN7761  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,808,700 - 55,808,947UniSTSGRCh37
Build 361055,478,706 - 55,478,953RGDNCBI36
Celera1049,071,610 - 49,071,857RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,790,126 - 49,790,373UniSTS
REN7762  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,808,925 - 55,809,193UniSTSGRCh37
Build 361055,478,931 - 55,479,199RGDNCBI36
Celera1049,071,835 - 49,072,103RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,790,351 - 49,790,619UniSTS
REN7763  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,809,110 - 55,809,361UniSTSGRCh37
Build 361055,479,116 - 55,479,367RGDNCBI36
Celera1049,072,020 - 49,072,271RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,790,536 - 49,790,787UniSTS
REN7764  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,809,565 - 55,809,789UniSTSGRCh37
Build 361055,479,571 - 55,479,795RGDNCBI36
Celera1049,072,475 - 49,072,699RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,790,992 - 49,791,216UniSTS
REN7765  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,809,768 - 55,810,036UniSTSGRCh37
Build 361055,479,774 - 55,480,042RGDNCBI36
Celera1049,072,678 - 49,072,946RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,791,195 - 49,791,463UniSTS
REN7766  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,809,924 - 55,810,189UniSTSGRCh37
Build 361055,479,930 - 55,480,195RGDNCBI36
Celera1049,072,834 - 49,073,099RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,791,351 - 49,791,616UniSTS
REN7767  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,810,165 - 55,810,415UniSTSGRCh37
Build 361055,480,171 - 55,480,421RGDNCBI36
Celera1049,073,075 - 49,073,325RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,791,592 - 49,791,842UniSTS
REN7768  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,810,352 - 55,810,613UniSTSGRCh37
Build 361055,480,358 - 55,480,619RGDNCBI36
Celera1049,073,262 - 49,073,523RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,791,779 - 49,792,040UniSTS
REN7769  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,810,505 - 55,810,752UniSTSGRCh37
Build 361055,480,511 - 55,480,758RGDNCBI36
Celera1049,073,415 - 49,073,662RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,791,932 - 49,792,179UniSTS
REN7770  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,810,728 - 55,810,970UniSTSGRCh37
Build 361055,480,734 - 55,480,976RGDNCBI36
Celera1049,073,638 - 49,073,880RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,792,155 - 49,792,397UniSTS
REN7771  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,810,960 - 55,811,212UniSTSGRCh37
Build 361055,480,966 - 55,481,218RGDNCBI36
Celera1049,073,870 - 49,074,122RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,792,387 - 49,792,639UniSTS
REN7772  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,811,150 - 55,811,399UniSTSGRCh37
Build 361055,481,156 - 55,481,405RGDNCBI36
Celera1049,074,060 - 49,074,309RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,792,577 - 49,792,826UniSTS
REN7773  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,811,357 - 55,811,606UniSTSGRCh37
Build 361055,481,363 - 55,481,612RGDNCBI36
Celera1049,074,267 - 49,074,516RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,792,784 - 49,793,033UniSTS
REN7774  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,811,581 - 55,811,831UniSTSGRCh37
Build 361055,481,587 - 55,481,837RGDNCBI36
Celera1049,074,491 - 49,074,741RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,793,008 - 49,793,258UniSTS
REN7775  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,811,805 - 55,812,033UniSTSGRCh37
Build 361055,481,811 - 55,482,039RGDNCBI36
Celera1049,074,715 - 49,074,943RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,793,232 - 49,793,460UniSTS
REN7776  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,812,011 - 55,812,238UniSTSGRCh37
Build 361055,482,017 - 55,482,244RGDNCBI36
Celera1049,074,921 - 49,075,148RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,793,438 - 49,793,665UniSTS
REN7777  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,812,202 - 55,812,426UniSTSGRCh37
GRCh37751,627,521 - 51,627,746UniSTSGRCh37
Build 36751,595,015 - 51,595,240RGDNCBI36
Celera751,685,740 - 51,685,965RGD
Celera1049,075,112 - 49,075,336UniSTS
Cytogenetic Map10q21.1UniSTS
HuRef751,475,602 - 51,475,827UniSTS
HuRef1049,793,629 - 49,793,853UniSTS
CRA_TCAGchr7v2751,633,038 - 51,633,263UniSTS
REN7778  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,812,404 - 55,812,671UniSTSGRCh37
Build 361055,482,410 - 55,482,677RGDNCBI36
Celera1049,075,314 - 49,075,581RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,793,831 - 49,794,098UniSTS
REN7779  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,812,661 - 55,812,918UniSTSGRCh37
Build 361055,482,667 - 55,482,924RGDNCBI36
Celera1049,075,571 - 49,075,828RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,794,088 - 49,794,345UniSTS
REN7780  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,812,891 - 55,813,148UniSTSGRCh37
Build 361055,482,897 - 55,483,154RGDNCBI36
Celera1049,075,801 - 49,076,058RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,794,318 - 49,794,575UniSTS
REN7781  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,813,127 - 55,813,359UniSTSGRCh37
Build 361055,483,133 - 55,483,365RGDNCBI36
Celera1049,076,037 - 49,076,269RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,794,554 - 49,794,786UniSTS
REN7782  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,813,334 - 55,813,582UniSTSGRCh37
Build 361055,483,340 - 55,483,588RGDNCBI36
Celera1049,076,244 - 49,076,492RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,794,761 - 49,795,009UniSTS
REN7783  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,813,558 - 55,813,816UniSTSGRCh37
Build 361055,483,564 - 55,483,822RGDNCBI36
Celera1049,076,468 - 49,076,726RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,794,985 - 49,795,243UniSTS
REN7784  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,813,769 - 55,814,019UniSTSGRCh37
Build 361055,483,775 - 55,484,025RGDNCBI36
Celera1049,076,679 - 49,076,929RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,795,196 - 49,795,446UniSTS
REN7785  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,813,992 - 55,814,252UniSTSGRCh37
Build 361055,483,998 - 55,484,258RGDNCBI36
Celera1049,076,902 - 49,077,162RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,795,419 - 49,795,679UniSTS
REN7786  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,814,236 - 55,814,488UniSTSGRCh37
Build 361055,484,242 - 55,484,494RGDNCBI36
Celera1049,077,146 - 49,077,398RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,795,663 - 49,795,915UniSTS
REN7787  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,814,459 - 55,814,710UniSTSGRCh37
Build 361055,484,465 - 55,484,716RGDNCBI36
Celera1049,077,369 - 49,077,620RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,795,886 - 49,796,137UniSTS
REN7788  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,814,695 - 55,814,922UniSTSGRCh37
Build 361055,484,701 - 55,484,928RGDNCBI36
Celera1049,077,605 - 49,077,832RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,796,122 - 49,796,349UniSTS
REN7789  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,814,884 - 55,815,118UniSTSGRCh37
Build 361055,484,890 - 55,485,124RGDNCBI36
Celera1049,077,794 - 49,078,028RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,796,311 - 49,796,545UniSTS
REN7790  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,815,094 - 55,815,360UniSTSGRCh37
Build 361055,485,100 - 55,485,366RGDNCBI36
Celera1049,078,004 - 49,078,270RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,796,521 - 49,796,787UniSTS
REN7791  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,815,258 - 55,815,514UniSTSGRCh37
Build 361055,485,264 - 55,485,520RGDNCBI36
Celera1049,078,168 - 49,078,424RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,796,685 - 49,796,943UniSTS
REN7792  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,815,496 - 55,815,726UniSTSGRCh37
Build 361055,485,502 - 55,485,732RGDNCBI36
Celera1049,078,406 - 49,078,636RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,796,925 - 49,797,155UniSTS
REN7793  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,815,723 - 55,815,975UniSTSGRCh37
Build 361055,485,729 - 55,485,981RGDNCBI36
Celera1049,078,633 - 49,078,885RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,797,152 - 49,797,404UniSTS
REN7794  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,815,843 - 55,816,069UniSTSGRCh37
Build 361055,485,849 - 55,486,075RGDNCBI36
Celera1049,078,753 - 49,078,979RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,797,272 - 49,797,498UniSTS
REN7795  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,816,004 - 55,816,228UniSTSGRCh37
Build 361055,486,010 - 55,486,234RGDNCBI36
Celera1049,078,914 - 49,079,138RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,797,433 - 49,797,657UniSTS
REN7796  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,816,481 - 55,816,744UniSTSGRCh37
Build 361055,486,487 - 55,486,750RGDNCBI36
Celera1049,079,391 - 49,079,654RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,797,910 - 49,798,173UniSTS
REN7797  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,816,718 - 55,816,950UniSTSGRCh37
Build 361055,486,724 - 55,486,956RGDNCBI36
Celera1049,079,628 - 49,079,860RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,798,147 - 49,798,379UniSTS
REN7798  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,816,840 - 55,817,105UniSTSGRCh37
Build 361055,486,846 - 55,487,111RGDNCBI36
Celera1049,079,750 - 49,080,015RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,798,269 - 49,798,534UniSTS
REN7799  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,817,080 - 55,817,319UniSTSGRCh37
Build 361055,487,086 - 55,487,325RGDNCBI36
Celera1049,079,990 - 49,080,229RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,798,509 - 49,798,748UniSTS
REN7800  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,817,287 - 55,817,539UniSTSGRCh37
Build 361055,487,293 - 55,487,545RGDNCBI36
Celera1049,080,197 - 49,080,449RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,798,716 - 49,798,968UniSTS
REN7801  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,817,507 - 55,817,754UniSTSGRCh37
Build 361055,487,513 - 55,487,760RGDNCBI36
Celera1049,080,417 - 49,080,664RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,798,936 - 49,799,183UniSTS
REN7802  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,817,626 - 55,817,863UniSTSGRCh37
Build 361055,487,632 - 55,487,869RGDNCBI36
Celera1049,080,536 - 49,080,773RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,799,055 - 49,799,292UniSTS
REN7804  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,817,965 - 55,818,192UniSTSGRCh37
Build 361055,487,971 - 55,488,198RGDNCBI36
Celera1049,080,875 - 49,081,102RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,799,394 - 49,799,621UniSTS
REN7805  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,818,164 - 55,818,415UniSTSGRCh37
GRCh371055,818,164 - 55,818,368UniSTSGRCh37
Build 361055,488,170 - 55,488,374RGDNCBI36
Celera1049,081,074 - 49,081,278RGD
Celera1049,081,074 - 49,081,325UniSTS
Cytogenetic Map10q21.1UniSTS
HuRef1049,799,593 - 49,799,797UniSTS
HuRef1049,799,593 - 49,799,844UniSTS
REN7806  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,818,580 - 55,818,805UniSTSGRCh37
Build 361055,488,586 - 55,488,811RGDNCBI36
Celera1049,081,490 - 49,081,715RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,800,009 - 49,800,234UniSTS
REN7807  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,818,787 - 55,819,037UniSTSGRCh37
Build 361055,488,793 - 55,489,043RGDNCBI36
Celera1049,081,697 - 49,081,947RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,800,216 - 49,800,466UniSTS
REN7808  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,819,002 - 55,819,257UniSTSGRCh37
Build 361055,489,008 - 55,489,263RGDNCBI36
Celera1049,081,912 - 49,082,167RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,800,431 - 49,800,686UniSTS
REN7809  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,819,229 - 55,819,492UniSTSGRCh37
Build 361055,489,235 - 55,489,498RGDNCBI36
Celera1049,082,139 - 49,082,402RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,800,658 - 49,800,921UniSTS
REN7810  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,819,483 - 55,819,730UniSTSGRCh37
Build 361055,489,489 - 55,489,736RGDNCBI36
Celera1049,082,393 - 49,082,640RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,800,912 - 49,801,159UniSTS
REN7811  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,819,718 - 55,819,949UniSTSGRCh37
Build 361055,489,724 - 55,489,955RGDNCBI36
Celera1049,082,628 - 49,082,859RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,801,147 - 49,801,378UniSTS
REN7812  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,819,926 - 55,820,174UniSTSGRCh37
Build 361055,489,932 - 55,490,180RGDNCBI36
Celera1049,082,836 - 49,083,084RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,801,355 - 49,801,603UniSTS
REN7813  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,820,148 - 55,820,392UniSTSGRCh37
Build 361055,490,154 - 55,490,398RGDNCBI36
Celera1049,083,058 - 49,083,302RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,801,577 - 49,801,821UniSTS
REN7814  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,820,369 - 55,820,619UniSTSGRCh37
Build 361055,490,375 - 55,490,625RGDNCBI36
Celera1049,083,279 - 49,083,529RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,801,798 - 49,802,048UniSTS
REN7815  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,820,596 - 55,820,837UniSTSGRCh37
Build 361055,490,602 - 55,490,843RGDNCBI36
Celera1049,083,506 - 49,083,747RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,802,025 - 49,802,266UniSTS
REN7816  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,820,819 - 55,821,043UniSTSGRCh37
Build 361055,490,825 - 55,491,049RGDNCBI36
Celera1049,083,729 - 49,083,953RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,802,248 - 49,802,472UniSTS
REN7817  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,821,023 - 55,821,252UniSTSGRCh37
Build 361055,491,029 - 55,491,258RGDNCBI36
Celera1049,083,933 - 49,084,162RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,802,452 - 49,802,681UniSTS
REN7818  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,821,224 - 55,821,456UniSTSGRCh37
Build 361055,491,230 - 55,491,462RGDNCBI36
Celera1049,084,134 - 49,084,366RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,802,653 - 49,802,885UniSTS
REN7819  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,821,426 - 55,821,656UniSTSGRCh37
Build 361055,491,432 - 55,491,662RGDNCBI36
Celera1049,084,336 - 49,084,565RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,802,855 - 49,803,084UniSTS
REN7820  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,821,630 - 55,821,867UniSTSGRCh37
Build 361055,491,636 - 55,491,873RGDNCBI36
Celera1049,084,539 - 49,084,776RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,803,058 - 49,803,295UniSTS
REN7821  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,821,798 - 55,822,048UniSTSGRCh37
Build 361055,491,804 - 55,492,054RGDNCBI36
Celera1049,084,707 - 49,084,957RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,803,226 - 49,803,481UniSTS
REN7822  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,822,026 - 55,822,274UniSTSGRCh37
Build 361055,492,032 - 55,492,280RGDNCBI36
Celera1049,084,935 - 49,085,183RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,803,459 - 49,803,707UniSTS
REN7823  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,822,254 - 55,822,490UniSTSGRCh37
Build 361055,492,260 - 55,492,496RGDNCBI36
Celera1049,085,163 - 49,085,399RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,803,687 - 49,803,923UniSTS
REN7824  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,822,396 - 55,822,649UniSTSGRCh37
Build 361055,492,402 - 55,492,655RGDNCBI36
Celera1049,085,305 - 49,085,557RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,803,829 - 49,804,081UniSTS
REN7825  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,822,639 - 55,822,886UniSTSGRCh37
Build 361055,492,645 - 55,492,892RGDNCBI36
Celera1049,085,547 - 49,085,794RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,804,071 - 49,804,318UniSTS
REN7826  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,822,872 - 55,823,115UniSTSGRCh37
Build 361055,492,878 - 55,493,121RGDNCBI36
Celera1049,085,780 - 49,086,023RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,804,304 - 49,804,547UniSTS
REN7827  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,823,114 - 55,823,338UniSTSGRCh37
Build 361055,493,120 - 55,493,344RGDNCBI36
Celera1049,086,022 - 49,086,246RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,804,546 - 49,804,770UniSTS
REN7828  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,823,305 - 55,823,539UniSTSGRCh37
Build 361055,493,311 - 55,493,545RGDNCBI36
Celera1049,086,213 - 49,086,447RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,804,737 - 49,804,971UniSTS
REN7829  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,823,513 - 55,823,766UniSTSGRCh37
Build 361055,493,519 - 55,493,772RGDNCBI36
Celera1049,086,421 - 49,086,674RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,804,945 - 49,805,198UniSTS
REN7830  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,823,757 - 55,824,015UniSTSGRCh37
Build 361055,493,763 - 55,494,021RGDNCBI36
Celera1049,086,665 - 49,086,923RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,805,189 - 49,805,447UniSTS
REN7831  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,823,944 - 55,824,188UniSTSGRCh37
Build 361055,493,950 - 55,494,194RGDNCBI36
Celera1049,086,852 - 49,087,096RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,805,376 - 49,805,620UniSTS
REN7832  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,824,164 - 55,824,415UniSTSGRCh37
Build 361055,494,170 - 55,494,421RGDNCBI36
Celera1049,087,072 - 49,087,323RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,805,596 - 49,805,847UniSTS
REN7833  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,824,361 - 55,824,622UniSTSGRCh37
Build 361055,494,367 - 55,494,628RGDNCBI36
Celera1049,087,269 - 49,087,530RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,805,793 - 49,806,054UniSTS
REN7834  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,824,600 - 55,824,856UniSTSGRCh37
Build 361055,494,606 - 55,494,862RGDNCBI36
Celera1049,087,508 - 49,087,764RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,806,032 - 49,806,288UniSTS
REN7835  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,824,855 - 55,825,095UniSTSGRCh37
Build 361055,494,861 - 55,495,101RGDNCBI36
Celera1049,087,763 - 49,088,003RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,806,287 - 49,806,527UniSTS
REN7836  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,825,073 - 55,825,328UniSTSGRCh37
Build 361055,495,079 - 55,495,334RGDNCBI36
Celera1049,087,981 - 49,088,236RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,806,505 - 49,806,760UniSTS
REN7837  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,825,321 - 55,825,571UniSTSGRCh37
Build 361055,495,327 - 55,495,577RGDNCBI36
Celera1049,088,229 - 49,088,479RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,806,753 - 49,807,003UniSTS
REN7838  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,825,548 - 55,825,807UniSTSGRCh37
Build 361055,495,554 - 55,495,813RGDNCBI36
Celera1049,088,456 - 49,088,715RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,806,980 - 49,807,239UniSTS
REN7839  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,825,803 - 55,826,038UniSTSGRCh37
Build 361055,495,809 - 55,496,044RGDNCBI36
Celera1049,088,711 - 49,088,946RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,807,235 - 49,807,470UniSTS
REN7840  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,825,984 - 55,826,208UniSTSGRCh37
Build 361055,495,990 - 55,496,214RGDNCBI36
Celera1049,088,892 - 49,089,116RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,807,416 - 49,807,640UniSTS
REN7841  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,826,183 - 55,826,424UniSTSGRCh37
Build 361055,496,189 - 55,496,430RGDNCBI36
Celera1049,089,091 - 49,089,332RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,807,615 - 49,807,856UniSTS
REN7842  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,826,402 - 55,826,653UniSTSGRCh37
Build 361055,496,408 - 55,496,659RGDNCBI36
Celera1049,089,310 - 49,089,561RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,807,834 - 49,808,085UniSTS
REN7843  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,826,623 - 55,826,863UniSTSGRCh37
Build 361055,496,629 - 55,496,869RGDNCBI36
Celera1049,089,531 - 49,089,771RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,808,055 - 49,808,295UniSTS
REN7844  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,826,855 - 55,827,093UniSTSGRCh37
Build 361055,496,861 - 55,497,099RGDNCBI36
Celera1049,089,763 - 49,090,001RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,808,287 - 49,808,525UniSTS
REN7845  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,827,066 - 55,827,322UniSTSGRCh37
Build 361055,497,072 - 55,497,328RGDNCBI36
Celera1049,089,974 - 49,090,230RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,808,498 - 49,808,754UniSTS
REN7846  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,827,307 - 55,827,566UniSTSGRCh37
Build 361055,497,313 - 55,497,572RGDNCBI36
Celera1049,090,215 - 49,090,474RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,808,739 - 49,808,998UniSTS
REN7847  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,827,561 - 55,827,798UniSTSGRCh37
Build 361055,497,567 - 55,497,804RGDNCBI36
Celera1049,090,469 - 49,090,706RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,808,993 - 49,809,230UniSTS
REN7848  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,827,775 - 55,828,003UniSTSGRCh37
Build 361055,497,781 - 55,498,009RGDNCBI36
Celera1049,090,683 - 49,090,911RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,809,207 - 49,809,435UniSTS
REN7849  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,827,981 - 55,828,217UniSTSGRCh37
Build 361055,497,987 - 55,498,223RGDNCBI36
Celera1049,090,889 - 49,091,125RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,809,413 - 49,809,649UniSTS
REN7850  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,828,158 - 55,828,421UniSTSGRCh37
Build 361055,498,164 - 55,498,427RGDNCBI36
Celera1049,091,066 - 49,091,329RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,809,590 - 49,809,853UniSTS
REN7851  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,828,398 - 55,828,655UniSTSGRCh37
Build 361055,498,404 - 55,498,661RGDNCBI36
Celera1049,091,306 - 49,091,563RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,809,830 - 49,810,087UniSTS
REN7852  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,828,586 - 55,828,856UniSTSGRCh37
Build 361055,498,592 - 55,498,862RGDNCBI36
Celera1049,091,494 - 49,091,764RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,810,018 - 49,810,288UniSTS
REN7853  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,828,838 - 55,829,094UniSTSGRCh37
Build 361055,498,844 - 55,499,100RGDNCBI36
Celera1049,091,746 - 49,092,002RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,810,270 - 49,810,526UniSTS
REN7854  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,829,003 - 55,829,247UniSTSGRCh37
Build 361055,499,009 - 55,499,253RGDNCBI36
Celera1049,091,911 - 49,092,155RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,810,435 - 49,810,679UniSTS
REN7855  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,829,211 - 55,829,435UniSTSGRCh37
Build 361055,499,217 - 55,499,441RGDNCBI36
Celera1049,092,119 - 49,092,343RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,810,643 - 49,810,867UniSTS
REN7856  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,829,376 - 55,829,617UniSTSGRCh37
Build 361055,499,382 - 55,499,623RGDNCBI36
Celera1049,092,284 - 49,092,525RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,810,808 - 49,811,049UniSTS
REN7857  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,829,554 - 55,829,781UniSTSGRCh37
Build 361055,499,560 - 55,499,787RGDNCBI36
Celera1049,092,462 - 49,092,689RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,810,986 - 49,811,213UniSTS
REN7858  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,829,735 - 55,829,962UniSTSGRCh37
Build 361055,499,741 - 55,499,968RGDNCBI36
Celera1049,092,643 - 49,092,870RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,811,167 - 49,811,394UniSTS
REN7859  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,830,185 - 55,830,428UniSTSGRCh37
Build 361055,500,191 - 55,500,434RGDNCBI36
Celera1049,093,093 - 49,093,336RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,811,617 - 49,811,860UniSTS
REN7860  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,830,551 - 55,830,775UniSTSGRCh37
Build 361055,500,557 - 55,500,781RGDNCBI36
Celera1049,093,459 - 49,093,683RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,811,983 - 49,812,207UniSTS
REN7861  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,830,755 - 55,831,021UniSTSGRCh37
Build 361055,500,761 - 55,501,027RGDNCBI36
Celera1049,093,663 - 49,093,929RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,812,187 - 49,812,453UniSTS
REN7862  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,830,983 - 55,831,209UniSTSGRCh37
Build 361055,500,989 - 55,501,215RGDNCBI36
Celera1049,093,891 - 49,094,117RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,812,415 - 49,812,641UniSTS
REN7863  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,831,185 - 55,831,450UniSTSGRCh37
Build 361055,501,191 - 55,501,456RGDNCBI36
Celera1049,094,093 - 49,094,358RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,812,617 - 49,812,882UniSTS
REN7864  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,831,383 - 55,831,617UniSTSGRCh37
Build 361055,501,389 - 55,501,623RGDNCBI36
Celera1049,094,291 - 49,094,525RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,812,815 - 49,813,049UniSTS
REN7865  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,831,587 - 55,831,848UniSTSGRCh37
Build 361055,501,593 - 55,501,854RGDNCBI36
Celera1049,094,495 - 49,094,756RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,813,019 - 49,813,280UniSTS
REN7866  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,831,844 - 55,832,092UniSTSGRCh37
Build 361055,501,850 - 55,502,098RGDNCBI36
Celera1049,094,752 - 49,095,000RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,813,276 - 49,813,524UniSTS
REN7867  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,832,069 - 55,832,321UniSTSGRCh37
Build 361055,502,075 - 55,502,327RGDNCBI36
Celera1049,094,977 - 49,095,229RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,813,501 - 49,813,753UniSTS
REN7868  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,832,303 - 55,832,555UniSTSGRCh37
Build 361055,502,309 - 55,502,561RGDNCBI36
Celera1049,095,211 - 49,095,463RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,813,735 - 49,813,987UniSTS
REN7869  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,832,532 - 55,832,780UniSTSGRCh37
Build 361055,502,538 - 55,502,786RGDNCBI36
Celera1049,095,440 - 49,095,688RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,813,964 - 49,814,212UniSTS
REN7870  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,832,663 - 55,832,933UniSTSGRCh37
Build 361055,502,669 - 55,502,939RGDNCBI36
Celera1049,095,571 - 49,095,841RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,814,095 - 49,814,365UniSTS
REN7871  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,833,182 - 55,833,417UniSTSGRCh37
Build 361055,503,188 - 55,503,423RGDNCBI36
Celera1049,096,090 - 49,096,325RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,814,614 - 49,814,849UniSTS
REN7872  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,833,409 - 55,833,657UniSTSGRCh37
Build 361055,503,415 - 55,503,663RGDNCBI36
Celera1049,096,317 - 49,096,565RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,814,841 - 49,815,089UniSTS
REN7873  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,833,634 - 55,833,882UniSTSGRCh37
Build 361055,503,640 - 55,503,888RGDNCBI36
Celera1049,096,542 - 49,096,790RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,815,066 - 49,815,314UniSTS
REN7874  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,833,866 - 55,834,133UniSTSGRCh37
Build 361055,503,872 - 55,504,139RGDNCBI36
Celera1049,096,774 - 49,097,041RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,815,298 - 49,815,565UniSTS
REN7875  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,834,126 - 55,834,377UniSTSGRCh37
Build 361055,504,132 - 55,504,383RGDNCBI36
Celera1049,097,034 - 49,097,285RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,815,558 - 49,815,809UniSTS
REN7876  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,834,288 - 55,834,542UniSTSGRCh37
Build 361055,504,294 - 55,504,548RGDNCBI36
Celera1049,097,196 - 49,097,450RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,815,720 - 49,815,974UniSTS
REN7877  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,834,518 - 55,834,784UniSTSGRCh37
Build 361055,504,524 - 55,504,790RGDNCBI36
Celera1049,097,426 - 49,097,692RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,815,950 - 49,816,216UniSTS
REN7878  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,835,234 - 55,835,473UniSTSGRCh37
Build 361055,505,240 - 55,505,479RGDNCBI36
Celera1049,098,142 - 49,098,381RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,816,665 - 49,816,904UniSTS
REN7879  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,835,449 - 55,835,701UniSTSGRCh37
Build 361055,505,455 - 55,505,707RGDNCBI36
Celera1049,098,357 - 49,098,609RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,816,880 - 49,817,132UniSTS
REN7880  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,835,592 - 55,835,822UniSTSGRCh37
Build 361055,505,598 - 55,505,828RGDNCBI36
Celera1049,098,500 - 49,098,730RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,817,023 - 49,817,253UniSTS
REN7881  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,835,796 - 55,836,058UniSTSGRCh37
Build 361055,505,802 - 55,506,064RGDNCBI36
Celera1049,098,704 - 49,098,966RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,817,227 - 49,817,489UniSTS
REN7882  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,836,033 - 55,836,282UniSTSGRCh37
Build 361055,506,039 - 55,506,288RGDNCBI36
Celera1049,098,941 - 49,099,190RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,817,464 - 49,817,713UniSTS
REN7883  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,836,263 - 55,836,528UniSTSGRCh37
Build 361055,506,269 - 55,506,534RGDNCBI36
Celera1049,099,171 - 49,099,436RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,817,694 - 49,817,959UniSTS
REN7884  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,836,495 - 55,836,719UniSTSGRCh37
Build 361055,506,501 - 55,506,725RGDNCBI36
Celera1049,099,403 - 49,099,627RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,817,926 - 49,818,150UniSTS
REN7885  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,836,690 - 55,836,948UniSTSGRCh37
Build 361055,506,696 - 55,506,954RGDNCBI36
Celera1049,099,598 - 49,099,856RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,818,121 - 49,818,379UniSTS
REN7886  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,836,883 - 55,837,132UniSTSGRCh37
Build 361055,506,889 - 55,507,138RGDNCBI36
Celera1049,099,791 - 49,100,040RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,818,314 - 49,818,563UniSTS
REN7887  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,837,113 - 55,837,340UniSTSGRCh37
Build 361055,507,119 - 55,507,346RGDNCBI36
Celera1049,100,021 - 49,100,248RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,818,544 - 49,818,771UniSTS
REN7888  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,837,311 - 55,837,547UniSTSGRCh37
Build 361055,507,317 - 55,507,553RGDNCBI36
Celera1049,100,219 - 49,100,455RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,818,742 - 49,818,978UniSTS
REN7889  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,837,680 - 55,837,938UniSTSGRCh37
Build 361055,507,686 - 55,507,944RGDNCBI36
Celera1049,100,588 - 49,100,846RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,819,111 - 49,819,369UniSTS
REN7890  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,837,912 - 55,838,140UniSTSGRCh37
Build 361055,507,918 - 55,508,146RGDNCBI36
Celera1049,100,820 - 49,101,048RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,819,343 - 49,819,571UniSTS
REN7891  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,838,113 - 55,838,353UniSTSGRCh37
Build 361055,508,119 - 55,508,359RGDNCBI36
Celera1049,101,021 - 49,101,261RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,819,544 - 49,819,784UniSTS
REN7892  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,838,330 - 55,838,586UniSTSGRCh37
Build 361055,508,336 - 55,508,592RGDNCBI36
Celera1049,101,238 - 49,101,494RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,819,761 - 49,820,017UniSTS
REN7893  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,838,562 - 55,838,812UniSTSGRCh37
Build 361055,508,568 - 55,508,818RGDNCBI36
Celera1049,101,470 - 49,101,720RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,819,993 - 49,820,243UniSTS
REN7894  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,838,794 - 55,839,048UniSTSGRCh37
Build 361055,508,800 - 55,509,054RGDNCBI36
Celera1049,101,702 - 49,101,956RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,820,225 - 49,820,479UniSTS
REN7895  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,839,008 - 55,839,247UniSTSGRCh37
Build 361055,509,014 - 55,509,253RGDNCBI36
Celera1049,101,916 - 49,102,155RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,820,439 - 49,820,678UniSTS
REN7896  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,839,217 - 55,839,461UniSTSGRCh37
Build 361055,509,223 - 55,509,467RGDNCBI36
Celera1049,102,125 - 49,102,369RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,820,648 - 49,820,892UniSTS
REN7897  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,839,445 - 55,839,718UniSTSGRCh37
Build 361055,509,451 - 55,509,724RGDNCBI36
Celera1049,102,353 - 49,102,626RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,820,876 - 49,821,149UniSTS
REN7898  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,839,692 - 55,839,918UniSTSGRCh37
Build 361055,509,698 - 55,509,924RGDNCBI36
Celera1049,102,600 - 49,102,826RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,821,123 - 49,821,349UniSTS
REN7899  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,839,893 - 55,840,140UniSTSGRCh37
Build 361055,509,899 - 55,510,146RGDNCBI36
Celera1049,102,801 - 49,103,048RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,821,324 - 49,821,571UniSTS
REN7900  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,840,120 - 55,840,386UniSTSGRCh37
Build 361055,510,126 - 55,510,392RGDNCBI36
Celera1049,103,028 - 49,103,294RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,821,551 - 49,821,817UniSTS
REN7901  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,840,368 - 55,840,620UniSTSGRCh37
Build 361055,510,374 - 55,510,626RGDNCBI36
Celera1049,103,276 - 49,103,528RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,821,799 - 49,822,051UniSTS
REN7902  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,840,597 - 55,840,864UniSTSGRCh37
Build 361055,510,603 - 55,510,870RGDNCBI36
Celera1049,103,505 - 49,103,772RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,822,028 - 49,822,295UniSTS
REN7903  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,840,842 - 55,841,068UniSTSGRCh37
Build 361055,510,848 - 55,511,074RGDNCBI36
Celera1049,103,750 - 49,103,976RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,822,273 - 49,822,499UniSTS
REN7904  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,841,035 - 55,841,290UniSTSGRCh37
Build 361055,511,041 - 55,511,296RGDNCBI36
Celera1049,103,943 - 49,104,198RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,822,466 - 49,822,725UniSTS
REN7905  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,841,258 - 55,841,482UniSTSGRCh37
Build 361055,511,264 - 55,511,488RGDNCBI36
Celera1049,104,166 - 49,104,390RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,822,693 - 49,822,917UniSTS
REN7906  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,841,456 - 55,841,708UniSTSGRCh37
Build 361055,511,462 - 55,511,714RGDNCBI36
Celera1049,104,364 - 49,104,616RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,822,891 - 49,823,143UniSTS
REN7907  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,841,673 - 55,841,897UniSTSGRCh37
Build 361055,511,679 - 55,511,903RGDNCBI36
Celera1049,104,581 - 49,104,805RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,823,108 - 49,823,332UniSTS
REN7908  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,841,881 - 55,842,144UniSTSGRCh37
Build 361055,511,887 - 55,512,150RGDNCBI36
Celera1049,104,789 - 49,105,052RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,823,316 - 49,823,579UniSTS
REN7909  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,842,115 - 55,842,364UniSTSGRCh37
Build 361055,512,121 - 55,512,370RGDNCBI36
Celera1049,105,023 - 49,105,272RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,823,550 - 49,823,799UniSTS
REN7910  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,842,339 - 55,842,566UniSTSGRCh37
Build 361055,512,345 - 55,512,572RGDNCBI36
Celera1049,105,247 - 49,105,474RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,823,774 - 49,824,001UniSTS
REN7911  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,842,536 - 55,842,792UniSTSGRCh37
Build 361055,512,542 - 55,512,798RGDNCBI36
Celera1049,105,444 - 49,105,700RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,823,971 - 49,824,227UniSTS
REN7912  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,842,692 - 55,842,944UniSTSGRCh37
Build 361055,512,698 - 55,512,950RGDNCBI36
Celera1049,105,600 - 49,105,852RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,824,127 - 49,824,379UniSTS
REN7913  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,842,937 - 55,843,193UniSTSGRCh37
Build 361055,512,943 - 55,513,199RGDNCBI36
Celera1049,105,845 - 49,106,101RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,824,372 - 49,824,628UniSTS
REN7914  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,843,188 - 55,843,435UniSTSGRCh37
Build 361055,513,194 - 55,513,441RGDNCBI36
Celera1049,106,096 - 49,106,343RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,824,623 - 49,824,870UniSTS
REN7915  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,843,414 - 55,843,652UniSTSGRCh37
Build 361055,513,420 - 55,513,658RGDNCBI36
Celera1049,106,322 - 49,106,560RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,824,849 - 49,825,087UniSTS
REN7916  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,844,033 - 55,844,287UniSTSGRCh37
Build 361055,514,039 - 55,514,293RGDNCBI36
Celera1049,106,941 - 49,107,195RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,825,466 - 49,825,720UniSTS
REN7917  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,844,184 - 55,844,433UniSTSGRCh37
Build 361055,514,190 - 55,514,439RGDNCBI36
Celera1049,107,092 - 49,107,341RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,825,617 - 49,825,866UniSTS
REN7918  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,844,423 - 55,844,666UniSTSGRCh37
Build 361055,514,429 - 55,514,672RGDNCBI36
Celera1049,107,331 - 49,107,574RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,825,856 - 49,826,099UniSTS
REN7919  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,844,641 - 55,844,902UniSTSGRCh37
Build 361055,514,647 - 55,514,908RGDNCBI36
Celera1049,107,549 - 49,107,810RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,826,074 - 49,826,335UniSTS
REN7920  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,844,879 - 55,845,128UniSTSGRCh37
Build 361055,514,885 - 55,515,134RGDNCBI36
Celera1049,107,787 - 49,108,036RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,826,312 - 49,826,561UniSTS
REN7921  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,845,105 - 55,845,329UniSTSGRCh37
Build 361055,515,111 - 55,515,335RGDNCBI36
Celera1049,108,013 - 49,108,237RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,826,538 - 49,826,762UniSTS
REN7922  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,845,305 - 55,845,553UniSTSGRCh37
Build 361055,515,311 - 55,515,559RGDNCBI36
Celera1049,108,213 - 49,108,461RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,826,738 - 49,826,986UniSTS
REN7923  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,845,519 - 55,845,781UniSTSGRCh37
Build 361055,515,525 - 55,515,787RGDNCBI36
Celera1049,108,427 - 49,108,689RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,826,952 - 49,827,214UniSTS
REN7924  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,845,742 - 55,845,966UniSTSGRCh37
Build 361055,515,748 - 55,515,972RGDNCBI36
Celera1049,108,650 - 49,108,874RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,827,175 - 49,827,399UniSTS
REN7925  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,845,941 - 55,846,188UniSTSGRCh37
Build 361055,515,947 - 55,516,194RGDNCBI36
Celera1049,108,849 - 49,109,096RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,827,374 - 49,827,621UniSTS
REN7926  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,846,183 - 55,846,437UniSTSGRCh37
Build 361055,516,189 - 55,516,443RGDNCBI36
Celera1049,109,091 - 49,109,345RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,827,616 - 49,827,870UniSTS
REN7927  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,846,429 - 55,846,673UniSTSGRCh37
Build 361055,516,435 - 55,516,679RGDNCBI36
Celera1049,109,337 - 49,109,581RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,827,862 - 49,828,106UniSTS
REN7928  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,846,662 - 55,846,890UniSTSGRCh37
Build 361055,516,668 - 55,516,896RGDNCBI36
Celera1049,109,570 - 49,109,798RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,828,095 - 49,828,323UniSTS
REN7929  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,846,859 - 55,847,106UniSTSGRCh37
Build 361055,516,865 - 55,517,112RGDNCBI36
Celera1049,109,767 - 49,110,014RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,828,292 - 49,828,539UniSTS
REN7930  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,847,061 - 55,847,303UniSTSGRCh37
Build 361055,517,067 - 55,517,309RGDNCBI36
Celera1049,109,969 - 49,110,211RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,828,494 - 49,828,736UniSTS
REN7931  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,847,284 - 55,847,547UniSTSGRCh37
Build 361055,517,290 - 55,517,553RGDNCBI36
Celera1049,110,192 - 49,110,455RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,828,717 - 49,828,980UniSTS
REN7932  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,847,521 - 55,847,772UniSTSGRCh37
Build 361055,517,527 - 55,517,778RGDNCBI36
Celera1049,110,429 - 49,110,680RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,828,954 - 49,829,205UniSTS
REN7933  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,847,709 - 55,847,958UniSTSGRCh37
Build 361055,517,715 - 55,517,964RGDNCBI36
Celera1049,110,617 - 49,110,866RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,829,142 - 49,829,391UniSTS
REN7934  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,847,895 - 55,848,119UniSTSGRCh37
Build 361055,517,901 - 55,518,125RGDNCBI36
Celera1049,110,803 - 49,111,027RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,829,328 - 49,829,552UniSTS
REN7935  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,848,094 - 55,848,357UniSTSGRCh37
Build 361055,518,100 - 55,518,363RGDNCBI36
Celera1049,111,002 - 49,111,265RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,829,527 - 49,829,790UniSTS
REN7936  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,848,334 - 55,848,582UniSTSGRCh37
Build 361055,518,340 - 55,518,588RGDNCBI36
Celera1049,111,242 - 49,111,490RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,829,767 - 49,830,015UniSTS
REN7937  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,848,518 - 55,848,767UniSTSGRCh37
Build 361055,518,524 - 55,518,773RGDNCBI36
Celera1049,111,426 - 49,111,675RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,829,951 - 49,830,200UniSTS
REN7938  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,848,739 - 55,848,989UniSTSGRCh37
Build 361055,518,745 - 55,518,995RGDNCBI36
Celera1049,111,647 - 49,111,897RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,830,172 - 49,830,422UniSTS
REN7939  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,848,966 - 55,849,203UniSTSGRCh37
Build 361055,518,972 - 55,519,209RGDNCBI36
Celera1049,111,874 - 49,112,111RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,830,399 - 49,830,636UniSTS
REN7940  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,849,200 - 55,849,433UniSTSGRCh37
Build 361055,519,206 - 55,519,439RGDNCBI36
Celera1049,112,108 - 49,112,341RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,830,633 - 49,830,866UniSTS
REN7941  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,849,413 - 55,849,673UniSTSGRCh37
Build 361055,519,419 - 55,519,679RGDNCBI36
Celera1049,112,321 - 49,112,581RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,830,846 - 49,831,106UniSTS
REN7942  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,849,663 - 55,849,923UniSTSGRCh37
Build 361055,519,669 - 55,519,929RGDNCBI36
Celera1049,112,571 - 49,112,831RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,831,096 - 49,831,356UniSTS
REN7943  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,849,854 - 55,850,127UniSTSGRCh37
Build 361055,519,860 - 55,520,133RGDNCBI36
Celera1049,112,762 - 49,113,035RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,831,287 - 49,831,560UniSTS
REN7944  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,850,028 - 55,850,264UniSTSGRCh37
Build 361055,520,034 - 55,520,270RGDNCBI36
Celera1049,112,936 - 49,113,172RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,831,461 - 49,831,697UniSTS
REN7945  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,850,254 - 55,850,528UniSTSGRCh37
Build 361055,520,260 - 55,520,534RGDNCBI36
Celera1049,113,162 - 49,113,436RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,831,687 - 49,831,960UniSTS
REN7946  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,850,424 - 55,850,649UniSTSGRCh37
Build 361055,520,430 - 55,520,655RGDNCBI36
Celera1049,113,332 - 49,113,557RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,831,856 - 49,832,081UniSTS
REN7947  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,850,618 - 55,850,872UniSTSGRCh37
Build 361055,520,624 - 55,520,878RGDNCBI36
Celera1049,113,526 - 49,113,780RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,832,050 - 49,832,304UniSTS
REN7948  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,850,849 - 55,851,118UniSTSGRCh37
Build 361055,520,855 - 55,521,124RGDNCBI36
Celera1049,113,757 - 49,114,026RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,832,281 - 49,832,550UniSTS
REN7949  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,851,101 - 55,851,359UniSTSGRCh37
Build 361055,521,107 - 55,521,365RGDNCBI36
Celera1049,114,009 - 49,114,267RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,832,533 - 49,832,791UniSTS
REN7950  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,851,335 - 55,851,564UniSTSGRCh37
Build 361055,521,341 - 55,521,570RGDNCBI36
Celera1049,114,243 - 49,114,472RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,832,767 - 49,832,996UniSTS
REN7951  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,851,535 - 55,851,782UniSTSGRCh37
Build 361055,521,541 - 55,521,788RGDNCBI36
Celera1049,114,443 - 49,114,690RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,832,967 - 49,833,214UniSTS
REN7952  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,851,759 - 55,851,993UniSTSGRCh37
Build 361055,521,765 - 55,521,999RGDNCBI36
Celera1049,114,667 - 49,114,901RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,833,191 - 49,833,425UniSTS
REN7953  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,851,970 - 55,852,194UniSTSGRCh37
Build 361055,521,976 - 55,522,200RGDNCBI36
Celera1049,114,878 - 49,115,102RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,833,402 - 49,833,626UniSTS
REN7954  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,852,169 - 55,852,434UniSTSGRCh37
Build 361055,522,175 - 55,522,440RGDNCBI36
Celera1049,115,077 - 49,115,342RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,833,601 - 49,833,866UniSTS
REN7955  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,852,408 - 55,852,659UniSTSGRCh37
Build 361055,522,414 - 55,522,665RGDNCBI36
Celera1049,115,316 - 49,115,567RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,833,840 - 49,834,091UniSTS
REN7956  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,852,635 - 55,852,886UniSTSGRCh37
Build 361055,522,641 - 55,522,892RGDNCBI36
Celera1049,115,543 - 49,115,794RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,834,067 - 49,834,318UniSTS
REN7957  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,852,874 - 55,853,098UniSTSGRCh37
Build 361055,522,880 - 55,523,104RGDNCBI36
Celera1049,115,782 - 49,116,006RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,834,306 - 49,834,530UniSTS
REN7958  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,853,095 - 55,853,363UniSTSGRCh37
Build 361055,523,101 - 55,523,369RGDNCBI36
Celera1049,116,003 - 49,116,271RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,834,527 - 49,834,795UniSTS
REN7959  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,853,338 - 55,853,562UniSTSGRCh37
Build 361055,523,344 - 55,523,568RGDNCBI36
Celera1049,116,246 - 49,116,470RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,834,770 - 49,834,994UniSTS
REN7960  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,853,534 - 55,853,800UniSTSGRCh37
Build 361055,523,540 - 55,523,806RGDNCBI36
Celera1049,116,442 - 49,116,708RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,834,966 - 49,835,232UniSTS
REN7961  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,853,782 - 55,854,037UniSTSGRCh37
Build 361055,523,788 - 55,524,043RGDNCBI36
Celera1049,116,690 - 49,116,945RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,835,214 - 49,835,469UniSTS
REN7962  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,854,015 - 55,854,265UniSTSGRCh37
Build 361055,524,021 - 55,524,271RGDNCBI36
Celera1049,116,923 - 49,117,173RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,835,447 - 49,835,697UniSTS
REN7963  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,854,242 - 55,854,497UniSTSGRCh37
Build 361055,524,248 - 55,524,503RGDNCBI36
Celera1049,117,150 - 49,117,405RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,835,674 - 49,835,929UniSTS
REN7964  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,854,470 - 55,854,718UniSTSGRCh37
Build 361055,524,476 - 55,524,724RGDNCBI36
Celera1049,117,378 - 49,117,626RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,835,902 - 49,836,150UniSTS
REN7965  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,854,694 - 55,854,963UniSTSGRCh37
Build 361055,524,700 - 55,524,969RGDNCBI36
Celera1049,117,602 - 49,117,871RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,836,126 - 49,836,395UniSTS
REN7966  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,854,940 - 55,855,181UniSTSGRCh37
Build 361055,524,946 - 55,525,187RGDNCBI36
Celera1049,117,848 - 49,118,089RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,836,372 - 49,836,613UniSTS
REN7967  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,855,154 - 55,855,405UniSTSGRCh37
Build 361055,525,160 - 55,525,411RGDNCBI36
Celera1049,118,062 - 49,118,313RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,836,586 - 49,836,837UniSTS
REN7968  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,855,393 - 55,855,646UniSTSGRCh37
Build 361055,525,399 - 55,525,652RGDNCBI36
Celera1049,118,301 - 49,118,554RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,836,825 - 49,837,078UniSTS
REN7969  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,855,585 - 55,855,809UniSTSGRCh37
Build 361055,525,591 - 55,525,815RGDNCBI36
Celera1049,118,493 - 49,118,717RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,837,017 - 49,837,241UniSTS
REN7970  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,855,792 - 55,856,053UniSTSGRCh37
Build 361055,525,798 - 55,526,059RGDNCBI36
Celera1049,118,700 - 49,118,961RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,837,224 - 49,837,485UniSTS
REN7971  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,856,034 - 55,856,258UniSTSGRCh37
Build 361055,526,040 - 55,526,264RGDNCBI36
Celera1049,118,942 - 49,119,166RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,837,466 - 49,837,690UniSTS
REN7972  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,856,234 - 55,856,497UniSTSGRCh37
Build 361055,526,240 - 55,526,503RGDNCBI36
Celera1049,119,142 - 49,119,405RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,837,666 - 49,837,929UniSTS
REN7973  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,856,463 - 55,856,704UniSTSGRCh37
Build 361055,526,469 - 55,526,710RGDNCBI36
Celera1049,119,371 - 49,119,612RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,837,895 - 49,838,136UniSTS
REN7974  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,856,667 - 55,856,914UniSTSGRCh37
Build 361055,526,673 - 55,526,920RGDNCBI36
Celera1049,119,575 - 49,119,822RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,838,099 - 49,838,346UniSTS
REN7975  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,856,904 - 55,857,161UniSTSGRCh37
Build 361055,526,910 - 55,527,167RGDNCBI36
Celera1049,119,812 - 49,120,069RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,838,336 - 49,838,593UniSTS
REN7976  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,857,138 - 55,857,384UniSTSGRCh37
Build 361055,527,144 - 55,527,390RGDNCBI36
Celera1049,120,046 - 49,120,292RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,838,570 - 49,838,816UniSTS
REN7977  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,857,357 - 55,857,587UniSTSGRCh37
Build 361055,527,363 - 55,527,593RGDNCBI36
Celera1049,120,265 - 49,120,495RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,838,789 - 49,839,019UniSTS
REN7978  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,857,563 - 55,857,809UniSTSGRCh37
Build 361055,527,569 - 55,527,815RGDNCBI36
Celera1049,120,471 - 49,120,717RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,838,995 - 49,839,241UniSTS
REN7979  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,857,796 - 55,858,040UniSTSGRCh37
Build 361055,527,802 - 55,528,046RGDNCBI36
Celera1049,120,704 - 49,120,946RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,839,228 - 49,839,470UniSTS
REN7980  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,858,016 - 55,858,257UniSTSGRCh37
Build 361055,528,022 - 55,528,263RGDNCBI36
Celera1049,120,922 - 49,121,163RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,839,446 - 49,839,687UniSTS
REN7981  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,858,219 - 55,858,470UniSTSGRCh37
Build 361055,528,225 - 55,528,476RGDNCBI36
Celera1049,121,125 - 49,121,376RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,839,649 - 49,839,900UniSTS
REN7982  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,858,447 - 55,858,679UniSTSGRCh37
Build 361055,528,453 - 55,528,685RGDNCBI36
Celera1049,121,353 - 49,121,585RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,839,877 - 49,840,109UniSTS
REN7983  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,858,654 - 55,858,906UniSTSGRCh37
Build 361055,528,660 - 55,528,912RGDNCBI36
Celera1049,121,560 - 49,121,812RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,840,084 - 49,840,336UniSTS
REN7984  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,858,725 - 55,858,958UniSTSGRCh37
Build 361055,528,731 - 55,528,964RGDNCBI36
Celera1049,121,631 - 49,121,864RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,840,155 - 49,840,388UniSTS
REN7985  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,858,938 - 55,859,191UniSTSGRCh37
Build 361055,528,944 - 55,529,197RGDNCBI36
Celera1049,121,844 - 49,122,097RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,840,368 - 49,840,621UniSTS
REN7986  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,859,165 - 55,859,422UniSTSGRCh37
Build 361055,529,171 - 55,529,428RGDNCBI36
Celera1049,122,071 - 49,122,328RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,840,595 - 49,840,858UniSTS
REN7987  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,859,396 - 55,859,625UniSTSGRCh37
Build 361055,529,402 - 55,529,631RGDNCBI36
Celera1049,122,302 - 49,122,531RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,840,832 - 49,841,061UniSTS
REN7988  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,859,590 - 55,859,850UniSTSGRCh37
Build 361055,529,596 - 55,529,856RGDNCBI36
Celera1049,122,496 - 49,122,756RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,841,026 - 49,841,286UniSTS
REN7989  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,859,984 - 55,860,208UniSTSGRCh37
Build 361055,529,990 - 55,530,214RGDNCBI36
Celera1049,122,890 - 49,123,114RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,841,420 - 49,841,644UniSTS
REN7990  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,860,177 - 55,860,435UniSTSGRCh37
Build 361055,530,183 - 55,530,441RGDNCBI36
Celera1049,123,083 - 49,123,341RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,841,613 - 49,841,871UniSTS
REN7991  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,860,411 - 55,860,655UniSTSGRCh37
Build 361055,530,417 - 55,530,661RGDNCBI36
Celera1049,123,317 - 49,123,561RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,841,847 - 49,842,091UniSTS
REN7992  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,860,564 - 55,860,811UniSTSGRCh37
Build 361055,530,570 - 55,530,817RGDNCBI36
Celera1049,123,470 - 49,123,717RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,842,000 - 49,842,247UniSTS
REN7993  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,860,781 - 55,861,034UniSTSGRCh37
Build 361055,530,787 - 55,531,040RGDNCBI36
Celera1049,123,687 - 49,123,940RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,842,217 - 49,842,470UniSTS
REN7994  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,860,998 - 55,861,222UniSTSGRCh37
Build 361055,531,004 - 55,531,228RGDNCBI36
Celera1049,123,904 - 49,124,128RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,842,434 - 49,842,658UniSTS
REN7995  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,861,196 - 55,861,457UniSTSGRCh37
Build 361055,531,202 - 55,531,463RGDNCBI36
Celera1049,124,102 - 49,124,363RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,842,632 - 49,842,893UniSTS
REN7996  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,861,369 - 55,861,618UniSTSGRCh37
Build 361055,531,375 - 55,531,624RGDNCBI36
Celera1049,124,275 - 49,124,524RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,842,805 - 49,843,054UniSTS
REN7997  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,861,595 - 55,861,821UniSTSGRCh37
Build 361055,531,601 - 55,531,827RGDNCBI36
Celera1049,124,501 - 49,124,727RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,843,031 - 49,843,257UniSTS
REN7998  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,861,796 - 55,862,043UniSTSGRCh37
Build 361055,531,802 - 55,532,049RGDNCBI36
Celera1049,124,702 - 49,124,949RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,843,232 - 49,843,479UniSTS
REN7999  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,862,019 - 55,862,275UniSTSGRCh37
Build 361055,532,025 - 55,532,281RGDNCBI36
Celera1049,124,925 - 49,125,181RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,843,455 - 49,843,711UniSTS
REN8000  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,862,262 - 55,862,512UniSTSGRCh37
Build 361055,532,268 - 55,532,518RGDNCBI36
Celera1049,125,168 - 49,125,418RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,843,698 - 49,843,948UniSTS
REN8001  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,862,486 - 55,862,735UniSTSGRCh37
Build 361055,532,492 - 55,532,741RGDNCBI36
Celera1049,125,392 - 49,125,641RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,843,922 - 49,844,171UniSTS
REN8002  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,862,733 - 55,862,975UniSTSGRCh37
Build 361055,532,739 - 55,532,981RGDNCBI36
Celera1049,125,639 - 49,125,881RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,844,169 - 49,844,411UniSTS
REN8003  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,862,809 - 55,863,063UniSTSGRCh37
Build 361055,532,815 - 55,533,069RGDNCBI36
Celera1049,125,715 - 49,125,969RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,844,245 - 49,844,499UniSTS
REN8004  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,863,047 - 55,863,301UniSTSGRCh37
Build 361055,533,053 - 55,533,307RGDNCBI36
Celera1049,125,953 - 49,126,207RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,844,483 - 49,844,737UniSTS
REN8005  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,863,290 - 55,863,548UniSTSGRCh37
Build 361055,533,296 - 55,533,554RGDNCBI36
Celera1049,126,196 - 49,126,454RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,844,726 - 49,844,984UniSTS
REN8007  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,863,765 - 55,863,997UniSTSGRCh37
Build 361055,533,771 - 55,534,003RGDNCBI36
Celera1049,126,671 - 49,126,903RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,845,201 - 49,845,433UniSTS
REN8008  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,863,984 - 55,864,249UniSTSGRCh37
Build 361055,533,990 - 55,534,255RGDNCBI36
Celera1049,126,890 - 49,127,155RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,845,420 - 49,845,685UniSTS
REN8009  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,864,165 - 55,864,417UniSTSGRCh37
Build 361055,534,171 - 55,534,423RGDNCBI36
Celera1049,127,071 - 49,127,323RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,845,601 - 49,845,853UniSTS
REN8010  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,864,399 - 55,864,649UniSTSGRCh37
Build 361055,534,405 - 55,534,655RGDNCBI36
Celera1049,127,305 - 49,127,555RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,845,835 - 49,846,085UniSTS
REN8011  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,865,171 - 55,865,419UniSTSGRCh37
Build 361055,535,177 - 55,535,425RGDNCBI36
Celera1049,128,071 - 49,128,319RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,846,601 - 49,846,849UniSTS
REN8012  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,865,391 - 55,865,655UniSTSGRCh37
Build 361055,535,397 - 55,535,661RGDNCBI36
Celera1049,128,291 - 49,128,555RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,846,821 - 49,847,085UniSTS
REN8013  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,865,651 - 55,865,905UniSTSGRCh37
Build 361055,535,657 - 55,535,911RGDNCBI36
Celera1049,128,551 - 49,128,805RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,847,081 - 49,847,335UniSTS
REN8014  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,865,882 - 55,866,134UniSTSGRCh37
Build 361055,535,888 - 55,536,140RGDNCBI36
Celera1049,128,782 - 49,129,034RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,847,312 - 49,847,564UniSTS
REN8015  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,866,111 - 55,866,359UniSTSGRCh37
Build 361055,536,117 - 55,536,365RGDNCBI36
Celera1049,129,011 - 49,129,259RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,847,541 - 49,847,789UniSTS
REN8016  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,866,345 - 55,866,575UniSTSGRCh37
Build 361055,536,351 - 55,536,581RGDNCBI36
Celera1049,129,245 - 49,129,475RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,847,775 - 49,848,005UniSTS
REN8017  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,866,531 - 55,866,780UniSTSGRCh37
Build 361055,536,537 - 55,536,786RGDNCBI36
Celera1049,129,431 - 49,129,680RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,847,961 - 49,848,210UniSTS
REN8018  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,866,757 - 55,867,012UniSTSGRCh37
Build 361055,536,763 - 55,537,018RGDNCBI36
Celera1049,129,657 - 49,129,912RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,848,187 - 49,848,442UniSTS
REN8019  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,866,985 - 55,867,233UniSTSGRCh37
Build 361055,536,991 - 55,537,239RGDNCBI36
Celera1049,129,885 - 49,130,133RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,848,415 - 49,848,663UniSTS
REN8020  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,867,205 - 55,867,457UniSTSGRCh37
Build 361055,537,211 - 55,537,463RGDNCBI36
Celera1049,130,105 - 49,130,357RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,848,635 - 49,848,887UniSTS
REN8021  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,867,441 - 55,867,690UniSTSGRCh37
Build 361055,537,447 - 55,537,696RGDNCBI36
Celera1049,130,341 - 49,130,590RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,848,871 - 49,849,120UniSTS
REN8022  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,867,670 - 55,867,915UniSTSGRCh37
Build 361055,537,676 - 55,537,921RGDNCBI36
Celera1049,130,570 - 49,130,815RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,849,100 - 49,849,345UniSTS
REN8023  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,867,892 - 55,868,142UniSTSGRCh37
Build 361055,537,898 - 55,538,148RGDNCBI36
Celera1049,130,792 - 49,131,042RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,849,322 - 49,849,572UniSTS
REN8024  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,868,119 - 55,868,365UniSTSGRCh37
Build 361055,538,125 - 55,538,371RGDNCBI36
Celera1049,131,019 - 49,131,265RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,849,549 - 49,849,795UniSTS
REN8025  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,868,349 - 55,868,599UniSTSGRCh37
Build 361055,538,355 - 55,538,605RGDNCBI36
Celera1049,131,249 - 49,131,499RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,849,779 - 49,850,029UniSTS
REN8026  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,868,597 - 55,868,822UniSTSGRCh37
Build 361055,538,603 - 55,538,828RGDNCBI36
Celera1049,131,497 - 49,131,722RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,850,027 - 49,850,252UniSTS
REN8027  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,868,821 - 55,869,057UniSTSGRCh37
Build 361055,538,827 - 55,539,063RGDNCBI36
Celera1049,131,721 - 49,131,957RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,850,251 - 49,850,487UniSTS
REN8028  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,869,009 - 55,869,249UniSTSGRCh37
Build 361055,539,015 - 55,539,255RGDNCBI36
Celera1049,131,909 - 49,132,149RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,850,439 - 49,850,679UniSTS
REN8029  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,869,224 - 55,869,473UniSTSGRCh37
Build 361055,539,230 - 55,539,479RGDNCBI36
Celera1049,132,124 - 49,132,373RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,850,654 - 49,850,903UniSTS
REN8030  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,869,448 - 55,869,685UniSTSGRCh37
Build 361055,539,454 - 55,539,691RGDNCBI36
Celera1049,132,348 - 49,132,585RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,850,878 - 49,851,115UniSTS
REN8031  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,869,651 - 55,869,875UniSTSGRCh37
Build 361055,539,657 - 55,539,881RGDNCBI36
Celera1049,132,551 - 49,132,775RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,851,081 - 49,851,305UniSTS
REN8032  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,869,852 - 55,870,124UniSTSGRCh37
Build 361055,539,858 - 55,540,130RGDNCBI36
Celera1049,132,752 - 49,133,025RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,851,282 - 49,851,554UniSTS
REN8033  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,870,120 - 55,870,388UniSTSGRCh37
Build 361055,540,126 - 55,540,394RGDNCBI36
Celera1049,133,021 - 49,133,289RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,851,550 - 49,851,818UniSTS
REN8034  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,870,367 - 55,870,596UniSTSGRCh37
Build 361055,540,373 - 55,540,602RGDNCBI36
Celera1049,133,268 - 49,133,497RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,851,797 - 49,852,026UniSTS
REN8035  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,870,571 - 55,870,796UniSTSGRCh37
Build 361055,540,577 - 55,540,802RGDNCBI36
Celera1049,133,472 - 49,133,697RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,852,001 - 49,852,226UniSTS
REN8036  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,870,772 - 55,871,016UniSTSGRCh37
Build 361055,540,778 - 55,541,022RGDNCBI36
Celera1049,133,673 - 49,133,917RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,852,202 - 49,852,446UniSTS
REN8037  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,870,995 - 55,871,262UniSTSGRCh37
Build 361055,541,001 - 55,541,268RGDNCBI36
Celera1049,133,896 - 49,134,163RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,852,425 - 49,852,692UniSTS
REN8038  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,871,238 - 55,871,495UniSTSGRCh37
Build 361055,541,244 - 55,541,501RGDNCBI36
Celera1049,134,139 - 49,134,396RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,852,668 - 49,852,925UniSTS
REN8039  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,871,345 - 55,871,612UniSTSGRCh37
Build 361055,541,351 - 55,541,618RGDNCBI36
Celera1049,134,246 - 49,134,513RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,852,775 - 49,853,042UniSTS
REN8040  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,871,522 - 55,871,772UniSTSGRCh37
Build 361055,541,528 - 55,541,778RGDNCBI36
Celera1049,134,423 - 49,134,673RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,852,952 - 49,853,202UniSTS
REN8041  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,871,748 - 55,871,984UniSTSGRCh37
Build 361055,541,754 - 55,541,990RGDNCBI36
Celera1049,134,649 - 49,134,885RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,853,178 - 49,853,414UniSTS
REN8042  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,871,970 - 55,872,221UniSTSGRCh37
Build 361055,541,976 - 55,542,227RGDNCBI36
Celera1049,134,871 - 49,135,122RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,853,400 - 49,853,651UniSTS
REN8043  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,872,220 - 55,872,467UniSTSGRCh37
Build 361055,542,226 - 55,542,473RGDNCBI36
Celera1049,135,121 - 49,135,368RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,853,650 - 49,853,897UniSTS
REN8044  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,872,460 - 55,872,710UniSTSGRCh37
Build 361055,542,466 - 55,542,716RGDNCBI36
Celera1049,135,361 - 49,135,611RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,853,890 - 49,854,140UniSTS
REN8045  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,872,685 - 55,872,932UniSTSGRCh37
Build 361055,542,691 - 55,542,938RGDNCBI36
Celera1049,135,586 - 49,135,833RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,854,115 - 49,854,362UniSTS
REN8046  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,872,920 - 55,873,178UniSTSGRCh37
Build 361055,542,926 - 55,543,184RGDNCBI36
Celera1049,135,821 - 49,136,079RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,854,350 - 49,854,608UniSTS
REN8047  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,873,165 - 55,873,407UniSTSGRCh37
Build 361055,543,171 - 55,543,413RGDNCBI36
Celera1049,136,066 - 49,136,308RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,854,595 - 49,854,837UniSTS
REN8048  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,873,382 - 55,873,627UniSTSGRCh37
Build 361055,543,388 - 55,543,633RGDNCBI36
Celera1049,136,283 - 49,136,528RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,854,812 - 49,855,057UniSTS
REN8049  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,873,563 - 55,873,814UniSTSGRCh37
Build 361055,543,569 - 55,543,820RGDNCBI36
Celera1049,136,464 - 49,136,715RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,854,993 - 49,855,244UniSTS
REN8050  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,873,793 - 55,874,044UniSTSGRCh37
Build 361055,543,799 - 55,544,050RGDNCBI36
Celera1049,136,694 - 49,136,945RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,855,223 - 49,855,474UniSTS
REN8051  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,874,018 - 55,874,273UniSTSGRCh37
Build 361055,544,024 - 55,544,279RGDNCBI36
Celera1049,136,919 - 49,137,174RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,855,448 - 49,855,703UniSTS
REN8052  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,874,250 - 55,874,489UniSTSGRCh37
Build 361055,544,256 - 55,544,495RGDNCBI36
Celera1049,137,151 - 49,137,390RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,855,680 - 49,855,919UniSTS
REN8053  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,874,461 - 55,874,708UniSTSGRCh37
Build 361055,544,467 - 55,544,714RGDNCBI36
Celera1049,137,362 - 49,137,609RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,855,891 - 49,856,138UniSTS
REN8054  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,874,693 - 55,874,957UniSTSGRCh37
Build 361055,544,699 - 55,544,963RGDNCBI36
Celera1049,137,594 - 49,137,858RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,856,123 - 49,856,387UniSTS
REN8055  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,874,933 - 55,875,175UniSTSGRCh37
Build 361055,544,939 - 55,545,181RGDNCBI36
Celera1049,137,834 - 49,138,076RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,856,363 - 49,856,605UniSTS
REN8056  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,875,154 - 55,875,409UniSTSGRCh37
Build 361055,545,160 - 55,545,415RGDNCBI36
Celera1049,138,055 - 49,138,310RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,856,584 - 49,856,839UniSTS
REN8057  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,875,408 - 55,875,632UniSTSGRCh37
Build 361055,545,414 - 55,545,638RGDNCBI36
Celera1049,138,309 - 49,138,533RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,856,838 - 49,857,062UniSTS
REN8058  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,875,594 - 55,875,851UniSTSGRCh37
Build 361055,545,600 - 55,545,857RGDNCBI36
Celera1049,138,495 - 49,138,752RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,857,024 - 49,857,281UniSTS
REN8059  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,875,828 - 55,876,079UniSTSGRCh37
Build 361055,545,834 - 55,546,085RGDNCBI36
Celera1049,138,729 - 49,138,980RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,857,258 - 49,857,509UniSTS
REN8060  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,876,073 - 55,876,322UniSTSGRCh37
Build 361055,546,079 - 55,546,328RGDNCBI36
Celera1049,138,974 - 49,139,223RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,857,503 - 49,857,752UniSTS
REN8061  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,876,299 - 55,876,535UniSTSGRCh37
Build 361055,546,305 - 55,546,541RGDNCBI36
Celera1049,139,200 - 49,139,436RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,857,729 - 49,857,965UniSTS
REN8062  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,876,504 - 55,876,772UniSTSGRCh37
Build 361055,546,510 - 55,546,778RGDNCBI36
Celera1049,139,405 - 49,139,673RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,857,934 - 49,858,202UniSTS
REN8063  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,876,752 - 55,877,011UniSTSGRCh37
Build 361055,546,758 - 55,547,017RGDNCBI36
Celera1049,139,653 - 49,139,912RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,858,182 - 49,858,441UniSTS
REN8064  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,876,989 - 55,877,238UniSTSGRCh37
Build 361055,546,995 - 55,547,244RGDNCBI36
Celera1049,139,890 - 49,140,139RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,858,419 - 49,858,668UniSTS
REN8065  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,877,209 - 55,877,447UniSTSGRCh37
Build 361055,547,215 - 55,547,453RGDNCBI36
Celera1049,140,110 - 49,140,348RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,858,639 - 49,858,877UniSTS
REN8066  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,877,424 - 55,877,666UniSTSGRCh37
Build 361055,547,430 - 55,547,672RGDNCBI36
Celera1049,140,325 - 49,140,567RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,858,854 - 49,859,096UniSTS
REN8067  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,877,573 - 55,877,825UniSTSGRCh37
Build 361055,547,579 - 55,547,831RGDNCBI36
Celera1049,140,474 - 49,140,726RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,859,003 - 49,859,255UniSTS
REN8068  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,877,798 - 55,878,022UniSTSGRCh37
Build 361055,547,804 - 55,548,028RGDNCBI36
Celera1049,140,699 - 49,140,923RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,859,228 - 49,859,452UniSTS
REN8069  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,877,922 - 55,878,148UniSTSGRCh37
Build 361055,547,928 - 55,548,154RGDNCBI36
Celera1049,140,823 - 49,141,049RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,859,352 - 49,859,578UniSTS
REN8070  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,878,348 - 55,878,578UniSTSGRCh37
Build 361055,548,354 - 55,548,584RGDNCBI36
Celera1049,141,249 - 49,141,479RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,859,778 - 49,860,010UniSTS
REN8071  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,878,550 - 55,878,774UniSTSGRCh37
Build 361055,548,556 - 55,548,780RGDNCBI36
Celera1049,141,451 - 49,141,675RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,859,982 - 49,860,206UniSTS
REN8072  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,878,747 - 55,879,000UniSTSGRCh37
Build 361055,548,753 - 55,549,006RGDNCBI36
Celera1049,141,648 - 49,141,901RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,860,179 - 49,860,432UniSTS
REN8073  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,878,970 - 55,879,194UniSTSGRCh37
Build 361055,548,976 - 55,549,200RGDNCBI36
Celera1049,141,871 - 49,142,095RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,860,402 - 49,860,626UniSTS
REN8074  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,879,171 - 55,879,409UniSTSGRCh37
Build 361055,549,177 - 55,549,415RGDNCBI36
Celera1049,142,072 - 49,142,310RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,860,603 - 49,860,841UniSTS
REN8075  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,879,233 - 55,879,478UniSTSGRCh37
Build 361055,549,239 - 55,549,484RGDNCBI36
Celera1049,142,134 - 49,142,379RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,860,665 - 49,860,910UniSTS
REN8076  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,879,428 - 55,879,653UniSTSGRCh37
Build 361055,549,434 - 55,549,659RGDNCBI36
Celera1049,142,329 - 49,142,554RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,860,860 - 49,861,085UniSTS
REN8077  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,879,632 - 55,879,902UniSTSGRCh37
Build 361055,549,638 - 55,549,908RGDNCBI36
Celera1049,142,533 - 49,142,803RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,861,064 - 49,861,334UniSTS
REN8078  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,879,807 - 55,880,055UniSTSGRCh37
Build 361055,549,813 - 55,550,061RGDNCBI36
Celera1049,142,708 - 49,142,956RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,861,239 - 49,861,487UniSTS
REN8079  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,880,032 - 55,880,296UniSTSGRCh37
Build 361055,550,038 - 55,550,302RGDNCBI36
Celera1049,142,933 - 49,143,197RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,861,464 - 49,861,728UniSTS
REN8080  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,880,273 - 55,880,536UniSTSGRCh37
Build 361055,550,279 - 55,550,542RGDNCBI36
Celera1049,143,174 - 49,143,437RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,861,705 - 49,861,968UniSTS
REN8081  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,880,512 - 55,880,778UniSTSGRCh37
Build 361055,550,518 - 55,550,784RGDNCBI36
Celera1049,143,413 - 49,143,679RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,861,944 - 49,862,210UniSTS
REN8082  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,880,749 - 55,880,984UniSTSGRCh37
Build 361055,550,755 - 55,550,990RGDNCBI36
Celera1049,143,650 - 49,143,885RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,862,181 - 49,862,416UniSTS
REN8083  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,880,960 - 55,881,234UniSTSGRCh37
Build 361055,550,966 - 55,551,240RGDNCBI36
Celera1049,143,861 - 49,144,135RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,862,392 - 49,862,666UniSTS
REN8084  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,881,211 - 55,881,447UniSTSGRCh37
Build 361055,551,217 - 55,551,453RGDNCBI36
Celera1049,144,112 - 49,144,348RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,862,643 - 49,862,879UniSTS
REN8085  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,881,411 - 55,881,662UniSTSGRCh37
Build 361055,551,417 - 55,551,668RGDNCBI36
Celera1049,144,312 - 49,144,563RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,862,843 - 49,863,094UniSTS
REN8086  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,881,640 - 55,881,905UniSTSGRCh37
Build 361055,551,646 - 55,551,911RGDNCBI36
Celera1049,144,541 - 49,144,806RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,863,072 - 49,863,337UniSTS
REN8087  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,881,882 - 55,882,110UniSTSGRCh37
Build 361055,551,888 - 55,552,116RGDNCBI36
Celera1049,144,783 - 49,145,011RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,863,314 - 49,863,542UniSTS
REN8088  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,882,092 - 55,882,345UniSTSGRCh37
Build 361055,552,098 - 55,552,351RGDNCBI36
Celera1049,144,993 - 49,145,246RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,863,524 - 49,863,777UniSTS
REN8089  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,882,313 - 55,882,562UniSTSGRCh37
Build 361055,552,319 - 55,552,568RGDNCBI36
Celera1049,145,214 - 49,145,463RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,863,745 - 49,863,995UniSTS
REN8090  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,882,554 - 55,882,808UniSTSGRCh37
Build 361055,552,560 - 55,552,814RGDNCBI36
Celera1049,145,455 - 49,145,709RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,863,987 - 49,864,240UniSTS
REN8091  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,882,730 - 55,882,990UniSTSGRCh37
Build 361055,552,736 - 55,552,996RGDNCBI36
Celera1049,145,631 - 49,145,891RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,864,162 - 49,864,422UniSTS
REN8092  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,882,875 - 55,883,143UniSTSGRCh37
Build 361055,552,881 - 55,553,149RGDNCBI36
Celera1049,145,776 - 49,146,044RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,864,307 - 49,864,575UniSTS
REN8093  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,883,130 - 55,883,379UniSTSGRCh37
Build 361055,553,136 - 55,553,385RGDNCBI36
Celera1049,146,031 - 49,146,280RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,864,562 - 49,864,811UniSTS
REN8094  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,883,344 - 55,883,588UniSTSGRCh37
Build 361055,553,350 - 55,553,594RGDNCBI36
Celera1049,146,245 - 49,146,489RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,864,776 - 49,865,020UniSTS
REN8095  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,883,550 - 55,883,791UniSTSGRCh37
Build 361055,553,556 - 55,553,797RGDNCBI36
Celera1049,146,451 - 49,146,692RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,864,982 - 49,865,223UniSTS
REN8096  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,883,771 - 55,884,020UniSTSGRCh37
Build 361055,553,777 - 55,554,026RGDNCBI36
Celera1049,146,672 - 49,146,921RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,865,203 - 49,865,452UniSTS
REN8097  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,883,988 - 55,884,229UniSTSGRCh37
Build 361055,553,994 - 55,554,235RGDNCBI36
Celera1049,146,889 - 49,147,130RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,865,420 - 49,865,661UniSTS
REN8098  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,884,215 - 55,884,464UniSTSGRCh37
Build 361055,554,221 - 55,554,470RGDNCBI36
Celera1049,147,116 - 49,147,365RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,865,647 - 49,865,896UniSTS
REN8099  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,884,462 - 55,884,733UniSTSGRCh37
Build 361055,554,468 - 55,554,739RGDNCBI36
Celera1049,147,363 - 49,147,634RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,865,894 - 49,866,165UniSTS
REN8100  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,884,710 - 55,884,957UniSTSGRCh37
Build 361055,554,716 - 55,554,963RGDNCBI36
Celera1049,147,611 - 49,147,858RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,866,142 - 49,866,389UniSTS
REN8101  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,884,948 - 55,885,212UniSTSGRCh37
Build 361055,554,954 - 55,555,218RGDNCBI36
Celera1049,147,849 - 49,148,113RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,866,380 - 49,866,644UniSTS
REN8102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,885,190 - 55,885,440UniSTSGRCh37
Build 361055,555,196 - 55,555,446RGDNCBI36
Celera1049,148,091 - 49,148,341RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,866,622 - 49,866,872UniSTS
REN8103  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,885,402 - 55,885,626UniSTSGRCh37
Build 361055,555,408 - 55,555,632RGDNCBI36
Celera1049,148,303 - 49,148,527RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,866,834 - 49,867,058UniSTS
REN8104  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,885,597 - 55,885,821UniSTSGRCh37
Build 361055,555,603 - 55,555,827RGDNCBI36
Celera1049,148,498 - 49,148,722RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,867,029 - 49,867,253UniSTS
REN8105  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,885,790 - 55,886,064UniSTSGRCh37
Build 361055,555,796 - 55,556,070RGDNCBI36
Celera1049,148,691 - 49,148,966RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,867,222 - 49,867,497UniSTS
REN8106  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,886,031 - 55,886,255UniSTSGRCh37
Build 361055,556,037 - 55,556,261RGDNCBI36
Celera1049,148,933 - 49,149,157RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,867,464 - 49,867,688UniSTS
REN8107  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,886,110 - 55,886,356UniSTSGRCh37
Build 361055,556,116 - 55,556,362RGDNCBI36
Celera1049,149,012 - 49,149,258RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,867,543 - 49,867,789UniSTS
REN8108  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,886,331 - 55,886,587UniSTSGRCh37
Build 361055,556,337 - 55,556,593RGDNCBI36
Celera1049,149,233 - 49,149,489RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,867,764 - 49,868,020UniSTS
REN8109  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,886,561 - 55,886,833UniSTSGRCh37
Build 361055,556,567 - 55,556,839RGDNCBI36
Celera1049,149,463 - 49,149,735RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,867,994 - 49,868,266UniSTS
REN8110  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,886,813 - 55,887,065UniSTSGRCh37
Build 361055,556,819 - 55,557,071RGDNCBI36
Celera1049,149,715 - 49,149,967RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,868,246 - 49,868,498UniSTS
REN8111  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,887,016 - 55,887,257UniSTSGRCh37
Build 361055,557,022 - 55,557,263RGDNCBI36
Celera1049,149,918 - 49,150,159RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,868,449 - 49,868,690UniSTS
REN8112  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,887,240 - 55,887,473UniSTSGRCh37
Build 361055,557,246 - 55,557,479RGDNCBI36
Celera1049,150,142 - 49,150,375RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,868,673 - 49,868,906UniSTS
REN8113  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,887,351 - 55,887,597UniSTSGRCh37
Build 361055,557,357 - 55,557,603RGDNCBI36
Celera1049,150,253 - 49,150,499RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,868,784 - 49,869,030UniSTS
REN8114  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,887,581 - 55,887,824UniSTSGRCh37
Build 361055,557,587 - 55,557,830RGDNCBI36
Celera1049,150,483 - 49,150,726RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,869,014 - 49,869,257UniSTS
REN8115  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,887,801 - 55,888,052UniSTSGRCh37
Build 361055,557,807 - 55,558,058RGDNCBI36
Celera1049,150,703 - 49,150,954RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,869,234 - 49,869,485UniSTS
REN8116  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,888,030 - 55,888,291UniSTSGRCh37
Build 361055,558,036 - 55,558,297RGDNCBI36
Celera1049,150,932 - 49,151,193RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,869,463 - 49,869,724UniSTS
REN8117  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,888,265 - 55,888,515UniSTSGRCh37
Build 361055,558,271 - 55,558,521RGDNCBI36
Celera1049,151,167 - 49,151,417RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,869,698 - 49,869,948UniSTS
REN8118  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,888,491 - 55,888,715UniSTSGRCh37
Build 361055,558,497 - 55,558,721RGDNCBI36
Celera1049,151,393 - 49,151,617RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,869,924 - 49,870,148UniSTS
REN8119  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,888,697 - 55,888,939UniSTSGRCh37
Build 361055,558,703 - 55,558,945RGDNCBI36
Celera1049,151,599 - 49,151,841RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,870,130 - 49,870,372UniSTS
REN8120  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,888,898 - 55,889,137UniSTSGRCh37
Build 361055,558,904 - 55,559,143RGDNCBI36
Celera1049,151,800 - 49,152,039RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,870,331 - 49,870,570UniSTS
REN8121  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,889,092 - 55,889,330UniSTSGRCh37
Build 361055,559,098 - 55,559,336RGDNCBI36
Celera1049,151,994 - 49,152,232RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,870,525 - 49,870,763UniSTS
REN8122  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,889,306 - 55,889,557UniSTSGRCh37
Build 361055,559,312 - 55,559,563RGDNCBI36
Celera1049,152,208 - 49,152,459RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,870,739 - 49,870,990UniSTS
REN8123  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,889,545 - 55,889,796UniSTSGRCh37
Build 361055,559,551 - 55,559,802RGDNCBI36
Celera1049,152,447 - 49,152,698RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,870,978 - 49,871,229UniSTS
REN8124  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,889,780 - 55,890,024UniSTSGRCh37
Build 361055,559,786 - 55,560,030RGDNCBI36
Celera1049,152,682 - 49,152,926RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,871,213 - 49,871,457UniSTS
REN8125  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,890,000 - 55,890,254UniSTSGRCh37
Build 361055,560,006 - 55,560,260RGDNCBI36
Celera1049,152,902 - 49,153,156RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,871,433 - 49,871,687UniSTS
REN8126  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,890,231 - 55,890,472UniSTSGRCh37
Build 361055,560,237 - 55,560,478RGDNCBI36
Celera1049,153,133 - 49,153,374RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,871,664 - 49,871,905UniSTS
REN8127  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,890,459 - 55,890,702UniSTSGRCh37
Build 361055,560,465 - 55,560,708RGDNCBI36
Celera1049,153,361 - 49,153,604RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,871,892 - 49,872,135UniSTS
REN8128  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,890,692 - 55,890,947UniSTSGRCh37
Build 361055,560,698 - 55,560,953RGDNCBI36
Celera1049,153,594 - 49,153,849RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,872,125 - 49,872,380UniSTS
REN8129  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,890,945 - 55,891,169UniSTSGRCh37
Build 361055,560,951 - 55,561,175RGDNCBI36
Celera1049,153,847 - 49,154,071RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,872,378 - 49,872,602UniSTS
REN8130  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,891,142 - 55,891,409UniSTSGRCh37
Build 361055,561,148 - 55,561,415RGDNCBI36
Celera1049,154,044 - 49,154,311RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,872,575 - 49,872,842UniSTS
REN8131  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,891,386 - 55,891,632UniSTSGRCh37
Build 361055,561,392 - 55,561,638RGDNCBI36
Celera1049,154,288 - 49,154,534RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,872,819 - 49,873,065UniSTS
REN8132  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,891,605 - 55,891,845UniSTSGRCh37
Build 361055,561,611 - 55,561,851RGDNCBI36
Celera1049,154,507 - 49,154,747RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,873,038 - 49,873,278UniSTS
REN8133  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,891,834 - 55,892,067UniSTSGRCh37
Build 361055,561,840 - 55,562,073RGDNCBI36
Celera1049,154,736 - 49,154,969RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,873,267 - 49,873,500UniSTS
REN8134  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,892,053 - 55,892,299UniSTSGRCh37
Build 361055,562,059 - 55,562,305RGDNCBI36
Celera1049,154,955 - 49,155,201RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,873,486 - 49,873,732UniSTS
REN8135  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,892,276 - 55,892,527UniSTSGRCh37
Build 361055,562,282 - 55,562,533RGDNCBI36
Celera1049,155,178 - 49,155,429RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,873,709 - 49,873,960UniSTS
REN8136  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,892,506 - 55,892,769UniSTSGRCh37
Build 361055,562,512 - 55,562,775RGDNCBI36
Celera1049,155,408 - 49,155,673RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,873,939 - 49,874,202UniSTS
REN8137  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,892,709 - 55,892,947UniSTSGRCh37
Build 361055,562,715 - 55,562,953RGDNCBI36
Celera1049,155,613 - 49,155,851RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,874,142 - 49,875,166UniSTS
HuRef1049,874,142 - 49,874,380UniSTS
REN8138  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,892,918 - 55,893,171UniSTSGRCh37
Build 361055,562,924 - 55,563,177RGDNCBI36
Celera1049,155,822 - 49,156,075RGD
HuRef1049,875,137 - 49,875,390UniSTS
HuRef1049,874,351 - 49,874,604UniSTS
REN8139  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,893,155 - 55,893,408UniSTSGRCh37
Build 361055,563,161 - 55,563,414RGDNCBI36
Celera1049,156,059 - 49,156,312RGD
HuRef1049,875,374 - 49,875,627UniSTS
HuRef1049,876,677 - 49,876,930UniSTS
HuRef1049,874,588 - 49,874,841UniSTS
REN8140  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,893,371 - 55,893,597UniSTSGRCh37
Build 361055,563,377 - 55,563,603RGDNCBI36
Celera1049,156,275 - 49,156,501RGD
HuRef1049,876,893 - 49,877,119UniSTS
HuRef1049,875,590 - 49,875,816UniSTS
REN8141  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,893,576 - 55,893,840UniSTSGRCh37
Build 361055,563,582 - 55,563,846RGDNCBI36
Celera1049,156,480 - 49,156,744RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,875,795 - 49,876,059UniSTS
REN8142  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,893,977 - 55,894,234UniSTSGRCh37
Build 361055,563,983 - 55,564,240RGDNCBI36
Celera1049,156,881 - 49,157,138RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,876,196 - 49,877,304UniSTS
HuRef1049,876,196 - 49,876,453UniSTS
REN8143  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,893,982 - 55,894,236UniSTSGRCh37
Build 361055,563,988 - 55,564,242RGDNCBI36
Celera1049,156,886 - 49,157,140RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,876,201 - 49,877,306UniSTS
HuRef1049,876,201 - 49,876,455UniSTS
REN8144  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,894,854 - 55,895,086UniSTSGRCh37
Build 361055,564,860 - 55,565,092RGDNCBI36
Celera1049,157,758 - 49,157,990RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,877,924 - 49,878,156UniSTS
REN8145  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,895,061 - 55,895,315UniSTSGRCh37
Build 361055,565,067 - 55,565,321RGDNCBI36
Celera1049,157,965 - 49,158,219RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,878,131 - 49,878,385UniSTS
REN8146  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,895,305 - 55,895,559UniSTSGRCh37
Build 361055,565,311 - 55,565,565RGDNCBI36
Celera1049,158,209 - 49,158,463RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,878,375 - 49,878,629UniSTS
REN8147  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,895,553 - 55,895,797UniSTSGRCh37
Build 361055,565,559 - 55,565,803RGDNCBI36
Celera1049,158,457 - 49,158,701RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,878,623 - 49,878,867UniSTS
REN8148  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,895,791 - 55,896,040UniSTSGRCh37
Build 361055,565,797 - 55,566,046RGDNCBI36
Celera1049,158,695 - 49,158,944RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,878,861 - 49,879,110UniSTS
REN8149  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,896,037 - 55,896,268UniSTSGRCh37
Build 361055,566,043 - 55,566,274RGDNCBI36
Celera1049,158,941 - 49,159,172RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,879,107 - 49,879,338UniSTS
REN8150  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,896,242 - 55,896,491UniSTSGRCh37
Build 361055,566,248 - 55,566,497RGDNCBI36
Celera1049,159,146 - 49,159,395RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,879,312 - 49,879,561UniSTS
REN8151  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,896,468 - 55,896,728UniSTSGRCh37
Build 361055,566,474 - 55,566,734RGDNCBI36
Celera1049,159,372 - 49,159,632RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,879,538 - 49,879,798UniSTS
REN8152  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,896,702 - 55,896,970UniSTSGRCh37
Build 361055,566,708 - 55,566,976RGDNCBI36
Celera1049,159,606 - 49,159,874RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,879,772 - 49,880,040UniSTS
REN8153  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,896,960 - 55,897,184UniSTSGRCh37
Build 361055,566,966 - 55,567,190RGDNCBI36
Celera1049,159,864 - 49,160,088RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,880,030 - 49,880,254UniSTS
REN8154  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,897,153 - 55,897,395UniSTSGRCh37
Build 361055,567,159 - 55,567,401RGDNCBI36
Celera1049,160,057 - 49,160,299RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,880,223 - 49,880,465UniSTS
REN8155  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,897,382 - 55,897,631UniSTSGRCh37
Build 361055,567,388 - 55,567,637RGDNCBI36
Celera1049,160,286 - 49,160,535RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,880,452 - 49,880,701UniSTS
REN8156  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,897,617 - 55,897,870UniSTSGRCh37
Build 361055,567,623 - 55,567,876RGDNCBI36
Celera1049,160,521 - 49,160,774RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,880,687 - 49,880,940UniSTS
REN8157  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,897,852 - 55,898,116UniSTSGRCh37
Build 361055,567,858 - 55,568,122RGDNCBI36
Celera1049,160,756 - 49,161,020RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,880,922 - 49,881,186UniSTS
REN8158  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,898,114 - 55,898,367UniSTSGRCh37
Build 361055,568,120 - 55,568,373RGDNCBI36
Celera1049,161,018 - 49,161,271RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,881,184 - 49,881,437UniSTS
REN8159  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,898,340 - 55,898,565UniSTSGRCh37
Build 361055,568,346 - 55,568,571RGDNCBI36
Celera1049,161,244 - 49,161,469RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,881,410 - 49,881,635UniSTS
REN8160  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,898,522 - 55,898,771UniSTSGRCh37
Build 361055,568,528 - 55,568,777RGDNCBI36
Celera1049,161,426 - 49,161,675RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,881,592 - 49,881,841UniSTS
REN8161  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,898,748 - 55,899,004UniSTSGRCh37
Build 361055,568,754 - 55,569,010RGDNCBI36
Celera1049,161,652 - 49,161,908RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,881,818 - 49,882,074UniSTS
REN8162  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,898,980 - 55,899,252UniSTSGRCh37
Build 361055,568,986 - 55,569,258RGDNCBI36
Celera1049,161,884 - 49,162,156RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,882,050 - 49,882,322UniSTS
REN8163  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,899,241 - 55,899,504UniSTSGRCh37
Build 361055,569,247 - 55,569,510RGDNCBI36
Celera1049,162,145 - 49,162,408RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,882,311 - 49,882,574UniSTS
REN8164  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,899,495 - 55,899,733UniSTSGRCh37
Build 361055,569,501 - 55,569,739RGDNCBI36
Celera1049,162,399 - 49,162,637RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,882,565 - 49,882,803UniSTS
REN8165  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,899,706 - 55,899,959UniSTSGRCh37
Build 361055,569,712 - 55,569,965RGDNCBI36
Celera1049,162,610 - 49,162,863RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,882,776 - 49,883,029UniSTS
REN8166  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,899,938 - 55,900,176UniSTSGRCh37
Build 361055,569,944 - 55,570,182RGDNCBI36
Celera1049,162,842 - 49,163,080RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,883,008 - 49,883,246UniSTS
REN8167  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,900,153 - 55,900,387UniSTSGRCh37
Build 361055,570,159 - 55,570,393RGDNCBI36
Celera1049,163,057 - 49,163,291RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,883,223 - 49,883,457UniSTS
REN8168  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,900,208 - 55,900,454UniSTSGRCh37
Build 361055,570,214 - 55,570,460RGDNCBI36
Celera1049,163,112 - 49,163,358RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,883,278 - 49,883,524UniSTS
REN8169  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,900,428 - 55,900,694UniSTSGRCh37
Build 361055,570,434 - 55,570,700RGDNCBI36
Celera1049,163,332 - 49,163,598RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,883,498 - 49,883,764UniSTS
REN8170  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,900,673 - 55,900,929UniSTSGRCh37
Build 361055,570,679 - 55,570,935RGDNCBI36
Celera1049,163,577 - 49,163,833RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,883,743 - 49,883,999UniSTS
REN8171  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,900,745 - 55,900,988UniSTSGRCh37
Build 361055,570,751 - 55,570,994RGDNCBI36
Celera1049,163,649 - 49,163,892RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,883,815 - 49,884,058UniSTS
REN8172  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,900,965 - 55,901,214UniSTSGRCh37
Build 361055,570,971 - 55,571,220RGDNCBI36
Celera1049,163,869 - 49,164,118RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,884,035 - 49,884,284UniSTS
REN8173  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,901,176 - 55,901,422UniSTSGRCh37
Build 361055,571,182 - 55,571,428RGDNCBI36
Celera1049,164,080 - 49,164,326RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,884,246 - 49,884,492UniSTS
REN8174  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,901,393 - 55,901,650UniSTSGRCh37
Build 361055,571,399 - 55,571,656RGDNCBI36
Celera1049,164,297 - 49,164,554RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,884,463 - 49,884,720UniSTS
REN8175  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,901,625 - 55,901,861UniSTSGRCh37
GRCh37X87,787,096 - 87,787,636UniSTSGRCh37
Build 36X87,673,752 - 87,674,292RGDNCBI36
Celera1049,164,529 - 49,164,765UniSTS
CeleraX88,022,664 - 88,023,204RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,884,695 - 49,884,931UniSTS
HuRefX81,370,320 - 81,370,873UniSTS
REN8176  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,901,833 - 55,902,073UniSTSGRCh37
Build 361055,571,839 - 55,572,079RGDNCBI36
Celera1049,164,737 - 49,164,977RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,884,903 - 49,885,143UniSTS
REN8177  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,902,063 - 55,902,289UniSTSGRCh37
Build 361055,572,069 - 55,572,295RGDNCBI36
Celera1049,164,967 - 49,165,193RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,885,133 - 49,885,359UniSTS
REN8178  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,902,264 - 55,902,528UniSTSGRCh37
Build 361055,572,270 - 55,572,534RGDNCBI36
Celera1049,165,168 - 49,165,432RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,885,334 - 49,885,598UniSTS
REN8179  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,902,405 - 55,902,665UniSTSGRCh37
Build 361055,572,411 - 55,572,671RGDNCBI36
Celera1049,165,309 - 49,165,569RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,885,475 - 49,885,735UniSTS
REN8180  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,902,640 - 55,902,864UniSTSGRCh37
Build 361055,572,646 - 55,572,870RGDNCBI36
Celera1049,165,544 - 49,165,768RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,885,710 - 49,885,934UniSTS
REN8181  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,902,839 - 55,903,087UniSTSGRCh37
Build 361055,572,845 - 55,573,093RGDNCBI36
Celera1049,165,743 - 49,165,991RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,885,909 - 49,886,157UniSTS
REN8182  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,903,086 - 55,903,353UniSTSGRCh37
Build 361055,573,092 - 55,573,359RGDNCBI36
Celera1049,165,990 - 49,166,257RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,886,156 - 49,886,423UniSTS
REN8183  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,903,330 - 55,903,579UniSTSGRCh37
Build 361055,573,336 - 55,573,585RGDNCBI36
Celera1049,166,234 - 49,166,483RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,886,400 - 49,886,649UniSTS
REN8184  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,903,571 - 55,903,821UniSTSGRCh37
Build 361055,573,577 - 55,573,827RGDNCBI36
Celera1049,166,475 - 49,166,725RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,886,641 - 49,886,891UniSTS
REN8185  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,903,770 - 55,904,018UniSTSGRCh37
Build 361055,573,776 - 55,574,024RGDNCBI36
Celera1049,166,674 - 49,166,922RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,886,840 - 49,887,087UniSTS
REN8186  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,903,995 - 55,904,241UniSTSGRCh37
Build 361055,574,001 - 55,574,247RGDNCBI36
Celera1049,166,899 - 49,167,145RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,887,064 - 49,887,310UniSTS
REN8187  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,904,196 - 55,904,438UniSTSGRCh37
Build 361055,574,202 - 55,574,444RGDNCBI36
Celera1049,167,100 - 49,167,342RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,887,265 - 49,887,507UniSTS
REN8188  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,904,430 - 55,904,681UniSTSGRCh37
Build 361055,574,436 - 55,574,687RGDNCBI36
Celera1049,167,334 - 49,167,585RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,887,499 - 49,887,750UniSTS
REN8189  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,904,654 - 55,904,912UniSTSGRCh37
Build 361055,574,660 - 55,574,918RGDNCBI36
Celera1049,167,558 - 49,167,816RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,887,723 - 49,887,981UniSTS
REN8190  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,904,889 - 55,905,121UniSTSGRCh37
Build 361055,574,895 - 55,575,127RGDNCBI36
Celera1049,167,793 - 49,168,025RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,887,958 - 49,888,190UniSTS
REN8191  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,905,093 - 55,905,360UniSTSGRCh37
Build 361055,575,099 - 55,575,366RGDNCBI36
Celera1049,167,997 - 49,168,264RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,888,162 - 49,888,429UniSTS
REN8192  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,905,337 - 55,905,590UniSTSGRCh37
Build 361055,575,343 - 55,575,596RGDNCBI36
Celera1049,168,241 - 49,168,494RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,888,406 - 49,888,659UniSTS
REN8193  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,905,565 - 55,905,808UniSTSGRCh37
Build 361055,575,571 - 55,575,814RGDNCBI36
Celera1049,168,469 - 49,168,712RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,888,634 - 49,888,877UniSTS
REN8194  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,905,787 - 55,906,021UniSTSGRCh37
Build 361055,575,793 - 55,576,027RGDNCBI36
Celera1049,168,691 - 49,168,925RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,888,856 - 49,889,090UniSTS
REN8195  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,905,980 - 55,906,210UniSTSGRCh37
Build 361055,575,986 - 55,576,216RGDNCBI36
Celera1049,168,884 - 49,169,114RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,889,049 - 49,889,279UniSTS
REN8196  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,906,178 - 55,906,417UniSTSGRCh37
Build 361055,576,184 - 55,576,423RGDNCBI36
Celera1049,169,082 - 49,169,322RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,889,247 - 49,889,486UniSTS
REN8197  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,906,379 - 55,906,605UniSTSGRCh37
Build 361055,576,385 - 55,576,611RGDNCBI36
Celera1049,169,284 - 49,169,510RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,889,448 - 49,889,674UniSTS
REN8198  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,906,604 - 55,906,865UniSTSGRCh37
Build 361055,576,610 - 55,576,871RGDNCBI36
Celera1049,169,509 - 49,169,813RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,889,673 - 49,889,962UniSTS
REN8199  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,906,844 - 55,907,113UniSTSGRCh37
Build 361055,576,850 - 55,577,119RGDNCBI36
Celera1049,169,792 - 49,170,061RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,889,941 - 49,890,210UniSTS
REN8200  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,907,100 - 55,907,345UniSTSGRCh37
Build 361055,577,106 - 55,577,351RGDNCBI36
Celera1049,170,048 - 49,170,293RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,890,197 - 49,890,442UniSTS
REN8201  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,907,340 - 55,907,590UniSTSGRCh37
Build 361055,577,346 - 55,577,596RGDNCBI36
Celera1049,170,288 - 49,170,538RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,890,437 - 49,890,687UniSTS
REN8202  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,907,564 - 55,907,828UniSTSGRCh37
Build 361055,577,570 - 55,577,834RGDNCBI36
Celera1049,170,512 - 49,170,776RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,890,661 - 49,890,925UniSTS
REN8203  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,907,822 - 55,908,085UniSTSGRCh37
Build 361055,577,828 - 55,578,091RGDNCBI36
Celera1049,170,770 - 49,171,033RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,890,919 - 49,891,182UniSTS
REN8204  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,908,059 - 55,908,302UniSTSGRCh37
Build 361055,578,065 - 55,578,308RGDNCBI36
Celera1049,171,007 - 49,171,250RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,891,156 - 49,891,399UniSTS
REN8205  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,908,285 - 55,908,554UniSTSGRCh37
Build 361055,578,291 - 55,578,560RGDNCBI36
Celera1049,171,233 - 49,171,502RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,891,382 - 49,891,651UniSTS
REN8206  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,908,532 - 55,908,767UniSTSGRCh37
Build 361055,578,538 - 55,578,773RGDNCBI36
Celera1049,171,480 - 49,171,715RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,891,629 - 49,891,864UniSTS
REN8207  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,908,743 - 55,908,981UniSTSGRCh37
Build 361055,578,749 - 55,578,987RGDNCBI36
Celera1049,171,691 - 49,171,929RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,891,840 - 49,892,078UniSTS
REN8208  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,908,965 - 55,909,223UniSTSGRCh37
Build 361055,578,971 - 55,579,229RGDNCBI36
Celera1049,171,913 - 49,172,171RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,892,062 - 49,892,320UniSTS
REN8209  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,909,215 - 55,909,472UniSTSGRCh37
Build 361055,579,221 - 55,579,478RGDNCBI36
Celera1049,172,163 - 49,172,420RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,892,312 - 49,892,569UniSTS
REN8210  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,909,425 - 55,909,678UniSTSGRCh37
Build 361055,579,431 - 55,579,684RGDNCBI36
Celera1049,172,373 - 49,172,626RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,892,522 - 49,892,775UniSTS
REN8211  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,909,665 - 55,909,928UniSTSGRCh37
Build 361055,579,671 - 55,579,934RGDNCBI36
Celera1049,172,613 - 49,172,876RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,892,762 - 49,893,025UniSTS
REN8212  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,909,917 - 55,910,141UniSTSGRCh37
Build 361055,579,923 - 55,580,147RGDNCBI36
Celera1049,172,865 - 49,173,089RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,893,014 - 49,893,238UniSTS
REN8213  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,910,059 - 55,910,302UniSTSGRCh37
Build 361055,580,065 - 55,580,308RGDNCBI36
Celera1049,173,007 - 49,173,250RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,893,156 - 49,893,399UniSTS
REN8214  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,910,232 - 55,910,456UniSTSGRCh37
Build 361055,580,238 - 55,580,462RGDNCBI36
Celera1049,173,180 - 49,173,404RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,893,329 - 49,893,553UniSTS
REN8215  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,910,431 - 55,910,704UniSTSGRCh37
Build 361055,580,437 - 55,580,710RGDNCBI36
Celera1049,173,379 - 49,173,652RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,893,528 - 49,893,801UniSTS
REN8216  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,910,686 - 55,910,934UniSTSGRCh37
Build 361055,580,692 - 55,580,940RGDNCBI36
Celera1049,173,634 - 49,173,882RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,893,783 - 49,894,031UniSTS
REN8217  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,910,929 - 55,911,170UniSTSGRCh37
Build 361055,580,935 - 55,581,176RGDNCBI36
Celera1049,173,877 - 49,174,118RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,894,026 - 49,894,267UniSTS
REN8218  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,911,065 - 55,911,301UniSTSGRCh37
Build 361055,581,071 - 55,581,307RGDNCBI36
Celera1049,174,013 - 49,174,249RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,894,162 - 49,894,398UniSTS
REN8219  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,911,259 - 55,911,487UniSTSGRCh37
Build 361055,581,265 - 55,581,493RGDNCBI36
Celera1049,174,207 - 49,174,435RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,894,356 - 49,894,584UniSTS
REN8220  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,911,461 - 55,911,685UniSTSGRCh37
Build 361055,581,467 - 55,581,691RGDNCBI36
Celera1049,174,409 - 49,174,633RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,894,558 - 49,894,782UniSTS
REN8221  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,911,638 - 55,911,887UniSTSGRCh37
Build 361055,581,644 - 55,581,893RGDNCBI36
Celera1049,174,586 - 49,174,835RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,894,735 - 49,894,984UniSTS
REN8222  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,911,880 - 55,912,110UniSTSGRCh37
Build 361055,581,886 - 55,582,116RGDNCBI36
Celera1049,174,828 - 49,175,058RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,894,977 - 49,895,207UniSTS
REN8223  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,912,071 - 55,912,308UniSTSGRCh37
Build 361055,582,077 - 55,582,314RGDNCBI36
Celera1049,175,019 - 49,175,256RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,895,168 - 49,895,405UniSTS
REN8224  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,912,249 - 55,912,492UniSTSGRCh37
Build 361055,582,255 - 55,582,498RGDNCBI36
Celera1049,175,197 - 49,175,440RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,895,346 - 49,895,589UniSTS
REN8225  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,912,466 - 55,912,718UniSTSGRCh37
Build 361055,582,472 - 55,582,724RGDNCBI36
Celera1049,175,414 - 49,175,666RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,895,563 - 49,895,815UniSTS
REN8226  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,912,677 - 55,912,941UniSTSGRCh37
Build 361055,582,683 - 55,582,947RGDNCBI36
Celera1049,175,625 - 49,175,889RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,895,774 - 49,896,038UniSTS
REN8227  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,912,891 - 55,913,116UniSTSGRCh37
Build 361055,582,897 - 55,583,122RGDNCBI36
Celera1049,175,839 - 49,176,064RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,895,988 - 49,896,213UniSTS
REN8228  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,913,093 - 55,913,363UniSTSGRCh37
Build 361055,583,099 - 55,583,369RGDNCBI36
Celera1049,176,041 - 49,176,311RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,896,190 - 49,896,460UniSTS
REN8229  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,913,340 - 55,913,564UniSTSGRCh37
Build 361055,583,346 - 55,583,570RGDNCBI36
Celera1049,176,288 - 49,176,512RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,896,437 - 49,896,661UniSTS
REN8230  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,913,541 - 55,913,771UniSTSGRCh37
Build 361055,583,547 - 55,583,777RGDNCBI36
Celera1049,176,489 - 49,176,719RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,896,638 - 49,896,868UniSTS
REN8231  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,913,757 - 55,913,984UniSTSGRCh37
Build 361055,583,763 - 55,583,990RGDNCBI36
Celera1049,176,705 - 49,176,932RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,896,854 - 49,897,081UniSTS
REN8232  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,913,905 - 55,914,129UniSTSGRCh37
Build 361055,583,911 - 55,584,135RGDNCBI36
Celera1049,176,853 - 49,177,077RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,897,002 - 49,897,226UniSTS
REN8233  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,914,099 - 55,914,354UniSTSGRCh37
Build 361055,584,105 - 55,584,360RGDNCBI36
Celera1049,177,047 - 49,177,302RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,897,196 - 49,897,451UniSTS
REN8234  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,914,331 - 55,914,590UniSTSGRCh37
Build 361055,584,337 - 55,584,596RGDNCBI36
Celera1049,177,279 - 49,177,538RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,897,428 - 49,897,687UniSTS
REN8235  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,914,567 - 55,914,819UniSTSGRCh37
Build 361055,584,573 - 55,584,825RGDNCBI36
Celera1049,177,515 - 49,177,767RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,897,664 - 49,897,916UniSTS
REN8236  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,914,791 - 55,915,020UniSTSGRCh37
Build 361055,584,797 - 55,585,026RGDNCBI36
Celera1049,177,739 - 49,177,968RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,897,888 - 49,898,117UniSTS
REN8237  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,914,986 - 55,915,212UniSTSGRCh37
Build 361055,584,992 - 55,585,218RGDNCBI36
Celera1049,177,934 - 49,178,160RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,898,083 - 49,898,309UniSTS
REN8238  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,915,177 - 55,915,436UniSTSGRCh37
Build 361055,585,183 - 55,585,442RGDNCBI36
Celera1049,178,125 - 49,178,384RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,898,274 - 49,898,533UniSTS
REN8239  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,915,413 - 55,915,676UniSTSGRCh37
Build 361055,585,419 - 55,585,682RGDNCBI36
Celera1049,178,361 - 49,178,624RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,898,510 - 49,898,773UniSTS
REN8240  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,915,653 - 55,915,922UniSTSGRCh37
Build 361055,585,659 - 55,585,928RGDNCBI36
Celera1049,178,601 - 49,178,870RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,898,750 - 49,899,019UniSTS
REN8241  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,915,899 - 55,916,159UniSTSGRCh37
Build 361055,585,905 - 55,586,165RGDNCBI36
Celera1049,178,847 - 49,179,107RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,898,996 - 49,899,256UniSTS
REN8242  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,915,965 - 55,916,189UniSTSGRCh37
Build 361055,585,971 - 55,586,195RGDNCBI36
Celera1049,178,913 - 49,179,137RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,899,062 - 49,899,286UniSTS
REN8243  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,916,165 - 55,916,391UniSTSGRCh37
Build 361055,586,171 - 55,586,397RGDNCBI36
Celera1049,179,113 - 49,179,339RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,899,262 - 49,899,488UniSTS
REN8244  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,916,346 - 55,916,582UniSTSGRCh37
Build 361055,586,352 - 55,586,588RGDNCBI36
Celera1049,179,294 - 49,179,530RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,899,443 - 49,899,679UniSTS
REN8245  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,916,594 - 55,916,855UniSTSGRCh37
Build 361055,586,600 - 55,586,861RGDNCBI36
Celera1049,179,542 - 49,179,803RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,899,691 - 49,899,952UniSTS
REN8246  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,916,820 - 55,917,051UniSTSGRCh37
Build 361055,586,826 - 55,587,057RGDNCBI36
Celera1049,179,768 - 49,179,999RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,899,917 - 49,900,148UniSTS
REN8247  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,916,951 - 55,917,178UniSTSGRCh37
Build 361055,586,957 - 55,587,184RGDNCBI36
Celera1049,179,899 - 49,180,126RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,900,048 - 49,900,275UniSTS
REN8248  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,917,547 - 55,917,794UniSTSGRCh37
Build 361055,587,553 - 55,587,800RGDNCBI36
Celera1049,180,495 - 49,180,742RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,900,644 - 49,900,891UniSTS
REN8249  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,917,834 - 55,918,081UniSTSGRCh37
Build 361055,587,840 - 55,588,087RGDNCBI36
Celera1049,180,782 - 49,181,029RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,900,931 - 49,901,178UniSTS
REN8250  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,918,070 - 55,918,341UniSTSGRCh37
Build 361055,588,076 - 55,588,347RGDNCBI36
Celera1049,181,018 - 49,181,289RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,901,167 - 49,901,438UniSTS
REN8251  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,918,275 - 55,918,541UniSTSGRCh37
Build 361055,588,281 - 55,588,547RGDNCBI36
Celera1049,181,223 - 49,181,489RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,901,372 - 49,901,638UniSTS
REN8252  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,918,421 - 55,918,683UniSTSGRCh37
Build 361055,588,427 - 55,588,689RGDNCBI36
Celera1049,181,369 - 49,181,631RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,901,518 - 49,901,780UniSTS
REN8253  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,918,574 - 55,918,807UniSTSGRCh37
Build 361055,588,580 - 55,588,813RGDNCBI36
Celera1049,181,522 - 49,181,755RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,901,671 - 49,901,904UniSTS
REN8254  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,918,785 - 55,919,045UniSTSGRCh37
Build 361055,588,791 - 55,589,051RGDNCBI36
Celera1049,181,733 - 49,181,993RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,901,882 - 49,902,145UniSTS
REN8255  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,919,039 - 55,919,263UniSTSGRCh37
Build 361055,589,045 - 55,589,269RGDNCBI36
Celera1049,181,987 - 49,182,211RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,902,139 - 49,902,363UniSTS
REN8256  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,919,240 - 55,919,511UniSTSGRCh37
Build 361055,589,246 - 55,589,517RGDNCBI36
Celera1049,182,188 - 49,182,459RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,902,340 - 49,902,611UniSTS
REN8257  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,919,476 - 55,919,709UniSTSGRCh37
Build 361055,589,482 - 55,589,715RGDNCBI36
Celera1049,182,424 - 49,182,657RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,902,576 - 49,902,809UniSTS
REN8258  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,919,678 - 55,919,923UniSTSGRCh37
Build 361055,589,684 - 55,589,929RGDNCBI36
Celera1049,182,626 - 49,182,871RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,902,778 - 49,903,023UniSTS
REN8259  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,919,909 - 55,920,164UniSTSGRCh37
Build 361055,589,915 - 55,590,170RGDNCBI36
Celera1049,182,857 - 49,183,112RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,903,009 - 49,903,264UniSTS
REN8260  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,920,054 - 55,920,284UniSTSGRCh37
Build 361055,590,060 - 55,590,290RGDNCBI36
Celera1049,183,002 - 49,183,232RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,903,154 - 49,903,384UniSTS
REN8261  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,920,246 - 55,920,485UniSTSGRCh37
Build 361055,590,252 - 55,590,491RGDNCBI36
Celera1049,183,194 - 49,183,433RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,903,346 - 49,903,585UniSTS
REN8262  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,920,539 - 55,920,773UniSTSGRCh37
Build 361055,590,545 - 55,590,779RGDNCBI36
Celera1049,183,487 - 49,183,721RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,903,639 - 49,903,873UniSTS
REN8263  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,920,743 - 55,921,011UniSTSGRCh37
Build 361055,590,749 - 55,591,017RGDNCBI36
Celera1049,183,691 - 49,183,959RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,903,843 - 49,904,111UniSTS
REN8264  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,920,998 - 55,921,263UniSTSGRCh37
Build 361055,591,004 - 55,591,269RGDNCBI36
Celera1049,183,946 - 49,184,211RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,904,098 - 49,904,363UniSTS
REN8265  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,921,237 - 55,921,465UniSTSGRCh37
Build 361055,591,243 - 55,591,471RGDNCBI36
Celera1049,184,185 - 49,184,408RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,904,337 - 49,904,560UniSTS
REN8266  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,921,446 - 55,921,714UniSTSGRCh37
Build 361055,591,452 - 55,591,720RGDNCBI36
Celera1049,184,389 - 49,184,657RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,904,541 - 49,904,809UniSTS
REN8267  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,921,657 - 55,921,908UniSTSGRCh37
Build 361055,591,663 - 55,591,914RGDNCBI36
Celera1049,184,600 - 49,184,851RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,904,752 - 49,905,003UniSTS
REN8268  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,921,885 - 55,922,127UniSTSGRCh37
Build 361055,591,891 - 55,592,133RGDNCBI36
Celera1049,184,828 - 49,185,070RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,904,980 - 49,905,222UniSTS
REN8269  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,922,104 - 55,922,358UniSTSGRCh37
Build 361055,592,110 - 55,592,364RGDNCBI36
Celera1049,185,047 - 49,185,301RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,905,199 - 49,905,453UniSTS
REN8270  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,922,335 - 55,922,597UniSTSGRCh37
Build 361055,592,341 - 55,592,603RGDNCBI36
Celera1049,185,278 - 49,185,540RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,905,430 - 49,905,692UniSTS
REN8271  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,922,594 - 55,922,836UniSTSGRCh37
Build 361055,592,600 - 55,592,842RGDNCBI36
Celera1049,185,537 - 49,185,779RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,905,689 - 49,905,931UniSTS
REN8272  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,922,816 - 55,923,069UniSTSGRCh37
Build 361055,592,822 - 55,593,075RGDNCBI36
Celera1049,185,759 - 49,186,012RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,905,911 - 49,906,164UniSTS
REN8273  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,923,021 - 55,923,282UniSTSGRCh37
Build 361055,593,027 - 55,593,288RGDNCBI36
Celera1049,185,964 - 49,186,225RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,906,116 - 49,906,377UniSTS
REN8274  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,923,265 - 55,923,512UniSTSGRCh37
Build 361055,593,271 - 55,593,518RGDNCBI36
Celera1049,186,208 - 49,186,455RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,906,360 - 49,906,607UniSTS
REN8275  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,923,486 - 55,923,713UniSTSGRCh37
Build 361055,593,492 - 55,593,719RGDNCBI36
Celera1049,186,429 - 49,186,656RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,906,581 - 49,906,808UniSTS
REN8276  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,923,684 - 55,923,937UniSTSGRCh37
Build 361055,593,690 - 55,593,943RGDNCBI36
Celera1049,186,627 - 49,186,880RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,906,779 - 49,907,032UniSTS
REN8277  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,923,915 - 55,924,184UniSTSGRCh37
Build 361055,593,921 - 55,594,190RGDNCBI36
Celera1049,186,858 - 49,187,127RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,907,010 - 49,907,279UniSTS
REN8278  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,924,154 - 55,924,403UniSTSGRCh37
Build 361055,594,160 - 55,594,409RGDNCBI36
Celera1049,187,097 - 49,187,346RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,907,249 - 49,907,498UniSTS
REN8279  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,924,391 - 55,924,641UniSTSGRCh37
Build 361055,594,397 - 55,594,647RGDNCBI36
Celera1049,187,334 - 49,187,584RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,907,486 - 49,907,736UniSTS
REN8280  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,924,618 - 55,924,867UniSTSGRCh37
Build 361055,594,624 - 55,594,873RGDNCBI36
Celera1049,187,561 - 49,187,810RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,907,713 - 49,907,962UniSTS
REN8281  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,924,805 - 55,925,055UniSTSGRCh37
Build 361055,594,811 - 55,595,061RGDNCBI36
Celera1049,187,748 - 49,187,998RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,907,900 - 49,908,150UniSTS
REN8282  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,925,041 - 55,925,277UniSTSGRCh37
Build 361055,595,047 - 55,595,283RGDNCBI36
Celera1049,187,984 - 49,188,220RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,908,136 - 49,908,372UniSTS
REN8283  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,925,251 - 55,925,477UniSTSGRCh37
Build 361055,595,257 - 55,595,483RGDNCBI36
Celera1049,188,194 - 49,188,420RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,908,346 - 49,908,572UniSTS
REN8284  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,925,446 - 55,925,679UniSTSGRCh37
Build 361055,595,452 - 55,595,685RGDNCBI36
Celera1049,188,389 - 49,188,622RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,908,541 - 49,908,774UniSTS
REN8285  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,925,666 - 55,925,915UniSTSGRCh37
Build 361055,595,672 - 55,595,921RGDNCBI36
Celera1049,188,609 - 49,188,858RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,908,761 - 49,909,010UniSTS
REN8286  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,925,879 - 55,926,136UniSTSGRCh37
Build 361055,595,885 - 55,596,142RGDNCBI36
Celera1049,188,822 - 49,189,079RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,908,974 - 49,909,231UniSTS
REN8287  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,926,109 - 55,926,374UniSTSGRCh37
Build 361055,596,115 - 55,596,380RGDNCBI36
Celera1049,189,052 - 49,189,317RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,909,204 - 49,909,469UniSTS
REN8288  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,926,406 - 55,926,650UniSTSGRCh37
Build 361055,596,412 - 55,596,656RGDNCBI36
Celera1049,189,349 - 49,189,593RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,909,501 - 49,909,744UniSTS
REN8292  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,932,024 - 55,932,294UniSTSGRCh37
Build 361055,602,030 - 55,602,300RGDNCBI36
Celera1049,194,967 - 49,195,237RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,915,202 - 49,915,472UniSTS
REN8293  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,932,280 - 55,932,510UniSTSGRCh37
Build 361055,602,286 - 55,602,516RGDNCBI36
Celera1049,195,223 - 49,195,453RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,915,458 - 49,915,688UniSTS
REN8294  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,932,475 - 55,932,743UniSTSGRCh37
Build 361055,602,481 - 55,602,749RGDNCBI36
Celera1049,195,418 - 49,195,686RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,915,653 - 49,915,921UniSTS
REN8295  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,932,617 - 55,932,873UniSTSGRCh37
Build 361055,602,623 - 55,602,879RGDNCBI36
Celera1049,195,560 - 49,195,816RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,915,795 - 49,916,051UniSTS
REN8296  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,932,843 - 55,933,089UniSTSGRCh37
Build 361055,602,849 - 55,603,095RGDNCBI36
Celera1049,195,786 - 49,196,032RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,916,021 - 49,916,267UniSTS
REN8297  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,932,935 - 55,933,160UniSTSGRCh37
Build 361055,602,941 - 55,603,166RGDNCBI36
Celera1049,195,878 - 49,196,103RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,916,113 - 49,916,338UniSTS
REN8298  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,933,131 - 55,933,355UniSTSGRCh37
Build 361055,603,137 - 55,603,361RGDNCBI36
Celera1049,196,074 - 49,196,298RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,916,309 - 49,916,533UniSTS
REN8299  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,933,330 - 55,933,604UniSTSGRCh37
Build 361055,603,336 - 55,603,610RGDNCBI36
Celera1049,196,273 - 49,196,547RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,916,508 - 49,916,782UniSTS
REN8300  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,933,582 - 55,933,826UniSTSGRCh37
Build 361055,603,588 - 55,603,832RGDNCBI36
Celera1049,196,525 - 49,196,769RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,916,760 - 49,917,004UniSTS
REN8301  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,933,774 - 55,934,001UniSTSGRCh37
Build 361055,603,780 - 55,604,007RGDNCBI36
Celera1049,196,717 - 49,196,944RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,916,952 - 49,917,179UniSTS
REN8302  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,934,339 - 55,934,563UniSTSGRCh37
Build 361055,604,345 - 55,604,569RGDNCBI36
Celera1049,197,282 - 49,197,506RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,917,517 - 49,917,741UniSTS
REN8303  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,934,548 - 55,934,773UniSTSGRCh37
Build 361055,604,554 - 55,604,779RGDNCBI36
Celera1049,197,491 - 49,197,716RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,917,726 - 49,917,951UniSTS
REN8304  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,934,745 - 55,935,000UniSTSGRCh37
Build 361055,604,751 - 55,605,006RGDNCBI36
Celera1049,197,688 - 49,197,943RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,917,923 - 49,918,178UniSTS
REN8305  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,934,965 - 55,935,195UniSTSGRCh37
Build 361055,604,971 - 55,605,201RGDNCBI36
Celera1049,197,908 - 49,198,138RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,918,143 - 49,918,373UniSTS
REN8306  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,935,151 - 55,935,400UniSTSGRCh37
Build 361055,605,157 - 55,605,406RGDNCBI36
Celera1049,198,094 - 49,198,343RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,918,329 - 49,918,578UniSTS
REN8307  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,935,317 - 55,935,545UniSTSGRCh37
Build 361055,605,323 - 55,605,551RGDNCBI36
Celera1049,198,260 - 49,198,488RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,918,495 - 49,918,723UniSTS
REN8308  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,935,503 - 55,935,771UniSTSGRCh37
Build 361055,605,509 - 55,605,777RGDNCBI36
Celera1049,198,446 - 49,198,714RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,918,681 - 49,918,949UniSTS
REN8309  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,935,741 - 55,935,965UniSTSGRCh37
Build 361055,605,747 - 55,605,971RGDNCBI36
Celera1049,198,684 - 49,198,908RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,918,919 - 49,919,143UniSTS
REN8310  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,935,926 - 55,936,150UniSTSGRCh37
Build 361055,605,932 - 55,606,156RGDNCBI36
Celera1049,198,869 - 49,199,093RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,919,104 - 49,919,328UniSTS
REN8311  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,936,102 - 55,936,348UniSTSGRCh37
Build 361055,606,108 - 55,606,354RGDNCBI36
Celera1049,199,045 - 49,199,291RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,919,280 - 49,919,526UniSTS
REN8312  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,936,315 - 55,936,555UniSTSGRCh37
Build 361055,606,321 - 55,606,561RGDNCBI36
Celera1049,199,258 - 49,199,498RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,919,493 - 49,919,733UniSTS
REN8313  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,936,531 - 55,936,780UniSTSGRCh37
Build 361055,606,537 - 55,606,786RGDNCBI36
Celera1049,199,474 - 49,199,724RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,919,709 - 49,919,959UniSTS
REN8314  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,936,724 - 55,936,982UniSTSGRCh37
Build 361055,606,730 - 55,606,988RGDNCBI36
Celera1049,199,668 - 49,199,926RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,919,903 - 49,920,161UniSTS
REN8315  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,936,980 - 55,937,206UniSTSGRCh37
Build 361055,606,986 - 55,607,212RGDNCBI36
Celera1049,199,924 - 49,200,150RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,920,159 - 49,920,385UniSTS
REN8316  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,937,183 - 55,937,450UniSTSGRCh37
Build 361055,607,189 - 55,607,456RGDNCBI36
Celera1049,200,127 - 49,200,394RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,920,362 - 49,920,629UniSTS
REN8317  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,937,427 - 55,937,682UniSTSGRCh37
Build 361055,607,433 - 55,607,688RGDNCBI36
Celera1049,200,371 - 49,200,626RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,920,606 - 49,920,861UniSTS
REN8318  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,937,670 - 55,937,898UniSTSGRCh37
Build 361055,607,676 - 55,607,904RGDNCBI36
Celera1049,200,614 - 49,200,842RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,920,849 - 49,921,077UniSTS
REN8319  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,937,881 - 55,938,147UniSTSGRCh37
Build 361055,607,887 - 55,608,153RGDNCBI36
Celera1049,200,825 - 49,201,091RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,921,060 - 49,921,326UniSTS
REN8320  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,938,139 - 55,938,363UniSTSGRCh37
Build 361055,608,145 - 55,608,369RGDNCBI36
Celera1049,201,083 - 49,201,307RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,921,318 - 49,921,542UniSTS
REN8321  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,938,240 - 55,938,475UniSTSGRCh37
Build 361055,608,246 - 55,608,481RGDNCBI36
Celera1049,201,184 - 49,201,419RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,921,419 - 49,921,654UniSTS
REN8322  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,939,404 - 55,939,631UniSTSGRCh37
Build 361055,609,410 - 55,609,637RGDNCBI36
Celera1049,202,348 - 49,202,575RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,922,583 - 49,922,810UniSTS
REN8323  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,939,620 - 55,939,864UniSTSGRCh37
Build 361055,609,626 - 55,609,870RGDNCBI36
Celera1049,202,564 - 49,202,808RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,922,799 - 49,923,043UniSTS
REN8324  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,939,839 - 55,940,099UniSTSGRCh37
Build 361055,609,845 - 55,610,105RGDNCBI36
Celera1049,202,783 - 49,203,043RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,923,018 - 49,923,278UniSTS
REN8325  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,940,091 - 55,940,336UniSTSGRCh37
Build 361055,610,097 - 55,610,342RGDNCBI36
Celera1049,203,035 - 49,203,280RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,923,270 - 49,923,515UniSTS
REN8326  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,940,310 - 55,940,535UniSTSGRCh37
Build 361055,610,316 - 55,610,541RGDNCBI36
Celera1049,203,254 - 49,203,479RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,923,489 - 49,923,714UniSTS
REN8327  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,940,494 - 55,940,749UniSTSGRCh37
Build 361055,610,500 - 55,610,755RGDNCBI36
Celera1049,203,438 - 49,203,693RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,923,673 - 49,923,928UniSTS
REN8328  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,940,734 - 55,941,002UniSTSGRCh37
Build 361055,610,740 - 55,611,008RGDNCBI36
Celera1049,203,678 - 49,203,946RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,923,913 - 49,924,181UniSTS
REN8329  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,940,951 - 55,941,205UniSTSGRCh37
Build 361055,610,957 - 55,611,211RGDNCBI36
Celera1049,203,895 - 49,204,149RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,924,130 - 49,924,384UniSTS
REN8330  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,941,177 - 55,941,417UniSTSGRCh37
Build 361055,611,183 - 55,611,423RGDNCBI36
Celera1049,204,121 - 49,204,361RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,924,356 - 49,924,596UniSTS
REN8331  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,941,376 - 55,941,617UniSTSGRCh37
Build 361055,611,382 - 55,611,623RGDNCBI36
Celera1049,204,320 - 49,204,561RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,924,555 - 49,924,796UniSTS
REN8332  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,941,461 - 55,941,716UniSTSGRCh37
Build 361055,611,467 - 55,611,722RGDNCBI36
Celera1049,204,405 - 49,204,660RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,924,640 - 49,924,895UniSTS
REN8333  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,941,936 - 55,942,179UniSTSGRCh37
Build 361055,611,942 - 55,612,185RGDNCBI36
Celera1049,204,880 - 49,205,123RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,925,115 - 49,925,358UniSTS
REN8334  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,942,171 - 55,942,398UniSTSGRCh37
Build 361055,612,177 - 55,612,404RGDNCBI36
Celera1049,205,115 - 49,205,342RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,925,350 - 49,925,579UniSTS
REN8335  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,942,369 - 55,942,614UniSTSGRCh37
Build 361055,612,375 - 55,612,620RGDNCBI36
Celera1049,205,313 - 49,205,558RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,925,550 - 49,925,795UniSTS
REN8336  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,942,466 - 55,942,703UniSTSGRCh37
Build 361055,612,472 - 55,612,709RGDNCBI36
Celera1049,205,410 - 49,205,647RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,925,647 - 49,925,884UniSTS
REN8337  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,942,689 - 55,942,942UniSTSGRCh37
Build 361055,612,695 - 55,612,948RGDNCBI36
Celera1049,205,633 - 49,205,886RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,925,870 - 49,926,124UniSTS
REN8338  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,942,919 - 55,943,177UniSTSGRCh37
Build 361055,612,925 - 55,613,183RGDNCBI36
Celera1049,205,863 - 49,206,121RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,926,101 - 49,926,359UniSTS
REN8339  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,943,135 - 55,943,369UniSTSGRCh37
Build 361055,613,141 - 55,613,375RGDNCBI36
Celera1049,206,079 - 49,206,313RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,926,317 - 49,926,551UniSTS
REN8340  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,943,342 - 55,943,589UniSTSGRCh37
Build 361055,613,348 - 55,613,595RGDNCBI36
Celera1049,206,286 - 49,206,533RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,926,524 - 49,926,771UniSTS
REN8341  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,943,570 - 55,943,812UniSTSGRCh37
Build 361055,613,576 - 55,613,818RGDNCBI36
Celera1049,206,514 - 49,206,756RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,926,752 - 49,926,994UniSTS
REN8342  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,943,810 - 55,944,054UniSTSGRCh37
Build 361055,613,816 - 55,614,060RGDNCBI36
Celera1049,206,754 - 49,206,998RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,926,992 - 49,927,236UniSTS
REN8343  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,944,007 - 55,944,254UniSTSGRCh37
Build 361055,614,013 - 55,614,260RGDNCBI36
Celera1049,206,951 - 49,207,198RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,927,189 - 49,927,437UniSTS
REN8344  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,944,223 - 55,944,486UniSTSGRCh37
Build 361055,614,229 - 55,614,492RGDNCBI36
Celera1049,207,167 - 49,207,430RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,927,406 - 49,927,669UniSTS
REN8345  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,944,462 - 55,944,705UniSTSGRCh37
Build 361055,614,468 - 55,614,711RGDNCBI36
Celera1049,207,406 - 49,207,649RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,927,645 - 49,927,888UniSTS
REN8346  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,944,671 - 55,944,922UniSTSGRCh37
Build 361055,614,677 - 55,614,928RGDNCBI36
Celera1049,207,615 - 49,207,866RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,927,854 - 49,928,105UniSTS
REN8347  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,944,810 - 55,945,034UniSTSGRCh37
Build 361055,614,816 - 55,615,040RGDNCBI36
Celera1049,207,754 - 49,207,978RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,927,993 - 49,928,217UniSTS
REN8348  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,945,012 - 55,945,268UniSTSGRCh37
Build 361055,615,018 - 55,615,274RGDNCBI36
Celera1049,207,956 - 49,208,212RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,928,195 - 49,928,451UniSTS
REN8349  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,945,355 - 55,945,579UniSTSGRCh37
Build 361055,615,361 - 55,615,585RGDNCBI36
Celera1049,208,299 - 49,208,523RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,928,538 - 49,928,762UniSTS
REN8350  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,945,551 - 55,945,775UniSTSGRCh37
Build 361055,615,557 - 55,615,781RGDNCBI36
Celera1049,208,495 - 49,208,719RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,928,734 - 49,928,958UniSTS
REN8351  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,945,753 - 55,945,978UniSTSGRCh37
Build 361055,615,759 - 55,615,984RGDNCBI36
Celera1049,208,697 - 49,208,922RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,928,936 - 49,929,161UniSTS
REN8352  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,945,951 - 55,946,223UniSTSGRCh37
Build 361055,615,957 - 55,616,229RGDNCBI36
Celera1049,208,895 - 49,209,167RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,929,134 - 49,929,406UniSTS
REN8353  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,946,221 - 55,946,484UniSTSGRCh37
Build 361055,616,227 - 55,616,490RGDNCBI36
Celera1049,209,165 - 49,209,428RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,929,404 - 49,929,667UniSTS
REN8354  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,946,346 - 55,946,570UniSTSGRCh37
Build 361055,616,352 - 55,616,576RGDNCBI36
Celera1049,209,290 - 49,209,514RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,929,529 - 49,929,753UniSTS
REN8355  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,946,520 - 55,946,793UniSTSGRCh37
Build 361055,616,526 - 55,616,799RGDNCBI36
Celera1049,209,464 - 49,209,737RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,929,703 - 49,929,976UniSTS
REN8356  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,946,779 - 55,947,040UniSTSGRCh37
Build 361055,616,785 - 55,617,046RGDNCBI36
Celera1049,209,723 - 49,209,984RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,929,962 - 49,930,223UniSTS
REN8357  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,947,017 - 55,947,260UniSTSGRCh37
Build 361055,617,023 - 55,617,266RGDNCBI36
Celera1049,209,961 - 49,210,204RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,930,200 - 49,930,443UniSTS
REN8358  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,947,250 - 55,947,474UniSTSGRCh37
Build 361055,617,256 - 55,617,480RGDNCBI36
Celera1049,210,194 - 49,210,418RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,930,433 - 49,930,657UniSTS
REN8359  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,947,445 - 55,947,703UniSTSGRCh37
Build 361055,617,451 - 55,617,709RGDNCBI36
Celera1049,210,389 - 49,210,647RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,930,628 - 49,930,886UniSTS
REN8360  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,947,677 - 55,947,902UniSTSGRCh37
Build 361055,617,683 - 55,617,908RGDNCBI36
Celera1049,210,621 - 49,210,846RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,930,860 - 49,931,085UniSTS
REN8361  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,947,884 - 55,948,131UniSTSGRCh37
Build 361055,617,890 - 55,618,137RGDNCBI36
Celera1049,210,828 - 49,211,075RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,931,067 - 49,931,314UniSTS
REN8362  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,948,045 - 55,948,304UniSTSGRCh37
Build 361055,618,051 - 55,618,310RGDNCBI36
Celera1049,210,989 - 49,211,248RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,931,228 - 49,931,487UniSTS
REN8363  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,948,237 - 55,948,499UniSTSGRCh37
Build 361055,618,243 - 55,618,505RGDNCBI36
Celera1049,211,181 - 49,211,443RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,931,420 - 49,931,682UniSTS
REN8364  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,948,470 - 55,948,720UniSTSGRCh37
Build 361055,618,476 - 55,618,726RGDNCBI36
Celera1049,211,414 - 49,211,664RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,931,653 - 49,931,903UniSTS
REN8365  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,948,639 - 55,948,864UniSTSGRCh37
Build 361055,618,645 - 55,618,870RGDNCBI36
Celera1049,211,583 - 49,211,808RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,931,822 - 49,932,047UniSTS
REN8366  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,948,837 - 55,949,082UniSTSGRCh37
Build 361055,618,843 - 55,619,088RGDNCBI36
Celera1049,211,781 - 49,212,026RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,932,020 - 49,932,265UniSTS
REN8367  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,949,080 - 55,949,306UniSTSGRCh37
Build 361055,619,086 - 55,619,312RGDNCBI36
Celera1049,212,024 - 49,212,250RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,932,263 - 49,932,489UniSTS
REN8368  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,949,276 - 55,949,538UniSTSGRCh37
Build 361055,619,282 - 55,619,544RGDNCBI36
Celera1049,212,220 - 49,212,482RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,932,459 - 49,932,721UniSTS
REN8369  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,949,391 - 55,949,639UniSTSGRCh37
Build 361055,619,397 - 55,619,645RGDNCBI36
Celera1049,212,335 - 49,212,583RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,932,574 - 49,932,822UniSTS
REN8370  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,949,615 - 55,949,874UniSTSGRCh37
Build 361055,619,621 - 55,619,880RGDNCBI36
Celera1049,212,559 - 49,212,818RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,932,798 - 49,933,053UniSTS
REN8371  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,949,851 - 55,950,100UniSTSGRCh37
Build 361055,619,857 - 55,620,106RGDNCBI36
Celera1049,212,795 - 49,213,044RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,933,030 - 49,933,279UniSTS
REN8372  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,950,077 - 55,950,317UniSTSGRCh37
Build 361055,620,083 - 55,620,323RGDNCBI36
Celera1049,213,021 - 49,213,261RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,933,256 - 49,933,496UniSTS
REN8373  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,950,280 - 55,950,504UniSTSGRCh37
Build 361055,620,286 - 55,620,510RGDNCBI36
Celera1049,213,224 - 49,213,448RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,933,459 - 49,933,683UniSTS
REN8374  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,950,492 - 55,950,739UniSTSGRCh37
Build 361055,620,498 - 55,620,745RGDNCBI36
Celera1049,213,436 - 49,213,683RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,933,671 - 49,933,918UniSTS
REN8375  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,950,713 - 55,950,943UniSTSGRCh37
Build 361055,620,719 - 55,620,949RGDNCBI36
Celera1049,213,657 - 49,213,887RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,933,892 - 49,934,122UniSTS
REN8376  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,950,919 - 55,951,184UniSTSGRCh37
Build 361055,620,925 - 55,621,190RGDNCBI36
Celera1049,213,863 - 49,214,128RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,934,098 - 49,934,363UniSTS
REN8377  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,951,160 - 55,951,403UniSTSGRCh37
Build 361055,621,166 - 55,621,409RGDNCBI36
Celera1049,214,104 - 49,214,347RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,934,339 - 49,934,582UniSTS
REN8378  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,951,380 - 55,951,641UniSTSGRCh37
Build 361055,621,386 - 55,621,647RGDNCBI36
Celera1049,214,324 - 49,214,585RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,934,559 - 49,934,821UniSTS
REN8379  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,951,564 - 55,951,806UniSTSGRCh37
Build 361055,621,570 - 55,621,812RGDNCBI36
Celera1049,214,508 - 49,214,750RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,934,744 - 49,934,986UniSTS
REN8380  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,951,783 - 55,952,048UniSTSGRCh37
Build 361055,621,789 - 55,622,054RGDNCBI36
Celera1049,214,727 - 49,214,992RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,934,963 - 49,935,228UniSTS
REN8381  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,952,000 - 55,952,237UniSTSGRCh37
Build 361055,622,006 - 55,622,243RGDNCBI36
Celera1049,214,944 - 49,215,181RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,935,180 - 49,935,417UniSTS
REN8382  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,952,226 - 55,952,491UniSTSGRCh37
Build 361055,622,232 - 55,622,497RGDNCBI36
Celera1049,215,170 - 49,215,435RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,935,406 - 49,935,671UniSTS
REN8383  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,952,471 - 55,952,711UniSTSGRCh37
Build 361055,622,477 - 55,622,717RGDNCBI36
Celera1049,215,415 - 49,215,655RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,935,651 - 49,935,891UniSTS
REN8384  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,952,684 - 55,952,947UniSTSGRCh37
Build 361055,622,690 - 55,622,953RGDNCBI36
Celera1049,215,628 - 49,215,891RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,935,864 - 49,936,127UniSTS
REN8385  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,952,924 - 55,953,187UniSTSGRCh37
Build 361055,622,930 - 55,623,193RGDNCBI36
Celera1049,215,868 - 49,216,131RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,936,104 - 49,936,367UniSTS
REN8386  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,953,179 - 55,953,435UniSTSGRCh37
Build 361055,623,185 - 55,623,441RGDNCBI36
Celera1049,216,123 - 49,216,379RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,936,359 - 49,936,615UniSTS
REN8387  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,953,425 - 55,953,668UniSTSGRCh37
Build 361055,623,431 - 55,623,674RGDNCBI36
Celera1049,216,369 - 49,216,612RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,936,605 - 49,936,848UniSTS
REN8388  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,953,652 - 55,953,905UniSTSGRCh37
Build 361055,623,658 - 55,623,911RGDNCBI36
Celera1049,216,596 - 49,216,849RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,936,832 - 49,937,084UniSTS
REN8389  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,953,801 - 55,954,063UniSTSGRCh37
Build 361055,623,807 - 55,624,069RGDNCBI36
Celera1049,216,745 - 49,217,007RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,936,981 - 49,937,242UniSTS
REN8390  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,954,050 - 55,954,276UniSTSGRCh37
Build 361055,624,056 - 55,624,282RGDNCBI36
Celera1049,216,994 - 49,217,220RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,937,229 - 49,937,455UniSTS
REN8391  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,954,334 - 55,954,573UniSTSGRCh37
Build 361055,624,340 - 55,624,579RGDNCBI36
Celera1049,217,278 - 49,217,523RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,937,513 - 49,937,758UniSTS
REN8392  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,954,550 - 55,954,812UniSTSGRCh37
Build 361055,624,556 - 55,624,818RGDNCBI36
Celera1049,217,500 - 49,217,762RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,937,735 - 49,937,997UniSTS
REN8393  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,954,807 - 55,955,049UniSTSGRCh37
Build 361055,624,813 - 55,625,055RGDNCBI36
Celera1049,217,757 - 49,217,999RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,937,992 - 49,938,234UniSTS
REN8394  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,955,043 - 55,955,268UniSTSGRCh37
Build 361055,625,049 - 55,625,274RGDNCBI36
Celera1049,217,993 - 49,218,218RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,938,228 - 49,938,453UniSTS
REN8395  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,955,229 - 55,955,467UniSTSGRCh37
Build 361055,625,235 - 55,625,473RGDNCBI36
Celera1049,218,179 - 49,218,417RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,938,414 - 49,938,652UniSTS
REN8396  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,955,442 - 55,955,667UniSTSGRCh37
Build 361055,625,448 - 55,625,673RGDNCBI36
Celera1049,218,392 - 49,218,617RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,938,627 - 49,938,852UniSTS
REN8397  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,955,625 - 55,955,849UniSTSGRCh37
Build 361055,625,631 - 55,625,855RGDNCBI36
Celera1049,218,575 - 49,218,799RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,938,810 - 49,939,034UniSTS
REN8398  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,955,780 - 55,956,004UniSTSGRCh37
Build 361055,625,786 - 55,626,010RGDNCBI36
Celera1049,218,730 - 49,218,954RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,938,965 - 49,939,189UniSTS
REN8399  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,955,981 - 55,956,245UniSTSGRCh37
Build 361055,625,987 - 55,626,251RGDNCBI36
Celera1049,218,931 - 49,219,195RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,939,166 - 49,939,430UniSTS
REN8400  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,956,225 - 55,956,489UniSTSGRCh37
Build 361055,626,231 - 55,626,495RGDNCBI36
Celera1049,219,175 - 49,219,439RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,939,410 - 49,939,674UniSTS
REN8401  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,956,469 - 55,956,719UniSTSGRCh37
Build 361055,626,475 - 55,626,725RGDNCBI36
Celera1049,219,419 - 49,219,669RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,939,654 - 49,939,904UniSTS
REN8402  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,956,646 - 55,956,896UniSTSGRCh37
Build 361055,626,652 - 55,626,902RGDNCBI36
Celera1049,219,596 - 49,219,846RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,939,831 - 49,940,081UniSTS
REN8403  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,956,817 - 55,957,055UniSTSGRCh37
Build 361055,626,823 - 55,627,061RGDNCBI36
Celera1049,219,767 - 49,220,005RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,940,002 - 49,940,240UniSTS
REN8404  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,957,021 - 55,957,265UniSTSGRCh37
Build 361055,627,027 - 55,627,271RGDNCBI36
Celera1049,219,971 - 49,220,215RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,940,206 - 49,940,450UniSTS
REN8405  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,957,258 - 55,957,517UniSTSGRCh37
Build 361055,627,264 - 55,627,523RGDNCBI36
Celera1049,220,208 - 49,220,467RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,940,443 - 49,940,702UniSTS
REN8406  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,957,510 - 55,957,779UniSTSGRCh37
Build 361055,627,516 - 55,627,785RGDNCBI36
Celera1049,220,460 - 49,220,729RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,940,695 - 49,940,964UniSTS
REN8407  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,957,758 - 55,958,005UniSTSGRCh37
Build 361055,627,764 - 55,628,011RGDNCBI36
Celera1049,220,708 - 49,220,955RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,940,943 - 49,941,190UniSTS
REN8408  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,957,996 - 55,958,239UniSTSGRCh37
Build 361055,628,002 - 55,628,245RGDNCBI36
Celera1049,220,946 - 49,221,189RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,941,181 - 49,941,424UniSTS
REN8409  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,958,550 - 55,958,802UniSTSGRCh37
Build 361055,628,556 - 55,628,808RGDNCBI36
Celera1049,221,500 - 49,221,752RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,941,743 - 49,941,995UniSTS
REN8410  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,958,801 - 55,959,049UniSTSGRCh37
Build 361055,628,807 - 55,629,055RGDNCBI36
Celera1049,221,751 - 49,221,999RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,941,994 - 49,942,242UniSTS
REN8411  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,959,032 - 55,959,256UniSTSGRCh37
Build 361055,629,038 - 55,629,262RGDNCBI36
Celera1049,221,982 - 49,222,206RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,942,225 - 49,942,449UniSTS
REN8412  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,959,228 - 55,959,473UniSTSGRCh37
Build 361055,629,234 - 55,629,479RGDNCBI36
Celera1049,222,178 - 49,222,429RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,942,421 - 49,942,678UniSTS
REN8413  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,959,445 - 55,959,683UniSTSGRCh37
Build 361055,629,451 - 55,629,689RGDNCBI36
Celera1049,222,401 - 49,222,639RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,942,650 - 49,942,888UniSTS
REN8414  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,959,663 - 55,959,919UniSTSGRCh37
Build 361055,629,669 - 55,629,925RGDNCBI36
Celera1049,222,619 - 49,222,875RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,942,868 - 49,943,124UniSTS
REN8415  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,959,847 - 55,960,110UniSTSGRCh37
Build 361055,629,853 - 55,630,116RGDNCBI36
Celera1049,222,803 - 49,223,066RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,943,052 - 49,943,316UniSTS
REN8416  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,960,089 - 55,960,345UniSTSGRCh37
Build 361055,630,095 - 55,630,351RGDNCBI36
Celera1049,223,045 - 49,223,301RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,943,295 - 49,943,551UniSTS
REN8417  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,960,330 - 55,960,569UniSTSGRCh37
Build 361055,630,336 - 55,630,575RGDNCBI36
Celera1049,223,286 - 49,223,525RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,943,536 - 49,943,775UniSTS
REN8418  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,960,563 - 55,960,806UniSTSGRCh37
Build 361055,630,569 - 55,630,812RGDNCBI36
Celera1049,223,519 - 49,223,762RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,943,769 - 49,944,012UniSTS
REN8419  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,960,774 - 55,961,004UniSTSGRCh37
Build 361055,630,780 - 55,631,010RGDNCBI36
Celera1049,223,730 - 49,223,960RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,943,980 - 49,944,210UniSTS
REN8420  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,960,885 - 55,961,125UniSTSGRCh37
Build 361055,630,891 - 55,631,131RGDNCBI36
Celera1049,223,841 - 49,224,081RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,944,091 - 49,944,331UniSTS
REN8421  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,961,099 - 55,961,356UniSTSGRCh37
Build 361055,631,105 - 55,631,362RGDNCBI36
Celera1049,224,055 - 49,224,312RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,944,305 - 49,944,562UniSTS
REN8422  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,961,338 - 55,961,574UniSTSGRCh37
Build 361055,631,344 - 55,631,580RGDNCBI36
Celera1049,224,294 - 49,224,528RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,944,544 - 49,944,778UniSTS
REN8423  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,961,521 - 55,961,753UniSTSGRCh37
Build 361055,631,527 - 55,631,759RGDNCBI36
Celera1049,224,475 - 49,224,707RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,944,725 - 49,944,957UniSTS
REN8424  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,961,728 - 55,961,972UniSTSGRCh37
Build 361055,631,734 - 55,631,978RGDNCBI36
Celera1049,224,682 - 49,224,926RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,944,932 - 49,945,176UniSTS
REN8425  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,961,948 - 55,962,192UniSTSGRCh37
Build 361055,631,954 - 55,632,198RGDNCBI36
Celera1049,224,902 - 49,225,146RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,945,152 - 49,945,396UniSTS
REN8426  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,962,151 - 55,962,404UniSTSGRCh37
Build 361055,632,157 - 55,632,410RGDNCBI36
Celera1049,225,105 - 49,225,358RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,945,355 - 49,945,608UniSTS
REN8427  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,962,381 - 55,962,628UniSTSGRCh37
Build 361055,632,387 - 55,632,634RGDNCBI36
Celera1049,225,335 - 49,225,583RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,945,585 - 49,945,833UniSTS
REN8428  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,962,605 - 55,962,853UniSTSGRCh37
Build 361055,632,611 - 55,632,859RGDNCBI36
Celera1049,225,560 - 49,225,808RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,945,810 - 49,946,058UniSTS
REN8429  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,962,784 - 55,963,032UniSTSGRCh37
Build 361055,632,790 - 55,633,038RGDNCBI36
Celera1049,225,739 - 49,225,987RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,945,989 - 49,946,237UniSTS
REN8430  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,963,021 - 55,963,268UniSTSGRCh37
Build 361055,633,027 - 55,633,274RGDNCBI36
Celera1049,225,976 - 49,226,223RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,946,226 - 49,946,473UniSTS
REN8431  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,963,239 - 55,963,475UniSTSGRCh37
Build 361055,633,245 - 55,633,481RGDNCBI36
Celera1049,226,194 - 49,226,430RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,946,444 - 49,946,680UniSTS
REN8432  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,963,445 - 55,963,693UniSTSGRCh37
Build 361055,633,451 - 55,633,699RGDNCBI36
Celera1049,226,400 - 49,226,648RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,946,650 - 49,946,898UniSTS
REN8433  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,963,680 - 55,963,906UniSTSGRCh37
Build 361055,633,686 - 55,633,912RGDNCBI36
Celera1049,226,635 - 49,226,861RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,946,885 - 49,947,111UniSTS
REN8434  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,963,877 - 55,964,112UniSTSGRCh37
Build 361055,633,883 - 55,634,118RGDNCBI36
Celera1049,226,832 - 49,227,067RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,947,082 - 49,947,317UniSTS
REN8435  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,963,998 - 55,964,247UniSTSGRCh37
Build 361055,634,004 - 55,634,253RGDNCBI36
Celera1049,226,953 - 49,227,201RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,947,203 - 49,947,451UniSTS
REN8436  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,964,224 - 55,964,485UniSTSGRCh37
Build 361055,634,230 - 55,634,491RGDNCBI36
Celera1049,227,178 - 49,227,439RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,947,428 - 49,947,689UniSTS
REN8437  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,964,471 - 55,964,706UniSTSGRCh37
Build 361055,634,477 - 55,634,712RGDNCBI36
Celera1049,227,425 - 49,227,660RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,947,675 - 49,947,910UniSTS
REN8438  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,964,705 - 55,964,954UniSTSGRCh37
Build 361055,634,711 - 55,634,960RGDNCBI36
Celera1049,227,659 - 49,227,908RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,947,909 - 49,948,158UniSTS
REN8439  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,964,948 - 55,965,204UniSTSGRCh37
Build 361055,634,954 - 55,635,210RGDNCBI36
Celera1049,227,902 - 49,228,158RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,948,152 - 49,948,408UniSTS
REN8440  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,965,192 - 55,965,449UniSTSGRCh37
Build 361055,635,198 - 55,635,455RGDNCBI36
Celera1049,228,146 - 49,228,403RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,948,396 - 49,948,653UniSTS
REN8441  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,965,430 - 55,965,679UniSTSGRCh37
Build 361055,635,436 - 55,635,685RGDNCBI36
Celera1049,228,384 - 49,228,633RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,948,634 - 49,948,883UniSTS
REN8442  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,965,658 - 55,965,921UniSTSGRCh37
Build 361055,635,664 - 55,635,927RGDNCBI36
Celera1049,228,612 - 49,228,875RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,948,862 - 49,949,125UniSTS
REN8443  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,965,917 - 55,966,164UniSTSGRCh37
Build 361055,635,923 - 55,636,170RGDNCBI36
Celera1049,228,871 - 49,229,118RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,949,121 - 49,949,368UniSTS
REN8444  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,966,150 - 55,966,374UniSTSGRCh37
Build 361055,636,156 - 55,636,380RGDNCBI36
Celera1049,229,104 - 49,229,328RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,949,354 - 49,949,578UniSTS
REN8445  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,966,338 - 55,966,602UniSTSGRCh37
Build 361055,636,344 - 55,636,608RGDNCBI36
Celera1049,229,292 - 49,229,553RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,949,542 - 49,949,803UniSTS
REN8446  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,966,598 - 55,966,838UniSTSGRCh37
Build 361055,636,604 - 55,636,844RGDNCBI36
Celera1049,229,549 - 49,229,789RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,949,799 - 49,950,039UniSTS
REN8447  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,966,820 - 55,967,075UniSTSGRCh37
Build 361055,636,826 - 55,637,081RGDNCBI36
Celera1049,229,771 - 49,230,026RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,950,021 - 49,950,276UniSTS
REN8448  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,966,969 - 55,967,225UniSTSGRCh37
Build 361055,636,975 - 55,637,231RGDNCBI36
Celera1049,229,920 - 49,230,167RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,950,170 - 49,950,412UniSTS
REN8449  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,967,199 - 55,967,448UniSTSGRCh37
Build 361055,637,205 - 55,637,454RGDNCBI36
Cytogenetic Map10q21.1UniSTS
REN8450  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,967,425 - 55,967,668UniSTSGRCh37
Build 361055,637,431 - 55,637,674RGDNCBI36
Celera1049,230,367 - 49,230,610RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,950,612 - 49,950,855UniSTS
REN8451  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,967,643 - 55,967,906UniSTSGRCh37
Build 361055,637,649 - 55,637,912RGDNCBI36
Celera1049,230,585 - 49,230,848RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,950,830 - 49,951,093UniSTS
REN8452  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,967,900 - 55,968,124UniSTSGRCh37
Build 361055,637,906 - 55,638,130RGDNCBI36
Celera1049,230,842 - 49,231,066RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,951,087 - 49,951,311UniSTS
REN8453  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,968,103 - 55,968,365UniSTSGRCh37
Build 361055,638,109 - 55,638,371RGDNCBI36
Celera1049,231,045 - 49,231,307RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,951,290 - 49,951,552UniSTS
REN8454  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,968,356 - 55,968,611UniSTSGRCh37
Build 361055,638,362 - 55,638,617RGDNCBI36
Celera1049,231,298 - 49,231,553RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,951,543 - 49,951,798UniSTS
REN8455  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,968,510 - 55,968,770UniSTSGRCh37
Build 361055,638,516 - 55,638,776RGDNCBI36
Celera1049,231,452 - 49,231,712RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,951,697 - 49,951,957UniSTS
REN8456  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,968,735 - 55,968,980UniSTSGRCh37
Build 361055,638,741 - 55,638,986RGDNCBI36
Celera1049,231,677 - 49,231,922RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,951,922 - 49,952,167UniSTS
REN8457  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,968,957 - 55,969,212UniSTSGRCh37
Build 361055,638,963 - 55,639,218RGDNCBI36
Celera1049,231,899 - 49,232,154RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,952,144 - 49,952,399UniSTS
REN8458  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,969,192 - 55,969,444UniSTSGRCh37
Build 361055,639,198 - 55,639,450RGDNCBI36
Celera1049,232,134 - 49,232,386RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,952,379 - 49,952,631UniSTS
REN8459  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,969,433 - 55,969,689UniSTSGRCh37
Build 361055,639,439 - 55,639,695RGDNCBI36
Celera1049,232,375 - 49,232,631RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,952,620 - 49,952,876UniSTS
REN8460  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,969,667 - 55,969,918UniSTSGRCh37
Build 361055,639,673 - 55,639,924RGDNCBI36
Celera1049,232,609 - 49,232,860RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,952,854 - 49,953,105UniSTS
REN8461  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,969,896 - 55,970,164UniSTSGRCh37
Build 361055,639,902 - 55,640,170RGDNCBI36
Celera1049,232,838 - 49,233,106RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,953,083 - 49,953,351UniSTS
REN8462  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,970,147 - 55,970,395UniSTSGRCh37
Build 361055,640,153 - 55,640,401RGDNCBI36
Celera1049,233,089 - 49,233,337RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,953,334 - 49,953,582UniSTS
REN8463  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,970,374 - 55,970,625UniSTSGRCh37
Build 361055,640,380 - 55,640,631RGDNCBI36
Celera1049,233,316 - 49,233,567RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,953,561 - 49,953,812UniSTS
REN8464  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,970,578 - 55,970,804UniSTSGRCh37
Build 361055,640,584 - 55,640,810RGDNCBI36
Celera1049,233,520 - 49,233,746RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,953,765 - 49,953,991UniSTS
REN8465  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,970,768 - 55,971,010UniSTSGRCh37
Build 361055,640,774 - 55,641,016RGDNCBI36
Celera1049,233,710 - 49,233,952RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,953,955 - 49,954,197UniSTS
REN8466  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,970,992 - 55,971,252UniSTSGRCh37
Build 361055,640,998 - 55,641,258RGDNCBI36
Celera1049,233,934 - 49,234,194RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,954,179 - 49,954,439UniSTS
REN8467  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,971,230 - 55,971,465UniSTSGRCh37
Build 361055,641,236 - 55,641,471RGDNCBI36
Celera1049,234,172 - 49,234,407RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,954,417 - 49,954,652UniSTS
REN8468  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,971,442 - 55,971,680UniSTSGRCh37
Build 361055,641,448 - 55,641,686RGDNCBI36
Celera1049,234,384 - 49,234,622RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,954,629 - 49,954,867UniSTS
REN8469  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,971,648 - 55,971,901UniSTSGRCh37
Build 361055,641,654 - 55,641,907RGDNCBI36
Celera1049,234,590 - 49,234,843RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,954,835 - 49,955,088UniSTS
REN8470  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,971,884 - 55,972,136UniSTSGRCh37
Build 361055,641,890 - 55,642,142RGDNCBI36
Celera1049,234,826 - 49,235,078RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,955,071 - 49,955,323UniSTS
REN8471  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,972,120 - 55,972,382UniSTSGRCh37
Build 361055,642,126 - 55,642,388RGDNCBI36
Celera1049,235,062 - 49,235,324RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,955,307 - 49,955,569UniSTS
REN8472  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,972,359 - 55,972,596UniSTSGRCh37
Build 361055,642,365 - 55,642,602RGDNCBI36
Celera1049,235,301 - 49,235,538RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,955,546 - 49,955,783UniSTS
REN8473  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,972,573 - 55,972,802UniSTSGRCh37
Build 361055,642,579 - 55,642,808RGDNCBI36
Celera1049,235,515 - 49,235,744RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,955,760 - 49,955,989UniSTS
REN8474  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,972,778 - 55,973,041UniSTSGRCh37
Build 361055,642,784 - 55,643,047RGDNCBI36
Celera1049,235,720 - 49,235,982RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,955,965 - 49,956,228UniSTS
REN8475  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,973,020 - 55,973,244UniSTSGRCh37
Build 361055,643,026 - 55,643,250RGDNCBI36
Celera1049,235,961 - 49,236,185RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,956,207 - 49,956,431UniSTS
REN8476  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,973,202 - 55,973,455UniSTSGRCh37
Build 361055,643,208 - 55,643,461RGDNCBI36
Celera1049,236,143 - 49,236,396RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,956,389 - 49,956,642UniSTS
REN8477  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,973,441 - 55,973,679UniSTSGRCh37
Build 361055,643,447 - 55,643,685RGDNCBI36
Celera1049,236,382 - 49,236,620RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,956,628 - 49,956,866UniSTS
REN8478  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,973,647 - 55,973,893UniSTSGRCh37
Build 361055,643,653 - 55,643,899RGDNCBI36
Celera1049,236,588 - 49,236,834RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,956,834 - 49,957,080UniSTS
REN8479  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,973,885 - 55,974,113UniSTSGRCh37
Build 361055,643,891 - 55,644,119RGDNCBI36
Celera1049,236,826 - 49,237,054RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,957,072 - 49,957,300UniSTS
REN8480  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,974,080 - 55,974,346UniSTSGRCh37
Build 361055,644,086 - 55,644,352RGDNCBI36
Celera1049,237,021 - 49,237,287RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,957,267 - 49,957,533UniSTS
REN8481  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,974,316 - 55,974,555UniSTSGRCh37
Build 361055,644,322 - 55,644,561RGDNCBI36
Celera1049,237,257 - 49,237,496RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,957,503 - 49,957,742UniSTS
REN8482  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,974,531 - 55,974,760UniSTSGRCh37
Build 361055,644,537 - 55,644,766RGDNCBI36
Celera1049,237,472 - 49,237,701RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,957,718 - 49,957,947UniSTS
REN8483  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,974,738 - 55,974,984UniSTSGRCh37
Build 361055,644,744 - 55,644,990RGDNCBI36
Celera1049,237,679 - 49,237,925RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,957,925 - 49,958,167UniSTS
REN8484  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,974,960 - 55,975,210UniSTSGRCh37
Build 361055,644,966 - 55,645,216RGDNCBI36
Celera1049,237,901 - 49,238,151RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,958,143 - 49,958,392UniSTS
REN8485  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,975,124 - 55,975,382UniSTSGRCh37
Build 361055,645,130 - 55,645,388RGDNCBI36
Celera1049,238,065 - 49,238,323RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,958,306 - 49,958,564UniSTS
REN8486  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,975,369 - 55,975,625UniSTSGRCh37
Build 361055,645,375 - 55,645,631RGDNCBI36
Celera1049,238,310 - 49,238,566RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,958,551 - 49,958,807UniSTS
REN8487  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,975,604 - 55,975,866UniSTSGRCh37
Build 361055,645,610 - 55,645,872RGDNCBI36
Celera1049,238,545 - 49,238,807RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,958,786 - 49,959,056UniSTS
REN8488  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,976,143 - 55,976,398UniSTSGRCh37
Build 361055,646,149 - 55,646,404RGDNCBI36
Celera1049,239,084 - 49,239,339RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,959,333 - 49,959,588UniSTS
REN8489  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,976,383 - 55,976,632UniSTSGRCh37
Build 361055,646,389 - 55,646,638RGDNCBI36
Celera1049,239,324 - 49,239,573RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,959,573 - 49,959,822UniSTS
REN8490  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,976,627 - 55,976,879UniSTSGRCh37
Build 361055,646,633 - 55,646,885RGDNCBI36
Celera1049,239,568 - 49,239,820RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,959,817 - 49,960,069UniSTS
REN8491  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,976,872 - 55,977,110UniSTSGRCh37
Build 361055,646,878 - 55,647,116RGDNCBI36
Celera1049,239,813 - 49,240,051RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,960,062 - 49,960,300UniSTS
REN8492  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,977,094 - 55,977,363UniSTSGRCh37
Build 361055,647,100 - 55,647,369RGDNCBI36
Celera1049,240,035 - 49,240,304RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,960,284 - 49,960,553UniSTS
REN8493  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,977,351 - 55,977,607UniSTSGRCh37
Build 361055,647,357 - 55,647,613RGDNCBI36
Celera1049,240,292 - 49,240,548RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,960,541 - 49,960,797UniSTS
REN8494  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,977,586 - 55,977,834UniSTSGRCh37
Build 361055,647,592 - 55,647,840RGDNCBI36
Celera1049,240,527 - 49,240,775RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,960,776 - 49,961,024UniSTS
REN8495  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,977,800 - 55,978,033UniSTSGRCh37
Build 361055,647,806 - 55,648,039RGDNCBI36
Celera1049,240,741 - 49,240,974RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,960,990 - 49,961,223UniSTS
REN8496  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,978,009 - 55,978,258UniSTSGRCh37
Build 361055,648,015 - 55,648,264RGDNCBI36
Celera1049,240,950 - 49,241,199RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,961,199 - 49,961,448UniSTS
REN8497  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,978,225 - 55,978,477UniSTSGRCh37
Build 361055,648,231 - 55,648,483RGDNCBI36
Celera1049,241,166 - 49,241,418RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,961,415 - 49,961,667UniSTS
REN8498  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,978,451 - 55,978,722UniSTSGRCh37
Build 361055,648,457 - 55,648,728RGDNCBI36
Celera1049,241,392 - 49,241,663RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,961,641 - 49,961,912UniSTS
REN8499  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,978,505 - 55,978,739UniSTSGRCh37
Build 361055,648,511 - 55,648,745RGDNCBI36
Celera1049,241,446 - 49,241,680RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,961,695 - 49,961,929UniSTS
REN8500  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,979,377 - 55,979,601UniSTSGRCh37
Build 361055,649,383 - 55,649,607RGDNCBI36
Celera1049,242,318 - 49,242,542RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,962,567 - 49,962,791UniSTS
REN8501  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,979,572 - 55,979,844UniSTSGRCh37
Build 361055,649,578 - 55,649,850RGDNCBI36
Celera1049,242,513 - 49,242,785RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,962,762 - 49,963,034UniSTS
REN8502  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,979,837 - 55,980,093UniSTSGRCh37
Build 361055,649,843 - 55,650,099RGDNCBI36
Celera1049,242,778 - 49,243,034RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,963,027 - 49,963,283UniSTS
REN8503  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,980,081 - 55,980,348UniSTSGRCh37
Build 361055,650,087 - 55,650,354RGDNCBI36
Celera1049,243,022 - 49,243,289RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,963,271 - 49,963,538UniSTS
REN8504  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,980,639 - 55,980,863UniSTSGRCh37
Build 361055,650,645 - 55,650,869RGDNCBI36
Celera1049,243,580 - 49,243,804RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,963,833 - 49,964,057UniSTS
REN8505  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,980,842 - 55,981,081UniSTSGRCh37
Build 361055,650,848 - 55,651,087RGDNCBI36
Celera1049,243,783 - 49,244,022RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,964,036 - 49,964,275UniSTS
REN8506  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,981,058 - 55,981,306UniSTSGRCh37
Build 361055,651,064 - 55,651,312RGDNCBI36
Celera1049,243,999 - 49,244,247RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,964,252 - 49,964,500UniSTS
REN8507  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,981,219 - 55,981,448UniSTSGRCh37
Build 361055,651,225 - 55,651,454RGDNCBI36
Celera1049,244,160 - 49,244,389RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,964,413 - 49,964,642UniSTS
REN8508  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,981,677 - 55,981,904UniSTSGRCh37
Build 361055,651,683 - 55,651,910RGDNCBI36
Celera1049,244,618 - 49,244,845RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,964,871 - 49,965,098UniSTS
REN8509  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,981,868 - 55,982,114UniSTSGRCh37
Build 361055,651,874 - 55,652,120RGDNCBI36
Celera1049,244,809 - 49,245,055RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,965,062 - 49,965,308UniSTS
REN8510  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,982,091 - 55,982,350UniSTSGRCh37
Build 361055,652,097 - 55,652,356RGDNCBI36
Celera1049,245,032 - 49,245,291RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,965,285 - 49,965,544UniSTS
REN8511  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,982,238 - 55,982,487UniSTSGRCh37
Build 361055,652,244 - 55,652,493RGDNCBI36
Celera1049,245,179 - 49,245,428RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,965,432 - 49,965,681UniSTS
REN8512  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,982,433 - 55,982,701UniSTSGRCh37
Build 361055,652,439 - 55,652,707RGDNCBI36
Celera1049,245,374 - 49,245,642RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,965,627 - 49,965,895UniSTS
REN8513  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,982,677 - 55,982,934UniSTSGRCh37
Build 361055,652,683 - 55,652,940RGDNCBI36
Celera1049,245,618 - 49,245,875RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,965,871 - 49,966,128UniSTS
REN8514  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,982,744 - 55,982,974UniSTSGRCh37
Build 361055,652,750 - 55,652,980RGDNCBI36
Celera1049,245,685 - 49,245,915RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,965,938 - 49,966,168UniSTS
REN8515  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,982,944 - 55,983,212UniSTSGRCh37
Build 361055,652,950 - 55,653,218RGDNCBI36
Celera1049,245,885 - 49,246,153RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,966,138 - 49,966,406UniSTS
REN8516  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,983,204 - 55,983,443UniSTSGRCh37
Build 361055,653,210 - 55,653,449RGDNCBI36
Celera1049,246,145 - 49,246,384RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,966,398 - 49,966,637UniSTS
REN8517  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,983,420 - 55,983,673UniSTSGRCh37
Build 361055,653,426 - 55,653,679RGDNCBI36
Celera1049,246,361 - 49,246,614RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,966,614 - 49,966,867UniSTS
REN8518  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,983,650 - 55,983,923UniSTSGRCh37
Build 361055,653,656 - 55,653,929RGDNCBI36
Celera1049,246,591 - 49,246,864RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,966,844 - 49,967,117UniSTS
REN8519  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,983,885 - 55,984,113UniSTSGRCh37
Build 361055,653,891 - 55,654,119RGDNCBI36
Celera1049,246,826 - 49,247,054RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,967,079 - 49,967,307UniSTS
D10S1584  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371056,467,014 - 56,467,226UniSTSGRCh37
Build 361056,137,020 - 56,137,232RGDNCBI36
Celera1049,730,210 - 49,730,422RGD
Cytogenetic Map10q21.1UniSTS
HuRef1050,451,160 - 50,451,372UniSTS
Whitehead-RH Map10410.1UniSTS
Whitehead-YAC Contig Map10 UniSTS
L18135  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,944,747 - 55,944,922UniSTSGRCh37
Build 361055,614,753 - 55,614,928RGDNCBI36
Celera1049,207,691 - 49,207,866RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,927,930 - 49,928,105UniSTS
stSG617833  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,562,035 - 55,563,518UniSTSGRCh37
Build 361055,232,041 - 55,233,524RGDNCBI36
Celera1048,825,004 - 48,826,487RGD
HuRef1049,543,634 - 49,545,117UniSTS
stSG617834  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,563,499 - 55,564,926UniSTSGRCh37
Build 361055,233,505 - 55,234,932RGDNCBI36
Celera1048,826,468 - 48,827,895RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,545,098 - 49,546,525UniSTS
stSG617835  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,564,907 - 55,565,952UniSTSGRCh37
Build 361055,234,913 - 55,235,958RGDNCBI36
Celera1048,827,876 - 48,828,921RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,546,506 - 49,547,555UniSTS
stSG617836  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,565,933 - 55,566,970UniSTSGRCh37
Build 361055,235,939 - 55,236,976RGDNCBI36
Celera1048,828,902 - 48,829,939RGD
HuRef1049,547,536 - 49,548,573UniSTS
stSG617838  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,568,388 - 55,569,401UniSTSGRCh37
Build 361055,238,394 - 55,239,407RGDNCBI36
Celera1048,831,357 - 48,832,370RGD
HuRef1049,549,986 - 49,550,999UniSTS
stSG617839  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,569,382 - 55,570,523UniSTSGRCh37
Build 361055,239,388 - 55,240,529RGDNCBI36
Celera1048,832,351 - 48,833,492RGD
HuRef1049,550,980 - 49,552,121UniSTS
stSG617840  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,570,512 - 55,571,916UniSTSGRCh37
Build 361055,240,518 - 55,241,922RGDNCBI36
Celera1048,833,481 - 48,834,885RGD
HuRef1049,552,110 - 49,553,514UniSTS
stSG617841  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,571,902 - 55,573,082UniSTSGRCh37
Build 361055,241,908 - 55,243,088RGDNCBI36
Celera1048,834,871 - 48,836,051RGD
HuRef1049,553,500 - 49,554,680UniSTS
stSG617842  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,573,061 - 55,574,406UniSTSGRCh37
Build 361055,243,067 - 55,244,412RGDNCBI36
Celera1048,836,030 - 48,837,375RGD
HuRef1049,554,659 - 49,556,004UniSTS
stSG617843  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,574,402 - 55,575,546UniSTSGRCh37
Build 361055,244,408 - 55,245,552RGDNCBI36
Celera1048,837,371 - 48,838,515RGD
HuRef1049,556,000 - 49,557,147UniSTS
stSG617844  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,575,527 - 55,576,657UniSTSGRCh37
Build 361055,245,533 - 55,246,663RGDNCBI36
Celera1048,838,496 - 48,839,626RGD
HuRef1049,557,128 - 49,558,258UniSTS
stSG617845  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,576,642 - 55,577,782UniSTSGRCh37
Build 361055,246,648 - 55,247,788RGDNCBI36
Celera1048,839,611 - 48,840,751RGD
HuRef1049,558,243 - 49,559,383UniSTS
stSG617846  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,577,764 - 55,578,838UniSTSGRCh37
Build 361055,247,770 - 55,248,844RGDNCBI36
Celera1048,840,733 - 48,841,807RGD
HuRef1049,559,365 - 49,560,439UniSTS
stSG617847  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,578,819 - 55,579,132UniSTSGRCh37
Build 361055,248,825 - 55,249,138RGDNCBI36
Celera1048,841,788 - 48,842,101RGD
HuRef1049,560,420 - 49,560,733UniSTS
stSG617848  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,579,159 - 55,580,222UniSTSGRCh37
Build 361055,249,165 - 55,250,228RGDNCBI36
Celera1048,842,128 - 48,843,191RGD
HuRef1049,560,760 - 49,561,823UniSTS
stSG617849  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,580,205 - 55,581,317UniSTSGRCh37
Build 361055,250,211 - 55,251,323RGDNCBI36
Celera1048,843,174 - 48,844,286RGD
HuRef1049,561,806 - 49,562,918UniSTS
stSG617850  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,581,298 - 55,582,679UniSTSGRCh37
Build 361055,251,304 - 55,252,685RGDNCBI36
Celera1048,844,267 - 48,845,648RGD
Cytogenetic Map10q21.1UniSTS
HuRef1049,562,899 - 49,564,280UniSTS
stSG617851  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,582,660 - 55,584,046UniSTSGRCh37
Build 361055,252,666 - 55,254,052RGDNCBI36
Celera1048,845,629 - 48,847,014RGD
HuRef1049,564,261 - 49,565,646UniSTS
stSG617852  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,584,042 - 55,585,203UniSTSGRCh37
Build 361055,254,048 - 55,255,209RGDNCBI36
Celera1048,847,010 - 48,848,171RGD
HuRef1049,565,642 - 49,566,801UniSTS
stSG617853  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,585,189 - 55,586,524UniSTSGRCh37
Build 361055,255,195 - 55,256,530RGDNCBI36
Celera1048,848,157 - 48,849,492RGD
HuRef1049,566,787 - 49,568,126UniSTS
stSG617855  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,587,492 - 55,588,729UniSTSGRCh37
Build 361055,257,498 - 55,258,735RGDNCBI36
Celera1048,850,460 - 48,851,696RGD
HuRef1049,569,094 - 49,570,330UniSTS
stSG617856  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,588,676 - 55,589,704UniSTSGRCh37
Build 361055,258,682 - 55,259,710RGDNCBI36
Celera1048,851,643 - 48,852,671RGD
HuRef1049,570,277 - 49,571,305UniSTS
stSG617857  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,589,556 - 55,590,752UniSTSGRCh37
Build 361055,259,562 - 55,260,758RGDNCBI36
Celera1048,852,523 - 48,853,719RGD
HuRef1049,571,157 - 49,572,353UniSTS
stSG617858  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,590,733 - 55,591,747UniSTSGRCh37
Build 361055,260,739 - 55,261,753RGDNCBI36
Celera1048,853,700 - 48,854,714RGD
HuRef1049,572,334 - 49,573,348UniSTS
stSG617859  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,591,725 - 55,593,169UniSTSGRCh37
Build 361055,261,731 - 55,263,175RGDNCBI36
Celera1048,854,692 - 48,856,136RGD
HuRef1049,573,326 - 49,574,770UniSTS
stSG617860  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,593,150 - 55,594,153UniSTSGRCh37
Build 361055,263,156 - 55,264,159RGDNCBI36
Celera1048,856,117 - 48,857,120RGD
HuRef1049,574,751 - 49,575,750UniSTS
stSG617861  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,594,134 - 55,595,594UniSTSGRCh37
Build 361055,264,140 - 55,265,600RGDNCBI36
Celera1048,857,101 - 48,858,562RGD
HuRef1049,575,731 - 49,577,193UniSTS
stSG617862  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,595,589 - 55,597,054UniSTSGRCh37
Build 361055,265,595 - 55,267,060RGDNCBI36
Celera1048,858,557 - 48,860,022RGD
HuRef1049,577,188 - 49,578,653UniSTS
stSG617863  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,597,036 - 55,598,089UniSTSGRCh37
Build 361055,267,042 - 55,268,095RGDNCBI36
Celera1048,860,004 - 48,861,055RGD
HuRef1049,578,635 - 49,579,680UniSTS
stSG617865  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,599,605 - 55,600,760UniSTSGRCh37
Build 361055,269,611 - 55,270,766RGDNCBI36
Celera1048,862,570 - 48,863,725RGD
HuRef1049,581,196 - 49,582,351UniSTS
stSG617866  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,600,741 - 55,601,862UniSTSGRCh37
Build 361055,270,747 - 55,271,868RGDNCBI36
Celera1048,863,706 - 48,864,827RGD
HuRef1049,582,332 - 49,583,453UniSTS
stSG617867  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,601,845 - 55,603,191UniSTSGRCh37
Build 361055,271,851 - 55,273,197RGDNCBI36
Celera1048,864,810 - 48,866,156RGD
HuRef1049,583,436 - 49,584,782UniSTS
stSG617868  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,602,646 - 55,604,117UniSTSGRCh37
Build 361055,272,652 - 55,274,123RGDNCBI36
Celera1048,865,611 - 48,867,082RGD
HuRef1049,584,237 - 49,585,708UniSTS
stSG617869  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,605,833 - 55,607,052UniSTSGRCh37
Build 361055,275,839 - 55,277,058RGDNCBI36
Celera1048,868,798 - 48,870,017RGD
HuRef1049,587,424 - 49,588,643UniSTS
stSG617870  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,607,079 - 55,608,281UniSTSGRCh37
Build 361055,277,085 - 55,278,287RGDNCBI36
Celera1048,870,044 - 48,871,246RGD
HuRef1049,588,670 - 49,589,872UniSTS
stSG617872  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,609,230 - 55,610,506UniSTSGRCh37
Build 361055,279,236 - 55,280,512RGDNCBI36
Celera1048,872,195 - 48,873,470RGD
HuRef1049,590,821 - 49,592,095UniSTS
stSG617873  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,610,487 - 55,611,628UniSTSGRCh37
Build 361055,280,493 - 55,281,634RGDNCBI36
Celera1048,873,451 - 48,874,592RGD
HuRef1049,592,076 - 49,593,197UniSTS
stSG617874  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,611,611 - 55,612,754UniSTSGRCh37
Build 361055,281,617 - 55,282,760RGDNCBI36
Celera1048,874,575 - 48,875,718RGD
HuRef1049,593,180 - 49,594,323UniSTS
stSG617876  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,614,198 - 55,615,440UniSTSGRCh37
Build 361055,284,204 - 55,285,446RGDNCBI36
Celera1048,877,162 - 48,878,404RGD
HuRef1049,595,767 - 49,597,009UniSTS
stSG617877  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,615,423 - 55,616,612UniSTSGRCh37
Build 361055,285,429 - 55,286,618RGDNCBI36
Celera1048,878,387 - 48,879,582RGD
HuRef1049,596,992 - 49,598,187UniSTS
stSG617878  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,616,968 - 55,618,037UniSTSGRCh37
Build 361055,286,974 - 55,288,043RGDNCBI36
Celera1048,879,938 - 48,881,007RGD
HuRef1049,598,543 - 49,599,612UniSTS
stSG617879  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,618,017 - 55,619,069UniSTSGRCh37
Build 361055,288,023 - 55,289,075RGDNCBI36
Celera1048,880,987 - 48,882,039RGD
HuRef1049,599,592 - 49,600,644UniSTS
stSG617880  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,618,917 - 55,619,923UniSTSGRCh37
Build 361055,288,923 - 55,289,929RGDNCBI36
Celera1048,881,887 - 48,882,893RGD
HuRef1049,600,492 - 49,601,498UniSTS
stSG617881  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,619,684 - 55,620,714UniSTSGRCh37
Build 361055,289,690 - 55,290,720RGDNCBI36
Celera1048,882,654 - 48,883,684RGD
HuRef1049,601,259 - 49,602,289UniSTS
stSG617882  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,620,704 - 55,621,205UniSTSGRCh37
Build 361055,290,710 - 55,291,211RGDNCBI36
Celera1048,883,674 - 48,884,175RGD
HuRef1049,602,279 - 49,602,780UniSTS
stSG617883  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,621,606 - 55,622,655UniSTSGRCh37
Build 361055,291,612 - 55,292,661RGDNCBI36
Celera1048,884,576 - 48,885,625RGD
HuRef1049,603,181 - 49,604,230UniSTS
stSG617884  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,625,377 - 55,626,445UniSTSGRCh37
Build 361055,295,383 - 55,296,451RGDNCBI36
Celera1048,888,347 - 48,889,415RGD
HuRef1049,606,952 - 49,608,025UniSTS
stSG617885  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,626,426 - 55,627,811UniSTSGRCh37
Build 361055,296,432 - 55,297,817RGDNCBI36
Celera1048,889,396 - 48,890,781RGD
HuRef1049,608,006 - 49,609,391UniSTS
stSG617886  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,627,792 - 55,628,907UniSTSGRCh37
Build 361055,297,798 - 55,298,913RGDNCBI36
Celera1048,890,762 - 48,891,877RGD
HuRef1049,609,372 - 49,610,487UniSTS
stSG617887  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,628,928 - 55,630,399UniSTSGRCh37
Build 361055,298,934 - 55,300,405RGDNCBI36
Celera1048,891,898 - 48,893,369RGD
HuRef1049,610,508 - 49,611,979UniSTS
stSG617888  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,630,380 - 55,631,793UniSTSGRCh37
Build 361055,300,386 - 55,301,799RGDNCBI36
Celera1048,893,350 - 48,894,774RGD
HuRef1049,611,960 - 49,613,383UniSTS
stSG617889  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,631,774 - 55,633,045UniSTSGRCh37
Build 361055,301,780 - 55,303,051RGDNCBI36
Celera1048,894,755 - 48,896,026RGD
HuRef1049,613,364 - 49,614,636UniSTS
stSG617890  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,633,031 - 55,634,196UniSTSGRCh37
Build 361055,303,037 - 55,304,202RGDNCBI36
Celera1048,896,012 - 48,897,177RGD
HuRef1049,614,622 - 49,615,787UniSTS
stSG617891  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,634,214 - 55,635,645UniSTSGRCh37
Build 361055,304,220 - 55,305,651RGDNCBI36
Celera1048,897,195 - 48,898,630RGD
HuRef1049,615,805 - 49,617,241UniSTS
stSG617892  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,635,627 - 55,636,884UniSTSGRCh37
Build 361055,305,633 - 55,306,890RGDNCBI36
Celera1048,898,612 - 48,899,871RGD
HuRef1049,617,223 - 49,618,482UniSTS
stSG617894  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,638,166 - 55,639,182UniSTSGRCh37
Build 361055,308,172 - 55,309,188RGDNCBI36
Celera1048,901,153 - 48,902,168RGD
HuRef1049,619,773 - 49,620,792UniSTS
stSG617895  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,639,167 - 55,640,257UniSTSGRCh37
Build 361055,309,173 - 55,310,263RGDNCBI36
Celera1048,902,153 - 48,903,243RGD
HuRef1049,620,777 - 49,621,867UniSTS
stSG617896  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,640,238 - 55,641,515UniSTSGRCh37
Build 361055,310,244 - 55,311,521RGDNCBI36
Celera1048,903,224 - 48,904,500RGD
HuRef1049,621,848 - 49,623,124UniSTS
stSG617897  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,641,496 - 55,642,716UniSTSGRCh37
Build 361055,311,502 - 55,312,722RGDNCBI36
Celera1048,904,481 - 48,905,681RGD
HuRef1049,623,105 - 49,624,304UniSTS
stSG617898  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,642,697 - 55,643,958UniSTSGRCh37
Build 361055,312,703 - 55,313,964RGDNCBI36
Celera1048,905,662 - 48,906,925RGD
HuRef1049,624,285 - 49,625,549UniSTS
stSG617899  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,643,939 - 55,645,249UniSTSGRCh37
Build 361055,313,945 - 55,315,255RGDNCBI36
Celera1048,906,906 - 48,908,216RGD
HuRef1049,625,530 - 49,626,840UniSTS
stSG617900  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,645,230 - 55,646,319UniSTSGRCh37
Build 361055,315,236 - 55,316,325RGDNCBI36
Celera1048,908,197 - 48,909,286RGD
HuRef1049,626,821 - 49,627,910UniSTS
stSG617901  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,646,339 - 55,647,819UniSTSGRCh37
Build 361055,316,345 - 55,317,825RGDNCBI36
Celera1048,909,306 - 48,910,783RGD
HuRef1049,627,930 - 49,629,407UniSTS
stSG617903  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,649,026 - 55,650,512UniSTSGRCh37
Build 361055,319,032 - 55,320,518RGDNCBI36
Celera1048,911,985 - 48,913,471RGD
HuRef1049,630,660 - 49,632,146UniSTS
stSG617904  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,650,503 - 55,651,771UniSTSGRCh37
Build 361055,320,509 - 55,321,777RGDNCBI36
stSG617905  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,652,094 - 55,653,111UniSTSGRCh37
Build 361055,322,100 - 55,323,117RGDNCBI36
Celera1048,915,010 - 48,916,027RGD
HuRef1049,634,026 - 49,635,043UniSTS
stSG617906  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,653,094 - 55,654,221UniSTSGRCh37
Build 361055,323,100 - 55,324,227RGDNCBI36
Celera1048,916,010 - 48,917,137RGD
HuRef1049,635,026 - 49,636,153UniSTS
stSG617907  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,654,202 - 55,655,572UniSTSGRCh37
Build 361055,324,208 - 55,325,578RGDNCBI36
Celera1048,917,118 - 48,918,488RGD
HuRef1049,636,134 - 49,637,504UniSTS
stSG617908  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,655,553 - 55,657,013UniSTSGRCh37
Build 361055,325,559 - 55,327,019RGDNCBI36
Celera1048,918,469 - 48,919,929RGD
HuRef1049,637,485 - 49,638,946UniSTS
stSG617909  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,656,994 - 55,658,219UniSTSGRCh37
Build 361055,327,000 - 55,328,225RGDNCBI36
Celera1048,919,910 - 48,921,134RGD
HuRef1049,638,927 - 49,640,144UniSTS
stSG617910  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,658,200 - 55,659,496UniSTSGRCh37
Build 361055,328,206 - 55,329,502RGDNCBI36
Celera1048,921,115 - 48,922,412RGD
stSG617911  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,659,600 - 55,660,981UniSTSGRCh37
Build 361055,329,606 - 55,330,987RGDNCBI36
Celera1048,922,516 - 48,923,896RGD
stSG617912  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,661,005 - 55,662,029UniSTSGRCh37
Build 361055,331,011 - 55,332,035RGDNCBI36
Celera1048,923,920 - 48,924,944RGD
HuRef1049,642,527 - 49,643,551UniSTS
stSG617913  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,662,010 - 55,663,183UniSTSGRCh37
Build 361055,332,016 - 55,333,189RGDNCBI36
Celera1048,924,925 - 48,926,099RGD
HuRef1049,643,532 - 49,644,705UniSTS
stSG617914  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,663,164 - 55,664,309UniSTSGRCh37
Build 361055,333,170 - 55,334,315RGDNCBI36
Celera1048,926,080 - 48,927,226RGD
HuRef1049,644,686 - 49,645,833UniSTS
stSG617915  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,664,290 - 55,665,556UniSTSGRCh37
Build 361055,334,296 - 55,335,562RGDNCBI36
Celera1048,927,207 - 48,928,473RGD
HuRef1049,645,814 - 49,647,078UniSTS
stSG617916  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,665,540 - 55,666,674UniSTSGRCh37
Build 361055,335,546 - 55,336,680RGDNCBI36
Celera1048,928,457 - 48,929,590RGD
HuRef1049,647,062 - 49,648,195UniSTS
stSG617917  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,666,880 - 55,668,173UniSTSGRCh37
Build 361055,336,886 - 55,338,179RGDNCBI36
Celera1048,929,796 - 48,931,089RGD
HuRef1049,648,401 - 49,649,694UniSTS
stSG617918  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,668,170 - 55,669,202UniSTSGRCh37
Build 361055,338,176 - 55,339,208RGDNCBI36
Celera1048,931,086 - 48,932,118RGD
HuRef1049,649,691 - 49,650,723UniSTS
stSG617919  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,675,036 - 55,676,210UniSTSGRCh37
Build 361055,345,042 - 55,346,216RGDNCBI36
Celera1048,937,949 - 48,939,123RGD
HuRef1049,656,554 - 49,657,728UniSTS
stSG617920  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,676,246 - 55,677,338UniSTSGRCh37
Build 361055,346,252 - 55,347,344RGDNCBI36
Celera1048,939,159 - 48,940,254RGD
HuRef1049,657,764 - 49,658,859UniSTS
stSG617923  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,679,930 - 55,681,226UniSTSGRCh37
Build 361055,349,936 - 55,351,232RGDNCBI36
Celera1048,942,821 - 48,944,118RGD
HuRef1049,661,425 - 49,662,722UniSTS
stSG617924  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,681,207 - 55,682,257UniSTSGRCh37
Build 361055,351,213 - 55,352,263RGDNCBI36
Celera1048,944,099 - 48,945,149RGD
HuRef1049,662,703 - 49,663,753UniSTS
stSG617925  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,682,246 - 55,683,725UniSTSGRCh37
Build 361055,352,252 - 55,353,731RGDNCBI36
Celera1048,945,138 - 48,946,617RGD
HuRef1049,663,742 - 49,665,221UniSTS
stSG617926  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,685,300 - 55,686,350UniSTSGRCh37
Build 361055,355,306 - 55,356,356RGDNCBI36
Celera1048,948,192 - 48,949,242RGD
HuRef1049,666,796 - 49,667,846UniSTS
stSG617927  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,686,330 - 55,687,626UniSTSGRCh37
Build 361055,356,336 - 55,357,632RGDNCBI36
Celera1048,949,222 - 48,950,522RGD
HuRef1049,667,826 - 49,669,126UniSTS
stSG617928  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,687,607 - 55,688,919UniSTSGRCh37
Build 361055,357,613 - 55,358,925RGDNCBI36
Celera1048,950,503 - 48,951,815RGD
HuRef1049,669,107 - 49,670,419UniSTS
stSG617929  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,688,912 - 55,690,272UniSTSGRCh37
Build 361055,358,918 - 55,360,278RGDNCBI36
Celera1048,951,808 - 48,953,166RGD
HuRef1049,670,412 - 49,671,770UniSTS
stSG617930  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,690,253 - 55,691,597UniSTSGRCh37
Build 361055,360,259 - 55,361,603RGDNCBI36
Celera1048,953,147 - 48,954,491RGD
HuRef1049,671,751 - 49,673,095UniSTS
stSG617931  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,691,432 - 55,692,453UniSTSGRCh37
Build 361055,361,438 - 55,362,459RGDNCBI36
Celera1048,954,326 - 48,955,347RGD
HuRef1049,672,930 - 49,673,951UniSTS
stSG617933  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,693,896 - 55,694,083UniSTSGRCh37
Build 361055,363,902 - 55,364,089RGDNCBI36
Celera1048,956,790 - 48,956,977RGD
HuRef1049,675,394 - 49,675,581UniSTS
stSG617934  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,694,085 - 55,695,179UniSTSGRCh37
Build 361055,364,091 - 55,365,185RGDNCBI36
Celera1048,956,979 - 48,958,073RGD
HuRef1049,675,583 - 49,676,677UniSTS
stSG617935  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,695,173 - 55,696,595UniSTSGRCh37
Build 361055,365,179 - 55,366,601RGDNCBI36
Celera1048,958,067 - 48,959,489RGD
HuRef1049,676,671 - 49,678,093UniSTS
stSG617936  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,696,651 - 55,697,662UniSTSGRCh37
Build 361055,366,657 - 55,367,668RGDNCBI36
Celera1048,959,545 - 48,960,556RGD
HuRef1049,678,149 - 49,679,160UniSTS
stSG617937  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,697,652 - 55,698,873UniSTSGRCh37
Build 361055,367,658 - 55,368,879RGDNCBI36
Celera1048,960,546 - 48,961,767RGD
HuRef1049,679,150 - 49,680,371UniSTS
stSG617939  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,700,298 - 55,701,713UniSTSGRCh37
Build 361055,370,304 - 55,371,719RGDNCBI36
Celera1048,963,192 - 48,964,607RGD
HuRef1049,681,796 - 49,683,211UniSTS
stSG617940  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,701,804 - 55,702,924UniSTSGRCh37
Build 361055,371,810 - 55,372,930RGDNCBI36
Celera1048,964,698 - 48,965,817RGD
HuRef1049,683,302 - 49,684,421UniSTS
stSG617941  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,702,916 - 55,704,201UniSTSGRCh37
Build 361055,372,922 - 55,374,207RGDNCBI36
Celera1048,965,809 - 48,967,095RGD
HuRef1049,684,413 - 49,685,698UniSTS
stSG617942  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,703,873 - 55,704,984UniSTSGRCh37
Build 361055,373,879 - 55,374,990RGDNCBI36
Celera1048,966,767 - 48,967,878RGD
HuRef1049,685,370 - 49,686,481UniSTS
stSG617944  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,706,474 - 55,707,773UniSTSGRCh37
Build 361055,376,480 - 55,377,779RGDNCBI36
Celera1048,969,357 - 48,970,656RGD
HuRef1049,687,960 - 49,689,259UniSTS
stSG617945  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,707,758 - 55,708,938UniSTSGRCh37
Build 361055,377,764 - 55,378,944RGDNCBI36
Celera1048,970,641 - 48,971,821RGD
HuRef1049,689,244 - 49,690,424UniSTS
stSG617946  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,708,926 - 55,710,315UniSTSGRCh37
Build 361055,378,932 - 55,380,321RGDNCBI36
Celera1048,971,809 - 48,973,198RGD
HuRef1049,690,412 - 49,691,801UniSTS
stSG617947  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,710,295 - 55,711,382UniSTSGRCh37
Build 361055,380,301 - 55,381,388RGDNCBI36
Celera1048,973,178 - 48,974,265RGD
HuRef1049,691,781 - 49,692,868UniSTS
stSG617948  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,712,915 - 55,713,919UniSTSGRCh37
Build 361055,382,921 - 55,383,925RGDNCBI36
Celera1048,975,798 - 48,976,802RGD
HuRef1049,694,401 - 49,695,405UniSTS
stSG617949  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,713,900 - 55,715,037UniSTSGRCh37
Build 361055,383,906 - 55,385,043RGDNCBI36
Celera1048,976,783 - 48,977,920RGD
HuRef1049,695,386 - 49,696,523UniSTS
stSG617950  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,715,019 - 55,716,499UniSTSGRCh37
Build 361055,385,025 - 55,386,505RGDNCBI36
Celera1048,977,902 - 48,979,382RGD
HuRef1049,696,505 - 49,697,985UniSTS
stSG617951  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,716,481 - 55,716,706UniSTSGRCh37
Build 361055,386,487 - 55,386,712RGDNCBI36
Celera1048,979,364 - 48,979,589RGD
HuRef1049,697,967 - 49,698,192UniSTS
stSG617952  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,716,749 - 55,717,824UniSTSGRCh37
Build 361055,386,755 - 55,387,830RGDNCBI36
Celera1048,979,632 - 48,980,712RGD
HuRef1049,698,235 - 49,699,315UniSTS
stSG617953  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,717,806 - 55,719,165UniSTSGRCh37
Build 361055,387,812 - 55,389,171RGDNCBI36
Celera1048,980,694 - 48,982,053RGD
HuRef1049,699,297 - 49,700,655UniSTS
stSG617954  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,719,146 - 55,720,410UniSTSGRCh37
Build 361055,389,152 - 55,390,416RGDNCBI36
Celera1048,982,034 - 48,983,298RGD
HuRef1049,700,636 - 49,701,900UniSTS
stSG617955  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,720,471 - 55,721,646UniSTSGRCh37
Build 361055,390,477 - 55,391,652RGDNCBI36
Celera1048,983,359 - 48,984,534RGD
HuRef1049,701,961 - 49,703,136UniSTS
stSG617956  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,721,898 - 55,722,963UniSTSGRCh37
Build 361055,391,904 - 55,392,969RGDNCBI36
Celera1048,984,786 - 48,985,851RGD
HuRef1049,703,389 - 49,704,454UniSTS
stSG617957  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,722,944 - 55,724,348UniSTSGRCh37
Build 361055,392,950 - 55,394,354RGDNCBI36
Celera1048,985,832 - 48,987,239RGD
HuRef1049,704,435 - 49,705,842UniSTS
stSG617958  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,724,329 - 55,725,442UniSTSGRCh37
Build 361055,394,335 - 55,395,448RGDNCBI36
Celera1048,987,220 - 48,988,331RGD
HuRef1049,705,823 - 49,706,934UniSTS
stSG617959  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,725,330 - 55,726,392UniSTSGRCh37
Build 361055,395,336 - 55,396,398RGDNCBI36
Celera1048,988,219 - 48,989,281RGD
HuRef1049,706,822 - 49,707,797UniSTS
stSG617960  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,733,234 - 55,734,126UniSTSGRCh37
Build 361055,403,240 - 55,404,132RGDNCBI36
Celera1048,996,122 - 48,997,014RGD
HuRef1049,714,640 - 49,715,528UniSTS
stSG617961  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,736,034 - 55,737,224UniSTSGRCh37
Build 361055,406,040 - 55,407,230RGDNCBI36
Celera1048,998,922 - 49,000,112RGD
HuRef1049,717,436 - 49,718,627UniSTS
stSG617962  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,739,268 - 55,740,416UniSTSGRCh37
Build 361055,409,274 - 55,410,422RGDNCBI36
Celera1049,002,155 - 49,003,304RGD
HuRef1049,720,670 - 49,721,818UniSTS
stSG617963  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,740,397 - 55,740,843UniSTSGRCh37
Build 361055,410,403 - 55,410,849RGDNCBI36
Celera1049,003,285 - 49,003,731RGD
HuRef1049,721,799 - 49,722,245UniSTS
stSG617964  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,742,629 - 55,743,737UniSTSGRCh37
Build 361055,412,635 - 55,413,743RGDNCBI36
Celera1049,005,517 - 49,006,625RGD
HuRef1049,724,031 - 49,725,139UniSTS
stSG617965  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,743,729 - 55,745,092UniSTSGRCh37
Build 361055,413,735 - 55,415,098RGDNCBI36
Celera1049,006,617 - 49,007,980RGD
HuRef1049,725,131 - 49,726,496UniSTS
stSG617966  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,744,521 - 55,745,524UniSTSGRCh37
Build 361055,414,527 - 55,415,530RGDNCBI36
Celera1049,007,409 - 49,008,412RGD
HuRef1049,725,925 - 49,726,928UniSTS
stSG617967  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,747,379 - 55,748,429UniSTSGRCh37
Build 361055,417,385 - 55,418,435RGDNCBI36
Celera1049,010,267 - 49,011,317RGD
HuRef1049,728,783 - 49,729,833UniSTS
stSG617968  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,748,555 - 55,749,745UniSTSGRCh37
Build 361055,418,561 - 55,419,751RGDNCBI36
Celera1049,011,443 - 49,012,633RGD
HuRef1049,729,959 - 49,731,149UniSTS
stSG617969  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,749,726 - 55,749,965UniSTSGRCh37
Build 361055,419,732 - 55,419,971RGDNCBI36
Celera1049,012,614 - 49,012,853RGD
HuRef1049,731,130 - 49,731,369UniSTS
stSG617970  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,749,946 - 55,750,153UniSTSGRCh37
Build 361055,419,952 - 55,420,159RGDNCBI36
Celera1049,012,834 - 49,013,041RGD
HuRef1049,731,350 - 49,731,557UniSTS
stSG617971  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,752,237 - 55,753,256UniSTSGRCh37
Build 361055,422,243 - 55,423,262RGDNCBI36
Celera1049,015,125 - 49,016,144RGD
HuRef1049,733,654 - 49,734,673UniSTS
stSG617972  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,753,237 - 55,754,555UniSTSGRCh37
Build 361055,423,243 - 55,424,561RGDNCBI36
Celera1049,016,125 - 49,017,443RGD
HuRef1049,734,654 - 49,735,972UniSTS
stSG617973  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,754,536 - 55,755,898UniSTSGRCh37
Build 361055,424,542 - 55,425,904RGDNCBI36
Celera1049,017,424 - 49,018,786RGD
HuRef1049,735,953 - 49,737,315UniSTS
stSG617974  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,755,879 - 55,757,127UniSTSGRCh37
Build 361055,425,885 - 55,427,133RGDNCBI36
Celera1049,018,767 - 49,020,015RGD
HuRef1049,737,296 - 49,738,546UniSTS
stSG617975  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,757,108 - 55,758,153UniSTSGRCh37
Build 361055,427,114 - 55,428,159RGDNCBI36
Celera1049,019,996 - 49,021,041RGD
HuRef1049,738,527 - 49,739,572UniSTS
stSG617976  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,758,134 - 55,759,224UniSTSGRCh37
Build 361055,428,140 - 55,429,230RGDNCBI36
Celera1049,021,022 - 49,022,111RGD
HuRef1049,739,553 - 49,740,641UniSTS
stSG617977  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,762,441 - 55,762,628UniSTSGRCh37
GRCh37686,685,511 - 86,685,695UniSTSGRCh37
Build 36686,742,230 - 86,742,414RGDNCBI36
Celera1049,025,324 - 49,025,511UniSTS
Celera687,110,714 - 87,110,898RGD
HuRef1049,743,854 - 49,744,041UniSTS
HuRef683,907,767 - 83,907,951UniSTS
stSG617978  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,765,796 - 55,766,902UniSTSGRCh37
Build 361055,435,802 - 55,436,908RGDNCBI36
Celera1049,028,691 - 49,029,797RGD
HuRef1049,747,208 - 49,748,314UniSTS
stSG617979  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,766,882 - 55,768,352UniSTSGRCh37
Build 361055,436,888 - 55,438,358RGDNCBI36
Celera1049,029,777 - 49,031,247RGD
HuRef1049,748,294 - 49,749,764UniSTS
stSG617980  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,768,240 - 55,769,246UniSTSGRCh37
Build 361055,438,246 - 55,439,252RGDNCBI36
Celera1049,031,135 - 49,032,140RGD
HuRef1049,749,652 - 49,750,657UniSTS
stSG617981  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,776,688 - 55,777,936UniSTSGRCh37
Build 361055,446,694 - 55,447,942RGDNCBI36
Celera1049,039,589 - 49,040,837RGD
HuRef1049,758,106 - 49,759,354UniSTS
stSG617982  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,777,916 - 55,778,141UniSTSGRCh37
Build 361055,447,922 - 55,448,147RGDNCBI36
Celera1049,040,817 - 49,041,042RGD
HuRef1049,759,334 - 49,759,559UniSTS
stSG617983  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,778,251 - 55,779,275UniSTSGRCh37
Build 361055,448,257 - 55,449,281RGDNCBI36
Celera1049,041,152 - 49,042,176RGD
HuRef1049,759,669 - 49,760,693UniSTS
stSG617984  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,779,256 - 55,780,269UniSTSGRCh37
Build 361055,449,262 - 55,450,275RGDNCBI36
Celera1049,042,157 - 49,043,170RGD
HuRef1049,760,674 - 49,761,687UniSTS
stSG617985  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,780,344 - 55,781,646UniSTSGRCh37
Build 361055,450,350 - 55,451,652RGDNCBI36
Celera1049,043,245 - 49,044,547RGD
HuRef1049,761,762 - 49,763,064UniSTS
stSG617986  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,781,749 - 55,783,085UniSTSGRCh37
Build 361055,451,755 - 55,453,091RGDNCBI36
Celera1049,044,650 - 49,045,985RGD
HuRef1049,763,167 - 49,764,502UniSTS
stSG617987  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,783,067 - 55,784,089UniSTSGRCh37
Build 361055,453,073 - 55,454,095RGDNCBI36
Celera1049,045,967 - 49,046,989RGD
HuRef1049,764,484 - 49,765,504UniSTS
stSG617988  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,783,769 - 55,784,905UniSTSGRCh37
Build 361055,453,775 - 55,454,911RGDNCBI36
Celera1049,046,669 - 49,047,805RGD
HuRef1049,765,184 - 49,766,320UniSTS
stSG617989  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,784,886 - 55,786,218UniSTSGRCh37
Build 361055,454,892 - 55,456,224RGDNCBI36
Celera1049,047,786 - 49,049,118RGD
HuRef1049,766,301 - 49,767,633UniSTS
stSG617990  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,788,723 - 55,789,722UniSTSGRCh37
Build 361055,458,729 - 55,459,728RGDNCBI36
Celera1049,051,622 - 49,052,621RGD
HuRef1049,770,138 - 49,771,137UniSTS
stSG617991  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,789,715 - 55,790,817UniSTSGRCh37
Build 361055,459,721 - 55,460,823RGDNCBI36
Celera1049,052,614 - 49,053,715RGD
HuRef1049,771,130 - 49,772,232UniSTS
stSG617992  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,790,798 - 55,792,099UniSTSGRCh37
Build 361055,460,804 - 55,462,105RGDNCBI36
Celera1049,053,696 - 49,054,996RGD
HuRef1049,772,213 - 49,773,514UniSTS
stSG617993  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,792,080 - 55,793,460UniSTSGRCh37
Build 361055,462,086 - 55,463,466RGDNCBI36
Celera1049,054,977 - 49,056,357RGD
HuRef1049,773,495 - 49,774,875UniSTS
stSG617994  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,793,443 - 55,794,570UniSTSGRCh37
Build 361055,463,449 - 55,464,576RGDNCBI36
Celera1049,056,340 - 49,057,479RGD
HuRef1049,774,858 - 49,775,997UniSTS
stSG617995  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,793,910 - 55,794,921UniSTSGRCh37
Build 361055,463,916 - 55,464,927RGDNCBI36
Celera1049,056,807 - 49,057,830RGD
HuRef1049,775,325 - 49,776,348UniSTS
stSG617996  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,797,635 - 55,798,741UniSTSGRCh37
Build 361055,467,641 - 55,468,747RGDNCBI36
Celera1049,060,544 - 49,061,650RGD
HuRef1049,779,062 - 49,780,168UniSTS
stSG617997  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,798,737 - 55,799,741UniSTSGRCh37
Build 361055,468,743 - 55,469,747RGDNCBI36
Celera1049,061,646 - 49,062,650RGD
HuRef1049,780,164 - 49,781,168UniSTS
stSG617998  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,799,722 - 55,801,175UniSTSGRCh37
Build 361055,469,728 - 55,471,181RGDNCBI36
Celera1049,062,631 - 49,064,084RGD
HuRef1049,781,149 - 49,782,602UniSTS
stSG617999  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,800,462 - 55,801,585UniSTSGRCh37
Build 361055,470,468 - 55,471,591RGDNCBI36
Celera1049,063,371 - 49,064,494RGD
HuRef1049,781,889 - 49,783,012UniSTS
stSG618000  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,801,581 - 55,802,878UniSTSGRCh37
Build 361055,471,587 - 55,472,884RGDNCBI36
Celera1049,064,490 - 49,065,787RGD
HuRef1049,783,008 - 49,784,305UniSTS
stSG618001  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,802,870 - 55,804,219UniSTSGRCh37
Build 361055,472,876 - 55,474,225RGDNCBI36
Celera1049,065,779 - 49,067,128RGD
HuRef1049,784,297 - 49,785,646UniSTS
stSG618002  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,804,203 - 55,805,453UniSTSGRCh37
Build 361055,474,209 - 55,475,459RGDNCBI36
Celera1049,067,112 - 49,068,362RGD
HuRef1049,785,630 - 49,786,880UniSTS
stSG618003  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,805,438 - 55,806,669UniSTSGRCh37
Build 361055,475,444 - 55,476,675RGDNCBI36
Celera1049,068,347 - 49,069,579RGD
HuRef1049,786,865 - 49,788,095UniSTS
stSG618005  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,812,968 - 55,814,106UniSTSGRCh37
Build 361055,482,974 - 55,484,112RGDNCBI36
Celera1049,075,878 - 49,077,016RGD
HuRef1049,794,395 - 49,795,533UniSTS
stSG618006  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,814,087 - 55,815,426UniSTSGRCh37
Build 361055,484,093 - 55,485,432RGDNCBI36
Celera1049,076,997 - 49,078,336RGD
stSG618007  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,814,810 - 55,815,855UniSTSGRCh37
Build 361055,484,816 - 55,485,861RGDNCBI36
Celera1049,077,720 - 49,078,765RGD
HuRef1049,796,237 - 49,797,284UniSTS
stSG618009  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,820,107 - 55,821,149UniSTSGRCh37
Build 361055,490,113 - 55,491,155RGDNCBI36
Celera1049,083,017 - 49,084,059RGD
HuRef1049,801,536 - 49,802,578UniSTS
stSG618010  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,821,127 - 55,822,339UniSTSGRCh37
Build 361055,491,133 - 55,492,345RGDNCBI36
Celera1049,084,037 - 49,085,248RGD
HuRef1049,802,556 - 49,803,772UniSTS
stSG618012  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,824,821 - 55,825,832UniSTSGRCh37
Build 361055,494,827 - 55,495,838RGDNCBI36
Celera1049,087,729 - 49,088,740RGD
HuRef1049,806,253 - 49,807,264UniSTS
stSG618013  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,825,813 - 55,826,960UniSTSGRCh37
Build 361055,495,819 - 55,496,966RGDNCBI36
Celera1049,088,721 - 49,089,868RGD
HuRef1049,807,245 - 49,808,392UniSTS
stSG618014  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,826,949 - 55,828,031UniSTSGRCh37
Build 361055,496,955 - 55,498,037RGDNCBI36
Celera1049,089,857 - 49,090,939RGD
HuRef1049,808,381 - 49,809,463UniSTS
stSG618018  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,832,186 - 55,833,650UniSTSGRCh37
Build 361055,502,192 - 55,503,656RGDNCBI36
Celera1049,095,094 - 49,096,558RGD
HuRef1049,813,618 - 49,815,082UniSTS
stSG618019  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,833,631 - 55,833,908UniSTSGRCh37
Build 361055,503,637 - 55,503,914RGDNCBI36
Celera1049,096,539 - 49,096,816RGD
HuRef1049,815,063 - 49,815,340UniSTS
stSG618020  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,836,366 - 55,837,435UniSTSGRCh37
Build 361055,506,372 - 55,507,441RGDNCBI36
Celera1049,099,274 - 49,100,343RGD
HuRef1049,817,797 - 49,818,866UniSTS
stSG618021  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,837,419 - 55,838,461UniSTSGRCh37
Build 361055,507,425 - 55,508,467RGDNCBI36
Celera1049,100,327 - 49,101,369RGD
HuRef1049,818,850 - 49,819,892UniSTS
stSG618022  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,838,442 - 55,839,914UniSTSGRCh37
Build 361055,508,448 - 55,509,920RGDNCBI36
Celera1049,101,350 - 49,102,822RGD
HuRef1049,819,873 - 49,821,345UniSTS
stSG618023  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,839,896 - 55,841,282UniSTSGRCh37
Build 361055,509,902 - 55,511,288RGDNCBI36
Celera1049,102,804 - 49,104,190RGD
HuRef1049,821,327 - 49,822,717UniSTS
stSG618024  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,841,263 - 55,841,457UniSTSGRCh37
Build 361055,511,269 - 55,511,463RGDNCBI36
Celera1049,104,171 - 49,104,365RGD
HuRef1049,822,698 - 49,822,892UniSTS
stSG618025  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,843,592 - 55,844,724UniSTSGRCh37
Build 361055,513,598 - 55,514,730RGDNCBI36
Celera1049,106,500 - 49,107,632RGD
HuRef1049,825,027 - 49,826,157UniSTS
stSG618026  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,844,640 - 55,845,656UniSTSGRCh37
Build 361055,514,646 - 55,515,662RGDNCBI36
Celera1049,107,548 - 49,108,564RGD
HuRef1049,826,073 - 49,827,089UniSTS
stSG618027  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,845,635 - 55,846,828UniSTSGRCh37
Build 361055,515,641 - 55,516,834RGDNCBI36
Celera1049,108,543 - 49,109,736RGD
HuRef1049,827,068 - 49,828,261UniSTS
stSG618028  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,848,833 - 55,849,874UniSTSGRCh37
Build 361055,518,839 - 55,519,880RGDNCBI36
Celera1049,111,741 - 49,112,782RGD
HuRef1049,830,266 - 49,831,307UniSTS
stSG618029  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,849,946 - 55,851,063UniSTSGRCh37
Build 361055,519,952 - 55,521,069RGDNCBI36
Celera1049,112,854 - 49,113,971RGD
HuRef1049,831,379 - 49,832,495UniSTS
stSG618030  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,851,062 - 55,852,230UniSTSGRCh37
Build 361055,521,068 - 55,522,236RGDNCBI36
Celera1049,113,970 - 49,115,138RGD
HuRef1049,832,494 - 49,833,662UniSTS
stSG618031  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,852,212 - 55,853,547UniSTSGRCh37
Build 361055,522,218 - 55,523,553RGDNCBI36
Celera1049,115,120 - 49,116,455RGD
HuRef1049,833,644 - 49,834,979UniSTS
stSG618032  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,853,533 - 55,854,711UniSTSGRCh37
Build 361055,523,539 - 55,524,717RGDNCBI36
Celera1049,116,441 - 49,117,619RGD
HuRef1049,834,965 - 49,836,143UniSTS
stSG618033  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,854,692 - 55,855,732UniSTSGRCh37
Build 361055,524,698 - 55,525,738RGDNCBI36
Celera1049,117,600 - 49,118,640RGD
HuRef1049,836,124 - 49,837,164UniSTS
stSG618034  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,857,449 - 55,858,466UniSTSGRCh37
Build 361055,527,455 - 55,528,472RGDNCBI36
Celera1049,120,357 - 49,121,372RGD
HuRef1049,838,881 - 49,839,896UniSTS
stSG618035  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,858,445 - 55,859,684UniSTSGRCh37
Build 361055,528,451 - 55,529,690RGDNCBI36
Celera1049,121,351 - 49,122,590RGD
HuRef1049,839,875 - 49,841,120UniSTS
stSG618036  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,859,674 - 55,860,683UniSTSGRCh37
Build 361055,529,680 - 55,530,689RGDNCBI36
Celera1049,122,580 - 49,123,589RGD
HuRef1049,841,110 - 49,842,119UniSTS
stSG618037  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,860,664 - 55,861,346UniSTSGRCh37
Build 361055,530,670 - 55,531,352RGDNCBI36
Celera1049,123,570 - 49,124,252RGD
HuRef1049,842,100 - 49,842,782UniSTS
stSG618038  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,866,103 - 55,867,166UniSTSGRCh37
Build 361055,536,109 - 55,537,172RGDNCBI36
Celera1049,129,003 - 49,130,066RGD
HuRef1049,847,533 - 49,848,596UniSTS
stSG618040  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,867,808 - 55,869,208UniSTSGRCh37
Build 361055,537,814 - 55,539,214RGDNCBI36
Celera1049,130,708 - 49,132,108RGD
HuRef1049,849,238 - 49,850,638UniSTS
stSG618041  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,869,187 - 55,870,326UniSTSGRCh37
Build 361055,539,193 - 55,540,332RGDNCBI36
Celera1049,132,087 - 49,133,227RGD
HuRef1049,850,617 - 49,851,756UniSTS
stSG618042  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,870,374 - 55,871,534UniSTSGRCh37
Build 361055,540,380 - 55,541,540RGDNCBI36
Celera1049,133,275 - 49,134,435RGD
HuRef1049,851,804 - 49,852,964UniSTS
stSG618043  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,871,517 - 55,872,882UniSTSGRCh37
Build 361055,541,523 - 55,542,888RGDNCBI36
Celera1049,134,418 - 49,135,783RGD
HuRef1049,852,947 - 49,854,312UniSTS
stSG618044  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,872,864 - 55,874,179UniSTSGRCh37
Build 361055,542,870 - 55,544,185RGDNCBI36
Celera1049,135,765 - 49,137,080RGD
HuRef1049,854,294 - 49,855,609UniSTS
stSG618045  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,876,410 - 55,876,692UniSTSGRCh37
Build 361055,546,416 - 55,546,698RGDNCBI36
Celera1049,139,311 - 49,139,593RGD
HuRef1049,857,840 - 49,858,122UniSTS
stSG618046  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,884,278 - 55,885,313UniSTSGRCh37
Build 361055,554,284 - 55,555,319RGDNCBI36
Celera1049,147,179 - 49,148,214RGD
HuRef1049,865,710 - 49,866,745UniSTS
stSG618047  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,885,301 - 55,886,717UniSTSGRCh37
Build 361055,555,307 - 55,556,723RGDNCBI36
Celera1049,148,202 - 49,149,619RGD
HuRef1049,866,733 - 49,868,150UniSTS
stSG618048  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,886,699 - 55,888,173UniSTSGRCh37
Build 361055,556,705 - 55,558,179RGDNCBI36
Celera1049,149,601 - 49,151,075RGD
HuRef1049,868,132 - 49,869,606UniSTS
stSG618049  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,888,158 - 55,889,408UniSTSGRCh37
Build 361055,558,164 - 55,559,414RGDNCBI36
Celera1049,151,060 - 49,152,310RGD
HuRef1049,869,591 - 49,870,841UniSTS
stSG618050  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,889,395 - 55,890,642UniSTSGRCh37
Build 361055,559,401 - 55,560,648RGDNCBI36
Celera1049,152,297 - 49,153,544RGD
HuRef1049,870,828 - 49,872,075UniSTS
stSG618051  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,890,624 - 55,891,706UniSTSGRCh37
Build 361055,560,630 - 55,561,712RGDNCBI36
Celera1049,153,526 - 49,154,608RGD
HuRef1049,872,057 - 49,873,139UniSTS
stSG618052  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,891,687 - 55,892,771UniSTSGRCh37
Build 361055,561,693 - 55,562,777RGDNCBI36
Celera1049,154,589 - 49,155,675RGD
HuRef1049,873,120 - 49,874,204UniSTS
stSG618053  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,892,714 - 55,893,713UniSTSGRCh37
Build 361055,562,720 - 55,563,719RGDNCBI36
Celera1049,155,618 - 49,156,617RGD
stSG618055  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,895,232 - 55,896,233UniSTSGRCh37
Build 361055,565,238 - 55,566,239RGDNCBI36
Celera1049,158,136 - 49,159,137RGD
HuRef1049,878,302 - 49,879,303UniSTS
stSG618056  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,896,128 - 55,897,133UniSTSGRCh37
Build 361055,566,134 - 55,567,139RGDNCBI36
Celera1049,159,032 - 49,160,037RGD
HuRef1049,879,198 - 49,880,203UniSTS
stSG618057  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,904,665 - 55,905,788UniSTSGRCh37
Build 361055,574,671 - 55,575,794RGDNCBI36
Celera1049,167,569 - 49,168,692RGD
HuRef1049,887,734 - 49,888,857UniSTS
stSG618060  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,907,141 - 55,908,610UniSTSGRCh37
Build 361055,577,147 - 55,578,616RGDNCBI36
Celera1049,170,089 - 49,171,558RGD
HuRef1049,890,238 - 49,891,707UniSTS
stSG618063  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,911,608 - 55,912,797UniSTSGRCh37
Build 361055,581,614 - 55,582,803RGDNCBI36
Celera1049,174,556 - 49,175,745RGD
HuRef1049,894,705 - 49,895,894UniSTS
stSG618064  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,912,778 - 55,913,928UniSTSGRCh37
Build 361055,582,784 - 55,583,934RGDNCBI36
Celera1049,175,726 - 49,176,876RGD
HuRef1049,895,875 - 49,897,025UniSTS
stSG618065  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,913,913 - 55,915,359UniSTSGRCh37
Build 361055,583,919 - 55,585,365RGDNCBI36
Celera1049,176,861 - 49,178,307RGD
HuRef1049,897,010 - 49,898,456UniSTS
stSG618066  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,914,640 - 55,915,816UniSTSGRCh37
Build 361055,584,646 - 55,585,822RGDNCBI36
Celera1049,177,588 - 49,178,764RGD
HuRef1049,897,737 - 49,898,913UniSTS
stSG618067  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,915,798 - 55,915,984UniSTSGRCh37
Build 361055,585,804 - 55,585,990RGDNCBI36
Celera1049,178,746 - 49,178,932RGD
HuRef1049,898,895 - 49,899,081UniSTS
stSG618068  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,918,267 - 55,919,327UniSTSGRCh37
Build 361055,588,273 - 55,589,333RGDNCBI36
Celera1049,181,215 - 49,182,275RGD
HuRef1049,901,364 - 49,902,427UniSTS
stSG618069  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,919,399 - 55,919,610UniSTSGRCh37
Build 361055,589,405 - 55,589,616RGDNCBI36
Celera1049,182,347 - 49,182,558RGD
HuRef1049,902,499 - 49,902,710UniSTS
stSG618070  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,921,826 - 55,922,868UniSTSGRCh37
Build 361055,591,832 - 55,592,874RGDNCBI36
Celera1049,184,769 - 49,185,811RGD
HuRef1049,904,921 - 49,905,963UniSTS
stSG618072  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,923,911 - 55,925,152UniSTSGRCh37
Build 361055,593,917 - 55,595,158RGDNCBI36
Celera1049,186,854 - 49,188,095RGD
HuRef1049,907,006 - 49,908,247UniSTS
stSG618073  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,925,136 - 55,926,292UniSTSGRCh37
Build 361055,595,142 - 55,596,298RGDNCBI36
Celera1049,188,079 - 49,189,235RGD
HuRef1049,908,231 - 49,909,387UniSTS
stSG618074  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,932,280 - 55,932,593UniSTSGRCh37
Build 361055,602,286 - 55,602,599RGDNCBI36
Celera1049,195,223 - 49,195,536RGD
HuRef1049,915,458 - 49,915,771UniSTS
stSG618075  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,932,595 - 55,933,740UniSTSGRCh37
Build 361055,602,601 - 55,603,746RGDNCBI36
Celera1049,195,538 - 49,196,683RGD
HuRef1049,915,773 - 49,916,918UniSTS
stSG618076  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,933,840 - 55,934,906UniSTSGRCh37
Build 361055,603,846 - 55,604,912RGDNCBI36
Celera1049,196,783 - 49,197,849RGD
HuRef1049,917,018 - 49,918,084UniSTS
stSG618077  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,934,889 - 55,936,078UniSTSGRCh37
Build 361055,604,895 - 55,606,084RGDNCBI36
Celera1049,197,832 - 49,199,021RGD
HuRef1049,918,067 - 49,919,256UniSTS
stSG618078  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,936,098 - 55,937,481UniSTSGRCh37
Build 361055,606,104 - 55,607,487RGDNCBI36
Celera1049,199,041 - 49,200,425RGD
HuRef1049,919,276 - 49,920,660UniSTS
stSG618079  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,937,439 - 55,938,440UniSTSGRCh37
Build 361055,607,445 - 55,608,446RGDNCBI36
Celera1049,200,383 - 49,201,384RGD
HuRef1049,920,618 - 49,921,619UniSTS
stSG618080  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,938,419 - 55,939,616UniSTSGRCh37
Build 361055,608,425 - 55,609,622RGDNCBI36
Celera1049,201,363 - 49,202,560RGD
HuRef1049,921,598 - 49,922,795UniSTS
stSG618081  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,939,595 - 55,940,595UniSTSGRCh37
Build 361055,609,601 - 55,610,601RGDNCBI36
Celera1049,202,539 - 49,203,539RGD
HuRef1049,922,774 - 49,923,774UniSTS
stSG618082  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,940,587 - 55,941,614UniSTSGRCh37
Build 361055,610,593 - 55,611,620RGDNCBI36
Celera1049,203,531 - 49,204,558RGD
HuRef1049,923,766 - 49,924,793UniSTS
stSG618083  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,941,028 - 55,942,245UniSTSGRCh37
Build 361055,611,034 - 55,612,251RGDNCBI36
Celera1049,203,972 - 49,205,189RGD
HuRef1049,924,207 - 49,925,424UniSTS
stSG618084  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,942,226 - 55,943,292UniSTSGRCh37
Build 361055,612,232 - 55,613,298RGDNCBI36
Celera1049,205,170 - 49,206,236RGD
HuRef1049,925,405 - 49,926,474UniSTS
stSG618085  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,943,273 - 55,944,308UniSTSGRCh37
Build 361055,613,279 - 55,614,314RGDNCBI36
Celera1049,206,217 - 49,207,252RGD
HuRef1049,926,455 - 49,927,491UniSTS
stSG618087  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,945,778 - 55,946,924UniSTSGRCh37
Build 361055,615,784 - 55,616,930RGDNCBI36
Celera1049,208,722 - 49,209,868RGD
HuRef1049,928,961 - 49,930,107UniSTS
stSG618088  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,946,905 - 55,947,966UniSTSGRCh37
Build 361055,616,911 - 55,617,972RGDNCBI36
Celera1049,209,849 - 49,210,910RGD
HuRef1049,930,088 - 49,931,149UniSTS
stSG618089  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,947,957 - 55,949,155UniSTSGRCh37
Build 361055,617,963 - 55,619,161RGDNCBI36
Celera1049,210,901 - 49,212,099RGD
HuRef1049,931,140 - 49,932,338UniSTS
stSG618090  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,949,136 - 55,950,164UniSTSGRCh37
Build 361055,619,142 - 55,620,170RGDNCBI36
Celera1049,212,080 - 49,213,108RGD
HuRef1049,932,319 - 49,933,343UniSTS
stSG618091  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,950,144 - 55,951,311UniSTSGRCh37
Build 361055,620,150 - 55,621,317RGDNCBI36
Celera1049,213,088 - 49,214,255RGD
HuRef1049,933,323 - 49,934,490UniSTS
stSG618092  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,951,292 - 55,952,596UniSTSGRCh37
Build 361055,621,298 - 55,622,602RGDNCBI36
Celera1049,214,236 - 49,215,540RGD
HuRef1049,934,471 - 49,935,776UniSTS
stSG618093  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,952,578 - 55,953,924UniSTSGRCh37
Build 361055,622,584 - 55,623,930RGDNCBI36
Celera1049,215,522 - 49,216,868RGD
HuRef1049,935,758 - 49,937,103UniSTS
stSG618094  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,953,907 - 55,954,975UniSTSGRCh37
Build 361055,623,913 - 55,624,981RGDNCBI36
Celera1049,216,851 - 49,217,925RGD
HuRef1049,937,086 - 49,938,160UniSTS
stSG618095  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,954,960 - 55,956,297UniSTSGRCh37
Build 361055,624,966 - 55,626,303RGDNCBI36
Celera1049,217,910 - 49,219,247RGD
HuRef1049,938,145 - 49,939,482UniSTS
stSG618096  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,956,276 - 55,957,417UniSTSGRCh37
Build 361055,626,282 - 55,627,423RGDNCBI36
Celera1049,219,226 - 49,220,367RGD
HuRef1049,939,461 - 49,940,602UniSTS
stSG618097  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,957,397 - 55,958,625UniSTSGRCh37
Build 361055,627,403 - 55,628,631RGDNCBI36
Celera1049,220,347 - 49,221,575RGD
HuRef1049,940,582 - 49,941,818UniSTS
stSG618098  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,958,623 - 55,959,816UniSTSGRCh37
Build 361055,628,629 - 55,629,822RGDNCBI36
Celera1049,221,573 - 49,222,772RGD
HuRef1049,941,816 - 49,943,021UniSTS
stSG618099  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,959,226 - 55,960,285UniSTSGRCh37
Build 361055,629,232 - 55,630,291RGDNCBI36
Celera1049,222,176 - 49,223,241RGD
HuRef1049,942,419 - 49,943,491UniSTS
stSG618100  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,960,270 - 55,961,744UniSTSGRCh37
Build 361055,630,276 - 55,631,750RGDNCBI36
Celera1049,223,226 - 49,224,698RGD
HuRef1049,943,476 - 49,944,948UniSTS
stSG618101  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,961,816 - 55,962,054UniSTSGRCh37
Build 361055,631,822 - 55,632,060RGDNCBI36
Celera1049,224,770 - 49,225,008RGD
HuRef1049,945,020 - 49,945,258UniSTS
stSG618102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,962,094 - 55,963,144UniSTSGRCh37
Build 361055,632,100 - 55,633,150RGDNCBI36
Celera1049,225,048 - 49,226,099RGD
HuRef1049,945,298 - 49,946,349UniSTS
stSG618103  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,963,137 - 55,964,502UniSTSGRCh37
Build 361055,633,143 - 55,634,508RGDNCBI36
Celera1049,226,092 - 49,227,456RGD
HuRef1049,946,342 - 49,947,706UniSTS
stSG618104  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,964,483 - 55,965,921UniSTSGRCh37
Build 361055,634,489 - 55,635,927RGDNCBI36
Celera1049,227,437 - 49,228,875RGD
HuRef1049,947,687 - 49,949,125UniSTS
stSG618106  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,966,101 - 55,967,408UniSTSGRCh37
Build 361055,636,107 - 55,637,414RGDNCBI36
Celera1049,229,055 - 49,230,350RGD
HuRef1049,949,305 - 49,950,595UniSTS
stSG618107  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,967,390 - 55,968,636UniSTSGRCh37
Build 361055,637,396 - 55,638,642RGDNCBI36
Celera1049,230,332 - 49,231,578RGD
HuRef1049,950,577 - 49,951,823UniSTS
stSG618108  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,968,617 - 55,969,701UniSTSGRCh37
Build 361055,638,623 - 55,639,707RGDNCBI36
Celera1049,231,559 - 49,232,643RGD
HuRef1049,951,804 - 49,952,888UniSTS
stSG618109  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,969,684 - 55,971,075UniSTSGRCh37
Build 361055,639,690 - 55,641,081RGDNCBI36
Celera1049,232,626 - 49,234,017RGD
HuRef1049,952,871 - 49,954,262UniSTS
stSG618110  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,971,062 - 55,972,395UniSTSGRCh37
Build 361055,641,068 - 55,642,401RGDNCBI36
Celera1049,234,004 - 49,235,337RGD
HuRef1049,954,249 - 49,955,582UniSTS
stSG618111  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,972,376 - 55,973,775UniSTSGRCh37
Build 361055,642,382 - 55,643,781RGDNCBI36
Celera1049,235,318 - 49,236,716RGD
HuRef1049,955,563 - 49,956,962UniSTS
stSG618112  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,973,773 - 55,975,037UniSTSGRCh37
Build 361055,643,779 - 55,645,043RGDNCBI36
Celera1049,236,714 - 49,237,978RGD
HuRef1049,956,960 - 49,958,220UniSTS
stSG618113  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,974,739 - 55,975,916UniSTSGRCh37
Build 361055,644,745 - 55,645,922RGDNCBI36
Celera1049,237,680 - 49,238,857RGD
HuRef1049,957,926 - 49,959,106UniSTS
stSG618115  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,979,857 - 55,981,078UniSTSGRCh37
Build 361055,649,863 - 55,651,084RGDNCBI36
Celera1049,242,798 - 49,244,019RGD
HuRef1049,963,047 - 49,964,272UniSTS
stSG618116  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,980,961 - 55,982,009UniSTSGRCh37
Build 361055,650,967 - 55,652,015RGDNCBI36
Celera1049,243,902 - 49,244,950RGD
HuRef1049,964,155 - 49,965,203UniSTS
stSG618117  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371055,981,991 - 55,983,438UniSTSGRCh37
Build 361055,651,997 - 55,653,444RGDNCBI36
Celera1049,244,932 - 49,246,379RGD
HuRef1049,965,185 - 49,966,632UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
renal system
reproductive system
respiratory system
sensory system
visual system
775 2119 1705 1609 4637 1198 1509 186 773 108 1758 4101 4071 23 3609 493 1284 1238 83 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_009191 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001142763 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001142764 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001142765 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001142766 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001142767 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001142768 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001142769 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001142770 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001142771 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001142772 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001142773 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001354404 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001354411 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001354420 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001354429 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001354430 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001384140 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_033056 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017016573 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425663 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047425664 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366620 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054366621 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001747192 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001747193 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB839113 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB839114 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB839115 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB839116 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB839117 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB839118 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC013737 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC016817 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC016822 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC024073 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC027671 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC051618 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC069545 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC074322 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC079271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK126923 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL353784 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL355314 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL356114 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL360214 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL365496 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL390785 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL391356 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL603835 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL834134 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW005431 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY029205 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY029237 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY388963 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM675194 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471083 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068268 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU718480 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU718481 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EU718482 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF455239 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000320301   ⟹   ENSP00000322604
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,821,099 - 54,801,231 (-)Ensembl
Ensembl Acc Id: ENST00000361849   ⟹   ENSP00000354950
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,821,110 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000373955   ⟹   ENSP00000363066
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,994,579 - 54,801,188 (-)Ensembl
Ensembl Acc Id: ENST00000373956   ⟹   ENSP00000363067
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,821,110 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000373957   ⟹   ENSP00000363068
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,821,110 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000373965   ⟹   ENSP00000363076
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,802,771 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000395430   ⟹   ENSP00000378818
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,821,110 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000395432   ⟹   ENSP00000378820
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,821,100 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000395433   ⟹   ENSP00000378821
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,821,110 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000395438   ⟹   ENSP00000378826
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,808,692 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000395440   ⟹   ENSP00000378827
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,808,070 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000395442   ⟹   ENSP00000378829
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,808,070 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000395445   ⟹   ENSP00000378832
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,808,070 - 54,801,231 (-)Ensembl
Ensembl Acc Id: ENST00000395446   ⟹   ENSP00000378833
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,808,085 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000409834   ⟹   ENSP00000386693
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,808,108 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000414367   ⟹   ENSP00000412531
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,808,131 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000414778   ⟹   ENSP00000410304
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,802,771 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000437009   ⟹   ENSP00000412628
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,821,110 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000448885   ⟹   ENSP00000412320
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,821,110 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000458638   ⟹   ENSP00000394465
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1054,378,823 - 55,319,614 (-)Ensembl
Ensembl Acc Id: ENST00000463095
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,821,276 - 53,907,217 (-)Ensembl
Ensembl Acc Id: ENST00000476074
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,806,986 - 53,818,384 (-)Ensembl
Ensembl Acc Id: ENST00000495484   ⟹   ENSP00000480780
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,806,325 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000612394   ⟹   ENSP00000482921
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,808,692 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000613346   ⟹   ENSP00000481211
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1054,378,816 - 55,627,942 (-)Ensembl
Ensembl Acc Id: ENST00000613657   ⟹   ENSP00000482794
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,808,070 - 54,801,231 (-)Ensembl
Ensembl Acc Id: ENST00000614895   ⟹   ENSP00000478512
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,802,771 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000615043   ⟹   ENSP00000478551
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,808,522 - 53,810,664 (-)Ensembl
Ensembl Acc Id: ENST00000616114   ⟹   ENSP00000483745
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,806,156 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000617051   ⟹   ENSP00000484703
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,821,100 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000617271   ⟹   ENSP00000478076
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,808,070 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000618301   ⟹   ENSP00000482780
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,806,501 - 53,857,206 (-)Ensembl
Ensembl Acc Id: ENST00000621708   ⟹   ENSP00000484454
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,806,323 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000622048   ⟹   ENSP00000482329
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,821,100 - 54,801,291 (-)Ensembl
Ensembl Acc Id: ENST00000642496   ⟹   ENSP00000495930
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,806,326 - 54,195,846 (-)Ensembl
Ensembl Acc Id: ENST00000644397   ⟹   ENSP00000495195
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1053,802,771 - 54,801,231 (-)Ensembl
RefSeq Acc Id: NM_001142763   ⟹   NP_001136235
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381053,821,099 - 54,801,231 (-)NCBI
GRCh371055,562,531 - 56,561,051 (-)ENTREZGENE
HuRef1049,544,130 - 50,545,244 (-)ENTREZGENE
CHM1_11055,862,344 - 56,842,749 (-)NCBI
T2T-CHM13v2.01054,669,972 - 55,651,057 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001142764   ⟹   NP_001136236
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381053,821,099 - 54,801,231 (-)NCBI
GRCh371055,562,531 - 56,561,051 (-)ENTREZGENE
HuRef1049,544,130 - 50,545,244 (-)ENTREZGENE
CHM1_11055,862,344 - 56,842,749 (-)NCBI
T2T-CHM13v2.01054,669,972 - 55,651,057 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001142765   ⟹   NP_001136237
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381053,821,099 - 54,801,231 (-)NCBI
GRCh371055,562,531 - 56,561,051 (-)ENTREZGENE
HuRef1049,544,130 - 50,545,244 (-)ENTREZGENE
CHM1_11055,862,344 - 56,842,749 (-)NCBI
T2T-CHM13v2.01054,669,972 - 55,651,057 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001142766   ⟹   NP_001136238
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381053,821,099 - 54,801,231 (-)NCBI
GRCh371055,562,531 - 56,561,051 (-)ENTREZGENE
HuRef1049,544,130 - 50,545,244 (-)ENTREZGENE
CHM1_11055,862,344 - 56,842,749 (-)NCBI
T2T-CHM13v2.01054,669,972 - 55,651,057 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001142767   ⟹   NP_001136239
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381053,821,099 - 54,801,231 (-)NCBI
GRCh371055,562,531 - 56,561,051 (-)ENTREZGENE
HuRef1049,544,130 - 50,545,244 (-)ENTREZGENE
CHM1_11055,862,344 - 56,842,749 (-)NCBI
T2T-CHM13v2.01054,669,972 - 55,651,057 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001142768   ⟹   NP_001136240
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381053,821,099 - 54,801,231 (-)NCBI
GRCh371055,562,531 - 56,561,051 (-)ENTREZGENE
HuRef1049,544,130 - 50,545,244 (-)ENTREZGENE
CHM1_11055,862,344 - 56,842,749 (-)NCBI
T2T-CHM13v2.01054,669,972 - 55,651,057 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001142769   ⟹   NP_001136241
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381053,808,070 - 54,801,231 (-)NCBI
GRCh371055,562,531 - 56,561,051 (-)ENTREZGENE
HuRef1049,544,130 - 50,545,244 (-)ENTREZGENE
CHM1_11055,849,936 - 56,842,749 (-)NCBI
T2T-CHM13v2.01054,656,948 - 55,651,057 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001142770   ⟹   NP_001136242
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381053,808,070 - 54,801,231 (-)NCBI
GRCh371055,562,531 - 56,561,051 (-)NCBI
HuRef1049,544,130 - 50,545,244 (-)ENTREZGENE
CHM1_11055,849,936 - 56,842,749 (-)NCBI
T2T-CHM13v2.01054,656,948 - 55,651,057 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001142771   ⟹   NP_001136243
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381053,802,771 - 54,801,231 (-)NCBI
GRCh371055,562,531 - 56,561,051 (-)NCBI
HuRef1049,544,130 - 50,545,244 (-)ENTREZGENE
CHM1_11055,844,015 - 56,842,749 (-)NCBI
T2T-CHM13v2.01054,651,649 - 55,651,057 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001142772   ⟹   NP_001136244
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381053,802,771 - 54,801,231 (-)NCBI
GRCh371055,562,531 - 56,561,051 (-)NCBI
HuRef1049,544,130 - 50,545,244 (-)ENTREZGENE
CHM1_11055,844,015 - 56,842,749 (-)NCBI
T2T-CHM13v2.01054,651,649 - 55,651,057 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001142773   ⟹   NP_001136245
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381053,821,099 - 54,801,231 (-)NCBI
GRCh371055,562,531 - 56,561,051 (-)ENTREZGENE
HuRef1049,544,130 - 50,545,244 (-)ENTREZGENE
CHM1_11055,862,344 - 56,842,749 (-)NCBI
T2T-CHM13v2.01054,669,972 - 55,651,057 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001354404   ⟹   NP_001341333
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381053,821,099 - 55,627,942 (-)NCBI
T2T-CHM13v2.01054,669,972 - 56,478,314 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001354411   ⟹   NP_001341340
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381053,808,070 - 54,801,231 (-)NCBI
T2T-CHM13v2.01054,656,948 - 55,651,057 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001354420   ⟹   NP_001341349
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381053,802,771 - 54,801,231 (-)NCBI
T2T-CHM13v2.01054,651,649 - 55,651,057 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001354429   ⟹   NP_001341358
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381053,802,771 - 54,801,231 (-)NCBI
T2T-CHM13v2.01054,651,649 - 55,651,057 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001354430   ⟹   NP_001341359
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381053,994,572 - 54,801,231 (-)NCBI
T2T-CHM13v2.01054,843,365 - 55,651,057 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001384140   ⟹   NP_001371069
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381053,802,771 - 54,801,231 (-)NCBI
T2T-CHM13v2.01054,651,649 - 55,651,057 (-)NCBI
Sequence:
RefSeq Acc Id: NM_033056   ⟹   NP_149045
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381053,821,099 - 54,801,231 (-)NCBI
GRCh371055,562,531 - 56,561,051 (-)ENTREZGENE
Build 361055,250,866 - 56,231,057 (-)NCBI Archive
HuRef1049,544,130 - 50,545,244 (-)ENTREZGENE
CHM1_11055,862,344 - 56,842,749 (-)NCBI
T2T-CHM13v2.01054,669,972 - 55,651,057 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047425663   ⟹   XP_047281619
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381053,802,771 - 54,801,231 (-)NCBI
RefSeq Acc Id: XM_047425664   ⟹   XP_047281620
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381053,808,331 - 54,801,231 (-)NCBI
RefSeq Acc Id: XM_054366620   ⟹   XP_054222595
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01054,651,649 - 55,651,057 (-)NCBI
RefSeq Acc Id: XM_054366621   ⟹   XP_054222596
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01054,657,208 - 56,479,356 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001136235 (Get FASTA)   NCBI Sequence Viewer  
  NP_001136236 (Get FASTA)   NCBI Sequence Viewer  
  NP_001136237 (Get FASTA)   NCBI Sequence Viewer  
  NP_001136238 (Get FASTA)   NCBI Sequence Viewer  
  NP_001136239 (Get FASTA)   NCBI Sequence Viewer  
  NP_001136240 (Get FASTA)   NCBI Sequence Viewer  
  NP_001136241 (Get FASTA)   NCBI Sequence Viewer  
  NP_001136242 (Get FASTA)   NCBI Sequence Viewer  
  NP_001136243 (Get FASTA)   NCBI Sequence Viewer  
  NP_001136244 (Get FASTA)   NCBI Sequence Viewer  
  NP_001136245 (Get FASTA)   NCBI Sequence Viewer  
  NP_001341333 (Get FASTA)   NCBI Sequence Viewer  
  NP_001341340 (Get FASTA)   NCBI Sequence Viewer  
  NP_001341349 (Get FASTA)   NCBI Sequence Viewer  
  NP_001341358 (Get FASTA)   NCBI Sequence Viewer  
  NP_001341359 (Get FASTA)   NCBI Sequence Viewer  
  NP_001371069 (Get FASTA)   NCBI Sequence Viewer  
  NP_149045 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281619 (Get FASTA)   NCBI Sequence Viewer  
  XP_047281620 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222595 (Get FASTA)   NCBI Sequence Viewer  
  XP_054222596 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAK31581 (Get FASTA)   NCBI Sequence Viewer  
  AAK31804 (Get FASTA)   NCBI Sequence Viewer  
  AAR26468 (Get FASTA)   NCBI Sequence Viewer  
  ACF76476 (Get FASTA)   NCBI Sequence Viewer  
  ACF76477 (Get FASTA)   NCBI Sequence Viewer  
  ACF76478 (Get FASTA)   NCBI Sequence Viewer  
  BAG54399 (Get FASTA)   NCBI Sequence Viewer  
  CAD38850 (Get FASTA)   NCBI Sequence Viewer  
  EAW54151 (Get FASTA)   NCBI Sequence Viewer  
  EAW54152 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000322604
  ENSP00000322604.6
  ENSP00000354950
  ENSP00000354950.3
  ENSP00000363066
  ENSP00000363066.1
  ENSP00000363067.4
  ENSP00000363068
  ENSP00000363068.4
  ENSP00000363076
  ENSP00000363076.3
  ENSP00000378818
  ENSP00000378818.1
  ENSP00000378821
  ENSP00000378821.1
  ENSP00000378827.1
  ENSP00000378829.1
  ENSP00000378832
  ENSP00000378832.2
  ENSP00000378833.1
  ENSP00000386693.1
  ENSP00000394465.1
  ENSP00000412320.1
  ENSP00000412531.1
  ENSP00000412628
  ENSP00000412628.2
  ENSP00000478076
  ENSP00000478076.1
  ENSP00000478551.1
  ENSP00000480780.1
  ENSP00000481211.1
  ENSP00000482780.1
  ENSP00000482794
  ENSP00000482794.1
  ENSP00000483745
  ENSP00000483745.1
  ENSP00000484454
  ENSP00000484454.1
  ENSP00000495195
  ENSP00000495195.1
  ENSP00000495930.1
GenBank Protein Q96QU1 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_001136244   ⟸   NM_001142772
- Peptide Label: isoform CD3-2 precursor
- UniProtKB: A9Z1W1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001136243   ⟸   NM_001142771
- Peptide Label: isoform CD3-1 precursor
- UniProtKB: A0A087X1T6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001136242   ⟸   NM_001142770
- Peptide Label: isoform CD2-2 precursor
- UniProtKB: A0A087WTR6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001136241   ⟸   NM_001142769
- Peptide Label: isoform CD2-1 precursor
- UniProtKB: A0A087WZN9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001136245   ⟸   NM_001142773
- Peptide Label: isoform CD1-10 precursor
- UniProtKB: A2A3E8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001136240   ⟸   NM_001142768
- Peptide Label: isoform CD1-9 precursor
- Sequence:
RefSeq Acc Id: NP_001136239   ⟸   NM_001142767
- Peptide Label: isoform CD1-8 precursor
- UniProtKB: E7EMG0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001136237   ⟸   NM_001142765
- Peptide Label: isoform CD1-6 precursor
- UniProtKB: E7EM53 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001136238   ⟸   NM_001142766
- Peptide Label: isoform CD1-7 precursor
- UniProtKB: A2A3E6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_149045   ⟸   NM_033056
- Peptide Label: isoform CD1-4 precursor
- UniProtKB: Q8NDB9 (UniProtKB/Swiss-Prot),   Q6TRH8 (UniProtKB/Swiss-Prot),   Q5VY39 (UniProtKB/Swiss-Prot),   Q5VY38 (UniProtKB/Swiss-Prot),   C6ZEF7 (UniProtKB/Swiss-Prot),   C6ZEF6 (UniProtKB/Swiss-Prot),   C6ZEF5 (UniProtKB/Swiss-Prot),   A6NL19 (UniProtKB/Swiss-Prot),   Q96QT8 (UniProtKB/Swiss-Prot),   Q96QU1 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001136236   ⟸   NM_001142764
- Peptide Label: isoform CD1-2 precursor
- UniProtKB: A2A3E7 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001136235   ⟸   NM_001142763
- Peptide Label: isoform CD1-1 precursor
- UniProtKB: A2A3D8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001341349   ⟸   NM_001354420
- Peptide Label: isoform CD3-a precursor
- Sequence:
RefSeq Acc Id: NP_001341358   ⟸   NM_001354429
- Peptide Label: isoform CD3-b precursor
- Sequence:
RefSeq Acc Id: NP_001341340   ⟸   NM_001354411
- Peptide Label: isoform CD2-a precursor
- Sequence:
RefSeq Acc Id: NP_001341333   ⟸   NM_001354404
- Peptide Label: isoform CD1-a precursor
- Sequence:
RefSeq Acc Id: NP_001341359   ⟸   NM_001354430
- Peptide Label: isoform CD-Sa precursor
- Sequence:
Ensembl Acc Id: ENSP00000484454   ⟸   ENST00000621708
Ensembl Acc Id: ENSP00000482329   ⟸   ENST00000622048
Ensembl Acc Id: ENSP00000363067   ⟸   ENST00000373956
Ensembl Acc Id: ENSP00000363066   ⟸   ENST00000373955
Ensembl Acc Id: ENSP00000363068   ⟸   ENST00000373957
Ensembl Acc Id: ENSP00000363076   ⟸   ENST00000373965
Ensembl Acc Id: ENSP00000322604   ⟸   ENST00000320301
Ensembl Acc Id: ENSP00000412531   ⟸   ENST00000414367
Ensembl Acc Id: ENSP00000410304   ⟸   ENST00000414778
Ensembl Acc Id: ENSP00000354950   ⟸   ENST00000361849
Ensembl Acc Id: ENSP00000482921   ⟸   ENST00000612394
Ensembl Acc Id: ENSP00000481211   ⟸   ENST00000613346
Ensembl Acc Id: ENSP00000482794   ⟸   ENST00000613657
Ensembl Acc Id: ENSP00000480780   ⟸   ENST00000495484
Ensembl Acc Id: ENSP00000478512   ⟸   ENST00000614895
Ensembl Acc Id: ENSP00000394465   ⟸   ENST00000458638
Ensembl Acc Id: ENSP00000478551   ⟸   ENST00000615043
Ensembl Acc Id: ENSP00000483745   ⟸   ENST00000616114
Ensembl Acc Id: ENSP00000484703   ⟸   ENST00000617051
Ensembl Acc Id: ENSP00000495930   ⟸   ENST00000642496
Ensembl Acc Id: ENSP00000478076   ⟸   ENST00000617271
Ensembl Acc Id: ENSP00000482780   ⟸   ENST00000618301
Ensembl Acc Id: ENSP00000495195   ⟸   ENST00000644397
Ensembl Acc Id: ENSP00000386693   ⟸   ENST00000409834
Ensembl Acc Id: ENSP00000412320   ⟸   ENST00000448885
Ensembl Acc Id: ENSP00000378826   ⟸   ENST00000395438
Ensembl Acc Id: ENSP00000378820   ⟸   ENST00000395432
Ensembl Acc Id: ENSP00000378821   ⟸   ENST00000395433
Ensembl Acc Id: ENSP00000378818   ⟸   ENST00000395430
Ensembl Acc Id: ENSP00000378832   ⟸   ENST00000395445
Ensembl Acc Id: ENSP00000378833   ⟸   ENST00000395446
Ensembl Acc Id: ENSP00000378829   ⟸   ENST00000395442
Ensembl Acc Id: ENSP00000378827   ⟸   ENST00000395440
Ensembl Acc Id: ENSP00000412628   ⟸   ENST00000437009
RefSeq Acc Id: NP_001371069   ⟸   NM_001384140
- Peptide Label: soform CD3-c precursor
- UniProtKB: A0A2R8Y6C0 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047281619   ⟸   XM_047425663
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047281620   ⟸   XM_047425664
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054222595   ⟸   XM_054366620
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054222596   ⟸   XM_054366621
- Peptide Label: isoform X2
Protein Domains
Cadherin   Extracellular cadherin

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q96QU1-F1-model_v2 AlphaFold Q96QU1 1-1955 view protein structure

Promoters
RGD ID:7217571
Promoter ID:EPDNEW_H14531
Type:single initiation site
Name:PCDH15_2
Description:protocadherin related 15
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H14532  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381054,739,224 - 54,739,284EPDNEW
RGD ID:7217573
Promoter ID:EPDNEW_H14532
Type:initiation region
Name:PCDH15_1
Description:protocadherin related 15
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H14531  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381054,801,202 - 54,801,262EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:14674 AgrOrtholog
COSMIC PCDH15 COSMIC
Ensembl Genes ENSG00000150275 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000320301 ENTREZGENE
  ENST00000320301.11 UniProtKB/Swiss-Prot
  ENST00000361849 ENTREZGENE
  ENST00000361849.7 UniProtKB/TrEMBL
  ENST00000373955 ENTREZGENE
  ENST00000373955.5 UniProtKB/Swiss-Prot
  ENST00000373956.7 UniProtKB/TrEMBL
  ENST00000373957 ENTREZGENE
  ENST00000373957.7 UniProtKB/TrEMBL
  ENST00000373965 ENTREZGENE
  ENST00000373965.6 UniProtKB/TrEMBL
  ENST00000395430 ENTREZGENE
  ENST00000395430.5 UniProtKB/TrEMBL
  ENST00000395433 ENTREZGENE
  ENST00000395433.5 UniProtKB/TrEMBL
  ENST00000395440.5 UniProtKB/TrEMBL
  ENST00000395442.5 UniProtKB/TrEMBL
  ENST00000395445 ENTREZGENE
  ENST00000395445.6 UniProtKB/Swiss-Prot
  ENST00000395446.5 UniProtKB/TrEMBL
  ENST00000409834.5 UniProtKB/TrEMBL
  ENST00000414367.5 UniProtKB/TrEMBL
  ENST00000437009 ENTREZGENE
  ENST00000437009.5 UniProtKB/TrEMBL
  ENST00000448885.5 UniProtKB/TrEMBL
  ENST00000458638.1 UniProtKB/TrEMBL
  ENST00000495484.5 UniProtKB/TrEMBL
  ENST00000613346.4 UniProtKB/TrEMBL
  ENST00000613657 ENTREZGENE
  ENST00000613657.6 UniProtKB/TrEMBL
  ENST00000615043.1 UniProtKB/TrEMBL
  ENST00000616114 ENTREZGENE
  ENST00000616114.4 UniProtKB/Swiss-Prot
  ENST00000617271 ENTREZGENE
  ENST00000617271.4 UniProtKB/TrEMBL
  ENST00000618301.4 UniProtKB/TrEMBL
  ENST00000621708 ENTREZGENE
  ENST00000621708.4 UniProtKB/TrEMBL
  ENST00000642496.1 UniProtKB/TrEMBL
  ENST00000644397 ENTREZGENE
  ENST00000644397.2 UniProtKB/TrEMBL
Gene3D-CATH 2.60.40.3430 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cadherins UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000150275 GTEx
HGNC ID HGNC:14674 ENTREZGENE
Human Proteome Map PCDH15 Human Proteome Map
InterPro Cadherin UniProtKB/TrEMBL
  Cadherin-domain_protein UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cadherin-like_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cadherin-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cadherin_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EC_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Protocadherin-15 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:65217 UniProtKB/Swiss-Prot
NCBI Gene 65217 ENTREZGENE
OMIM 605514 OMIM
PANTHER CADHERIN DOMAIN-CONTAINING PROTEIN UniProtKB/TrEMBL
  CADHERIN-23 UniProtKB/TrEMBL
  CADHERIN-99C UniProtKB/TrEMBL
  DESMOGLEIN FAMILY MEMBER UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  FAT ATYPICAL CADHERIN-RELATED UniProtKB/TrEMBL
  NEURAL-CADHERIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Cadherin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ECD UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA32999 PharmGKB
PRINTS CADHERIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PRICHEXTENSN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE CADHERIN_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CADHERIN_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART SM00112 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF49313 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A087WTR6 ENTREZGENE, UniProtKB/TrEMBL
  A0A087WUC7_HUMAN UniProtKB/TrEMBL
  A0A087WX70_HUMAN UniProtKB/TrEMBL
  A0A087WXQ6_HUMAN UniProtKB/TrEMBL
  A0A087WZN4_HUMAN UniProtKB/TrEMBL
  A0A087WZN9 ENTREZGENE, UniProtKB/TrEMBL
  A0A087X1T6 ENTREZGENE, UniProtKB/TrEMBL
  A0A2R8Y6C0 ENTREZGENE, UniProtKB/TrEMBL
  A0A2R8YEV2_HUMAN UniProtKB/TrEMBL
  A2A3D8 ENTREZGENE, UniProtKB/TrEMBL
  A2A3D9_HUMAN UniProtKB/TrEMBL
  A2A3E1_HUMAN UniProtKB/TrEMBL
  A2A3E4_HUMAN UniProtKB/TrEMBL
  A2A3E5_HUMAN UniProtKB/TrEMBL
  A2A3E6 ENTREZGENE, UniProtKB/TrEMBL
  A2A3E7 ENTREZGENE, UniProtKB/TrEMBL
  A2A3E8 ENTREZGENE, UniProtKB/TrEMBL
  A6NL19 ENTREZGENE
  A9Z1W1 ENTREZGENE, UniProtKB/TrEMBL
  B7ZBT8_HUMAN UniProtKB/TrEMBL
  C6ZEF5 ENTREZGENE
  C6ZEF6 ENTREZGENE
  C6ZEF7 ENTREZGENE
  E7EM53 ENTREZGENE, UniProtKB/TrEMBL
  E7EM97_HUMAN UniProtKB/TrEMBL
  E7EMG0 ENTREZGENE
  E7EMG8_HUMAN UniProtKB/TrEMBL
  PCD15_HUMAN UniProtKB/Swiss-Prot
  Q5VY38 ENTREZGENE
  Q5VY39 ENTREZGENE
  Q6TRH8 ENTREZGENE
  Q8NDB9 ENTREZGENE
  Q96QT8 ENTREZGENE
  Q96QU1 ENTREZGENE
UniProt Secondary A6NL19 UniProtKB/Swiss-Prot
  C6ZEF5 UniProtKB/Swiss-Prot
  C6ZEF6 UniProtKB/Swiss-Prot
  C6ZEF7 UniProtKB/Swiss-Prot
  F8WCD8 UniProtKB/TrEMBL
  Q5VY38 UniProtKB/Swiss-Prot
  Q5VY39 UniProtKB/Swiss-Prot
  Q6TRH8 UniProtKB/Swiss-Prot
  Q8NDB9 UniProtKB/Swiss-Prot
  Q96QT8 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-06-21 PCDH15  protocadherin related 15  PCDH15  protocadherin-related 15  Symbol and/or name change 5135510 APPROVED
2011-07-27 PCDH15  protocadherin-related 15  PCDH15  protocadherin 15  Symbol and/or name change 5135510 APPROVED