SCAMP4 (secretory carrier membrane protein 4) - Rat Genome Database

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Gene: SCAMP4 (secretory carrier membrane protein 4) Homo sapiens
Analyze
Symbol: SCAMP4
Name: secretory carrier membrane protein 4
RGD ID: 1345872
HGNC Page HGNC:30385
Description: Predicted to be involved in protein transport. Predicted to be located in membrane. Predicted to be active in recycling endosome membrane and trans-Golgi network membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: FLJ33847; FLJ90105; SCAMP-4; secretory carrier-associated membrane protein 4
RGD Orthologs
Mouse
Rat
Bonobo
Dog
Squirrel
Pig
Green Monkey
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
GRCh38191,905,399 - 1,926,013 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl191,905,214 - 1,926,013 (+)EnsemblGRCh38hg38GRCh38
GRCh37191,905,398 - 1,926,012 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36191,856,373 - 1,877,012 (+)NCBINCBI36Build 36hg18NCBI36
Build 34191,856,372 - 1,877,011NCBI
Celera191,839,456 - 1,860,087 (+)NCBICelera
Cytogenetic Map19p13.3NCBI
HuRef191,676,855 - 1,697,510 (+)NCBIHuRef
CHM1_1191,904,962 - 1,925,465 (+)NCBICHM1_1
T2T-CHM13v2.0191,876,716 - 1,897,325 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process
protein transport  (IBA,IEA)

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
4. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11.
Additional References at PubMed
PMID:11050114   PMID:11295240   PMID:14702039   PMID:15489334   PMID:16105885   PMID:16303743   PMID:19322201   PMID:20379614   PMID:21516116   PMID:21873635   PMID:22810586   PMID:26496610  
PMID:26638075   PMID:28298427   PMID:28514442   PMID:29117863   PMID:29967290   PMID:31073040   PMID:32296183   PMID:32807901   PMID:32814053   PMID:33845483   PMID:33961781   PMID:34079125  
PMID:35044719   PMID:35271311   PMID:37314216   PMID:37499664   PMID:38569033  


Genomics

Comparative Map Data
SCAMP4
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38191,905,399 - 1,926,013 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl191,905,214 - 1,926,013 (+)EnsemblGRCh38hg38GRCh38
GRCh37191,905,398 - 1,926,012 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36191,856,373 - 1,877,012 (+)NCBINCBI36Build 36hg18NCBI36
Build 34191,856,372 - 1,877,011NCBI
Celera191,839,456 - 1,860,087 (+)NCBICelera
Cytogenetic Map19p13.3NCBI
HuRef191,676,855 - 1,697,510 (+)NCBIHuRef
CHM1_1191,904,962 - 1,925,465 (+)NCBICHM1_1
T2T-CHM13v2.0191,876,716 - 1,897,325 (+)NCBIT2T-CHM13v2.0
Scamp4
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391080,438,716 - 80,451,617 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1080,438,706 - 80,451,617 (+)EnsemblGRCm39 Ensembl
GRCm381080,602,882 - 80,615,783 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1080,602,872 - 80,615,783 (+)EnsemblGRCm38mm10GRCm38
MGSCv371080,065,627 - 80,078,528 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361080,006,011 - 80,018,912 (+)NCBIMGSCv36mm8
Celera1081,620,706 - 81,633,607 (+)NCBICelera
Cytogenetic Map10C1NCBI
cM Map1039.72NCBI
Scamp4
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr879,752,193 - 9,764,614 (-)NCBIGRCr8
mRatBN7.279,101,504 - 9,113,929 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl79,101,489 - 9,113,967 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx711,979,727 - 11,992,191 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0713,855,239 - 13,867,703 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0711,721,307 - 11,733,744 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0711,969,720 - 11,982,141 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl711,969,720 - 11,982,141 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0712,137,245 - 12,149,666 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4710,612,354 - 10,624,775 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1710,612,353 - 10,624,775 (-)NCBI
Celera77,283,714 - 7,296,113 (-)NCBICelera
Cytogenetic Map7q11NCBI
SCAMP4
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2206,276,368 - 6,297,165 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1195,507,395 - 5,528,107 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v019914,220 - 925,244 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1191,893,577 - 1,904,452 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl191,893,577 - 1,904,452 (+)Ensemblpanpan1.1panPan2
SCAMP4
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12057,047,022 - 57,061,274 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2057,048,026 - 57,063,245 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2056,840,199 - 56,868,306 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02057,778,113 - 57,806,269 (-)NCBIROS_Cfam_1.0
UMICH_Zoey_3.12056,835,107 - 56,863,078 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02057,315,013 - 57,343,088 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02057,515,962 - 57,544,107 (-)NCBIUU_Cfam_GSD_1.0
Scamp4
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024405118216,715,026 - 216,730,688 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365881,104,098 - 1,119,778 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365881,104,098 - 1,119,761 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SCAMP4
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl276,615,000 - 76,634,264 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1276,614,984 - 76,634,314 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2277,320,048 - 77,339,367 (-)NCBISscrofa10.2Sscrofa10.2susScr3
SCAMP4
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.161,695,545 - 1,718,633 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl61,695,876 - 1,719,189 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660817,067,161 - 7,090,361 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in SCAMP4
122 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19p13.3(chr19:259395-2555149)x3 copy number gain See cases [RCV000051044] Chr19:259395..2555149 [GRCh38]
Chr19:259395..2555147 [GRCh37]
Chr19:210395..2506147 [NCBI36]
Chr19:19p13.3		 pathogenic
GRCh38/hg38 19p13.3-13.2(chr19:265917-8564134)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052876]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052876]|See cases [RCV000052876] Chr19:265917..8564134 [GRCh38]
Chr19:265917..8629018 [GRCh37]
Chr19:216917..8535018 [NCBI36]
Chr19:19p13.3-13.2		 pathogenic
GRCh38/hg38 19p13.3(chr19:1565575-4108128)x3 copy number gain See cases [RCV000052878] Chr19:1565575..4108128 [GRCh38]
Chr19:1565574..4108126 [GRCh37]
Chr19:1516574..4059126 [NCBI36]
Chr19:19p13.3		 pathogenic
GRCh38/hg38 19p13.3(chr19:259395-1952650)x3 copy number gain See cases [RCV000052875] Chr19:259395..1952650 [GRCh38]
Chr19:259395..1952649 [GRCh37]
Chr19:210395..1903649 [NCBI36]
Chr19:19p13.3		 pathogenic
GRCh38/hg38 19p13.3(chr19:233565-4699472)x3 copy number gain See cases [RCV000052575] Chr19:233565..4699472 [GRCh38]
Chr19:233565..4699484 [GRCh37]
Chr19:184565..4650484 [NCBI36]
Chr19:19p13.3		 pathogenic
GRCh38/hg38 19p13.3(chr19:945098-1972299)x1 copy number loss See cases [RCV000053938] Chr19:945098..1972299 [GRCh38]
Chr19:945098..1972298 [GRCh37]
Chr19:896098..1923298 [NCBI36]
Chr19:19p13.3		 pathogenic
GRCh38/hg38 19p13.3(chr19:1727562-2306496)x1 copy number loss See cases [RCV000053941] Chr19:1727562..2306496 [GRCh38]
Chr19:1727561..2306495 [GRCh37]
Chr19:1678561..2257495 [NCBI36]
Chr19:19p13.3		 pathogenic
SCAMP4:c.-41-2114C>T single nucleotide variant Malignant melanoma [RCV000072017] Chr19:1912865 [GRCh38]
Chr19:1912864 [GRCh37]
Chr19:1863864 [NCBI36]
Chr19:19p13.3		 not provided
SCAMP4:c.-41-2082C>G single nucleotide variant Malignant melanoma [RCV000063465] Chr19:1912897 [GRCh38]
Chr19:1912896 [GRCh37]
Chr19:1863896 [NCBI36]
Chr19:19p13.3		 not provided
NM_138422.4(ADAT3):c.1069G>C (p.Glu357Gln) single nucleotide variant Inborn genetic diseases [RCV003263910]|Intellectual disability [RCV001251870]|not specified [RCV001819959] Chr19:1913116 [GRCh38]
Chr19:1913115 [GRCh37]
Chr19:19p13.3		 likely benign|uncertain significance
GRCh38/hg38 19p13.3(chr19:1549144-4288720)x1 copy number loss See cases [RCV000134795] Chr19:1549144..4288720 [GRCh38]
Chr19:1549143..4288717 [GRCh37]
Chr19:1500143..4239717 [NCBI36]
Chr19:19p13.3		 pathogenic
GRCh38/hg38 19p13.3(chr19:421537-2897921)x3 copy number gain See cases [RCV000134894] Chr19:421537..2897921 [GRCh38]
Chr19:421537..2897919 [GRCh37]
Chr19:372537..2848919 [NCBI36]
Chr19:19p13.3		 likely pathogenic
GRCh38/hg38 19p13.3(chr19:259395-2068507)x3 copy number gain See cases [RCV000135433] Chr19:259395..2068507 [GRCh38]
Chr19:259395..2068506 [GRCh37]
Chr19:210395..2019506 [NCBI36]
Chr19:19p13.3		 pathogenic
GRCh38/hg38 19p13.3(chr19:1351163-2555149)x3 copy number gain See cases [RCV000136880] Chr19:1351163..2555149 [GRCh38]
Chr19:1351162..2555147 [GRCh37]
Chr19:1302162..2506147 [NCBI36]
Chr19:19p13.3		 uncertain significance
GRCh38/hg38 19p13.3(chr19:1911810-1952591)x3 copy number gain See cases [RCV000140197] Chr19:1911810..1952591 [GRCh38]
Chr19:1911809..1952590 [GRCh37]
Chr19:1862809..1903590 [NCBI36]
Chr19:19p13.3		 benign
GRCh38/hg38 19p13.3(chr19:259395-6795611)x3 copy number gain See cases [RCV000142627] Chr19:259395..6795611 [GRCh38]
Chr19:259395..6795622 [GRCh37]
Chr19:210395..6746622 [NCBI36]
Chr19:19p13.3		 pathogenic
NM_138422.4(ADAT3):c.430G>A (p.Val144Met) single nucleotide variant Intellectual disability-strabismus syndrome [RCV000162122]|not provided [RCV000254727] Chr19:1912477 [GRCh38]
Chr19:1912476 [GRCh37]
Chr19:19p13.3		 pathogenic|likely pathogenic|conflicting interpretations of pathogenicity
GRCh37/hg19 19p13.3(chr19:277373-2555164)x3 copy number gain See cases [RCV000240507] Chr19:277373..2555164 [GRCh37]
Chr19:19p13.3		 pathogenic
NM_138422.4(ADAT3):c.383G>T (p.Arg128Leu) single nucleotide variant ADAT3-related disorder [RCV003925560]|Inborn genetic diseases [RCV002525157]|not provided [RCV000766848]|not specified [RCV000521772] Chr19:1912430 [GRCh38]
Chr19:1912429 [GRCh37]
Chr19:19p13.3		 benign|likely benign|conflicting interpretations of pathogenicity|uncertain significance
NM_138422.4(ADAT3):c.667G>A (p.Val223Met) single nucleotide variant Inborn genetic diseases [RCV004023561]|not provided [RCV000523582] Chr19:1912714 [GRCh38]
Chr19:1912713 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.548C>T (p.Thr183Met) single nucleotide variant ADAT3-related disorder [RCV003925418]|not provided [RCV000488362] Chr19:1912595 [GRCh38]
Chr19:1912594 [GRCh37]
Chr19:19p13.3		 benign|conflicting interpretations of pathogenicity|uncertain significance
NM_138422.4(ADAT3):c.586_587delinsTT (p.Ala196Leu) indel not provided [RCV000599503] Chr19:1912633..1912634 [GRCh38]
Chr19:1912632..1912633 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.274A>C (p.Lys92Gln) single nucleotide variant not provided [RCV000593679] Chr19:1912321 [GRCh38]
Chr19:1912320 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.604C>T (p.Arg202Trp) single nucleotide variant not provided [RCV000435540] Chr19:1912651 [GRCh38]
Chr19:1912650 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.761G>A (p.Arg254His) single nucleotide variant ADAT3-related disorder [RCV003932782]|not provided [RCV000479359] Chr19:1912808 [GRCh38]
Chr19:1912807 [GRCh37]
Chr19:19p13.3		 likely benign|uncertain significance
NM_138422.4(ADAT3):c.1093C>G (p.Pro365Ala) single nucleotide variant not provided [RCV000485456] Chr19:1913140 [GRCh38]
Chr19:1913139 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.59C>T (p.Ala20Val) single nucleotide variant Intellectual disability-strabismus syndrome [RCV001335386]|not specified [RCV000503250] Chr19:1912106 [GRCh38]
Chr19:1912105 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.716A>C (p.His239Pro) single nucleotide variant not specified [RCV000503321] Chr19:1912763 [GRCh38]
Chr19:1912762 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.440G>A (p.Arg147Gln) single nucleotide variant Inborn genetic diseases [RCV004609408]|Intellectual disability-strabismus syndrome [RCV003139702]|not specified [RCV000501535] Chr19:1912487 [GRCh38]
Chr19:1912486 [GRCh37]
Chr19:19p13.3		 likely benign|uncertain significance
NM_138422.4(ADAT3):c.862G>A (p.Glu288Lys) single nucleotide variant not specified [RCV000501696] Chr19:1912909 [GRCh38]
Chr19:1912908 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.62C>G (p.Pro21Arg) single nucleotide variant not specified [RCV000499858] Chr19:1912109 [GRCh38]
Chr19:1912108 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.854A>C (p.Asp285Ala) single nucleotide variant ADAT3-related disorder [RCV003942620]|Inborn genetic diseases [RCV002524142]|not provided [RCV000514261]|not specified [RCV000499886] Chr19:1912901 [GRCh38]
Chr19:1912900 [GRCh37]
Chr19:19p13.3		 likely benign
GRCh37/hg19 19p13.3(chr19:260911-1965786)x3 copy number gain See cases [RCV000511452] Chr19:260911..1965786 [GRCh37]
Chr19:19p13.3		 likely pathogenic
NM_138422.4(ADAT3):c.314C>G (p.Ala105Gly) single nucleotide variant Inborn genetic diseases [RCV003291928] Chr19:1912361 [GRCh38]
Chr19:1912360 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.16C>T (p.Arg6Cys) single nucleotide variant not provided [RCV000594825] Chr19:1912063 [GRCh38]
Chr19:1912062 [GRCh37]
Chr19:19p13.3		 uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain See cases [RCV000511289] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic|uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) copy number gain See cases [RCV000512296] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
NM_138422.4(ADAT3):c.586del (p.Ala196fs) deletion Intellectual disability-strabismus syndrome [RCV002245055]|not provided [RCV000627469] Chr19:1912631 [GRCh38]
Chr19:1912630 [GRCh37]
Chr19:19p13.3		 likely pathogenic|uncertain significance
NM_138422.4(ADAT3):c.99_106dup (p.Glu36fs) duplication Intellectual disability-strabismus syndrome [RCV000664409] Chr19:1912141..1912142 [GRCh38]
Chr19:1912140..1912141 [GRCh37]
Chr19:19p13.3		 pathogenic
GRCh37/hg19 19p13.3(chr19:259395-3152419) copy number gain Global developmental delay [RCV000626520] Chr19:259395..3152419 [GRCh37]
Chr19:19p13.3		 likely pathogenic
GRCh37/hg19 19p13.3(chr19:260911-3200875)x3 copy number gain not provided [RCV000684094] Chr19:260911..3200875 [GRCh37]
Chr19:19p13.3		 pathogenic
NM_138422.4(ADAT3):c.751G>A (p.Gly251Ser) single nucleotide variant Inborn genetic diseases [RCV002568720]|Intellectual disability [RCV001251871]|Intellectual disability-strabismus syndrome [RCV001335387] Chr19:1912798 [GRCh38]
Chr19:1912797 [GRCh37]
Chr19:19p13.3		 likely benign|uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3 copy number gain not provided [RCV000752444] Chr19:260912..59097160 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 copy number gain not provided [RCV000752439] Chr19:68029..59110290 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
NM_138422.4(ADAT3):c.940C>T (p.Leu314=) single nucleotide variant ADAT3-related disorder [RCV003976060]|not provided [RCV001707880] Chr19:1912987 [GRCh38]
Chr19:1912986 [GRCh37]
Chr19:19p13.3		 benign
GRCh37/hg19 19p13.3(chr19:1822668-1912976)x3 copy number gain not provided [RCV000752501] Chr19:1822668..1912976 [GRCh37]
Chr19:19p13.3		 benign
GRCh37/hg19 19p13.3(chr19:1822668-1914795)x3 copy number gain not provided [RCV000752502] Chr19:1822668..1914795 [GRCh37]
Chr19:19p13.3		 benign
GRCh37/hg19 19p13.3(chr19:1823760-1914795)x4 copy number gain not provided [RCV000752503] Chr19:1823760..1914795 [GRCh37]
Chr19:19p13.3		 benign
GRCh37/hg19 19p13.3(chr19:1827304-1912976)x4 copy number gain not provided [RCV000752504] Chr19:1827304..1912976 [GRCh37]
Chr19:19p13.3		 benign
GRCh37/hg19 19p13.3(chr19:1827304-1914795)x3 copy number gain not provided [RCV000752505] Chr19:1827304..1914795 [GRCh37]
Chr19:19p13.3		 benign
GRCh37/hg19 19p13.3(chr19:1827503-1912976)x3 copy number gain not provided [RCV000752506] Chr19:1827503..1912976 [GRCh37]
Chr19:19p13.3		 benign
NM_138422.4(ADAT3):c.111T>G (p.Pro37=) single nucleotide variant not provided [RCV000900495] Chr19:1912158 [GRCh38]
Chr19:1912157 [GRCh37]
Chr19:19p13.3		 likely benign
NM_138422.4(ADAT3):c.441G>A (p.Arg147=) single nucleotide variant not provided [RCV000925669] Chr19:1912488 [GRCh38]
Chr19:1912487 [GRCh37]
Chr19:19p13.3		 likely benign
NM_138422.4(ADAT3):c.216C>G (p.Thr72=) single nucleotide variant not provided [RCV000970342] Chr19:1912263 [GRCh38]
Chr19:1912262 [GRCh37]
Chr19:19p13.3		 benign|likely benign
NM_138422.4(ADAT3):c.831C>T (p.Arg277=) single nucleotide variant not provided [RCV000970343] Chr19:1912878 [GRCh38]
Chr19:1912877 [GRCh37]
Chr19:19p13.3		 benign|likely benign
NM_138422.4(ADAT3):c.978G>A (p.Ala326=) single nucleotide variant not provided [RCV000927770] Chr19:1913025 [GRCh38]
Chr19:1913024 [GRCh37]
Chr19:19p13.3		 likely benign
NM_138422.4(ADAT3):c.36G>A (p.Ser12=) single nucleotide variant not provided [RCV000950836] Chr19:1912083 [GRCh38]
Chr19:1912082 [GRCh37]
Chr19:19p13.3		 likely benign
NM_138422.4(ADAT3):c.363G>A (p.Ser121=) single nucleotide variant ADAT3-related disorder [RCV003905851]|not provided [RCV000962602] Chr19:1912410 [GRCh38]
Chr19:1912409 [GRCh37]
Chr19:19p13.3		 benign
NM_138422.4(ADAT3):c.724A>G (p.Met242Val) single nucleotide variant not provided [RCV000880172] Chr19:1912771 [GRCh38]
Chr19:1912770 [GRCh37]
Chr19:19p13.3		 benign
GRCh37/hg19 19p13.3(chr19:260911-4788357)x3 copy number gain not provided [RCV000846988] Chr19:260911..4788357 [GRCh37]
Chr19:19p13.3		 pathogenic
NC_000019.9:g.1406030_3597207dup duplication Neurodevelopmental disorder [RCV000787423] Chr19:1406030..3597207 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.870C>T (p.Gly290=) single nucleotide variant not provided [RCV000893167] Chr19:1912917 [GRCh38]
Chr19:1912916 [GRCh37]
Chr19:19p13.3		 likely benign
GRCh37/hg19 19p13.3(chr19:1772993-1990715)x1 copy number loss not provided [RCV000847336] Chr19:1772993..1990715 [GRCh37]
Chr19:19p13.3		 uncertain significance
GRCh37/hg19 19p13.3(chr19:1816218-2152190)x3 copy number gain not provided [RCV000849885] Chr19:1816218..2152190 [GRCh37]
Chr19:19p13.3		 uncertain significance
NC_000019.9:g.(?_589946)_(2151333_?)dup duplication Cyclical neutropenia [RCV003107569] Chr19:589946..2151333 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.888T>C (p.Thr296=) single nucleotide variant Intellectual disability-strabismus syndrome [RCV001544466]|not provided [RCV001685499] Chr19:1912935 [GRCh38]
Chr19:1912934 [GRCh37]
Chr19:19p13.3		 benign
NM_138422.4(ADAT3):c.258C>T (p.Pro86=) single nucleotide variant not provided [RCV000907366] Chr19:1912305 [GRCh38]
Chr19:1912304 [GRCh37]
Chr19:19p13.3		 likely benign
NM_138422.4(ADAT3):c.522C>T (p.Ser174=) single nucleotide variant not provided [RCV000955027]|not specified [RCV001818996] Chr19:1912569 [GRCh38]
Chr19:1912568 [GRCh37]
Chr19:19p13.3		 benign
NM_138422.4(ADAT3):c.117G>A (p.Pro39=) single nucleotide variant not provided [RCV000891166] Chr19:1912164 [GRCh38]
Chr19:1912163 [GRCh37]
Chr19:19p13.3		 benign|likely benign
GRCh37/hg19 19p13.3(chr19:260911-3501271)x3 copy number gain not provided [RCV001007025] Chr19:260911..3501271 [GRCh37]
Chr19:19p13.3		 pathogenic
GRCh37/hg19 19p13.3(chr19:260912-4384674)x3 copy number gain See cases [RCV001007443] Chr19:260912..4384674 [GRCh37]
Chr19:19p13.3		 pathogenic
GRCh37/hg19 19p13.3(chr19:1075192-2256387)x3 copy number gain not provided [RCV001007026] Chr19:1075192..2256387 [GRCh37]
Chr19:19p13.3		 likely pathogenic
NM_138422.4(ADAT3):c.356C>T (p.Pro119Leu) single nucleotide variant Microcephaly [RCV001252922] Chr19:1912403 [GRCh38]
Chr19:1912402 [GRCh37]
Chr19:19p13.3		 uncertain significance
GRCh37/hg19 19p13.3(chr19:260911-2256387)x3 copy number gain See cases [RCV002285065] Chr19:260911..2256387 [GRCh37]
Chr19:19p13.3		 pathogenic
NM_138422.4(ADAT3):c.973G>C (p.Gly325Arg) single nucleotide variant not provided [RCV001764863] Chr19:1913020 [GRCh38]
Chr19:1913019 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.820dup (p.Gln274fs) duplication Intellectual disability-strabismus syndrome [RCV001262927]|not provided [RCV002307716] Chr19:1912861..1912862 [GRCh38]
Chr19:1912860..1912861 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.1001G>T (p.Gly334Val) single nucleotide variant Intellectual disability-strabismus syndrome [RCV001334517] Chr19:1913048 [GRCh38]
Chr19:1913047 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.239C>A (p.Ser80Ter) single nucleotide variant Mental retardation, autosomal recessive 36 [RCV001328577] Chr19:1912286 [GRCh38]
Chr19:1912285 [GRCh37]
Chr19:19p13.3		 pathogenic
NM_138422.4(ADAT3):c.988G>A (p.Asp330Asn) single nucleotide variant ADAT3-related disorder [RCV003953625]|not provided [RCV004590298]|not specified [RCV001280550] Chr19:1913035 [GRCh38]
Chr19:1913034 [GRCh37]
Chr19:19p13.3		 likely benign|uncertain significance
NM_138422.4(ADAT3):c.806C>T (p.Pro269Leu) single nucleotide variant not specified [RCV001280551] Chr19:1912853 [GRCh38]
Chr19:1912852 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.897C>G (p.Asp299Glu) single nucleotide variant Intellectual disability-strabismus syndrome [RCV001335388] Chr19:1912944 [GRCh38]
Chr19:1912943 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.338C>G (p.Ala113Gly) single nucleotide variant Intellectual disability-strabismus syndrome [RCV001334518] Chr19:1912385 [GRCh38]
Chr19:1912384 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.930C>A (p.Cys310Ter) single nucleotide variant Mental retardation, autosomal recessive 36 [RCV001335389] Chr19:1912977 [GRCh38]
Chr19:1912976 [GRCh37]
Chr19:19p13.3		 pathogenic
NM_138422.4(ADAT3):c.54G>C (p.Glu18Asp) single nucleotide variant Intellectual disability-strabismus syndrome [RCV001330347] Chr19:1912101 [GRCh38]
Chr19:1912100 [GRCh37]
Chr19:19p13.3		 uncertain significance
NC_000019.9:g.(?_589946)_(4818389_?)dup duplication not provided [RCV003105391] Chr19:589946..4818389 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.67C>T (p.Leu23Phe) single nucleotide variant not specified [RCV001817419] Chr19:1912114 [GRCh38]
Chr19:1912113 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.436_446del (p.Ala146fs) deletion not specified [RCV001817738] Chr19:1912481..1912491 [GRCh38]
Chr19:1912480..1912490 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.626G>A (p.Arg209Gln) single nucleotide variant not provided [RCV004692752]|not specified [RCV001820399] Chr19:1912673 [GRCh38]
Chr19:1912672 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.444G>A (p.Pro148=) single nucleotide variant ADAT3-related disorder [RCV003923328]|not provided [RCV003416477]|not specified [RCV001820596] Chr19:1912491 [GRCh38]
Chr19:1912490 [GRCh37]
Chr19:19p13.3		 likely benign
NM_138422.4(ADAT3):c.362C>T (p.Ser121Leu) single nucleotide variant not specified [RCV001822293] Chr19:1912409 [GRCh38]
Chr19:1912408 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.482_487dup (p.Trp162_Pro163insHisTrp) duplication Intellectual disability-strabismus syndrome [RCV001809275] Chr19:1912527..1912528 [GRCh38]
Chr19:1912526..1912527 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.922G>A (p.Ala308Thr) single nucleotide variant not specified [RCV001820400] Chr19:1912969 [GRCh38]
Chr19:1912968 [GRCh37]
Chr19:19p13.3		 likely benign
NM_138422.4(ADAT3):c.941T>C (p.Leu314Pro) single nucleotide variant Intellectual disability-strabismus syndrome [RCV001809276] Chr19:1912988 [GRCh38]
Chr19:1912987 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.24_37del (p.Pro10fs) deletion not provided [RCV001806899] Chr19:1912070..1912083 [GRCh38]
Chr19:1912069..1912082 [GRCh37]
Chr19:19p13.3		 likely pathogenic
NC_000019.9:g.(?_589946)_(5696788_?)dup duplication not provided [RCV003113597] Chr19:589946..5696788 [GRCh37]
Chr19:19p13.3		 uncertain significance
NC_000019.9:g.(?_1456055)_(2456931_?)dup duplication Progressive myoclonic epilepsy type 9 [RCV003122897] Chr19:1456055..2456931 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.748C>T (p.Arg250Cys) single nucleotide variant Intellectual disability-strabismus syndrome [RCV002272936] Chr19:1912795 [GRCh38]
Chr19:1912794 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.427C>G (p.Pro143Ala) single nucleotide variant Intellectual disability-strabismus syndrome [RCV002286362] Chr19:1912474 [GRCh38]
Chr19:1912473 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.292C>G (p.Arg98Gly) single nucleotide variant Intellectual disability-strabismus syndrome [RCV002288381] Chr19:1912339 [GRCh38]
Chr19:1912338 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.875C>T (p.Pro292Leu) single nucleotide variant Inborn genetic diseases [RCV004047604]|Intellectual disability-strabismus syndrome [RCV002288382] Chr19:1912922 [GRCh38]
Chr19:1912921 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.877T>A (p.Tyr293Asn) single nucleotide variant Intellectual disability-strabismus syndrome [RCV002289487] Chr19:1912924 [GRCh38]
Chr19:1912923 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.803C>G (p.Ala268Gly) single nucleotide variant Inborn genetic diseases [RCV002729870] Chr19:1912850 [GRCh38]
Chr19:1912849 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_079834.4(SCAMP4):c.214G>A (p.Gly72Ser) single nucleotide variant not specified [RCV004215347] Chr19:1918204 [GRCh38]
Chr19:1918203 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.151A>C (p.Lys51Gln) single nucleotide variant Inborn genetic diseases [RCV002818256] Chr19:1912198 [GRCh38]
Chr19:1912197 [GRCh37]
Chr19:19p13.3		 likely benign
NM_079834.4(SCAMP4):c.608C>T (p.Ala203Val) single nucleotide variant not specified [RCV004101639] Chr19:1924202 [GRCh38]
Chr19:1924201 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.181G>T (p.Ala61Ser) single nucleotide variant Inborn genetic diseases [RCV002946155]|not provided [RCV003883917] Chr19:1912228 [GRCh38]
Chr19:1912227 [GRCh37]
Chr19:19p13.3		 likely benign|uncertain significance
NM_138422.4(ADAT3):c.1013G>A (p.Arg338His) single nucleotide variant Inborn genetic diseases [RCV002779151] Chr19:1913060 [GRCh38]
Chr19:1913059 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.215C>T (p.Thr72Ile) single nucleotide variant Inborn genetic diseases [RCV002906154] Chr19:1912262 [GRCh38]
Chr19:1912261 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.1025G>T (p.Arg342Leu) single nucleotide variant Inborn genetic diseases [RCV002772616] Chr19:1913072 [GRCh38]
Chr19:1913071 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.962G>C (p.Arg321Pro) single nucleotide variant Inborn genetic diseases [RCV002973082] Chr19:1913009 [GRCh38]
Chr19:1913008 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_079834.4(SCAMP4):c.662G>T (p.Ser221Ile) single nucleotide variant not specified [RCV004129715] Chr19:1924256 [GRCh38]
Chr19:1924255 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.545C>T (p.Ser182Phe) single nucleotide variant Intellectual disability-strabismus syndrome [RCV002463425] Chr19:1912592 [GRCh38]
Chr19:1912591 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.551A>G (p.Gln184Arg) single nucleotide variant Intellectual disability-strabismus syndrome [RCV002463426] Chr19:1912598 [GRCh38]
Chr19:1912597 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.596C>T (p.Ala199Val) single nucleotide variant Inborn genetic diseases [RCV002973879] Chr19:1912643 [GRCh38]
Chr19:1912642 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_079834.4(SCAMP4):c.412A>G (p.Ile138Val) single nucleotide variant not specified [RCV004124992] Chr19:1923086 [GRCh38]
Chr19:1923085 [GRCh37]
Chr19:19p13.3		 likely benign
NM_079834.4(SCAMP4):c.266G>C (p.Trp89Ser) single nucleotide variant not specified [RCV004149244] Chr19:1918256 [GRCh38]
Chr19:1918255 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_079834.4(SCAMP4):c.434C>T (p.Pro145Leu) single nucleotide variant not specified [RCV004235081] Chr19:1923108 [GRCh38]
Chr19:1923107 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.116C>T (p.Pro39Leu) single nucleotide variant Inborn genetic diseases [RCV002712947] Chr19:1912163 [GRCh38]
Chr19:1912162 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.706C>T (p.Pro236Ser) single nucleotide variant Inborn genetic diseases [RCV002764205] Chr19:1912753 [GRCh38]
Chr19:1912752 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_079834.4(SCAMP4):c.119T>G (p.Ile40Ser) single nucleotide variant not specified [RCV004135476] Chr19:1917805 [GRCh38]
Chr19:1917804 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_079834.4(SCAMP4):c.502G>A (p.Ala168Thr) single nucleotide variant not specified [RCV004202289] Chr19:1923176 [GRCh38]
Chr19:1923175 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.529G>A (p.Ala177Thr) single nucleotide variant Inborn genetic diseases [RCV002825982] Chr19:1912576 [GRCh38]
Chr19:1912575 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_079834.4(SCAMP4):c.166A>G (p.Ile56Val) single nucleotide variant not specified [RCV004225507] Chr19:1918156 [GRCh38]
Chr19:1918155 [GRCh37]
Chr19:19p13.3		 likely benign
NM_138422.4(ADAT3):c.251C>G (p.Pro84Arg) single nucleotide variant Inborn genetic diseases [RCV002921857] Chr19:1912298 [GRCh38]
Chr19:1912297 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.676A>C (p.Thr226Pro) single nucleotide variant Inborn genetic diseases [RCV002702712] Chr19:1912723 [GRCh38]
Chr19:1912722 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.78G>T (p.Gln26His) single nucleotide variant Inborn genetic diseases [RCV002809691] Chr19:1912125 [GRCh38]
Chr19:1912124 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.701A>C (p.Asp234Ala) single nucleotide variant Inborn genetic diseases [RCV002652595] Chr19:1912748 [GRCh38]
Chr19:1912747 [GRCh37]
Chr19:19p13.3		 likely benign
NM_079834.4(SCAMP4):c.478G>A (p.Val160Met) single nucleotide variant not specified [RCV004105551] Chr19:1923152 [GRCh38]
Chr19:1923151 [GRCh37]
Chr19:19p13.3		 likely benign
NM_138422.4(ADAT3):c.355C>A (p.Pro119Thr) single nucleotide variant Inborn genetic diseases [RCV002656945] Chr19:1912402 [GRCh38]
Chr19:1912401 [GRCh37]
Chr19:19p13.3		 uncertain significance
NC_000019.9:g.(?_1206913)_(3771740_?)dup duplication not provided [RCV003154903] Chr19:1206913..3771740 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.777C>A (p.Phe259Leu) single nucleotide variant not provided [RCV003228424] Chr19:1912824 [GRCh38]
Chr19:1912823 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.947A>C (p.His316Pro) single nucleotide variant Intellectual disability-strabismus syndrome [RCV003141205] Chr19:1912994 [GRCh38]
Chr19:1912993 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.874C>T (p.Pro292Ser) single nucleotide variant Intellectual disability-strabismus syndrome [RCV003141204] Chr19:1912921 [GRCh38]
Chr19:1912920 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.56C>T (p.Pro19Leu) single nucleotide variant Inborn genetic diseases [RCV003284465] Chr19:1912103 [GRCh38]
Chr19:1912102 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.108G>C (p.Glu36Asp) single nucleotide variant Inborn genetic diseases [RCV004285624]|not provided [RCV003228558] Chr19:1912155 [GRCh38]
Chr19:1912154 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_079834.4(SCAMP4):c.563C>T (p.Thr188Met) single nucleotide variant not specified [RCV004259498] Chr19:1924157 [GRCh38]
Chr19:1924156 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.726G>A (p.Met242Ile) single nucleotide variant Inborn genetic diseases [RCV003359098] Chr19:1912773 [GRCh38]
Chr19:1912772 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_079834.4(SCAMP4):c.604G>C (p.Glu202Gln) single nucleotide variant not specified [RCV004353296] Chr19:1924198 [GRCh38]
Chr19:1924197 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.304A>G (p.Ser102Gly) single nucleotide variant Inborn genetic diseases [RCV003385560] Chr19:1912351 [GRCh38]
Chr19:1912350 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.87C>G (p.Cys29Trp) single nucleotide variant Inborn genetic diseases [RCV003367533] Chr19:1912134 [GRCh38]
Chr19:1912133 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.161G>A (p.Gly54Glu) single nucleotide variant Inborn genetic diseases [RCV003370572] Chr19:1912208 [GRCh38]
Chr19:1912207 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.424G>A (p.Val142Met) single nucleotide variant Inborn genetic diseases [RCV003374618] Chr19:1912471 [GRCh38]
Chr19:1912470 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.601C>T (p.Arg201Trp) single nucleotide variant Inborn genetic diseases [RCV003351545] Chr19:1912648 [GRCh38]
Chr19:1912647 [GRCh37]
Chr19:19p13.3		 uncertain significance
GRCh37/hg19 19p13.3-13.2(chr19:260912-7246777)x3 copy number gain not provided [RCV003485190] Chr19:260912..7246777 [GRCh37]
Chr19:19p13.3-13.2		 pathogenic
NM_079834.4(SCAMP4):c.246G>A (p.Thr82=) single nucleotide variant not provided [RCV003423175] Chr19:1918236 [GRCh38]
Chr19:1918235 [GRCh37]
Chr19:19p13.3		 likely benign
NM_079834.4(SCAMP4):c.482C>T (p.Ser161Leu) single nucleotide variant not provided [RCV003421717] Chr19:1923156 [GRCh38]
Chr19:1923155 [GRCh37]
Chr19:19p13.3		 likely benign
NM_138422.4(ADAT3):c.867C>T (p.Asp289=) single nucleotide variant not provided [RCV003413515] Chr19:1912914 [GRCh38]
Chr19:1912913 [GRCh37]
Chr19:19p13.3		 likely benign
GRCh37/hg19 19p13.3(chr19:1773489-2186237)x3 copy number gain not specified [RCV003986105] Chr19:1773489..2186237 [GRCh37]
Chr19:19p13.3		 uncertain significance
GRCh37/hg19 19p13.3(chr19:1648089-2302433)x3 copy number gain not specified [RCV003986124] Chr19:1648089..2302433 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.904G>A (p.Val302Met) single nucleotide variant Inborn genetic diseases [RCV004375502] Chr19:1912951 [GRCh38]
Chr19:1912950 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.908C>T (p.Thr303Ile) single nucleotide variant Inborn genetic diseases [RCV004375508] Chr19:1912955 [GRCh38]
Chr19:1912954 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.910C>T (p.Arg304Cys) single nucleotide variant Inborn genetic diseases [RCV004375511] Chr19:1912957 [GRCh38]
Chr19:1912956 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.925A>G (p.Met309Val) single nucleotide variant Inborn genetic diseases [RCV004375514] Chr19:1912972 [GRCh38]
Chr19:1912971 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.718G>A (p.Ala240Thr) single nucleotide variant Inborn genetic diseases [RCV004375465] Chr19:1912765 [GRCh38]
Chr19:1912764 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.640G>A (p.Val214Met) single nucleotide variant Intellectual disability-strabismus syndrome [RCV003988692] Chr19:1912687 [GRCh38]
Chr19:1912686 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.147C>T (p.Ser49=) single nucleotide variant not provided [RCV003885123] Chr19:1912194 [GRCh38]
Chr19:1912193 [GRCh37]
Chr19:19p13.3		 likely benign
NM_138422.4(ADAT3):c.626GGGCCGTGG[1] (p.Gly212_Val214del) microsatellite not provided [RCV003885578] Chr19:1912673..1912681 [GRCh38]
Chr19:1912672..1912680 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.1057C>T (p.Arg353Cys) single nucleotide variant Inborn genetic diseases [RCV004375398] Chr19:1913104 [GRCh38]
Chr19:1913103 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.1100C>T (p.Thr367Met) single nucleotide variant Inborn genetic diseases [RCV004375404] Chr19:1913147 [GRCh38]
Chr19:1913146 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.436G>A (p.Ala146Thr) single nucleotide variant Inborn genetic diseases [RCV004375441] Chr19:1912483 [GRCh38]
Chr19:1912482 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.579G>A (p.Met193Ile) single nucleotide variant Inborn genetic diseases [RCV004375447] Chr19:1912626 [GRCh38]
Chr19:1912625 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.802G>A (p.Ala268Thr) single nucleotide variant Inborn genetic diseases [RCV004375485] Chr19:1912849 [GRCh38]
Chr19:1912848 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.118G>T (p.Ala40Ser) single nucleotide variant Inborn genetic diseases [RCV004375482] Chr19:1912165 [GRCh38]
Chr19:1912164 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.278G>A (p.Arg93Gln) single nucleotide variant Inborn genetic diseases [RCV004375417] Chr19:1912325 [GRCh38]
Chr19:1912324 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.820C>G (p.Gln274Glu) single nucleotide variant Inborn genetic diseases [RCV004375489] Chr19:1912867 [GRCh38]
Chr19:1912866 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.739C>G (p.Leu247Val) single nucleotide variant Inborn genetic diseases [RCV004375473]|not provided [RCV004775550] Chr19:1912786 [GRCh38]
Chr19:1912785 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.888T>G (p.Thr296=) single nucleotide variant ADAT3-related disorder [RCV003914653] Chr19:1912935 [GRCh38]
Chr19:1912934 [GRCh37]
Chr19:19p13.3		 likely benign
NM_138422.4(ADAT3):c.551A>C (p.Gln184Pro) single nucleotide variant Inborn genetic diseases [RCV004375446] Chr19:1912598 [GRCh38]
Chr19:1912597 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_079834.4(SCAMP4):c.508A>G (p.Met170Val) single nucleotide variant not specified [RCV004452607] Chr19:1923182 [GRCh38]
Chr19:1923181 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_079834.4(SCAMP4):c.655G>A (p.Val219Met) single nucleotide variant not specified [RCV004452611] Chr19:1924249 [GRCh38]
Chr19:1924248 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_079834.4(SCAMP4):c.653C>G (p.Thr218Ser) single nucleotide variant not specified [RCV004452610] Chr19:1924247 [GRCh38]
Chr19:1924246 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_079834.4(SCAMP4):c.578G>A (p.Gly193Asp) single nucleotide variant not specified [RCV004452608] Chr19:1924172 [GRCh38]
Chr19:1924171 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_079834.4(SCAMP4):c.581C>T (p.Thr194Ile) single nucleotide variant not specified [RCV004452609] Chr19:1924175 [GRCh38]
Chr19:1924174 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.296A>T (p.Asp99Val) single nucleotide variant Inborn genetic diseases [RCV004608291] Chr19:1912343 [GRCh38]
Chr19:1912342 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.205A>C (p.Lys69Gln) single nucleotide variant Inborn genetic diseases [RCV004610805] Chr19:1912252 [GRCh38]
Chr19:1912251 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.437C>T (p.Ala146Val) single nucleotide variant Inborn genetic diseases [RCV004608301] Chr19:1912484 [GRCh38]
Chr19:1912483 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.1066C>G (p.Leu356Val) single nucleotide variant Inborn genetic diseases [RCV004608340] Chr19:1913113 [GRCh38]
Chr19:1913112 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.826G>A (p.Val276Ile) single nucleotide variant Inborn genetic diseases [RCV004610784] Chr19:1912873 [GRCh38]
Chr19:1912872 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.58G>A (p.Ala20Thr) single nucleotide variant Inborn genetic diseases [RCV004610795] Chr19:1912105 [GRCh38]
Chr19:1912104 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_079834.4(SCAMP4):c.413T>C (p.Ile138Thr) single nucleotide variant not specified [RCV004658627] Chr19:1923087 [GRCh38]
Chr19:1923086 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.820C>A (p.Gln274Lys) single nucleotide variant Inborn genetic diseases [RCV004608320] Chr19:1912867 [GRCh38]
Chr19:1912866 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.1058G>A (p.Arg353His) single nucleotide variant Inborn genetic diseases [RCV004608281] Chr19:1913105 [GRCh38]
Chr19:1913104 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_079834.4(SCAMP4):c.497C>T (p.Ala166Val) single nucleotide variant not specified [RCV004658628] Chr19:1923171 [GRCh38]
Chr19:1923170 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.1037A>G (p.Asn346Ser) single nucleotide variant Inborn genetic diseases [RCV004608330] Chr19:1913084 [GRCh38]
Chr19:1913083 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_079834.4(SCAMP4):c.433C>T (p.Pro145Ser) single nucleotide variant not specified [RCV004674531] Chr19:1923107 [GRCh38]
Chr19:1923106 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.238T>C (p.Ser80Pro) single nucleotide variant not provided [RCV004727598] Chr19:1912285 [GRCh38]
Chr19:1912284 [GRCh37]
Chr19:19p13.3		 uncertain significance
NM_138422.4(ADAT3):c.319G>A (p.Glu107Lys) single nucleotide variant Intellectual disability-strabismus syndrome [RCV004764407] Chr19:1912366 [GRCh38]
Chr19:1912365 [GRCh37]
Chr19:19p13.3		 likely pathogenic
NM_138422.4(ADAT3):c.159_160del (p.Asp55fs) deletion Intellectual disability-strabismus syndrome [RCV004764612] Chr19:1912206..1912207 [GRCh38]
Chr19:1912205..1912206 [GRCh37]
Chr19:19p13.3		 likely pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:5735
Count of miRNA genes:1101
Interacting mature miRNAs:1395
Transcripts:ENST00000316097, ENST00000409472, ENST00000411971, ENST00000414057, ENST00000452128, ENST00000460767, ENST00000472442, ENST00000489554, ENST00000585335, ENST00000588555, ENST00000588907, ENST00000590266
Prediction methods:Miranda, Rnahybrid
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
1298499UAE1_HUrinary albumin excretion QTL 1 (human)2.730.0009Urinary albumin excretionurine albumin:creatinine ratio (ACR)19116075902Human
1643451SLIPL6_HSerum lipid level QTL 6 (human)2.190.0008Lipid level19116075902Human
1581534BP76_HBlood pressure QTL 76 (human)20.001Blood pressurepulse pressure19116075902Human
1581535BP65_HBlood pressure QTL 65 (human)3.10.001Blood pressurepulse pressure19116075902Human
2314591INSUL4_HInsulin level QTL 4 (human)3.80.000038Insulin levelfasting19116075902Human
1298476BP3_HBlood pressure QTL 3 (human)2.4Blood pressuresystolic19116075902Human

Markers in Region
RH11579  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37191,925,707 - 1,925,880UniSTSGRCh37
Build 36191,876,707 - 1,876,880RGDNCBI36
Celera191,859,782 - 1,859,955RGD
Cytogenetic Map19p13.3UniSTS
HuRef191,697,206 - 1,697,379UniSTS
GeneMap99-GB4 RH Map1917.75UniSTS
L17971  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map1q21UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map3p25UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic MapXq22UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map18q21.31UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map20p11.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map9q34.13UniSTS
L18426  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10p11UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map2p23.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map17q21-q22UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map12q24.1-q24.3UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map9p24.2UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map6q25.1-q26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17q23.1UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map1q41-q42.2UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map11p11.11UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map21q22.1UniSTS
Cytogenetic Map4q25-q27UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map18p11.22UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map21q21.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map12p12.3UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map22q12UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map1p13-p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map10q21.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map20p11.21UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map16p13.13-p13.12UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map14q22-q24UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map10q11UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map12q21.31UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map9p21.1UniSTS
D10S275  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map13q12.13UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map14q22-q24UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10p11UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map6q24UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map3p25UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map20pter-q11.23UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map10p12.3UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map3q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map1q24-q25.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map12q24.32UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map11p14.3UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map4q13UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map6q12-q13UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map2p14UniSTS
D1S1361  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map6p21.1-p12.1UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map5q21UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map5q22.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map17q21UniSTS
D11S2921  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map10q24.33UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic MapXp11.4-p11.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map1q24.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map18pter-p11.3UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map4q34.1UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map7q21.12UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map17q21-q22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map11p13-p12UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map5q12-q13UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map15q15-q21.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic MapXq25-q26.3UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map18p11.32UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map9p24.1-p23UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map20q12-q13.12UniSTS
Cytogenetic Map1q24-q25.3UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map6q25.1-q26UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map12p11.22UniSTS
Cytogenetic Map17q23.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map9p11UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map11p11.11UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map15q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map15q22-qterUniSTS
Cytogenetic Map10q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map5p15.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map19p13.2-cenUniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map9q33UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map4q25-q27UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic MapXq26.2UniSTS
Cytogenetic Map8q13.2UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic MapXq21.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map5p13.1-p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map6q14.3-q16.1UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map6q14.3UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q21.1-q21.3UniSTS
Cytogenetic Map6q11.1UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map12p13.2-p12.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map10q24-q25UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map14q11.2-q21UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map5p14.3UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map9p13.1UniSTS
Cytogenetic Map9q34.13UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
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Cytogenetic Map3p21.31UniSTS
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Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS
D1S1425  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map8q12.1UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map6q25.2-q25.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map2p23-p22UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic Map2p11.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map2p12-p11.2UniSTS
Cytogenetic Map3q11.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map18p11.3-p11.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map2p24UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map12q24.32UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map15q11-q12UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map15q21.1-q21.2UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map12p13.33UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map4q31.21UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map10p15-p14UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map15q24-q25UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map6pter-p12.1UniSTS
Cytogenetic Map6q16UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map11q23.1-q23.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map16q24.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic MapXq21.1UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2439 2788 2253 4974 1726 2351 6 624 1951 465 2270 7306 6472 53 3734 1 852 1744 1617 175 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001329539 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001329540 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_079834 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC012615 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF109187 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF173896 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK074586 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK074967 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK091166 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK092056 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK307641 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK307700 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL832731 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC007958 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC011747 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC016509 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC016685 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC062598 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX647235 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA417608 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471139 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CQ782937 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000316097   ⟹   ENSP00000316007
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl191,905,399 - 1,926,013 (+)Ensembl
Ensembl Acc Id: ENST00000409472   ⟹   ENSP00000386865
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl191,905,214 - 1,926,013 (+)Ensembl
Ensembl Acc Id: ENST00000411971   ⟹   ENSP00000388185
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl191,908,264 - 1,918,965 (+)Ensembl
Ensembl Acc Id: ENST00000414057   ⟹   ENSP00000479672
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl191,905,378 - 1,925,016 (+)Ensembl
Ensembl Acc Id: ENST00000452128
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl191,905,372 - 1,919,204 (+)Ensembl
Ensembl Acc Id: ENST00000460767   ⟹   ENSP00000481989
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl191,905,391 - 1,918,961 (+)Ensembl
Ensembl Acc Id: ENST00000472442
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl191,922,113 - 1,926,005 (+)Ensembl
Ensembl Acc Id: ENST00000489554
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl191,905,399 - 1,920,743 (+)Ensembl
Ensembl Acc Id: ENST00000585335
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl191,918,644 - 1,922,156 (+)Ensembl
Ensembl Acc Id: ENST00000588555
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl191,905,400 - 1,907,184 (+)Ensembl
Ensembl Acc Id: ENST00000588907   ⟹   ENSP00000478264
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl191,908,281 - 1,918,189 (+)Ensembl
Ensembl Acc Id: ENST00000590266   ⟹   ENSP00000465199
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl191,913,090 - 1,918,161 (+)Ensembl
Ensembl Acc Id: ENST00000621748   ⟹   ENSP00000479083
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl191,914,521 - 1,924,701 (+)Ensembl
RefSeq Acc Id: NM_001329539   ⟹   NP_001316468
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38191,905,399 - 1,926,013 (+)NCBI
T2T-CHM13v2.0191,876,716 - 1,897,325 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001329540   ⟹   NP_001316469
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38191,905,399 - 1,926,013 (+)NCBI
T2T-CHM13v2.0191,876,716 - 1,897,325 (+)NCBI
Sequence:
RefSeq Acc Id: NM_079834   ⟹   NP_524558
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38191,905,399 - 1,926,013 (+)NCBI
GRCh37191,905,213 - 1,926,012 (+)NCBI
Build 36191,856,373 - 1,877,012 (+)NCBI Archive
Celera191,839,456 - 1,860,087 (+)RGD
HuRef191,676,855 - 1,697,510 (+)RGD
CHM1_1191,904,962 - 1,925,465 (+)NCBI
T2T-CHM13v2.0191,876,716 - 1,897,325 (+)NCBI
Sequence:
RefSeq Acc Id: NP_524558   ⟸   NM_079834
- Peptide Label: isoform 1
- UniProtKB: Q8N2N1 (UniProtKB/Swiss-Prot),   Q8NAV0 (UniProtKB/Swiss-Prot),   Q969E2 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001316469   ⟸   NM_001329540
- Peptide Label: isoform 3
- UniProtKB: Q969E2 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001316468   ⟸   NM_001329539
- Peptide Label: isoform 2
- UniProtKB: Q969E2 (UniProtKB/Swiss-Prot)
- Sequence:
Ensembl Acc Id: ENSP00000479083   ⟸   ENST00000621748
Ensembl Acc Id: ENSP00000388185   ⟸   ENST00000411971
Ensembl Acc Id: ENSP00000479672   ⟸   ENST00000414057
Ensembl Acc Id: ENSP00000478264   ⟸   ENST00000588907
Ensembl Acc Id: ENSP00000465199   ⟸   ENST00000590266
Ensembl Acc Id: ENSP00000316007   ⟸   ENST00000316097
Ensembl Acc Id: ENSP00000386865   ⟸   ENST00000409472
Ensembl Acc Id: ENSP00000481989   ⟸   ENST00000460767

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q969E2-F1-model_v2 AlphaFold Q969E2 1-229 view protein structure

Promoters
RGD ID:6796023
Promoter ID:HG_KWN:28427
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_079834,   OTTHUMT00000336212,   OTTHUMT00000336214,   OTTHUMT00000336215,   UC002LUH.1,   UC002LUI.1,   UC002LUK.1,   UC010DSS.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36191,855,621 - 1,856,807 (+)MPROMDB
RGD ID:6796024
Promoter ID:HG_KWN:28428
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000336216,   OTTHUMT00000336218
Position:
Human AssemblyChrPosition (strand)Source
Build 36191,858,751 - 1,859,251 (+)MPROMDB
RGD ID:7237885
Promoter ID:EPDNEW_H24688
Type:initiation region
Name:SCAMP4_1
Description:secretory carrier membrane protein 4
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38191,905,400 - 1,905,460EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:30385 AgrOrtholog
COSMIC SCAMP4 COSMIC
Ensembl Genes ENSG00000227500 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000316097 ENTREZGENE
  ENST00000316097.13 UniProtKB/Swiss-Prot
  ENST00000409472 ENTREZGENE
  ENST00000409472.6 UniProtKB/Swiss-Prot
  ENST00000411971.5 UniProtKB/TrEMBL
  ENST00000414057.6 UniProtKB/TrEMBL
  ENST00000460767.5 UniProtKB/TrEMBL
  ENST00000588907.2 UniProtKB/TrEMBL
  ENST00000590266.5 UniProtKB/TrEMBL
  ENST00000621748.1 UniProtKB/Swiss-Prot
GTEx ENSG00000227500 GTEx
HGNC ID HGNC:30385 ENTREZGENE
Human Proteome Map SCAMP4 Human Proteome Map
InterPro SCAMP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:113178 UniProtKB/Swiss-Prot
NCBI Gene 113178 ENTREZGENE
OMIM 613764 OMIM
PANTHER PTHR10687 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SECRETORY CARRIER-ASSOCIATED MEMBRANE PROTEIN 4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam SCAMP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134983341 PharmGKB
UniProt A0A087WU01_HUMAN UniProtKB/TrEMBL
  A0A087WVT5_HUMAN UniProtKB/TrEMBL
  A0A087WYP4_HUMAN UniProtKB/TrEMBL
  C9JWM2_HUMAN UniProtKB/TrEMBL
  K7EJJ4_HUMAN UniProtKB/TrEMBL
  Q8N2N1 ENTREZGENE
  Q8NAV0 ENTREZGENE
  Q969E2 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary Q8N2N1 UniProtKB/Swiss-Prot
  Q8NAV0 UniProtKB/Swiss-Prot