NUP188 (nucleoporin 188) - Rat Genome Database

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Gene: NUP188 (nucleoporin 188) Homo sapiens
Analyze
Symbol: NUP188
Name: nucleoporin 188
RGD ID: 1348104
HGNC Page HGNC:17859
Description: Predicted to be a structural constituent of nuclear pore. Involved in protein import into nucleus. Located in nuclear envelope. Implicated in Sandestig-Stefanova syndrome and respiratory failure.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: FLJ21639; hNup188; KIAA0169; nucleoporin 188kDa; nucleoporin NUP188; nucleoporin NUP188 homolog; SANDSTEF
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh389128,947,699 - 129,007,096 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl9128,947,699 - 129,007,096 (+)EnsemblGRCh38hg38GRCh38
GRCh379131,709,978 - 131,769,375 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 369130,749,798 - 130,809,195 (+)NCBINCBI36Build 36hg18NCBI36
Build 349128,789,563 - 128,848,928NCBI
Celera9102,361,838 - 102,421,686 (+)NCBICelera
Cytogenetic Map9q34.11NCBI
HuRef9101,317,691 - 101,376,696 (+)NCBIHuRef
CHM1_19131,861,021 - 131,920,403 (+)NCBICHM1_1
T2T-CHM13v2.09141,151,108 - 141,210,530 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
cytosol  (TAS)
membrane  (HDA)
nuclear envelope  (IDA,TAS)
nuclear pore  (IEA,NAS)
nuclear pore inner ring  (IBA,IEA)
nucleus  (IEA)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. Bi-allelic Loss-of-Function Variants in NUP188 Cause a Recognizable Syndrome Characterized by Neurologic, Ocular, and Cardiac Abnormalities. Muir AM, etal., Am J Hum Genet. 2020 May 7;106(5):623-631. doi: 10.1016/j.ajhg.2020.03.009. Epub 2020 Apr 9.
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8724849   PMID:10668806   PMID:11029043   PMID:12477932   PMID:15146197   PMID:17353931   PMID:17567994   PMID:19596235   PMID:19615732   PMID:19738201   PMID:19946888   PMID:20360068  
PMID:21565611   PMID:21873635   PMID:22586326   PMID:22623428   PMID:22863883   PMID:22939629   PMID:22990118   PMID:23602568   PMID:24315095   PMID:24457600   PMID:24711643   PMID:24927568  
PMID:25582440   PMID:25693804   PMID:25921289   PMID:26186194   PMID:26344197   PMID:26496610   PMID:26878725   PMID:26972000   PMID:27016207   PMID:27025967   PMID:27593162   PMID:28192407  
PMID:28611094   PMID:28675297   PMID:29117863   PMID:29180619   PMID:29229926   PMID:29395067   PMID:29478914   PMID:29507755   PMID:29568061   PMID:29676528   PMID:29955894   PMID:30154076  
PMID:30804502   PMID:30833792   PMID:30948266   PMID:31073040   PMID:31091453   PMID:31527135   PMID:31586073   PMID:31753913   PMID:31980649   PMID:31995728   PMID:32211895   PMID:32344865  
PMID:32694731   PMID:32707033   PMID:32780723   PMID:32814769   PMID:32877691   PMID:33239621   PMID:33545068   PMID:33766124   PMID:33845483   PMID:33903120   PMID:33961781   PMID:34079125  
PMID:34244565   PMID:34299191   PMID:34591612   PMID:34709727   PMID:35032548   PMID:35271311   PMID:35384245   PMID:35439318   PMID:35563538   PMID:35676246   PMID:35679425   PMID:35748872  
PMID:35831314   PMID:35944360   PMID:36114006   PMID:36180527   PMID:36215168   PMID:36282215   PMID:36597993   PMID:36736316   PMID:37827155  


Genomics

Comparative Map Data
NUP188
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh389128,947,699 - 129,007,096 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl9128,947,699 - 129,007,096 (+)EnsemblGRCh38hg38GRCh38
GRCh379131,709,978 - 131,769,375 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 369130,749,798 - 130,809,195 (+)NCBINCBI36Build 36hg18NCBI36
Build 349128,789,563 - 128,848,928NCBI
Celera9102,361,838 - 102,421,686 (+)NCBICelera
Cytogenetic Map9q34.11NCBI
HuRef9101,317,691 - 101,376,696 (+)NCBIHuRef
CHM1_19131,861,021 - 131,920,403 (+)NCBICHM1_1
T2T-CHM13v2.09141,151,108 - 141,210,530 (+)NCBIT2T-CHM13v2.0
Nup188
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39230,176,419 - 30,234,278 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl230,176,409 - 30,234,278 (+)EnsemblGRCm39 Ensembl
GRCm38230,286,407 - 30,344,266 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl230,286,397 - 30,344,266 (+)EnsemblGRCm38mm10GRCm38
MGSCv37230,141,953 - 30,199,782 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36230,108,442 - 30,166,271 (+)NCBIMGSCv36mm8
Celera229,991,190 - 30,049,297 (+)NCBICelera
Cytogenetic Map2BNCBI
cM Map221.49NCBI
Nup188
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8333,957,778 - 34,014,122 (+)NCBIGRCr8
mRatBN7.2313,559,917 - 13,616,313 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl313,559,990 - 13,616,307 (+)EnsemblmRatBN7.2 Ensembl
Rnor_6.038,852,271 - 8,908,608 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl38,873,933 - 8,908,438 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0314,205,251 - 14,261,382 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.439,331,812 - 9,388,204 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera38,326,493 - 8,382,816 (+)NCBICelera
Cytogenetic Map3p12NCBI
Nup188
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049555701,312,998 - 1,369,513 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049555701,312,998 - 1,369,513 (+)NCBIChiLan1.0ChiLan1.0
NUP188
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21110,346,228 - 10,404,809 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1910,348,576 - 10,407,139 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v09100,069,656 - 100,130,521 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.19128,733,749 - 128,791,252 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl9128,733,780 - 128,791,252 (+)Ensemblpanpan1.1panPan2
NUP188
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1954,657,520 - 54,712,900 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl954,657,682 - 54,712,827 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha953,853,072 - 53,908,426 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0955,578,563 - 55,633,941 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl955,578,567 - 55,633,921 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1954,340,129 - 54,395,076 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0954,652,331 - 54,707,442 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0954,745,638 - 54,800,996 (-)NCBIUU_Cfam_GSD_1.0
Nup188
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404947196,639,939 - 196,694,386 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493648716,408,518 - 16,462,923 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493648716,408,523 - 16,462,916 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
NUP188
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1269,259,519 - 269,312,862 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11269,259,496 - 269,312,872 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21303,275,625 - 303,328,996 (+)NCBISscrofa10.2Sscrofa10.2susScr3
NUP188
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1129,150,603 - 9,213,512 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl129,151,005 - 9,208,452 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666096299,833 - 407,072 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Nup188
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247606,111,621 - 6,118,084 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla_female_1.0 EnsemblNW_0046247606,061,130 - 6,106,853 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247606,061,130 - 6,120,597 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in NUP188
175 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 copy number gain See cases [RCV000050348] Chr9:193412..138179445 [GRCh38]
Chr9:204193..141073897 [GRCh37]
Chr9:194193..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9q33.2-34.3(chr9:121112395-138075224)x3 copy number gain See cases [RCV000051009] Chr9:121112395..138075224 [GRCh38]
Chr9:123874673..140969676 [GRCh37]
Chr9:122914494..140089497 [NCBI36]
Chr9:9q33.2-34.3		 pathogenic
GRCh38/hg38 9q33.2-34.3(chr9:122792658-138124532)x3 copy number gain See cases [RCV000051040] Chr9:122792658..138124532 [GRCh38]
Chr9:125554937..141018984 [GRCh37]
Chr9:124594758..140138805 [NCBI36]
Chr9:9q33.2-34.3		 pathogenic
GRCh38/hg38 9q34.11(chr9:128808545-129002107)x3 copy number gain See cases [RCV000052257] Chr9:128808545..129002107 [GRCh38]
Chr9:131570824..131764386 [GRCh37]
Chr9:130610645..130804207 [NCBI36]
Chr9:9q34.11		 uncertain significance
GRCh38/hg38 9q33.3-34.11(chr9:125993583-129682375)x1 copy number loss See cases [RCV000052923] Chr9:125993583..129682375 [GRCh38]
Chr9:128755862..132444654 [GRCh37]
Chr9:127795683..131484475 [NCBI36]
Chr9:9q33.3-34.11		 pathogenic
GRCh38/hg38 9q34.11(chr9:127874581-130421811)x1 copy number loss See cases [RCV000052934] Chr9:127874581..130421811 [GRCh38]
Chr9:130636860..133297198 [GRCh37]
Chr9:129676681..132287019 [NCBI36]
Chr9:9q34.11		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124532)x3 copy number gain See cases [RCV000053745] Chr9:193412..138124532 [GRCh38]
Chr9:204193..141018984 [GRCh37]
Chr9:194193..140138805 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138114463)x3 copy number gain See cases [RCV000053746] Chr9:193412..138114463 [GRCh38]
Chr9:214367..141008915 [GRCh37]
Chr9:204367..140128736 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053748]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053748]|See cases [RCV000053748] Chr9:193412..138179445 [GRCh38]
Chr9:266045..141073897 [GRCh37]
Chr9:256045..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9q33.2-34.3(chr9:121586837-138179445)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053776]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053776]|See cases [RCV000053776] Chr9:121586837..138179445 [GRCh38]
Chr9:124349116..141073897 [GRCh37]
Chr9:123388937..140193718 [NCBI36]
Chr9:9q33.2-34.3		 pathogenic
GRCh38/hg38 9q34.11(chr9:127919476-130079974)x3 copy number gain See cases [RCV000053777] Chr9:127919476..130079974 [GRCh38]
Chr9:130681755..132842253 [GRCh37]
Chr9:129721576..131882074 [NCBI36]
Chr9:9q34.11		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:204193-138179445) copy number gain See cases [RCV000133791] Chr9:204193..138179445 [GRCh38]
Chr9:204193..141073897 [GRCh37]
Chr9:194193..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9q33.2-34.3(chr9:121073102-138179445)x3 copy number gain See cases [RCV000134920] Chr9:121073102..138179445 [GRCh38]
Chr9:123835380..141073897 [GRCh37]
Chr9:122875201..140193718 [NCBI36]
Chr9:9q33.2-34.3		 pathogenic
GRCh38/hg38 9q34.11(chr9:128610170-129368351)x1 copy number loss See cases [RCV000138126] Chr9:128610170..129368351 [GRCh38]
Chr9:131372449..132130630 [GRCh37]
Chr9:130412270..131170451 [NCBI36]
Chr9:9q34.11		 uncertain significance
GRCh38/hg38 9q34.11-34.12(chr9:128839676-130912873)x3 copy number gain See cases [RCV000137775] Chr9:128839676..130912873 [GRCh38]
Chr9:131601955..133788260 [GRCh37]
Chr9:130641776..132778081 [NCBI36]
Chr9:9q34.11-34.12		 uncertain significance
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124524)x3 copy number gain See cases [RCV000138783] Chr9:193412..138124524 [GRCh38]
Chr9:204090..141018976 [GRCh37]
Chr9:194090..140138797 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p11.2-q34.3(chr9:193412-138159073)x3 copy number gain See cases [RCV000139207] Chr9:193412..138159073 [GRCh38]
Chr9:68420641..141053525 [GRCh37]
Chr9:67910461..140173346 [NCBI36]
Chr9:9p11.2-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138159073)x3 copy number gain See cases [RCV000138962] Chr9:193412..138159073 [GRCh38]
Chr9:204104..141053525 [GRCh37]
Chr9:194104..140173346 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic|conflicting data from submitters
GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3 copy number gain See cases [RCV000141876] Chr9:203861..138125937 [GRCh38]
Chr9:203861..141020389 [GRCh37]
Chr9:193861..140140210 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:203862-138125937)x3 copy number gain See cases [RCV000143476] Chr9:203862..138125937 [GRCh38]
Chr9:203862..141020389 [GRCh37]
Chr9:193862..140140210 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 copy number gain See cases [RCV000148113] Chr9:193412..138179445 [GRCh38]
Chr9:204193..141073897 [GRCh37]
Chr9:194193..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q34.11(chr9:131550680-131775355)x3 copy number gain See cases [RCV000240044] Chr9:131550680..131775355 [GRCh37]
Chr9:9q34.11		 uncertain significance
GRCh37/hg19 9p24.3-q34.3(chr9:163131-141122114)x3 copy number gain See cases [RCV000240081] Chr9:163131..141122114 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
NM_015354.3(NUP188):c.-6G>A single nucleotide variant DK1-congenital disorder of glycosylation [RCV000323596] Chr9:128947714 [GRCh38]
Chr9:131709993 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.-13C>T single nucleotide variant DK1-congenital disorder of glycosylation [RCV000287303]|not provided [RCV000839153] Chr9:128947707 [GRCh38]
Chr9:131709986 [GRCh37]
Chr9:9q34.11		 benign|likely benign
NM_015354.3(NUP188):c.8C>T (p.Ala3Val) single nucleotide variant DK1-congenital disorder of glycosylation [RCV000378227]|Inborn genetic diseases [RCV002523737] Chr9:128947727 [GRCh38]
Chr9:131710006 [GRCh37]
Chr9:9q34.11		 uncertain significance
GRCh37/hg19 9q34.11(chr9:131282528-131720659)x3 copy number gain not provided [RCV001270669] Chr9:131282528..131720659 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.19G>A (p.Gly7Arg) single nucleotide variant Congenital disorder of glycosylation [RCV000316700]|not provided [RCV001672746] Chr9:128947738 [GRCh38]
Chr9:131710017 [GRCh37]
Chr9:9q34.11		 benign|likely benign
GRCh37/hg19 9p24.3-q34.3(chr9:62525-141006407) copy number gain See cases [RCV000449375] Chr9:62525..141006407 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3 copy number gain not specified [RCV003986800] Chr9:203861..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q33.3-34.3(chr9:128652785-141044751)x3 copy number gain See cases [RCV000447080] Chr9:128652785..141044751 [GRCh37]
Chr9:9q33.3-34.3		 pathogenic
GRCh37/hg19 9q34.11(chr9:130390139-132760275)x1 copy number loss See cases [RCV000445837] Chr9:130390139..132760275 [GRCh37]
Chr9:9q34.11		 pathogenic
GRCh37/hg19 9q33.2-34.3(chr9:124642754-141146461)x3 copy number gain See cases [RCV000448784] Chr9:124642754..141146461 [GRCh37]
Chr9:9q33.2-34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203864-141020389)x3 copy number gain See cases [RCV000448978] Chr9:203864..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
NM_015354.3(NUP188):c.4044+6A>C single nucleotide variant NUP188-related condition [RCV003972730]|Sandestig-stefanova syndrome [RCV001788219]|not provided [RCV001613280]|not specified [RCV000454604] Chr9:129001735 [GRCh38]
Chr9:131764014 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.3516-14A>G single nucleotide variant Sandestig-stefanova syndrome [RCV001788217]|not specified [RCV000455127] Chr9:128999158 [GRCh38]
Chr9:131761437 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.4596A>C (p.Ser1532=) single nucleotide variant NUP188-related condition [RCV003983072]|Sandestig-stefanova syndrome [RCV001788220]|not specified [RCV000455292] Chr9:129005389 [GRCh38]
Chr9:131767668 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.3662-4A>G single nucleotide variant NUP188-related condition [RCV003972729]|Sandestig-stefanova syndrome [RCV001788218]|not specified [RCV000455839] Chr9:128999620 [GRCh38]
Chr9:131761899 [GRCh37]
Chr9:9q34.11		 benign
GRCh37/hg19 9q34.11-34.13(chr9:131670024-134514071) copy number loss not provided [RCV000767561] Chr9:131670024..134514071 [GRCh37]
Chr9:9q34.11-34.13		 likely pathogenic
NM_015354.3(NUP188):c.2821G>A (p.Val941Ile) single nucleotide variant Inborn genetic diseases [RCV003259637] Chr9:128993377 [GRCh38]
Chr9:131755656 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2338A>G (p.Ile780Val) single nucleotide variant Inborn genetic diseases [RCV003266900] Chr9:128987662 [GRCh38]
Chr9:131749941 [GRCh37]
Chr9:9q34.11		 uncertain significance
GRCh37/hg19 9q21.11-34.3(chr9:71069743-140999928) copy number gain Global developmental delay [RCV000626548] Chr9:71069743..140999928 [GRCh37]
Chr9:9q21.11-34.3		 likely pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203862-141020389) copy number gain See cases [RCV000512392] Chr9:203862..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q33.3-34.12(chr9:129370440-133866894)x1 copy number loss not provided [RCV000748671] Chr9:129370440..133866894 [GRCh37]
Chr9:9q33.3-34.12		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141122247)x3 copy number gain not provided [RCV000748055] Chr9:10590..141122247 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q34.11-34.12(chr9:131413885-133866894)x1 copy number loss not provided [RCV000748699] Chr9:131413885..133866894 [GRCh37]
Chr9:9q34.11-34.12		 benign
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141107672)x3 copy number gain not provided [RCV000748053] Chr9:10590..141107672 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:46587-141066491)x3 copy number gain not provided [RCV000748063] Chr9:46587..141066491 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141114095)x2 copy number gain not provided [RCV000748054] Chr9:10590..141114095 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
NM_015354.3(NUP188):c.4734T>G (p.Asp1578Glu) single nucleotide variant NUP188-related condition [RCV003930549]|not provided [RCV000881742] Chr9:129005527 [GRCh38]
Chr9:131767806 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.3974G>A (p.Arg1325His) single nucleotide variant NUP188-related condition [RCV003936137]|not provided [RCV000971914] Chr9:129001659 [GRCh38]
Chr9:131763938 [GRCh37]
Chr9:9q34.11		 benign|likely benign
GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020388)x3 copy number gain not provided [RCV000845900] Chr9:203861..141020388 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
NM_015354.3(NUP188):c.1205A>G (p.Asp402Gly) single nucleotide variant not provided [RCV000906157] Chr9:128979263 [GRCh38]
Chr9:131741542 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.426C>T (p.His142=) single nucleotide variant not provided [RCV000981215] Chr9:128958855 [GRCh38]
Chr9:131721134 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.2393+6G>T single nucleotide variant NUP188-related condition [RCV003928981]|not provided [RCV003312742] Chr9:128987723 [GRCh38]
Chr9:131750002 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.32+156A>G single nucleotide variant not provided [RCV000832790] Chr9:128947907 [GRCh38]
Chr9:131710186 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.87G>A (p.Leu29=) single nucleotide variant not provided [RCV000840230] Chr9:128949243 [GRCh38]
Chr9:131711522 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.32+95A>G single nucleotide variant not provided [RCV000835730] Chr9:128947846 [GRCh38]
Chr9:131710125 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.5239A>T (p.Met1747Leu) single nucleotide variant not provided [RCV000891614] Chr9:129006667 [GRCh38]
Chr9:131768946 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.337C>T (p.Gln113Ter) single nucleotide variant Sandestig-stefanova syndrome [RCV001007636]|not provided [RCV000999238] Chr9:128958019 [GRCh38]
Chr9:131720298 [GRCh37]
Chr9:9q34.11		 pathogenic|likely pathogenic
NM_015354.3(NUP188):c.4078C>T (p.Gln1360Ter) single nucleotide variant Sandestig-stefanova syndrome [RCV001175261] Chr9:129001917 [GRCh38]
Chr9:131764196 [GRCh37]
Chr9:9q34.11		 pathogenic
GRCh37/hg19 9q21.11-34.3(chr9:71416475-141020389)x3 copy number gain not provided [RCV000847808] Chr9:71416475..141020389 [GRCh37]
Chr9:9q21.11-34.3		 pathogenic
NM_015354.3(NUP188):c.3977T>C (p.Met1326Thr) single nucleotide variant Inborn genetic diseases [RCV003275232] Chr9:129001662 [GRCh38]
Chr9:131763941 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3814C>T (p.Arg1272Trp) single nucleotide variant Inborn genetic diseases [RCV003246574] Chr9:128999776 [GRCh38]
Chr9:131762055 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3144C>G (p.Tyr1048Ter) single nucleotide variant Sandestig-stefanova syndrome [RCV001175258] Chr9:128994912 [GRCh38]
Chr9:131757191 [GRCh37]
Chr9:9q34.11		 pathogenic
NM_015354.3(NUP188):c.5032dup (p.Arg1678fs) duplication Sandestig-stefanova syndrome [RCV001175259] Chr9:129006322..129006323 [GRCh38]
Chr9:131768601..131768602 [GRCh37]
Chr9:9q34.11		 pathogenic
GRCh37/hg19 9q34.11(chr9:131094304-131863858)x3 copy number gain not provided [RCV001006275] Chr9:131094304..131863858 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3962A>C (p.Glu1321Ala) single nucleotide variant Inborn genetic diseases [RCV003292588] Chr9:129001647 [GRCh38]
Chr9:131763926 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3503G>A (p.Arg1168Gln) single nucleotide variant Inborn genetic diseases [RCV003251300] Chr9:128998611 [GRCh38]
Chr9:131760890 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.32+311C>T single nucleotide variant not provided [RCV001687777] Chr9:128948062 [GRCh38]
Chr9:131710341 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.3186A>C (p.Thr1062=) single nucleotide variant not provided [RCV000953610] Chr9:128995349 [GRCh38]
Chr9:131757628 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.1170C>T (p.Thr390=) single nucleotide variant NUP188-related condition [RCV003975607]|not provided [RCV000889222] Chr9:128973216 [GRCh38]
Chr9:131735495 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.5025G>C (p.Val1675=) single nucleotide variant not provided [RCV000933825] Chr9:129006320 [GRCh38]
Chr9:131768599 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.287dup (p.Tyr96Ter) duplication Sandestig-stefanova syndrome [RCV001007635]|not provided [RCV001092375] Chr9:128956991..128956992 [GRCh38]
Chr9:131719270..131719271 [GRCh37]
Chr9:9q34.11		 pathogenic|uncertain significance
NM_015354.3(NUP188):c.32+137G>A single nucleotide variant not provided [RCV001676682] Chr9:128947888 [GRCh38]
Chr9:131710167 [GRCh37]
Chr9:9q34.11		 benign
GRCh37/hg19 9q34.11(chr9:130957344-132310210)x1 copy number loss not provided [RCV001006274] Chr9:130957344..132310210 [GRCh37]
Chr9:9q34.11		 pathogenic
NM_015354.3(NUP188):c.904_907del (p.Ile302fs) deletion Sandestig-stefanova syndrome [RCV001175257] Chr9:128969504..128969507 [GRCh38]
Chr9:131731783..131731786 [GRCh37]
Chr9:9q34.11		 pathogenic
NM_015354.3(NUP188):c.1890G>A (p.Trp630Ter) single nucleotide variant Sandestig-stefanova syndrome [RCV001175260] Chr9:128983479 [GRCh38]
Chr9:131745758 [GRCh37]
Chr9:9q34.11		 pathogenic
NM_015354.3(NUP188):c.3515+1G>A single nucleotide variant Microcephaly [RCV001526559]|Sandestig-stefanova syndrome [RCV003151861] Chr9:128998624 [GRCh38]
Chr9:131760903 [GRCh37]
Chr9:9q34.11		 likely pathogenic
NM_015354.3(NUP188):c.1851_1852delinsG (p.Cys617fs) indel Microcephaly [RCV001526560]|Sandestig-stefanova syndrome [RCV003151862] Chr9:128983347..128983348 [GRCh38]
Chr9:131745626..131745627 [GRCh37]
Chr9:9q34.11		 likely pathogenic
NM_015354.3(NUP188):c.4987A>C (p.Ile1663Leu) single nucleotide variant not provided [RCV001779647] Chr9:129006282 [GRCh38]
Chr9:131768561 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.1203+31T>C single nucleotide variant Sandestig-stefanova syndrome [RCV001788898] Chr9:128973280 [GRCh38]
Chr9:131735559 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.1797-24T>C single nucleotide variant Sandestig-stefanova syndrome [RCV001788899] Chr9:128983269 [GRCh38]
Chr9:131745548 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.3230G>A (p.Gly1077Glu) single nucleotide variant not provided [RCV001770843] Chr9:128995393 [GRCh38]
Chr9:131757672 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3460C>T (p.Arg1154Cys) single nucleotide variant not provided [RCV001771498] Chr9:128998568 [GRCh38]
Chr9:131760847 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3820C>T (p.Arg1274Trp) single nucleotide variant not provided [RCV001771499] Chr9:128999782 [GRCh38]
Chr9:131762061 [GRCh37]
Chr9:9q34.11		 uncertain significance
GRCh37/hg19 9q33.3-34.11(chr9:128523763-132604808)x3 copy number gain not provided [RCV001832977] Chr9:128523763..132604808 [GRCh37]
Chr9:9q33.3-34.11		 pathogenic
GRCh37/hg19 9q34.11(chr9:130390139-132760275) copy number loss not specified [RCV002052848] Chr9:130390139..132760275 [GRCh37]
Chr9:9q34.11		 pathogenic
NM_015354.3(NUP188):c.3881G>T (p.Cys1294Phe) single nucleotide variant not provided [RCV001825174] Chr9:129001566 [GRCh38]
Chr9:131763845 [GRCh37]
Chr9:9q34.11		 not provided
GRCh37/hg19 9p24.3-q34.3(chr9:353349-141020389) copy number gain not specified [RCV002053823] Chr9:353349..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q32-34.11(chr9:116422275-131713233) copy number gain not specified [RCV002052831] Chr9:116422275..131713233 [GRCh37]
Chr9:9q32-34.11		 pathogenic
NC_000009.11:g.(?_131087402)_(141016451_?)dup duplication Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome [RCV003119700] Chr9:131087402..141016451 [GRCh37]
Chr9:9q34.11-34.3		 uncertain significance
NM_015354.3(NUP188):c.3780G>T (p.Glu1260Asp) single nucleotide variant NUP188-related condition [RCV003973373]|not provided [RCV002263520] Chr9:128999742 [GRCh38]
Chr9:131762021 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.4948C>T (p.Leu1650Phe) single nucleotide variant Inborn genetic diseases [RCV003299799] Chr9:129006243 [GRCh38]
Chr9:131768522 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.880C>T (p.His294Tyr) single nucleotide variant not provided [RCV002474019] Chr9:128969482 [GRCh38]
Chr9:131731761 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.1516+1G>T single nucleotide variant not provided [RCV002474219] Chr9:128981391 [GRCh38]
Chr9:131743670 [GRCh37]
Chr9:9q34.11		 likely pathogenic
NM_015354.3(NUP188):c.1053G>C (p.Gln351His) single nucleotide variant Inborn genetic diseases [RCV002749437] Chr9:128970898 [GRCh38]
Chr9:131733177 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.1504C>T (p.Leu502Phe) single nucleotide variant Inborn genetic diseases [RCV002777030] Chr9:128981378 [GRCh38]
Chr9:131743657 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.1996C>T (p.Leu666Phe) single nucleotide variant Inborn genetic diseases [RCV002748778] Chr9:128984934 [GRCh38]
Chr9:131747213 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.1741T>C (p.Ser581Pro) single nucleotide variant Inborn genetic diseases [RCV002687264]|NUP188-related condition [RCV003404146] Chr9:128982973 [GRCh38]
Chr9:131745252 [GRCh37]
Chr9:9q34.11		 likely benign|uncertain significance
NM_015354.3(NUP188):c.4102A>G (p.Ser1368Gly) single nucleotide variant Inborn genetic diseases [RCV003012970] Chr9:129001941 [GRCh38]
Chr9:131764220 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3619T>A (p.Phe1207Ile) single nucleotide variant Inborn genetic diseases [RCV002946966] Chr9:128999275 [GRCh38]
Chr9:131761554 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3193A>C (p.Lys1065Gln) single nucleotide variant Inborn genetic diseases [RCV002864063] Chr9:128995356 [GRCh38]
Chr9:131757635 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3221A>G (p.Tyr1074Cys) single nucleotide variant Inborn genetic diseases [RCV002973812] Chr9:128995384 [GRCh38]
Chr9:131757663 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.585+5G>A single nucleotide variant Inborn genetic diseases [RCV002864380] Chr9:128959139 [GRCh38]
Chr9:131721418 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.1973T>A (p.Met658Lys) single nucleotide variant Inborn genetic diseases [RCV002816739] Chr9:128984911 [GRCh38]
Chr9:131747190 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3278G>A (p.Ser1093Asn) single nucleotide variant Inborn genetic diseases [RCV002727855] Chr9:128995441 [GRCh38]
Chr9:131757720 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.4286G>A (p.Arg1429Gln) single nucleotide variant Inborn genetic diseases [RCV002772655] Chr9:129002965 [GRCh38]
Chr9:131765244 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.4696C>T (p.Arg1566Cys) single nucleotide variant Inborn genetic diseases [RCV002818898] Chr9:129005489 [GRCh38]
Chr9:131767768 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.4034G>A (p.Arg1345His) single nucleotide variant Inborn genetic diseases [RCV002974771] Chr9:129001719 [GRCh38]
Chr9:131763998 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.722A>G (p.Glu241Gly) single nucleotide variant Inborn genetic diseases [RCV002793793] Chr9:128968642 [GRCh38]
Chr9:131730921 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.908G>A (p.Cys303Tyr) single nucleotide variant Inborn genetic diseases [RCV002906081] Chr9:128969510 [GRCh38]
Chr9:131731789 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2485CCT[1] (p.Pro830del) microsatellite Inborn genetic diseases [RCV002992264] Chr9:128988138..128988140 [GRCh38]
Chr9:131750417..131750419 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2084T>G (p.Leu695Arg) single nucleotide variant Inborn genetic diseases [RCV002973636] Chr9:128986565 [GRCh38]
Chr9:131748844 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.1657G>A (p.Val553Ile) single nucleotide variant Inborn genetic diseases [RCV002864237] Chr9:128982689 [GRCh38]
Chr9:131744968 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2737C>T (p.Arg913Cys) single nucleotide variant Inborn genetic diseases [RCV002754634] Chr9:128993293 [GRCh38]
Chr9:131755572 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3598G>A (p.Glu1200Lys) single nucleotide variant Inborn genetic diseases [RCV002845472] Chr9:128999254 [GRCh38]
Chr9:131761533 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.4462T>C (p.Cys1488Arg) single nucleotide variant Inborn genetic diseases [RCV002888959] Chr9:129005174 [GRCh38]
Chr9:131767453 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.4931C>T (p.Thr1644Ile) single nucleotide variant Inborn genetic diseases [RCV002759161] Chr9:129006111 [GRCh38]
Chr9:131768390 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3298T>G (p.Tyr1100Asp) single nucleotide variant Inborn genetic diseases [RCV002707910] Chr9:128995461 [GRCh38]
Chr9:131757740 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3749G>A (p.Arg1250His) single nucleotide variant Inborn genetic diseases [RCV003001752] Chr9:128999711 [GRCh38]
Chr9:131761990 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.471A>C (p.Glu157Asp) single nucleotide variant Inborn genetic diseases [RCV002924222] Chr9:128959020 [GRCh38]
Chr9:131721299 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2497G>A (p.Val833Met) single nucleotide variant Inborn genetic diseases [RCV002783861] Chr9:128988150 [GRCh38]
Chr9:131750429 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.190A>G (p.Asn64Asp) single nucleotide variant Inborn genetic diseases [RCV002976772]|NUP188-related condition [RCV003928917] Chr9:128956378 [GRCh38]
Chr9:131718657 [GRCh37]
Chr9:9q34.11		 benign|likely benign
NM_015354.3(NUP188):c.690T>G (p.Ser230Arg) single nucleotide variant Inborn genetic diseases [RCV002703918] Chr9:128968610 [GRCh38]
Chr9:131730889 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.5111G>T (p.Arg1704Leu) single nucleotide variant Inborn genetic diseases [RCV002887130] Chr9:129006539 [GRCh38]
Chr9:131768818 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3815G>A (p.Arg1272Gln) single nucleotide variant Inborn genetic diseases [RCV002822004] Chr9:128999777 [GRCh38]
Chr9:131762056 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2440G>C (p.Val814Leu) single nucleotide variant Inborn genetic diseases [RCV002782218] Chr9:128988093 [GRCh38]
Chr9:131750372 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.890C>T (p.Ala297Val) single nucleotide variant Inborn genetic diseases [RCV002870219] Chr9:128969492 [GRCh38]
Chr9:131731771 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3798G>C (p.Glu1266Asp) single nucleotide variant Inborn genetic diseases [RCV002950806] Chr9:128999760 [GRCh38]
Chr9:131762039 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.4241A>G (p.Asn1414Ser) single nucleotide variant Inborn genetic diseases [RCV002644856] Chr9:129002920 [GRCh38]
Chr9:131765199 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2326A>T (p.Thr776Ser) single nucleotide variant Inborn genetic diseases [RCV002768408] Chr9:128987650 [GRCh38]
Chr9:131749929 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.572A>G (p.His191Arg) single nucleotide variant Inborn genetic diseases [RCV002854627] Chr9:128959121 [GRCh38]
Chr9:131721400 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.1754G>T (p.Cys585Phe) single nucleotide variant Inborn genetic diseases [RCV002830323] Chr9:128982986 [GRCh38]
Chr9:131745265 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.1235C>T (p.Ala412Val) single nucleotide variant Inborn genetic diseases [RCV002874308] Chr9:128979293 [GRCh38]
Chr9:131741572 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2269A>T (p.Thr757Ser) single nucleotide variant Inborn genetic diseases [RCV002701640] Chr9:128987593 [GRCh38]
Chr9:131749872 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.1483C>T (p.Arg495Trp) single nucleotide variant Inborn genetic diseases [RCV002768138] Chr9:128981357 [GRCh38]
Chr9:131743636 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2390G>A (p.Arg797Gln) single nucleotide variant Inborn genetic diseases [RCV002698856] Chr9:128987714 [GRCh38]
Chr9:131749993 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.1021G>A (p.Val341Met) single nucleotide variant Inborn genetic diseases [RCV002743780] Chr9:128970866 [GRCh38]
Chr9:131733145 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.1019G>A (p.Ser340Asn) single nucleotide variant Inborn genetic diseases [RCV002696686] Chr9:128970864 [GRCh38]
Chr9:131733143 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3923G>A (p.Arg1308His) single nucleotide variant Inborn genetic diseases [RCV002986673] Chr9:129001608 [GRCh38]
Chr9:131763887 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.4177T>C (p.Trp1393Arg) single nucleotide variant Inborn genetic diseases [RCV002986719] Chr9:129002856 [GRCh38]
Chr9:131765135 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.1900C>T (p.Arg634Cys) single nucleotide variant Inborn genetic diseases [RCV003003955]|NUP188-related condition [RCV003427661]|Sandestig-stefanova syndrome [RCV003135266] Chr9:128983489 [GRCh38]
Chr9:131745768 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3211C>T (p.Arg1071Cys) single nucleotide variant Inborn genetic diseases [RCV002698960] Chr9:128995374 [GRCh38]
Chr9:131757653 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2666G>C (p.Cys889Ser) single nucleotide variant Inborn genetic diseases [RCV002803116] Chr9:128993222 [GRCh38]
Chr9:131755501 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.17G>C (p.Gly6Ala) single nucleotide variant Inborn genetic diseases [RCV002955605]|NUP188-related condition [RCV003963750] Chr9:128947736 [GRCh38]
Chr9:131710015 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.2053C>T (p.Arg685Cys) single nucleotide variant Inborn genetic diseases [RCV002697785] Chr9:128984991 [GRCh38]
Chr9:131747270 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2683G>A (p.Ala895Thr) single nucleotide variant Inborn genetic diseases [RCV002853495] Chr9:128993239 [GRCh38]
Chr9:131755518 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.2590G>T (p.Asp864Tyr) single nucleotide variant Inborn genetic diseases [RCV002645010] Chr9:128990176 [GRCh38]
Chr9:131752455 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.5225C>T (p.Ala1742Val) single nucleotide variant Inborn genetic diseases [RCV002767720] Chr9:129006653 [GRCh38]
Chr9:131768932 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2038A>G (p.Thr680Ala) single nucleotide variant Inborn genetic diseases [RCV002764600] Chr9:128984976 [GRCh38]
Chr9:131747255 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.1591C>T (p.Arg531Cys) single nucleotide variant Inborn genetic diseases [RCV002719924] Chr9:128982623 [GRCh38]
Chr9:131744902 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.553G>A (p.Ala185Thr) single nucleotide variant Inborn genetic diseases [RCV002703513] Chr9:128959102 [GRCh38]
Chr9:131721381 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.273G>T (p.Gln91His) single nucleotide variant Inborn genetic diseases [RCV002965879] Chr9:128956978 [GRCh38]
Chr9:131719257 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.463A>G (p.Arg155Gly) single nucleotide variant Inborn genetic diseases [RCV002719789] Chr9:128958892 [GRCh38]
Chr9:131721171 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2896A>G (p.Ile966Val) single nucleotide variant Inborn genetic diseases [RCV002673589] Chr9:128993573 [GRCh38]
Chr9:131755852 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.5143C>T (p.Leu1715Phe) single nucleotide variant Inborn genetic diseases [RCV002652178] Chr9:129006571 [GRCh38]
Chr9:131768850 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.446A>G (p.Asp149Gly) single nucleotide variant Inborn genetic diseases [RCV002855476] Chr9:128958875 [GRCh38]
Chr9:131721154 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.4737+5T>G single nucleotide variant Inborn genetic diseases [RCV002717727]|NUP188-related condition [RCV003973736] Chr9:129005535 [GRCh38]
Chr9:131767814 [GRCh37]
Chr9:9q34.11		 likely benign|uncertain significance
NM_015354.3(NUP188):c.2020C>T (p.Gln674Ter) single nucleotide variant not provided [RCV003063642] Chr9:128984958 [GRCh38]
Chr9:131747237 [GRCh37]
Chr9:9q34.11		 pathogenic
NM_015354.3(NUP188):c.4104T>A (p.Ser1368Arg) single nucleotide variant Inborn genetic diseases [RCV002921433] Chr9:129001943 [GRCh38]
Chr9:131764222 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2009G>A (p.Ser670Asn) single nucleotide variant Inborn genetic diseases [RCV002935226] Chr9:128984947 [GRCh38]
Chr9:131747226 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3389G>C (p.Arg1130Pro) single nucleotide variant Inborn genetic diseases [RCV002703192] Chr9:128998188 [GRCh38]
Chr9:131760467 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.4033C>T (p.Arg1345Cys) single nucleotide variant Inborn genetic diseases [RCV002855702] Chr9:129001718 [GRCh38]
Chr9:131763997 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.605G>A (p.Arg202His) single nucleotide variant Inborn genetic diseases [RCV002669287] Chr9:128968525 [GRCh38]
Chr9:131730804 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3748C>T (p.Arg1250Cys) single nucleotide variant Inborn genetic diseases [RCV002960683] Chr9:128999710 [GRCh38]
Chr9:131761989 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.25T>G (p.Cys9Gly) single nucleotide variant Inborn genetic diseases [RCV002896001] Chr9:128947744 [GRCh38]
Chr9:131710023 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3969C>G (p.Ser1323Arg) single nucleotide variant Inborn genetic diseases [RCV002669404] Chr9:129001654 [GRCh38]
Chr9:131763933 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.724C>A (p.Gln242Lys) single nucleotide variant Inborn genetic diseases [RCV003008656] Chr9:128968644 [GRCh38]
Chr9:131730923 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2554A>G (p.Ile852Val) single nucleotide variant Inborn genetic diseases [RCV002809874] Chr9:128990140 [GRCh38]
Chr9:131752419 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3821G>A (p.Arg1274Gln) single nucleotide variant Inborn genetic diseases [RCV002989113] Chr9:128999783 [GRCh38]
Chr9:131762062 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.62T>C (p.Leu21Pro) single nucleotide variant Inborn genetic diseases [RCV002920810] Chr9:128949218 [GRCh38]
Chr9:131711497 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.796G>A (p.Gly266Ser) single nucleotide variant Inborn genetic diseases [RCV002723097] Chr9:128968716 [GRCh38]
Chr9:131730995 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.1217C>G (p.Thr406Arg) single nucleotide variant Inborn genetic diseases [RCV002723354] Chr9:128979275 [GRCh38]
Chr9:131741554 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3377_3378del (p.Ser1126fs) microsatellite Sandestig-stefanova syndrome [RCV003235772]|not provided [RCV002606417] Chr9:128998174..128998175 [GRCh38]
Chr9:131760453..131760454 [GRCh37]
Chr9:9q34.11		 pathogenic|likely pathogenic
NM_015354.3(NUP188):c.1979C>T (p.Ala660Val) single nucleotide variant Inborn genetic diseases [RCV002678460] Chr9:128984917 [GRCh38]
Chr9:131747196 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.172G>C (p.Ala58Pro) single nucleotide variant Inborn genetic diseases [RCV003192564] Chr9:128956360 [GRCh38]
Chr9:131718639 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3145T>C (p.Tyr1049His) single nucleotide variant Inborn genetic diseases [RCV003183033] Chr9:128994913 [GRCh38]
Chr9:131757192 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.5234G>C (p.Arg1745Pro) single nucleotide variant Inborn genetic diseases [RCV003211717] Chr9:129006662 [GRCh38]
Chr9:131768941 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2007C>G (p.Asn669Lys) single nucleotide variant Inborn genetic diseases [RCV003207702] Chr9:128984945 [GRCh38]
Chr9:131747224 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.1408A>G (p.Lys470Glu) single nucleotide variant Inborn genetic diseases [RCV003196618] Chr9:128981282 [GRCh38]
Chr9:131743561 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3835C>T (p.Arg1279Cys) single nucleotide variant Inborn genetic diseases [RCV003181119] Chr9:128999797 [GRCh38]
Chr9:131762076 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3910C>G (p.Leu1304Val) single nucleotide variant not provided [RCV003227236] Chr9:129001595 [GRCh38]
Chr9:131763874 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.4478A>G (p.His1493Arg) single nucleotide variant Inborn genetic diseases [RCV003258240] Chr9:129005190 [GRCh38]
Chr9:131767469 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2929C>T (p.Pro977Ser) single nucleotide variant Inborn genetic diseases [RCV003205041] Chr9:128993606 [GRCh38]
Chr9:131755885 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.1355G>A (p.Arg452Gln) single nucleotide variant Sandestig-stefanova syndrome [RCV003133092] Chr9:128980691 [GRCh38]
Chr9:131742970 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.700G>C (p.Val234Leu) single nucleotide variant Inborn genetic diseases [RCV003185066] Chr9:128968620 [GRCh38]
Chr9:131730899 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.4550G>A (p.Arg1517Gln) single nucleotide variant not provided [RCV003319687] Chr9:129005343 [GRCh38]
Chr9:131767622 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2440G>A (p.Val814Met) single nucleotide variant not provided [RCV003319685] Chr9:128988093 [GRCh38]
Chr9:131750372 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2477G>A (p.Arg826Gln) single nucleotide variant Inborn genetic diseases [RCV003379165] Chr9:128988130 [GRCh38]
Chr9:131750409 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3605C>A (p.Thr1202Asn) single nucleotide variant Inborn genetic diseases [RCV003343520] Chr9:128999261 [GRCh38]
Chr9:131761540 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.989G>A (p.Arg330His) single nucleotide variant Inborn genetic diseases [RCV003346058] Chr9:128970834 [GRCh38]
Chr9:131733113 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.4912A>C (p.Ser1638Arg) single nucleotide variant Inborn genetic diseases [RCV003347779] Chr9:129006092 [GRCh38]
Chr9:131768371 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2776G>A (p.Val926Ile) single nucleotide variant Inborn genetic diseases [RCV003364826] Chr9:128993332 [GRCh38]
Chr9:131755611 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2437A>C (p.Thr813Pro) single nucleotide variant Inborn genetic diseases [RCV003366409] Chr9:128988090 [GRCh38]
Chr9:131750369 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.4511A>G (p.Asn1504Ser) single nucleotide variant Inborn genetic diseases [RCV003364863] Chr9:129005304 [GRCh38]
Chr9:131767583 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2165G>A (p.Arg722His) single nucleotide variant Inborn genetic diseases [RCV003347724] Chr9:128986646 [GRCh38]
Chr9:131748925 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.4201A>G (p.Met1401Val) single nucleotide variant Inborn genetic diseases [RCV003347872] Chr9:129002880 [GRCh38]
Chr9:131765159 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3767G>A (p.Gly1256Asp) single nucleotide variant Inborn genetic diseases [RCV003349213] Chr9:128999729 [GRCh38]
Chr9:131762008 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2347A>G (p.Ile783Val) single nucleotide variant not specified [RCV003479920] Chr9:128987671 [GRCh38]
Chr9:131749950 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2640+19C>A single nucleotide variant not specified [RCV003479921] Chr9:128990245 [GRCh38]
Chr9:131752524 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.1002C>G (p.Asn334Lys) single nucleotide variant not provided [RCV003430277] Chr9:128970847 [GRCh38]
Chr9:131733126 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.124C>T (p.Arg42Ter) single nucleotide variant not provided [RCV003430275] Chr9:128952809 [GRCh38]
Chr9:131715088 [GRCh37]
Chr9:9q34.11		 pathogenic
NM_015354.3(NUP188):c.4902A>C (p.Ala1634=) single nucleotide variant not provided [RCV003425815] Chr9:129006082 [GRCh38]
Chr9:131768361 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.1075A>T (p.Thr359Ser) single nucleotide variant not provided [RCV003443926] Chr9:128970920 [GRCh38]
Chr9:131733199 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.1684T>C (p.Cys562Arg) single nucleotide variant not provided [RCV003430279] Chr9:128982916 [GRCh38]
Chr9:131745195 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.4260G>A (p.Leu1420=) single nucleotide variant NUP188-related condition [RCV003954208]|not provided [RCV003430284] Chr9:129002939 [GRCh38]
Chr9:131765218 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.5215T>C (p.Leu1739=) single nucleotide variant NUP188-related condition [RCV003946618]|not provided [RCV003430287] Chr9:129006643 [GRCh38]
Chr9:131768922 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.5003G>A (p.Arg1668Gln) single nucleotide variant NUP188-related condition [RCV003402845]|not provided [RCV003429086] Chr9:129006298 [GRCh38]
Chr9:131768577 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.3261C>T (p.Ala1087=) single nucleotide variant NUP188-related condition [RCV003939038]|not provided [RCV003430282] Chr9:128995424 [GRCh38]
Chr9:131757703 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.3839A>G (p.Asp1280Gly) single nucleotide variant NUP188-related condition [RCV003966436]|not provided [RCV003430283] Chr9:128999801 [GRCh38]
Chr9:131762080 [GRCh37]
Chr9:9q34.11		 benign|likely benign
NM_015354.3(NUP188):c.891G>A (p.Ala297=) single nucleotide variant not provided [RCV003430276] Chr9:128969493 [GRCh38]
Chr9:131731772 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.1998C>A (p.Leu666=) single nucleotide variant not provided [RCV003430280] Chr9:128984936 [GRCh38]
Chr9:131747215 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.4574C>T (p.Ala1525Val) single nucleotide variant not provided [RCV003430285] Chr9:129005367 [GRCh38]
Chr9:131767646 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.4638C>G (p.Ala1546=) single nucleotide variant not provided [RCV003430286] Chr9:129005431 [GRCh38]
Chr9:131767710 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.3297G>A (p.Glu1099=) single nucleotide variant not provided [RCV003425811] Chr9:128995460 [GRCh38]
Chr9:131757739 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.1140T>C (p.Cys380=) single nucleotide variant not provided [RCV003425809] Chr9:128973186 [GRCh38]
Chr9:131735465 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.4256C>T (p.Ala1419Val) single nucleotide variant NUP188-related condition [RCV003919232]|not provided [RCV003425812] Chr9:129002935 [GRCh38]
Chr9:131765214 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.4761C>G (p.Asn1587Lys) single nucleotide variant NUP188-related condition [RCV003908968]|not provided [RCV003425814] Chr9:129005668 [GRCh38]
Chr9:131767947 [GRCh37]
Chr9:9q34.11		 benign|likely benign
NM_015354.3(NUP188):c.609G>C (p.Trp203Cys) single nucleotide variant not provided [RCV003425808] Chr9:128968529 [GRCh38]
Chr9:131730808 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.2067C>A (p.Thr689=) single nucleotide variant not provided [RCV003425810] Chr9:128985005 [GRCh38]
Chr9:131747284 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.4510-1G>T single nucleotide variant not provided [RCV003425813] Chr9:129005302 [GRCh38]
Chr9:131767581 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.5018C>T (p.Pro1673Leu) single nucleotide variant NUP188-related condition [RCV003402748] Chr9:129006313 [GRCh38]
Chr9:131768592 [GRCh37]
Chr9:9q34.11		 uncertain significance
NM_015354.3(NUP188):c.1432T>C (p.Tyr478His) single nucleotide variant not provided [RCV003430278] Chr9:128981306 [GRCh38]
Chr9:131743585 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.3255C>T (p.His1085=) single nucleotide variant NUP188-related condition [RCV003939037]|not provided [RCV003430281] Chr9:128995418 [GRCh38]
Chr9:131757697 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.1743G>A (p.Ser581=) single nucleotide variant NUP188-related condition [RCV003931362]|not provided [RCV003884875] Chr9:128982975 [GRCh38]
Chr9:131745254 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.3204C>T (p.Ile1068=) single nucleotide variant NUP188-related condition [RCV003941935] Chr9:128995367 [GRCh38]
Chr9:131757646 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.4369C>T (p.Leu1457=) single nucleotide variant NUP188-related condition [RCV003942297] Chr9:129003389 [GRCh38]
Chr9:131765668 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.4347G>A (p.Ala1449=) single nucleotide variant not provided [RCV003885265] Chr9:129003367 [GRCh38]
Chr9:131765646 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.4036A>G (p.Thr1346Ala) single nucleotide variant NUP188-related condition [RCV003917401] Chr9:129001721 [GRCh38]
Chr9:131764000 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.825G>A (p.Glu275=) single nucleotide variant not provided [RCV003885037] Chr9:128969427 [GRCh38]
Chr9:131731706 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.1759C>T (p.Leu587=) single nucleotide variant NUP188-related condition [RCV003926946] Chr9:128982991 [GRCh38]
Chr9:131745270 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.4125C>T (p.Asn1375=) single nucleotide variant NUP188-related condition [RCV003962153] Chr9:129001964 [GRCh38]
Chr9:131764243 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.4509+7G>A single nucleotide variant NUP188-related condition [RCV003917087] Chr9:129005228 [GRCh38]
Chr9:131767507 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.2094C>T (p.Thr698=) single nucleotide variant NUP188-related condition [RCV003934696] Chr9:128986575 [GRCh38]
Chr9:131748854 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.3386G>A (p.Arg1129His) single nucleotide variant NUP188-related condition [RCV003931543] Chr9:128998185 [GRCh38]
Chr9:131760464 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.4914C>T (p.Ser1638=) single nucleotide variant NUP188-related condition [RCV003936859] Chr9:129006094 [GRCh38]
Chr9:131768373 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.3133T>C (p.Leu1045=) single nucleotide variant not provided [RCV003887527] Chr9:128994901 [GRCh38]
Chr9:131757180 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.5074-5T>C single nucleotide variant NUP188-related condition [RCV003926826] Chr9:129006497 [GRCh38]
Chr9:131768776 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.837C>T (p.Ile279=) single nucleotide variant NUP188-related condition [RCV003926901] Chr9:128969439 [GRCh38]
Chr9:131731718 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.5079G>A (p.Thr1693=) single nucleotide variant NUP188-related condition [RCV003914110] Chr9:129006507 [GRCh38]
Chr9:131768786 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.592C>A (p.Arg198Ser) single nucleotide variant NUP188-related condition [RCV003921966] Chr9:128968512 [GRCh38]
Chr9:131730791 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.784G>A (p.Val262Ile) single nucleotide variant NUP188-related condition [RCV003929809] Chr9:128968704 [GRCh38]
Chr9:131730983 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.1567T>C (p.Leu523=) single nucleotide variant NUP188-related condition [RCV003981389] Chr9:128982599 [GRCh38]
Chr9:131744878 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.3624A>G (p.Ser1208=) single nucleotide variant NUP188-related condition [RCV003951542] Chr9:128999280 [GRCh38]
Chr9:131761559 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.614T>C (p.Val205Ala) single nucleotide variant NUP188-related condition [RCV003959562] Chr9:128968534 [GRCh38]
Chr9:131730813 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.2935C>T (p.Leu979=) single nucleotide variant NUP188-related condition [RCV003919445] Chr9:128993612 [GRCh38]
Chr9:131755891 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.4738-3C>T single nucleotide variant NUP188-related condition [RCV003959725] Chr9:129005642 [GRCh38]
Chr9:131767921 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.2640+10T>C single nucleotide variant NUP188-related condition [RCV003934416] Chr9:128990236 [GRCh38]
Chr9:131752515 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.1563A>G (p.Val521=) single nucleotide variant not provided [RCV003884116] Chr9:128982595 [GRCh38]
Chr9:131744874 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.3088-10A>G single nucleotide variant NUP188-related condition [RCV003914453] Chr9:128994846 [GRCh38]
Chr9:131757125 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.4737+4C>T single nucleotide variant NUP188-related condition [RCV003981750] Chr9:129005534 [GRCh38]
Chr9:131767813 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.1231T>C (p.Leu411=) single nucleotide variant NUP188-related condition [RCV003972040] Chr9:128979289 [GRCh38]
Chr9:131741568 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.5226G>A (p.Ala1742=) single nucleotide variant NUP188-related condition [RCV003977096] Chr9:129006654 [GRCh38]
Chr9:131768933 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.1005A>G (p.Pro335=) single nucleotide variant not provided [RCV003887631] Chr9:128970850 [GRCh38]
Chr9:131733129 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.2223T>C (p.His741=) single nucleotide variant NUP188-related condition [RCV003894755] Chr9:128986834 [GRCh38]
Chr9:131749113 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.5094C>G (p.Leu1698=) single nucleotide variant NUP188-related condition [RCV003971686] Chr9:129006522 [GRCh38]
Chr9:131768801 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.2580C>T (p.Tyr860=) single nucleotide variant NUP188-related condition [RCV003979764] Chr9:128990166 [GRCh38]
Chr9:131752445 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.456C>T (p.His152=) single nucleotide variant NUP188-related condition [RCV003951734] Chr9:128958885 [GRCh38]
Chr9:131721164 [GRCh37]
Chr9:9q34.11		 benign
NM_015354.3(NUP188):c.2264+5T>C single nucleotide variant NUP188-related condition [RCV003967310] Chr9:128986880 [GRCh38]
Chr9:131749159 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.4077C>T (p.Thr1359=) single nucleotide variant NUP188-related condition [RCV003954625] Chr9:129001916 [GRCh38]
Chr9:131764195 [GRCh37]
Chr9:9q34.11		 likely benign
NM_015354.3(NUP188):c.4357G>A (p.Val1453Met) single nucleotide variant Inborn genetic diseases [RCV003341470] Chr9:129003377 [GRCh38]
Chr9:131765656 [GRCh37]
Chr9:9q34.11		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2052
Count of miRNA genes:986
Interacting mature miRNAs:1210
Transcripts:ENST00000372577, ENST00000464729, ENST00000465344, ENST00000467044, ENST00000477069, ENST00000485158, ENST00000487952, ENST00000491502, ENST00000491990, ENST00000495726, ENST00000550219
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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

Markers in Region
D9S260  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,718,424 - 131,718,604UniSTSGRCh37
GRCh379131,718,420 - 131,718,601UniSTSGRCh37
Build 369130,758,241 - 130,758,422RGDNCBI36
Celera9102,370,737 - 102,370,918RGD
Celera9102,370,741 - 102,370,921UniSTS
Cytogenetic Map9q34.11UniSTS
HuRef9101,326,144 - 101,326,325UniSTS
HuRef9101,326,148 - 101,326,328UniSTS
Marshfield Genetic Map9140.86UniSTS
Marshfield Genetic Map9140.86RGD
Genethon Genetic Map9141.1UniSTS
TNG Radiation Hybrid Map949711.0UniSTS
Whitehead-YAC Contig Map9 UniSTS
RH35819  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,755,326 - 131,755,502UniSTSGRCh37
Build 369130,795,147 - 130,795,323RGDNCBI36
Celera9102,407,638 - 102,407,814RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,362,670 - 101,362,846UniSTS
GeneMap99-GB4 RH Map9391.66UniSTS
RH98324  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,769,202 - 131,769,324UniSTSGRCh37
Build 369130,809,023 - 130,809,145RGDNCBI36
Celera9102,421,514 - 102,421,636RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,376,523 - 101,376,645UniSTS
GeneMap99-GB4 RH Map9392.45UniSTS
RH25386  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,769,132 - 131,769,293UniSTSGRCh37
Build 369130,808,953 - 130,809,114RGDNCBI36
Celera9102,421,444 - 102,421,605RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,376,453 - 101,376,614UniSTS
GeneMap99-GB4 RH Map9392.76UniSTS
ECD00465  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,763,865 - 131,764,769UniSTSGRCh37
Build 369130,803,686 - 130,804,590RGDNCBI36
Celera9102,416,177 - 102,417,081RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,371,186 - 101,372,090UniSTS
ECD00690  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,744,814 - 131,745,707UniSTSGRCh37
Build 369130,784,635 - 130,785,528RGDNCBI36
Celera9102,397,129 - 102,398,022RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,352,505 - 101,353,398UniSTS
ECD00796  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,749,727 - 131,750,616UniSTSGRCh37
Build 369130,789,548 - 130,790,437RGDNCBI36
Celera9102,402,040 - 102,402,929RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,357,422 - 101,358,311UniSTS
ECD01480  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,718,581 - 131,719,444UniSTSGRCh37
Build 369130,758,402 - 130,759,265RGDNCBI36
Celera9102,370,898 - 102,371,761RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,326,305 - 101,327,168UniSTS
ECD04390  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,760,362 - 131,761,127UniSTSGRCh37
Build 369130,800,183 - 130,800,948RGDNCBI36
Celera9102,412,674 - 102,413,439RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,367,706 - 101,368,471UniSTS
ECD05630  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,767,359 - 131,768,089UniSTSGRCh37
Build 369130,807,180 - 130,807,910RGDNCBI36
Celera9102,419,671 - 102,420,401RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,374,680 - 101,375,410UniSTS
ECD06138  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,768,335 - 131,769,051UniSTSGRCh37
Build 369130,808,156 - 130,808,872RGDNCBI36
Celera9102,420,647 - 102,421,363RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,375,656 - 101,376,372UniSTS
ECD06521  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,756,898 - 131,757,604UniSTSGRCh37
Build 369130,796,719 - 130,797,425RGDNCBI36
Celera9102,409,210 - 102,409,916RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,364,242 - 101,364,948UniSTS
ECD06635  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,757,679 - 131,758,382UniSTSGRCh37
Build 369130,797,500 - 130,798,203RGDNCBI36
Celera9102,409,991 - 102,410,694RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,365,023 - 101,365,726UniSTS
ECD06702  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,756,168 - 131,756,869UniSTSGRCh37
Build 369130,795,989 - 130,796,690RGDNCBI36
Celera9102,408,480 - 102,409,181RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,363,512 - 101,364,213UniSTS
ECD06829  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,769,097 - 131,769,794UniSTSGRCh37
Build 369130,808,918 - 130,809,615RGDNCBI36
Celera9102,421,409 - 102,422,106RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,376,418 - 101,377,115UniSTS
ECD07700  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,742,258 - 131,742,932UniSTSGRCh37
Build 369130,782,079 - 130,782,753RGDNCBI36
Celera9102,394,573 - 102,395,247RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,349,949 - 101,350,623UniSTS
ECD07733  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,746,705 - 131,747,378UniSTSGRCh37
Build 369130,786,526 - 130,787,199RGDNCBI36
Celera9102,399,020 - 102,399,693RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,354,396 - 101,355,069UniSTS
ECD07809  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,742,974 - 131,743,645UniSTSGRCh37
Build 369130,782,795 - 130,783,466RGDNCBI36
Celera9102,395,289 - 102,395,960RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,350,665 - 101,351,336UniSTS
ECD07840  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,708,593 - 131,709,263UniSTSGRCh37
Build 369130,748,414 - 130,749,084RGDNCBI36
Celera9102,360,454 - 102,361,124RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,316,312 - 101,316,982UniSTS
ECD09036  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,761,469 - 131,762,107UniSTSGRCh37
Build 369130,801,290 - 130,801,928RGDNCBI36
Celera9102,413,781 - 102,414,419RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,368,813 - 101,369,451UniSTS
ECD10151  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,755,319 - 131,755,928UniSTSGRCh37
Build 369130,795,140 - 130,795,749RGDNCBI36
Celera9102,407,631 - 102,408,240RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,362,663 - 101,363,272UniSTS
ECD10329  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,709,266 - 131,709,870UniSTSGRCh37
Build 369130,749,087 - 130,749,691RGDNCBI36
Celera9102,361,127 - 102,361,731RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,316,985 - 101,317,589UniSTS
ECD10910  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,732,742 - 131,733,329UniSTSGRCh37
Build 369130,772,563 - 130,773,150RGDNCBI36
Celera9102,385,057 - 102,385,644RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,340,392 - 101,340,979UniSTS
ECD11198  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,710,063 - 131,710,642UniSTSGRCh37
Build 369130,749,884 - 130,750,463RGDNCBI36
Celera9102,361,924 - 102,362,503RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,317,782 - 101,318,361UniSTS
ECD12085  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,735,051 - 131,735,604UniSTSGRCh37
Build 369130,774,872 - 130,775,425RGDNCBI36
Celera9102,387,366 - 102,387,919RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,342,701 - 101,343,254UniSTS
ECD13684  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,720,136 - 131,720,647UniSTSGRCh37
Build 369130,759,957 - 130,760,468RGDNCBI36
Celera9102,372,453 - 102,372,964RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,327,860 - 101,328,371UniSTS
ECD13760  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,764,925 - 131,765,434UniSTSGRCh37
Build 369130,804,746 - 130,805,255RGDNCBI36
Celera9102,417,237 - 102,417,746RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,372,246 - 101,372,755UniSTS
ECD14082  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,765,479 - 131,765,980UniSTSGRCh37
Build 369130,805,300 - 130,805,801RGDNCBI36
Celera9102,417,791 - 102,418,292RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,372,800 - 101,373,301UniSTS
ECD16033  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,730,769 - 131,731,224UniSTSGRCh37
Build 369130,770,590 - 130,771,045RGDNCBI36
Celera9102,383,084 - 102,383,539RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,338,419 - 101,338,874UniSTS
ECD16063  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,748,385 - 131,748,839UniSTSGRCh37
Build 369130,788,206 - 130,788,660RGDNCBI36
Celera9102,400,700 - 102,401,154RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,356,076 - 101,356,530UniSTS
ECD16117  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,748,853 - 131,749,305UniSTSGRCh37
Build 369130,788,674 - 130,789,126RGDNCBI36
Celera9102,401,168 - 102,401,620RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,356,544 - 101,356,996UniSTS
ECD16647  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,720,736 - 131,721,167UniSTSGRCh37
Build 369130,760,557 - 130,760,988RGDNCBI36
Celera9102,373,053 - 102,373,484RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,328,460 - 101,328,891UniSTS
ECD17357  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,715,053 - 131,715,454UniSTSGRCh37
Build 369130,754,874 - 130,755,275RGDNCBI36
Celera9102,367,366 - 102,367,767RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,322,773 - 101,323,174UniSTS
ECD17358  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,752,173 - 131,752,574UniSTSGRCh37
Build 369130,791,994 - 130,792,395RGDNCBI36
Celera9102,404,485 - 102,404,886RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,359,838 - 101,360,239UniSTS
ECD19013  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,763,389 - 131,763,726UniSTSGRCh37
Build 369130,803,210 - 130,803,547RGDNCBI36
Celera9102,415,701 - 102,416,038RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,370,710 - 101,371,047UniSTS
ECD19043  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,758,759 - 131,759,095UniSTSGRCh37
Build 369130,798,580 - 130,798,916RGDNCBI36
Celera9102,411,071 - 102,411,407RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,366,103 - 101,366,439UniSTS
ECD19440  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,731,596 - 131,731,917UniSTSGRCh37
Build 369130,771,417 - 130,771,738RGDNCBI36
Celera9102,383,911 - 102,384,232RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,339,246 - 101,339,567UniSTS
ECD23487  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,711,384 - 131,711,571UniSTSGRCh37
Build 369130,751,205 - 130,751,392RGDNCBI36
Celera9102,363,246 - 102,363,433RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,319,104 - 101,319,291UniSTS
ECD24216  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,741,493 - 131,741,644UniSTSGRCh37
Build 369130,781,314 - 130,781,465RGDNCBI36
Celera9102,393,808 - 102,393,959RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,349,184 - 101,349,335UniSTS
STS-H17411  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,755,302 - 131,755,500UniSTSGRCh37
Build 369130,795,123 - 130,795,321RGDNCBI36
Celera9102,407,614 - 102,407,812RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,362,646 - 101,362,844UniSTS
GeneMap99-GB4 RH Map9392.76UniSTS
REN36567  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,769,414 - 131,769,674UniSTSGRCh37
Build 369130,809,235 - 130,809,495RGDNCBI36
Celera9102,421,726 - 102,421,986RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,376,735 - 101,376,995UniSTS
REN36568  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,769,159 - 131,769,425UniSTSGRCh37
Build 369130,808,980 - 130,809,246RGDNCBI36
Celera9102,421,471 - 102,421,737RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,376,480 - 101,376,746UniSTS
REN36569  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,768,949 - 131,769,181UniSTSGRCh37
Build 369130,808,770 - 130,809,002RGDNCBI36
Celera9102,421,261 - 102,421,493RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,376,270 - 101,376,502UniSTS
REN36570  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,768,729 - 131,768,971UniSTSGRCh37
Build 369130,808,550 - 130,808,792RGDNCBI36
Celera9102,421,041 - 102,421,283RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,376,050 - 101,376,292UniSTS
REN36571  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,768,514 - 131,768,742UniSTSGRCh37
Build 369130,808,335 - 130,808,563RGDNCBI36
Celera9102,420,826 - 102,421,054RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,375,835 - 101,376,063UniSTS
REN36572  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,768,244 - 131,768,472UniSTSGRCh37
Build 369130,808,065 - 130,808,293RGDNCBI36
Celera9102,420,556 - 102,420,784RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,375,565 - 101,375,793UniSTS
REN36573  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,768,041 - 131,768,265UniSTSGRCh37
Build 369130,807,862 - 130,808,086RGDNCBI36
Celera9102,420,353 - 102,420,577RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,375,362 - 101,375,586UniSTS
REN36574  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,767,793 - 131,768,019UniSTSGRCh37
Build 369130,807,614 - 130,807,840RGDNCBI36
Celera9102,420,105 - 102,420,331RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,375,114 - 101,375,340UniSTS
REN36575  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,767,551 - 131,767,790UniSTSGRCh37
Build 369130,807,372 - 130,807,611RGDNCBI36
Celera9102,419,863 - 102,420,102RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,374,872 - 101,375,111UniSTS
REN36576  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,767,335 - 131,767,572UniSTSGRCh37
Build 369130,807,156 - 130,807,393RGDNCBI36
Celera9102,419,647 - 102,419,884RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,374,656 - 101,374,893UniSTS
REN36577  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,767,076 - 131,767,323UniSTSGRCh37
Build 369130,806,897 - 130,807,144RGDNCBI36
Celera9102,419,388 - 102,419,635RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,374,397 - 101,374,644UniSTS
REN36578  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,766,198 - 131,766,460UniSTSGRCh37
Build 369130,806,019 - 130,806,281RGDNCBI36
Celera9102,418,510 - 102,418,772RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,373,519 - 101,373,781UniSTS
REN36579  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,765,810 - 131,766,047UniSTSGRCh37
Build 369130,805,631 - 130,805,868RGDNCBI36
Celera9102,418,122 - 102,418,359RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,373,131 - 101,373,368UniSTS
REN36580  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,765,604 - 131,765,833UniSTSGRCh37
Build 369130,805,425 - 130,805,654RGDNCBI36
Celera9102,417,916 - 102,418,145RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,372,925 - 101,373,154UniSTS
REN36581  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,765,388 - 131,765,628UniSTSGRCh37
Build 369130,805,209 - 130,805,449RGDNCBI36
Celera9102,417,700 - 102,417,940RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,372,709 - 101,372,949UniSTS
REN36582  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,765,180 - 131,765,408UniSTSGRCh37
Build 369130,805,001 - 130,805,229RGDNCBI36
Celera9102,417,492 - 102,417,720RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,372,501 - 101,372,729UniSTS
REN36583  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,764,918 - 131,765,163UniSTSGRCh37
Build 369130,804,739 - 130,804,984RGDNCBI36
Celera9102,417,230 - 102,417,475RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,372,239 - 101,372,484UniSTS
REN36584  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,764,682 - 131,764,941UniSTSGRCh37
Build 369130,804,503 - 130,804,762RGDNCBI36
Celera9102,416,994 - 102,417,253RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,372,003 - 101,372,262UniSTS
REN36585  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,764,455 - 131,764,705UniSTSGRCh37
Build 369130,804,276 - 130,804,526RGDNCBI36
Celera9102,416,767 - 102,417,017RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,371,776 - 101,372,026UniSTS
REN36586  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,764,223 - 131,764,470UniSTSGRCh37
Build 369130,804,044 - 130,804,291RGDNCBI36
Celera9102,416,535 - 102,416,782RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,371,544 - 101,371,791UniSTS
REN36587  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,763,996 - 131,764,236UniSTSGRCh37
Build 369130,803,817 - 130,804,057RGDNCBI36
Celera9102,416,308 - 102,416,548RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,371,317 - 101,371,557UniSTS
REN36588  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,763,780 - 131,764,018UniSTSGRCh37
Build 369130,803,601 - 130,803,839RGDNCBI36
Celera9102,416,092 - 102,416,330RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,371,101 - 101,371,339UniSTS
REN36589  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,763,573 - 131,763,804UniSTSGRCh37
Build 369130,803,394 - 130,803,625RGDNCBI36
Celera9102,415,885 - 102,416,116RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,370,894 - 101,371,125UniSTS
REN36590  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,763,362 - 131,763,594UniSTSGRCh37
Build 369130,803,183 - 130,803,415RGDNCBI36
Celera9102,415,674 - 102,415,906RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,370,683 - 101,370,915UniSTS
REN36591  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,762,365 - 131,762,609UniSTSGRCh37
Build 369130,802,186 - 130,802,430RGDNCBI36
Celera9102,414,677 - 102,414,921RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,369,709 - 101,369,953UniSTS
REN36592  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,762,083 - 131,762,320UniSTSGRCh37
Build 369130,801,904 - 130,802,141RGDNCBI36
Celera9102,414,395 - 102,414,632RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,369,427 - 101,369,664UniSTS
REN36593  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,761,876 - 131,762,105UniSTSGRCh37
Build 369130,801,697 - 130,801,926RGDNCBI36
Celera9102,414,188 - 102,414,417RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,369,220 - 101,369,449UniSTS
REN36594  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,761,673 - 131,761,899UniSTSGRCh37
Build 369130,801,494 - 130,801,720RGDNCBI36
Celera9102,413,985 - 102,414,211RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,369,017 - 101,369,243UniSTS
REN36595  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,761,425 - 131,761,650UniSTSGRCh37
Build 369130,801,246 - 130,801,471RGDNCBI36
Celera9102,413,737 - 102,413,962RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,368,769 - 101,368,994UniSTS
REN36596  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,761,052 - 131,761,289UniSTSGRCh37
Build 369130,800,873 - 130,801,110RGDNCBI36
Celera9102,413,364 - 102,413,601RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,368,396 - 101,368,633UniSTS
REN36597  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,760,772 - 131,761,022UniSTSGRCh37
Build 369130,800,593 - 130,800,843RGDNCBI36
Celera9102,413,084 - 102,413,334RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,368,116 - 101,368,366UniSTS
REN36598  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,760,549 - 131,760,778UniSTSGRCh37
Build 369130,800,370 - 130,800,599RGDNCBI36
Celera9102,412,861 - 102,413,090RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,367,893 - 101,368,122UniSTS
REN36599  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,760,315 - 131,760,539UniSTSGRCh37
Build 369130,800,136 - 130,800,360RGDNCBI36
Celera9102,412,627 - 102,412,851RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,367,659 - 101,367,883UniSTS
REN36600  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,759,578 - 131,759,824UniSTSGRCh37
Build 369130,799,399 - 130,799,645RGDNCBI36
Celera9102,411,890 - 102,412,136RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,366,922 - 101,367,168UniSTS
REN36601  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,759,364 - 131,759,597UniSTSGRCh37
Build 369130,799,185 - 130,799,418RGDNCBI36
Celera9102,411,676 - 102,411,909RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,366,708 - 101,366,941UniSTS
REN36602  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,759,147 - 131,759,384UniSTSGRCh37
Build 369130,798,968 - 130,799,205RGDNCBI36
Celera9102,411,459 - 102,411,696RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,366,491 - 101,366,728UniSTS
REN36603  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,758,939 - 131,759,167UniSTSGRCh37
Build 369130,798,760 - 130,798,988RGDNCBI36
Celera9102,411,251 - 102,411,479RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,366,283 - 101,366,511UniSTS
REN36604  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,758,739 - 131,758,963UniSTSGRCh37
Build 369130,798,560 - 130,798,784RGDNCBI36
Celera9102,411,051 - 102,411,275RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,366,083 - 101,366,307UniSTS
REN36605  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,758,091 - 131,758,318UniSTSGRCh37
Build 369130,797,912 - 130,798,139RGDNCBI36
Celera9102,410,403 - 102,410,630RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,365,435 - 101,365,662UniSTS
REN36606  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,757,837 - 131,758,083UniSTSGRCh37
Build 369130,797,658 - 130,797,904RGDNCBI36
Celera9102,410,149 - 102,410,395RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,365,181 - 101,365,427UniSTS
REN36607  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,757,631 - 131,757,858UniSTSGRCh37
Build 369130,797,452 - 130,797,679RGDNCBI36
Celera9102,409,943 - 102,410,170RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,364,975 - 101,365,202UniSTS
REN36608  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,757,388 - 131,757,613UniSTSGRCh37
Build 369130,797,209 - 130,797,434RGDNCBI36
Celera9102,409,700 - 102,409,925RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,364,732 - 101,364,957UniSTS
REN36609  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,757,155 - 131,757,411UniSTSGRCh37
Build 369130,796,976 - 130,797,232RGDNCBI36
Celera9102,409,467 - 102,409,723RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,364,499 - 101,364,755UniSTS
REN36610  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,756,938 - 131,757,174UniSTSGRCh37
Build 369130,796,759 - 130,796,995RGDNCBI36
Celera9102,409,250 - 102,409,486RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,364,282 - 101,364,518UniSTS
REN36611  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,756,709 - 131,756,942UniSTSGRCh37
Build 369130,796,530 - 130,796,763RGDNCBI36
Celera9102,409,021 - 102,409,254RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,364,053 - 101,364,286UniSTS
REN36612  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,756,456 - 131,756,694UniSTSGRCh37
Build 369130,796,277 - 130,796,515RGDNCBI36
Celera9102,408,768 - 102,409,006RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,363,800 - 101,364,038UniSTS
REN36613  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,756,172 - 131,756,423UniSTSGRCh37
Build 369130,795,993 - 130,796,244RGDNCBI36
Celera9102,408,484 - 102,408,735RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,363,516 - 101,363,767UniSTS
REN36614  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,755,960 - 131,756,193UniSTSGRCh37
Build 369130,795,781 - 130,796,014RGDNCBI36
Celera9102,408,272 - 102,408,505RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,363,304 - 101,363,537UniSTS
REN36615  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,755,684 - 131,755,943UniSTSGRCh37
Build 369130,795,505 - 130,795,764RGDNCBI36
Celera9102,407,996 - 102,408,255RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,363,028 - 101,363,287UniSTS
REN36616  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,755,482 - 131,755,706UniSTSGRCh37
Build 369130,795,303 - 130,795,527RGDNCBI36
Celera9102,407,794 - 102,408,018RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,362,826 - 101,363,050UniSTS
REN36617  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,755,252 - 131,755,505UniSTSGRCh37
Build 369130,795,073 - 130,795,326RGDNCBI36
Celera9102,407,564 - 102,407,817RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,362,596 - 101,362,849UniSTS
REN36618  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,755,021 - 131,755,272UniSTSGRCh37
Build 369130,794,842 - 130,795,093RGDNCBI36
Celera9102,407,333 - 102,407,584RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,362,365 - 101,362,616UniSTS
REN36619  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,754,815 - 131,755,045UniSTSGRCh37
Build 369130,794,636 - 130,794,866RGDNCBI36
Celera9102,407,127 - 102,407,357RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,362,159 - 101,362,389UniSTS
REN36620  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,754,582 - 131,754,814UniSTSGRCh37
Build 369130,794,403 - 130,794,635RGDNCBI36
Celera9102,406,894 - 102,407,126RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,361,926 - 101,362,158UniSTS
REN36621  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,753,489 - 131,753,749UniSTSGRCh37
Build 369130,793,310 - 130,793,570RGDNCBI36
Celera9102,405,801 - 102,406,061RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,361,154 - 101,361,414UniSTS
REN36622  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,753,050 - 131,753,310UniSTSGRCh37
Build 369130,792,871 - 130,793,131RGDNCBI36
Celera9102,405,362 - 102,405,622RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,360,715 - 101,360,975UniSTS
REN36623  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,752,375 - 131,752,622UniSTSGRCh37
Build 369130,792,196 - 130,792,443RGDNCBI36
Celera9102,404,687 - 102,404,934RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,360,040 - 101,360,287UniSTS
REN36624  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,752,152 - 131,752,377UniSTSGRCh37
Build 369130,791,973 - 130,792,198RGDNCBI36
Celera9102,404,464 - 102,404,689RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,359,817 - 101,360,042UniSTS
REN36625  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,751,216 - 131,751,458UniSTSGRCh37
Build 369130,791,037 - 130,791,279RGDNCBI36
Celera9102,403,528 - 102,403,770RGD
Cytogenetic Map9q34.11UniSTS
REN36626  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,750,933 - 131,751,165UniSTSGRCh37
Build 369130,790,754 - 130,790,986RGDNCBI36
Celera9102,403,246 - 102,403,477RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,358,628 - 101,358,859UniSTS
REN36627  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,750,713 - 131,750,937UniSTSGRCh37
Build 369130,790,534 - 130,790,758RGDNCBI36
Celera9102,403,026 - 102,403,250RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,358,408 - 101,358,632UniSTS
REN36628  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,750,385 - 131,750,636UniSTSGRCh37
Build 369130,790,206 - 130,790,457RGDNCBI36
Celera9102,402,698 - 102,402,949RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,358,080 - 101,358,331UniSTS
REN36629  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,750,131 - 131,750,388UniSTSGRCh37
Build 369130,789,952 - 130,790,209RGDNCBI36
Celera9102,402,444 - 102,402,701RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,357,826 - 101,358,083UniSTS
REN36630  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,749,909 - 131,750,143UniSTSGRCh37
Build 369130,789,730 - 130,789,964RGDNCBI36
Celera9102,402,222 - 102,402,456RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,357,604 - 101,357,838UniSTS
REN36631  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,749,684 - 131,749,932UniSTSGRCh37
Build 369130,789,505 - 130,789,753RGDNCBI36
Celera9102,401,997 - 102,402,245RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,357,379 - 101,357,627UniSTS
REN36632  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,749,457 - 131,749,705UniSTSGRCh37
Build 369130,789,278 - 130,789,526RGDNCBI36
Celera9102,401,770 - 102,402,018RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,357,152 - 101,357,400UniSTS
REN36633  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,749,236 - 131,749,479UniSTSGRCh37
Build 369130,789,057 - 130,789,300RGDNCBI36
Celera9102,401,551 - 102,401,792RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,356,927 - 101,357,174UniSTS
REN36634  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,748,947 - 131,749,189UniSTSGRCh37
Build 369130,788,768 - 130,789,010RGDNCBI36
Celera9102,401,262 - 102,401,504RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,356,638 - 101,356,880UniSTS
REN36635  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,748,741 - 131,748,971UniSTSGRCh37
Build 369130,788,562 - 130,788,792RGDNCBI36
Celera9102,401,056 - 102,401,286RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,356,432 - 101,356,662UniSTS
REN36636  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,748,526 - 131,748,765UniSTSGRCh37
Build 369130,788,347 - 130,788,586RGDNCBI36
Celera9102,400,841 - 102,401,080RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,356,217 - 101,356,456UniSTS
REN36637  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,748,288 - 131,748,536UniSTSGRCh37
Build 369130,788,109 - 130,788,357RGDNCBI36
Celera9102,400,603 - 102,400,851RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,355,979 - 101,356,227UniSTS
REN36638  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,747,716 - 131,747,951UniSTSGRCh37
Build 369130,787,537 - 130,787,772RGDNCBI36
Celera9102,400,031 - 102,400,266RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,355,407 - 101,355,642UniSTS
REN36639  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,747,514 - 131,747,739UniSTSGRCh37
Build 369130,787,335 - 130,787,560RGDNCBI36
Celera9102,399,829 - 102,400,054RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,355,205 - 101,355,430UniSTS
REN36640  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,747,247 - 131,747,489UniSTSGRCh37
Build 369130,787,068 - 130,787,310RGDNCBI36
Celera9102,399,562 - 102,399,804RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,354,938 - 101,355,180UniSTS
REN36641  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,747,024 - 131,747,265UniSTSGRCh37
Build 369130,786,845 - 130,787,086RGDNCBI36
Celera9102,399,339 - 102,399,580RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,354,715 - 101,354,956UniSTS
REN36642  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,746,805 - 131,747,048UniSTSGRCh37
Build 369130,786,626 - 130,786,869RGDNCBI36
Celera9102,399,120 - 102,399,363RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,354,496 - 101,354,739UniSTS
REN36643  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,746,561 - 131,746,801UniSTSGRCh37
Build 369130,786,382 - 130,786,622RGDNCBI36
Celera9102,398,876 - 102,399,116RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,354,252 - 101,354,492UniSTS
REN36644  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,746,004 - 131,746,247UniSTSGRCh37
Build 369130,785,825 - 130,786,068RGDNCBI36
Celera9102,398,319 - 102,398,562RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,353,695 - 101,353,938UniSTS
REN36645  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,745,757 - 131,746,027UniSTSGRCh37
Build 369130,785,578 - 130,785,848RGDNCBI36
Celera9102,398,072 - 102,398,342RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,353,448 - 101,353,718UniSTS
REN36646  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,745,480 - 131,745,716UniSTSGRCh37
Build 369130,785,301 - 130,785,537RGDNCBI36
Celera9102,397,795 - 102,398,031RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,353,171 - 101,353,407UniSTS
REN36647  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,745,231 - 131,745,487UniSTSGRCh37
Build 369130,785,052 - 130,785,308RGDNCBI36
Celera9102,397,546 - 102,397,802RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,352,922 - 101,353,178UniSTS
REN36648  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,744,981 - 131,745,226UniSTSGRCh37
Build 369130,784,802 - 130,785,047RGDNCBI36
Celera9102,397,296 - 102,397,541RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,352,672 - 101,352,917UniSTS
REN36649  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,744,739 - 131,744,980UniSTSGRCh37
Build 369130,784,560 - 130,784,801RGDNCBI36
Celera9102,397,054 - 102,397,295RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,352,430 - 101,352,671UniSTS
REN36650  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,744,514 - 131,744,746UniSTSGRCh37
Build 369130,784,335 - 130,784,567RGDNCBI36
Celera9102,396,829 - 102,397,061RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,352,205 - 101,352,437UniSTS
REN36651  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,743,849 - 131,744,074UniSTSGRCh37
Build 369130,783,670 - 130,783,895RGDNCBI36
Celera9102,396,164 - 102,396,389RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,351,540 - 101,351,765UniSTS
REN36652  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,743,641 - 131,743,870UniSTSGRCh37
Build 369130,783,462 - 130,783,691RGDNCBI36
Celera9102,395,956 - 102,396,185RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,351,332 - 101,351,561UniSTS
REN36653  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,743,329 - 131,743,554UniSTSGRCh37
Build 369130,783,150 - 130,783,375RGDNCBI36
Celera9102,395,644 - 102,395,869RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,351,020 - 101,351,245UniSTS
REN36654  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,743,106 - 131,743,349UniSTSGRCh37
Build 369130,782,927 - 130,783,170RGDNCBI36
Celera9102,395,421 - 102,395,664RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,350,797 - 101,351,040UniSTS
REN36655  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,742,855 - 131,743,099UniSTSGRCh37
Build 369130,782,676 - 130,782,920RGDNCBI36
Celera9102,395,170 - 102,395,414RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,350,546 - 101,350,790UniSTS
REN36656  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,742,640 - 131,742,879UniSTSGRCh37
Build 369130,782,461 - 130,782,700RGDNCBI36
Celera9102,394,955 - 102,395,194RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,350,331 - 101,350,570UniSTS
REN36657  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,742,416 - 131,742,654UniSTSGRCh37
Build 369130,782,237 - 130,782,475RGDNCBI36
Celera9102,394,731 - 102,394,969RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,350,107 - 101,350,345UniSTS
REN36658  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,742,207 - 131,742,440UniSTSGRCh37
Build 369130,782,028 - 130,782,261RGDNCBI36
Celera9102,394,522 - 102,394,755RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,349,898 - 101,350,131UniSTS
REN36659  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,741,519 - 131,741,766UniSTSGRCh37
Build 369130,781,340 - 130,781,587RGDNCBI36
Celera9102,393,834 - 102,394,081RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,349,210 - 101,349,457UniSTS
REN36660  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,741,286 - 131,741,518UniSTSGRCh37
Build 369130,781,107 - 130,781,339RGDNCBI36
Celera9102,393,601 - 102,393,833RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,348,977 - 101,349,209UniSTS
REN36661  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,741,067 - 131,741,309UniSTSGRCh37
Build 369130,780,888 - 130,781,130RGDNCBI36
Celera9102,393,382 - 102,393,624RGD
Cytogenetic Map9q34.11UniSTS
REN36662  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,740,864 - 131,741,091UniSTSGRCh37
Build 369130,780,685 - 130,780,912RGDNCBI36
Celera9102,393,179 - 102,393,406RGD
Cytogenetic Map9q34.11UniSTS
REN36663  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,740,124 - 131,740,378UniSTSGRCh37
Build 369130,779,945 - 130,780,199RGDNCBI36
Celera9102,392,439 - 102,392,693RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,347,774 - 101,348,028UniSTS
REN36664  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,739,907 - 131,740,132UniSTSGRCh37
Build 369130,779,728 - 130,779,953RGDNCBI36
Celera9102,392,222 - 102,392,447RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,347,557 - 101,347,782UniSTS
REN36665  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,739,706 - 131,739,930UniSTSGRCh37
Build 369130,779,527 - 130,779,751RGDNCBI36
Celera9102,392,021 - 102,392,245RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,347,356 - 101,347,580UniSTS
REN36666  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,739,036 - 131,739,283UniSTSGRCh37
Build 369130,778,857 - 130,779,104RGDNCBI36
Celera9102,391,351 - 102,391,598RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,346,686 - 101,346,933UniSTS
REN36667  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,738,361 - 131,738,598UniSTSGRCh37
Build 369130,778,182 - 130,778,419RGDNCBI36
Celera9102,390,676 - 102,390,913RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,346,011 - 101,346,248UniSTS
REN36668  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,738,156 - 131,738,384UniSTSGRCh37
Build 369130,777,977 - 130,778,205RGDNCBI36
Celera9102,390,471 - 102,390,699RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,345,806 - 101,346,034UniSTS
REN36669  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,737,855 - 131,738,108UniSTSGRCh37
Build 369130,777,676 - 130,777,929RGDNCBI36
Celera9102,390,170 - 102,390,423RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,345,505 - 101,345,758UniSTS
REN36670  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,736,941 - 131,737,169UniSTSGRCh37
Build 369130,776,762 - 130,776,990RGDNCBI36
Celera9102,389,256 - 102,389,484RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,344,591 - 101,344,819UniSTS
REN36671  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,736,738 - 131,736,965UniSTSGRCh37
Build 369130,776,559 - 130,776,786RGDNCBI36
Celera9102,389,053 - 102,389,280RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,344,388 - 101,344,615UniSTS
REN36672  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,736,535 - 131,736,761UniSTSGRCh37
Build 369130,776,356 - 130,776,582RGDNCBI36
Celera9102,388,850 - 102,389,076RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,344,185 - 101,344,411UniSTS
REN36673  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,736,079 - 131,736,336UniSTSGRCh37
Build 369130,775,900 - 130,776,157RGDNCBI36
Celera9102,388,394 - 102,388,651RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,343,729 - 101,343,986UniSTS
REN36674  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,735,623 - 131,735,872UniSTSGRCh37
Build 369130,775,444 - 130,775,693RGDNCBI36
Celera9102,387,938 - 102,388,187RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,343,273 - 101,343,522UniSTS
REN36675  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,735,417 - 131,735,645UniSTSGRCh37
Build 369130,775,238 - 130,775,466RGDNCBI36
Celera9102,387,732 - 102,387,960RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,343,067 - 101,343,295UniSTS
REN36676  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,735,185 - 131,735,439UniSTSGRCh37
Build 369130,775,006 - 130,775,260RGDNCBI36
Celera9102,387,500 - 102,387,754RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,342,835 - 101,343,089UniSTS
REN36677  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,734,955 - 131,735,208UniSTSGRCh37
Build 369130,774,776 - 130,775,029RGDNCBI36
Celera9102,387,270 - 102,387,523RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,342,605 - 101,342,858UniSTS
REN36678  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,734,715 - 131,734,966UniSTSGRCh37
Build 369130,774,536 - 130,774,787RGDNCBI36
Celera9102,387,030 - 102,387,281RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,342,365 - 101,342,616UniSTS
REN36679  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,734,470 - 131,734,730UniSTSGRCh37
Build 369130,774,291 - 130,774,551RGDNCBI36
Celera9102,386,785 - 102,387,045RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,342,120 - 101,342,380UniSTS
REN36680  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,734,259 - 131,734,489UniSTSGRCh37
Build 369130,774,080 - 130,774,310RGDNCBI36
Celera9102,386,574 - 102,386,804RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,341,909 - 101,342,139UniSTS
REN36681  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,733,458 - 131,733,684UniSTSGRCh37
Build 369130,773,279 - 130,773,505RGDNCBI36
Celera9102,385,773 - 102,385,999RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,341,108 - 101,341,334UniSTS
REN36682  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,733,184 - 131,733,434UniSTSGRCh37
Build 369130,773,005 - 130,773,255RGDNCBI36
Celera9102,385,499 - 102,385,749RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,340,834 - 101,341,084UniSTS
REN36683  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,732,955 - 131,733,207UniSTSGRCh37
Build 369130,772,776 - 130,773,028RGDNCBI36
Celera9102,385,270 - 102,385,522RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,340,605 - 101,340,857UniSTS
REN36684  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,732,742 - 131,732,972UniSTSGRCh37
Build 369130,772,563 - 130,772,793RGDNCBI36
Celera9102,385,057 - 102,385,287RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,340,392 - 101,340,622UniSTS
REN36685  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,732,498 - 131,732,724UniSTSGRCh37
Build 369130,772,319 - 130,772,545RGDNCBI36
Celera9102,384,813 - 102,385,039RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,340,148 - 101,340,374UniSTS
REN36686  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,731,890 - 131,732,143UniSTSGRCh37
Build 369130,771,711 - 130,771,964RGDNCBI36
Celera9102,384,205 - 102,384,458RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,339,540 - 101,339,793UniSTS
REN36687  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,731,563 - 131,731,804UniSTSGRCh37
Build 369130,771,384 - 130,771,625RGDNCBI36
Celera9102,383,878 - 102,384,119RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,339,213 - 101,339,454UniSTS
REN36688  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,731,315 - 131,731,586UniSTSGRCh37
Build 369130,771,136 - 130,771,407RGDNCBI36
Celera9102,383,630 - 102,383,901RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,338,965 - 101,339,236UniSTS
REN36689  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,731,088 - 131,731,339UniSTSGRCh37
Build 369130,770,909 - 130,771,160RGDNCBI36
Celera9102,383,403 - 102,383,654RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,338,738 - 101,338,989UniSTS
REN36690  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,730,868 - 131,731,100UniSTSGRCh37
Build 369130,770,689 - 130,770,921RGDNCBI36
Celera9102,383,183 - 102,383,415RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,338,518 - 101,338,750UniSTS
REN36691  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,730,623 - 131,730,850UniSTSGRCh37
Build 369130,770,444 - 130,770,671RGDNCBI36
Celera9102,382,938 - 102,383,165RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,338,273 - 101,338,500UniSTS
REN36692  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,730,346 - 131,730,610UniSTSGRCh37
Build 369130,770,167 - 130,770,431RGDNCBI36
Celera9102,382,661 - 102,382,925RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,337,996 - 101,338,260UniSTS
REN36693  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,730,101 - 131,730,338UniSTSGRCh37
Build 369130,769,922 - 130,770,159RGDNCBI36
Celera9102,382,416 - 102,382,653RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,337,751 - 101,337,988UniSTS
REN36694  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,729,342 - 131,729,588UniSTSGRCh37
Build 369130,769,163 - 130,769,409RGDNCBI36
Celera9102,381,657 - 102,381,903RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,336,992 - 101,337,238UniSTS
REN36695  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,729,123 - 131,729,357UniSTSGRCh37
Build 369130,768,944 - 130,769,178RGDNCBI36
Celera9102,381,438 - 102,381,672RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,336,773 - 101,337,007UniSTS
REN36696  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,728,796 - 131,729,061UniSTSGRCh37
Build 369130,768,617 - 130,768,882RGDNCBI36
Celera9102,381,111 - 102,381,376RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,336,446 - 101,336,711UniSTS
REN36697  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,728,587 - 131,728,814UniSTSGRCh37
Build 369130,768,408 - 130,768,635RGDNCBI36
Celera9102,380,902 - 102,381,129RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,336,237 - 101,336,464UniSTS
REN36698  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,728,387 - 131,728,611UniSTSGRCh37
Build 369130,768,208 - 130,768,432RGDNCBI36
Celera9102,380,704 - 102,380,926RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,336,037 - 101,336,261UniSTS
REN36699  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,727,803 - 131,728,045UniSTSGRCh37
Build 369130,767,624 - 130,767,866RGDNCBI36
Celera9102,380,120 - 102,380,362RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,335,453 - 101,335,695UniSTS
REN36700  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,727,544 - 131,727,785UniSTSGRCh37
Build 369130,767,365 - 130,767,606RGDNCBI36
Celera9102,379,861 - 102,380,102RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,335,194 - 101,335,435UniSTS
REN36701  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,727,339 - 131,727,566UniSTSGRCh37
Build 369130,767,160 - 130,767,387RGDNCBI36
Celera9102,379,656 - 102,379,883RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,334,989 - 101,335,216UniSTS
REN36702  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,727,137 - 131,727,362UniSTSGRCh37
Build 369130,766,958 - 130,767,183RGDNCBI36
Celera9102,379,454 - 102,379,679RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,334,787 - 101,335,012UniSTS
REN36703  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,726,934 - 131,727,158UniSTSGRCh37
Build 369130,766,755 - 130,766,979RGDNCBI36
Celera9102,379,251 - 102,379,475RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,334,584 - 101,334,808UniSTS
REN36704  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,726,660 - 131,726,904UniSTSGRCh37
Build 369130,766,481 - 130,766,725RGDNCBI36
Celera9102,378,977 - 102,379,221RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,334,310 - 101,334,554UniSTS
REN36705  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,726,379 - 131,726,629UniSTSGRCh37
Build 369130,766,200 - 130,766,450RGDNCBI36
Celera9102,378,696 - 102,378,946RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,334,029 - 101,334,279UniSTS
REN36706  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,725,825 - 131,726,049UniSTSGRCh37
Build 369130,765,646 - 130,765,870RGDNCBI36
Celera9102,378,142 - 102,378,366RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,333,549 - 101,333,699UniSTS
REN36707  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,725,024 - 131,725,298UniSTSGRCh37
Build 369130,764,845 - 130,765,119RGDNCBI36
Celera9102,377,341 - 102,377,615RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,332,748 - 101,333,022UniSTS
REN36708  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,724,822 - 131,725,048UniSTSGRCh37
Build 369130,764,643 - 130,764,869RGDNCBI36
Celera9102,377,139 - 102,377,365RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,332,546 - 101,332,772UniSTS
REN36709  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,724,505 - 131,724,768UniSTSGRCh37
Build 369130,764,326 - 130,764,589RGDNCBI36
Celera9102,376,822 - 102,377,085RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,332,229 - 101,332,492UniSTS
REN36710  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,723,703 - 131,723,970UniSTSGRCh37
Build 369130,763,524 - 130,763,791RGDNCBI36
Celera9102,376,020 - 102,376,287RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,331,427 - 101,331,694UniSTS
REN36711  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,722,583 - 131,722,834UniSTSGRCh37
Build 369130,762,404 - 130,762,655RGDNCBI36
Celera9102,374,900 - 102,375,151RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,330,307 - 101,330,558UniSTS
REN36712  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,722,105 - 131,722,329UniSTSGRCh37
Build 369130,761,926 - 130,762,150RGDNCBI36
Celera9102,374,422 - 102,374,646RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,329,829 - 101,330,053UniSTS
REN36713  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,721,836 - 131,722,085UniSTSGRCh37
Build 369130,761,657 - 130,761,906RGDNCBI36
Celera9102,374,153 - 102,374,402RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,329,560 - 101,329,809UniSTS
REN36714  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,721,519 - 131,721,770UniSTSGRCh37
Build 369130,761,340 - 130,761,591RGDNCBI36
Celera9102,373,836 - 102,374,087RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,329,243 - 101,329,494UniSTS
REN36715  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,721,302 - 131,721,542UniSTSGRCh37
Build 369130,761,123 - 130,761,363RGDNCBI36
Celera9102,373,619 - 102,373,859RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,329,026 - 101,329,266UniSTS
REN36716  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,721,057 - 131,721,326UniSTSGRCh37
Build 369130,760,878 - 130,761,147RGDNCBI36
Celera9102,373,374 - 102,373,643RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,328,781 - 101,329,050UniSTS
REN36717  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,720,777 - 131,721,006UniSTSGRCh37
Build 369130,760,598 - 130,760,827RGDNCBI36
Celera9102,373,094 - 102,373,323RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,328,501 - 101,328,730UniSTS
REN36718  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,720,513 - 131,720,761UniSTSGRCh37
Build 369130,760,334 - 130,760,582RGDNCBI36
Celera9102,372,830 - 102,373,078RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,328,237 - 101,328,485UniSTS
REN36719  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,720,252 - 131,720,508UniSTSGRCh37
Build 369130,760,073 - 130,760,329RGDNCBI36
Celera9102,372,569 - 102,372,825RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,327,976 - 101,328,232UniSTS
REN36720  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,720,037 - 131,720,271UniSTSGRCh37
Build 369130,759,858 - 130,760,092RGDNCBI36
Celera9102,372,354 - 102,372,588RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,327,761 - 101,327,995UniSTS
REN36721  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,719,413 - 131,719,672UniSTSGRCh37
Build 369130,759,234 - 130,759,493RGDNCBI36
Celera9102,371,730 - 102,371,989RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,327,137 - 101,327,396UniSTS
REN36722  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,719,126 - 131,719,350UniSTSGRCh37
Build 369130,758,947 - 130,759,171RGDNCBI36
Celera9102,371,443 - 102,371,667RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,326,850 - 101,327,074UniSTS
REN36723  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,718,884 - 131,719,121UniSTSGRCh37
Build 369130,758,705 - 130,758,942RGDNCBI36
Celera9102,371,201 - 102,371,438RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,326,608 - 101,326,845UniSTS
REN36724  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,718,666 - 131,718,903UniSTSGRCh37
Build 369130,758,487 - 130,758,724RGDNCBI36
Celera9102,370,983 - 102,371,220RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,326,390 - 101,326,627UniSTS
REN36725  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,718,425 - 131,718,682UniSTSGRCh37
Build 369130,758,246 - 130,758,503RGDNCBI36
Celera9102,370,742 - 102,370,999RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,326,149 - 101,326,406UniSTS
REN36726  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,718,106 - 131,718,340UniSTSGRCh37
Build 369130,757,927 - 130,758,161RGDNCBI36
Celera9102,370,419 - 102,370,657RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,325,826 - 101,326,064UniSTS
REN36727  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,717,878 - 131,718,115UniSTSGRCh37
Build 369130,757,699 - 130,757,936RGDNCBI36
Celera9102,370,191 - 102,370,428RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,325,598 - 101,325,835UniSTS
REN36728  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,717,672 - 131,717,897UniSTSGRCh37
Build 369130,757,493 - 130,757,718RGDNCBI36
Celera9102,369,985 - 102,370,210RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,325,392 - 101,325,617UniSTS
REN36729  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,717,423 - 131,717,647UniSTSGRCh37
Build 369130,757,244 - 130,757,468RGDNCBI36
Celera9102,369,736 - 102,369,960RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,325,143 - 101,325,367UniSTS
REN36730  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,716,966 - 131,717,190UniSTSGRCh37
Build 369130,756,787 - 130,757,011RGDNCBI36
Celera9102,369,279 - 102,369,503RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,324,686 - 101,324,910UniSTS
REN36731  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,716,163 - 131,716,407UniSTSGRCh37
Build 369130,755,984 - 130,756,228RGDNCBI36
Celera9102,368,476 - 102,368,720RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,323,883 - 101,324,127UniSTS
REN36732  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,715,739 - 131,715,998UniSTSGRCh37
Build 369130,755,560 - 130,755,819RGDNCBI36
Celera9102,368,052 - 102,368,311RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,323,459 - 101,323,718UniSTS
REN36733  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,715,528 - 131,715,753UniSTSGRCh37
Build 369130,755,349 - 130,755,574RGDNCBI36
Celera9102,367,841 - 102,368,066RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,323,248 - 101,323,473UniSTS
REN36734  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,715,255 - 131,715,479UniSTSGRCh37
Build 369130,755,076 - 130,755,300RGDNCBI36
Celera9102,367,568 - 102,367,792RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,322,975 - 101,323,199UniSTS
REN36735  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,715,021 - 131,715,259UniSTSGRCh37
Build 369130,754,842 - 130,755,080RGDNCBI36
Celera9102,367,334 - 102,367,572RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,322,741 - 101,322,979UniSTS
REN36736  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,713,886 - 131,714,116UniSTSGRCh37
Build 369130,753,707 - 130,753,937RGDNCBI36
Celera9102,365,748 - 102,365,978RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,321,606 - 101,321,836UniSTS
REN36737  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,713,611 - 131,713,857UniSTSGRCh37
Build 369130,753,432 - 130,753,678RGDNCBI36
Celera9102,365,473 - 102,365,719RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,321,331 - 101,321,577UniSTS
REN36738  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,713,068 - 131,713,313UniSTSGRCh37
Build 369130,752,889 - 130,753,134RGDNCBI36
Celera9102,364,930 - 102,365,175RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,320,788 - 101,321,033UniSTS
REN36739  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,712,828 - 131,713,088UniSTSGRCh37
Build 369130,752,649 - 130,752,909RGDNCBI36
Celera9102,364,690 - 102,364,950RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,320,548 - 101,320,808UniSTS
REN36740  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,711,958 - 131,712,183UniSTSGRCh37
Build 369130,751,779 - 130,752,004RGDNCBI36
Celera9102,363,820 - 102,364,045RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,319,678 - 101,319,903UniSTS
REN36741  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,710,734 - 131,710,958UniSTSGRCh37
Build 369130,750,555 - 130,750,779RGDNCBI36
Celera9102,362,595 - 102,362,819RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,318,453 - 101,318,677UniSTS
REN36742  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,710,497 - 131,710,743UniSTSGRCh37
Build 369130,750,318 - 130,750,564RGDNCBI36
Celera9102,362,358 - 102,362,604RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,318,216 - 101,318,462UniSTS
REN36743  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,710,287 - 131,710,517UniSTSGRCh37
Build 369130,750,108 - 130,750,338RGDNCBI36
Celera9102,362,148 - 102,362,378RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,318,006 - 101,318,236UniSTS
REN36744  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,710,063 - 131,710,292UniSTSGRCh37
Build 369130,749,884 - 130,750,113RGDNCBI36
Celera9102,361,924 - 102,362,153RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,317,782 - 101,318,011UniSTS
REN36745  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,709,809 - 131,710,039UniSTSGRCh37
Build 369130,749,630 - 130,749,860RGDNCBI36
Celera9102,361,670 - 102,361,900RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,317,528 - 101,317,758UniSTS
REN36746  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,709,579 - 131,709,832UniSTSGRCh37
Build 369130,749,400 - 130,749,653RGDNCBI36
Celera9102,361,440 - 102,361,693RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,317,298 - 101,317,551UniSTS
REN36747  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,709,356 - 131,709,601UniSTSGRCh37
Build 369130,749,177 - 130,749,422RGDNCBI36
Celera9102,361,217 - 102,361,462RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,317,075 - 101,317,320UniSTS
REN36748  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,709,150 - 131,709,376UniSTSGRCh37
Build 369130,748,971 - 130,749,197RGDNCBI36
Celera9102,361,011 - 102,361,237RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,316,869 - 101,317,095UniSTS
REN36749  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,708,927 - 131,709,174UniSTSGRCh37
Build 369130,748,748 - 130,748,995RGDNCBI36
Celera9102,360,788 - 102,361,035RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,316,646 - 101,316,893UniSTS
REN36750  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,708,708 - 131,708,949UniSTSGRCh37
Build 369130,748,529 - 130,748,770RGDNCBI36
Celera9102,360,569 - 102,360,810RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,316,427 - 101,316,668UniSTS
REN36751  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,708,455 - 131,708,718UniSTSGRCh37
Build 369130,748,276 - 130,748,539RGDNCBI36
Celera9102,360,316 - 102,360,579RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,316,174 - 101,316,437UniSTS
REN36752  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,708,212 - 131,708,477UniSTSGRCh37
Build 369130,748,033 - 130,748,298RGDNCBI36
Celera9102,360,073 - 102,360,338RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,315,931 - 101,316,196UniSTS
REN36753  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,707,997 - 131,708,234UniSTSGRCh37
Build 369130,747,818 - 130,748,055RGDNCBI36
Celera9102,359,858 - 102,360,095RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,315,716 - 101,315,953UniSTS
NUP188_9358  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,768,841 - 131,769,439UniSTSGRCh37
Build 369130,808,662 - 130,809,260RGDNCBI36
Celera9102,421,153 - 102,421,751RGD
HuRef9101,376,162 - 101,376,760UniSTS
WI-21818  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,755,251 - 131,755,543UniSTSGRCh37
Build 369130,795,072 - 130,795,364RGDNCBI36
Celera9102,407,563 - 102,407,855RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,362,595 - 101,362,887UniSTS
GeneMap99-GB4 RH Map9392.55UniSTS
Whitehead-RH Map9474.0UniSTS
SHGC-33284  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,730,246 - 131,730,373UniSTSGRCh37
Build 369130,770,067 - 130,770,194RGDNCBI36
Celera9102,382,561 - 102,382,688RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,337,896 - 101,338,023UniSTS
TNG Radiation Hybrid Map949721.0UniSTS
GeneMap99-GB4 RH Map9392.35UniSTS
Whitehead-RH Map9474.0UniSTS
GeneMap99-G3 RH Map94590.0UniSTS
stSG628088  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,708,924 - 131,710,311UniSTSGRCh37
Build 369130,748,745 - 130,750,132RGDNCBI36
Celera9102,360,785 - 102,362,172RGD
HuRef9101,316,643 - 101,318,030UniSTS
stSG628089  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,710,292 - 131,711,563UniSTSGRCh37
Build 369130,750,113 - 130,751,384RGDNCBI36
Celera9102,362,153 - 102,363,425RGD
HuRef9101,318,011 - 101,319,283UniSTS
stSG628090  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,715,069 - 131,715,687UniSTSGRCh37
Build 369130,754,890 - 130,755,508RGDNCBI36
Celera9102,367,382 - 102,368,000RGD
HuRef9101,322,789 - 101,323,407UniSTS
stSG628091  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,718,426 - 131,719,443UniSTSGRCh37
Build 369130,758,247 - 130,759,264RGDNCBI36
Celera9102,370,743 - 102,371,760RGD
HuRef9101,326,150 - 101,327,167UniSTS
stSG628094  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,721,745 - 131,722,838UniSTSGRCh37
Build 369130,761,566 - 130,762,659RGDNCBI36
Celera9102,374,062 - 102,375,155RGD
HuRef9101,329,469 - 101,330,562UniSTS
stSG628095  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,728,539 - 131,728,621UniSTSGRCh37
GRCh379131,728,406 - 131,728,621UniSTSGRCh37
Build 369130,768,227 - 130,768,442RGDNCBI36
Celera9102,380,854 - 102,380,936UniSTS
Celera9102,380,723 - 102,380,936RGD
HuRef9101,336,187 - 101,336,271UniSTS
HuRef9101,336,056 - 101,336,271UniSTS
stSG628096  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,730,776 - 131,731,791UniSTSGRCh37
Build 369130,770,597 - 130,771,612RGDNCBI36
Celera9102,383,091 - 102,384,106RGD
HuRef9101,338,426 - 101,339,441UniSTS
stSG628097  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,731,772 - 131,733,174UniSTSGRCh37
Build 369130,771,593 - 130,772,995RGDNCBI36
Celera9102,384,087 - 102,385,489RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,339,422 - 101,340,824UniSTS
stSG628098  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,732,967 - 131,734,021UniSTSGRCh37
Build 369130,772,788 - 130,773,842RGDNCBI36
Celera9102,385,282 - 102,386,336RGD
HuRef9101,340,617 - 101,341,671UniSTS
stSG628099  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,734,001 - 131,735,148UniSTSGRCh37
Build 369130,773,822 - 130,774,969RGDNCBI36
Celera9102,386,316 - 102,387,463RGD
HuRef9101,341,651 - 101,342,798UniSTS
stSG628101  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,736,649 - 131,737,035UniSTSGRCh37
Build 369130,776,470 - 130,776,856RGDNCBI36
Celera9102,388,964 - 102,389,350RGD
HuRef9101,344,299 - 101,344,685UniSTS
stSG628102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,739,031 - 131,740,335UniSTSGRCh37
Build 369130,778,852 - 130,780,156RGDNCBI36
Celera9102,391,346 - 102,392,650RGD
HuRef9101,346,681 - 101,347,985UniSTS
stSG628103  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,740,315 - 131,741,577UniSTSGRCh37
Build 369130,780,136 - 130,781,398RGDNCBI36
Celera9102,392,630 - 102,393,892RGD
HuRef9101,347,965 - 101,349,268UniSTS
stSG628105  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,742,639 - 131,743,655UniSTSGRCh37
Build 369130,782,460 - 130,783,476RGDNCBI36
Celera9102,394,954 - 102,395,970RGD
HuRef9101,350,330 - 101,351,346UniSTS
stSG628106  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,743,636 - 131,744,867UniSTSGRCh37
Build 369130,783,457 - 130,784,688RGDNCBI36
Celera9102,395,951 - 102,397,182RGD
Cytogenetic Map9q34.11UniSTS
HuRef9101,351,327 - 101,352,558UniSTS
stSG628107  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,744,865 - 131,745,868UniSTSGRCh37
Build 369130,784,686 - 130,785,689RGDNCBI36
Celera9102,397,180 - 102,398,183RGD
HuRef9101,352,556 - 101,353,559UniSTS
stSG628108  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,745,849 - 131,746,926UniSTSGRCh37
Build 369130,785,670 - 130,786,747RGDNCBI36
Celera9102,398,164 - 102,399,241RGD
HuRef9101,353,540 - 101,354,617UniSTS
stSG628109  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,746,917 - 131,747,997UniSTSGRCh37
Build 369130,786,738 - 130,787,818RGDNCBI36
Celera9102,399,232 - 102,400,312RGD
HuRef9101,354,608 - 101,355,688UniSTS
stSG628110  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,747,992 - 131,749,239UniSTSGRCh37
Build 369130,787,813 - 130,789,060RGDNCBI36
Celera9102,400,307 - 102,401,554RGD
HuRef9101,355,683 - 101,356,930UniSTS
stSG628111  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,749,220 - 131,750,394UniSTSGRCh37
Build 369130,789,041 - 130,790,215RGDNCBI36
Celera9102,401,535 - 102,402,707RGD
HuRef9101,356,911 - 101,358,089UniSTS
stSG628112  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,750,375 - 131,750,624UniSTSGRCh37
Build 369130,790,196 - 130,790,445RGDNCBI36
Celera9102,402,688 - 102,402,937RGD
HuRef9101,358,070 - 101,358,319UniSTS
stSG628113  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,752,178 - 131,753,444UniSTSGRCh37
Build 369130,791,999 - 130,793,265RGDNCBI36
Celera9102,404,490 - 102,405,756RGD
HuRef9101,359,843 - 101,361,109UniSTS
stSG628114  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,753,468 - 131,754,839UniSTSGRCh37
Build 369130,793,289 - 130,794,660RGDNCBI36
Celera9102,405,780 - 102,407,151RGD
HuRef9101,361,133 - 101,362,183UniSTS
stSG628115  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,754,837 - 131,755,869UniSTSGRCh37
Build 369130,794,658 - 130,795,690RGDNCBI36
Celera9102,407,149 - 102,408,181RGD
HuRef9101,362,181 - 101,363,213UniSTS
stSG628116  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,755,850 - 131,756,882UniSTSGRCh37
Build 369130,795,671 - 130,796,703RGDNCBI36
Celera9102,408,162 - 102,409,194RGD
HuRef9101,363,194 - 101,364,226UniSTS
stSG628117  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,756,863 - 131,757,895UniSTSGRCh37
Build 369130,796,684 - 130,797,716RGDNCBI36
Celera9102,409,175 - 102,410,207RGD
HuRef9101,364,207 - 101,365,239UniSTS
stSG628118  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,757,876 - 131,758,889UniSTSGRCh37
Build 369130,797,697 - 130,798,710RGDNCBI36
Celera9102,410,188 - 102,411,201RGD
HuRef9101,365,220 - 101,366,233UniSTS
stSG628119  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,758,993 - 131,760,381UniSTSGRCh37
Build 369130,798,814 - 130,800,202RGDNCBI36
Celera9102,411,305 - 102,412,693RGD
HuRef9101,366,337 - 101,367,725UniSTS
stSG628120  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,760,362 - 131,761,678UniSTSGRCh37
Build 369130,800,183 - 130,801,499RGDNCBI36
Celera9102,412,674 - 102,413,990RGD
HuRef9101,367,706 - 101,369,022UniSTS
stSG628121  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,761,108 - 131,762,355UniSTSGRCh37
Build 369130,800,929 - 130,802,176RGDNCBI36
Celera9102,413,420 - 102,414,667RGD
HuRef9101,368,452 - 101,369,699UniSTS
stSG628122  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,762,519 - 131,763,769UniSTSGRCh37
Build 369130,802,340 - 130,803,590RGDNCBI36
Celera9102,414,831 - 102,416,081RGD
HuRef9101,369,863 - 101,371,090UniSTS
stSG628123  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,763,750 - 131,765,115UniSTSGRCh37
Build 369130,803,571 - 130,804,936RGDNCBI36
Celera9102,416,062 - 102,417,427RGD
HuRef9101,371,071 - 101,372,436UniSTS
stSG628124  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,764,925 - 131,765,929UniSTSGRCh37
Build 369130,804,746 - 130,805,750RGDNCBI36
Celera9102,417,237 - 102,418,241RGD
HuRef9101,372,246 - 101,373,250UniSTS
stSG628125  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,765,910 - 131,767,398UniSTSGRCh37
Build 369130,805,731 - 130,807,219RGDNCBI36
Celera9102,418,222 - 102,419,710RGD
HuRef9101,373,231 - 101,374,719UniSTS
stSG628126  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379131,767,380 - 131,768,673UniSTSGRCh37
Build 369130,807,201 - 130,808,494RGDNCBI36
Celera9102,419,692 - 102,420,985RGD
HuRef9101,374,701 - 101,375,994UniSTS
D1S1423  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map10p12.1-p11.2UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map6p22.3-p21.32UniSTS
Cytogenetic Map6q22.33UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map7q11.2UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map9q12UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map18q22.1UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map10p14-p13UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map11q23-q24UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map22cen-q12.3UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map15q11.2-q21.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map4q28UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map1q41-q42UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map11q24.1UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map3q13UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map3q26UniSTS
Cytogenetic Map9p21.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic MapXq27.2UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map4q31UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map12q14.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map20q11.21-q11.23UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map4q31.23UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map13q33.3UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map4p15.31UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map4q26UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map4q24UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map10pter-q25.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map11q13.1-q13.3UniSTS
Cytogenetic Map16p13UniSTS
Cytogenetic Map15q26UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map4p15.1-p14UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map7q32.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map9p13UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map3q21-q24UniSTS
Cytogenetic Map4q13UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map8q24.12UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map6q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map20pter-p12UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map18p11.22UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map14q22.2UniSTS
Cytogenetic Map20p11.22-p11.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map6p22-p21UniSTS
Cytogenetic Map17q21.1-q21.3UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12p13.2-p12.3UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map5q22.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map4p15.3UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map12q13.1-q13.2UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map6q22.32UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map10q22.3-q23.2UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map3q12.1UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map2p13.2UniSTS
Cytogenetic Map3p12.3UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map3q11.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map6p24.2UniSTS
Cytogenetic Map20q13.33UniSTS
D9S260  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map9q34.11UniSTS
TNG Radiation Hybrid Map949711.0UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component
High
Medium 2326 1782 1350 260 1306 105 3993 1481 1993 255 1437 1597 169 1198 2427 3
Low 106 1200 373 362 640 359 362 712 1726 163 13 11 3 6 361 1
Below cutoff 1 4 1 2 8 4 1 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000372577   ⟹   ENSP00000361658
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9128,947,699 - 129,007,096 (+)Ensembl
RefSeq Acc Id: ENST00000464729
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9128,948,959 - 128,952,895 (+)Ensembl
RefSeq Acc Id: ENST00000465344
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9128,983,514 - 128,985,262 (+)Ensembl
RefSeq Acc Id: ENST00000467044
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9128,993,095 - 128,994,890 (+)Ensembl
RefSeq Acc Id: ENST00000477069
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9128,984,971 - 129,003,993 (+)Ensembl
RefSeq Acc Id: ENST00000485158
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9128,994,396 - 128,995,200 (+)Ensembl
RefSeq Acc Id: ENST00000487952
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9128,999,601 - 129,001,891 (+)Ensembl
RefSeq Acc Id: ENST00000491502
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9128,986,589 - 128,993,230 (+)Ensembl
RefSeq Acc Id: ENST00000491990
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9128,947,707 - 128,958,054 (+)Ensembl
RefSeq Acc Id: ENST00000495726
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9128,995,136 - 128,998,596 (+)Ensembl
RefSeq Acc Id: ENST00000550219
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9128,948,017 - 128,957,011 (+)Ensembl
RefSeq Acc Id: NM_015354   ⟹   NP_056169
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389128,947,699 - 129,007,096 (+)NCBI
GRCh379131,709,972 - 131,769,375 (+)NCBI
Build 369130,749,798 - 130,809,195 (+)NCBI Archive
Celera9102,361,838 - 102,421,686 (+)RGD
HuRef9101,317,691 - 101,376,696 (+)NCBI
CHM1_19131,861,021 - 131,920,403 (+)NCBI
T2T-CHM13v2.09141,151,108 - 141,210,530 (+)NCBI
Sequence:
Reference Protein Sequences
RefSeq Acc Id: NP_056169   ⟸   NM_015354
- UniProtKB: Q7Z3K8 (UniProtKB/Swiss-Prot),   Q2TA87 (UniProtKB/Swiss-Prot),   Q14675 (UniProtKB/Swiss-Prot),   Q8IWF1 (UniProtKB/Swiss-Prot),   Q5SRE5 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000361658   ⟸   ENST00000372577
Protein Domains
Nucleoporin Nup188 N-terminal subdomain III

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q5SRE5-F1-model_v2 AlphaFold Q5SRE5 1-1749 view protein structure

Promoters
RGD ID:7216343
Promoter ID:EPDNEW_H13917
Type:initiation region
Name:NUP188_1
Description:nucleoporin 188
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H13918  EPDNEW_H13919  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh389128,947,699 - 128,947,759EPDNEW
RGD ID:7216345
Promoter ID:EPDNEW_H13918
Type:initiation region
Name:NUP188_3
Description:nucleoporin 188
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H13917  EPDNEW_H13919  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh389128,947,907 - 128,947,967EPDNEW
RGD ID:7216347
Promoter ID:EPDNEW_H13919
Type:initiation region
Name:NUP188_2
Description:nucleoporin 188
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H13917  EPDNEW_H13918  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh389128,952,823 - 128,952,883EPDNEW
RGD ID:6807489
Promoter ID:HG_KWN:65202
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000356693,   OTTHUMT00000054529,   OTTHUMT00000054532,   OTTHUMT00000258045,   OTTHUMT00000317341,   OTTHUMT00000317342
Position:
Human AssemblyChrPosition (strand)Source
Build 369130,749,736 - 130,750,527 (+)MPROMDB
RGD ID:6807938
Promoter ID:HG_KWN:65203
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   K562
Transcripts:OTTHUMT00000106247
Position:
Human AssemblyChrPosition (strand)Source
Build 369130,784,764 - 130,785,264 (+)MPROMDB
RGD ID:6807940
Promoter ID:HG_KWN:65204
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Jurkat
Transcripts:UC004BWU.2
Position:
Human AssemblyChrPosition (strand)Source
Build 369130,787,246 - 130,787,746 (+)MPROMDB
RGD ID:6807937
Promoter ID:HG_KWN:65207
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell_2Hour
Transcripts:OTTHUMT00000054534
Position:
Human AssemblyChrPosition (strand)Source
Build 369130,795,406 - 130,795,906 (+)MPROMDB
RGD ID:6807939
Promoter ID:HG_KWN:65209
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   Lymphoblastoid
Transcripts:OTTHUMT00000315882
Position:
Human AssemblyChrPosition (strand)Source
Build 369130,801,511 - 130,802,011 (+)MPROMDB
RGD ID:6813674
Promoter ID:HG_ACW:82592
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:NUP188.JAPR07-UNSPLICED
Position:
Human AssemblyChrPosition (strand)Source
Build 369130,807,231 - 130,807,731 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:17859 AgrOrtholog
COSMIC NUP188 COSMIC
Ensembl Genes ENSG00000095319 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000372577 ENTREZGENE
  ENST00000372577.2 UniProtKB/Swiss-Prot
GTEx ENSG00000095319 GTEx
HGNC ID HGNC:17859 ENTREZGENE
Human Proteome Map NUP188 Human Proteome Map
InterPro ARM-type_fold UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Nucleoporin_Nup188 UniProtKB/Swiss-Prot
  Nup188 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Nup188_N-subdom_III UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:23511 UniProtKB/Swiss-Prot
NCBI Gene 23511 ENTREZGENE
OMIM 615587 OMIM
PANTHER NUCLEOPORIN NUP188 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR31431 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Nup188 UniProtKB/Swiss-Prot
  Nup188_N-subdom_III UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Nup188_SH3-like UniProtKB/Swiss-Prot
PharmGKB PA134908952 PharmGKB
Superfamily-SCOP SSF48371 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt NU188_HUMAN UniProtKB/Swiss-Prot
  Q14675 ENTREZGENE
  Q2TA87 ENTREZGENE
  Q5SRE5 ENTREZGENE
  Q7Z3K8 ENTREZGENE
  Q8IWF1 ENTREZGENE
  Q9BS12_HUMAN UniProtKB/TrEMBL
UniProt Secondary Q14675 UniProtKB/Swiss-Prot
  Q2TA87 UniProtKB/Swiss-Prot
  Q7Z3K8 UniProtKB/Swiss-Prot
  Q8IWF1 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-06-07 NUP188  nucleoporin 188    nucleoporin 188kDa  Symbol and/or name change 5135510 APPROVED