GAB3 (GRB2 associated binding protein 3) - Rat Genome Database

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Gene: GAB3 (GRB2 associated binding protein 3) Homo sapiens
Analyze
Symbol: GAB3
Name: GRB2 associated binding protein 3
RGD ID: 1353554
HGNC Page HGNC
Description: Predicted to be involved in macrophage differentiation.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: DOS/Gab family member 3; Gab3 scaffolding protein; GRB2-associated binder 3; GRB2-associated binding protein 3; GRB2-associated-binding protein 3; growth factor receptor bound protein 2-associated protein 3
RGD Orthologs
Mouse
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
GRCh38.p13 EnsemblX154,675,249 - 154,751,583 (-)EnsemblGRCh38hg38GRCh38
GRCh38X154,675,249 - 154,751,566 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X153,903,526 - 153,979,841 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X153,556,720 - 153,632,542 (-)NCBINCBI36hg18NCBI36
Build 34X153,467,233 - 153,543,036NCBI
CeleraX154,061,594 - 154,137,916 (-)NCBI
Cytogenetic MapXq28NCBI
HuRefX142,447,630 - 142,523,043 (-)NCBIHuRef
CHM1_1X153,815,233 - 153,891,531 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Schizophrenia  (IAGP)
References

Additional References at PubMed
PMID:11739737   PMID:11943184   PMID:11997510   PMID:12640125   PMID:12773374   PMID:16344560   PMID:16386802   PMID:17567994   PMID:18235045   PMID:19430480   PMID:19913121   PMID:20237496  
PMID:20628086   PMID:22163099   PMID:23431498   PMID:28115166   PMID:28291820  


Genomics

Comparative Map Data
GAB3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 EnsemblX154,675,249 - 154,751,583 (-)EnsemblGRCh38hg38GRCh38
GRCh38X154,675,249 - 154,751,566 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X153,903,526 - 153,979,841 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X153,556,720 - 153,632,542 (-)NCBINCBI36hg18NCBI36
Build 34X153,467,233 - 153,543,036NCBI
CeleraX154,061,594 - 154,137,916 (-)NCBI
Cytogenetic MapXq28NCBI
HuRefX142,447,630 - 142,523,043 (-)NCBIHuRef
CHM1_1X153,815,233 - 153,891,531 (-)NCBICHM1_1
Gab3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39X74,032,151 - 74,128,511 (-)NCBIGRCm39mm39
GRCm39 EnsemblX74,010,449 - 74,129,064 (-)Ensembl
GRCm38X74,988,545 - 75,084,905 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 EnsemblX74,966,843 - 75,085,458 (-)EnsemblGRCm38mm10GRCm38
MGSCv37X72,233,884 - 72,330,244 (-)NCBIGRCm37mm9NCBIm37
MGSCv36X71,241,241 - 71,337,625 (-)NCBImm8
CeleraX66,394,016 - 66,489,831 (-)NCBICelera
Cytogenetic MapXA7.3NCBI
Gab3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955594912,108 - 956,037 (+)EnsemblChiLan1.0
ChiLan1.0NW_004955594882,921 - 955,079 (+)NCBIChiLan1.0ChiLan1.0
GAB3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1X153,993,736 - 154,073,529 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 EnsemblX153,993,736 - 154,038,529 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v0X144,150,062 - 144,232,216 (-)NCBIMhudiblu_PPA_v0panPan3
GAB3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1X122,741,199 - 122,822,446 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 EnsemblX122,741,197 - 122,779,143 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_TashaX107,734,458 - 107,815,671 (-)NCBI
ROS_Cfam_1.0X125,869,755 - 125,948,703 (-)NCBI
UMICH_Zoey_3.1X121,615,438 - 121,696,660 (-)NCBI
UNSW_CanFamBas_1.0X124,138,699 - 124,223,143 (-)NCBI
UU_Cfam_GSD_1.0X123,869,043 - 123,912,968 (-)NCBI
Gab3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2X119,709,450 - 119,765,746 (-)NCBI
SpeTri2.0NW_00493692768,506 - 93,899 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
GAB3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 EnsemblX125,158,148 - 125,209,036 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1X125,158,148 - 125,209,080 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2X143,274,129 - 143,302,751 (+)NCBISscrofa10.2Sscrofa10.2susScr3
GAB3
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1X128,904,743 - 129,004,596 (-)NCBI
ChlSab1.1 EnsemblX128,902,420 - 128,973,550 (-)Ensembl
Gab3
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_004624963492,210 - 573,887 (+)NCBI

Position Markers
RH80376  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,924,350 - 153,924,573UniSTSGRCh37
Build 36X153,577,544 - 153,577,767RGDNCBI36
CeleraX154,082,935 - 154,083,158RGD
Cytogenetic MapXq28UniSTS
HuRefX142,468,409 - 142,468,632UniSTS
GeneMap99-GB4 RH MapX354.15UniSTS
RH99020  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,903,616 - 153,903,767UniSTSGRCh37
Build 36X153,556,810 - 153,556,961RGDNCBI36
CeleraX154,061,684 - 154,061,835RGD
Cytogenetic MapXq28UniSTS
HuRefX142,447,720 - 142,447,871UniSTS
GeneMap99-GB4 RH MapX352.15UniSTS
RH80611  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,903,544 - 153,903,786UniSTSGRCh37
Build 36X153,556,738 - 153,556,980RGDNCBI36
CeleraX154,061,612 - 154,061,854RGD
Cytogenetic MapXq28UniSTS
HuRefX142,447,648 - 142,447,890UniSTS
GeneMap99-GB4 RH MapX352.37UniSTS
SHGC-149514  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,927,816 - 153,928,161UniSTSGRCh37
Build 36X153,581,010 - 153,581,355RGDNCBI36
CeleraX154,086,401 - 154,086,746RGD
Cytogenetic MapXq28UniSTS
HuRefX142,471,875 - 142,472,220UniSTS
GAB3_1528  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,903,509 - 153,904,350UniSTSGRCh37
Build 36X153,556,703 - 153,557,544RGDNCBI36
CeleraX154,061,577 - 154,062,418RGD
HuRefX142,447,613 - 142,448,454UniSTS
ECD00503  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,904,680 - 153,905,582UniSTSGRCh37
Build 36X153,557,874 - 153,558,776RGDNCBI36
CeleraX154,062,748 - 154,063,650RGD
Cytogenetic MapXq28UniSTS
HuRefX142,448,784 - 142,449,686UniSTS
ECD00614  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,903,748 - 153,904,645UniSTSGRCh37
Build 36X153,556,942 - 153,557,839RGDNCBI36
CeleraX154,061,816 - 154,062,713RGD
Cytogenetic MapXq28UniSTS
HuRefX142,447,852 - 142,448,749UniSTS
ECD01500  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,942,735 - 153,943,598UniSTSGRCh37
Build 36X153,595,929 - 153,596,792RGDNCBI36
CeleraX154,101,318 - 154,102,181RGD
Cytogenetic MapXq28UniSTS
HuRefX142,486,662 - 142,487,525UniSTS
ECD03315  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,964,790 - 153,965,589UniSTSGRCh37
Build 36X153,617,984 - 153,618,783RGDNCBI36
CeleraX154,123,369 - 154,124,168RGD
Cytogenetic MapXq28UniSTS
HuRefX142,508,638 - 142,509,437UniSTS
ECD03346  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,978,295 - 153,979,093UniSTSGRCh37
Build 36X153,631,489 - 153,632,287RGDNCBI36
CeleraX154,136,863 - 154,137,661RGD
Cytogenetic MapXq28UniSTS
HuRefX142,522,037 - 142,522,835UniSTS
ECD04121  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,976,648 - 153,977,422UniSTSGRCh37
Build 36X153,629,842 - 153,630,616RGDNCBI36
CeleraX154,135,216 - 154,135,990RGD
Cytogenetic MapXq28UniSTS
HuRefX142,520,390 - 142,521,164UniSTS
ECD04213  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,977,442 - 153,978,213UniSTSGRCh37
Build 36X153,630,636 - 153,631,407RGDNCBI36
CeleraX154,136,010 - 154,136,781RGD
Cytogenetic MapXq28UniSTS
HuRefX142,521,184 - 142,521,955UniSTS
ECD04476  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,941,215 - 153,941,978UniSTSGRCh37
Build 36X153,594,409 - 153,595,172RGDNCBI36
CeleraX154,099,798 - 154,100,561RGD
Cytogenetic MapXq28UniSTS
HuRefX142,485,150 - 142,485,913UniSTS
ECD04543  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,940,371 - 153,941,132UniSTSGRCh37
Build 36X153,593,565 - 153,594,326RGDNCBI36
CeleraX154,098,954 - 154,099,715RGD
Cytogenetic MapXq28UniSTS
HuRefX142,484,306 - 142,485,067UniSTS
ECD05238  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,939,624 - 153,940,365UniSTSGRCh37
Build 36X153,592,818 - 153,593,559RGDNCBI36
CeleraX154,098,207 - 154,098,948RGD
Cytogenetic MapXq28UniSTS
HuRefX142,483,559 - 142,484,300UniSTS
ECD06412  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,962,562 - 153,963,271UniSTSGRCh37
Build 36X153,615,756 - 153,616,465RGDNCBI36
CeleraX154,121,145 - 154,121,854RGD
Cytogenetic MapXq28UniSTS
HuRefX142,506,414 - 142,507,123UniSTS
ECD06813  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,927,154 - 153,927,852UniSTSGRCh37
Build 36X153,580,348 - 153,581,046RGDNCBI36
CeleraX154,085,739 - 154,086,437RGD
Cytogenetic MapXq28UniSTS
HuRefX142,471,213 - 142,471,911UniSTS
ECD07127  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,923,868 - 153,924,558UniSTSGRCh37
Build 36X153,577,062 - 153,577,752RGDNCBI36
CeleraX154,082,453 - 154,083,143RGD
Cytogenetic MapXq28UniSTS
HuRefX142,467,927 - 142,468,617UniSTS
ECD07299  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,923,132 - 153,923,817UniSTSGRCh37
Build 36X153,576,326 - 153,577,011RGDNCBI36
CeleraX154,081,717 - 154,082,402RGD
Cytogenetic MapXq28UniSTS
HuRefX142,467,191 - 142,467,876UniSTS
ECD07713  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,961,866 - 153,962,540UniSTSGRCh37
Build 36X153,615,060 - 153,615,734RGDNCBI36
CeleraX154,120,449 - 154,121,123RGD
Cytogenetic MapXq28UniSTS
HuRefX142,505,718 - 142,506,392UniSTS
ECD08097  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,926,486 - 153,927,150UniSTSGRCh37
Build 36X153,579,680 - 153,580,344RGDNCBI36
CeleraX154,085,071 - 154,085,735RGD
Cytogenetic MapXq28UniSTS
HuRefX142,470,545 - 142,471,209UniSTS
ECD08612  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,927,902 - 153,928,552UniSTSGRCh37
Build 36X153,581,096 - 153,581,746RGDNCBI36
CeleraX154,086,487 - 154,087,137RGD
Cytogenetic MapXq28UniSTS
HuRefX142,471,961 - 142,472,611UniSTS
ECD10273  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,946,835 - 153,947,441UniSTSGRCh37
Build 36X153,600,029 - 153,600,635RGDNCBI36
CeleraX154,105,418 - 154,106,024RGD
Cytogenetic MapXq28UniSTS
ECD10274  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,979,493 - 153,980,099UniSTSGRCh37
Build 36X153,632,687 - 153,633,293RGDNCBI36
CeleraX154,138,061 - 154,138,667RGD
Cytogenetic MapXq28UniSTS
HuRefX142,523,362 - 142,523,968UniSTS
ECD10531  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,908,392 - 153,908,991UniSTSGRCh37
Build 36X153,561,586 - 153,562,185RGDNCBI36
CeleraX154,066,460 - 154,067,059RGD
Cytogenetic MapXq28UniSTS
HuRefX142,452,496 - 142,453,095UniSTS
ECD11432  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,958,799 - 153,959,371UniSTSGRCh37
Build 36X153,611,993 - 153,612,565RGDNCBI36
CeleraX154,117,382 - 154,117,954RGD
Cytogenetic MapXq28UniSTS
HuRefX142,502,651 - 142,503,223UniSTS
ECD11604  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,958,217 - 153,958,784UniSTSGRCh37
Build 36X153,611,411 - 153,611,978RGDNCBI36
CeleraX154,116,800 - 154,117,367RGD
Cytogenetic MapXq28UniSTS
HuRefX142,502,069 - 142,502,636UniSTS
ECD12444  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,938,921 - 153,939,464UniSTSGRCh37
Build 36X153,592,115 - 153,592,658RGDNCBI36
CeleraX154,097,504 - 154,098,047RGD
Cytogenetic MapXq28UniSTS
HuRefX142,482,856 - 142,483,399UniSTS
ECD13575  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,924,598 - 153,925,112UniSTSGRCh37
Build 36X153,577,792 - 153,578,306RGDNCBI36
CeleraX154,083,183 - 154,083,697RGD
Cytogenetic MapXq28UniSTS
HuRefX142,468,657 - 142,469,171UniSTS
ECD13907  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,925,186 - 153,925,692UniSTSGRCh37
Build 36X153,578,380 - 153,578,886RGDNCBI36
CeleraX154,083,771 - 154,084,277RGD
Cytogenetic MapXq28UniSTS
HuRefX142,469,245 - 142,469,751UniSTS
ECD14146  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,945,690 - 153,946,190UniSTSGRCh37
Build 36X153,598,884 - 153,599,384RGDNCBI36
CeleraX154,104,273 - 154,104,773RGD
Cytogenetic MapXq28UniSTS
HuRefX142,489,617 - 142,490,117UniSTS
ECD14503  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,946,226 - 153,946,718UniSTSGRCh37
Build 36X153,599,420 - 153,599,912RGDNCBI36
CeleraX154,104,809 - 154,105,301RGD
Cytogenetic MapXq28UniSTS
HuRefX142,490,153 - 142,490,645UniSTS
ECD15061  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,960,837 - 153,961,316UniSTSGRCh37
Build 36X153,614,031 - 153,614,510RGDNCBI36
CeleraX154,119,420 - 154,119,899RGD
Cytogenetic MapXq28UniSTS
HuRefX142,504,689 - 142,505,168UniSTS
ECD15111  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,956,517 - 153,956,995UniSTSGRCh37
Build 36X153,609,711 - 153,610,189RGDNCBI36
CeleraX154,115,100 - 154,115,578RGD
Cytogenetic MapXq28UniSTS
HuRefX142,500,471 - 142,500,949UniSTS
ECD15308  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,956,010 - 153,956,483UniSTSGRCh37
Build 36X153,609,204 - 153,609,677RGDNCBI36
CeleraX154,114,593 - 154,115,066RGD
Cytogenetic MapXq28UniSTS
HuRefX142,499,964 - 142,500,437UniSTS
ECD15346  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,951,580 - 153,952,052UniSTSGRCh37
Build 36X153,604,774 - 153,605,246RGDNCBI36
CeleraX154,110,163 - 154,110,635RGD
Cytogenetic MapXq28UniSTS
HuRefX142,495,536 - 142,496,008UniSTS
ECD15563  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,943,735 - 153,944,202UniSTSGRCh37
Build 36X153,596,929 - 153,597,396RGDNCBI36
CeleraX154,102,318 - 154,102,785RGD
Cytogenetic MapXq28UniSTS
HuRefX142,487,662 - 142,488,129UniSTS
ECD15938  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,922,111 - 153,922,569UniSTSGRCh37
Build 36X153,575,305 - 153,575,763RGDNCBI36
CeleraX154,080,696 - 154,081,154RGD
Cytogenetic MapXq28UniSTS
HuRefX142,466,170 - 142,466,628UniSTS
ECD15939  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,944,257 - 153,944,715UniSTSGRCh37
Build 36X153,597,451 - 153,597,909RGDNCBI36
CeleraX154,102,840 - 154,103,298RGD
Cytogenetic MapXq28UniSTS
HuRefX142,488,184 - 142,488,642UniSTS
ECD18641  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,952,810 - 153,953,162UniSTSGRCh37
Build 36X153,606,004 - 153,606,356RGDNCBI36
CeleraX154,111,393 - 154,111,745RGD
Cytogenetic MapXq28UniSTS
HuRefX142,496,766 - 142,497,118UniSTS
ECD18725  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,947,765 - 153,948,114UniSTSGRCh37
Build 36X153,600,959 - 153,601,308RGDNCBI36
CeleraX154,106,348 - 154,106,697RGD
Cytogenetic MapXq28UniSTS
HuRefX142,491,720 - 142,492,069UniSTS
ECD18939  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,957,709 - 153,958,050UniSTSGRCh37
Build 36X153,610,903 - 153,611,244RGDNCBI36
CeleraX154,116,292 - 154,116,633RGD
Cytogenetic MapXq28UniSTS
HuRefX142,501,561 - 142,501,902UniSTS
ECD19365  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,961,383 - 153,961,707UniSTSGRCh37
Build 36X153,614,577 - 153,614,901RGDNCBI36
CeleraX154,119,966 - 154,120,290RGD
Cytogenetic MapXq28UniSTS
HuRefX142,505,235 - 142,505,559UniSTS
ECD19947  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,960,318 - 153,960,621UniSTSGRCh37
Build 36X153,613,512 - 153,613,815RGDNCBI36
CeleraX154,118,901 - 154,119,204RGD
Cytogenetic MapXq28UniSTS
HuRefX142,504,170 - 142,504,473UniSTS
ECD20170  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,906,426 - 153,906,720UniSTSGRCh37
Build 36X153,559,620 - 153,559,914RGDNCBI36
CeleraX154,064,494 - 154,064,788RGD
Cytogenetic MapXq28UniSTS
HuRefX142,450,530 - 142,450,824UniSTS
ECD21286  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,906,106 - 153,906,360UniSTSGRCh37
Build 36X153,559,300 - 153,559,554RGDNCBI36
CeleraX154,064,174 - 154,064,428RGD
Cytogenetic MapXq28UniSTS
HuRefX142,450,210 - 142,450,464UniSTS
ECD21980  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,967,264 - 153,967,497UniSTSGRCh37
Build 36X153,620,458 - 153,620,691RGDNCBI36
CeleraX154,125,843 - 154,126,076RGD
Cytogenetic MapXq28UniSTS
HuRefX142,511,112 - 142,511,345UniSTS
ECD22080  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,913,581 - 153,913,811UniSTSGRCh37
Build 36X153,566,775 - 153,567,005RGDNCBI36
CeleraX154,071,650 - 154,071,880RGD
Cytogenetic MapXq28UniSTS
HuRefX142,457,685 - 142,457,915UniSTS
ECD22398  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,925,823 - 153,926,043UniSTSGRCh37
Build 36X153,579,017 - 153,579,237RGDNCBI36
CeleraX154,084,408 - 154,084,628RGD
Cytogenetic MapXq28UniSTS
HuRefX142,469,882 - 142,470,102UniSTS
ECD22729  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,964,238 - 153,964,448UniSTSGRCh37
Build 36X153,617,432 - 153,617,642RGDNCBI36
CeleraX154,122,817 - 154,123,027RGD
Cytogenetic MapXq28UniSTS
HuRefX142,508,086 - 142,508,296UniSTS
ECD22844  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,963,528 - 153,963,734UniSTSGRCh37
Build 36X153,616,722 - 153,616,928RGDNCBI36
CeleraX154,122,107 - 154,122,313RGD
Cytogenetic MapXq28UniSTS
HuRefX142,507,376 - 142,507,582UniSTS
ECD23004  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,942,311 - 153,942,512UniSTSGRCh37
Build 36X153,595,505 - 153,595,706RGDNCBI36
CeleraX154,100,894 - 154,101,095RGD
Cytogenetic MapXq28UniSTS
HuRefX142,486,238 - 142,486,439UniSTS
ECD23229  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,929,550 - 153,929,745UniSTSGRCh37
Build 36X153,582,744 - 153,582,939RGDNCBI36
CeleraX154,088,135 - 154,088,330RGD
Cytogenetic MapXq28UniSTS
ECD23373  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,907,671 - 153,907,862UniSTSGRCh37
Build 36X153,560,865 - 153,561,056RGDNCBI36
CeleraX154,065,739 - 154,065,930RGD
Cytogenetic MapXq28UniSTS
HuRefX142,451,775 - 142,451,966UniSTS
ECD24232  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,959,585 - 153,959,735UniSTSGRCh37
Build 36X153,612,779 - 153,612,929RGDNCBI36
CeleraX154,118,168 - 154,118,318RGD
Cytogenetic MapXq28UniSTS
HuRefX142,503,437 - 142,503,587UniSTS
REN90211  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,903,205 - 153,903,462UniSTSGRCh37
Build 36X153,556,399 - 153,556,656RGDNCBI36
CeleraX154,061,273 - 154,061,530RGD
Cytogenetic MapXq28UniSTS
HuRefX142,447,309 - 142,447,566UniSTS
REN90212  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,903,456 - 153,903,706UniSTSGRCh37
Build 36X153,556,650 - 153,556,900RGDNCBI36
CeleraX154,061,524 - 154,061,774RGD
Cytogenetic MapXq28UniSTS
HuRefX142,447,560 - 142,447,810UniSTS
REN90213  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,903,699 - 153,903,929UniSTSGRCh37
Build 36X153,556,893 - 153,557,123RGDNCBI36
CeleraX154,061,767 - 154,061,997RGD
Cytogenetic MapXq28UniSTS
HuRefX142,447,803 - 142,448,033UniSTS
REN90214  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,903,905 - 153,904,169UniSTSGRCh37
Build 36X153,557,099 - 153,557,363RGDNCBI36
CeleraX154,061,973 - 154,062,237RGD
Cytogenetic MapXq28UniSTS
HuRefX142,448,009 - 142,448,273UniSTS
REN90215  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,904,146 - 153,904,385UniSTSGRCh37
Build 36X153,557,340 - 153,557,579RGDNCBI36
CeleraX154,062,214 - 154,062,453RGD
Cytogenetic MapXq28UniSTS
HuRefX142,448,250 - 142,448,489UniSTS
REN90216  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,904,348 - 153,904,599UniSTSGRCh37
Build 36X153,557,542 - 153,557,793RGDNCBI36
CeleraX154,062,416 - 154,062,667RGD
Cytogenetic MapXq28UniSTS
HuRefX142,448,452 - 142,448,703UniSTS
REN90217  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,904,555 - 153,904,799UniSTSGRCh37
Build 36X153,557,749 - 153,557,993RGDNCBI36
CeleraX154,062,623 - 154,062,867RGD
Cytogenetic MapXq28UniSTS
HuRefX142,448,659 - 142,448,903UniSTS
REN90218  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,904,766 - 153,905,000UniSTSGRCh37
Build 36X153,557,960 - 153,558,194RGDNCBI36
CeleraX154,062,834 - 154,063,068RGD
Cytogenetic MapXq28UniSTS
HuRefX142,448,870 - 142,449,104UniSTS
REN90219  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,904,984 - 153,905,234UniSTSGRCh37
Build 36X153,558,178 - 153,558,428RGDNCBI36
CeleraX154,063,052 - 154,063,302RGD
Cytogenetic MapXq28UniSTS
HuRefX142,449,088 - 142,449,338UniSTS
REN90220  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,905,219 - 153,905,467UniSTSGRCh37
Build 36X153,558,413 - 153,558,661RGDNCBI36
CeleraX154,063,287 - 154,063,535RGD
Cytogenetic MapXq28UniSTS
HuRefX142,449,323 - 142,449,571UniSTS
REN90221  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,905,444 - 153,905,696UniSTSGRCh37
Build 36X153,558,638 - 153,558,890RGDNCBI36
CeleraX154,063,512 - 154,063,764RGD
Cytogenetic MapXq28UniSTS
HuRefX142,449,548 - 142,449,800UniSTS
REN90222  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,905,673 - 153,905,911UniSTSGRCh37
Build 36X153,558,867 - 153,559,105RGDNCBI36
CeleraX154,063,741 - 154,063,979RGD
Cytogenetic MapXq28UniSTS
HuRefX142,449,777 - 142,450,015UniSTS
REN90223  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,905,885 - 153,906,128UniSTSGRCh37
Build 36X153,559,079 - 153,559,322RGDNCBI36
CeleraX154,063,953 - 154,064,196RGD
Cytogenetic MapXq28UniSTS
HuRefX142,449,989 - 142,450,232UniSTS
REN90224  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,906,103 - 153,906,355UniSTSGRCh37
Build 36X153,559,297 - 153,559,549RGDNCBI36
CeleraX154,064,171 - 154,064,423RGD
Cytogenetic MapXq28UniSTS
HuRefX142,450,207 - 142,450,459UniSTS
REN90225  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,906,332 - 153,906,585UniSTSGRCh37
Build 36X153,559,526 - 153,559,779RGDNCBI36
CeleraX154,064,400 - 154,064,653RGD
Cytogenetic MapXq28UniSTS
HuRefX142,450,436 - 142,450,689UniSTS
REN90226  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,906,562 - 153,906,803UniSTSGRCh37
Build 36X153,559,756 - 153,559,997RGDNCBI36
CeleraX154,064,630 - 154,064,871RGD
Cytogenetic MapXq28UniSTS
HuRefX142,450,666 - 142,450,907UniSTS
REN90227  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,906,749 - 153,906,981UniSTSGRCh37
Build 36X153,559,943 - 153,560,175RGDNCBI36
CeleraX154,064,817 - 154,065,049RGD
Cytogenetic MapXq28UniSTS
HuRefX142,450,853 - 142,451,085UniSTS
REN90228  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,907,123 - 153,907,369UniSTSGRCh37
Build 36X153,560,317 - 153,560,563RGDNCBI36
CeleraX154,065,191 - 154,065,437RGD
Cytogenetic MapXq28UniSTS
HuRefX142,451,227 - 142,451,473UniSTS
REN90229  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,907,345 - 153,907,611UniSTSGRCh37
Build 36X153,560,539 - 153,560,805RGDNCBI36
CeleraX154,065,413 - 154,065,679RGD
Cytogenetic MapXq28UniSTS
HuRefX142,451,449 - 142,451,715UniSTS
REN90230  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,907,584 - 153,907,826UniSTSGRCh37
Build 36X153,560,778 - 153,561,020RGDNCBI36
CeleraX154,065,652 - 154,065,894RGD
Cytogenetic MapXq28UniSTS
HuRefX142,451,688 - 142,451,930UniSTS
REN90231  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,907,822 - 153,908,062UniSTSGRCh37
Build 36X153,561,016 - 153,561,256RGDNCBI36
CeleraX154,065,890 - 154,066,130RGD
Cytogenetic MapXq28UniSTS
HuRefX142,451,926 - 142,452,166UniSTS
REN90232  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,908,037 - 153,908,286UniSTSGRCh37
Build 36X153,561,231 - 153,561,480RGDNCBI36
CeleraX154,066,105 - 154,066,354RGD
Cytogenetic MapXq28UniSTS
HuRefX142,452,141 - 142,452,390UniSTS
REN90233  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,908,267 - 153,908,539UniSTSGRCh37
Build 36X153,561,461 - 153,561,733RGDNCBI36
CeleraX154,066,335 - 154,066,607RGD
Cytogenetic MapXq28UniSTS
HuRefX142,452,371 - 142,452,643UniSTS
REN90234  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,908,532 - 153,908,774UniSTSGRCh37
Build 36X153,561,726 - 153,561,968RGDNCBI36
CeleraX154,066,600 - 154,066,842RGD
Cytogenetic MapXq28UniSTS
HuRefX142,452,636 - 142,452,878UniSTS
REN90235  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,908,752 - 153,908,989UniSTSGRCh37
Build 36X153,561,946 - 153,562,183RGDNCBI36
CeleraX154,066,820 - 154,067,057RGD
Cytogenetic MapXq28UniSTS
HuRefX142,452,856 - 142,453,093UniSTS
REN90236  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,908,969 - 153,909,219UniSTSGRCh37
Build 36X153,562,163 - 153,562,413RGDNCBI36
CeleraX154,067,037 - 154,067,287RGD
Cytogenetic MapXq28UniSTS
HuRefX142,453,073 - 142,453,323UniSTS
REN90237  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,909,196 - 153,909,430UniSTSGRCh37
Build 36X153,562,390 - 153,562,624RGDNCBI36
CeleraX154,067,264 - 154,067,498RGD
Cytogenetic MapXq28UniSTS
HuRefX142,453,300 - 142,453,534UniSTS
REN90238  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,909,402 - 153,909,655UniSTSGRCh37
Build 36X153,562,596 - 153,562,849RGDNCBI36
CeleraX154,067,470 - 154,067,723RGD
Cytogenetic MapXq28UniSTS
HuRefX142,453,506 - 142,453,759UniSTS
REN90239  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,909,653 - 153,909,877UniSTSGRCh37
Build 36X153,562,847 - 153,563,071RGDNCBI36
CeleraX154,067,721 - 154,067,945RGD
Cytogenetic MapXq28UniSTS
HuRefX142,453,757 - 142,453,981UniSTS
REN90240  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,909,839 - 153,910,104UniSTSGRCh37
Build 36X153,563,033 - 153,563,298RGDNCBI36
CeleraX154,067,907 - 154,068,172RGD
Cytogenetic MapXq28UniSTS
HuRefX142,453,943 - 142,454,208UniSTS
REN90241  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,910,065 - 153,910,289UniSTSGRCh37
Build 36X153,563,259 - 153,563,483RGDNCBI36
CeleraX154,068,133 - 154,068,357RGD
Cytogenetic MapXq28UniSTS
HuRefX142,454,169 - 142,454,393UniSTS
REN90242  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,910,265 - 153,910,504UniSTSGRCh37
Build 36X153,563,459 - 153,563,698RGDNCBI36
CeleraX154,068,333 - 154,068,572RGD
Cytogenetic MapXq28UniSTS
HuRefX142,454,369 - 142,454,608UniSTS
REN90243  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,910,441 - 153,910,669UniSTSGRCh37
Build 36X153,563,635 - 153,563,863RGDNCBI36
CeleraX154,068,509 - 154,068,737RGD
Cytogenetic MapXq28UniSTS
HuRefX142,454,545 - 142,454,773UniSTS
REN90244  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,910,624 - 153,910,888UniSTSGRCh37
Build 36X153,563,818 - 153,564,082RGDNCBI36
CeleraX154,068,692 - 154,068,956RGD
Cytogenetic MapXq28UniSTS
HuRefX142,454,728 - 142,454,992UniSTS
REN90245  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,911,282 - 153,911,506UniSTSGRCh37
Build 36X153,564,476 - 153,564,700RGDNCBI36
CeleraX154,069,350 - 154,069,574RGD
Cytogenetic MapXq28UniSTS
HuRefX142,455,386 - 142,455,610UniSTS
REN90246  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,911,480 - 153,911,734UniSTSGRCh37
Build 36X153,564,674 - 153,564,928RGDNCBI36
CeleraX154,069,548 - 154,069,802RGD
Cytogenetic MapXq28UniSTS
HuRefX142,455,584 - 142,455,838UniSTS
REN90247  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,911,711 - 153,911,936UniSTSGRCh37
Build 36X153,564,905 - 153,565,130RGDNCBI36
CeleraX154,069,779 - 154,070,004RGD
Cytogenetic MapXq28UniSTS
HuRefX142,455,815 - 142,456,040UniSTS
REN90248  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,911,901 - 153,912,150UniSTSGRCh37
Build 36X153,565,095 - 153,565,344RGDNCBI36
CeleraX154,069,969 - 154,070,218RGD
Cytogenetic MapXq28UniSTS
HuRefX142,456,005 - 142,456,254UniSTS
REN90249  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,912,140 - 153,912,397UniSTSGRCh37
Build 36X153,565,334 - 153,565,591RGDNCBI36
CeleraX154,070,208 - 154,070,465RGD
Cytogenetic MapXq28UniSTS
HuRefX142,456,244 - 142,456,501UniSTS
REN90250  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,912,351 - 153,912,609UniSTSGRCh37
Build 36X153,565,545 - 153,565,803RGDNCBI36
CeleraX154,070,419 - 154,070,677RGD
Cytogenetic MapXq28UniSTS
HuRefX142,456,455 - 142,456,713UniSTS
REN90251  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,912,520 - 153,912,766UniSTSGRCh37
Build 36X153,565,714 - 153,565,960RGDNCBI36
CeleraX154,070,588 - 154,070,834RGD
Cytogenetic MapXq28UniSTS
HuRefX142,456,624 - 142,456,870UniSTS
REN90252  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,912,747 - 153,913,017UniSTSGRCh37
Build 36X153,565,941 - 153,566,211RGDNCBI36
CeleraX154,070,815 - 154,071,085RGD
Cytogenetic MapXq28UniSTS
HuRefX142,456,851 - 142,457,121UniSTS
REN90253  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,913,000 - 153,913,247UniSTSGRCh37
Build 36X153,566,194 - 153,566,441RGDNCBI36
CeleraX154,071,068 - 154,071,315RGD
Cytogenetic MapXq28UniSTS
HuRefX142,457,104 - 142,457,351UniSTS
REN90254  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,913,225 - 153,913,471UniSTSGRCh37
Build 36X153,566,419 - 153,566,665RGDNCBI36
CeleraX154,071,293 - 154,071,540RGD
Cytogenetic MapXq28UniSTS
HuRefX142,457,329 - 142,457,575UniSTS
REN90255  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,913,437 - 153,913,661UniSTSGRCh37
Build 36X153,566,631 - 153,566,855RGDNCBI36
CeleraX154,071,506 - 154,071,730RGD
Cytogenetic MapXq28UniSTS
HuRefX142,457,541 - 142,457,765UniSTS
REN90256  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,913,627 - 153,913,881UniSTSGRCh37
Build 36X153,566,821 - 153,567,075RGDNCBI36
CeleraX154,071,696 - 154,071,950RGD
Cytogenetic MapXq28UniSTS
HuRefX142,457,731 - 142,457,985UniSTS
REN90257  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,913,787 - 153,914,013UniSTSGRCh37
Build 36X153,566,981 - 153,567,207RGDNCBI36
CeleraX154,071,856 - 154,072,082RGD
Cytogenetic MapXq28UniSTS
HuRefX142,457,891 - 142,458,117UniSTS
REN90258  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,913,990 - 153,914,256UniSTSGRCh37
Build 36X153,567,184 - 153,567,450RGDNCBI36
CeleraX154,072,059 - 154,072,325RGD
Cytogenetic MapXq28UniSTS
HuRefX142,458,094 - 142,458,360UniSTS
REN90259  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,914,249 - 153,914,498UniSTSGRCh37
Build 36X153,567,443 - 153,567,692RGDNCBI36
CeleraX154,072,318 - 154,072,567RGD
Cytogenetic MapXq28UniSTS
HuRefX142,458,353 - 142,458,602UniSTS
REN90260  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,914,360 - 153,914,613UniSTSGRCh37
Build 36X153,567,554 - 153,567,807RGDNCBI36
CeleraX154,072,429 - 154,072,682RGD
Cytogenetic MapXq28UniSTS
HuRefX142,458,464 - 142,458,717UniSTS
REN90261  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,914,549 - 153,914,800UniSTSGRCh37
Build 36X153,567,743 - 153,567,994RGDNCBI36
CeleraX154,072,618 - 154,072,869RGD
Cytogenetic MapXq28UniSTS
REN90262  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,914,771 - 153,915,016UniSTSGRCh37
Build 36X153,567,965 - 153,568,210RGDNCBI36
CeleraX154,072,840 - 154,073,085RGD
REN90263  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,914,954 - 153,915,191UniSTSGRCh37
Build 36X153,568,148 - 153,568,385RGDNCBI36
CeleraX154,073,023 - 154,073,813UniSTS
Cytogenetic MapXq28UniSTS
REN90264  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,915,159 - 153,915,389UniSTSGRCh37
Build 36X153,568,353 - 153,568,583RGDNCBI36
Cytogenetic MapXq28UniSTS
REN90265  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,915,377 - 153,915,636UniSTSGRCh37
Build 36X153,568,571 - 153,568,830RGDNCBI36
CeleraX154,073,999 - 154,074,258RGD
Cytogenetic MapXq28UniSTS
REN90266  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,915,963 - 153,916,189UniSTSGRCh37
Build 36X153,569,157 - 153,569,383RGDNCBI36
Cytogenetic MapXq28UniSTS
REN90267  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,916,165 - 153,916,420UniSTSGRCh37
Build 36X153,569,359 - 153,569,614RGDNCBI36
Cytogenetic MapXq28UniSTS
HuRefX142,460,223 - 142,460,478UniSTS
REN90268  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,916,299 - 153,916,544UniSTSGRCh37
Build 36X153,569,493 - 153,569,738RGDNCBI36
CeleraX154,074,884 - 154,075,129RGD
Cytogenetic MapXq28UniSTS
HuRefX142,460,357 - 142,460,602UniSTS
REN90269  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,916,855 - 153,917,083UniSTSGRCh37
Build 36X153,570,049 - 153,570,277RGDNCBI36
CeleraX154,075,440 - 154,075,668RGD
Cytogenetic MapXq28UniSTS
HuRefX142,460,913 - 142,461,141UniSTS
REN90271  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,919,741 - 153,919,965UniSTSGRCh37
Build 36X153,572,935 - 153,573,159RGDNCBI36
CeleraX154,078,326 - 154,078,550RGD
Cytogenetic MapXq28UniSTS
HuRefX142,463,799 - 142,464,023UniSTS
REN90272  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,919,898 - 153,920,164UniSTSGRCh37
Build 36X153,573,092 - 153,573,358RGDNCBI36
CeleraX154,078,483 - 154,078,749RGD
Cytogenetic MapXq28UniSTS
HuRefX142,463,956 - 142,464,222UniSTS
REN90273  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,920,141 - 153,920,376UniSTSGRCh37
Build 36X153,573,335 - 153,573,570RGDNCBI36
CeleraX154,078,726 - 154,078,961RGD
Cytogenetic MapXq28UniSTS
HuRefX142,464,199 - 142,464,434UniSTS
REN90274  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,920,222 - 153,920,481UniSTSGRCh37
Build 36X153,573,416 - 153,573,675RGDNCBI36
CeleraX154,078,807 - 154,079,066RGD
Cytogenetic MapXq28UniSTS
HuRefX142,464,280 - 142,464,539UniSTS
REN90275  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,920,407 - 153,920,643UniSTSGRCh37
Build 36X153,573,601 - 153,573,837RGDNCBI36
CeleraX154,078,992 - 154,079,228RGD
Cytogenetic MapXq28UniSTS
HuRefX142,464,465 - 142,464,701UniSTS
REN90276  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,920,537 - 153,920,765UniSTSGRCh37
Build 36X153,573,731 - 153,573,959RGDNCBI36
CeleraX154,079,122 - 154,079,350RGD
Cytogenetic MapXq28UniSTS
REN90277  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,921,105 - 153,921,340UniSTSGRCh37
Build 36X153,574,299 - 153,574,534RGDNCBI36
CeleraX154,079,690 - 154,079,925RGD
Cytogenetic MapXq28UniSTS
HuRefX142,465,164 - 142,465,399UniSTS
REN90278  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,921,314 - 153,921,539UniSTSGRCh37
Build 36X153,574,508 - 153,574,733RGDNCBI36
CeleraX154,079,899 - 154,080,124RGD
Cytogenetic MapXq28UniSTS
HuRefX142,465,373 - 142,465,598UniSTS
REN90279  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,921,509 - 153,921,763UniSTSGRCh37
Build 36X153,574,703 - 153,574,957RGDNCBI36
CeleraX154,080,094 - 154,080,348RGD
Cytogenetic MapXq28UniSTS
HuRefX142,465,568 - 142,465,822UniSTS
REN90280  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,921,746 - 153,921,997UniSTSGRCh37
Build 36X153,574,940 - 153,575,191RGDNCBI36
CeleraX154,080,331 - 154,080,582RGD
Cytogenetic MapXq28UniSTS
HuRefX142,465,805 - 142,466,056UniSTS
REN90281  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,921,985 - 153,922,259UniSTSGRCh37
Build 36X153,575,179 - 153,575,453RGDNCBI36
CeleraX154,080,570 - 154,080,844RGD
Cytogenetic MapXq28UniSTS
HuRefX142,466,044 - 142,466,318UniSTS
REN90282  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,922,239 - 153,922,483UniSTSGRCh37
Build 36X153,575,433 - 153,575,677RGDNCBI36
CeleraX154,080,824 - 154,081,068RGD
Cytogenetic MapXq28UniSTS
HuRefX142,466,298 - 142,466,542UniSTS
REN90283  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,922,409 - 153,922,658UniSTSGRCh37
Build 36X153,575,603 - 153,575,852RGDNCBI36
CeleraX154,080,994 - 154,081,243RGD
Cytogenetic MapXq28UniSTS
HuRefX142,466,468 - 142,466,717UniSTS
REN90284  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,922,498 - 153,922,747UniSTSGRCh37
Build 36X153,575,692 - 153,575,941RGDNCBI36
CeleraX154,081,083 - 154,081,332RGD
Cytogenetic MapXq28UniSTS
HuRefX142,466,557 - 142,466,806UniSTS
REN90285  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,922,965 - 153,923,189UniSTSGRCh37
Build 36X153,576,159 - 153,576,383RGDNCBI36
CeleraX154,081,550 - 154,081,774RGD
Cytogenetic MapXq28UniSTS
HuRefX142,467,024 - 142,467,248UniSTS
REN90286  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,923,139 - 153,923,395UniSTSGRCh37
Build 36X153,576,333 - 153,576,589RGDNCBI36
CeleraX154,081,724 - 154,081,980RGD
Cytogenetic MapXq28UniSTS
HuRefX142,467,198 - 142,467,454UniSTS
REN90287  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,923,375 - 153,923,629UniSTSGRCh37
Build 36X153,576,569 - 153,576,823RGDNCBI36
CeleraX154,081,960 - 154,082,214RGD
Cytogenetic MapXq28UniSTS
HuRefX142,467,434 - 142,467,688UniSTS
REN90288  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,923,606 - 153,923,856UniSTSGRCh37
Build 36X153,576,800 - 153,577,050RGDNCBI36
CeleraX154,082,191 - 154,082,441RGD
Cytogenetic MapXq28UniSTS
HuRefX142,467,665 - 142,467,915UniSTS
REN90289  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,923,846 - 153,924,085UniSTSGRCh37
Build 36X153,577,040 - 153,577,279RGDNCBI36
CeleraX154,082,431 - 154,082,670RGD
Cytogenetic MapXq28UniSTS
HuRefX142,467,905 - 142,468,144UniSTS
REN90290  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,924,062 - 153,924,302UniSTSGRCh37
Build 36X153,577,256 - 153,577,496RGDNCBI36
CeleraX154,082,647 - 154,082,887RGD
Cytogenetic MapXq28UniSTS
HuRefX142,468,121 - 142,468,361UniSTS
REN90291  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,924,279 - 153,924,538UniSTSGRCh37
Build 36X153,577,473 - 153,577,732RGDNCBI36
CeleraX154,082,864 - 154,083,123RGD
Cytogenetic MapXq28UniSTS
HuRefX142,468,338 - 142,468,597UniSTS
REN90292  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,924,533 - 153,924,763UniSTSGRCh37
Build 36X153,577,727 - 153,577,957RGDNCBI36
CeleraX154,083,118 - 154,083,348RGD
Cytogenetic MapXq28UniSTS
HuRefX142,468,592 - 142,468,822UniSTS
REN90293  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,924,740 - 153,924,993UniSTSGRCh37
Build 36X153,577,934 - 153,578,187RGDNCBI36
CeleraX154,083,325 - 154,083,578RGD
Cytogenetic MapXq28UniSTS
HuRefX142,468,799 - 142,469,052UniSTS
REN90294  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,924,974 - 153,925,222UniSTSGRCh37
Build 36X153,578,168 - 153,578,416RGDNCBI36
CeleraX154,083,559 - 154,083,807RGD
Cytogenetic MapXq28UniSTS
HuRefX142,469,033 - 142,469,281UniSTS
REN90295  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,925,195 - 153,925,445UniSTSGRCh37
Build 36X153,578,389 - 153,578,639RGDNCBI36
CeleraX154,083,780 - 154,084,030RGD
Cytogenetic MapXq28UniSTS
HuRefX142,469,254 - 142,469,504UniSTS
REN90296  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,925,422 - 153,925,686UniSTSGRCh37
Build 36X153,578,616 - 153,578,880RGDNCBI36
CeleraX154,084,007 - 154,084,271RGD
Cytogenetic MapXq28UniSTS
HuRefX142,469,481 - 142,469,745UniSTS
REN90297  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,925,664 - 153,925,912UniSTSGRCh37
Build 36X153,578,858 - 153,579,106RGDNCBI36
CeleraX154,084,249 - 154,084,497RGD
Cytogenetic MapXq28UniSTS
HuRefX142,469,723 - 142,469,971UniSTS
REN90298  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,925,902 - 153,926,150UniSTSGRCh37
Build 36X153,579,096 - 153,579,344RGDNCBI36
CeleraX154,084,487 - 154,084,735RGD
Cytogenetic MapXq28UniSTS
HuRefX142,469,961 - 142,470,209UniSTS
REN90299  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,926,109 - 153,926,347UniSTSGRCh37
Build 36X153,579,303 - 153,579,541RGDNCBI36
CeleraX154,084,694 - 154,084,932RGD
Cytogenetic MapXq28UniSTS
HuRefX142,470,168 - 142,470,406UniSTS
REN90300  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,926,324 - 153,926,574UniSTSGRCh37
Build 36X153,579,518 - 153,579,768RGDNCBI36
CeleraX154,084,909 - 154,085,159RGD
Cytogenetic MapXq28UniSTS
HuRefX142,470,383 - 142,470,633UniSTS
REN90301  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,926,557 - 153,926,820UniSTSGRCh37
Build 36X153,579,751 - 153,580,014RGDNCBI36
CeleraX154,085,142 - 154,085,405RGD
Cytogenetic MapXq28UniSTS
HuRefX142,470,616 - 142,470,879UniSTS
REN90302  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,926,790 - 153,927,024UniSTSGRCh37
Build 36X153,579,984 - 153,580,218RGDNCBI36
CeleraX154,085,375 - 154,085,609RGD
Cytogenetic MapXq28UniSTS
HuRefX142,470,849 - 142,471,083UniSTS
REN90303  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,927,000 - 153,927,238UniSTSGRCh37
Build 36X153,580,194 - 153,580,432RGDNCBI36
CeleraX154,085,585 - 154,085,823RGD
Cytogenetic MapXq28UniSTS
HuRefX142,471,059 - 142,471,297UniSTS
REN90304  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,927,210 - 153,927,460UniSTSGRCh37
Build 36X153,580,404 - 153,580,654RGDNCBI36
CeleraX154,085,795 - 154,086,045RGD
Cytogenetic MapXq28UniSTS
HuRefX142,471,269 - 142,471,519UniSTS
REN90305  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,927,429 - 153,927,671UniSTSGRCh37
Build 36X153,580,623 - 153,580,865RGDNCBI36
CeleraX154,086,014 - 154,086,256RGD
Cytogenetic MapXq28UniSTS
HuRefX142,471,488 - 142,471,730UniSTS
REN90306  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,927,667 - 153,927,922UniSTSGRCh37
Build 36X153,580,861 - 153,581,116RGDNCBI36
CeleraX154,086,252 - 154,086,507RGD
Cytogenetic MapXq28UniSTS
HuRefX142,471,726 - 142,471,981UniSTS
REN90307  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,927,913 - 153,928,164UniSTSGRCh37
Build 36X153,581,107 - 153,581,358RGDNCBI36
CeleraX154,086,498 - 154,086,749RGD
Cytogenetic MapXq28UniSTS
HuRefX142,471,972 - 142,472,223UniSTS
REN90308  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,928,157 - 153,928,405UniSTSGRCh37
Build 36X153,581,351 - 153,581,599RGDNCBI36
CeleraX154,086,742 - 154,086,990RGD
Cytogenetic MapXq28UniSTS
HuRefX142,472,216 - 142,472,464UniSTS
REN90309  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,928,400 - 153,928,636UniSTSGRCh37
Build 36X153,581,594 - 153,581,830RGDNCBI36
CeleraX154,086,985 - 154,087,221RGD
Cytogenetic MapXq28UniSTS
HuRefX142,472,459 - 142,472,695UniSTS
REN90310  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,928,605 - 153,928,830UniSTSGRCh37
Build 36X153,581,799 - 153,582,024RGDNCBI36
CeleraX154,087,190 - 154,087,415RGD
Cytogenetic MapXq28UniSTS
HuRefX142,472,664 - 142,472,889UniSTS
REN90311  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,928,801 - 153,929,059UniSTSGRCh37
Build 36X153,581,995 - 153,582,253RGDNCBI36
CeleraX154,087,386 - 154,087,644RGD
Cytogenetic MapXq28UniSTS
HuRefX142,472,860 - 142,473,118UniSTS
REN90312  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,929,005 - 153,929,243UniSTSGRCh37
Build 36X153,582,199 - 153,582,437RGDNCBI36
CeleraX154,087,590 - 154,087,828RGD
Cytogenetic MapXq28UniSTS
HuRefX142,473,064 - 142,473,302UniSTS
REN90313  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,929,219 - 153,929,489UniSTSGRCh37
Build 36X153,582,413 - 153,582,683RGDNCBI36
CeleraX154,087,804 - 154,088,074RGD
Cytogenetic MapXq28UniSTS
HuRefX142,473,278 - 142,473,548UniSTS
REN90314  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,929,485 - 153,929,729UniSTSGRCh37
Build 36X153,582,679 - 153,582,923RGDNCBI36
CeleraX154,088,070 - 154,088,314RGD
Cytogenetic MapXq28UniSTS
HuRefX142,473,544 - 142,473,664UniSTS
REN90315  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,929,706 - 153,929,956UniSTSGRCh37
Build 36X153,582,900 - 153,583,150RGDNCBI36
CeleraX154,088,291 - 154,088,541RGD
Cytogenetic MapXq28UniSTS
HuRefX142,473,641 - 142,473,891UniSTS
REN90316  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,929,857 - 153,930,128UniSTSGRCh37
Build 36X153,583,051 - 153,583,322RGDNCBI36
CeleraX154,088,442 - 154,088,713RGD
Cytogenetic MapXq28UniSTS
HuRefX142,473,792 - 142,474,063UniSTS
REN90317  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,930,245 - 153,930,482UniSTSGRCh37
Build 36X153,583,439 - 153,583,676RGDNCBI36
CeleraX154,088,830 - 154,089,067RGD
Cytogenetic MapXq28UniSTS
HuRefX142,474,180 - 142,474,417UniSTS
REN90318  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,930,297 - 153,930,567UniSTSGRCh37
Build 36X153,583,491 - 153,583,761RGDNCBI36
CeleraX154,088,882 - 154,089,152RGD
Cytogenetic MapXq28UniSTS
HuRefX142,474,232 - 142,474,502UniSTS
REN90319  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,930,738 - 153,930,987UniSTSGRCh37
Build 36X153,583,932 - 153,584,181RGDNCBI36
CeleraX154,089,323 - 154,089,572RGD
Cytogenetic MapXq28UniSTS
HuRefX142,474,673 - 142,474,922UniSTS
REN90320  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,930,832 - 153,931,080UniSTSGRCh37
Build 36X153,584,026 - 153,584,274RGDNCBI36
CeleraX154,089,417 - 154,089,665RGD
Cytogenetic MapXq28UniSTS
HuRefX142,474,767 - 142,475,015UniSTS
REN90321  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,931,011 - 153,931,238UniSTSGRCh37
Build 36X153,584,205 - 153,584,432RGDNCBI36
CeleraX154,089,596 - 154,089,823RGD
Cytogenetic MapXq28UniSTS
HuRefX142,474,946 - 142,475,173UniSTS
REN90322  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,931,203 - 153,931,430UniSTSGRCh37
Build 36X153,584,397 - 153,584,624RGDNCBI36
CeleraX154,089,788 - 154,090,015RGD
Cytogenetic MapXq28UniSTS
HuRefX142,475,138 - 142,475,365UniSTS
REN90323  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,931,390 - 153,931,647UniSTSGRCh37
Build 36X153,584,584 - 153,584,841RGDNCBI36
CeleraX154,089,975 - 154,090,232RGD
Cytogenetic MapXq28UniSTS
HuRefX142,475,325 - 142,475,582UniSTS
REN90324  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,931,643 - 153,931,881UniSTSGRCh37
Build 36X153,584,837 - 153,585,075RGDNCBI36
CeleraX154,090,228 - 154,090,466RGD
Cytogenetic MapXq28UniSTS
HuRefX142,475,578 - 142,475,816UniSTS
REN90325  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,931,771 - 153,931,996UniSTSGRCh37
Build 36X153,584,965 - 153,585,190RGDNCBI36
CeleraX154,090,356 - 154,090,581RGD
Cytogenetic MapXq28UniSTS
HuRefX142,475,706 - 142,475,931UniSTS
REN90326  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,931,973 - 153,932,197UniSTSGRCh37
Build 36X153,585,167 - 153,585,391RGDNCBI36
CeleraX154,090,558 - 154,090,782RGD
Cytogenetic MapXq28UniSTS
HuRefX142,475,908 - 142,476,132UniSTS
REN90327  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,932,172 - 153,932,417UniSTSGRCh37
Build 36X153,585,366 - 153,585,611RGDNCBI36
CeleraX154,090,757 - 154,091,002RGD
Cytogenetic MapXq28UniSTS
HuRefX142,476,107 - 142,476,352UniSTS
REN90328  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,932,376 - 153,932,633UniSTSGRCh37
Build 36X153,585,570 - 153,585,827RGDNCBI36
CeleraX154,090,961 - 154,091,218RGD
Cytogenetic MapXq28UniSTS
HuRefX142,476,311 - 142,476,568UniSTS
REN90329  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,932,605 - 153,932,839UniSTSGRCh37
Build 36X153,585,799 - 153,586,033RGDNCBI36
CeleraX154,091,190 - 154,091,424RGD
Cytogenetic MapXq28UniSTS
HuRefX142,476,540 - 142,476,774UniSTS
REN90330  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,932,821 - 153,933,048UniSTSGRCh37
Build 36X153,586,015 - 153,586,242RGDNCBI36
CeleraX154,091,406 - 154,091,633RGD
Cytogenetic MapXq28UniSTS
HuRefX142,476,756 - 142,476,983UniSTS
REN90331  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,933,023 - 153,933,271UniSTSGRCh37
Build 36X153,586,217 - 153,586,465RGDNCBI36
CeleraX154,091,608 - 154,091,856RGD
Cytogenetic MapXq28UniSTS
HuRefX142,476,958 - 142,477,206UniSTS
REN90332  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,933,128 - 153,933,354UniSTSGRCh37
GRCh37X153,933,128 - 153,933,309UniSTSGRCh37
GRCh37X153,933,128 - 153,933,307UniSTSGRCh37
Build 36X153,586,322 - 153,586,503RGDNCBI36
CeleraX154,091,713 - 154,091,892UniSTS
CeleraX154,091,713 - 154,091,939UniSTS
CeleraX154,091,713 - 154,091,894RGD
Cytogenetic MapXq28UniSTS
HuRefX142,477,063 - 142,477,289UniSTS
HuRefX142,477,063 - 142,477,242UniSTS
HuRefX142,477,063 - 142,477,244UniSTS
REN90333  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,933,325 - 153,933,573UniSTSGRCh37
Build 36X153,586,519 - 153,586,767RGDNCBI36
CeleraX154,091,910 - 154,092,158RGD
Cytogenetic MapXq28UniSTS
HuRefX142,477,260 - 142,477,508UniSTS
REN90334  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,933,495 - 153,933,740UniSTSGRCh37
Build 36X153,586,689 - 153,586,934RGDNCBI36
CeleraX154,092,080 - 154,092,325RGD
Cytogenetic MapXq28UniSTS
HuRefX142,477,430 - 142,477,675UniSTS
REN90335  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,933,717 - 153,933,977UniSTSGRCh37
Build 36X153,586,911 - 153,587,171RGDNCBI36
CeleraX154,092,302 - 154,092,562RGD
Cytogenetic MapXq28UniSTS
HuRefX142,477,652 - 142,477,912UniSTS
REN90336  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,933,908 - 153,934,132UniSTSGRCh37
Build 36X153,587,102 - 153,587,326RGDNCBI36
CeleraX154,092,493 - 154,092,717RGD
Cytogenetic MapXq28UniSTS
HuRefX142,477,843 - 142,478,067UniSTS
REN90337  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,934,105 - 153,934,329UniSTSGRCh37
Build 36X153,587,299 - 153,587,523RGDNCBI36
CeleraX154,092,690 - 154,092,914RGD
Cytogenetic MapXq28UniSTS
HuRefX142,478,040 - 142,478,264UniSTS
REN90338  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,934,555 - 153,934,779UniSTSGRCh37
Build 36X153,587,749 - 153,587,973RGDNCBI36
CeleraX154,093,140 - 154,093,363RGD
Cytogenetic MapXq28UniSTS
HuRefX142,478,490 - 142,478,713UniSTS
REN90339  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,934,730 - 153,934,959UniSTSGRCh37
Build 36X153,587,924 - 153,588,153RGDNCBI36
CeleraX154,093,314 - 154,093,543RGD
Cytogenetic MapXq28UniSTS
HuRefX142,478,664 - 142,478,893UniSTS
REN90340  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,934,895 - 153,935,132UniSTSGRCh37
Build 36X153,588,089 - 153,588,326RGDNCBI36
CeleraX154,093,479 - 154,093,716RGD
Cytogenetic MapXq28UniSTS
HuRefX142,478,829 - 142,479,066UniSTS
REN90341  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,935,045 - 153,935,293UniSTSGRCh37
Build 36X153,588,239 - 153,588,487RGDNCBI36
CeleraX154,093,629 - 154,093,877RGD
Cytogenetic MapXq28UniSTS
HuRefX142,478,979 - 142,479,228UniSTS
REN90342  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,935,282 - 153,935,539UniSTSGRCh37
Build 36X153,588,476 - 153,588,733RGDNCBI36
CeleraX154,093,866 - 154,094,123RGD
Cytogenetic MapXq28UniSTS
HuRefX142,479,217 - 142,479,474UniSTS
REN90343  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,935,457 - 153,935,688UniSTSGRCh37
Build 36X153,588,651 - 153,588,882RGDNCBI36
CeleraX154,094,041 - 154,094,272RGD
Cytogenetic MapXq28UniSTS
HuRefX142,479,392 - 142,479,623UniSTS
REN90344  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,935,611 - 153,935,878UniSTSGRCh37
Build 36X153,588,805 - 153,589,072RGDNCBI36
CeleraX154,094,195 - 154,094,462RGD
Cytogenetic MapXq28UniSTS
HuRefX142,479,546 - 142,479,813UniSTS
REN90345  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,935,852 - 153,936,091UniSTSGRCh37
Build 36X153,589,046 - 153,589,285RGDNCBI36
CeleraX154,094,436 - 154,094,675RGD
Cytogenetic MapXq28UniSTS
HuRefX142,479,787 - 142,480,026UniSTS
REN90346  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,936,067 - 153,936,293UniSTSGRCh37
Build 36X153,589,261 - 153,589,487RGDNCBI36
CeleraX154,094,651 - 154,094,877RGD
Cytogenetic MapXq28UniSTS
HuRefX142,480,002 - 142,480,228UniSTS
REN90347  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,936,263 - 153,936,487UniSTSGRCh37
Build 36X153,589,457 - 153,589,681RGDNCBI36
CeleraX154,094,847 - 154,095,071RGD
Cytogenetic MapXq28UniSTS
HuRefX142,480,198 - 142,480,422UniSTS
REN90348  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,936,439 - 153,936,692UniSTSGRCh37
Build 36X153,589,633 - 153,589,886RGDNCBI36
CeleraX154,095,023 - 154,095,276RGD
Cytogenetic MapXq28UniSTS
HuRefX142,480,374 - 142,480,627UniSTS
REN90349  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,936,669 - 153,936,912UniSTSGRCh37
Build 36X153,589,863 - 153,590,106RGDNCBI36
CeleraX154,095,253 - 154,095,496RGD
Cytogenetic MapXq28UniSTS
HuRefX142,480,604 - 142,480,847UniSTS
REN90350  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,936,782 - 153,937,021UniSTSGRCh37
Build 36X153,589,976 - 153,590,215RGDNCBI36
CeleraX154,095,366 - 154,095,605RGD
Cytogenetic MapXq28UniSTS
HuRefX142,480,717 - 142,480,956UniSTS
REN90351  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,936,986 - 153,937,230UniSTSGRCh37
Build 36X153,590,180 - 153,590,424RGDNCBI36
CeleraX154,095,570 - 154,095,814RGD
Cytogenetic MapXq28UniSTS
HuRefX142,480,921 - 142,481,165UniSTS
REN90352  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,937,579 - 153,937,831UniSTSGRCh37
Build 36X153,590,773 - 153,591,025RGDNCBI36
CeleraX154,096,163 - 154,096,414RGD
Cytogenetic MapXq28UniSTS
HuRefX142,481,514 - 142,481,765UniSTS
REN90353  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,937,806 - 153,938,067UniSTSGRCh37
Build 36X153,591,000 - 153,591,261RGDNCBI36
CeleraX154,096,389 - 154,096,650RGD
Cytogenetic MapXq28UniSTS
HuRefX142,481,740 - 142,482,001UniSTS
REN90354  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,938,043 - 153,938,281UniSTSGRCh37
Build 36X153,591,237 - 153,591,475RGDNCBI36
CeleraX154,096,626 - 154,096,864RGD
Cytogenetic MapXq28UniSTS
HuRefX142,481,977 - 142,482,215UniSTS
REN90355  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,938,254 - 153,938,507UniSTSGRCh37
Build 36X153,591,448 - 153,591,701RGDNCBI36
CeleraX154,096,837 - 154,097,090RGD
Cytogenetic MapXq28UniSTS
HuRefX142,482,188 - 142,482,442UniSTS
REN90356  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,938,482 - 153,938,742UniSTSGRCh37
Build 36X153,591,676 - 153,591,936RGDNCBI36
CeleraX154,097,065 - 154,097,325RGD
Cytogenetic MapXq28UniSTS
HuRefX142,482,417 - 142,482,677UniSTS
REN90357  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,938,741 - 153,938,982UniSTSGRCh37
Build 36X153,591,935 - 153,592,176RGDNCBI36
CeleraX154,097,324 - 154,097,565RGD
Cytogenetic MapXq28UniSTS
HuRefX142,482,676 - 142,482,917UniSTS
REN90358  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,938,978 - 153,939,223UniSTSGRCh37
Build 36X153,592,172 - 153,592,417RGDNCBI36
CeleraX154,097,561 - 154,097,806RGD
Cytogenetic MapXq28UniSTS
HuRefX142,482,913 - 142,483,158UniSTS
REN90359  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,939,193 - 153,939,447UniSTSGRCh37
Build 36X153,592,387 - 153,592,641RGDNCBI36
CeleraX154,097,776 - 154,098,030RGD
Cytogenetic MapXq28UniSTS
HuRefX142,483,128 - 142,483,382UniSTS
REN90360  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,939,444 - 153,939,687UniSTSGRCh37
Build 36X153,592,638 - 153,592,881RGDNCBI36
CeleraX154,098,027 - 154,098,270RGD
Cytogenetic MapXq28UniSTS
HuRefX142,483,379 - 142,483,622UniSTS
REN90361  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,939,661 - 153,939,912UniSTSGRCh37
Build 36X153,592,855 - 153,593,106RGDNCBI36
CeleraX154,098,244 - 154,098,495RGD
Cytogenetic MapXq28UniSTS
HuRefX142,483,596 - 142,483,847UniSTS
REN90362  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,939,904 - 153,940,161UniSTSGRCh37
Build 36X153,593,098 - 153,593,355RGDNCBI36
CeleraX154,098,487 - 154,098,744RGD
Cytogenetic MapXq28UniSTS
HuRefX142,483,839 - 142,484,096UniSTS
REN90363  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,940,159 - 153,940,395UniSTSGRCh37
Build 36X153,593,353 - 153,593,589RGDNCBI36
CeleraX154,098,742 - 154,098,978RGD
Cytogenetic MapXq28UniSTS
HuRefX142,484,094 - 142,484,330UniSTS
REN90364  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,940,388 - 153,940,635UniSTSGRCh37
Build 36X153,593,582 - 153,593,829RGDNCBI36
CeleraX154,098,971 - 154,099,218RGD
Cytogenetic MapXq28UniSTS
HuRefX142,484,323 - 142,484,570UniSTS
REN90365  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,940,612 - 153,940,876UniSTSGRCh37
Build 36X153,593,806 - 153,594,070RGDNCBI36
CeleraX154,099,195 - 154,099,459RGD
Cytogenetic MapXq28UniSTS
HuRefX142,484,547 - 142,484,811UniSTS
REN90366  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,940,855 - 153,941,113UniSTSGRCh37
Build 36X153,594,049 - 153,594,307RGDNCBI36
CeleraX154,099,438 - 154,099,696RGD
Cytogenetic MapXq28UniSTS
HuRefX142,484,790 - 142,485,048UniSTS
REN90367  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,941,106 - 153,941,351UniSTSGRCh37
Build 36X153,594,300 - 153,594,545RGDNCBI36
CeleraX154,099,689 - 154,099,934RGD
Cytogenetic MapXq28UniSTS
HuRefX142,485,041 - 142,485,286UniSTS
REN90368  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,941,328 - 153,941,579UniSTSGRCh37
Build 36X153,594,522 - 153,594,773RGDNCBI36
CeleraX154,099,911 - 154,100,162RGD
Cytogenetic MapXq28UniSTS
HuRefX142,485,263 - 142,485,514UniSTS
REN90369  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,941,556 - 153,941,807UniSTSGRCh37
Build 36X153,594,750 - 153,595,001RGDNCBI36
CeleraX154,100,139 - 154,100,390RGD
Cytogenetic MapXq28UniSTS
HuRefX142,485,491 - 142,485,742UniSTS
REN90370  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,941,756 - 153,941,997UniSTSGRCh37
Build 36X153,594,950 - 153,595,191RGDNCBI36
CeleraX154,100,339 - 154,100,580RGD
Cytogenetic MapXq28UniSTS
HuRefX142,485,691 - 142,485,932UniSTS
REN90371  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,941,978 - 153,942,232UniSTSGRCh37
Build 36X153,595,172 - 153,595,426RGDNCBI36
CeleraX154,100,561 - 154,100,815RGD
Cytogenetic MapXq28UniSTS
HuRefX142,485,913 - 142,486,159UniSTS
REN90372  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,942,209 - 153,942,456UniSTSGRCh37
Build 36X153,595,403 - 153,595,650RGDNCBI36
CeleraX154,100,792 - 154,101,039RGD
Cytogenetic MapXq28UniSTS
HuRefX142,486,136 - 142,486,383UniSTS
REN90373  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,942,442 - 153,942,695UniSTSGRCh37
Build 36X153,595,636 - 153,595,889RGDNCBI36
CeleraX154,101,025 - 154,101,278RGD
Cytogenetic MapXq28UniSTS
HuRefX142,486,369 - 142,486,622UniSTS
REN90374  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,942,672 - 153,942,899UniSTSGRCh37
Build 36X153,595,866 - 153,596,093RGDNCBI36
CeleraX154,101,255 - 154,101,482RGD
Cytogenetic MapXq28UniSTS
HuRefX142,486,599 - 142,486,826UniSTS
REN90375  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,942,877 - 153,943,137UniSTSGRCh37
Build 36X153,596,071 - 153,596,331RGDNCBI36
CeleraX154,101,460 - 154,101,720RGD
Cytogenetic MapXq28UniSTS
HuRefX142,486,804 - 142,487,064UniSTS
REN90376  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,943,134 - 153,943,388UniSTSGRCh37
Build 36X153,596,328 - 153,596,582RGDNCBI36
CeleraX154,101,717 - 154,101,971RGD
Cytogenetic MapXq28UniSTS
HuRefX142,487,061 - 142,487,315UniSTS
REN90377  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,943,374 - 153,943,617UniSTSGRCh37
Build 36X153,596,568 - 153,596,811RGDNCBI36
CeleraX154,101,957 - 154,102,200RGD
Cytogenetic MapXq28UniSTS
HuRefX142,487,301 - 142,487,544UniSTS
REN90378  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,943,594 - 153,943,841UniSTSGRCh37
Build 36X153,596,788 - 153,597,035RGDNCBI36
CeleraX154,102,177 - 154,102,424RGD
Cytogenetic MapXq28UniSTS
HuRefX142,487,521 - 142,487,768UniSTS
REN90379  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,943,837 - 153,944,090UniSTSGRCh37
Build 36X153,597,031 - 153,597,284RGDNCBI36
CeleraX154,102,420 - 154,102,673RGD
Cytogenetic MapXq28UniSTS
HuRefX142,487,764 - 142,488,017UniSTS
REN90380  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,944,066 - 153,944,316UniSTSGRCh37
Build 36X153,597,260 - 153,597,510RGDNCBI36
CeleraX154,102,649 - 154,102,899RGD
Cytogenetic MapXq28UniSTS
HuRefX142,487,993 - 142,488,243UniSTS
REN90381  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,944,286 - 153,944,542UniSTSGRCh37
Build 36X153,597,480 - 153,597,736RGDNCBI36
CeleraX154,102,869 - 154,103,125RGD
Cytogenetic MapXq28UniSTS
HuRefX142,488,213 - 142,488,469UniSTS
REN90382  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,944,534 - 153,944,784UniSTSGRCh37
Build 36X153,597,728 - 153,597,978RGDNCBI36
CeleraX154,103,117 - 154,103,367RGD
Cytogenetic MapXq28UniSTS
HuRefX142,488,461 - 142,488,711UniSTS
REN90383  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,944,766 - 153,945,028UniSTSGRCh37
Build 36X153,597,960 - 153,598,222RGDNCBI36
CeleraX154,103,349 - 154,103,611RGD
Cytogenetic MapXq28UniSTS
HuRefX142,488,693 - 142,488,955UniSTS
REN90384  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,945,005 - 153,945,253UniSTSGRCh37
Build 36X153,598,199 - 153,598,447RGDNCBI36
CeleraX154,103,588 - 154,103,836RGD
Cytogenetic MapXq28UniSTS
HuRefX142,488,932 - 142,489,180UniSTS
REN90385  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,945,241 - 153,945,487UniSTSGRCh37
Build 36X153,598,435 - 153,598,681RGDNCBI36
CeleraX154,103,824 - 154,104,070RGD
Cytogenetic MapXq28UniSTS
HuRefX142,489,168 - 142,489,414UniSTS
REN90386  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,945,460 - 153,945,706UniSTSGRCh37
Build 36X153,598,654 - 153,598,900RGDNCBI36
CeleraX154,104,043 - 154,104,289RGD
Cytogenetic MapXq28UniSTS
HuRefX142,489,387 - 142,489,633UniSTS
REN90387  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,945,682 - 153,945,935UniSTSGRCh37
Build 36X153,598,876 - 153,599,129RGDNCBI36
CeleraX154,104,265 - 154,104,518RGD
Cytogenetic MapXq28UniSTS
HuRefX142,489,609 - 142,489,862UniSTS
REN90388  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,945,912 - 153,946,147UniSTSGRCh37
Build 36X153,599,106 - 153,599,341RGDNCBI36
CeleraX154,104,495 - 154,104,730RGD
Cytogenetic MapXq28UniSTS
HuRefX142,489,839 - 142,490,074UniSTS
REN90389  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,946,108 - 153,946,371UniSTSGRCh37
Build 36X153,599,302 - 153,599,565RGDNCBI36
CeleraX154,104,691 - 154,104,954RGD
Cytogenetic MapXq28UniSTS
HuRefX142,490,035 - 142,490,298UniSTS
REN90390  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,946,357 - 153,946,601UniSTSGRCh37
Build 36X153,599,551 - 153,599,795RGDNCBI36
CeleraX154,104,940 - 154,105,184RGD
Cytogenetic MapXq28UniSTS
HuRefX142,490,284 - 142,490,528UniSTS
REN90391  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,946,575 - 153,946,826UniSTSGRCh37
Build 36X153,599,769 - 153,600,020RGDNCBI36
CeleraX154,105,158 - 154,105,409RGD
Cytogenetic MapXq28UniSTS
REN90392  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,946,800 - 153,947,056UniSTSGRCh37
Build 36X153,599,994 - 153,600,250RGDNCBI36
CeleraX154,105,383 - 154,105,639RGD
Cytogenetic MapXq28UniSTS
REN90393  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,947,041 - 153,947,293UniSTSGRCh37
Build 36X153,600,235 - 153,600,487RGDNCBI36
CeleraX154,105,624 - 154,105,876RGD
Cytogenetic MapXq28UniSTS
REN90394  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,947,290 - 153,947,540UniSTSGRCh37
Build 36X153,600,484 - 153,600,734RGDNCBI36
CeleraX154,105,873 - 154,106,123RGD
Cytogenetic MapXq28UniSTS
HuRefX142,491,245 - 142,491,495UniSTS
REN90395  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,947,515 - 153,947,787UniSTSGRCh37
Build 36X153,600,709 - 153,600,981RGDNCBI36
CeleraX154,106,098 - 154,106,370RGD
Cytogenetic MapXq28UniSTS
HuRefX142,491,470 - 142,491,742UniSTS
REN90396  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,947,773 - 153,948,030UniSTSGRCh37
Build 36X153,600,967 - 153,601,224RGDNCBI36
CeleraX154,106,356 - 154,106,613RGD
Cytogenetic MapXq28UniSTS
HuRefX142,491,728 - 142,491,985UniSTS
REN90397  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,948,022 - 153,948,262UniSTSGRCh37
Build 36X153,601,216 - 153,601,456RGDNCBI36
CeleraX154,106,605 - 154,106,845RGD
Cytogenetic MapXq28UniSTS
HuRefX142,491,977 - 142,492,217UniSTS
REN90398  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,948,251 - 153,948,486UniSTSGRCh37
Build 36X153,601,445 - 153,601,680RGDNCBI36
CeleraX154,106,834 - 154,107,069RGD
Cytogenetic MapXq28UniSTS
HuRefX142,492,206 - 142,492,441UniSTS
REN90399  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,948,456 - 153,948,701UniSTSGRCh37
Build 36X153,601,650 - 153,601,895RGDNCBI36
CeleraX154,107,039 - 154,107,284RGD
Cytogenetic MapXq28UniSTS
HuRefX142,492,411 - 142,492,656UniSTS
REN90400  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,948,921 - 153,949,149UniSTSGRCh37
Build 36X153,602,115 - 153,602,343RGDNCBI36
CeleraX154,107,504 - 154,107,732RGD
Cytogenetic MapXq28UniSTS
HuRefX142,492,876 - 142,493,104UniSTS
REN90401  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,949,119 - 153,949,374UniSTSGRCh37
Build 36X153,602,313 - 153,602,568RGDNCBI36
CeleraX154,107,702 - 154,107,957RGD
Cytogenetic MapXq28UniSTS
HuRefX142,493,074 - 142,493,329UniSTS
REN90402  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,949,353 - 153,949,607UniSTSGRCh37
Build 36X153,602,547 - 153,602,801RGDNCBI36
CeleraX154,107,936 - 154,108,190RGD
Cytogenetic MapXq28UniSTS
HuRefX142,493,308 - 142,493,562UniSTS
REN90403  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,949,526 - 153,949,781UniSTSGRCh37
Build 36X153,602,720 - 153,602,975RGDNCBI36
CeleraX154,108,109 - 154,108,364RGD
Cytogenetic MapXq28UniSTS
HuRefX142,493,481 - 142,493,736UniSTS
REN90404  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,949,780 - 153,950,046UniSTSGRCh37
Build 36X153,602,974 - 153,603,240RGDNCBI36
CeleraX154,108,363 - 154,108,629RGD
Cytogenetic MapXq28UniSTS
HuRefX142,493,735 - 142,494,001UniSTS
REN90405  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,950,023 - 153,950,287UniSTSGRCh37
Build 36X153,603,217 - 153,603,481RGDNCBI36
CeleraX154,108,606 - 154,108,870RGD
Cytogenetic MapXq28UniSTS
HuRefX142,493,978 - 142,494,242UniSTS
REN90406  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,950,252 - 153,950,500UniSTSGRCh37
Build 36X153,603,446 - 153,603,694RGDNCBI36
CeleraX154,108,835 - 154,109,083RGD
Cytogenetic MapXq28UniSTS
HuRefX142,494,207 - 142,494,455UniSTS
REN90407  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,950,469 - 153,950,719UniSTSGRCh37
Build 36X153,603,663 - 153,603,913RGDNCBI36
CeleraX154,109,052 - 154,109,302RGD
Cytogenetic MapXq28UniSTS
HuRefX142,494,424 - 142,494,674UniSTS
REN90408  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,950,696 - 153,950,959UniSTSGRCh37
Build 36X153,603,890 - 153,604,153RGDNCBI36
CeleraX154,109,279 - 154,109,542RGD
Cytogenetic MapXq28UniSTS
HuRefX142,494,651 - 142,494,914UniSTS
REN90409  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,950,936 - 153,951,160UniSTSGRCh37
Build 36X153,604,130 - 153,604,354RGDNCBI36
CeleraX154,109,519 - 154,109,743RGD
Cytogenetic MapXq28UniSTS
HuRefX142,494,891 - 142,495,115UniSTS
REN90410  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,951,451 - 153,951,687UniSTSGRCh37
Build 36X153,604,645 - 153,604,881RGDNCBI36
CeleraX154,110,034 - 154,110,270RGD
Cytogenetic MapXq28UniSTS
HuRefX142,495,406 - 142,495,643UniSTS
REN90411  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,951,661 - 153,951,911UniSTSGRCh37
Build 36X153,604,855 - 153,605,105RGDNCBI36
CeleraX154,110,244 - 154,110,494RGD
Cytogenetic MapXq28UniSTS
HuRefX142,495,617 - 142,495,867UniSTS
REN90412  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,951,888 - 153,952,151UniSTSGRCh37
Build 36X153,605,082 - 153,605,345RGDNCBI36
CeleraX154,110,471 - 154,110,734RGD
Cytogenetic MapXq28UniSTS
HuRefX142,495,844 - 142,496,107UniSTS
REN90413  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,952,109 - 153,952,344UniSTSGRCh37
Build 36X153,605,303 - 153,605,538RGDNCBI36
CeleraX154,110,692 - 154,110,927RGD
Cytogenetic MapXq28UniSTS
HuRefX142,496,065 - 142,496,300UniSTS
REN90414  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,952,527 - 153,952,752UniSTSGRCh37
Build 36X153,605,721 - 153,605,946RGDNCBI36
CeleraX154,111,110 - 154,111,335RGD
Cytogenetic MapXq28UniSTS
HuRefX142,496,483 - 142,496,708UniSTS
REN90415  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,952,738 - 153,952,974UniSTSGRCh37
Build 36X153,605,932 - 153,606,168RGDNCBI36
CeleraX154,111,321 - 154,111,557RGD
Cytogenetic MapXq28UniSTS
HuRefX142,496,694 - 142,496,930UniSTS
REN90416  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,952,944 - 153,953,209UniSTSGRCh37
Build 36X153,606,138 - 153,606,403RGDNCBI36
CeleraX154,111,527 - 154,111,792RGD
Cytogenetic MapXq28UniSTS
HuRefX142,496,900 - 142,497,165UniSTS
REN90417  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,953,207 - 153,953,454UniSTSGRCh37
Build 36X153,606,401 - 153,606,648RGDNCBI36
CeleraX154,111,790 - 154,112,037RGD
Cytogenetic MapXq28UniSTS
HuRefX142,497,163 - 142,497,410UniSTS
REN90418  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,953,426 - 153,953,650UniSTSGRCh37
Build 36X153,606,620 - 153,606,844RGDNCBI36
CeleraX154,112,009 - 154,112,233RGD
Cytogenetic MapXq28UniSTS
HuRefX142,497,382 - 142,497,606UniSTS
REN90419  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,953,633 - 153,953,889UniSTSGRCh37
Build 36X153,606,827 - 153,607,083RGDNCBI36
CeleraX154,112,216 - 154,112,472RGD
Cytogenetic MapXq28UniSTS
HuRefX142,497,589 - 142,497,845UniSTS
REN90420  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,953,850 - 153,954,100UniSTSGRCh37
Build 36X153,607,044 - 153,607,294RGDNCBI36
CeleraX154,112,433 - 154,112,683RGD
Cytogenetic MapXq28UniSTS
HuRefX142,497,806 - 142,498,056UniSTS
REN90421  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,954,075 - 153,954,299UniSTSGRCh37
Build 36X153,607,269 - 153,607,493RGDNCBI36
CeleraX154,112,658 - 154,112,882RGD
Cytogenetic MapXq28UniSTS
HuRefX142,498,031 - 142,498,255UniSTS
REN90422  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,954,273 - 153,954,515UniSTSGRCh37
Build 36X153,607,467 - 153,607,709RGDNCBI36
CeleraX154,112,856 - 154,113,098RGD
Cytogenetic MapXq28UniSTS
HuRefX142,498,229 - 142,498,471UniSTS
REN90423  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,954,480 - 153,954,727UniSTSGRCh37
Build 36X153,607,674 - 153,607,921RGDNCBI36
CeleraX154,113,063 - 154,113,310RGD
Cytogenetic MapXq28UniSTS
HuRefX142,498,436 - 142,498,683UniSTS
REN90424  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,954,705 - 153,954,962UniSTSGRCh37
Build 36X153,607,899 - 153,608,156RGDNCBI36
CeleraX154,113,288 - 154,113,545RGD
Cytogenetic MapXq28UniSTS
REN90425  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,954,944 - 153,955,168UniSTSGRCh37
Build 36X153,608,138 - 153,608,362RGDNCBI36
CeleraX154,113,527 - 154,113,751RGD
Cytogenetic MapXq28UniSTS
REN90426  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,955,139 - 153,955,401UniSTSGRCh37
Build 36X153,608,333 - 153,608,595RGDNCBI36
CeleraX154,113,722 - 154,113,984RGD
Cytogenetic MapXq28UniSTS
REN90427  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,955,378 - 153,955,620UniSTSGRCh37
Build 36X153,608,572 - 153,608,814RGDNCBI36
CeleraX154,113,961 - 154,114,203RGD
Cytogenetic MapXq28UniSTS
HuRefX142,499,332 - 142,499,574UniSTS
REN90428  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,955,591 - 153,955,821UniSTSGRCh37
Build 36X153,608,785 - 153,609,015RGDNCBI36
CeleraX154,114,174 - 154,114,404RGD
Cytogenetic MapXq28UniSTS
HuRefX142,499,545 - 142,499,775UniSTS
REN90429  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,955,783 - 153,956,039UniSTSGRCh37
Build 36X153,608,977 - 153,609,233RGDNCBI36
CeleraX154,114,366 - 154,114,622RGD
Cytogenetic MapXq28UniSTS
HuRefX142,499,737 - 142,499,993UniSTS
REN90430  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,956,016 - 153,956,275UniSTSGRCh37
Build 36X153,609,210 - 153,609,469RGDNCBI36
CeleraX154,114,599 - 154,114,858RGD
Cytogenetic MapXq28UniSTS
HuRefX142,499,970 - 142,500,229UniSTS
REN90431  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,956,240 - 153,956,473UniSTSGRCh37
Build 36X153,609,434 - 153,609,667RGDNCBI36
CeleraX154,114,823 - 154,115,056RGD
Cytogenetic MapXq28UniSTS
HuRefX142,500,194 - 142,500,427UniSTS
REN90432  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,956,453 - 153,956,698UniSTSGRCh37
Build 36X153,609,647 - 153,609,892RGDNCBI36
CeleraX154,115,036 - 154,115,281RGD
Cytogenetic MapXq28UniSTS
HuRefX142,500,407 - 142,500,652UniSTS
REN90433  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,956,666 - 153,956,896UniSTSGRCh37
Build 36X153,609,860 - 153,610,090RGDNCBI36
CeleraX154,115,249 - 154,115,479RGD
Cytogenetic MapXq28UniSTS
HuRefX142,500,620 - 142,500,850UniSTS
REN90434  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,956,869 - 153,957,117UniSTSGRCh37
Build 36X153,610,063 - 153,610,311RGDNCBI36
CeleraX154,115,452 - 154,115,700RGD
Cytogenetic MapXq28UniSTS
REN90435  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,957,111 - 153,957,357UniSTSGRCh37
Build 36X153,610,305 - 153,610,551RGDNCBI36
CeleraX154,115,694 - 154,115,940RGD
Cytogenetic MapXq28UniSTS
REN90436  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,957,333 - 153,957,596UniSTSGRCh37
Build 36X153,610,527 - 153,610,790RGDNCBI36
CeleraX154,115,916 - 154,116,179RGD
Cytogenetic MapXq28UniSTS
HuRefX142,501,185 - 142,501,448UniSTS
REN90437  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,957,574 - 153,957,823UniSTSGRCh37
Build 36X153,610,768 - 153,611,017RGDNCBI36
CeleraX154,116,157 - 154,116,406RGD
Cytogenetic MapXq28UniSTS
HuRefX142,501,426 - 142,501,675UniSTS
REN90438  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,957,818 - 153,958,053UniSTSGRCh37
Build 36X153,611,012 - 153,611,247RGDNCBI36
CeleraX154,116,401 - 154,116,636RGD
Cytogenetic MapXq28UniSTS
HuRefX142,501,670 - 142,501,905UniSTS
REN90439  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,958,037 - 153,958,289UniSTSGRCh37
Build 36X153,611,231 - 153,611,483RGDNCBI36
CeleraX154,116,620 - 154,116,872RGD
Cytogenetic MapXq28UniSTS
HuRefX142,501,889 - 142,502,141UniSTS
REN90440  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,958,277 - 153,958,502UniSTSGRCh37
Build 36X153,611,471 - 153,611,696RGDNCBI36
CeleraX154,116,860 - 154,117,085RGD
Cytogenetic MapXq28UniSTS
HuRefX142,502,129 - 142,502,354UniSTS
REN90441  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,958,498 - 153,958,747UniSTSGRCh37
Build 36X153,611,692 - 153,611,941RGDNCBI36
CeleraX154,117,081 - 154,117,330RGD
Cytogenetic MapXq28UniSTS
HuRefX142,502,350 - 142,502,599UniSTS
REN90442  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,958,719 - 153,958,970UniSTSGRCh37
Build 36X153,611,913 - 153,612,164RGDNCBI36
CeleraX154,117,302 - 154,117,553RGD
Cytogenetic MapXq28UniSTS
HuRefX142,502,571 - 142,502,822UniSTS
REN90443  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,958,949 - 153,959,202UniSTSGRCh37
Build 36X153,612,143 - 153,612,396RGDNCBI36
CeleraX154,117,532 - 154,117,785RGD
Cytogenetic MapXq28UniSTS
HuRefX142,502,801 - 142,503,054UniSTS
REN90444  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,959,200 - 153,959,452UniSTSGRCh37
Build 36X153,612,394 - 153,612,646RGDNCBI36
CeleraX154,117,783 - 154,118,035RGD
Cytogenetic MapXq28UniSTS
HuRefX142,503,052 - 142,503,304UniSTS
REN90445  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,959,430 - 153,959,687UniSTSGRCh37
Build 36X153,612,624 - 153,612,881RGDNCBI36
CeleraX154,118,013 - 154,118,270RGD
Cytogenetic MapXq28UniSTS
HuRefX142,503,282 - 142,503,539UniSTS
REN90446  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,959,668 - 153,959,913UniSTSGRCh37
Build 36X153,612,862 - 153,613,107RGDNCBI36
CeleraX154,118,251 - 154,118,496RGD
Cytogenetic MapXq28UniSTS
HuRefX142,503,520 - 142,503,765UniSTS
REN90447  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,959,858 - 153,960,103UniSTSGRCh37
Build 36X153,613,052 - 153,613,297RGDNCBI36
CeleraX154,118,441 - 154,118,686RGD
Cytogenetic MapXq28UniSTS
HuRefX142,503,710 - 142,503,955UniSTS
REN90448  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,960,078 - 153,960,334UniSTSGRCh37
Build 36X153,613,272 - 153,613,528RGDNCBI36
CeleraX154,118,661 - 154,118,917RGD
Cytogenetic MapXq28UniSTS
HuRefX142,503,930 - 142,504,186UniSTS
REN90449  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,960,331 - 153,960,555UniSTSGRCh37
Build 36X153,613,525 - 153,613,749RGDNCBI36
CeleraX154,118,914 - 154,119,138RGD
Cytogenetic MapXq28UniSTS
HuRefX142,504,183 - 142,504,407UniSTS
REN90450  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,960,535 - 153,960,790UniSTSGRCh37
Build 36X153,613,729 - 153,613,984RGDNCBI36
CeleraX154,119,118 - 154,119,373RGD
Cytogenetic MapXq28UniSTS
HuRefX142,504,387 - 142,504,642UniSTS
REN90451  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,960,765 - 153,961,028UniSTSGRCh37
Build 36X153,613,959 - 153,614,222RGDNCBI36
CeleraX154,119,348 - 154,119,611RGD
Cytogenetic MapXq28UniSTS
HuRefX142,504,617 - 142,504,880UniSTS
REN90452  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,961,018 - 153,961,255UniSTSGRCh37
Build 36X153,614,212 - 153,614,449RGDNCBI36
CeleraX154,119,601 - 154,119,838RGD
Cytogenetic MapXq28UniSTS
HuRefX142,504,870 - 142,505,107UniSTS
REN90453  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,961,254 - 153,961,485UniSTSGRCh37
Build 36X153,614,448 - 153,614,679RGDNCBI36
CeleraX154,119,837 - 154,120,068RGD
Cytogenetic MapXq28UniSTS
HuRefX142,505,106 - 142,505,337UniSTS
REN90454  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,961,455 - 153,961,702UniSTSGRCh37
Build 36X153,614,649 - 153,614,896RGDNCBI36
CeleraX154,120,038 - 154,120,285RGD
Cytogenetic MapXq28UniSTS
HuRefX142,505,307 - 142,505,554UniSTS
REN90455  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,961,679 - 153,961,931UniSTSGRCh37
Build 36X153,614,873 - 153,615,125RGDNCBI36
CeleraX154,120,262 - 154,120,514RGD
Cytogenetic MapXq28UniSTS
HuRefX142,505,531 - 142,505,783UniSTS
REN90456  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,961,930 - 153,962,165UniSTSGRCh37
Build 36X153,615,124 - 153,615,359RGDNCBI36
CeleraX154,120,513 - 154,120,748RGD
Cytogenetic MapXq28UniSTS
HuRefX142,505,782 - 142,506,017UniSTS
REN90457  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,962,147 - 153,962,392UniSTSGRCh37
Build 36X153,615,341 - 153,615,586RGDNCBI36
CeleraX154,120,730 - 154,120,975RGD
Cytogenetic MapXq28UniSTS
HuRefX142,505,999 - 142,506,244UniSTS
REN90458  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,962,368 - 153,962,625UniSTSGRCh37
Build 36X153,615,562 - 153,615,819RGDNCBI36
CeleraX154,120,951 - 154,121,208RGD
Cytogenetic MapXq28UniSTS
HuRefX142,506,220 - 142,506,477UniSTS
REN90459  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,962,604 - 153,962,858UniSTSGRCh37
Build 36X153,615,798 - 153,616,052RGDNCBI36
CeleraX154,121,187 - 154,121,441RGD
Cytogenetic MapXq28UniSTS
HuRefX142,506,456 - 142,506,710UniSTS
REN90460  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,962,849 - 153,963,101UniSTSGRCh37
Build 36X153,616,043 - 153,616,295RGDNCBI36
CeleraX154,121,432 - 154,121,684RGD
Cytogenetic MapXq28UniSTS
HuRefX142,506,701 - 142,506,953UniSTS
REN90461  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,963,037 - 153,963,293UniSTSGRCh37
Build 36X153,616,231 - 153,616,487RGDNCBI36
CeleraX154,121,620 - 154,121,876RGD
Cytogenetic MapXq28UniSTS
HuRefX142,506,889 - 142,507,145UniSTS
REN90462  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,963,226 - 153,963,462UniSTSGRCh37
Build 36X153,616,420 - 153,616,656RGDNCBI36
CeleraX154,121,809 - 154,122,041RGD
Cytogenetic MapXq28UniSTS
HuRefX142,507,078 - 142,507,310UniSTS
REN90463  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,963,436 - 153,963,691UniSTSGRCh37
Build 36X153,616,630 - 153,616,885RGDNCBI36
CeleraX154,122,015 - 154,122,270RGD
Cytogenetic MapXq28UniSTS
HuRefX142,507,284 - 142,507,539UniSTS
REN90464  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,963,669 - 153,963,905UniSTSGRCh37
Build 36X153,616,863 - 153,617,099RGDNCBI36
CeleraX154,122,248 - 154,122,484RGD
Cytogenetic MapXq28UniSTS
HuRefX142,507,517 - 142,507,753UniSTS
REN90465  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,963,885 - 153,964,136UniSTSGRCh37
Build 36X153,617,079 - 153,617,330RGDNCBI36
CeleraX154,122,464 - 154,122,715RGD
Cytogenetic MapXq28UniSTS
HuRefX142,507,733 - 142,507,984UniSTS
REN90466  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,964,113 - 153,964,349UniSTSGRCh37
Build 36X153,617,307 - 153,617,543RGDNCBI36
CeleraX154,122,692 - 154,122,928RGD
Cytogenetic MapXq28UniSTS
HuRefX142,507,961 - 142,508,197UniSTS
REN90467  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,964,306 - 153,964,560UniSTSGRCh37
Build 36X153,617,500 - 153,617,754RGDNCBI36
CeleraX154,122,885 - 154,123,139RGD
Cytogenetic MapXq28UniSTS
HuRefX142,508,154 - 142,508,408UniSTS
REN90468  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,964,557 - 153,964,816UniSTSGRCh37
Build 36X153,617,751 - 153,618,010RGDNCBI36
CeleraX154,123,136 - 154,123,395RGD
Cytogenetic MapXq28UniSTS
HuRefX142,508,405 - 142,508,664UniSTS
REN90469  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,964,793 - 153,965,020UniSTSGRCh37
Build 36X153,617,987 - 153,618,214RGDNCBI36
CeleraX154,123,372 - 154,123,599RGD
Cytogenetic MapXq28UniSTS
HuRefX142,508,641 - 142,508,868UniSTS
REN90470  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,964,995 - 153,965,262UniSTSGRCh37
Build 36X153,618,189 - 153,618,456RGDNCBI36
CeleraX154,123,574 - 154,123,841RGD
Cytogenetic MapXq28UniSTS
HuRefX142,508,843 - 142,509,110UniSTS
REN90471  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,965,250 - 153,965,507UniSTSGRCh37
Build 36X153,618,444 - 153,618,701RGDNCBI36
CeleraX154,123,829 - 154,124,086RGD
Cytogenetic MapXq28UniSTS
HuRefX142,509,098 - 142,509,355UniSTS
REN90472  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,965,489 - 153,965,737UniSTSGRCh37
Build 36X153,618,683 - 153,618,931RGDNCBI36
CeleraX154,124,068 - 154,124,316RGD
Cytogenetic MapXq28UniSTS
HuRefX142,509,337 - 142,509,585UniSTS
REN90473  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,965,714 - 153,965,953UniSTSGRCh37
Build 36X153,618,908 - 153,619,147RGDNCBI36
CeleraX154,124,293 - 154,124,532RGD
Cytogenetic MapXq28UniSTS
HuRefX142,509,562 - 142,509,801UniSTS
REN90474  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,965,928 - 153,966,163UniSTSGRCh37
Build 36X153,619,122 - 153,619,357RGDNCBI36
CeleraX154,124,507 - 154,124,742RGD
Cytogenetic MapXq28UniSTS
HuRefX142,509,776 - 142,510,011UniSTS
REN90475  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,966,137 - 153,966,361UniSTSGRCh37
Build 36X153,619,331 - 153,619,555RGDNCBI36
CeleraX154,124,716 - 154,124,940RGD
Cytogenetic MapXq28UniSTS
HuRefX142,509,985 - 142,510,209UniSTS
REN90476  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,966,360 - 153,966,606UniSTSGRCh37
Build 36X153,619,554 - 153,619,800RGDNCBI36
CeleraX154,124,939 - 154,125,185RGD
Cytogenetic MapXq28UniSTS
HuRefX142,510,208 - 142,510,454UniSTS
REN90477  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,966,586 - 153,966,827UniSTSGRCh37
Build 36X153,619,780 - 153,620,021RGDNCBI36
CeleraX154,125,165 - 154,125,406RGD
Cytogenetic MapXq28UniSTS
HuRefX142,510,434 - 142,510,675UniSTS
REN90478  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,966,801 - 153,967,045UniSTSGRCh37
Build 36X153,619,995 - 153,620,239RGDNCBI36
CeleraX154,125,380 - 154,125,624RGD
Cytogenetic MapXq28UniSTS
HuRefX142,510,649 - 142,510,893UniSTS
REN90479  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,967,028 - 153,967,287UniSTSGRCh37
Build 36X153,620,222 - 153,620,481RGDNCBI36
CeleraX154,125,607 - 154,125,866RGD
Cytogenetic MapXq28UniSTS
HuRefX142,510,876 - 142,511,135UniSTS
REN90480  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,967,283 - 153,967,509UniSTSGRCh37
Build 36X153,620,477 - 153,620,703RGDNCBI36
CeleraX154,125,862 - 154,126,088RGD
Cytogenetic MapXq28UniSTS
HuRefX142,511,131 - 142,511,357UniSTS
REN90481  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,967,388 - 153,967,612UniSTSGRCh37
Build 36X153,620,582 - 153,620,806RGDNCBI36
CeleraX154,125,967 - 154,126,191RGD
Cytogenetic MapXq28UniSTS
HuRefX142,511,236 - 142,511,460UniSTS
REN90482  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,967,540 - 153,967,793UniSTSGRCh37
Build 36X153,620,734 - 153,620,987RGDNCBI36
CeleraX154,126,119 - 154,126,372RGD
Cytogenetic MapXq28UniSTS
HuRefX142,511,388 - 142,511,641UniSTS
REN90483  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,967,752 - 153,967,996UniSTSGRCh37
Build 36X153,620,946 - 153,621,190RGDNCBI36
CeleraX154,126,331 - 154,126,575RGD
Cytogenetic MapXq28UniSTS
HuRefX142,511,600 - 142,511,844UniSTS
REN90484  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,967,973 - 153,968,232UniSTSGRCh37
Build 36X153,621,167 - 153,621,426RGDNCBI36
CeleraX154,126,552 - 154,126,811RGD
Cytogenetic MapXq28UniSTS
HuRefX142,511,821 - 142,512,080UniSTS
REN90485  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,968,206 - 153,968,476UniSTSGRCh37
Build 36X153,621,400 - 153,621,670RGDNCBI36
CeleraX154,126,785 - 154,127,055RGD
Cytogenetic MapXq28UniSTS
HuRefX142,512,054 - 142,512,324UniSTS
REN90486  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,968,474 - 153,968,738UniSTSGRCh37
Build 36X153,621,668 - 153,621,932RGDNCBI36
CeleraX154,127,053 - 154,127,317RGD
Cytogenetic MapXq28UniSTS
HuRefX142,512,322 - 142,512,586UniSTS
REN90487  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,968,715 - 153,968,953UniSTSGRCh37
Build 36X153,621,909 - 153,622,147RGDNCBI36
CeleraX154,127,294 - 154,127,532RGD
Cytogenetic MapXq28UniSTS
HuRefX142,512,563 - 142,512,801UniSTS
REN90488  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,968,936 - 153,969,198UniSTSGRCh37
Build 36X153,622,130 - 153,622,392RGDNCBI36
CeleraX154,127,515 - 154,127,777RGD
Cytogenetic MapXq28UniSTS
HuRefX142,512,784 - 142,513,046UniSTS
REN90489  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,969,144 - 153,969,389UniSTSGRCh37
Build 36X153,622,338 - 153,622,583RGDNCBI36
CeleraX154,127,723 - 154,127,968RGD
Cytogenetic MapXq28UniSTS
HuRefX142,512,992 - 142,513,237UniSTS
REN90491  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,970,058 - 153,970,314UniSTSGRCh37
Build 36X153,623,252 - 153,623,508RGDNCBI36
CeleraX154,128,637 - 154,128,893RGD
Cytogenetic MapXq28UniSTS
HuRefX142,513,906 - 142,514,162UniSTS
REN90492  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,970,282 - 153,970,525UniSTSGRCh37
Build 36X153,623,476 - 153,623,719RGDNCBI36
CeleraX154,128,861 - 154,129,104RGD
Cytogenetic MapXq28UniSTS
HuRefX142,514,130 - 142,514,373UniSTS
REN90493  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,970,411 - 153,970,635UniSTSGRCh37
Build 36X153,623,605 - 153,623,829RGDNCBI36
CeleraX154,128,990 - 154,129,214RGD
Cytogenetic MapXq28UniSTS
HuRefX142,514,259 - 142,514,483UniSTS
REN90494  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,970,588 - 153,970,838UniSTSGRCh37
Build 36X153,623,782 - 153,624,032RGDNCBI36
CeleraX154,129,167 - 154,129,417RGD
Cytogenetic MapXq28UniSTS
HuRefX142,514,436 - 142,514,686UniSTS
REN90495  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,970,809 - 153,971,033UniSTSGRCh37
Build 36X153,624,003 - 153,624,227RGDNCBI36
CeleraX154,129,388 - 154,129,612RGD
Cytogenetic MapXq28UniSTS
REN90496  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,971,005 - 153,971,257UniSTSGRCh37
Build 36X153,624,199 - 153,624,451RGDNCBI36
CeleraX154,129,584 - 154,129,836RGD
Cytogenetic MapXq28UniSTS
REN90497  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,971,233 - 153,971,459UniSTSGRCh37
Build 36X153,624,427 - 153,624,653RGDNCBI36
CeleraX154,129,812 - 154,130,038RGD
Cytogenetic MapXq28UniSTS
REN90498  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,971,447 - 153,971,712UniSTSGRCh37
Build 36X153,624,641 - 153,624,906RGDNCBI36
CeleraX154,130,026 - 154,130,291RGD
Cytogenetic MapXq28UniSTS
HuRefX142,515,274 - 142,515,539UniSTS
REN90499  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,971,655 - 153,971,879UniSTSGRCh37
Build 36X153,624,849 - 153,625,073RGDNCBI36
CeleraX154,130,234 - 154,130,458RGD
Cytogenetic MapXq28UniSTS
HuRefX142,515,482 - 142,515,706UniSTS
REN90500  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,971,849 - 153,972,087UniSTSGRCh37
Build 36X153,625,043 - 153,625,281RGDNCBI36
CeleraX154,130,428 - 154,130,666RGD
Cytogenetic MapXq28UniSTS
HuRefX142,515,676 - 142,515,914UniSTS
REN90501  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,971,966 - 153,972,212UniSTSGRCh37
Build 36X153,625,160 - 153,625,406RGDNCBI36
CeleraX154,130,545 - 154,130,791RGD
Cytogenetic MapXq28UniSTS
HuRefX142,515,793 - 142,516,039UniSTS
REN90502  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,972,186 - 153,972,419UniSTSGRCh37
Build 36X153,625,380 - 153,625,613RGDNCBI36
CeleraX154,130,765 - 154,130,998RGD
Cytogenetic MapXq28UniSTS
HuRefX142,516,013 - 142,516,246UniSTS
REN90503  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,972,388 - 153,972,631UniSTSGRCh37
Build 36X153,625,582 - 153,625,825RGDNCBI36
CeleraX154,130,967 - 154,131,199RGD
Cytogenetic MapXq28UniSTS
HuRefX142,516,215 - 142,516,447UniSTS
REN90504  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,972,609 - 153,972,849UniSTSGRCh37
Build 36X153,625,803 - 153,626,043RGDNCBI36
CeleraX154,131,177 - 154,131,417RGD
Cytogenetic MapXq28UniSTS
HuRefX142,516,425 - 142,516,665UniSTS
REN90505  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,972,845 - 153,973,077UniSTSGRCh37
Build 36X153,626,039 - 153,626,271RGDNCBI36
CeleraX154,131,413 - 154,131,645RGD
Cytogenetic MapXq28UniSTS
HuRefX142,516,661 - 142,516,893UniSTS
REN90506  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,973,041 - 153,973,290UniSTSGRCh37
Build 36X153,626,235 - 153,626,484RGDNCBI36
CeleraX154,131,609 - 154,131,858RGD
Cytogenetic MapXq28UniSTS
HuRefX142,516,857 - 142,517,106UniSTS
REN90507  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,973,102 - 153,973,327UniSTSGRCh37
Build 36X153,626,296 - 153,626,521RGDNCBI36
CeleraX154,131,670 - 154,131,895RGD
Cytogenetic MapXq28UniSTS
HuRefX142,516,918 - 142,517,143UniSTS
REN90508  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,973,582 - 153,973,829UniSTSGRCh37
Build 36X153,626,776 - 153,627,023RGDNCBI36
CeleraX154,132,150 - 154,132,397RGD
Cytogenetic MapXq28UniSTS
HuRefX142,517,398 - 142,517,645UniSTS
REN90509  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,973,806 - 153,974,053UniSTSGRCh37
Build 36X153,627,000 - 153,627,247RGDNCBI36
CeleraX154,132,374 - 154,132,621RGD
Cytogenetic MapXq28UniSTS
HuRefX142,517,622 - 142,517,869UniSTS
REN90510  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,974,361 - 153,974,586UniSTSGRCh37
Build 36X153,627,555 - 153,627,780RGDNCBI36
CeleraX154,132,929 - 154,133,154RGD
Cytogenetic MapXq28UniSTS
HuRefX142,518,103 - 142,518,328UniSTS
REN90511  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,974,575 - 153,974,829UniSTSGRCh37
Build 36X153,627,769 - 153,628,023RGDNCBI36
CeleraX154,133,143 - 154,133,397RGD
Cytogenetic MapXq28UniSTS
HuRefX142,518,317 - 142,518,571UniSTS
REN90512  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,974,806 - 153,975,047UniSTSGRCh37
Build 36X153,628,000 - 153,628,241RGDNCBI36
CeleraX154,133,374 - 154,133,615RGD
Cytogenetic MapXq28UniSTS
HuRefX142,518,548 - 142,518,789UniSTS
REN90513  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,974,987 - 153,975,232UniSTSGRCh37
Build 36X153,628,181 - 153,628,426RGDNCBI36
CeleraX154,133,555 - 154,133,800RGD
Cytogenetic MapXq28UniSTS
HuRefX142,518,729 - 142,518,974UniSTS
REN90514  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,975,075 - 153,975,323UniSTSGRCh37
Build 36X153,628,269 - 153,628,517RGDNCBI36
CeleraX154,133,643 - 154,133,891RGD
Cytogenetic MapXq28UniSTS
HuRefX142,518,817 - 142,519,065UniSTS
REN90515  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,975,569 - 153,975,807UniSTSGRCh37
Build 36X153,628,763 - 153,629,001RGDNCBI36
CeleraX154,134,137 - 154,134,375RGD
Cytogenetic MapXq28UniSTS
HuRefX142,519,311 - 142,519,549UniSTS
REN90516  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,975,783 - 153,976,041UniSTSGRCh37
Build 36X153,628,977 - 153,629,235RGDNCBI36
CeleraX154,134,351 - 154,134,609RGD
Cytogenetic MapXq28UniSTS
HuRefX142,519,525 - 142,519,783UniSTS
REN90517  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,976,020 - 153,976,269UniSTSGRCh37
Build 36X153,629,214 - 153,629,463RGDNCBI36
CeleraX154,134,588 - 154,134,837RGD
Cytogenetic MapXq28UniSTS
HuRefX142,519,762 - 142,520,011UniSTS
REN90518  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,976,247 - 153,976,510UniSTSGRCh37
Build 36X153,629,441 - 153,629,704RGDNCBI36
CeleraX154,134,815 - 154,135,078RGD
Cytogenetic MapXq28UniSTS
HuRefX142,519,989 - 142,520,252UniSTS
REN90519  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,976,451 - 153,976,680UniSTSGRCh37
Build 36X153,629,645 - 153,629,874RGDNCBI36
CeleraX154,135,019 - 154,135,248RGD
Cytogenetic MapXq28UniSTS
HuRefX142,520,193 - 142,520,422UniSTS
REN90520  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,976,657 - 153,976,922UniSTSGRCh37
Build 36X153,629,851 - 153,630,116RGDNCBI36
CeleraX154,135,225 - 154,135,490RGD
Cytogenetic MapXq28UniSTS
HuRefX142,520,399 - 142,520,664UniSTS
REN90521  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,976,898 - 153,977,138UniSTSGRCh37
Build 36X153,630,092 - 153,630,332RGDNCBI36
CeleraX154,135,466 - 154,135,706RGD
Cytogenetic MapXq28UniSTS
HuRefX142,520,640 - 142,520,880UniSTS
REN90522  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,977,111 - 153,977,364UniSTSGRCh37
Build 36X153,630,305 - 153,630,558RGDNCBI36
CeleraX154,135,679 - 154,135,932RGD
Cytogenetic MapXq28UniSTS
HuRefX142,520,853 - 142,521,106UniSTS
REN90523  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,977,340 - 153,977,606UniSTSGRCh37
Build 36X153,630,534 - 153,630,800RGDNCBI36
CeleraX154,135,908 - 154,136,174RGD
Cytogenetic MapXq28UniSTS
HuRefX142,521,082 - 142,521,348UniSTS
REN90524  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,977,602 - 153,977,850UniSTSGRCh37
Build 36X153,630,796 - 153,631,044RGDNCBI36
CeleraX154,136,170 - 154,136,418RGD
Cytogenetic MapXq28UniSTS
HuRefX142,521,344 - 142,521,592UniSTS
REN90525  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,977,827 - 153,978,069UniSTSGRCh37
Build 36X153,631,021 - 153,631,263RGDNCBI36
CeleraX154,136,395 - 154,136,637RGD
Cytogenetic MapXq28UniSTS
HuRefX142,521,569 - 142,521,811UniSTS
REN90526  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,978,048 - 153,978,296UniSTSGRCh37
Build 36X153,631,242 - 153,631,490RGDNCBI36
CeleraX154,136,616 - 154,136,864RGD
Cytogenetic MapXq28UniSTS
HuRefX142,521,790 - 142,522,038UniSTS
REN90527  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,978,293 - 153,978,539UniSTSGRCh37
Build 36X153,631,487 - 153,631,733RGDNCBI36
CeleraX154,136,861 - 154,137,107RGD
Cytogenetic MapXq28UniSTS
HuRefX142,522,035 - 142,522,281UniSTS
REN90528  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,978,530 - 153,978,779UniSTSGRCh37
Build 36X153,631,724 - 153,631,973RGDNCBI36
CeleraX154,137,098 - 154,137,347RGD
Cytogenetic MapXq28UniSTS
HuRefX142,522,272 - 142,522,521UniSTS
REN90529  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,978,739 - 153,978,994UniSTSGRCh37
Build 36X153,631,933 - 153,632,188RGDNCBI36
CeleraX154,137,307 - 154,137,562RGD
Cytogenetic MapXq28UniSTS
HuRefX142,522,481 - 142,522,736UniSTS
REN90530  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,978,987 - 153,979,242UniSTSGRCh37
Build 36X153,632,181 - 153,632,436RGDNCBI36
CeleraX154,137,555 - 154,137,810RGD
Cytogenetic MapXq28UniSTS
HuRefX142,522,729 - 142,522,984UniSTS
REN90531  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,979,517 - 153,979,768UniSTSGRCh37
Build 36X153,632,711 - 153,632,962RGDNCBI36
CeleraX154,138,085 - 154,138,336RGD
Cytogenetic MapXq28UniSTS
HuRefX142,523,386 - 142,523,637UniSTS
REN90532  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,979,746 - 153,979,996UniSTSGRCh37
Build 36X153,632,940 - 153,633,190RGDNCBI36
CeleraX154,138,314 - 154,138,564RGD
Cytogenetic MapXq28UniSTS
HuRefX142,523,615 - 142,523,865UniSTS
REN90533  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,979,964 - 153,980,218UniSTSGRCh37
Build 36X153,633,158 - 153,633,412RGDNCBI36
CeleraX154,138,532 - 154,138,786RGD
Cytogenetic MapXq28UniSTS
HuRefX142,523,833 - 142,524,087UniSTS
REN90534  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,980,179 - 153,980,426UniSTSGRCh37
Build 36X153,633,373 - 153,633,620RGDNCBI36
CeleraX154,138,747 - 154,138,994RGD
Cytogenetic MapXq28UniSTS
HuRefX142,524,048 - 142,524,295UniSTS
REN90535  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,980,414 - 153,980,676UniSTSGRCh37
Build 36X153,633,608 - 153,633,870RGDNCBI36
CeleraX154,138,982 - 154,139,244RGD
Cytogenetic MapXq28UniSTS
HuRefX142,524,283 - 142,524,545UniSTS
REN90536  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,980,665 - 153,980,915UniSTSGRCh37
Build 36X153,633,859 - 153,634,109RGDNCBI36
CeleraX154,139,233 - 154,139,483RGD
Cytogenetic MapXq28UniSTS
HuRefX142,524,534 - 142,524,784UniSTS
REN90537  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,980,905 - 153,981,173UniSTSGRCh37
Build 36X153,634,099 - 153,634,367RGDNCBI36
CeleraX154,139,473 - 154,139,741RGD
Cytogenetic MapXq28UniSTS
HuRefX142,524,774 - 142,525,042UniSTS
stSG604223  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,904,278 - 153,905,582UniSTSGRCh37
Build 36X153,557,472 - 153,558,776RGDNCBI36
CeleraX154,062,346 - 154,063,650RGD
Cytogenetic MapXq28UniSTS
HuRefX142,448,382 - 142,449,686UniSTS
stSG604224  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,905,577 - 153,906,685UniSTSGRCh37
Build 36X153,558,771 - 153,559,879RGDNCBI36
CeleraX154,063,645 - 154,064,753RGD
HuRefX142,449,681 - 142,450,789UniSTS
stSG604225  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,906,699 - 153,908,053UniSTSGRCh37
Build 36X153,559,893 - 153,561,247RGDNCBI36
CeleraX154,064,767 - 154,066,121RGD
HuRefX142,450,803 - 142,452,157UniSTS
stSG604226  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,907,839 - 153,908,991UniSTSGRCh37
Build 36X153,561,033 - 153,562,185RGDNCBI36
CeleraX154,065,907 - 154,067,059RGD
HuRefX142,451,943 - 142,453,095UniSTS
stSG604228  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,912,992 - 153,913,599UniSTSGRCh37
Build 36X153,566,186 - 153,566,793RGDNCBI36
CeleraX154,071,060 - 154,071,668RGD
HuRefX142,457,096 - 142,457,703UniSTS
stSG604229  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,913,606 - 153,913,807UniSTSGRCh37
Build 36X153,566,800 - 153,567,001RGDNCBI36
CeleraX154,071,675 - 154,071,876RGD
HuRefX142,457,710 - 142,457,911UniSTS
stSG604230  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,922,108 - 153,923,153UniSTSGRCh37
Build 36X153,575,302 - 153,576,347RGDNCBI36
CeleraX154,080,693 - 154,081,738RGD
HuRefX142,466,167 - 142,467,212UniSTS
stSG604231  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,923,132 - 153,924,497UniSTSGRCh37
Build 36X153,576,326 - 153,577,691RGDNCBI36
CeleraX154,081,717 - 154,083,082RGD
HuRefX142,467,191 - 142,468,556UniSTS
stSG604232  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,924,478 - 153,924,661UniSTSGRCh37
Build 36X153,577,672 - 153,577,855RGDNCBI36
CeleraX154,083,063 - 154,083,246RGD
HuRefX142,468,537 - 142,468,720UniSTS
stSG604233  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,924,677 - 153,925,985UniSTSGRCh37
Build 36X153,577,871 - 153,579,179RGDNCBI36
CeleraX154,083,262 - 154,084,570RGD
HuRefX142,468,736 - 142,470,044UniSTS
stSG604234  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,925,966 - 153,927,190UniSTSGRCh37
Build 36X153,579,160 - 153,580,384RGDNCBI36
CeleraX154,084,551 - 154,085,775RGD
HuRefX142,470,025 - 142,471,249UniSTS
stSG604235  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,927,174 - 153,928,322UniSTSGRCh37
Build 36X153,580,368 - 153,581,516RGDNCBI36
CeleraX154,085,759 - 154,086,907RGD
HuRefX142,471,233 - 142,472,381UniSTS
stSG604236  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,928,303 - 153,929,573UniSTSGRCh37
Build 36X153,581,497 - 153,582,767RGDNCBI36
CeleraX154,086,888 - 154,088,158RGD
stSG604237  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,929,559 - 153,929,743UniSTSGRCh37
Build 36X153,582,753 - 153,582,937RGDNCBI36
CeleraX154,088,144 - 154,088,328RGD
stSG604238  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,938,917 - 153,939,937UniSTSGRCh37
Build 36X153,592,111 - 153,593,131RGDNCBI36
CeleraX154,097,500 - 154,098,520RGD
HuRefX142,482,852 - 142,483,872UniSTS
stSG604240  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,941,398 - 153,942,398UniSTSGRCh37
Build 36X153,594,592 - 153,595,592RGDNCBI36
CeleraX154,099,981 - 154,100,981RGD
HuRefX142,485,333 - 142,486,325UniSTS
stSG604241  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,942,379 - 153,943,598UniSTSGRCh37
Build 36X153,595,573 - 153,596,792RGDNCBI36
CeleraX154,100,962 - 154,102,181RGD
HuRefX142,486,306 - 142,487,525UniSTS
stSG604242  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,943,584 - 153,945,042UniSTSGRCh37
Build 36X153,596,778 - 153,598,236RGDNCBI36
CeleraX154,102,167 - 154,103,625RGD
HuRefX142,487,511 - 142,488,969UniSTS
stSG604243  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,945,023 - 153,946,146UniSTSGRCh37
Build 36X153,598,217 - 153,599,340RGDNCBI36
CeleraX154,103,606 - 154,104,729RGD
HuRefX142,488,950 - 142,490,073UniSTS
stSG604244  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,946,127 - 153,947,390UniSTSGRCh37
Build 36X153,599,321 - 153,600,584RGDNCBI36
CeleraX154,104,710 - 154,105,973RGD
HuRefX142,490,054 - 142,491,345UniSTS
stSG604245  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,947,329 - 153,948,333UniSTSGRCh37
Build 36X153,600,523 - 153,601,527RGDNCBI36
CeleraX154,105,912 - 154,106,916RGD
HuRefX142,491,284 - 142,492,288UniSTS
stSG604246  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,948,089 - 153,949,228UniSTSGRCh37
Build 36X153,601,283 - 153,602,422RGDNCBI36
CeleraX154,106,672 - 154,107,811RGD
HuRefX142,492,044 - 142,493,183UniSTS
stSG604247  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,950,878 - 153,951,920UniSTSGRCh37
Build 36X153,604,072 - 153,605,114RGDNCBI36
CeleraX154,109,461 - 154,110,503RGD
HuRefX142,494,833 - 142,495,876UniSTS
stSG604248  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,951,901 - 153,953,162UniSTSGRCh37
Build 36X153,605,095 - 153,606,356RGDNCBI36
CeleraX154,110,484 - 154,111,745RGD
HuRefX142,495,857 - 142,497,118UniSTS
stSG604249  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,952,799 - 153,953,798UniSTSGRCh37
Build 36X153,605,993 - 153,606,992RGDNCBI36
CeleraX154,111,382 - 154,112,381RGD
HuRefX142,496,755 - 142,497,754UniSTS
stSG604250  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,953,773 - 153,954,781UniSTSGRCh37
Build 36X153,606,967 - 153,607,975RGDNCBI36
CeleraX154,112,356 - 154,113,364RGD
HuRefX142,497,729 - 142,498,737UniSTS
stSG604251  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,954,767 - 153,956,219UniSTSGRCh37
Build 36X153,607,961 - 153,609,413RGDNCBI36
CeleraX154,113,350 - 154,114,802RGD
HuRefX142,498,723 - 142,500,173UniSTS
stSG604252  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,956,202 - 153,956,383UniSTSGRCh37
Build 36X153,609,396 - 153,609,577RGDNCBI36
CeleraX154,114,785 - 154,114,966RGD
HuRefX142,500,156 - 142,500,337UniSTS
stSG604253  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,956,400 - 153,957,713UniSTSGRCh37
Build 36X153,609,594 - 153,610,907RGDNCBI36
CeleraX154,114,983 - 154,116,296RGD
HuRefX142,500,354 - 142,501,565UniSTS
stSG604254  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,957,709 - 153,959,120UniSTSGRCh37
Build 36X153,610,903 - 153,612,314RGDNCBI36
CeleraX154,116,292 - 154,117,703RGD
HuRefX142,501,561 - 142,502,972UniSTS
stSG604255  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,959,104 - 153,960,462UniSTSGRCh37
Build 36X153,612,298 - 153,613,656RGDNCBI36
CeleraX154,117,687 - 154,119,045RGD
HuRefX142,502,956 - 142,504,314UniSTS
stSG604256  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,960,443 - 153,961,579UniSTSGRCh37
Build 36X153,613,637 - 153,614,773RGDNCBI36
CeleraX154,119,026 - 154,120,162RGD
HuRefX142,504,295 - 142,505,431UniSTS
stSG604257  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,961,560 - 153,963,049UniSTSGRCh37
Build 36X153,614,754 - 153,616,243RGDNCBI36
CeleraX154,120,143 - 154,121,632RGD
HuRefX142,505,412 - 142,506,901UniSTS
stSG604258  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,963,091 - 153,964,317UniSTSGRCh37
Build 36X153,616,285 - 153,617,511RGDNCBI36
CeleraX154,121,674 - 154,122,896RGD
HuRefX142,506,943 - 142,508,165UniSTS
stSG604259  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,964,298 - 153,965,421UniSTSGRCh37
Build 36X153,617,492 - 153,618,615RGDNCBI36
CeleraX154,122,877 - 154,124,000RGD
HuRefX142,508,146 - 142,509,269UniSTS
stSG604260  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,965,402 - 153,966,881UniSTSGRCh37
Build 36X153,618,596 - 153,620,075RGDNCBI36
CeleraX154,123,981 - 154,125,460RGD
HuRefX142,509,250 - 142,510,729UniSTS
stSG604261  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,966,879 - 153,968,120UniSTSGRCh37
Build 36X153,620,073 - 153,621,314RGDNCBI36
CeleraX154,125,458 - 154,126,699RGD
HuRefX142,510,727 - 142,511,968UniSTS
stSG604262  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,968,096 - 153,969,095UniSTSGRCh37
Build 36X153,621,290 - 153,622,289RGDNCBI36
CeleraX154,126,675 - 154,127,674RGD
HuRefX142,511,944 - 142,512,943UniSTS
stSG604263  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,970,954 - 153,971,378UniSTSGRCh37
Build 36X153,624,148 - 153,624,572RGDNCBI36
CeleraX154,129,533 - 154,129,957RGD
HuRefX142,514,802 - 142,515,205UniSTS
stSG604264  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,976,614 - 153,977,738UniSTSGRCh37
Build 36X153,629,808 - 153,630,932RGDNCBI36
CeleraX154,135,182 - 154,136,306RGD
HuRefX142,520,356 - 142,521,480UniSTS
stSG604265  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,977,719 - 153,978,756UniSTSGRCh37
Build 36X153,630,913 - 153,631,950RGDNCBI36
CeleraX154,136,287 - 154,137,324RGD
HuRefX142,521,461 - 142,522,498UniSTS
stSG604267  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,979,755 - 153,980,931UniSTSGRCh37
Build 36X153,632,949 - 153,634,125RGDNCBI36
CeleraX154,138,323 - 154,139,499RGD
HuRefX142,523,624 - 142,524,800UniSTS
RH69764  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,962,225 - 153,962,393UniSTSGRCh37
Build 36X153,615,419 - 153,615,587RGDNCBI36
CeleraX154,120,808 - 154,120,976RGD
Cytogenetic MapXq28UniSTS
HuRefX142,506,077 - 142,506,245UniSTS
GeneMap99-GB4 RH MapX354.94UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3320
Count of miRNA genes:1180
Interacting mature miRNAs:1453
Transcripts:ENST00000369568, ENST00000369575, ENST00000424127, ENST00000454973, ENST00000475685, ENST00000496390
Prediction methods:Miranda, Pita, 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.


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 pharyngeal arch
High
Medium 129 1003 202 14 1050 15 354 178 29 4 295 687 427 70
Low 2202 1988 1481 572 874 408 3844 1981 3465 362 1072 829 168 1 777 2697 4 2
Below cutoff 47 36 32 21 34 152 35 232 49 68 69 5 21

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_012834 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001081573 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001282283 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_080612 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_104114 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005274648 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006724804 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011531103 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011531105 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011531106 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017029276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001755655 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_938505 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA808085 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC107450 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC109993 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC244107 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI799102 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK126283 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK307927 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL832051 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY057989 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ574803 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471172 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CN481476 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB065120 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DQ656063 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HF548023 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY029412 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000369568   ⟹   ENSP00000358581
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,676,169 - 154,751,073 (-)Ensembl
RefSeq Acc Id: ENST00000369575   ⟹   ENSP00000358588
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,675,253 - 154,751,057 (-)Ensembl
RefSeq Acc Id: ENST00000424127   ⟹   ENSP00000399588
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,675,249 - 154,751,077 (-)Ensembl
RefSeq Acc Id: ENST00000454973   ⟹   ENSP00000412258
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,678,978 - 154,680,219 (-)Ensembl
RefSeq Acc Id: ENST00000475685
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,678,290 - 154,696,092 (-)Ensembl
RefSeq Acc Id: ENST00000496390
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,675,249 - 154,751,583 (-)Ensembl
RefSeq Acc Id: NM_001081573   ⟹   NP_001075042
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,675,249 - 154,751,077 (-)NCBI
GRCh37X153,903,526 - 153,979,855 (-)NCBI
Build 36X153,556,720 - 153,632,542 (-)NCBI Archive
CeleraX154,061,594 - 154,137,916 (-)RGD
HuRefX142,447,630 - 142,523,727 (-)NCBI
CHM1_1X153,815,233 - 153,891,033 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001282283   ⟹   NP_001269212
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,675,249 - 154,751,077 (-)NCBI
HuRefX142,447,630 - 142,523,727 (-)NCBI
CHM1_1X153,815,233 - 153,891,033 (-)NCBI
Sequence:
RefSeq Acc Id: NM_080612   ⟹   NP_542179
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,675,249 - 154,751,077 (-)NCBI
GRCh37X153,903,526 - 153,979,855 (-)NCBI
Build 36X153,556,720 - 153,632,542 (-)NCBI Archive
CeleraX154,061,594 - 154,137,916 (-)RGD
HuRefX142,447,630 - 142,523,727 (-)NCBI
CHM1_1X153,815,233 - 153,891,033 (-)NCBI
Sequence:
RefSeq Acc Id: NR_104114
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,675,249 - 154,751,566 (-)NCBI
HuRefX142,447,630 - 142,523,727 (-)NCBI
CHM1_1X153,815,233 - 153,891,531 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005274648   ⟹   XP_005274705
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,675,249 - 154,751,050 (-)NCBI
GRCh37X153,903,526 - 153,979,855 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006724804   ⟹   XP_006724867
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,675,249 - 154,751,050 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011531103   ⟹   XP_011529405
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,675,249 - 154,751,050 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011531105   ⟹   XP_011529407
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,675,249 - 154,751,050 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011531106   ⟹   XP_011529408
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,675,249 - 154,751,050 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017029276   ⟹   XP_016884765
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,675,249 - 154,751,050 (-)NCBI
Sequence:
RefSeq Acc Id: XR_001755655
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,697,132 - 154,751,050 (-)NCBI
Sequence:
RefSeq Acc Id: XR_938505
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,675,249 - 154,751,050 (-)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_001075042   ⟸   NM_001081573
- Peptide Label: isoform 1
- UniProtKB: Q8WWW8 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_542179   ⟸   NM_080612
- Peptide Label: isoform 2
- UniProtKB: Q8WWW8 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005274705   ⟸   XM_005274648
- Peptide Label: isoform X3
- UniProtKB: Q8WWW8 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001269212   ⟸   NM_001282283
- Peptide Label: isoform 3
- UniProtKB: Q8WWW8 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_006724867   ⟸   XM_006724804
- Peptide Label: isoform X3
- UniProtKB: Q8WWW8 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011529408   ⟸   XM_011531106
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_011529407   ⟸   XM_011531105
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_011529405   ⟸   XM_011531103
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_016884765   ⟸   XM_017029276
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: ENSP00000399588   ⟸   ENST00000424127
RefSeq Acc Id: ENSP00000412258   ⟸   ENST00000454973
RefSeq Acc Id: ENSP00000358588   ⟸   ENST00000369575
RefSeq Acc Id: ENSP00000358581   ⟸   ENST00000369568
Protein Domains
PH

Promoters
RGD ID:6808870
Promoter ID:HG_KWN:68695
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid,   NB4
Transcripts:NM_001081573,   NM_080612,   UC004FML.1,   UC010NVE.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36X153,632,436 - 153,632,972 (-)MPROMDB
RGD ID:13628664
Promoter ID:EPDNEW_H29570
Type:initiation region
Name:GAB3_1
Description:GRB2 associated binding protein 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H29571  EPDNEW_H29574  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,751,077 - 154,751,137EPDNEW
RGD ID:13628666
Promoter ID:EPDNEW_H29571
Type:initiation region
Name:GAB3_2
Description:GRB2 associated binding protein 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H29570  EPDNEW_H29574  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,751,531 - 154,751,591EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 Xp22.33-q28(chrX:10701-156003242)x3 copy number gain See cases [RCV000133911] ChrX:10701..156003242 [GRCh38]
ChrX:60701..155232907 [GRCh37]
ChrX:701..154886101 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic|likely pathogenic|conflicting data from submitters
GRCh38/hg38 Xp22.33-q28(chrX:20140-155699618)x3 copy number gain See cases [RCV000050810] ChrX:20140..155699618 [GRCh38]
ChrX:70140..154929279 [GRCh37]
ChrX:10140..154582473 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:3092486-155699618)x2 copy number gain See cases [RCV000050889] ChrX:3092486..155699618 [GRCh38]
ChrX:3010527..154929279 [GRCh37]
ChrX:3020527..154582473 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xq28(chrX:150036146-156022206)x3 copy number gain See cases [RCV000050946] ChrX:150036146..156022206 [GRCh38]
ChrX:149298619..155251871 [GRCh37]
ChrX:148955035..154905065 [NCBI36]
ChrX:Xq28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:20140-155699618)x1 copy number loss See cases [RCV000050811] ChrX:20140..155699618 [GRCh38]
ChrX:70140..154929279 [GRCh37]
ChrX:10140..154582473 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156022206)x1 copy number loss See cases [RCV000050699] ChrX:10679..156022206 [GRCh38]
ChrX:60679..155251871 [GRCh37]
ChrX:679..154905065 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic|conflicting interpretations of pathogenicity|conflicting data from submitters
GRCh38/hg38 Xp22.33-q28(chrX:10679-156013167)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050385]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050385]|See cases [RCV000050385] ChrX:10679..156013167 [GRCh38]
ChrX:60679..155242832 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xq28(chrX:149989929-156022206)x3 copy number gain See cases [RCV000050657] ChrX:149989929..156022206 [GRCh38]
ChrX:149158160..155251871 [GRCh37]
ChrX:148908818..154905065 [NCBI36]
ChrX:Xq28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156013167)x1 copy number loss Global developmental delay [RCV000050386]|See cases [RCV000050386] ChrX:10679..156013167 [GRCh38]
ChrX:60679..155242832 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156022206)x3 copy number gain See cases [RCV000050697] ChrX:10679..156022206 [GRCh38]
ChrX:60679..155251871 [GRCh37]
ChrX:679..154905065 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic|conflicting interpretations of pathogenicity|conflicting data from submitters
GRCh38/hg38 Xq23-28(chrX:115417992-156022206)x1 copy number loss See cases [RCV000051160] ChrX:115417992..156022206 [GRCh38]
ChrX:114652461..155251871 [GRCh37]
ChrX:114558717..154905065 [NCBI36]
ChrX:Xq23-28		 pathogenic
GRCh38/hg38 Xq27.3-28(chrX:145879711-156022206)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051747]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051747]|See cases [RCV000051747] ChrX:145879711..156022206 [GRCh38]
ChrX:146715565..155251871 [GRCh37]
ChrX:144768921..154905065 [NCBI36]
ChrX:Xq27.3-28		 pathogenic
GRCh38/hg38 Xq28(chrX:153296806-155699618)x1 copy number loss See cases [RCV000051750] ChrX:153296806..155699618 [GRCh38]
ChrX:152568327..154929279 [GRCh37]
ChrX:152215458..154582473 [NCBI36]
ChrX:Xq28		 pathogenic
GRCh38/hg38 Xp11.21-q28(chrX:57372584-155996431)x1 copy number loss See cases [RCV000051665] ChrX:57372584..155996431 [GRCh38]
ChrX:57399017..155226096 [GRCh37]
ChrX:57415742..154879290 [NCBI36]
ChrX:Xp11.21-q28		 pathogenic
GRCh38/hg38 Xq23-28(chrX:116264813-155980575)x1 copy number loss See cases [RCV000051728] ChrX:116264813..155980575 [GRCh38]
ChrX:115396069..155210240 [GRCh37]
ChrX:115310097..154863434 [NCBI36]
ChrX:Xq23-28		 pathogenic
GRCh38/hg38 Xq11.1-28(chrX:63279794-155939524)x1 copy number loss See cases [RCV000051666] ChrX:63279794..155939524 [GRCh38]
ChrX:62499671..155169188 [GRCh37]
ChrX:62416396..154822382 [NCBI36]
ChrX:Xq11.1-28		 pathogenic
GRCh38/hg38 Xq25-28(chrX:126537861-155996431)x1 copy number loss See cases [RCV000051729] ChrX:126537861..155996431 [GRCh38]
ChrX:125671844..155226096 [GRCh37]
ChrX:125499525..154879290 [NCBI36]
ChrX:Xq25-28		 pathogenic
GRCh38/hg38 Xq26.3-28(chrX:136956500-156020993)x1 copy number loss See cases [RCV000051732] ChrX:136956500..156020993 [GRCh38]
ChrX:136038659..155250658 [GRCh37]
ChrX:135866325..154903852 [NCBI36]
ChrX:Xq26.3-28		 pathogenic
GRCh38/hg38 Xq22.1-28(chrX:100524562-155669954)x1 copy number loss See cases [RCV000051713] ChrX:100524562..155669954 [GRCh38]
ChrX:99779559..154785891 [GRCh37]
ChrX:99666215..154552809 [NCBI36]
ChrX:Xq22.1-28		 pathogenic
GRCh38/hg38 Xq27.1-28(chrX:140445228-155998166)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051746]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051746]|See cases [RCV000051746] ChrX:140445228..155998166 [GRCh38]
ChrX:139527393..155227831 [GRCh37]
ChrX:139355059..154881025 [NCBI36]
ChrX:Xq27.1-28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:40704-156022362)x3 copy number gain See cases [RCV000052325] ChrX:40704..156022362 [GRCh38]
ChrX:90704..155252027 [GRCh37]
ChrX:30704..154905221 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:26101-155999293)x3 copy number gain See cases [RCV000052322] ChrX:26101..155999293 [GRCh38]
ChrX:76101..155228958 [GRCh37]
ChrX:16101..154882152 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:2790845-155699618)x3 copy number gain See cases [RCV000052359] ChrX:2790845..155699618 [GRCh38]
ChrX:2708886..154929279 [GRCh37]
ChrX:2718886..154582473 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:237659-156022362)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052327]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052327]|See cases [RCV000052327] ChrX:237659..156022362 [GRCh38]
ChrX:154326..155252027 [GRCh37]
ChrX:94326..154905221 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:27245-155996431)x3 copy number gain See cases [RCV000052324] ChrX:27245..155996431 [GRCh38]
ChrX:77245..155226096 [GRCh37]
ChrX:17245..154879290 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xq28(chrX:153932045-155611794)x3 copy number gain See cases [RCV000052529] ChrX:153932045..155611794 [GRCh38]
ChrX:152850692..154494649 [NCBI36]
ChrX:Xq28		 pathogenic
GRCh38/hg38 Xq28(chrX:152932818-156022206)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052490]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052490]|See cases [RCV000052490] ChrX:152932818..156022206 [GRCh38]
ChrX:152173071..155251871 [GRCh37]
ChrX:151852018..154905065 [NCBI36]
ChrX:Xq28		 pathogenic
GRCh38/hg38 Xq28(chrX:153395425-155687381)x2 copy number gain See cases [RCV000052491] ChrX:153395425..155687381 [GRCh38]
ChrX:152314077..154570236 [NCBI36]
ChrX:Xq28		 pathogenic
GRCh38/hg38 Xq25-28(chrX:123731372-155687381)x3 copy number gain See cases [RCV000052445] ChrX:123731372..155687381 [GRCh38]
ChrX:122865222..154917042 [GRCh37]
ChrX:122692903..154570236 [NCBI36]
ChrX:Xq25-28		 pathogenic
GRCh38/hg38 Xq27.1-28(chrX:140226495-155687381)x2 copy number gain See cases [RCV000052471] ChrX:140226495..155687381 [GRCh38]
ChrX:139308651..154917042 [GRCh37]
ChrX:139136317..154570236 [NCBI36]
ChrX:Xq27.1-28		 pathogenic
GRCh38/hg38 Xq27.1-28(chrX:141160282-155699618)x3 copy number gain See cases [RCV000052475] ChrX:141160282..155699618 [GRCh38]
ChrX:140254480..154929279 [GRCh37]
ChrX:140082146..154582473 [NCBI36]
ChrX:Xq27.1-28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:26102-155996431)x1 copy number loss Global developmental delay [RCV000052986]|Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052987]|Intellectual functioning disability [RCV000052988]|Global developmental delay [RCV000052989]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052987]|See cases [RCV000052986] ChrX:26102..155996431 [GRCh38]
ChrX:76102..155226096 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:14245-155999293)x1 copy number loss Hypoplastic left heart [RCV000052982]|See cases [RCV000052982] ChrX:14245..155999293 [GRCh38]
ChrX:64245..155228958 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:26102-155996431)x3 copy number gain Global developmental delay [RCV000052984]|Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052985]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052985]|See cases [RCV000052984] ChrX:26102..155996431 [GRCh38]
ChrX:76102..155226096 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
NM_001081573.2(GAB3):c.1441T>G (p.Phe481Val) single nucleotide variant Malignant melanoma [RCV000073130] ChrX:154696006 [GRCh38]
ChrX:153924281 [GRCh37]
ChrX:153577475 [NCBI36]
ChrX:Xq28		 not provided
GRCh37/hg19 Xq28(chrX:153576750-154563104)x1 copy number loss See cases [RCV000663390] ChrX:153576750..154563104 [GRCh37]
ChrX:Xq28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156022826)x4 copy number gain See cases [RCV000133654] ChrX:10679..156022826 [GRCh38]
ChrX:60679..155252491 [GRCh37]
ChrX:679..154905685 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xq27.1-28(chrX:139333024-155978689)x1 copy number loss See cases [RCV000133818] ChrX:139333024..155978689 [GRCh38]
ChrX:138415183..155208354 [GRCh37]
ChrX:138242849..154861548 [NCBI36]
ChrX:Xq27.1-28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10701-155978689)x1 copy number loss See cases [RCV000133792] ChrX:10701..155978689 [GRCh38]
ChrX:60701..155208354 [GRCh37]
ChrX:701..154861548 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156013167)x1 copy number loss See cases [RCV000050386] ChrX:10679..156013167 [GRCh38]
ChrX:60679..155242832 [GRCh37]
ChrX:679..154896026 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156013167)x3 copy number gain See cases [RCV000050385] ChrX:10679..156013167 [GRCh38]
ChrX:60679..155242832 [GRCh37]
ChrX:679..154896026 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:14245-155999293)x1 copy number loss See cases [RCV000052982] ChrX:14245..155999293 [GRCh38]
ChrX:64245..155228958 [GRCh37]
ChrX:4245..154882152 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:26102-155996431)x1 copy number loss See cases [RCV000052986] ChrX:26102..155996431 [GRCh38]
ChrX:76102..155226096 [GRCh37]
ChrX:16102..154879290 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:26102-155996431)x3 copy number gain See cases [RCV000052984] ChrX:26102..155996431 [GRCh38]
ChrX:76102..155226096 [GRCh37]
ChrX:16102..154879290 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xq27.3-28(chrX:144627217-155434735)x3 copy number gain See cases [RCV000133725] ChrX:144627217..155434735 [GRCh38]
ChrX:146715565..154664396 [GRCh37]
ChrX:143516380..154317590 [NCBI36]
ChrX:Xq27.3-28		 pathogenic
GRCh38/hg38 Xq21.1-28(chrX:85123740-156022206)x3 copy number gain See cases [RCV000133744] ChrX:85123740..156022206 [GRCh38]
ChrX:84378746..155251871 [GRCh37]
ChrX:84265402..154905065 [NCBI36]
ChrX:Xq21.1-28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:20297-155999253)x3 copy number gain See cases [RCV000134564] ChrX:20297..155999253 [GRCh38]
ChrX:70297..155228918 [GRCh37]
ChrX:10297..154882112 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xq21.1-28(chrX:78605009-156016560)x1 copy number loss See cases [RCV000134570] ChrX:78605009..156016560 [GRCh38]
ChrX:77860506..155246225 [GRCh37]
ChrX:77747162..154899419 [NCBI36]
ChrX:Xq21.1-28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10701-156003242)x1 copy number loss See cases [RCV000133947] ChrX:10701..156003242 [GRCh38]
ChrX:60701..155232907 [GRCh37]
ChrX:701..154886101 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic|conflicting interpretations of pathogenicity|conflicting data from submitters
GRCh38/hg38 Xq11.1-28(chrX:62712230-155978888)x3 copy number gain See cases [RCV000134025] ChrX:62712230..155978888 [GRCh38]
ChrX:61931700..155208553 [GRCh37]
ChrX:61848425..154861747 [NCBI36]
ChrX:Xq11.1-28		 pathogenic
GRCh38/hg38 Xp21.1-q28(chrX:37076284-156016920)x1 copy number loss See cases [RCV000135300] ChrX:37076284..156016920 [GRCh38]
ChrX:37094357..155246585 [GRCh37]
ChrX:37004278..154899779 [NCBI36]
ChrX:Xp21.1-q28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:20297-156026127)x1 copy number loss See cases [RCV000135321] ChrX:20297..156026127 [GRCh38]
ChrX:70297..155255792 [GRCh37]
ChrX:10297..154908986 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xq21.31-28(chrX:92222680-156016920)x1 copy number loss See cases [RCV000135307] ChrX:92222680..156016920 [GRCh38]
ChrX:91477679..155246585 [GRCh37]
ChrX:91364335..154899779 [NCBI36]
ChrX:Xq21.31-28		 pathogenic
GRCh38/hg38 Xq23-28(chrX:114533139-156022206)x1 copy number loss See cases [RCV000134947] ChrX:114533139..156022206 [GRCh38]
ChrX:113767592..155251871 [GRCh37]
ChrX:113673848..154905065 [NCBI36]
ChrX:Xq23-28		 pathogenic
GRCh38/hg38 Xq13.2-28(chrX:74510116-156022206)x1 copy number loss See cases [RCV000134958] ChrX:74510116..156022206 [GRCh38]
ChrX:73729951..155251871 [GRCh37]
ChrX:73646676..154905065 [NCBI36]
ChrX:Xq13.2-28		 pathogenic
GRCh38/hg38 Xp21.1-q28(chrX:36237706-156022206)x1 copy number loss See cases [RCV000135552] ChrX:36237706..156022206 [GRCh38]
ChrX:36255823..155251871 [GRCh37]
ChrX:36165744..154905065 [NCBI36]
ChrX:Xp21.1-q28		 pathogenic
GRCh38/hg38 Xq21.1-28(chrX:77369933-156013167)x1 copy number loss See cases [RCV000135454] ChrX:77369933..156013167 [GRCh38]
ChrX:76634813..155242832 [GRCh37]
ChrX:76507069..154896026 [NCBI36]
ChrX:Xq21.1-28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10701-156003229)x1 copy number loss See cases [RCV000136097] ChrX:10701..156003229 [GRCh38]
ChrX:60701..155232894 [GRCh37]
ChrX:701..154886088 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xq21.33-28(chrX:94462929-156001635)x3 copy number gain See cases [RCV000136552] ChrX:94462929..156001635 [GRCh38]
ChrX:93717928..155231300 [GRCh37]
ChrX:93604584..154884494 [NCBI36]
ChrX:Xq21.33-28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:40904-155998166)x1 copy number loss See cases [RCV000136478] ChrX:40904..155998166 [GRCh38]
ChrX:90904..155227831 [GRCh37]
ChrX:30904..154881025 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xq21.1-28(chrX:79093152-156003229)x1 copy number loss See cases [RCV000136083] ChrX:79093152..156003229 [GRCh38]
ChrX:78348649..155232894 [GRCh37]
ChrX:78235305..154886088 [NCBI36]
ChrX:Xq21.1-28		 pathogenic
GRCh38/hg38 Xq28(chrX:154679854-156003229)x1 copy number loss See cases [RCV000136031] ChrX:154679854..156003229 [GRCh38]
ChrX:153908131..155232894 [GRCh37]
ChrX:153561325..154886088 [NCBI36]
ChrX:Xq28		 pathogenic
GRCh38/hg38 Xq25-28(chrX:128473235-156003229)x1 copy number loss See cases [RCV000136095] ChrX:128473235..156003229 [GRCh38]
ChrX:127607213..155232894 [GRCh37]
ChrX:127434894..154886088 [NCBI36]
ChrX:Xq25-28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10001-156030895)x1 copy number loss See cases [RCV000136005] ChrX:10001..156030895 [GRCh38]
ChrX:60001..155260560 [GRCh37]
ChrX:1..154913754 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xq27.1-28(chrX:140783390-155611114)x2 copy number gain See cases [RCV000135881] ChrX:140783390..155611114 [GRCh38]
ChrX:139865555..154785891 [GRCh37]
ChrX:139693221..154493969 [NCBI36]
ChrX:Xq27.1-28		 pathogenic
GRCh38/hg38 Xq27.2-28(chrX:141650284-156022206)x1 copy number loss See cases [RCV000136912] ChrX:141650284..156022206 [GRCh38]
ChrX:140738414..155251871 [GRCh37]
ChrX:140566080..154905065 [NCBI36]
ChrX:Xq27.2-28		 pathogenic
GRCh38/hg38 Xq13.3-28(chrX:75086417-156022206)x1 copy number loss See cases [RCV000137113] ChrX:75086417..156022206 [GRCh38]
ChrX:74306252..155251871 [GRCh37]
ChrX:74222977..154905065 [NCBI36]
ChrX:Xq13.3-28		 pathogenic
GRCh38/hg38 Xq28(chrX:153322656-155522304)x2 copy number gain See cases [RCV000136716] ChrX:153322656..155522304 [GRCh38]
ChrX:152864376..154751965 [GRCh37]
ChrX:152241308..154405159 [NCBI36]
ChrX:Xq28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:2782275-155611794)x2 copy number gain See cases [RCV000136841] ChrX:2782275..155611794 [GRCh38]
ChrX:2700316..154785891 [GRCh37]
ChrX:2710316..154494649 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xq28(chrX:151750863-155522304)x1 copy number loss See cases [RCV000136718] ChrX:151750863..155522304 [GRCh38]
ChrX:150919335..154751965 [GRCh37]
ChrX:150669991..154405159 [NCBI36]
ChrX:Xq28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:2765636-155522304)x3 copy number gain See cases [RCV000136791] ChrX:2765636..155522304 [GRCh38]
ChrX:2683677..154751965 [GRCh37]
ChrX:2693677..154405159 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xq11.1-28(chrX:62561604-156003242)x3 copy number gain See cases [RCV000137553] ChrX:62561604..156003242 [GRCh38]
ChrX:61781074..155232907 [GRCh37]
ChrX:61697799..154886101 [NCBI36]
ChrX:Xq11.1-28		 pathogenic
GRCh38/hg38 Xq28(chrX:153276277-156003242)x3 copy number gain See cases [RCV000137498] ChrX:153276277..156003242 [GRCh38]
ChrX:152465185..155232907 [GRCh37]
ChrX:152118379..154886101 [NCBI36]
ChrX:Xq28		 pathogenic
GRCh38/hg38 Xq22.1-28(chrX:102197284-156003242)x1 copy number loss See cases [RCV000137415] ChrX:102197284..156003242 [GRCh38]
ChrX:101452257..155232907 [GRCh37]
ChrX:101338913..154886101 [NCBI36]
ChrX:Xq22.1-28		 pathogenic
GRCh38/hg38 Xq13.3-28(chrX:76604011-156022206)x1 copy number loss See cases [RCV000137138] ChrX:76604011..156022206 [GRCh38]
ChrX:75824420..155251871 [GRCh37]
ChrX:75740824..154905065 [NCBI36]
ChrX:Xq13.3-28		 pathogenic
GRCh38/hg38 Xq26.3-28(chrX:137118983-156003242)x1 copy number loss See cases [RCV000137257] ChrX:137118983..156003242 [GRCh38]
ChrX:136201142..155232907 [GRCh37]
ChrX:136028808..154886101 [NCBI36]
ChrX:Xq26.3-28		 pathogenic|uncertain significance
GRCh38/hg38 Xq25-28(chrX:123793526-156022206)x1 copy number loss See cases [RCV000137167] ChrX:123793526..156022206 [GRCh38]
ChrX:122927376..155251871 [GRCh37]
ChrX:122755057..154905065 [NCBI36]
ChrX:Xq25-28		 pathogenic|uncertain significance
GRCh38/hg38 Xq28(chrX:154604412-154935279)x3 copy number gain See cases [RCV000137292] ChrX:154604412..154935279 [GRCh38]
ChrX:153485859..153816748 [NCBI36]
ChrX:Xq28		 likely pathogenic
GRCh38/hg38 Xq21.33-28(chrX:95846285-156003242)x3 copy number gain See cases [RCV000138020] ChrX:95846285..156003242 [GRCh38]
ChrX:95101284..155232907 [GRCh37]
ChrX:94987940..154886101 [NCBI36]
ChrX:Xq21.33-28		 pathogenic
GRCh38/hg38 Xq22.3-28(chrX:106127173-156003242)x1 copy number loss See cases [RCV000137887] ChrX:106127173..156003242 [GRCh38]
ChrX:105371166..155232907 [GRCh37]
ChrX:105257822..154886101 [NCBI36]
ChrX:Xq22.3-28		 pathogenic
GRCh38/hg38 Xq27.3-28(chrX:143553831-156003229)x1 copy number loss See cases [RCV000138679] ChrX:143553831..156003229 [GRCh38]
ChrX:142641674..155232894 [GRCh37]
ChrX:142469340..154886088 [NCBI36]
ChrX:Xq27.3-28		 pathogenic
GRCh38/hg38 Xq21.1-28(chrX:79911061-156003229)x1 copy number loss See cases [RCV000138787] ChrX:79911061..156003229 [GRCh38]
ChrX:79166568..155232894 [GRCh37]
ChrX:79053224..154886088 [NCBI36]
ChrX:Xq21.1-28		 pathogenic
GRCh38/hg38 Xq22.3-28(chrX:106465610-156003242)x1 copy number loss See cases [RCV000138541] ChrX:106465610..156003242 [GRCh38]
ChrX:105708840..155232907 [GRCh37]
ChrX:105595496..154886101 [NCBI36]
ChrX:Xq22.3-28		 pathogenic
GRCh38/hg38 Xq21.1-28(chrX:82211310-156003229)x1 copy number loss See cases [RCV000139400] ChrX:82211310..156003229 [GRCh38]
ChrX:81466759..155232894 [GRCh37]
ChrX:81353415..154886088 [NCBI36]
ChrX:Xq21.1-28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:1085618-155699644)x1 copy number loss See cases [RCV000139278] ChrX:1085618..155699644 [GRCh38]
ChrX:1118268..154929305 [GRCh37]
ChrX:1038268..154582499 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xq21.31-28(chrX:88339926-156003242)x1 copy number loss See cases [RCV000139351] ChrX:88339926..156003242 [GRCh38]
ChrX:87594927..155232907 [GRCh37]
ChrX:87481583..154886101 [NCBI36]
ChrX:Xq21.31-28		 pathogenic|likely benign
GRCh38/hg38 Xq11.1-28(chrX:62712219-156003242)x3 copy number gain See cases [RCV000139416] ChrX:62712219..156003242 [GRCh38]
ChrX:61931689..155232907 [GRCh37]
ChrX:61848414..154886101 [NCBI36]
ChrX:Xq11.1-28		 pathogenic|likely benign
GRCh38/hg38 Xp22.33-q28(chrX:251880-156004181)x3 copy number gain See cases [RCV000139888] ChrX:251880..156004181 [GRCh38]
ChrX:168547..155233846 [GRCh37]
ChrX:108547..154887040 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xq28(chrX:154559495-154736598)x2 copy number gain See cases [RCV000140472] ChrX:154559495..154736598 [GRCh38]
ChrX:153787710..153964873 [GRCh37]
ChrX:153440904..153618067 [NCBI36]
ChrX:Xq28		 benign
GRCh38/hg38 Xq28(chrX:154348522-154770053)x2 copy number gain See cases [RCV000140492] ChrX:154348522..154770053 [GRCh38]
ChrX:153576890..153998328 [GRCh37]
ChrX:153230084..153651522 [NCBI36]
ChrX:Xq28		 pathogenic
GRCh38/hg38 Xq27.1-28(chrX:139530928-156003229)x1 copy number loss See cases [RCV000139724] ChrX:139530928..156003229 [GRCh38]
ChrX:138613087..155232894 [GRCh37]
ChrX:138440753..154886088 [NCBI36]
ChrX:Xq27.1-28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:2299223-155992188)x3 copy number gain See cases [RCV000141400] ChrX:2299223..155992188 [GRCh38]
ChrX:2217264..155221853 [GRCh37]
ChrX:2227264..154875047 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:20297-156016920)x3 copy number gain See cases [RCV000141401] ChrX:20297..156016920 [GRCh38]
ChrX:70297..155246585 [GRCh37]
ChrX:10297..154899779 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251880-156004066)x4 copy number gain See cases [RCV000140786] ChrX:251880..156004066 [GRCh38]
ChrX:168547..155233731 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251880-156004066)x1 copy number loss See cases [RCV000140787] ChrX:251880..156004066 [GRCh38]
ChrX:168547..155233731 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic|conflicting data from submitters
GRCh38/hg38 Xq21.1-28(chrX:82096719-156004066)x1 copy number loss See cases [RCV000141825] ChrX:82096719..156004066 [GRCh38]
ChrX:81352168..155233731 [GRCh37]
ChrX:81238824..154886925 [NCBI36]
ChrX:Xq21.1-28		 pathogenic
GRCh38/hg38 Xq21.31-28(chrX:89557622-156004066)x1 copy number loss See cases [RCV000142016] ChrX:89557622..156004066 [GRCh38]
ChrX:88812621..155233731 [GRCh37]
ChrX:88699277..154886925 [NCBI36]
ChrX:Xq21.31-28		 pathogenic
GRCh38/hg38 Xq24-28(chrX:119297670-156004066)x1 copy number loss See cases [RCV000141743] ChrX:119297670..156004066 [GRCh38]
ChrX:118431633..155233731 [GRCh37]
ChrX:118315661..154886925 [NCBI36]
ChrX:Xq24-28		 pathogenic
GRCh38/hg38 Xq21.1-28(chrX:78187188-156004066)x1 copy number loss See cases [RCV000142337] ChrX:78187188..156004066 [GRCh38]
ChrX:77442685..155233731 [GRCh37]
ChrX:77329341..154886925 [NCBI36]
ChrX:Xq21.1-28		 pathogenic
GRCh38/hg38 Xq22.3-28(chrX:106722296-156004066)x1 copy number loss See cases [RCV000142190] ChrX:106722296..156004066 [GRCh38]
ChrX:105965526..155233731 [GRCh37]
ChrX:105852182..154886925 [NCBI36]
ChrX:Xq22.3-28		 pathogenic
GRCh38/hg38 Xq24-28(chrX:118856574-156004066)x1 copy number loss See cases [RCV000142137] ChrX:118856574..156004066 [GRCh38]
ChrX:117990537..155233731 [GRCh37]
ChrX:117874565..154886925 [NCBI36]
ChrX:Xq24-28		 pathogenic
GRCh38/hg38 Xq21.2-28(chrX:86626431-156004066)x1 copy number loss See cases [RCV000142037] ChrX:86626431..156004066 [GRCh38]
ChrX:85881434..155233731 [GRCh37]
ChrX:85768090..154886925 [NCBI36]
ChrX:Xq21.2-28		 pathogenic
GRCh38/hg38 Xq28(chrX:148951460-155434653)x2 copy number gain See cases [RCV000143002] ChrX:148951460..155434653 [GRCh38]
ChrX:148956425..154664314 [GRCh37]
ChrX:147840690..154317508 [NCBI36]
ChrX:Xq28		 pathogenic
GRCh38/hg38 Xq23-28(chrX:111050385-156022206)x1 copy number loss See cases [RCV000142577] ChrX:111050385..156022206 [GRCh38]
ChrX:110293613..155251871 [GRCh37]
ChrX:110180269..154905065 [NCBI36]
ChrX:Xq23-28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10701-156003229)x3 copy number gain See cases [RCV000142625] ChrX:10701..156003229 [GRCh38]
ChrX:60701..155232894 [GRCh37]
ChrX:701..154886088 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xq13.2-28(chrX:74684615-156004066)x1 copy number loss See cases [RCV000143424] ChrX:74684615..156004066 [GRCh38]
ChrX:73904450..155233731 [GRCh37]
ChrX:73821175..154886925 [NCBI36]
ChrX:Xq13.2-28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251879-156004066)x1 copy number loss See cases [RCV000143441] ChrX:251879..156004066 [GRCh38]
ChrX:168546..155233731 [GRCh37]
ChrX:108546..154886925 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xp11.22-q28(chrX:53144751-156003242)x1 copy number loss See cases [RCV000143349] ChrX:53144751..156003242 [GRCh38]
ChrX:53321095..155232907 [GRCh37]
ChrX:53190658..154886101 [NCBI36]
ChrX:Xp11.22-q28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251879-156004066)x3 copy number gain See cases [RCV000143433] ChrX:251879..156004066 [GRCh38]
ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251880-156004066)x3 copy number gain See cases [RCV000143219] ChrX:251880..156004066 [GRCh38]
ChrX:168547..155233731 [GRCh37]
ChrX:108547..154886925 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xq13.3-28(chrX:76557425-156004066)x1 copy number loss See cases [RCV000143132] ChrX:76557425..156004066 [GRCh38]
ChrX:75777833..155233731 [GRCh37]
ChrX:75694237..154886925 [NCBI36]
ChrX:Xq13.3-28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156022206)x1 copy number loss See cases [RCV000148135] ChrX:10679..156022206 [GRCh38]
ChrX:60679..155251871 [GRCh37]
ChrX:679..154905065 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156022206)x3 copy number gain See cases [RCV000148141] ChrX:10679..156022206 [GRCh38]
ChrX:60679..155251871 [GRCh37]
ChrX:679..154905065 [NCBI36]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:71267-155246643)x3 copy number gain See cases [RCV000240122] ChrX:71267..155246643 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xq11.1-28(chrX:62063537-155246643)x3 copy number gain See cases [RCV000240143] ChrX:62063537..155246643 [GRCh37]
ChrX:Xq11.1-28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:176426-155250222)x3 copy number gain See cases [RCV000239843] ChrX:176426..155250222 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:71267-155255839)x1 copy number loss See cases [RCV000239832] ChrX:71267..155255839 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp22.2-q28(chrX:13147668-155250222)x3 copy number gain See cases [RCV000239798] ChrX:13147668..155250222 [GRCh37]
ChrX:Xp22.2-q28		 pathogenic
GRCh37/hg19 Xq28(chrX:153627408-154089925)x2 copy number gain See cases [RCV000240046] ChrX:153627408..154089925 [GRCh37]
ChrX:Xq28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:71267-155234036)x2 copy number gain See cases [RCV000239874] ChrX:71267..155234036 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:70297-155255839)x3 copy number gain See cases [RCV000239934] ChrX:70297..155255839 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:150002-155234036)x2 copy number gain See cases [RCV000240106] ChrX:150002..155234036 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:71267-155224766)x1 copy number loss See cases [RCV000239902] ChrX:71267..155224766 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60701-155246271)x3 copy number gain See cases [RCV000239989] ChrX:60701..155246271 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xq28(chrX:153928244-154065414)x3 copy number gain See cases [RCV000240020] ChrX:153928244..154065414 [GRCh37]
ChrX:Xq28		 uncertain significance
GRCh37/hg19 Xq27.3-28(chrX:142174780-155250222)x2 copy number gain See cases [RCV000240530] ChrX:142174780..155250222 [GRCh37]
ChrX:Xq27.3-28		 pathogenic
GRCh37/hg19 Xq11.1-28(chrX:62063537-155250222)x3 copy number gain See cases [RCV000240148] ChrX:62063537..155250222 [GRCh37]
ChrX:Xq11.1-28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:2707626-155250222)x2 copy number gain See cases [RCV000240541] ChrX:2707626..155250222 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xq25-28(chrX:121022022-155211482)x1 copy number loss See cases [RCV000240337] ChrX:121022022..155211482 [GRCh37]
ChrX:Xq25-28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:176426-155236656)x3 copy number gain See cases [RCV000240552] ChrX:176426..155236656 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:225816-155234036)x2 copy number gain See cases [RCV000240464] ChrX:225816..155234036 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:150002-155234036)x3 copy number gain See cases [RCV000240314] ChrX:150002..155234036 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:70297-155255792) copy number loss See cases [RCV000449461] ChrX:70297..155255792 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xq21.33-28(chrX:94043221-155246585)x1 copy number loss See cases [RCV000449365] ChrX:94043221..155246585 [GRCh37]
ChrX:Xq21.33-28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-154930047)x3 copy number gain See cases [RCV000449437] ChrX:168546..154930047 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x3 copy number gain See cases [RCV000449330] ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:71267-155255792)x1 copy number loss See cases [RCV000446197] ChrX:71267..155255792 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:318707-155224707)x1 copy number loss See cases [RCV000446667] ChrX:318707..155224707 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xq28(chrX:152228560-154930047)x2 copy number gain See cases [RCV000447331] ChrX:152228560..154930047 [GRCh37]
ChrX:Xq28		 pathogenic
GRCh37/hg19 Xq13.3-28(chrX:74787886-155233731)x1 copy number loss See cases [RCV000447490] ChrX:74787886..155233731 [GRCh37]
ChrX:Xq13.3-28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x4 copy number gain See cases [RCV000446932] ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp11.1-q28(chrX:58140271-155046703)x3 copy number gain See cases [RCV000446151] ChrX:58140271..155046703 [GRCh37]
ChrX:Xp11.1-q28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155196888)x3 copy number gain See cases [RCV000446310] ChrX:168546..155196888 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155081533)x3 copy number gain See cases [RCV000447253] ChrX:168546..155081533 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60701-155246225)x3 copy number gain See cases [RCV000446270] ChrX:60701..155246225 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xq28(chrX:150253008-155233731)x1 copy number loss See cases [RCV000446761] ChrX:150253008..155233731 [GRCh37]
ChrX:Xq28		 pathogenic
GRCh37/hg19 Xq13.1-28(chrX:68701338-155233731)x3 copy number gain See cases [RCV000446471] ChrX:68701338..155233731 [GRCh37]
ChrX:Xq13.1-28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:2703632-155233731)x1 copy number loss See cases [RCV000446712] ChrX:2703632..155233731 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xq22.3-28(chrX:105694656-155224707)x1 copy number loss See cases [RCV000445891] ChrX:105694656..155224707 [GRCh37]
ChrX:Xq22.3-28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168566-155233731)x1 copy number loss See cases [RCV000445720] ChrX:168566..155233731 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:553069-155233731)x1 copy number loss See cases [RCV000446026] ChrX:553069..155233731 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1 copy number loss See cases [RCV000448393] ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:70297-155255792)x4 copy number gain See cases [RCV000448034] ChrX:70297..155255792 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xq25-28(chrX:126773628-155233731)x1 copy number loss See cases [RCV000448724] ChrX:126773628..155233731 [GRCh37]
ChrX:Xq25-28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:70297-155246585)x1 copy number loss See cases [RCV000448652] ChrX:70297..155246585 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xq26.3-28(chrX:134114063-155233731)x1 copy number loss See cases [RCV000448865] ChrX:134114063..155233731 [GRCh37]
ChrX:Xq26.3-28		 pathogenic
GRCh37/hg19 Xq28(chrX:151201777-154741703)x2 copy number gain See cases [RCV000510478] ChrX:151201777..154741703 [GRCh37]
ChrX:Xq28		 pathogenic
GRCh37/hg19 Xp21.2-q28(chrX:31088082-155233731)x1 copy number loss See cases [RCV000511413] ChrX:31088082..155233731 [GRCh37]
ChrX:Xp21.2-q28		 pathogenic
GRCh37/hg19 Xq23-28(chrX:112474054-155233731)x1 copy number loss See cases [RCV000511572] ChrX:112474054..155233731 [GRCh37]
ChrX:Xq23-28		 pathogenic
GRCh37/hg19 Xq24-28(chrX:116621104-155233731)x1 copy number loss See cases [RCV000511936] ChrX:116621104..155233731 [GRCh37]
ChrX:Xq24-28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168547-155233731) copy number gain See cases [RCV000512020] ChrX:168547..155233731 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xq21.1-28(chrX:79862302-155233731)x1 copy number loss See cases [RCV000511482] ChrX:79862302..155233731 [GRCh37]
ChrX:Xq21.1-28		 pathogenic
GRCh37/hg19 Xq21.31-28(chrX:86900388-155233731)x1 copy number loss See cases [RCV000511490] ChrX:86900388..155233731 [GRCh37]
ChrX:Xq21.31-28		 pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:55000501-155230750)x3 copy number gain See cases [RCV000511787] ChrX:55000501..155230750 [GRCh37]
ChrX:Xp11.21-q28		 pathogenic
GRCh37/hg19 Xq27.3-28(chrX:146232592-155233731)x1 copy number loss See cases [RCV000511228] ChrX:146232592..155233731 [GRCh37]
ChrX:Xq27.3-28		 pathogenic
GRCh37/hg19 Xq26.3-28(chrX:133944147-155233731)x3 copy number gain See cases [RCV000511034] ChrX:133944147..155233731 [GRCh37]
ChrX:Xq26.3-28		 pathogenic
GRCh37/hg19 Xq21.1-28(chrX:78230501-155233731)x1 copy number loss See cases [RCV000510820] ChrX:78230501..155233731 [GRCh37]
ChrX:Xq21.1-28		 pathogenic
GRCh37/hg19 Xq28(chrX:151963528-155233731)x1 copy number loss See cases [RCV000510866] ChrX:151963528..155233731 [GRCh37]
ChrX:Xq28		 pathogenic
GRCh37/hg19 Xq28(chrX:151311551-155233731)x1 copy number loss See cases [RCV000510920] ChrX:151311551..155233731 [GRCh37]
ChrX:Xq28		 pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:57511767-155233731)x3 copy number gain See cases [RCV000510826] ChrX:57511767..155233731 [GRCh37]
ChrX:Xp11.21-q28		 pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:56457791-155233731)x3 copy number gain See cases [RCV000511307] ChrX:56457791..155233731 [GRCh37]
ChrX:Xp11.21-q28		 pathogenic
GRCh37/hg19 Xq22.1-28(chrX:98495811-155233731)x1 copy number loss See cases [RCV000512372] ChrX:98495811..155233731 [GRCh37]
ChrX:Xq22.1-28		 pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:57415659-155233731)x3 copy number gain See cases [RCV000512173] ChrX:57415659..155233731 [GRCh37]
ChrX:Xp11.21-q28		 pathogenic
GRCh37/hg19 Xq27.1-28(chrX:138331745-155233731)x1 copy number loss not provided [RCV000684397] ChrX:138331745..155233731 [GRCh37]
ChrX:Xq27.1-28		 pathogenic
GRCh37/hg19 Xq27.2-28(chrX:140388077-155233731)x3 copy number gain not provided [RCV000684402] ChrX:140388077..155233731 [GRCh37]
ChrX:Xq27.2-28		 pathogenic
GRCh37/hg19 Xq21.31-28(chrX:91140025-155233731)x1 copy number loss not provided [RCV000684357] ChrX:91140025..155233731 [GRCh37]
ChrX:Xq21.31-28		 pathogenic
GRCh37/hg19 Xq27.1-28(chrX:139504488-155233731)x1 copy number loss not provided [RCV000684401] ChrX:139504488..155233731 [GRCh37]
ChrX:Xq27.1-28		 pathogenic
GRCh37/hg19 Xq22.3-28(chrX:107823442-155233731)x1 copy number loss not provided [RCV000684373] ChrX:107823442..155233731 [GRCh37]
ChrX:Xq22.3-28		 pathogenic
GRCh37/hg19 Xq22.1-28(chrX:99324651-155233731)x1 copy number loss not provided [RCV000684363] ChrX:99324651..155233731 [GRCh37]
ChrX:Xq22.1-28		 pathogenic
GRCh37/hg19 Xq28(chrX:153749360-155233731)x3 copy number gain not provided [RCV000684416] ChrX:153749360..155233731 [GRCh37]
ChrX:Xq28		 pathogenic
GRCh37/hg19 Xq25-28(chrX:125733292-155233846)x1 copy number loss not provided [RCV000684386] ChrX:125733292..155233846 [GRCh37]
ChrX:Xq25-28		 pathogenic
GRCh37/hg19 Xq25-28(chrX:122924044-155233731)x1 copy number loss not provided [RCV000849097] ChrX:122924044..155233731 [GRCh37]
ChrX:Xq25-28		 pathogenic
GRCh37/hg19 Xq22.3-28(chrX:104098124-155233731)x1 copy number loss not provided [RCV000846958] ChrX:104098124..155233731 [GRCh37]
ChrX:Xq22.3-28		 pathogenic
GRCh37/hg19 Xq28(chrX:153904473-155090513)x0 copy number loss not provided [RCV000753943] ChrX:153904473..155090513 [GRCh37]
ChrX:Xq28		 benign
GRCh37/hg19 Xq27.1-28(chrX:138750575-155246749)x1 copy number loss not provided [RCV000753810] ChrX:138750575..155246749 [GRCh37]
ChrX:Xq27.1-28		 pathogenic
GRCh37/hg19 Xq27.1-28(chrX:139504958-155254881)x1 copy number loss not provided [RCV000753815] ChrX:139504958..155254881 [GRCh37]
ChrX:Xq27.1-28		 pathogenic
GRCh37/hg19 Xq13.2-28(chrX:73472626-155254881)x1 copy number loss not provided [RCV000753606] ChrX:73472626..155254881 [GRCh37]
ChrX:Xq13.2-28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:181779-155171702)x1 copy number loss not provided [RCV000753278] ChrX:181779..155171702 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60262-155245765)x1 copy number loss not provided [RCV000753271] ChrX:60262..155245765 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
Single allele duplication Autistic disorder of childhood onset [RCV000754365] ChrX:1..156040895 [GRCh38]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60814-155254881)x2 copy number gain not provided [RCV000753277] ChrX:60814..155254881 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60262-155245765)x3 copy number gain not provided [RCV000753272] ChrX:60262..155245765 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60814-155236712)x2 copy number gain not provided [RCV000753276] ChrX:60814..155236712 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xq11.1-28(chrX:61694576-155254881)x1 copy number loss not provided [RCV000753556] ChrX:61694576..155254881 [GRCh37]
ChrX:Xq11.1-28		 pathogenic
GRCh37/hg19 Xq21.1-28(chrX:78444738-155233731)x1 copy number loss not provided [RCV001007318] ChrX:78444738..155233731 [GRCh37]
ChrX:Xq21.1-28		 pathogenic
GRCh37/hg19 Xq26.3-28(chrX:134975270-155233945) copy number gain not provided [RCV000767679] ChrX:134975270..155233945 [GRCh37]
ChrX:Xq26.3-28		 pathogenic
GRCh37/hg19 Xq28(chrX:153761240-155227607) copy number loss not provided [RCV000767811] ChrX:153761240..155227607 [GRCh37]
ChrX:Xq28		 likely pathogenic
NC_000023.10:g.(?_152954020)_(154096327_?)del deletion Adrenoleukodystrophy [RCV000815921] ChrX:152954020..154096327 [GRCh37]
ChrX:Xq28		 pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x4 copy number gain not provided [RCV000846039] ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xq28(chrX:153941568-154290231)x2 copy number gain not provided [RCV000846317] ChrX:153941568..154290231 [GRCh37]
ChrX:Xq28		 uncertain significance
GRCh37/hg19 Xq21.1-28(chrX:84387417-155233731)x1 copy number loss not provided [RCV001007322] ChrX:84387417..155233731 [GRCh37]
ChrX:Xq21.1-28		 pathogenic
NM_001081573.3(GAB3):c.1559G>C (p.Ser520Thr) single nucleotide variant not provided [RCV000960996] ChrX:154680220 [GRCh38]
ChrX:153908497 [GRCh37]
ChrX:Xq28		 benign
GRCh37/hg19 Xq21.32-28(chrX:92814516-155233731)x1 copy number loss not provided [RCV000845672] ChrX:92814516..155233731 [GRCh37]
ChrX:Xq21.32-28		 pathogenic
GRCh37/hg19 Xq25-28(chrX:122132166-155097214) copy number loss Intellectual disability [RCV001249592] ChrX:122132166..155097214 [GRCh37]
ChrX:Xq25-28		 likely pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1 copy number loss not provided [RCV000848828] ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-q28		 pathogenic
GRCh37/hg19 Xp11.1-q28(chrX:58455352-155233731)x1 copy number loss not provided [RCV000846274] ChrX:58455352..155233731 [GRCh37]
ChrX:Xp11.1-q28		 pathogenic
GRCh37/hg19 Xq24-28(chrX:118150047-155233731)x1 copy number loss not provided [RCV000847838] ChrX:118150047..155233731 [GRCh37]
ChrX:Xq24-28		 pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:54941868-155233731)x1 copy number loss not provided [RCV000848218] ChrX:54941868..155233731 [GRCh37]
ChrX:Xp11.21-q28		 uncertain significance
GRCh37/hg19 Xq25-28(chrX:122757437-155208244)x1 copy number loss Premature ovarian insufficiency [RCV000852349] ChrX:122757437..155208244 [GRCh37]
ChrX:Xq25-28		 likely pathogenic
NM_001081573.3(GAB3):c.829C>T (p.Leu277=) single nucleotide variant not provided [RCV000911337] ChrX:154712469 [GRCh38]
ChrX:153940744 [GRCh37]
ChrX:Xq28		 benign
GRCh37/hg19 Xp11.21-q28(chrX:55507789-155198481)x3 copy number gain See cases [RCV001263024] ChrX:55507789..155198481 [GRCh37]
ChrX:Xp11.21-q28		 pathogenic
GRCh37/hg19 Xq21.33-28(chrX:94264404-155233731)x1 copy number loss not provided [RCV001259012] ChrX:94264404..155233731 [GRCh37]
ChrX:Xq21.33-28		 pathogenic
GRCh37/hg19 Xp11.21-q28(chrX:56469080-155233731)x3 copy number gain not provided [RCV001281359] ChrX:56469080..155233731 [GRCh37]
ChrX:Xp11.21-q28		 pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:17515 AgrOrtholog
COSMIC GAB3 COSMIC
Ensembl Genes ENSG00000160219 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000358581 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000358588 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000399588 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000412258 UniProtKB/TrEMBL
Ensembl Transcript ENST00000369568 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000369575 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000424127 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000454973 UniProtKB/TrEMBL
  ENST00000496390 ENTREZGENE
Gene3D-CATH 2.30.29.30 UniProtKB/Swiss-Prot
GTEx ENSG00000160219 GTEx
HGNC ID HGNC:17515 ENTREZGENE
Human Proteome Map GAB3 Human Proteome Map
InterPro PH-like_dom_sf UniProtKB/Swiss-Prot
  PH_domain UniProtKB/Swiss-Prot
KEGG Report hsa:139716 UniProtKB/Swiss-Prot
NCBI Gene 139716 ENTREZGENE
OMIM 300482 OMIM
Pfam PF00169 UniProtKB/Swiss-Prot
PharmGKB PA28479 PharmGKB
PROSITE PH_DOMAIN UniProtKB/Swiss-Prot
SMART SM00233 UniProtKB/Swiss-Prot
UniProt GAB3_HUMAN UniProtKB/Swiss-Prot
  H7C3J9_HUMAN UniProtKB/TrEMBL
  L0R5B0_HUMAN UniProtKB/TrEMBL
  Q8WWW8 ENTREZGENE
UniProt Secondary A6NHF8 UniProtKB/Swiss-Prot
  E9PB44 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-11-24 GAB3  GRB2 associated binding protein 3    GRB2-associated binding protein 3  Symbol and/or name change 5135510 APPROVED
2011-09-01 GAB3  GRB2-associated binding protein 3  GAB3  GRB2-associated binding protein 3  Symbol and/or name change 5135510 APPROVED