CTAG1B (cancer/testis antigen 1B) - Rat Genome Database

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Gene: CTAG1B (cancer/testis antigen 1B) Homo sapiens
Analyze
No known orthologs.
Symbol: CTAG1B
Name: cancer/testis antigen 1B
RGD ID: 1353571
HGNC Page HGNC
Description: Exhibits identical protein binding activity. Predicted to be involved in positive regulation of transcription by RNA polymerase II and tRNA threonylcarbamoyladenosine metabolic process. Localizes to cytoplasm.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: autoimmunogenic cancer/testis antigen NY-ESO-1; cancer antigen 3; cancer/testis antigen 1; cancer/testis antigen 6.1; CT6.1; CTAG; CTAG1; CTAG1A; ESO1; l antigen family member 2; LAGE-2; LAGE2B; New York esophageal squamous cell carcinoma 1; NY-ESO-1
RGD Orthologs
Alliance Genes
More Info homologs ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 EnsemblX154,617,609 - 154,619,282 (-)EnsemblGRCh38hg38GRCh38
GRCh38X154,617,609 - 154,619,282 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X153,845,865 - 153,847,533 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X153,499,059 - 153,500,714 (-)NCBINCBI36hg18NCBI36
Build 34X153,409,569 - 153,411,224NCBI
CeleraX154,005,869 - 154,007,526 (-)NCBI
Cytogenetic MapXq28NCBI
HuRefX142,391,018 - 142,392,145 (-)NCBIHuRef
CHM1_1X153,757,593 - 153,759,255 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
cytoplasm  (IDA)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Schizophrenia  (IAGP)
References

References - curated
1. RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:9050879   PMID:9605863   PMID:9626360   PMID:9759882   PMID:10523621   PMID:10901371   PMID:11120859   PMID:11256614   PMID:11351307   PMID:11397121   PMID:11709543   PMID:11782380  
PMID:12065688   PMID:12138174   PMID:12209997   PMID:12445278   PMID:12452034   PMID:12477932   PMID:12853579   PMID:12889868   PMID:14503968   PMID:14522938   PMID:14559844   PMID:14583496  
PMID:15026363   PMID:15069548   PMID:15240519   PMID:15252201   PMID:15475443   PMID:15521719   PMID:15671442   PMID:15772651   PMID:16114059   PMID:16140944   PMID:16596224   PMID:16751374  
PMID:16951317   PMID:17023585   PMID:17137291   PMID:17208940   PMID:17488334   PMID:17625806   PMID:17640060   PMID:18396787   PMID:18923710   PMID:18982744   PMID:19030781   PMID:19155470  
PMID:19212631   PMID:19380770   PMID:19531622   PMID:19728336   PMID:19795170   PMID:20044626   PMID:20053942   PMID:20368442   PMID:20591578   PMID:20733200   PMID:21131422   PMID:21247062  
PMID:21556122   PMID:21873635   PMID:21900253   PMID:21933959   PMID:22323448   PMID:22388761   PMID:22529253   PMID:22936067   PMID:23312906   PMID:23454162   PMID:23599152   PMID:23645764  
PMID:23923079   PMID:24103781   PMID:24290058   PMID:24482145   PMID:24744590   PMID:24777967   PMID:24777968   PMID:24789172   PMID:24811699   PMID:25078248   PMID:25412843   PMID:25416956  
PMID:25954764   PMID:26191258   PMID:26324743   PMID:26413775   PMID:26903513   PMID:27070449   PMID:27140836   PMID:27466502   PMID:27793776   PMID:27993576   PMID:28105694   PMID:28536262  
PMID:28677424   PMID:28716148   PMID:29058035   PMID:29480665   PMID:30384365   PMID:30953385   PMID:31095042   PMID:31158427   PMID:31227504   PMID:31391242   PMID:32296183   PMID:32600281  


Genomics

Position Markers
DXS1073  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,828,908 - 153,829,128UniSTSGRCh37
Build 36X153,482,102 - 153,482,322RGDNCBI36
CeleraX153,988,914 - 153,989,132RGD
Cytogenetic MapXq27UniSTS
Cytogenetic MapXq28UniSTS
HuRefX142,374,111 - 142,374,331UniSTS
Marshfield Genetic MapX102.35UniSTS
Marshfield Genetic MapX102.35RGD
Genethon Genetic MapX196.5UniSTS
deCODE Assembly MapX188.22UniSTS
ECD03314  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,828,141 - 153,828,940UniSTSGRCh37
Build 36X153,481,335 - 153,482,134RGDNCBI36
CeleraX153,988,147 - 153,988,946RGD
Cytogenetic MapXq28UniSTS
HuRefX142,373,344 - 142,374,143UniSTS
ECD03580  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,827,278 - 153,828,068UniSTSGRCh37
Build 36X153,480,472 - 153,481,262RGDNCBI36
CeleraX153,987,284 - 153,988,074RGD
Cytogenetic MapXq28UniSTS
HuRefX142,372,481 - 142,373,271UniSTS
ECD04818  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,832,469 - 153,833,222UniSTSGRCh37
Build 36X153,485,663 - 153,486,416RGDNCBI36
CeleraX153,992,473 - 153,993,226RGD
Cytogenetic MapXq28UniSTS
HuRefX142,377,672 - 142,378,425UniSTS
ECD08940  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,847,951 - 153,848,592UniSTSGRCh37
GRCh37X153,812,348 - 153,812,989UniSTSGRCh37
Build 36X153,465,542 - 153,466,183RGDNCBI36
CeleraX153,972,274 - 153,972,915RGD
Cytogenetic MapXq28UniSTS
HuRefX142,392,574 - 142,393,215UniSTS
ECD09418  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,824,768 - 153,825,397UniSTSGRCh37
Build 36X153,477,962 - 153,478,591RGDNCBI36
CeleraX153,984,775 - 153,985,404RGD
Cytogenetic MapXq28UniSTS
HuRefX142,369,972 - 142,370,601UniSTS
ECD10017  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,824,108 - 153,824,721UniSTSGRCh37
Build 36X153,477,302 - 153,477,915RGDNCBI36
CeleraX153,984,115 - 153,984,728RGD
Cytogenetic MapXq28UniSTS
HuRefX142,369,312 - 142,369,925UniSTS
ECD10271  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,847,236 - 153,847,842UniSTSGRCh37
GRCh37X153,813,098 - 153,813,704UniSTSGRCh37
Build 36X153,466,292 - 153,466,898RGDNCBI36
Cytogenetic MapXq28UniSTS
HuRefX142,391,859 - 142,392,465UniSTS
ECD10991  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,830,170 - 153,830,755UniSTSGRCh37
Build 36X153,483,364 - 153,483,949RGDNCBI36
CeleraX153,990,174 - 153,990,759RGD
Cytogenetic MapXq28UniSTS
HuRefX142,375,373 - 142,375,958UniSTS
ECD11531  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,820,932 - 153,821,501UniSTSGRCh37
Build 36X153,474,126 - 153,474,695RGDNCBI36
CeleraX153,980,939 - 153,981,508RGD
Cytogenetic MapXq28UniSTS
HuRefX142,366,136 - 142,366,705UniSTS
ECD13187  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,846,048 - 153,846,572UniSTSGRCh37
GRCh37X153,814,368 - 153,814,892UniSTSGRCh37
Build 36X153,467,562 - 153,468,086RGDNCBI36
CeleraX154,006,052 - 154,006,576RGD
Cytogenetic MapXq28UniSTS
ECD13456  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,829,539 - 153,830,056UniSTSGRCh37
Build 36X153,482,733 - 153,483,250RGDNCBI36
CeleraX153,989,543 - 153,990,060RGD
Cytogenetic MapXq28UniSTS
HuRefX142,374,742 - 142,375,259UniSTS
ECD13664  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,830,800 - 153,831,312UniSTSGRCh37
Build 36X153,483,994 - 153,484,506RGDNCBI36
CeleraX153,990,804 - 153,991,316RGD
Cytogenetic MapXq28UniSTS
HuRefX142,376,003 - 142,376,515UniSTS
ECD14025  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,822,713 - 153,823,216UniSTSGRCh37
Build 36X153,475,907 - 153,476,410RGDNCBI36
CeleraX153,982,720 - 153,983,223RGD
Cytogenetic MapXq28UniSTS
HuRefX142,367,917 - 142,368,420UniSTS
ECD14189  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,829,012 - 153,829,511UniSTSGRCh37
Build 36X153,482,206 - 153,482,705RGDNCBI36
CeleraX153,989,016 - 153,989,515RGD
Cytogenetic MapXq28UniSTS
HuRefX142,374,215 - 142,374,714UniSTS
ECD16916  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,834,950 - 153,835,370UniSTSGRCh37
Build 36X153,488,144 - 153,488,564RGDNCBI36
CeleraX153,994,954 - 153,995,374RGD
Cytogenetic MapXq28UniSTS
HuRefX142,380,153 - 142,380,573UniSTS
ECD19575  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,878,614 - 153,878,931UniSTSGRCh37
GRCh37X153,836,355 - 153,836,672UniSTSGRCh37
Build 36X153,489,549 - 153,489,866RGDNCBI36
CeleraX153,996,359 - 153,996,676RGD
CeleraX154,036,695 - 154,037,012UniSTS
Cytogenetic MapXq28UniSTS
HuRefX142,381,559 - 142,381,876UniSTS
HuRefX142,423,237 - 142,423,554UniSTS
ECD20147  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,821,917 - 153,822,212UniSTSGRCh37
Build 36X153,475,111 - 153,475,406RGDNCBI36
CeleraX153,981,924 - 153,982,219RGD
Cytogenetic MapXq28UniSTS
HuRefX142,367,121 - 142,367,416UniSTS
ECD20832  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,831,990 - 153,832,260UniSTSGRCh37
Build 36X153,485,184 - 153,485,454RGDNCBI36
CeleraX153,991,994 - 153,992,264RGD
Cytogenetic MapXq28UniSTS
HuRefX142,377,193 - 142,377,463UniSTS
ECD20854  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,834,126 - 153,834,395UniSTSGRCh37
Build 36X153,487,320 - 153,487,589RGDNCBI36
CeleraX153,994,130 - 153,994,399RGD
Cytogenetic MapXq28UniSTS
HuRefX142,379,329 - 142,379,598UniSTS
ECD21943  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,820,126 - 153,820,360UniSTSGRCh37
Build 36X153,473,320 - 153,473,554RGDNCBI36
CeleraX153,980,133 - 153,980,367RGD
Cytogenetic MapXq28UniSTS
HuRefX142,365,330 - 142,365,564UniSTS
ECD22079  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,826,136 - 153,826,366UniSTSGRCh37
Build 36X153,479,330 - 153,479,560RGDNCBI36
CeleraX153,986,143 - 153,986,373RGD
Cytogenetic MapXq28UniSTS
HuRefX142,371,340 - 142,371,570UniSTS
ECD23788  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,836,041 - 153,836,217UniSTSGRCh37
Build 36X153,489,235 - 153,489,411RGDNCBI36
CeleraX153,996,045 - 153,996,221RGD
Cytogenetic MapXq28UniSTS
HuRefX142,381,244 - 142,381,420UniSTS
ECD24456  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,846,714 - 153,846,837UniSTSGRCh37
GRCh37X153,814,103 - 153,814,226UniSTSGRCh37
Build 36X153,467,297 - 153,467,420RGDNCBI36
CeleraX154,006,718 - 154,006,841RGD
Cytogenetic MapXq28UniSTS
HuRefX142,391,337 - 142,391,460UniSTS
REN90033  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,819,890 - 153,820,125UniSTSGRCh37
Build 36X153,473,084 - 153,473,319RGDNCBI36
CeleraX153,979,897 - 153,980,132RGD
Cytogenetic MapXq28UniSTS
HuRefX142,365,094 - 142,365,329UniSTS
REN90034  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,820,081 - 153,820,325UniSTSGRCh37
Build 36X153,473,275 - 153,473,519RGDNCBI36
CeleraX153,980,088 - 153,980,332RGD
Cytogenetic MapXq28UniSTS
HuRefX142,365,285 - 142,365,529UniSTS
REN90035  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,820,244 - 153,820,501UniSTSGRCh37
Build 36X153,473,438 - 153,473,695RGDNCBI36
CeleraX153,980,251 - 153,980,508RGD
Cytogenetic MapXq28UniSTS
HuRefX142,365,448 - 142,365,705UniSTS
REN90036  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,820,341 - 153,820,589UniSTSGRCh37
Build 36X153,473,535 - 153,473,783RGDNCBI36
CeleraX153,980,348 - 153,980,596RGD
Cytogenetic MapXq28UniSTS
HuRefX142,365,545 - 142,365,793UniSTS
REN90037  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,820,566 - 153,820,814UniSTSGRCh37
Build 36X153,473,760 - 153,474,008RGDNCBI36
CeleraX153,980,573 - 153,980,821RGD
Cytogenetic MapXq28UniSTS
HuRefX142,365,770 - 142,366,018UniSTS
REN90038  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,820,786 - 153,821,050UniSTSGRCh37
Build 36X153,473,980 - 153,474,244RGDNCBI36
CeleraX153,980,793 - 153,981,057RGD
Cytogenetic MapXq28UniSTS
HuRefX142,365,990 - 142,366,254UniSTS
REN90039  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,821,027 - 153,821,280UniSTSGRCh37
Build 36X153,474,221 - 153,474,474RGDNCBI36
CeleraX153,981,034 - 153,981,287RGD
Cytogenetic MapXq28UniSTS
HuRefX142,366,231 - 142,366,484UniSTS
REN90040  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,821,260 - 153,821,498UniSTSGRCh37
Build 36X153,474,454 - 153,474,692RGDNCBI36
CeleraX153,981,267 - 153,981,505RGD
Cytogenetic MapXq28UniSTS
HuRefX142,366,464 - 142,366,702UniSTS
REN90041  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,821,490 - 153,821,749UniSTSGRCh37
Build 36X153,474,684 - 153,474,943RGDNCBI36
CeleraX153,981,497 - 153,981,756RGD
Cytogenetic MapXq28UniSTS
HuRefX142,366,694 - 142,366,953UniSTS
REN90042  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,821,730 - 153,821,971UniSTSGRCh37
Build 36X153,474,924 - 153,475,165RGDNCBI36
CeleraX153,981,737 - 153,981,978RGD
Cytogenetic MapXq28UniSTS
HuRefX142,366,934 - 142,367,175UniSTS
REN90043  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,821,947 - 153,822,197UniSTSGRCh37
Build 36X153,475,141 - 153,475,391RGDNCBI36
CeleraX153,981,954 - 153,982,204RGD
Cytogenetic MapXq28UniSTS
HuRefX142,367,151 - 142,367,401UniSTS
REN90044  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,822,141 - 153,822,405UniSTSGRCh37
Build 36X153,475,335 - 153,475,599RGDNCBI36
CeleraX153,982,148 - 153,982,412RGD
Cytogenetic MapXq28UniSTS
HuRefX142,367,345 - 142,367,609UniSTS
REN90045  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,822,397 - 153,822,655UniSTSGRCh37
Build 36X153,475,591 - 153,475,849RGDNCBI36
CeleraX153,982,404 - 153,982,662RGD
Cytogenetic MapXq28UniSTS
HuRefX142,367,601 - 142,367,859UniSTS
REN90046  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,822,632 - 153,822,867UniSTSGRCh37
Build 36X153,475,826 - 153,476,061RGDNCBI36
CeleraX153,982,639 - 153,982,874RGD
Cytogenetic MapXq28UniSTS
HuRefX142,367,836 - 142,368,071UniSTS
REN90047  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,822,844 - 153,823,099UniSTSGRCh37
Build 36X153,476,038 - 153,476,293RGDNCBI36
CeleraX153,982,851 - 153,983,106RGD
Cytogenetic MapXq28UniSTS
HuRefX142,368,048 - 142,368,303UniSTS
REN90048  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,823,075 - 153,823,338UniSTSGRCh37
Build 36X153,476,269 - 153,476,532RGDNCBI36
CeleraX153,983,082 - 153,983,345RGD
Cytogenetic MapXq28UniSTS
HuRefX142,368,279 - 142,368,542UniSTS
REN90049  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,823,337 - 153,823,587UniSTSGRCh37
Build 36X153,476,531 - 153,476,781RGDNCBI36
CeleraX153,983,344 - 153,983,594RGD
Cytogenetic MapXq28UniSTS
HuRefX142,368,541 - 142,368,791UniSTS
REN90050  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,823,568 - 153,823,817UniSTSGRCh37
Build 36X153,476,762 - 153,477,011RGDNCBI36
CeleraX153,983,575 - 153,983,824RGD
Cytogenetic MapXq28UniSTS
HuRefX142,368,772 - 142,369,021UniSTS
REN90051  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,823,730 - 153,823,971UniSTSGRCh37
Build 36X153,476,924 - 153,477,165RGDNCBI36
CeleraX153,983,737 - 153,983,978RGD
Cytogenetic MapXq28UniSTS
HuRefX142,368,934 - 142,369,175UniSTS
REN90052  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,823,981 - 153,824,189UniSTSGRCh37
GRCh37X153,823,936 - 153,824,189UniSTSGRCh37
Build 36X153,477,130 - 153,477,383RGDNCBI36
CeleraX153,983,943 - 153,984,196RGD
CeleraX153,983,988 - 153,984,196UniSTS
Cytogenetic MapXq28UniSTS
HuRefX142,369,140 - 142,369,393UniSTS
HuRefX142,369,185 - 142,369,393UniSTS
REN90053  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,824,171 - 153,824,422UniSTSGRCh37
Build 36X153,477,365 - 153,477,616RGDNCBI36
CeleraX153,984,178 - 153,984,429RGD
Cytogenetic MapXq28UniSTS
HuRefX142,369,375 - 142,369,626UniSTS
REN90054  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,824,397 - 153,824,645UniSTSGRCh37
Build 36X153,477,591 - 153,477,839RGDNCBI36
CeleraX153,984,404 - 153,984,652RGD
Cytogenetic MapXq28UniSTS
HuRefX142,369,601 - 142,369,849UniSTS
REN90055  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,824,610 - 153,824,853UniSTSGRCh37
Build 36X153,477,804 - 153,478,047RGDNCBI36
CeleraX153,984,617 - 153,984,860RGD
Cytogenetic MapXq28UniSTS
HuRefX142,369,814 - 142,370,057UniSTS
REN90056  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,824,834 - 153,825,088UniSTSGRCh37
Build 36X153,478,028 - 153,478,282RGDNCBI36
CeleraX153,984,841 - 153,985,095RGD
Cytogenetic MapXq28UniSTS
HuRefX142,370,038 - 142,370,292UniSTS
REN90057  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,825,052 - 153,825,282UniSTSGRCh37
Build 36X153,478,246 - 153,478,476RGDNCBI36
CeleraX153,985,059 - 153,985,289RGD
Cytogenetic MapXq28UniSTS
HuRefX142,370,256 - 142,370,486UniSTS
REN90058  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,825,213 - 153,825,461UniSTSGRCh37
Build 36X153,478,407 - 153,478,655RGDNCBI36
CeleraX153,985,220 - 153,985,468RGD
Cytogenetic MapXq28UniSTS
HuRefX142,370,417 - 142,370,665UniSTS
REN90059  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,825,329 - 153,825,597UniSTSGRCh37
Build 36X153,478,523 - 153,478,791RGDNCBI36
CeleraX153,985,336 - 153,985,604RGD
Cytogenetic MapXq28UniSTS
HuRefX142,370,533 - 142,370,801UniSTS
REN90060  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,825,570 - 153,825,815UniSTSGRCh37
Build 36X153,478,764 - 153,479,009RGDNCBI36
CeleraX153,985,577 - 153,985,822RGD
Cytogenetic MapXq28UniSTS
HuRefX142,370,774 - 142,371,019UniSTS
REN90061  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,825,804 - 153,826,054UniSTSGRCh37
Build 36X153,478,998 - 153,479,248RGDNCBI36
CeleraX153,985,811 - 153,986,061RGD
Cytogenetic MapXq28UniSTS
HuRefX142,371,008 - 142,371,258UniSTS
REN90062  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,826,036 - 153,826,290UniSTSGRCh37
Build 36X153,479,230 - 153,479,484RGDNCBI36
CeleraX153,986,043 - 153,986,297RGD
Cytogenetic MapXq28UniSTS
HuRefX142,371,240 - 142,371,494UniSTS
REN90063  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,826,267 - 153,826,520UniSTSGRCh37
Build 36X153,479,461 - 153,479,714RGDNCBI36
CeleraX153,986,274 - 153,986,527RGD
Cytogenetic MapXq28UniSTS
HuRefX142,371,471 - 142,371,724UniSTS
REN90064  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,826,500 - 153,826,724UniSTSGRCh37
Build 36X153,479,694 - 153,479,918RGDNCBI36
CeleraX153,986,507 - 153,986,731RGD
Cytogenetic MapXq28UniSTS
HuRefX142,371,704 - 142,371,928UniSTS
REN90065  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,826,873 - 153,827,137UniSTSGRCh37
Build 36X153,480,067 - 153,480,331RGDNCBI36
CeleraX153,986,880 - 153,987,143RGD
Cytogenetic MapXq28UniSTS
HuRefX142,372,077 - 142,372,340UniSTS
REN90066  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,827,118 - 153,827,372UniSTSGRCh37
Build 36X153,480,312 - 153,480,566RGDNCBI36
CeleraX153,987,124 - 153,987,378RGD
Cytogenetic MapXq28UniSTS
HuRefX142,372,321 - 142,372,575UniSTS
REN90067  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,827,360 - 153,827,610UniSTSGRCh37
Build 36X153,480,554 - 153,480,804RGDNCBI36
CeleraX153,987,366 - 153,987,616RGD
Cytogenetic MapXq28UniSTS
HuRefX142,372,563 - 142,372,813UniSTS
REN90068  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,827,597 - 153,827,838UniSTSGRCh37
Build 36X153,480,791 - 153,481,032RGDNCBI36
CeleraX153,987,603 - 153,987,844RGD
Cytogenetic MapXq28UniSTS
HuRefX142,372,800 - 142,373,041UniSTS
REN90069  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,827,815 - 153,828,067UniSTSGRCh37
Build 36X153,481,009 - 153,481,261RGDNCBI36
CeleraX153,987,821 - 153,988,073RGD
Cytogenetic MapXq28UniSTS
HuRefX142,373,018 - 142,373,270UniSTS
REN90070  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,828,045 - 153,828,289UniSTSGRCh37
Build 36X153,481,239 - 153,481,483RGDNCBI36
CeleraX153,988,051 - 153,988,295RGD
Cytogenetic MapXq28UniSTS
HuRefX142,373,248 - 142,373,492UniSTS
REN90071  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,828,270 - 153,828,506UniSTSGRCh37
Build 36X153,481,464 - 153,481,700RGDNCBI36
CeleraX153,988,276 - 153,988,512RGD
Cytogenetic MapXq28UniSTS
HuRefX142,373,473 - 142,373,709UniSTS
REN90072  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,828,485 - 153,828,734UniSTSGRCh37
Build 36X153,481,679 - 153,481,928RGDNCBI36
CeleraX153,988,491 - 153,988,740RGD
Cytogenetic MapXq28UniSTS
HuRefX142,373,688 - 142,373,937UniSTS
REN90073  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,828,704 - 153,828,939UniSTSGRCh37
Build 36X153,481,898 - 153,482,133RGDNCBI36
CeleraX153,988,710 - 153,988,945RGD
Cytogenetic MapXq28UniSTS
HuRefX142,373,907 - 142,374,142UniSTS
REN90074  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,828,901 - 153,829,160UniSTSGRCh37
Build 36X153,482,095 - 153,482,354RGDNCBI36
CeleraX153,988,907 - 153,989,164RGD
Cytogenetic MapXq28UniSTS
HuRefX142,374,104 - 142,374,363UniSTS
REN90075  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,829,137 - 153,829,398UniSTSGRCh37
Build 36X153,482,331 - 153,482,592RGDNCBI36
CeleraX153,989,141 - 153,989,402RGD
Cytogenetic MapXq28UniSTS
HuRefX142,374,340 - 142,374,601UniSTS
REN90076  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,829,395 - 153,829,630UniSTSGRCh37
Build 36X153,482,589 - 153,482,824RGDNCBI36
CeleraX153,989,399 - 153,989,634RGD
Cytogenetic MapXq28UniSTS
HuRefX142,374,598 - 142,374,833UniSTS
REN90077  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,829,569 - 153,829,793UniSTSGRCh37
Build 36X153,482,763 - 153,482,987RGDNCBI36
CeleraX153,989,573 - 153,989,797RGD
Cytogenetic MapXq28UniSTS
HuRefX142,374,772 - 142,374,996UniSTS
REN90078  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,829,748 - 153,830,008UniSTSGRCh37
Build 36X153,482,942 - 153,483,202RGDNCBI36
CeleraX153,989,752 - 153,990,012RGD
Cytogenetic MapXq28UniSTS
HuRefX142,374,951 - 142,375,211UniSTS
REN90079  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,829,985 - 153,830,250UniSTSGRCh37
Build 36X153,483,179 - 153,483,444RGDNCBI36
CeleraX153,989,989 - 153,990,254RGD
Cytogenetic MapXq28UniSTS
HuRefX142,375,188 - 142,375,453UniSTS
REN90080  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,830,225 - 153,830,458UniSTSGRCh37
Build 36X153,483,419 - 153,483,652RGDNCBI36
CeleraX153,990,229 - 153,990,462RGD
Cytogenetic MapXq28UniSTS
HuRefX142,375,428 - 142,375,661UniSTS
REN90081  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,830,426 - 153,830,650UniSTSGRCh37
Build 36X153,483,620 - 153,483,844RGDNCBI36
CeleraX153,990,430 - 153,990,654RGD
Cytogenetic MapXq28UniSTS
HuRefX142,375,629 - 142,375,853UniSTS
REN90082  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,830,621 - 153,830,870UniSTSGRCh37
Build 36X153,483,815 - 153,484,064RGDNCBI36
CeleraX153,990,625 - 153,990,874RGD
Cytogenetic MapXq28UniSTS
HuRefX142,375,824 - 142,376,073UniSTS
REN90083  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,830,846 - 153,831,085UniSTSGRCh37
Build 36X153,484,040 - 153,484,279RGDNCBI36
CeleraX153,990,850 - 153,991,089RGD
Cytogenetic MapXq28UniSTS
HuRefX142,376,049 - 142,376,288UniSTS
REN90084  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,831,059 - 153,831,326UniSTSGRCh37
Build 36X153,484,253 - 153,484,520RGDNCBI36
CeleraX153,991,063 - 153,991,330RGD
Cytogenetic MapXq28UniSTS
HuRefX142,376,262 - 142,376,529UniSTS
REN90085  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,831,230 - 153,831,488UniSTSGRCh37
Build 36X153,484,424 - 153,484,682RGDNCBI36
CeleraX153,991,234 - 153,991,492RGD
Cytogenetic MapXq28UniSTS
HuRefX142,376,433 - 142,376,691UniSTS
REN90086  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,831,463 - 153,831,714UniSTSGRCh37
Build 36X153,484,657 - 153,484,908RGDNCBI36
CeleraX153,991,467 - 153,991,718RGD
Cytogenetic MapXq28UniSTS
HuRefX142,376,666 - 142,376,917UniSTS
REN90087  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,831,703 - 153,831,938UniSTSGRCh37
Build 36X153,484,897 - 153,485,132RGDNCBI36
CeleraX153,991,707 - 153,991,942RGD
Cytogenetic MapXq28UniSTS
HuRefX142,376,906 - 142,377,141UniSTS
REN90088  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,831,927 - 153,832,190UniSTSGRCh37
Build 36X153,485,121 - 153,485,384RGDNCBI36
CeleraX153,991,931 - 153,992,194RGD
Cytogenetic MapXq28UniSTS
HuRefX142,377,130 - 142,377,393UniSTS
REN90089  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,832,167 - 153,832,417UniSTSGRCh37
Build 36X153,485,361 - 153,485,611RGDNCBI36
CeleraX153,992,171 - 153,992,421RGD
Cytogenetic MapXq28UniSTS
HuRefX142,377,370 - 142,377,620UniSTS
REN90090  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,832,394 - 153,832,643UniSTSGRCh37
Build 36X153,485,588 - 153,485,837RGDNCBI36
CeleraX153,992,398 - 153,992,647RGD
Cytogenetic MapXq28UniSTS
HuRefX142,377,597 - 142,377,846UniSTS
REN90091  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,832,628 - 153,832,877UniSTSGRCh37
Build 36X153,485,822 - 153,486,071RGDNCBI36
CeleraX153,992,632 - 153,992,881RGD
Cytogenetic MapXq28UniSTS
HuRefX142,377,831 - 142,378,080UniSTS
REN90092  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,832,838 - 153,833,071UniSTSGRCh37
Build 36X153,486,032 - 153,486,265RGDNCBI36
CeleraX153,992,842 - 153,993,075RGD
Cytogenetic MapXq28UniSTS
HuRefX142,378,041 - 142,378,274UniSTS
REN90093  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,833,054 - 153,833,297UniSTSGRCh37
Build 36X153,486,248 - 153,486,491RGDNCBI36
CeleraX153,993,058 - 153,993,301RGD
Cytogenetic MapXq28UniSTS
HuRefX142,378,257 - 142,378,500UniSTS
REN90094  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,833,734 - 153,833,974UniSTSGRCh37
Build 36X153,486,928 - 153,487,168RGDNCBI36
CeleraX153,993,738 - 153,993,978RGD
Cytogenetic MapXq28UniSTS
HuRefX142,378,937 - 142,379,177UniSTS
REN90095  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,833,955 - 153,834,203UniSTSGRCh37
Build 36X153,487,149 - 153,487,397RGDNCBI36
CeleraX153,993,959 - 153,994,207RGD
Cytogenetic MapXq28UniSTS
HuRefX142,379,158 - 142,379,406UniSTS
REN90096  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,834,196 - 153,834,457UniSTSGRCh37
Build 36X153,487,390 - 153,487,651RGDNCBI36
CeleraX153,994,200 - 153,994,461RGD
Cytogenetic MapXq28UniSTS
HuRefX142,379,399 - 142,379,660UniSTS
REN90097  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,834,434 - 153,834,675UniSTSGRCh37
Build 36X153,487,628 - 153,487,869RGDNCBI36
CeleraX153,994,438 - 153,994,679RGD
Cytogenetic MapXq28UniSTS
HuRefX142,379,637 - 142,379,878UniSTS
REN90098  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,834,656 - 153,834,920UniSTSGRCh37
Build 36X153,487,850 - 153,488,114RGDNCBI36
CeleraX153,994,660 - 153,994,924RGD
Cytogenetic MapXq28UniSTS
HuRefX142,379,859 - 142,380,123UniSTS
REN90099  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,834,918 - 153,835,157UniSTSGRCh37
Build 36X153,488,112 - 153,488,351RGDNCBI36
CeleraX153,994,922 - 153,995,161RGD
Cytogenetic MapXq28UniSTS
HuRefX142,380,121 - 142,380,360UniSTS
REN90100  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,835,132 - 153,835,364UniSTSGRCh37
Build 36X153,488,326 - 153,488,558RGDNCBI36
CeleraX153,995,136 - 153,995,368RGD
Cytogenetic MapXq28UniSTS
HuRefX142,380,335 - 142,380,567UniSTS
REN90101  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,835,334 - 153,835,569UniSTSGRCh37
Build 36X153,488,528 - 153,488,763RGDNCBI36
CeleraX153,995,338 - 153,995,573RGD
Cytogenetic MapXq28UniSTS
HuRefX142,380,537 - 142,380,772UniSTS
REN90102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,835,542 - 153,835,801UniSTSGRCh37
Build 36X153,488,736 - 153,488,995RGDNCBI36
CeleraX153,995,546 - 153,995,805RGD
Cytogenetic MapXq28UniSTS
HuRefX142,380,745 - 142,381,004UniSTS
REN90103  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,835,792 - 153,836,046UniSTSGRCh37
Build 36X153,488,986 - 153,489,240RGDNCBI36
CeleraX153,995,796 - 153,996,050RGD
Cytogenetic MapXq28UniSTS
HuRefX142,380,995 - 142,381,249UniSTS
REN90104  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,835,948 - 153,836,217UniSTSGRCh37
Build 36X153,489,142 - 153,489,411RGDNCBI36
CeleraX153,995,952 - 153,996,221RGD
Cytogenetic MapXq28UniSTS
HuRefX142,381,151 - 142,381,420UniSTS
REN90105  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,836,194 - 153,836,420UniSTSGRCh37
Build 36X153,489,388 - 153,489,614RGDNCBI36
CeleraX153,996,198 - 153,996,424RGD
Cytogenetic MapXq28UniSTS
HuRefX142,381,397 - 142,381,624UniSTS
REN90106  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,836,454 - 153,836,681UniSTSGRCh37
Build 36X153,489,648 - 153,489,875RGDNCBI36
CeleraX153,996,458 - 153,996,685RGD
Cytogenetic MapXq28UniSTS
HuRefX142,381,658 - 142,381,885UniSTS
REN90107  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,836,656 - 153,836,907UniSTSGRCh37
Build 36X153,489,850 - 153,490,101RGDNCBI36
CeleraX153,996,660 - 153,996,911RGD
Cytogenetic MapXq28UniSTS
HuRefX142,381,860 - 142,382,111UniSTS
REN90108  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,836,883 - 153,837,131UniSTSGRCh37
Build 36X153,490,077 - 153,490,325RGDNCBI36
CeleraX153,996,887 - 153,997,135RGD
Cytogenetic MapXq28UniSTS
HuRefX142,382,087 - 142,382,335UniSTS
REN90109  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,837,101 - 153,837,352UniSTSGRCh37
Build 36X153,490,295 - 153,490,546RGDNCBI36
CeleraX153,997,105 - 153,997,356RGD
Cytogenetic MapXq28UniSTS
HuRefX142,382,305 - 142,382,556UniSTS
REN90110  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,837,479 - 153,837,704UniSTSGRCh37
Build 36X153,490,673 - 153,490,898RGDNCBI36
CeleraX153,997,483 - 153,997,708RGD
Cytogenetic MapXq28UniSTS
HuRefX142,382,683 - 142,382,908UniSTS
REN90111  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,837,689 - 153,837,914UniSTSGRCh37
Build 36X153,490,883 - 153,491,108RGDNCBI36
CeleraX153,997,693 - 153,997,918RGD
Cytogenetic MapXq28UniSTS
HuRefX142,382,893 - 142,383,118UniSTS
REN90113  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,838,098 - 153,838,322UniSTSGRCh37
Build 36X153,491,292 - 153,491,516RGDNCBI36
CeleraX153,998,102 - 153,998,326RGD
Cytogenetic MapXq28UniSTS
HuRefX142,383,302 - 142,383,526UniSTS
REN90115  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,838,452 - 153,838,677UniSTSGRCh37
GRCh375154,017,320 - 154,017,546UniSTSGRCh37
Build 36X153,491,646 - 153,491,871RGDNCBI36
CeleraX153,998,456 - 153,998,681RGD
Celera5150,094,366 - 150,094,592UniSTS
Cytogenetic MapXq28UniSTS
HuRefX142,383,656 - 142,383,881UniSTS
REN90116  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,838,646 - 153,838,908UniSTSGRCh37
Build 36X153,491,840 - 153,492,102RGDNCBI36
CeleraX153,998,650 - 153,998,912RGD
Cytogenetic MapXq28UniSTS
HuRefX142,383,850 - 142,384,112UniSTS
REN90118  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,838,979 - 153,839,239UniSTSGRCh37
Build 36X153,492,173 - 153,492,433RGDNCBI36
CeleraX153,998,983 - 153,999,243RGD
Cytogenetic MapXq28UniSTS
HuRefX142,384,183 - 142,384,443UniSTS
REN90119  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,839,212 - 153,839,474UniSTSGRCh37
Build 36X153,492,406 - 153,492,668RGDNCBI36
CeleraX153,999,216 - 153,999,478RGD
Cytogenetic MapXq28UniSTS
HuRefX142,384,416 - 142,384,678UniSTS
REN90120  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371920,394,239 - 20,394,505UniSTSGRCh37
GRCh37X153,839,473 - 153,839,738UniSTSGRCh37
Build 36X153,492,667 - 153,492,932RGDNCBI36
Celera1920,300,362 - 20,300,628UniSTS
CeleraX153,999,477 - 153,999,742RGD
Cytogenetic Map19p12UniSTS
Cytogenetic MapXq28UniSTS
HuRef1919,956,275 - 19,956,541UniSTS
HuRefX142,384,677 - 142,384,942UniSTS
REN90122  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,839,779 - 153,840,003UniSTSGRCh37
Build 36X153,492,973 - 153,493,197RGDNCBI36
CeleraX153,999,783 - 154,000,007RGD
Cytogenetic MapXq28UniSTS
HuRefX142,384,983 - 142,385,207UniSTS
REN90123  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,840,394 - 153,840,626UniSTSGRCh37
Build 36X153,493,588 - 153,493,820RGDNCBI36
CeleraX154,000,398 - 154,000,630RGD
Cytogenetic MapXq28UniSTS
HuRefX142,385,598 - 142,385,830UniSTS
REN90124  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,840,660 - 153,840,884UniSTSGRCh37
Build 36X153,493,854 - 153,494,078RGDNCBI36
CeleraX154,000,664 - 154,000,888RGD
Cytogenetic MapXq28UniSTS
HuRefX142,385,864 - 142,386,088UniSTS
stSG604162  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,848,111 - 153,849,329UniSTSGRCh37
GRCh37X153,811,611 - 153,812,829UniSTSGRCh37
Build 36X153,464,805 - 153,466,023RGDNCBI36
CeleraX153,971,537 - 153,972,755RGD
Cytogenetic MapXq28UniSTS
HuRefX142,392,734 - 142,393,952UniSTS
stSG604166  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,818,694 - 153,820,145UniSTSGRCh37
Build 36X153,471,888 - 153,473,339RGDNCBI36
Cytogenetic MapXq28UniSTS
HuRefX142,363,898 - 142,365,349UniSTS
stSG604167  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,820,126 - 153,821,219UniSTSGRCh37
Build 36X153,473,320 - 153,474,413RGDNCBI36
CeleraX153,980,133 - 153,981,226RGD
Cytogenetic MapXq28UniSTS
HuRefX142,365,330 - 142,366,423UniSTS
stSG604168  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,821,200 - 153,822,205UniSTSGRCh37
Build 36X153,474,394 - 153,475,399RGDNCBI36
CeleraX153,981,207 - 153,982,212RGD
Cytogenetic MapXq28UniSTS
HuRefX142,366,404 - 142,367,409UniSTS
stSG604169  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,822,195 - 153,823,216UniSTSGRCh37
Build 36X153,475,389 - 153,476,410RGDNCBI36
CeleraX153,982,202 - 153,983,223RGD
Cytogenetic MapXq28UniSTS
HuRefX142,367,399 - 142,368,420UniSTS
stSG604170  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,823,200 - 153,824,425UniSTSGRCh37
Build 36X153,476,394 - 153,477,619RGDNCBI36
CeleraX153,983,207 - 153,984,432RGD
Cytogenetic MapXq28UniSTS
HuRefX142,368,404 - 142,369,629UniSTS
stSG604171  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,824,406 - 153,825,406UniSTSGRCh37
Build 36X153,477,600 - 153,478,600RGDNCBI36
CeleraX153,984,413 - 153,985,413RGD
Cytogenetic MapXq28UniSTS
HuRefX142,369,610 - 142,370,610UniSTS
stSG604172  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,825,371 - 153,826,376UniSTSGRCh37
Build 36X153,478,565 - 153,479,570RGDNCBI36
CeleraX153,985,378 - 153,986,383RGD
Cytogenetic MapXq28UniSTS
HuRefX142,370,575 - 142,371,580UniSTS
stSG604173  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,826,354 - 153,827,610UniSTSGRCh37
Build 36X153,479,548 - 153,480,804RGDNCBI36
CeleraX153,986,361 - 153,987,616RGD
Cytogenetic MapXq28UniSTS
HuRefX142,371,558 - 142,372,813UniSTS
stSG604174  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,827,596 - 153,828,718UniSTSGRCh37
Build 36X153,480,790 - 153,481,912RGDNCBI36
CeleraX153,987,602 - 153,988,724RGD
Cytogenetic MapXq28UniSTS
HuRefX142,372,799 - 142,373,921UniSTS
stSG604175  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,828,700 - 153,829,893UniSTSGRCh37
Build 36X153,481,894 - 153,483,087RGDNCBI36
CeleraX153,988,706 - 153,989,897RGD
Cytogenetic MapXq28UniSTS
HuRefX142,373,903 - 142,375,096UniSTS
stSG604176  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,830,017 - 153,831,231UniSTSGRCh37
Build 36X153,483,211 - 153,484,425RGDNCBI36
CeleraX153,990,021 - 153,991,235RGD
Cytogenetic MapXq28UniSTS
HuRefX142,375,220 - 142,376,434UniSTS
stSG604177  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,831,218 - 153,832,228UniSTSGRCh37
Build 36X153,484,412 - 153,485,422RGDNCBI36
CeleraX153,991,222 - 153,992,232RGD
Cytogenetic MapXq28UniSTS
HuRefX142,376,421 - 142,377,431UniSTS
stSG604178  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,832,209 - 153,833,222UniSTSGRCh37
Build 36X153,485,403 - 153,486,416RGDNCBI36
CeleraX153,992,213 - 153,993,226RGD
Cytogenetic MapXq28UniSTS
HuRefX142,377,412 - 142,378,425UniSTS
stSG604180  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,834,224 - 153,835,257UniSTSGRCh37
Build 36X153,487,418 - 153,488,451RGDNCBI36
CeleraX153,994,228 - 153,995,261RGD
Cytogenetic MapXq28UniSTS
HuRefX142,379,427 - 142,380,460UniSTS
stSG604181  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,835,245 - 153,836,465UniSTSGRCh37
Build 36X153,488,439 - 153,489,659RGDNCBI36
CeleraX153,995,249 - 153,996,469RGD
Cytogenetic MapXq28UniSTS
HuRefX142,380,448 - 142,381,669UniSTS
stSG604182  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X153,878,705 - 153,878,931UniSTSGRCh37
GRCh37X153,836,446 - 153,836,672UniSTSGRCh37
Build 36X153,489,640 - 153,489,866RGDNCBI36
CeleraX153,996,450 - 153,996,676RGD
CeleraX154,036,786 - 154,037,012UniSTS
Cytogenetic MapXq28UniSTS
HuRefX142,381,650 - 142,381,876UniSTS
HuRefX142,423,328 - 142,423,554UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:668
Count of miRNA genes:468
Interacting mature miRNAs:504
Transcripts:ENST00000328435, ENST00000359887
Prediction methods:Microtar, Miranda, Pita, Rnahybrid
Result types:miRGate_prediction

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

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


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 adipose tissue appendage
High
Medium
Low 25 25 1 2 13 15 4 8 1 1 13
Below cutoff 1473 1784 504 99 515 49 2133 1096 1278 36 944 549 50 547 1565

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000328435   ⟹   ENSP00000332602
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,617,609 - 154,619,271 (-)Ensembl
RefSeq Acc Id: ENST00000359887   ⟹   ENSP00000352953
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,617,609 - 154,619,282 (-)Ensembl
RefSeq Acc Id: NM_001327   ⟹   NP_001318
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,617,609 - 154,619,282 (-)NCBI
GRCh37X153,845,865 - 153,847,522 (-)ENTREZGENE
Build 36X153,499,059 - 153,500,714 (-)NCBI Archive
HuRefX142,391,018 - 142,392,145 (-)ENTREZGENE
CHM1_1X153,757,593 - 153,759,255 (-)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_001318   ⟸   NM_001327
- UniProtKB: P78358 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000352953   ⟸   ENST00000359887
RefSeq Acc Id: ENSP00000332602   ⟸   ENST00000328435

Promoters
RGD ID:13628656
Promoter ID:EPDNEW_H29568
Type:initiation region
Name:CTAG1B_1
Description:cancer/testis antigen 1B
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,619,283 - 154,619,343EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
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)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: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 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 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 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 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 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 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 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 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: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 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: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 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
GRCh38/hg38 Xq28(chrX:154336596-154642063)x2 copy number gain See cases [RCV000054320] ChrX:154336596..154642063 [GRCh38]
ChrX:153564946..153870337 [GRCh37]
ChrX:153218140..153523531 [NCBI36]
ChrX:Xq28
uncertain significance
GRCh38/hg38 Xq28(chrX:154394598-154626056)x2 copy number gain See cases [RCV000054322] ChrX:154394598..154626056 [GRCh38]
ChrX:153622940..153854307 [GRCh37]
ChrX:153276134..153507501 [NCBI36]
ChrX:Xq28
uncertain significance
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 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 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)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: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: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 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 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 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: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 Xq21.33-28(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: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 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 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 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 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 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 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: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 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 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 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 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 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 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 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 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 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 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 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 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 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 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)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 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 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: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 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:71267-155224766)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 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:71267-155234036)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:176426-155236656)x3 copy number gain See cases [RCV000240552] ChrX:176426..155236656 [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:225816-155234036)x2 copy number gain See cases [RCV000240464] ChrX:225816..155234036 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
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 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:2707626-155250222)x2 copy number gain See cases [RCV000240541] ChrX:2707626..155250222 [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: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:60701-155246225)x3 copy number gain See cases [RCV000446270] ChrX:60701..155246225 [GRCh37]
ChrX:Xp22.33-q28
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 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 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:168546-155233731)x4 copy number gain See cases [RCV000446932] ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-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 Xq28(chrX:150253008-155233731)x1 copy number loss See cases [RCV000446761] ChrX:150253008..155233731 [GRCh37]
ChrX:Xq28
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:168566-155233731)x1 copy number loss See cases [RCV000445720] ChrX:168566..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:168546-155233731)x1 copy number loss See cases [RCV000448393] ChrX:168546..155233731 [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:70297-155255792)x4 copy number gain See cases [RCV000448034] ChrX:70297..155255792 [GRCh37]
ChrX:Xp22.33-q28
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 Xp11.21-q28(chrX:55000501-155230750)x3 copy number gain See cases [RCV000511787] ChrX:55000501..155230750 [GRCh37]
ChrX:Xp11.21-q28
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 Xq21.1-28(chrX:79862302-155233731)x1 copy number loss See cases [RCV000511482] ChrX:79862302..155233731 [GRCh37]
ChrX:Xq21.1-28
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 Xq21.31-28(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:56457791-155233731)x3 copy number gain See cases [RCV000511307] ChrX:56457791..155233731 [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 Xq21.1-28(chrX:78230501-155233731)x1 copy number loss See cases [RCV000510820] ChrX:78230501..155233731 [GRCh37]
ChrX:Xq21.1-28
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 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 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 Xq25-28(chrX:125733292-155233846)x1 copy number loss not provided [RCV000684386] ChrX:125733292..155233846 [GRCh37]
ChrX:Xq25-28
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 Xq27.1-28(chrX:139504488-155233731)x1 copy number loss not provided [RCV000684401] ChrX:139504488..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 Xq28(chrX:153581543-153858492)x2 copy number gain not provided [RCV000684413] ChrX:153581543..153858492 [GRCh37]
ChrX:Xq28
pathogenic
GRCh37/hg19 Xq28(chrX:153621005-153868484)x4 copy number gain not provided [RCV000684414] ChrX:153621005..153868484 [GRCh37]
ChrX:Xq28
uncertain significance
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 Xq21.31-28(chrX:91140025-155233731)x1 copy number loss not provided [RCV000684357] ChrX:91140025..155233731 [GRCh37]
ChrX:Xq21.31-28
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 Xq28(chrX:153560741-153858492)x2,3 copy number gain not provided [RCV000684745] ChrX:153560741..153858492 [GRCh37]
ChrX:Xq28
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 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:153827637-153888797)x2 copy number gain not provided [RCV000753942] ChrX:153827637..153888797 [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 Xp22.33-q28(chrX:60814-155254881)x2 copy number gain not provided [RCV000753277] ChrX:60814..155254881 [GRCh37]
ChrX:Xp22.33-q28
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:60262-155245765)x1 copy number loss not provided [RCV000753271] ChrX:60262..155245765 [GRCh37]
ChrX:Xp22.33-q28
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:60814-155236712)x2 copy number gain not provided [RCV000753276] ChrX:60814..155236712 [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
Single allele duplication Autistic disorder of childhood onset [RCV000754365] ChrX:1..156040895 [GRCh38]
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 Xq25-28(chrX:122757437-155208244)x1 copy number loss Premature ovarian insufficiency [RCV000852349] ChrX:122757437..155208244 [GRCh37]
ChrX:Xq25-28
likely 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
GRCh37/hg19 Xq25-28(chrX:122924044-155233731)x1 copy number loss not provided [RCV000849097] ChrX:122924044..155233731 [GRCh37]
ChrX:Xq25-28
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:153556428-153868487)x2 copy number gain not provided [RCV000845970] ChrX:153556428..153868487 [GRCh37]
ChrX:Xq28
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 Xq21.32-28(chrX:92814516-155233731)x1 copy number loss not provided [RCV000845672] ChrX:92814516..155233731 [GRCh37]
ChrX:Xq21.32-28
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 Xp22.33-q28(chrX:168546-155233731)x1 copy number loss not provided [RCV000848828] ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xq21.1-28(chrX:84387417-155233731)x1 copy number loss not provided [RCV001007322] ChrX:84387417..155233731 [GRCh37]
ChrX:Xq21.1-28
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 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:55507789-155198481)x3 copy number gain See cases [RCV001263024] ChrX:55507789..155198481 [GRCh37]
ChrX:Xp11.21-q28
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:2491 AgrOrtholog
COSMIC CTAG1B COSMIC
Ensembl Genes ENSG00000184033 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
  ENSG00000268651 UniProtKB/Swiss-Prot
Ensembl Protein ENSP00000332602 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000352953 UniProtKB/Swiss-Prot
  ENSP00000469441 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000328435 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000359887 UniProtKB/Swiss-Prot
  ENST00000599837 UniProtKB/Swiss-Prot
GTEx ENSG00000184033 GTEx
  ENSG00000268651 GTEx
HGNC ID HGNC:2491 ENTREZGENE
Human Proteome Map CTAG1B Human Proteome Map
InterPro CTAG/Pcc1 UniProtKB/Swiss-Prot
KEGG Report hsa:1485 UniProtKB/Swiss-Prot
  hsa:246100 UniProtKB/Swiss-Prot
NCBI Gene 1485 ENTREZGENE
OMIM 300156 OMIM
PANTHER PTHR31283 UniProtKB/Swiss-Prot
Pfam Pcc1 UniProtKB/Swiss-Prot
PharmGKB PA26993 PharmGKB
UniProt CTG1B_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
UniProt Secondary A1L417 UniProtKB/Swiss-Prot
  B7WNL9 UniProtKB/Swiss-Prot
  Q7LBY4 UniProtKB/Swiss-Prot
  Q9NY13 UniProtKB/Swiss-Prot