F8A1 (coagulation factor VIII associated 1) - Rat Genome Database

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Gene: F8A1 (coagulation factor VIII associated 1) Homo sapiens
Analyze
Symbol: F8A1
Name: coagulation factor VIII associated 1
RGD ID: 1342562
HGNC Page HGNC
Description: Involved in negative regulation of proteasomal protein catabolic process. Localizes to early endosome and nucleus.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: coagulation factor VIII-associated (intronic transcript) 1; coagulation factor VIII-associated 1; cpG island protein; DXS522E; F8A; F8A2; F8A3; factor VIII associated protein; factor VIII intron 22 protein; HAP40; huntingtin-associated protein 40
RGD Orthologs
Rat
Bonobo
Squirrel
Pig
Green Monkey
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 EnsemblX154,886,349 - 154,888,061 (+)EnsemblGRCh38hg38GRCh38
GRCh38.p13 EnsemblX154,886,355 - 154,888,061 (+)EnsemblGRCh38hg38GRCh38
GRCh38X154,886,355 - 154,888,061 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X154,114,630 - 154,116,336 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36X153,767,829 - 153,769,530 (+)NCBINCBI36hg18NCBI36
Build 34X154,250,279 - 154,251,980NCBI
CeleraX154,273,254 - 154,274,955 (+)NCBI
Cytogenetic MapXq28NCBI
HuRefX142,658,135 - 143,157,866 (+)NCBIHuRef
CHM1_1X154,027,043 - 154,027,955 (+)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

Cellular Component
early endosome  (IBA,IDA)
nuclear body  (ISS)
nucleus  (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:1427887   PMID:1639415   PMID:2110545   PMID:8528212   PMID:11035034   PMID:11076863   PMID:11256614   PMID:12477932   PMID:15009463   PMID:15123239   PMID:15489334   PMID:15489336  
PMID:15687285   PMID:16381901   PMID:16476778   PMID:16482509   PMID:16513639   PMID:18299331   PMID:18419747   PMID:19139273   PMID:19913121   PMID:20628086   PMID:21873635   PMID:23414517  
PMID:23521092   PMID:26514267   PMID:27815841   PMID:28514442   PMID:29466333   PMID:32814053  


Genomics

Comparative Map Data
F8A1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 EnsemblX154,886,349 - 154,888,061 (+)EnsemblGRCh38hg38GRCh38
GRCh38.p13 EnsemblX154,886,355 - 154,888,061 (+)EnsemblGRCh38hg38GRCh38
GRCh38X154,886,355 - 154,888,061 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X154,114,630 - 154,116,336 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36X153,767,829 - 153,769,530 (+)NCBINCBI36hg18NCBI36
Build 34X154,250,279 - 154,251,980NCBI
CeleraX154,273,254 - 154,274,955 (+)NCBI
Cytogenetic MapXq28NCBI
HuRefX142,658,135 - 143,157,866 (+)NCBIHuRef
CHM1_1X154,027,043 - 154,027,955 (+)NCBICHM1_1
F8a1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2X150,957,357 - 150,958,871 (-)NCBI
Rnor_6.0 Ensembl1147,021,436 - 147,022,950 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.01147,021,436 - 147,022,950 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.01153,316,591 - 153,318,105 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4X159,089,210 - 159,090,724 (+)NCBIRGSC3.4rn4RGSC3.4
Celera1131,899,603 - 131,901,117 (+)NCBICelera
Cytogenetic Map1q31NCBI
F8A1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Mhudiblu_PPA_v0X144,366,123 - 144,367,842 (+)NCBIMhudiblu_PPA_v0panPan3
F8a1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2X119,875,412 - 119,878,722 (+)NCBI
SpeTri2.0NW_004936927234,162 - 236,881 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
F8A1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1X125,280,978 - 125,282,771 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2X143,200,367 - 143,202,144 (-)NCBISscrofa10.2Sscrofa10.2susScr3
F8A1
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1X129,131,267 - 129,133,575 (+)NCBI

Position Markers
SHGC-2526  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,289,962 - 154,290,124UniSTSGRCh37
Build 36X153,943,156 - 153,943,318RGDNCBI36
CeleraX154,448,679 - 154,448,841RGD
Cytogenetic MapXq28UniSTS
HuRefX142,835,196 - 142,835,358UniSTS
GeneMap99-G3 RH MapX3257.0UniSTS
WIAF-2536  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37525,829,400 - 25,829,568UniSTSGRCh37
GRCh37X154,467,831 - 154,467,991UniSTSGRCh37
Build 36X154,121,025 - 154,121,185RGDNCBI36
CeleraX154,626,309 - 154,626,469RGD
Cytogenetic MapXq28UniSTS
HuRefX143,011,835 - 143,011,995UniSTS
GeneMap99-GB4 RH MapX356.07UniSTS
DXS7035E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,287,488 - 154,287,572UniSTSGRCh37
Build 36X153,940,682 - 153,940,766RGDNCBI36
CeleraX154,446,203 - 154,446,287RGD
Cytogenetic MapXq28UniSTS
HuRefX142,832,722 - 142,832,806UniSTS
GeneMap99-GB4 RH MapX356.07UniSTS
RH36657  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,467,936 - 154,467,994UniSTSGRCh37
Build 36X154,121,130 - 154,121,188RGDNCBI36
CeleraX154,626,414 - 154,626,472RGD
Cytogenetic MapXq28UniSTS
HuRefX143,011,940 - 143,011,998UniSTS
RH92996  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,718,778 - 154,718,921UniSTSGRCh37
GRCh37X154,581,303 - 154,581,446UniSTSGRCh37
Build 36X154,234,497 - 154,234,640RGDNCBI36
CeleraX154,739,746 - 154,739,889RGD
Cytogenetic MapXq28UniSTS
HuRefX143,125,067 - 143,125,210UniSTS
GeneMap99-GB4 RH MapX356.07UniSTS
RH79163  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375175,737,294 - 175,737,474UniSTSGRCh37
GRCh37X154,350,762 - 154,350,942UniSTSGRCh37
Build 36X154,003,956 - 154,004,136RGDNCBI36
Celera5172,765,456 - 172,765,636UniSTS
CeleraX154,509,517 - 154,509,697RGD
Cytogenetic Map5q35.2UniSTS
Cytogenetic MapXq28UniSTS
HuRef5170,661,862 - 170,662,042UniSTS
HuRefX142,895,996 - 142,896,176UniSTS
RH79860  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,506,585 - 154,506,738UniSTSGRCh37
Build 36X154,159,779 - 154,159,932RGDNCBI36
CeleraX154,665,096 - 154,665,249RGD
Cytogenetic MapXq28UniSTS
HuRefX143,050,173 - 143,050,326UniSTS
RH15635  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,288,414 - 154,288,515UniSTSGRCh37
Build 36X153,941,608 - 153,941,709RGDNCBI36
CeleraX154,447,129 - 154,447,230RGD
Cytogenetic MapXq28UniSTS
HuRefX142,833,648 - 142,833,749UniSTS
G43495  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,697,172 - 154,697,295UniSTSGRCh37
GRCh37X154,602,731 - 154,602,854UniSTSGRCh37
Build 36X154,255,925 - 154,256,048RGDNCBI36
CeleraX154,761,555 - 154,761,678RGD
Cytogenetic MapXq28UniSTS
HuRefX143,146,899 - 143,147,022UniSTS
RH103007  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,506,660 - 154,506,846UniSTSGRCh37
Build 36X154,159,854 - 154,160,040RGDNCBI36
CeleraX154,665,171 - 154,665,357RGD
Cytogenetic MapXq28UniSTS
HuRefX143,050,248 - 143,050,434UniSTS
GeneMap99-GB4 RH MapX356.07UniSTS
GDB:450201  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,157,626 - 154,157,905UniSTSGRCh37
Build 36X153,810,820 - 153,811,099RGDNCBI36
CeleraX154,316,364 - 154,316,643RGD
Cytogenetic MapXq28UniSTS
HuRefX142,702,165 - 142,702,444UniSTS
GDB:452843  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,250,829 - 154,250,998UniSTSGRCh37
Build 36X153,904,023 - 153,904,192RGDNCBI36
CeleraX154,409,564 - 154,409,733RGD
Cytogenetic MapXq28UniSTS
HuRefX142,795,927 - 142,796,096UniSTS
sWXD2469  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,694,800 - 154,695,191UniSTSGRCh37
GRCh37X154,604,833 - 154,605,224UniSTSGRCh37
Build 36X154,258,027 - 154,258,418RGDNCBI36
CeleraX154,763,661 - 154,764,052RGD
Cytogenetic MapXq28UniSTS
HuRefX143,149,007 - 143,149,398UniSTS
G59503  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,467,655 - 154,467,764UniSTSGRCh37
Build 36X154,120,849 - 154,120,958RGDNCBI36
CeleraX154,626,133 - 154,626,242RGD
Cytogenetic MapXq28UniSTS
HuRefX143,011,659 - 143,011,768UniSTS
AU048852  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,696,858 - 154,697,279UniSTSGRCh37
GRCh37X154,602,747 - 154,603,166UniSTSGRCh37
Build 36X154,255,941 - 154,256,360RGDNCBI36
Celera5132,169,648 - 132,170,182UniSTS
CeleraX154,761,571 - 154,761,990RGD
Cytogenetic MapXq28UniSTS
HuRefX143,146,915 - 143,147,336UniSTS
GDB:177507  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,194,671 - 154,195,026UniSTSGRCh37
Build 36X153,847,865 - 153,848,220RGDNCBI36
CeleraX154,353,410 - 154,353,765RGD
Cytogenetic MapXq28UniSTS
HuRefX142,739,805 - 142,740,160UniSTS
GDB:177561  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,129,678 - 154,130,379UniSTSGRCh37
Build 36X153,782,872 - 153,783,573RGDNCBI36
CeleraX154,288,418 - 154,289,116RGD
Cytogenetic MapXq28UniSTS
HuRefX142,674,421 - 142,675,122UniSTS
GDB:177816  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,156,856 - 154,157,057UniSTSGRCh37
Build 36X153,810,050 - 153,810,251RGDNCBI36
CeleraX154,315,594 - 154,315,795RGD
Cytogenetic MapXq28UniSTS
HuRefX142,701,395 - 142,701,596UniSTS
GDB:196462  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,194,761 - 154,195,074UniSTSGRCh37
Build 36X153,847,955 - 153,848,268RGDNCBI36
CeleraX154,353,500 - 154,353,813RGD
Cytogenetic MapXq28UniSTS
HuRefX142,739,895 - 142,740,208UniSTS
SHGC-143362  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,185,403 - 154,185,711UniSTSGRCh37
Build 36X153,838,597 - 153,838,905RGDNCBI36
CeleraX154,344,142 - 154,344,450RGD
Cytogenetic MapXq28UniSTS
HuRefX142,730,153 - 142,730,461UniSTS
TNG Radiation Hybrid MapX28708.0UniSTS
HSC271_(M4)  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,124,759 - 154,124,891UniSTSGRCh37
Build 36X153,777,953 - 153,778,085RGDNCBI36
CeleraX154,283,563 - 154,283,695RGD
Cytogenetic MapXq28UniSTS
HuRefX142,669,502 - 142,669,634UniSTS
ECD00116  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,228,594 - 154,229,528UniSTSGRCh37
Build 36X153,881,788 - 153,882,722RGDNCBI36
CeleraX154,387,329 - 154,388,263RGD
Cytogenetic MapXq28UniSTS
HuRefX142,773,741 - 142,774,675UniSTS
ECD00153  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,227,583 - 154,228,513UniSTSGRCh37
Build 36X153,880,777 - 153,881,707RGDNCBI36
CeleraX154,386,318 - 154,387,248RGD
Cytogenetic MapXq28UniSTS
HuRefX142,772,730 - 142,773,660UniSTS
ECD00985  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,309,829 - 154,310,711UniSTSGRCh37
Build 36X153,963,023 - 153,963,905RGDNCBI36
CeleraX154,468,588 - 154,469,470RGD
Cytogenetic MapXq28UniSTS
HuRefX142,855,539 - 142,856,421UniSTS
ECD01065  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,306,569 - 154,307,448UniSTSGRCh37
Build 36X153,959,763 - 153,960,642RGDNCBI36
CeleraX154,465,329 - 154,466,208RGD
Cytogenetic MapXq28UniSTS
HuRefX142,851,286 - 142,852,165UniSTS
ECD01501  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,185,076 - 154,185,939UniSTSGRCh37
Build 36X153,838,270 - 153,839,133RGDNCBI36
CeleraX154,343,815 - 154,344,678RGD
Cytogenetic MapXq28UniSTS
HuRefX142,729,826 - 142,730,689UniSTS
ECD01666  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,236,133 - 154,236,990UniSTSGRCh37
Build 36X153,889,327 - 153,890,184RGDNCBI36
CeleraX154,394,867 - 154,395,724RGD
Cytogenetic MapXq28UniSTS
HuRefX142,781,130 - 142,781,987UniSTS
ECD02249  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,158,591 - 154,159,427UniSTSGRCh37
Build 36X153,811,785 - 153,812,621RGDNCBI36
CeleraX154,317,329 - 154,318,165RGD
Cytogenetic MapXq28UniSTS
HuRefX142,703,130 - 142,703,966UniSTS
ECD02345  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,289,813 - 154,290,646UniSTSGRCh37
Build 36X153,943,007 - 153,943,840RGDNCBI36
CeleraX154,448,530 - 154,449,363RGD
Cytogenetic MapXq28UniSTS
HuRefX142,835,047 - 142,835,880UniSTS
ECD02848  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,156,806 - 154,157,621UniSTSGRCh37
Build 36X153,810,000 - 153,810,815RGDNCBI36
CeleraX154,315,544 - 154,316,359RGD
Cytogenetic MapXq28UniSTS
HuRefX142,701,345 - 142,702,160UniSTS
ECD03143  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,180,003 - 154,180,807UniSTSGRCh37
Build 36X153,833,197 - 153,834,001RGDNCBI36
CeleraX154,338,742 - 154,339,546RGD
Cytogenetic MapXq28UniSTS
HuRefX142,724,753 - 142,725,557UniSTS
ECD03412  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,157,717 - 154,158,513UniSTSGRCh37
Build 36X153,810,911 - 153,811,707RGDNCBI36
CeleraX154,316,455 - 154,317,251RGD
Cytogenetic MapXq28UniSTS
HuRefX142,702,256 - 142,703,052UniSTS
ECD03445  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,175,834 - 154,176,629UniSTSGRCh37
Build 36X153,829,028 - 153,829,823RGDNCBI36
CeleraX154,334,573 - 154,335,368RGD
Cytogenetic MapXq28UniSTS
HuRefX142,720,585 - 142,721,380UniSTS
ECD03608  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,274,598 - 154,275,387UniSTSGRCh37
Build 36X153,927,792 - 153,928,581RGDNCBI36
CeleraX154,433,314 - 154,434,103RGD
Cytogenetic MapXq28UniSTS
HuRefX142,819,589 - 142,820,378UniSTS
ECD04214  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,314,936 - 154,315,707UniSTSGRCh37
Build 36X153,968,130 - 153,968,901RGDNCBI36
CeleraX154,473,695 - 154,474,466RGD
Cytogenetic MapXq28UniSTS
HuRefX142,860,655 - 142,861,426UniSTS
ECD04373  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,182,658 - 154,183,424UniSTSGRCh37
Build 36X153,835,852 - 153,836,618RGDNCBI36
CeleraX154,341,397 - 154,342,163RGD
Cytogenetic MapXq28UniSTS
HuRefX142,727,408 - 142,728,174UniSTS
ECD04921  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,226,282 - 154,227,032UniSTSGRCh37
Build 36X153,879,476 - 153,880,226RGDNCBI36
CeleraX154,385,017 - 154,385,767RGD
Cytogenetic MapXq28UniSTS
HuRefX142,771,429 - 142,772,179UniSTS
ECD05774  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,305,080 - 154,305,807UniSTSGRCh37
Build 36X153,958,274 - 153,959,001RGDNCBI36
CeleraX154,463,840 - 154,464,567RGD
Cytogenetic MapXq28UniSTS
HuRefX142,849,797 - 142,850,524UniSTS
ECD06004  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,130,722 - 154,131,442UniSTSGRCh37
Build 36X153,783,916 - 153,784,636RGDNCBI36
CeleraX154,289,459 - 154,290,179RGD
Cytogenetic MapXq28UniSTS
HuRefX142,675,465 - 142,676,185UniSTS
ECD06005  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,283,160 - 154,283,880UniSTSGRCh37
Build 36X153,936,354 - 153,937,074RGDNCBI36
CeleraX154,441,875 - 154,442,595RGD
Cytogenetic MapXq28UniSTS
HuRefX142,828,151 - 142,828,871UniSTS
ECD06300  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,147,744 - 154,148,456UniSTSGRCh37
Build 36X153,800,938 - 153,801,650RGDNCBI36
CeleraX154,306,482 - 154,307,194RGD
Cytogenetic MapXq28UniSTS
HuRefX142,692,486 - 142,693,198UniSTS
ECD06301  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,181,879 - 154,182,591UniSTSGRCh37
Build 36X153,835,073 - 153,835,785RGDNCBI36
CeleraX154,340,618 - 154,341,330RGD
Cytogenetic MapXq28UniSTS
HuRefX142,726,629 - 142,727,341UniSTS
ECD06493  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,133,051 - 154,133,758UniSTSGRCh37
Build 36X153,786,245 - 153,786,952RGDNCBI36
CeleraX154,291,788 - 154,292,495RGD
Cytogenetic MapXq28UniSTS
HuRefX142,677,794 - 142,678,501UniSTS
ECD06570  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,220,828 - 154,221,533UniSTSGRCh37
Build 36X153,874,022 - 153,874,727RGDNCBI36
CeleraX154,379,563 - 154,380,268RGD
Cytogenetic MapXq28UniSTS
HuRefX142,765,975 - 142,766,680UniSTS
ECD06939  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,129,945 - 154,130,639UniSTSGRCh37
Build 36X153,783,139 - 153,783,833RGDNCBI36
CeleraX154,288,682 - 154,289,376RGD
Cytogenetic MapXq28UniSTS
HuRefX142,674,688 - 142,675,382UniSTS
ECD07087  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,282,450 - 154,283,141UniSTSGRCh37
Build 36X153,935,644 - 153,936,335RGDNCBI36
CeleraX154,441,165 - 154,441,856RGD
Cytogenetic MapXq28UniSTS
HuRefX142,827,441 - 142,828,132UniSTS
ECD07267  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,367,389 - 154,368,075UniSTSGRCh37
Build 36X154,020,583 - 154,021,269RGDNCBI36
CeleraX154,526,235 - 154,526,921RGD
Cytogenetic MapXq28UniSTS
HuRefX142,912,363 - 142,913,049UniSTS
ECD07563  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,313,940 - 154,314,618UniSTSGRCh37
Build 36X153,967,134 - 153,967,812RGDNCBI36
CeleraX154,472,699 - 154,473,377RGD
Cytogenetic MapXq28UniSTS
HuRefX142,859,659 - 142,860,337UniSTS
ECD07564  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,375,864 - 154,376,542UniSTSGRCh37
Build 36X154,029,058 - 154,029,736RGDNCBI36
CeleraX154,534,711 - 154,535,389RGD
Cytogenetic MapXq28UniSTS
HuRefX142,920,771 - 142,921,449UniSTS
ECD07678  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,279,758 - 154,280,433UniSTSGRCh37
Build 36X153,932,952 - 153,933,627RGDNCBI36
CeleraX154,438,474 - 154,439,149RGD
Cytogenetic MapXq28UniSTS
HuRefX142,824,749 - 142,825,424UniSTS
ECD07679  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,294,235 - 154,294,910UniSTSGRCh37
Build 36X153,947,429 - 153,948,104RGDNCBI36
CeleraX154,452,952 - 154,453,627RGD
Cytogenetic MapXq28UniSTS
HuRefX142,839,594 - 142,840,269UniSTS
ECD07714  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,396,661 - 154,397,335UniSTSGRCh37
Build 36X154,049,855 - 154,050,529RGDNCBI36
CeleraX154,555,000 - 154,555,674RGD
Cytogenetic MapXq28UniSTS
HuRefX142,941,298 - 142,941,972UniSTS
ECD07752  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,293,555 - 154,294,228UniSTSGRCh37
Build 36X153,946,749 - 153,947,422RGDNCBI36
CeleraX154,452,272 - 154,452,945RGD
Cytogenetic MapXq28UniSTS
HuRefX142,838,914 - 142,839,587UniSTS
ECD07963  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,278,997 - 154,279,664UniSTSGRCh37
Build 36X153,932,191 - 153,932,858RGDNCBI36
CeleraX154,437,713 - 154,438,380RGD
Cytogenetic MapXq28UniSTS
HuRefX142,823,989 - 142,824,656UniSTS
ECD08012  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,344,547 - 154,345,213UniSTSGRCh37
Build 36X153,997,741 - 153,998,407RGDNCBI36
CeleraX154,503,303 - 154,503,969RGD
Cytogenetic MapXq28UniSTS
HuRefX142,889,782 - 142,890,448UniSTS
ECD08124  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,371,081 - 154,371,744UniSTSGRCh37
Build 36X154,024,275 - 154,024,938RGDNCBI36
CeleraX154,529,928 - 154,530,591RGD
Cytogenetic MapXq28UniSTS
HuRefX142,916,056 - 142,916,719UniSTS
ECD08413  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,371,808 - 154,372,463UniSTSGRCh37
Build 36X154,025,002 - 154,025,657RGDNCBI36
CeleraX154,530,655 - 154,531,310RGD
Cytogenetic MapXq28UniSTS
HuRefX142,916,783 - 142,917,438UniSTS
ECD08613  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,186,185 - 154,186,835UniSTSGRCh37
Build 36X153,839,379 - 153,840,029RGDNCBI36
CeleraX154,344,924 - 154,345,574RGD
Cytogenetic MapXq28UniSTS
HuRefX142,730,935 - 142,731,586UniSTS
ECD08805  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,188,892 - 154,189,537UniSTSGRCh37
Build 36X153,842,086 - 153,842,731RGDNCBI36
CeleraX154,347,631 - 154,348,276RGD
Cytogenetic MapXq28UniSTS
HuRefX142,733,643 - 142,734,288UniSTS
ECD08846  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,291,256 - 154,291,900UniSTSGRCh37
Build 36X153,944,450 - 153,945,094RGDNCBI36
CeleraX154,449,973 - 154,450,617RGD
Cytogenetic MapXq28UniSTS
HuRefX142,836,490 - 142,837,134UniSTS
ECD09059  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,347,277 - 154,347,915UniSTSGRCh37
Build 36X154,000,471 - 154,001,109RGDNCBI36
CeleraX154,506,032 - 154,506,670RGD
Cytogenetic MapXq28UniSTS
HuRefX142,892,511 - 142,893,149UniSTS
ECD09392  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,275,949 - 154,276,579UniSTSGRCh37
Build 36X153,929,143 - 153,929,773RGDNCBI36
CeleraX154,434,665 - 154,435,295RGD
Cytogenetic MapXq28UniSTS
HuRefX142,820,940 - 142,821,570UniSTS
ECD09419  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,347,922 - 154,348,551UniSTSGRCh37
Build 36X154,001,116 - 154,001,745RGDNCBI36
CeleraX154,506,677 - 154,507,306RGD
Cytogenetic MapXq28UniSTS
HuRefX142,893,156 - 142,893,785UniSTS
ECD09460  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,234,948 - 154,235,576UniSTSGRCh37
Build 36X153,888,142 - 153,888,770RGDNCBI36
CeleraX154,393,682 - 154,394,310RGD
Cytogenetic MapXq28UniSTS
HuRefX142,779,945 - 142,780,573UniSTS
ECD09541  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,375,232 - 154,375,858UniSTSGRCh37
Build 36X154,028,426 - 154,029,052RGDNCBI36
CeleraX154,534,079 - 154,534,705RGD
Cytogenetic MapXq28UniSTS
HuRefX142,920,139 - 142,920,765UniSTS
ECD09588  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,348,669 - 154,349,294UniSTSGRCh37
Build 36X154,001,863 - 154,002,488RGDNCBI36
CeleraX154,507,424 - 154,508,049RGD
Cytogenetic MapXq28UniSTS
HuRefX142,893,903 - 142,894,528UniSTS
ECD09786  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,132,156 - 154,132,776UniSTSGRCh37
Build 36X153,785,350 - 153,785,970RGDNCBI36
CeleraX154,290,893 - 154,291,513RGD
Cytogenetic MapXq28UniSTS
HuRefX142,676,899 - 142,677,519UniSTS
ECD09788  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,313,306 - 154,313,926UniSTSGRCh37
Build 36X153,966,500 - 153,967,120RGDNCBI36
CeleraX154,472,065 - 154,472,685RGD
Cytogenetic MapXq28UniSTS
HuRefX142,859,025 - 142,859,645UniSTS
ECD09884  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,376,559 - 154,377,176UniSTSGRCh37
Build 36X154,029,753 - 154,030,370RGDNCBI36
CeleraX154,535,406 - 154,536,023RGD
Cytogenetic MapXq28UniSTS
HuRefX142,921,466 - 142,922,083UniSTS
ECD10131  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,250,172 - 154,250,782UniSTSGRCh37
Build 36X153,903,366 - 153,903,976RGDNCBI36
CeleraX154,408,907 - 154,409,517RGD
Cytogenetic MapXq28UniSTS
HuRefX142,795,173 - 142,795,880UniSTS
ECD10689  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,196,749 - 154,197,343UniSTSGRCh37
Build 36X153,849,943 - 153,850,537RGDNCBI36
CeleraX154,355,488 - 154,356,082RGD
Cytogenetic MapXq28UniSTS
HuRefX142,741,883 - 142,742,477UniSTS
ECD10854  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,234,356 - 154,234,945UniSTSGRCh37
Build 36X153,887,550 - 153,888,139RGDNCBI36
CeleraX154,393,090 - 154,393,679RGD
Cytogenetic MapXq28UniSTS
HuRefX142,779,353 - 142,779,942UniSTS
ECD10855  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,369,138 - 154,369,727UniSTSGRCh37
Build 36X154,022,332 - 154,022,921RGDNCBI36
CeleraX154,527,984 - 154,528,573RGD
Cytogenetic MapXq28UniSTS
HuRefX142,914,112 - 142,914,701UniSTS
ECD11022  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,212,785 - 154,213,369UniSTSGRCh37
Build 36X153,865,979 - 153,866,563RGDNCBI36
CeleraX154,371,520 - 154,372,104RGD
Cytogenetic MapXq28UniSTS
HuRefX142,757,970 - 142,758,554UniSTS
ECD11247  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,298,603 - 154,299,181UniSTSGRCh37
Build 36X153,951,797 - 153,952,375RGDNCBI36
CeleraX154,457,320 - 154,457,898RGD
Cytogenetic MapXq28UniSTS
HuRefX142,843,905 - 142,844,483UniSTS
ECD11314  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,292,920 - 154,293,496UniSTSGRCh37
Build 36X153,946,114 - 153,946,690RGDNCBI36
CeleraX154,451,637 - 154,452,213RGD
Cytogenetic MapXq28UniSTS
HuRefX142,838,279 - 142,838,855UniSTS
ECD11433  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,197,410 - 154,197,982UniSTSGRCh37
Build 36X153,850,604 - 153,851,176RGDNCBI36
CeleraX154,356,149 - 154,356,721RGD
Cytogenetic MapXq28UniSTS
HuRefX142,742,544 - 142,743,116UniSTS
ECD11467  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,195,774 - 154,196,345UniSTSGRCh37
Build 36X153,848,968 - 153,849,539RGDNCBI36
CeleraX154,354,513 - 154,355,084RGD
Cytogenetic MapXq28UniSTS
HuRefX142,740,908 - 142,741,479UniSTS
ECD11532  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,370,412 - 154,370,981UniSTSGRCh37
Build 36X154,023,606 - 154,024,175RGDNCBI36
CeleraX154,529,259 - 154,529,828RGD
Cytogenetic MapXq28UniSTS
HuRefX142,915,387 - 142,915,956UniSTS
ECD12533  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,318,459 - 154,319,000UniSTSGRCh37
Build 36X153,971,653 - 153,972,194RGDNCBI36
CeleraX154,477,218 - 154,477,759RGD
Cytogenetic MapXq28UniSTS
HuRefX142,864,134 - 142,864,675UniSTS
ECD12714  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,250,797 - 154,251,333UniSTSGRCh37
Build 36X153,903,991 - 153,904,527RGDNCBI36
CeleraX154,409,532 - 154,410,068RGD
Cytogenetic MapXq28UniSTS
HuRefX142,795,895 - 142,796,431UniSTS
ECD13023  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,317,051 - 154,317,579UniSTSGRCh37
Build 36X153,970,245 - 153,970,773RGDNCBI36
CeleraX154,475,810 - 154,476,338RGD
Cytogenetic MapXq28UniSTS
HuRefX142,862,770 - 142,863,298UniSTS
ECD13105  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,224,194 - 154,224,720UniSTSGRCh37
Build 36X153,877,388 - 153,877,914RGDNCBI36
CeleraX154,382,929 - 154,383,455RGD
Cytogenetic MapXq28UniSTS
HuRefX142,769,341 - 142,769,867UniSTS
ECD13141  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,294,998 - 154,295,523UniSTSGRCh37
Build 36X153,948,192 - 153,948,717RGDNCBI36
CeleraX154,453,715 - 154,454,240RGD
Cytogenetic MapXq28UniSTS
HuRefX142,840,357 - 142,840,807UniSTS
ECD13301  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,308,334 - 154,308,855UniSTSGRCh37
Build 36X153,961,528 - 153,962,049RGDNCBI36
CeleraX154,467,094 - 154,467,614RGD
Cytogenetic MapXq28UniSTS
HuRefX142,854,044 - 142,854,564UniSTS
ECD13341  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,298,027 - 154,298,547UniSTSGRCh37
Build 36X153,951,221 - 153,951,741RGDNCBI36
CeleraX154,456,744 - 154,457,264RGD
Cytogenetic MapXq28UniSTS
HuRefX142,843,329 - 142,843,849UniSTS
ECD13417  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,216,911 - 154,217,429UniSTSGRCh37
Build 36X153,870,105 - 153,870,623RGDNCBI36
CeleraX154,375,646 - 154,376,164RGD
Cytogenetic MapXq28UniSTS
HuRefX142,762,095 - 142,762,613UniSTS
ECD13457  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,280,637 - 154,281,154UniSTSGRCh37
Build 36X153,933,831 - 153,934,348RGDNCBI36
CeleraX154,439,353 - 154,439,870RGD
Cytogenetic MapXq28UniSTS
HuRefX142,825,628 - 142,826,145UniSTS
ECD13623  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,261,440 - 154,261,956UniSTSGRCh37
Build 36X153,914,634 - 153,915,150RGDNCBI36
CeleraX154,420,179 - 154,420,695RGD
Cytogenetic MapXq28UniSTS
HuRefX142,806,474 - 142,806,990UniSTS
ECD13705  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,288,836 - 154,289,347UniSTSGRCh37
Build 36X153,942,030 - 153,942,541RGDNCBI36
CeleraX154,447,551 - 154,448,062RGD
Cytogenetic MapXq28UniSTS
HuRefX142,834,070 - 142,834,581UniSTS
ECD14102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,366,003 - 154,366,504UniSTSGRCh37
Build 36X154,019,197 - 154,019,698RGDNCBI36
CeleraX154,524,845 - 154,525,346RGD
Cytogenetic MapXq28UniSTS
HuRefX142,910,993 - 142,911,496UniSTS
ECD14272  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,238,088 - 154,238,585UniSTSGRCh37
Build 36X153,891,282 - 153,891,779RGDNCBI36
CeleraX154,396,822 - 154,397,319RGD
Cytogenetic MapXq28UniSTS
HuRefX142,783,085 - 142,783,582UniSTS
ECD14326  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,193,986 - 154,194,482UniSTSGRCh37
Build 36X153,847,180 - 153,847,676RGDNCBI36
CeleraX154,352,725 - 154,353,221RGD
Cytogenetic MapXq28UniSTS
HuRefX142,739,120 - 142,739,616UniSTS
ECD14504  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,297,088 - 154,297,580UniSTSGRCh37
Build 36X153,950,282 - 153,950,774RGDNCBI36
CeleraX154,455,805 - 154,456,297RGD
Cytogenetic MapXq28UniSTS
HuRefX142,842,390 - 142,842,882UniSTS
ECD14556  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,296,432 - 154,296,923UniSTSGRCh37
Build 36X153,949,626 - 153,950,117RGDNCBI36
CeleraX154,455,149 - 154,455,640RGD
Cytogenetic MapXq28UniSTS
HuRefX142,841,716 - 142,842,225UniSTS
ECD14635  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,238,631 - 154,239,120UniSTSGRCh37
Build 36X153,891,825 - 153,892,314RGDNCBI36
CeleraX154,397,365 - 154,397,854RGD
Cytogenetic MapXq28UniSTS
HuRefX142,783,628 - 142,784,117UniSTS
ECD14725  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,343,977 - 154,344,464UniSTSGRCh37
Build 36X153,997,171 - 153,997,658RGDNCBI36
CeleraX154,502,733 - 154,503,220RGD
Cytogenetic MapXq28UniSTS
HuRefX142,889,212 - 142,889,699UniSTS
ECD14814  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,343,423 - 154,343,908UniSTSGRCh37
Build 36X153,996,617 - 153,997,102RGDNCBI36
CeleraX154,502,179 - 154,502,664RGD
Cytogenetic MapXq28UniSTS
HuRefX142,888,658 - 142,889,143UniSTS
ECD15064  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,161,191 - 154,161,670UniSTSGRCh37
Build 36X153,814,385 - 153,814,864RGDNCBI36
CeleraX154,319,929 - 154,320,408RGD
Cytogenetic MapXq28UniSTS
HuRefX142,705,561 - 142,706,040UniSTS
ECD15065  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,355,477 - 154,355,956UniSTSGRCh37
Build 36X154,008,671 - 154,009,150RGDNCBI36
CeleraX154,514,233 - 154,514,712RGD
Cytogenetic MapXq28UniSTS
HuRefX142,900,547 - 142,901,026UniSTS
ECD15347  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,301,155 - 154,301,627UniSTSGRCh37
Build 36X153,954,349 - 153,954,821RGDNCBI36
CeleraX154,459,872 - 154,460,344RGD
Cytogenetic MapXq28UniSTS
HuRefX142,846,504 - 142,846,976UniSTS
ECD15390  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,194,499 - 154,194,970UniSTSGRCh37
Build 36X153,847,693 - 153,848,164RGDNCBI36
CeleraX154,353,238 - 154,353,709RGD
Cytogenetic MapXq28UniSTS
HuRefX142,739,633 - 142,740,104UniSTS
ECD15463  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,295,935 - 154,296,404UniSTSGRCh37
Build 36X153,949,129 - 153,949,598RGDNCBI36
CeleraX154,454,652 - 154,455,121RGD
Cytogenetic MapXq28UniSTS
HuRefX142,841,219 - 142,841,688UniSTS
ECD15617  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,366,588 - 154,367,054UniSTSGRCh37
Build 36X154,019,782 - 154,020,248RGDNCBI36
CeleraX154,525,434 - 154,525,900RGD
Cytogenetic MapXq28UniSTS
HuRefX142,911,562 - 142,912,028UniSTS
ECD16678  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,161,694 - 154,162,124UniSTSGRCh37
Build 36X153,814,888 - 153,815,318RGDNCBI36
CeleraX154,320,432 - 154,320,862RGD
Cytogenetic MapXq28UniSTS
HuRefX142,706,064 - 142,706,494UniSTS
ECD16740  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,215,304 - 154,215,731UniSTSGRCh37
Build 36X153,868,498 - 153,868,925RGDNCBI36
CeleraX154,374,039 - 154,374,466RGD
Cytogenetic MapXq28UniSTS
HuRefX142,760,489 - 142,760,916UniSTS
ECD16978  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,319,063 - 154,319,480UniSTSGRCh37
Build 36X153,972,257 - 153,972,674RGDNCBI36
CeleraX154,477,822 - 154,478,239RGD
Cytogenetic MapXq28UniSTS
HuRefX142,864,738 - 142,865,155UniSTS
ECD17150  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,373,209 - 154,373,620UniSTSGRCh37
Build 36X154,026,403 - 154,026,814RGDNCBI36
CeleraX154,532,056 - 154,532,467RGD
Cytogenetic MapXq28UniSTS
HuRefX142,918,184 - 142,918,595UniSTS
ECD17705  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,225,168 - 154,225,555UniSTSGRCh37
Build 36X153,878,362 - 153,878,749RGDNCBI36
CeleraX154,383,903 - 154,384,290RGD
Cytogenetic MapXq28UniSTS
HuRefX142,770,315 - 142,770,702UniSTS
ECD17738  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,254,576 - 154,254,962UniSTSGRCh37
Build 36X153,907,770 - 153,908,156RGDNCBI36
CeleraX154,413,312 - 154,413,698RGD
Cytogenetic MapXq28UniSTS
HuRefX142,799,547 - 142,799,933UniSTS
ECD18081  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,345,494 - 154,345,868UniSTSGRCh37
Build 36X153,998,688 - 153,999,062RGDNCBI36
CeleraX154,504,250 - 154,504,624RGD
Cytogenetic MapXq28UniSTS
HuRefX142,890,729 - 142,891,103UniSTS
ECD18539  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,147,085 - 154,147,441UniSTSGRCh37
Build 36X153,800,279 - 153,800,635RGDNCBI36
CeleraX154,305,823 - 154,306,179RGD
Cytogenetic MapXq28UniSTS
HuRefX142,691,827 - 142,692,183UniSTS
ECD18560  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,256,264 - 154,256,590UniSTSGRCh37
Build 36X153,909,458 - 153,909,784RGDNCBI36
CeleraX154,415,000 - 154,415,328RGD
Cytogenetic MapXq28UniSTS
HuRefX142,801,236 - 142,801,562UniSTS
ECD18835  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,357,091 - 154,357,436UniSTSGRCh37
Build 36X154,010,285 - 154,010,630RGDNCBI36
CeleraX154,515,847 - 154,516,192RGD
Cytogenetic MapXq28UniSTS
HuRefX142,902,161 - 142,902,506UniSTS
ECD19109  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,400,869 - 154,401,203UniSTSGRCh37
Build 36X154,054,063 - 154,054,397RGDNCBI36
CeleraX154,559,205 - 154,559,539RGD
Cytogenetic MapXq28UniSTS
HuRefX142,945,497 - 142,945,831UniSTS
ECD19159  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,227,132 - 154,227,464UniSTSGRCh37
Build 36X153,880,326 - 153,880,658RGDNCBI36
CeleraX154,385,867 - 154,386,199RGD
Cytogenetic MapXq28UniSTS
HuRefX142,772,279 - 142,772,611UniSTS
ECD19185  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,251,924 - 154,252,255UniSTSGRCh37
Build 36X153,905,118 - 153,905,449RGDNCBI36
CeleraX154,410,660 - 154,410,991RGD
Cytogenetic MapXq28UniSTS
HuRefX142,797,022 - 142,797,353UniSTS
ECD19304  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,312,299 - 154,312,625UniSTSGRCh37
Build 36X153,965,493 - 153,965,819RGDNCBI36
CeleraX154,471,058 - 154,471,384RGD
Cytogenetic MapXq28UniSTS
HuRefX142,858,009 - 142,858,344UniSTS
ECD19784  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,221,853 - 154,222,162UniSTSGRCh37
Build 36X153,875,047 - 153,875,356RGDNCBI36
CeleraX154,380,588 - 154,380,897RGD
Cytogenetic MapXq28UniSTS
HuRefX142,767,000 - 142,767,309UniSTS
ECD19968  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,316,325 - 154,316,627UniSTSGRCh37
Build 36X153,969,519 - 153,969,821RGDNCBI36
CeleraX154,475,084 - 154,475,386RGD
Cytogenetic MapXq28UniSTS
HuRefX142,862,044 - 142,862,346UniSTS
ECD20106  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,162,738 - 154,163,035UniSTSGRCh37
Build 36X153,815,932 - 153,816,229RGDNCBI36
CeleraX154,321,476 - 154,321,773RGD
Cytogenetic MapXq28UniSTS
HuRefX142,707,108 - 142,707,405UniSTS
ECD20222  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,222,349 - 154,222,641UniSTSGRCh37
Build 36X153,875,543 - 153,875,835RGDNCBI36
CeleraX154,381,084 - 154,381,376RGD
Cytogenetic MapXq28UniSTS
HuRefX142,767,496 - 142,767,788UniSTS
ECD20246  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,162,288 - 154,162,579UniSTSGRCh37
Build 36X153,815,482 - 153,815,773RGDNCBI36
CeleraX154,321,026 - 154,321,317RGD
Cytogenetic MapXq28UniSTS
HuRefX142,706,658 - 142,706,949UniSTS
ECD20614  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,253,285 - 154,253,563UniSTSGRCh37
Build 36X153,906,479 - 153,906,757RGDNCBI36
CeleraX154,412,021 - 154,412,299RGD
Cytogenetic MapXq28UniSTS
HuRefX142,798,383 - 142,798,661UniSTS
ECD20758  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,233,643 - 154,233,916UniSTSGRCh37
Build 36X153,886,837 - 153,887,110RGDNCBI36
CeleraX154,392,377 - 154,392,650RGD
Cytogenetic MapXq28UniSTS
HuRefX142,778,640 - 142,778,913UniSTS
ECD21071  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,151,390 - 154,151,652UniSTSGRCh37
Build 36X153,804,584 - 153,804,846RGDNCBI36
CeleraX154,310,128 - 154,310,390RGD
Cytogenetic MapXq28UniSTS
HuRefX142,696,132 - 142,696,394UniSTS
ECD21185  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,271,890 - 154,272,148UniSTSGRCh37
Build 36X153,925,084 - 153,925,342RGDNCBI36
CeleraX154,430,609 - 154,430,867RGD
Cytogenetic MapXq28UniSTS
HuRefX142,816,457 - 142,816,715UniSTS
ECD21379  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,384,949 - 154,385,200UniSTSGRCh37
Build 36X154,038,143 - 154,038,394RGDNCBI36
CeleraX154,543,796 - 154,544,047RGD
Cytogenetic MapXq28UniSTS
HuRefX142,929,856 - 142,930,107UniSTS
ECD21451  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,259,943 - 154,260,192UniSTSGRCh37
Build 36X153,913,137 - 153,913,386RGDNCBI36
CeleraX154,418,681 - 154,418,930RGD
Cytogenetic MapXq28UniSTS
HuRefX142,804,977 - 142,805,226UniSTS
ECD21482  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,177,055 - 154,177,303UniSTSGRCh37
Build 36X153,830,249 - 153,830,497RGDNCBI36
CeleraX154,335,794 - 154,336,042RGD
Cytogenetic MapXq28UniSTS
HuRefX142,721,806 - 142,722,054UniSTS
ECD21584  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,199,103 - 154,199,348UniSTSGRCh37
Build 36X153,852,297 - 153,852,542RGDNCBI36
CeleraX154,357,842 - 154,358,087RGD
Cytogenetic MapXq28UniSTS
HuRefX142,744,237 - 142,744,482UniSTS
ECD21791  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,129,565 - 154,129,805UniSTSGRCh37
Build 36X153,782,759 - 153,782,999RGDNCBI36
CeleraX154,288,305 - 154,288,544RGD
Cytogenetic MapXq28UniSTS
HuRefX142,674,308 - 142,674,548UniSTS
ECD21916  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,246,507 - 154,246,742UniSTSGRCh37
Build 36X153,899,701 - 153,899,936RGDNCBI36
CeleraX154,405,242 - 154,405,477RGD
Cytogenetic MapXq28UniSTS
HuRefX142,791,508 - 142,791,743UniSTS
ECD22301  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,275,555 - 154,275,778UniSTSGRCh37
Build 36X153,928,749 - 153,928,972RGDNCBI36
CeleraX154,434,271 - 154,434,494RGD
Cytogenetic MapXq28UniSTS
HuRefX142,820,546 - 142,820,769UniSTS
ECD22302  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,384,637 - 154,384,860UniSTSGRCh37
Build 36X154,037,831 - 154,038,054RGDNCBI36
CeleraX154,543,484 - 154,543,707RGD
Cytogenetic MapXq28UniSTS
HuRefX142,929,544 - 142,929,767UniSTS
ECD22399  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,284,166 - 154,284,386UniSTSGRCh37
Build 36X153,937,360 - 153,937,580RGDNCBI36
CeleraX154,442,881 - 154,443,101RGD
Cytogenetic MapXq28UniSTS
HuRefX142,829,157 - 142,829,377UniSTS
ECD22497  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,396,327 - 154,396,544UniSTSGRCh37
Build 36X154,049,521 - 154,049,738RGDNCBI36
CeleraX154,554,666 - 154,554,883RGD
Cytogenetic MapXq28UniSTS
HuRefX142,940,964 - 142,941,181UniSTS
ECD22603  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,311,357 - 154,311,571UniSTSGRCh37
Build 36X153,964,551 - 153,964,765RGDNCBI36
CeleraX154,470,116 - 154,470,330RGD
Cytogenetic MapXq28UniSTS
HuRefX142,857,067 - 142,857,281UniSTS
ECD22697  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,356,081 - 154,356,292UniSTSGRCh37
Build 36X154,009,275 - 154,009,486RGDNCBI36
CeleraX154,514,837 - 154,515,048RGD
Cytogenetic MapXq28UniSTS
HuRefX142,901,151 - 142,901,362UniSTS
ECD22698  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,403,336 - 154,403,547UniSTSGRCh37
Build 36X154,056,530 - 154,056,741RGDNCBI36
CeleraX154,561,672 - 154,561,883RGD
Cytogenetic MapXq28UniSTS
HuRefX142,947,965 - 142,948,176UniSTS
ECD22781  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,213,753 - 154,213,961UniSTSGRCh37
Build 36X153,866,947 - 153,867,155RGDNCBI36
CeleraX154,372,488 - 154,372,696RGD
Cytogenetic MapXq28UniSTS
HuRefX142,758,938 - 142,759,146UniSTS
ECD23286  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,214,861 - 154,215,054UniSTSGRCh37
Build 36X153,868,055 - 153,868,248RGDNCBI36
CeleraX154,373,596 - 154,373,789RGD
Cytogenetic MapXq28UniSTS
HuRefX142,760,046 - 142,760,239UniSTS
ECD23324  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,192,772 - 154,192,964UniSTSGRCh37
Build 36X153,845,966 - 153,846,158RGDNCBI36
CeleraX154,351,511 - 154,351,703RGD
Cytogenetic MapXq28UniSTS
HuRefX142,737,453 - 142,737,645UniSTS
ECD23325  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,281,762 - 154,281,954UniSTSGRCh37
Build 36X153,934,956 - 153,935,148RGDNCBI36
Cytogenetic MapXq28UniSTS
HuRefX142,826,753 - 142,826,945UniSTS
ECD23374  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,134,668 - 154,134,859UniSTSGRCh37
Build 36X153,787,862 - 153,788,053RGDNCBI36
CeleraX154,293,405 - 154,293,596RGD
Cytogenetic MapXq28UniSTS
HuRefX142,679,411 - 142,679,602UniSTS
ECD23375  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,352,811 - 154,353,002UniSTSGRCh37
Build 36X154,006,005 - 154,006,196RGDNCBI36
CeleraX154,511,566 - 154,511,757RGD
Cytogenetic MapXq28UniSTS
HuRefX142,898,046 - 142,898,237UniSTS
ECD23674  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,333,784 - 154,333,965UniSTSGRCh37
Build 36X153,986,978 - 153,987,159RGDNCBI36
CeleraX154,492,542 - 154,492,723RGD
Cytogenetic MapXq28UniSTS
HuRefX142,879,222 - 142,879,403UniSTS
ECD23789  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,309,112 - 154,309,288UniSTSGRCh37
Build 36X153,962,306 - 153,962,482RGDNCBI36
CeleraX154,467,871 - 154,468,047RGD
Cytogenetic MapXq28UniSTS
HuRefX142,854,821 - 142,854,997UniSTS
ECD23918  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,237,499 - 154,237,668UniSTSGRCh37
Build 36X153,890,693 - 153,890,862RGDNCBI36
CeleraX154,396,233 - 154,396,402RGD
Cytogenetic MapXq28UniSTS
HuRefX142,782,496 - 142,782,665UniSTS
ECD24151  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,391,838 - 154,391,995UniSTSGRCh37
Build 36X154,045,032 - 154,045,189RGDNCBI36
CeleraX154,550,366 - 154,550,523RGD
Cytogenetic MapXq28UniSTS
HuRefX142,936,745 - 142,936,902UniSTS
ECD24179  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,249,423 - 154,249,578UniSTSGRCh37
Build 36X153,902,617 - 153,902,772RGDNCBI36
CeleraX154,408,158 - 154,408,313RGD
Cytogenetic MapXq28UniSTS
HuRefX142,794,424 - 142,794,579UniSTS
ECD24296  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,281,501 - 154,281,646UniSTSGRCh37
Build 36X153,934,695 - 153,934,840RGDNCBI36
CeleraX154,440,217 - 154,440,362RGD
Cytogenetic MapXq28UniSTS
HuRefX142,826,492 - 142,826,637UniSTS
ECD24309  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,214,130 - 154,214,274UniSTSGRCh37
Build 36X153,867,324 - 153,867,468RGDNCBI36
CeleraX154,372,865 - 154,373,009RGD
Cytogenetic MapXq28UniSTS
HuRefX142,759,315 - 142,759,459UniSTS
ECD24477  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,354,895 - 154,355,014UniSTSGRCh37
Build 36X154,008,089 - 154,008,208RGDNCBI36
CeleraX154,513,651 - 154,513,770RGD
Cytogenetic MapXq28UniSTS
HuRefX142,899,965 - 142,900,084UniSTS
WI-15153  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,467,653 - 154,467,777UniSTSGRCh37
Build 36X154,120,847 - 154,120,971RGDNCBI36
CeleraX154,626,131 - 154,626,255RGD
Cytogenetic MapXq28UniSTS
HuRefX143,011,657 - 143,011,781UniSTS
GeneMap99-GB4 RH MapX356.07UniSTS
Whitehead-RH MapX327.9UniSTS
REN90020  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,236,640 - 154,236,906UniSTSGRCh37
GRCh37X153,780,965 - 153,781,231UniSTSGRCh37
Build 36X153,434,159 - 153,434,425RGDNCBI36
CeleraX153,942,014 - 153,942,280RGD
CeleraX154,395,374 - 154,395,640UniSTS
Cytogenetic MapXq28UniSTS
HuRefX142,357,475 - 142,357,741UniSTS
HuRefX142,781,637 - 142,781,903UniSTS
REN90981  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,129,381 - 154,129,626UniSTSGRCh37
Build 36X153,782,575 - 153,782,820RGDNCBI36
CeleraX154,288,121 - 154,288,366RGD
Cytogenetic MapXq28UniSTS
HuRefX142,674,124 - 142,674,369UniSTS
REN90982  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,129,602 - 154,129,854UniSTSGRCh37
Build 36X153,782,796 - 153,783,048RGDNCBI36
CeleraX154,288,342 - 154,288,592RGD
Cytogenetic MapXq28UniSTS
HuRefX142,674,345 - 142,674,597UniSTS
REN90983  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,129,834 - 154,130,083UniSTSGRCh37
Build 36X153,783,028 - 153,783,277RGDNCBI36
CeleraX154,288,572 - 154,288,820RGD
Cytogenetic MapXq28UniSTS
HuRefX142,674,577 - 142,674,826UniSTS
REN90984  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,130,058 - 154,130,306UniSTSGRCh37
Build 36X153,783,252 - 153,783,500RGDNCBI36
CeleraX154,288,795 - 154,289,043RGD
Cytogenetic MapXq28UniSTS
HuRefX142,674,801 - 142,675,049UniSTS
REN90985  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,130,284 - 154,130,516UniSTSGRCh37
Build 36X153,783,478 - 153,783,710RGDNCBI36
CeleraX154,289,021 - 154,289,253RGD
Cytogenetic MapXq28UniSTS
HuRefX142,675,027 - 142,675,259UniSTS
REN90986  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,130,513 - 154,130,755UniSTSGRCh37
Build 36X153,783,707 - 153,783,949RGDNCBI36
CeleraX154,289,250 - 154,289,492RGD
Cytogenetic MapXq28UniSTS
HuRefX142,675,256 - 142,675,498UniSTS
REN90987  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,130,733 - 154,130,960UniSTSGRCh37
Build 36X153,783,927 - 153,784,154RGDNCBI36
CeleraX154,289,470 - 154,289,697RGD
Cytogenetic MapXq28UniSTS
HuRefX142,675,476 - 142,675,703UniSTS
REN90988  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,130,950 - 154,131,201UniSTSGRCh37
Build 36X153,784,144 - 153,784,395RGDNCBI36
CeleraX154,289,687 - 154,289,938RGD
Cytogenetic MapXq28UniSTS
HuRefX142,675,693 - 142,675,944UniSTS
REN90989  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,131,179 - 154,131,437UniSTSGRCh37
Build 36X153,784,373 - 153,784,631RGDNCBI36
CeleraX154,289,916 - 154,290,174RGD
Cytogenetic MapXq28UniSTS
HuRefX142,675,922 - 142,676,180UniSTS
REN90991  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,131,567 - 154,131,791UniSTSGRCh37
Build 36X153,784,761 - 153,784,985RGDNCBI36
CeleraX154,290,304 - 154,290,528RGD
Cytogenetic MapXq28UniSTS
HuRefX142,676,310 - 142,676,534UniSTS
REN90992  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,131,766 - 154,132,032UniSTSGRCh37
Build 36X153,784,960 - 153,785,226RGDNCBI36
CeleraX154,290,503 - 154,290,769RGD
Cytogenetic MapXq28UniSTS
HuRefX142,676,509 - 142,676,775UniSTS
REN90993  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,132,001 - 154,132,246UniSTSGRCh37
Build 36X153,785,195 - 153,785,440RGDNCBI36
CeleraX154,290,738 - 154,290,983RGD
Cytogenetic MapXq28UniSTS
HuRefX142,676,744 - 142,676,989UniSTS
REN90994  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,132,231 - 154,132,461UniSTSGRCh37
Build 36X153,785,425 - 153,785,655RGDNCBI36
CeleraX154,290,968 - 154,291,198RGD
Cytogenetic MapXq28UniSTS
HuRefX142,676,974 - 142,677,204UniSTS
REN90995  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,132,444 - 154,132,689UniSTSGRCh37
Build 36X153,785,638 - 153,785,883RGDNCBI36
CeleraX154,291,181 - 154,291,426RGD
Cytogenetic MapXq28UniSTS
HuRefX142,677,187 - 142,677,432UniSTS
REN90996  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,132,654 - 154,132,893UniSTSGRCh37
Build 36X153,785,848 - 153,786,087RGDNCBI36
CeleraX154,291,391 - 154,291,630RGD
Cytogenetic MapXq28UniSTS
HuRefX142,677,397 - 142,677,636UniSTS
REN90997  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,132,891 - 154,133,118UniSTSGRCh37
Build 36X153,786,085 - 153,786,312RGDNCBI36
CeleraX154,291,628 - 154,291,855RGD
Cytogenetic MapXq28UniSTS
HuRefX142,677,634 - 142,677,861UniSTS
REN90999  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,133,278 - 154,133,526UniSTSGRCh37
Build 36X153,786,472 - 153,786,720RGDNCBI36
CeleraX154,292,015 - 154,292,263RGD
Cytogenetic MapXq28UniSTS
HuRefX142,678,021 - 142,678,269UniSTS
REN91000  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,133,504 - 154,133,748UniSTSGRCh37
Build 36X153,786,698 - 153,786,942RGDNCBI36
CeleraX154,292,241 - 154,292,485RGD
Cytogenetic MapXq28UniSTS
HuRefX142,678,247 - 142,678,491UniSTS
REN91001  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,133,616 - 154,133,877UniSTSGRCh37
Build 36X153,786,810 - 153,787,071RGDNCBI36
CeleraX154,292,353 - 154,292,614RGD
Cytogenetic MapXq28UniSTS
HuRefX142,678,359 - 142,678,620UniSTS
REN91002  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,133,778 - 154,134,029UniSTSGRCh37
Build 36X153,786,972 - 153,787,223RGDNCBI36
CeleraX154,292,515 - 154,292,766RGD
Cytogenetic MapXq28UniSTS
HuRefX142,678,521 - 142,678,772UniSTS
REN91003  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,134,004 - 154,134,240UniSTSGRCh37
Build 36X153,787,198 - 153,787,434RGDNCBI36
CeleraX154,292,741 - 154,292,977RGD
Cytogenetic MapXq28UniSTS
HuRefX142,678,747 - 142,678,983UniSTS
REN91004  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,134,216 - 154,134,481UniSTSGRCh37
Build 36X153,787,410 - 153,787,675RGDNCBI36
CeleraX154,292,953 - 154,293,218RGD
Cytogenetic MapXq28UniSTS
HuRefX142,678,959 - 142,679,224UniSTS
REN91006  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,134,676 - 154,134,929UniSTSGRCh37
Build 36X153,787,870 - 153,788,123RGDNCBI36
CeleraX154,293,413 - 154,293,666RGD
Cytogenetic MapXq28UniSTS
HuRefX142,679,419 - 142,679,672UniSTS
REN91007  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,134,899 - 154,135,162UniSTSGRCh37
Build 36X153,788,093 - 153,788,356RGDNCBI36
CeleraX154,293,636 - 154,293,899RGD
Cytogenetic MapXq28UniSTS
HuRefX142,679,642 - 142,679,905UniSTS
REN91008  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,135,145 - 154,135,376UniSTSGRCh37
Build 36X153,788,339 - 153,788,570RGDNCBI36
CeleraX154,293,882 - 154,294,113RGD
Cytogenetic MapXq28UniSTS
HuRefX142,679,888 - 142,680,119UniSTS
REN91009  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,135,375 - 154,135,647UniSTSGRCh37
Build 36X153,788,569 - 153,788,841RGDNCBI36
CeleraX154,294,112 - 154,294,384RGD
Cytogenetic MapXq28UniSTS
HuRefX142,680,118 - 142,680,390UniSTS
REN91010  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,135,625 - 154,135,863UniSTSGRCh37
Build 36X153,788,819 - 153,789,057RGDNCBI36
CeleraX154,294,362 - 154,294,600RGD
Cytogenetic MapXq28UniSTS
HuRefX142,680,368 - 142,680,606UniSTS
REN91011  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,135,829 - 154,136,090UniSTSGRCh37
Build 36X153,789,023 - 153,789,284RGDNCBI36
CeleraX154,294,566 - 154,294,827RGD
Cytogenetic MapXq28UniSTS
HuRefX142,680,572 - 142,680,833UniSTS
REN91012  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,136,085 - 154,136,327UniSTSGRCh37
Build 36X153,789,279 - 153,789,521RGDNCBI36
CeleraX154,294,822 - 154,295,064RGD
Cytogenetic MapXq28UniSTS
HuRefX142,680,828 - 142,681,070UniSTS
REN91014  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,136,573 - 154,136,821UniSTSGRCh37
Build 36X153,789,767 - 153,790,015RGDNCBI36
CeleraX154,295,310 - 154,295,558RGD
Cytogenetic MapXq28UniSTS
HuRefX142,681,316 - 142,681,564UniSTS
REN91016  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,144,188 - 154,144,431UniSTSGRCh37
Build 36X153,797,382 - 153,797,625RGDNCBI36
CeleraX154,302,925 - 154,303,168RGD
Cytogenetic MapXq28UniSTS
HuRefX142,688,931 - 142,689,174UniSTS
REN91017  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,144,401 - 154,144,635UniSTSGRCh37
Build 36X153,797,595 - 153,797,829RGDNCBI36
CeleraX154,303,138 - 154,303,372RGD
Cytogenetic MapXq28UniSTS
HuRefX142,689,144 - 142,689,378UniSTS
REN91018  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,144,556 - 154,144,784UniSTSGRCh37
Build 36X153,797,750 - 153,797,978RGDNCBI36
CeleraX154,303,293 - 154,303,521RGD
Cytogenetic MapXq28UniSTS
HuRefX142,689,299 - 142,689,527UniSTS
REN91019  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,144,688 - 154,144,951UniSTSGRCh37
Build 36X153,797,882 - 153,798,145RGDNCBI36
CeleraX154,303,425 - 154,303,688RGD
Cytogenetic MapXq28UniSTS
HuRefX142,689,431 - 142,689,694UniSTS
REN91021  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,145,137 - 154,145,382UniSTSGRCh37
Build 36X153,798,331 - 153,798,576RGDNCBI36
CeleraX154,303,874 - 154,304,119RGD
Cytogenetic MapXq28UniSTS
HuRefX142,689,880 - 142,690,125UniSTS
REN91022  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,145,359 - 154,145,611UniSTSGRCh37
Build 36X153,798,553 - 153,798,805RGDNCBI36
CeleraX154,304,096 - 154,304,348RGD
Cytogenetic MapXq28UniSTS
HuRefX142,690,102 - 142,690,354UniSTS
REN91023  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,145,576 - 154,145,831UniSTSGRCh37
Build 36X153,798,770 - 153,799,025RGDNCBI36
CeleraX154,304,313 - 154,304,568RGD
Cytogenetic MapXq28UniSTS
HuRefX142,690,319 - 142,690,574UniSTS
REN91024  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,145,808 - 154,146,049UniSTSGRCh37
Build 36X153,799,002 - 153,799,243RGDNCBI36
CeleraX154,304,545 - 154,304,786RGD
Cytogenetic MapXq28UniSTS
HuRefX142,690,551 - 142,690,792UniSTS
REN91025  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,146,034 - 154,146,307UniSTSGRCh37
Build 36X153,799,228 - 153,799,501RGDNCBI36
CeleraX154,304,771 - 154,305,044RGD
Cytogenetic MapXq28UniSTS
HuRefX142,690,777 - 142,691,050UniSTS
REN91026  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,146,301 - 154,146,549UniSTSGRCh37
Build 36X153,799,495 - 153,799,743RGDNCBI36
CeleraX154,305,038 - 154,305,286RGD
Cytogenetic MapXq28UniSTS
HuRefX142,691,044 - 142,691,292UniSTS
REN91027  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,146,526 - 154,146,767UniSTSGRCh37
Build 36X153,799,720 - 153,799,961RGDNCBI36
CeleraX154,305,263 - 154,305,504RGD
Cytogenetic MapXq28UniSTS
HuRefX142,691,269 - 142,691,510UniSTS
REN91029  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,146,949 - 154,147,217UniSTSGRCh37
Build 36X153,800,143 - 153,800,411RGDNCBI36
CeleraX154,305,686 - 154,305,955RGD
Cytogenetic MapXq28UniSTS
HuRefX142,691,692 - 142,691,959UniSTS
REN91030  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,147,207 - 154,147,449UniSTSGRCh37
Build 36X153,800,401 - 153,800,643RGDNCBI36
CeleraX154,305,945 - 154,306,187RGD
Cytogenetic MapXq28UniSTS
HuRefX142,691,949 - 142,692,191UniSTS
REN91031  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,147,425 - 154,147,656UniSTSGRCh37
Build 36X153,800,619 - 153,800,850RGDNCBI36
CeleraX154,306,163 - 154,306,394RGD
Cytogenetic MapXq28UniSTS
HuRefX142,692,167 - 142,692,398UniSTS
REN91032  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,147,617 - 154,147,868UniSTSGRCh37
Build 36X153,800,811 - 153,801,062RGDNCBI36
CeleraX154,306,355 - 154,306,606RGD
Cytogenetic MapXq28UniSTS
HuRefX142,692,359 - 142,692,610UniSTS
REN91033  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37516,451,770 - 16,453,255UniSTSGRCh37
GRCh37X154,147,845 - 154,148,102UniSTSGRCh37
Build 36X153,801,039 - 153,801,296RGDNCBI36
CeleraX154,306,583 - 154,306,840RGD
Celera516,475,385 - 16,476,870UniSTS
Cytogenetic Map5p15.1UniSTS
Cytogenetic MapXq28UniSTS
HuRef516,423,674 - 16,425,159UniSTS
HuRefX142,692,587 - 142,692,844UniSTS
REN91034  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,148,054 - 154,148,311UniSTSGRCh37
Build 36X153,801,248 - 153,801,505RGDNCBI36
CeleraX154,306,792 - 154,307,049RGD
Cytogenetic MapXq28UniSTS
HuRefX142,692,796 - 142,693,053UniSTS
REN91035  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,148,293 - 154,148,539UniSTSGRCh37
Build 36X153,801,487 - 153,801,733RGDNCBI36
CeleraX154,307,031 - 154,307,277RGD
Cytogenetic MapXq28UniSTS
HuRefX142,693,035 - 142,693,281UniSTS
REN91036  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,148,506 - 154,148,730UniSTSGRCh37
Build 36X153,801,700 - 153,801,924RGDNCBI36
CeleraX154,307,244 - 154,307,468RGD
Cytogenetic MapXq28UniSTS
HuRefX142,693,248 - 142,693,472UniSTS
REN91038  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,148,928 - 154,149,182UniSTSGRCh37
Build 36X153,802,122 - 153,802,376RGDNCBI36
CeleraX154,307,666 - 154,307,920RGD
Cytogenetic MapXq28UniSTS
HuRefX142,693,670 - 142,693,924UniSTS
REN91039  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,149,143 - 154,149,367UniSTSGRCh37
Build 36X153,802,337 - 153,802,561RGDNCBI36
CeleraX154,307,881 - 154,308,105RGD
Cytogenetic MapXq28UniSTS
HuRefX142,693,885 - 142,694,109UniSTS
REN91040  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,149,255 - 154,149,514UniSTSGRCh37
Build 36X153,802,449 - 153,802,708RGDNCBI36
CeleraX154,307,993 - 154,308,252RGD
Cytogenetic MapXq28UniSTS
HuRefX142,693,997 - 142,694,256UniSTS
REN91041  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,150,341 - 154,150,565UniSTSGRCh37
Build 36X153,803,535 - 153,803,759RGDNCBI36
CeleraX154,309,079 - 154,309,303RGD
Cytogenetic MapXq28UniSTS
HuRefX142,695,083 - 142,695,307UniSTS
REN91042  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,150,530 - 154,150,759UniSTSGRCh37
Build 36X153,803,724 - 153,803,953RGDNCBI36
CeleraX154,309,268 - 154,309,497RGD
Cytogenetic MapXq28UniSTS
HuRefX142,695,272 - 142,695,501UniSTS
REN91043  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,150,733 - 154,151,003UniSTSGRCh37
Build 36X153,803,927 - 153,804,197RGDNCBI36
CeleraX154,309,471 - 154,309,741RGD
Cytogenetic MapXq28UniSTS
HuRefX142,695,475 - 142,695,745UniSTS
REN91044  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,150,995 - 154,151,244UniSTSGRCh37
Build 36X153,804,189 - 153,804,438RGDNCBI36
CeleraX154,309,733 - 154,309,982RGD
Cytogenetic MapXq28UniSTS
HuRefX142,695,737 - 142,695,986UniSTS
REN91046  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,151,435 - 154,151,681UniSTSGRCh37
Build 36X153,804,629 - 153,804,875RGDNCBI36
CeleraX154,310,173 - 154,310,419RGD
Cytogenetic MapXq28UniSTS
HuRefX142,696,177 - 142,696,423UniSTS
REN91047  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,151,539 - 154,151,777UniSTSGRCh37
Build 36X153,804,733 - 153,804,971RGDNCBI36
CeleraX154,310,277 - 154,310,515RGD
Cytogenetic MapXq28UniSTS
HuRefX142,696,281 - 142,696,519UniSTS
REN91048  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,151,885 - 154,152,114UniSTSGRCh37
Build 36X153,805,079 - 153,805,308RGDNCBI36
CeleraX154,310,623 - 154,310,852RGD
Cytogenetic MapXq28UniSTS
HuRefX142,696,627 - 142,696,856UniSTS
REN91051  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,153,166 - 154,153,413UniSTSGRCh37
Build 36X153,806,360 - 153,806,607RGDNCBI36
CeleraX154,311,904 - 154,312,151RGD
Cytogenetic MapXq28UniSTS
HuRefX142,697,892 - 142,698,139UniSTS
REN91060  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,155,067 - 154,155,331UniSTSGRCh37
Build 36X153,808,261 - 153,808,525RGDNCBI36
CeleraX154,313,805 - 154,314,069RGD
Cytogenetic MapXq28UniSTS
HuRefX142,699,606 - 142,699,870UniSTS
REN91061  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,155,321 - 154,155,570UniSTSGRCh37
Build 36X153,808,515 - 153,808,764RGDNCBI36
CeleraX154,314,059 - 154,314,308RGD
Cytogenetic MapXq28UniSTS
HuRefX142,699,860 - 142,700,109UniSTS
REN91062  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,155,563 - 154,155,802UniSTSGRCh37
Build 36X153,808,757 - 153,808,996RGDNCBI36
CeleraX154,314,301 - 154,314,540RGD
Cytogenetic MapXq28UniSTS
HuRefX142,700,102 - 142,700,341UniSTS
REN91063  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,155,779 - 154,156,040UniSTSGRCh37
Build 36X153,808,973 - 153,809,234RGDNCBI36
CeleraX154,314,517 - 154,314,778RGD
Cytogenetic MapXq28UniSTS
HuRefX142,700,318 - 142,700,579UniSTS
REN91064  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,156,023 - 154,156,274UniSTSGRCh37
Build 36X153,809,217 - 153,809,468RGDNCBI36
CeleraX154,314,761 - 154,315,012RGD
Cytogenetic MapXq28UniSTS
HuRefX142,700,562 - 142,700,813UniSTS
REN91065  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,156,254 - 154,156,503UniSTSGRCh37
Build 36X153,809,448 - 153,809,697RGDNCBI36
CeleraX154,314,992 - 154,315,241RGD
Cytogenetic MapXq28UniSTS
HuRefX142,700,793 - 142,701,042UniSTS
REN91067  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,156,693 - 154,156,941UniSTSGRCh37
Build 36X153,809,887 - 153,810,135RGDNCBI36
CeleraX154,315,431 - 154,315,679RGD
Cytogenetic MapXq28UniSTS
HuRefX142,701,232 - 142,701,480UniSTS
REN91068  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,156,918 - 154,157,162UniSTSGRCh37
Build 36X153,810,112 - 153,810,356RGDNCBI36
CeleraX154,315,656 - 154,315,900RGD
Cytogenetic MapXq28UniSTS
HuRefX142,701,457 - 142,701,701UniSTS
REN91069  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,157,156 - 154,157,399UniSTSGRCh37
Build 36X153,810,350 - 153,810,593RGDNCBI36
CeleraX154,315,894 - 154,316,137RGD
Cytogenetic MapXq28UniSTS
HuRefX142,701,695 - 142,701,938UniSTS
REN91070  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,157,363 - 154,157,614UniSTSGRCh37
Build 36X153,810,557 - 153,810,808RGDNCBI36
CeleraX154,316,101 - 154,316,352RGD
Cytogenetic MapXq28UniSTS
HuRefX142,701,902 - 142,702,153UniSTS
REN91071  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,157,596 - 154,157,842UniSTSGRCh37
Build 36X153,810,790 - 153,811,036RGDNCBI36
CeleraX154,316,334 - 154,316,580RGD
Cytogenetic MapXq28UniSTS
HuRefX142,702,135 - 142,702,381UniSTS
REN91072  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,157,828 - 154,158,085UniSTSGRCh37
Build 36X153,811,022 - 153,811,279RGDNCBI36
CeleraX154,316,566 - 154,316,823RGD
Cytogenetic MapXq28UniSTS
HuRefX142,702,367 - 142,702,624UniSTS
REN91073  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,158,065 - 154,158,318UniSTSGRCh37
Build 36X153,811,259 - 153,811,512RGDNCBI36
CeleraX154,316,803 - 154,317,056RGD
Cytogenetic MapXq28UniSTS
HuRefX142,702,604 - 142,702,857UniSTS
REN91074  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,158,307 - 154,158,546UniSTSGRCh37
Build 36X153,811,501 - 153,811,740RGDNCBI36
CeleraX154,317,045 - 154,317,284RGD
Cytogenetic MapXq28UniSTS
HuRefX142,702,846 - 142,703,085UniSTS
REN91076  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,158,768 - 154,159,009UniSTSGRCh37
Build 36X153,811,962 - 153,812,203RGDNCBI36
CeleraX154,317,506 - 154,317,747RGD
Cytogenetic MapXq28UniSTS
HuRefX142,703,307 - 142,703,548UniSTS
REN91077  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,158,983 - 154,159,232UniSTSGRCh37
Build 36X153,812,177 - 153,812,426RGDNCBI36
CeleraX154,317,721 - 154,317,970RGD
Cytogenetic MapXq28UniSTS
HuRefX142,703,522 - 142,703,771UniSTS
REN91078  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,159,198 - 154,159,456UniSTSGRCh37
Build 36X153,812,392 - 153,812,650RGDNCBI36
CeleraX154,317,936 - 154,318,194RGD
Cytogenetic MapXq28UniSTS
HuRefX142,703,737 - 142,703,995UniSTS
REN91079  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,159,450 - 154,159,695UniSTSGRCh37
Build 36X153,812,644 - 153,812,889RGDNCBI36
CeleraX154,318,188 - 154,318,433RGD
Cytogenetic MapXq28UniSTS
HuRefX142,703,989 - 142,704,234UniSTS
REN91080  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,159,688 - 154,159,930UniSTSGRCh37
Build 36X153,812,882 - 153,813,124RGDNCBI36
CeleraX154,318,426 - 154,318,668RGD
Cytogenetic MapXq28UniSTS
HuRefX142,704,227 - 142,704,469UniSTS
REN91081  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,159,907 - 154,160,139UniSTSGRCh37
Build 36X153,813,101 - 153,813,333RGDNCBI36
CeleraX154,318,645 - 154,318,877RGD
Cytogenetic MapXq28UniSTS
HuRefX142,704,446 - 142,704,678UniSTS
REN91085  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,160,793 - 154,161,043UniSTSGRCh37
Build 36X153,813,987 - 153,814,237RGDNCBI36
CeleraX154,319,531 - 154,319,781RGD
Cytogenetic MapXq28UniSTS
HuRefX142,705,163 - 142,705,413UniSTS
REN91086  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,161,004 - 154,161,248UniSTSGRCh37
Build 36X153,814,198 - 153,814,442RGDNCBI36
CeleraX154,319,742 - 154,319,986RGD
Cytogenetic MapXq28UniSTS
HuRefX142,705,374 - 142,705,618UniSTS
REN91087  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,161,246 - 154,161,470UniSTSGRCh37
Build 36X153,814,440 - 153,814,664RGDNCBI36
CeleraX154,319,984 - 154,320,208RGD
Cytogenetic MapXq28UniSTS
HuRefX142,705,616 - 142,705,840UniSTS
REN91088  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,161,439 - 154,161,676UniSTSGRCh37
Build 36X153,814,633 - 153,814,870RGDNCBI36
CeleraX154,320,177 - 154,320,414RGD
Cytogenetic MapXq28UniSTS
HuRefX142,705,809 - 142,706,046UniSTS
REN91089  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,161,654 - 154,161,909UniSTSGRCh37
Build 36X153,814,848 - 153,815,103RGDNCBI36
CeleraX154,320,392 - 154,320,647RGD
Cytogenetic MapXq28UniSTS
HuRefX142,706,024 - 142,706,279UniSTS
REN91091  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,162,113 - 154,162,386UniSTSGRCh37
Build 36X153,815,307 - 153,815,580RGDNCBI36
CeleraX154,320,851 - 154,321,124RGD
Cytogenetic MapXq28UniSTS
HuRefX142,706,483 - 142,706,756UniSTS
REN91092  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,162,367 - 154,162,624UniSTSGRCh37
Build 36X153,815,561 - 153,815,818RGDNCBI36
CeleraX154,321,105 - 154,321,362RGD
Cytogenetic MapXq28UniSTS
HuRefX142,706,737 - 142,706,994UniSTS
REN91093  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,162,559 - 154,162,799UniSTSGRCh37
Build 36X153,815,753 - 153,815,993RGDNCBI36
CeleraX154,321,297 - 154,321,537RGD
Cytogenetic MapXq28UniSTS
HuRefX142,706,929 - 142,707,169UniSTS
REN91094  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,162,777 - 154,163,035UniSTSGRCh37
Build 36X153,815,971 - 153,816,229RGDNCBI36
CeleraX154,321,515 - 154,321,773RGD
Cytogenetic MapXq28UniSTS
HuRefX142,707,147 - 142,707,405UniSTS
REN91095  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,162,938 - 154,163,190UniSTSGRCh37
Build 36X153,816,132 - 153,816,384RGDNCBI36
CeleraX154,321,676 - 154,321,928RGD
Cytogenetic MapXq28UniSTS
HuRefX142,707,308 - 142,707,560UniSTS
REN91099  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,163,983 - 154,164,252UniSTSGRCh37
Build 36X153,817,177 - 153,817,446RGDNCBI36
CeleraX154,322,721 - 154,322,990RGD
Cytogenetic MapXq28UniSTS
HuRefX142,708,790 - 142,709,059UniSTS
REN91100  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,164,237 - 154,164,504UniSTSGRCh37
Build 36X153,817,431 - 153,817,698RGDNCBI36
CeleraX154,322,975 - 154,323,240RGD
Cytogenetic MapXq28UniSTS
HuRefX142,709,044 - 142,709,309UniSTS
REN91101  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,164,489 - 154,164,756UniSTSGRCh37
Build 36X153,817,683 - 153,817,950RGDNCBI36
CeleraX154,323,225 - 154,323,492RGD
Cytogenetic MapXq28UniSTS
HuRefX142,709,294 - 142,709,561UniSTS
REN91102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,164,728 - 154,164,952UniSTSGRCh37
Build 36X153,817,922 - 153,818,146RGDNCBI36
CeleraX154,323,464 - 154,323,688RGD
Cytogenetic MapXq28UniSTS
HuRefX142,709,533 - 142,709,757UniSTS
REN91105  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,165,208 - 154,165,475UniSTSGRCh37
Build 36X153,818,402 - 153,818,669RGDNCBI36
CeleraX154,323,944 - 154,324,211RGD
Cytogenetic MapXq28UniSTS
HuRefX142,710,013 - 142,710,280UniSTS
REN91107  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,165,569 - 154,165,828UniSTSGRCh37
Build 36X153,818,763 - 153,819,022RGDNCBI36
CeleraX154,324,305 - 154,324,564RGD
Cytogenetic MapXq28UniSTS
HuRefX142,710,374 - 142,710,599UniSTS
REN91108  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,165,819 - 154,166,090UniSTSGRCh37
Build 36X153,819,013 - 153,819,284RGDNCBI36
CeleraX154,324,555 - 154,324,826RGD
Cytogenetic MapXq28UniSTS
HuRefX142,710,590 - 142,710,861UniSTS
REN91109  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,166,077 - 154,166,341UniSTSGRCh37
Build 36X153,819,271 - 153,819,535RGDNCBI36
CeleraX154,324,813 - 154,325,077RGD
Cytogenetic MapXq28UniSTS
HuRefX142,710,848 - 142,711,112UniSTS
REN91110  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,166,316 - 154,166,542UniSTSGRCh37
Build 36X153,819,510 - 153,819,736RGDNCBI36
CeleraX154,325,052 - 154,325,278RGD
Cytogenetic MapXq28UniSTS
HuRefX142,711,087 - 142,711,313UniSTS
REN91111  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,166,508 - 154,166,755UniSTSGRCh37
Build 36X153,819,702 - 153,819,949RGDNCBI36
CeleraX154,325,244 - 154,325,491RGD
Cytogenetic MapXq28UniSTS
HuRefX142,711,279 - 142,711,526UniSTS
REN91112  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,166,730 - 154,166,994UniSTSGRCh37
Build 36X153,819,924 - 153,820,188RGDNCBI36
CeleraX154,325,466 - 154,325,730RGD
Cytogenetic MapXq28UniSTS
HuRefX142,711,501 - 142,711,765UniSTS
REN91113  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,166,919 - 154,167,142UniSTSGRCh37
Build 36X153,820,113 - 153,820,336RGDNCBI36
CeleraX154,325,655 - 154,325,879RGD
Cytogenetic MapXq28UniSTS
HuRefX142,711,690 - 142,711,913UniSTS
REN91114  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,167,058 - 154,167,305UniSTSGRCh37
Build 36X153,820,252 - 153,820,499RGDNCBI36
CeleraX154,325,795 - 154,326,044RGD
Cytogenetic MapXq28UniSTS
HuRefX142,711,829 - 142,712,076UniSTS
REN91115  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,173,453 - 154,173,686UniSTSGRCh37
Build 36X153,826,647 - 153,826,880RGDNCBI36
CeleraX154,332,192 - 154,332,425RGD
Cytogenetic MapXq28UniSTS
HuRefX142,718,225 - 142,718,458UniSTS
REN91116  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,173,625 - 154,173,884UniSTSGRCh37
Build 36X153,826,819 - 153,827,078RGDNCBI36
CeleraX154,332,364 - 154,332,623RGD
Cytogenetic MapXq28UniSTS
HuRefX142,718,397 - 142,718,635UniSTS
REN91117  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,173,856 - 154,174,095UniSTSGRCh37
Build 36X153,827,050 - 153,827,289RGDNCBI36
CeleraX154,332,595 - 154,332,834RGD
Cytogenetic MapXq28UniSTS
HuRefX142,718,607 - 142,718,846UniSTS
REN91118  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,174,204 - 154,174,468UniSTSGRCh37
Build 36X153,827,398 - 153,827,662RGDNCBI36
CeleraX154,332,943 - 154,333,207RGD
Cytogenetic MapXq28UniSTS
HuRefX142,718,955 - 142,719,219UniSTS
REN91119  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,174,454 - 154,174,692UniSTSGRCh37
Build 36X153,827,648 - 153,827,886RGDNCBI36
CeleraX154,333,193 - 154,333,431RGD
Cytogenetic MapXq28UniSTS
HuRefX142,719,205 - 142,719,443UniSTS
REN91120  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,174,650 - 154,174,901UniSTSGRCh37
GRCh37X154,140,587 - 154,140,840UniSTSGRCh37
Build 36X153,793,781 - 153,794,034RGDNCBI36
CeleraX154,299,324 - 154,299,577RGD
CeleraX154,333,389 - 154,333,640UniSTS
Cytogenetic MapXq28UniSTS
HuRefX142,685,330 - 142,685,583UniSTS
HuRefX142,719,401 - 142,719,652UniSTS
REN91121  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,174,874 - 154,175,123UniSTSGRCh37
GRCh37X154,140,362 - 154,140,614UniSTSGRCh37
Build 36X153,793,556 - 153,793,808RGDNCBI36
CeleraX154,299,099 - 154,299,351RGD
CeleraX154,333,613 - 154,333,862UniSTS
Cytogenetic MapXq28UniSTS
HuRefX142,685,105 - 142,685,357UniSTS
HuRefX142,719,625 - 142,719,874UniSTS
REN91122  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,174,967 - 154,175,200UniSTSGRCh37
Build 36X153,828,161 - 153,828,394RGDNCBI36
CeleraX154,333,706 - 154,333,939RGD
Cytogenetic MapXq28UniSTS
HuRefX142,719,718 - 142,719,951UniSTS
REN91123  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,175,599 - 154,175,863UniSTSGRCh37
Build 36X153,828,793 - 153,829,057RGDNCBI36
CeleraX154,334,338 - 154,334,602RGD
Cytogenetic MapXq28UniSTS
HuRefX142,720,350 - 142,720,614UniSTS
REN91124  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,175,852 - 154,176,101UniSTSGRCh37
Build 36X153,829,046 - 153,829,295RGDNCBI36
CeleraX154,334,591 - 154,334,840RGD
Cytogenetic MapXq28UniSTS
HuRefX142,720,603 - 142,720,852UniSTS
REN91125  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,176,076 - 154,176,300UniSTSGRCh37
Build 36X153,829,270 - 153,829,494RGDNCBI36
CeleraX154,334,815 - 154,335,039RGD
Cytogenetic MapXq28UniSTS
HuRefX142,720,827 - 142,721,051UniSTS
REN91127  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,176,507 - 154,176,755UniSTSGRCh37
Build 36X153,829,701 - 153,829,949RGDNCBI36
CeleraX154,335,246 - 154,335,494RGD
Cytogenetic MapXq28UniSTS
HuRefX142,721,258 - 142,721,506UniSTS
REN91128  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,176,731 - 154,176,986UniSTSGRCh37
Build 36X153,829,925 - 153,830,180RGDNCBI36
CeleraX154,335,470 - 154,335,725RGD
Cytogenetic MapXq28UniSTS
HuRefX142,721,482 - 142,721,737UniSTS
REN91129  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,176,963 - 154,177,220UniSTSGRCh37
Build 36X153,830,157 - 153,830,414RGDNCBI36
CeleraX154,335,702 - 154,335,959RGD
Cytogenetic MapXq28UniSTS
HuRefX142,721,714 - 142,721,971UniSTS
REN91130  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,177,218 - 154,177,468UniSTSGRCh37
Build 36X153,830,412 - 153,830,662RGDNCBI36
CeleraX154,335,957 - 154,336,207RGD
Cytogenetic MapXq28UniSTS
HuRefX142,721,969 - 142,722,219UniSTS
REN91131  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,177,465 - 154,177,714UniSTSGRCh37
Build 36X153,830,659 - 153,830,908RGDNCBI36
CeleraX154,336,204 - 154,336,453RGD
Cytogenetic MapXq28UniSTS
HuRefX142,722,216 - 142,722,465UniSTS
REN91132  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,177,677 - 154,177,927UniSTSGRCh37
Build 36X153,830,871 - 153,831,121RGDNCBI36
CeleraX154,336,416 - 154,336,666RGD
Cytogenetic MapXq28UniSTS
HuRefX142,722,428 - 142,722,678UniSTS
REN91133  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,177,916 - 154,178,161UniSTSGRCh37
Build 36X153,831,110 - 153,831,355RGDNCBI36
CeleraX154,336,655 - 154,336,900RGD
Cytogenetic MapXq28UniSTS
HuRefX142,722,667 - 142,722,912UniSTS
REN91134  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,178,334 - 154,178,566UniSTSGRCh37
Build 36X153,831,528 - 153,831,760RGDNCBI36
CeleraX154,337,073 - 154,337,305RGD
Cytogenetic MapXq28UniSTS
HuRefX142,723,084 - 142,723,316UniSTS
REN91135  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,178,530 - 154,178,777UniSTSGRCh37
Build 36X153,831,724 - 153,831,971RGDNCBI36
CeleraX154,337,269 - 154,337,516RGD
Cytogenetic MapXq28UniSTS
HuRefX142,723,280 - 142,723,527UniSTS
REN91136  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,178,754 - 154,179,019UniSTSGRCh37
Build 36X153,831,948 - 153,832,213RGDNCBI36
CeleraX154,337,493 - 154,337,758RGD
Cytogenetic MapXq28UniSTS
HuRefX142,723,504 - 142,723,769UniSTS
REN91137  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,178,996 - 154,179,250UniSTSGRCh37
Build 36X153,832,190 - 153,832,444RGDNCBI36
CeleraX154,337,735 - 154,337,989RGD
Cytogenetic MapXq28UniSTS
HuRefX142,723,746 - 142,724,000UniSTS
REN91138  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,179,228 - 154,179,485UniSTSGRCh37
Build 36X153,832,422 - 153,832,679RGDNCBI36
CeleraX154,337,967 - 154,338,224RGD
Cytogenetic MapXq28UniSTS
HuRefX142,723,978 - 142,724,235UniSTS
REN91139  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,179,464 - 154,179,710UniSTSGRCh37
Build 36X153,832,658 - 153,832,904RGDNCBI36
CeleraX154,338,203 - 154,338,449RGD
Cytogenetic MapXq28UniSTS
HuRefX142,724,214 - 142,724,460UniSTS
REN91140  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,179,683 - 154,179,946UniSTSGRCh37
Build 36X153,832,877 - 153,833,140RGDNCBI36
CeleraX154,338,422 - 154,338,685RGD
Cytogenetic MapXq28UniSTS
HuRefX142,724,433 - 142,724,696UniSTS
REN91141  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,179,923 - 154,180,159UniSTSGRCh37
Build 36X153,833,117 - 153,833,353RGDNCBI36
CeleraX154,338,662 - 154,338,898RGD
Cytogenetic MapXq28UniSTS
HuRefX142,724,673 - 142,724,909UniSTS
REN91142  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,180,117 - 154,180,346UniSTSGRCh37
Build 36X153,833,311 - 153,833,540RGDNCBI36
CeleraX154,338,856 - 154,339,085RGD
Cytogenetic MapXq28UniSTS
HuRefX142,724,867 - 142,725,096UniSTS
REN91144  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,180,512 - 154,180,770UniSTSGRCh37
Build 36X153,833,706 - 153,833,964RGDNCBI36
CeleraX154,339,251 - 154,339,509RGD
Cytogenetic MapXq28UniSTS
HuRefX142,725,262 - 142,725,520UniSTS
REN91145  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,180,578 - 154,180,806UniSTSGRCh37
Build 36X153,833,772 - 153,834,000RGDNCBI36
CeleraX154,339,317 - 154,339,545RGD
Cytogenetic MapXq28UniSTS
HuRefX142,725,328 - 142,725,556UniSTS
REN91146  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,181,129 - 154,181,357UniSTSGRCh37
Build 36X153,834,323 - 153,834,551RGDNCBI36
CeleraX154,339,868 - 154,340,096RGD
Cytogenetic MapXq28UniSTS
HuRefX142,725,879 - 142,726,107UniSTS
REN91147  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,181,343 - 154,181,602UniSTSGRCh37
Build 36X153,834,537 - 153,834,796RGDNCBI36
CeleraX154,340,082 - 154,340,341RGD
Cytogenetic MapXq28UniSTS
HuRefX142,726,093 - 142,726,352UniSTS
REN91148  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,181,584 - 154,181,824UniSTSGRCh37
Build 36X153,834,778 - 153,835,018RGDNCBI36
CeleraX154,340,323 - 154,340,563RGD
Cytogenetic MapXq28UniSTS
HuRefX142,726,334 - 142,726,574UniSTS
REN91149  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,181,789 - 154,182,025UniSTSGRCh37
Build 36X153,834,983 - 153,835,219RGDNCBI36
CeleraX154,340,528 - 154,340,764RGD
Cytogenetic MapXq28UniSTS
HuRefX142,726,539 - 142,726,775UniSTS
REN91150  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,182,003 - 154,182,244UniSTSGRCh37
Build 36X153,835,197 - 153,835,438RGDNCBI36
CeleraX154,340,742 - 154,340,983RGD
Cytogenetic MapXq28UniSTS
HuRefX142,726,753 - 142,726,994UniSTS
REN91151  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,182,243 - 154,182,492UniSTSGRCh37
Build 36X153,835,437 - 153,835,686RGDNCBI36
CeleraX154,340,982 - 154,341,231RGD
Cytogenetic MapXq28UniSTS
HuRefX142,726,993 - 142,727,242UniSTS
REN91152  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,182,479 - 154,182,748UniSTSGRCh37
Build 36X153,835,673 - 153,835,942RGDNCBI36
CeleraX154,341,218 - 154,341,487RGD
Cytogenetic MapXq28UniSTS
HuRefX142,727,229 - 142,727,498UniSTS
REN91153  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,182,725 - 154,182,952UniSTSGRCh37
Build 36X153,835,919 - 153,836,146RGDNCBI36
CeleraX154,341,464 - 154,341,691RGD
Cytogenetic MapXq28UniSTS
HuRefX142,727,475 - 142,727,702UniSTS
REN91154  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,182,908 - 154,183,167UniSTSGRCh37
Build 36X153,836,102 - 153,836,361RGDNCBI36
CeleraX154,341,647 - 154,341,906RGD
Cytogenetic MapXq28UniSTS
HuRefX142,727,658 - 142,727,917UniSTS
REN91155  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,183,142 - 154,183,378UniSTSGRCh37
Build 36X153,836,336 - 153,836,572RGDNCBI36
CeleraX154,341,881 - 154,342,117RGD
Cytogenetic MapXq28UniSTS
HuRefX142,727,892 - 142,728,128UniSTS
REN91156  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,183,239 - 154,183,491UniSTSGRCh37
Build 36X153,836,433 - 153,836,685RGDNCBI36
CeleraX154,341,978 - 154,342,230RGD
Cytogenetic MapXq28UniSTS
HuRefX142,727,989 - 142,728,241UniSTS
REN91157  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,183,625 - 154,183,861UniSTSGRCh37
Build 36X153,836,819 - 153,837,055RGDNCBI36
CeleraX154,342,364 - 154,342,600RGD
Cytogenetic MapXq28UniSTS
HuRefX142,728,375 - 142,728,611UniSTS
REN91159  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,184,050 - 154,184,295UniSTSGRCh37
Build 36X153,837,244 - 153,837,489RGDNCBI36
CeleraX154,342,789 - 154,343,034RGD
Cytogenetic MapXq28UniSTS
HuRefX142,728,800 - 142,729,045UniSTS
REN91161  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,184,650 - 154,184,901UniSTSGRCh37
Build 36X153,837,844 - 153,838,095RGDNCBI36
CeleraX154,343,389 - 154,343,640RGD
Cytogenetic MapXq28UniSTS
HuRefX142,729,400 - 142,729,651UniSTS
REN91162  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,184,891 - 154,185,125UniSTSGRCh37
Build 36X153,838,085 - 153,838,319RGDNCBI36
CeleraX154,343,630 - 154,343,864RGD
Cytogenetic MapXq28UniSTS
HuRefX142,729,641 - 142,729,875UniSTS
REN91163  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,185,084 - 154,185,344UniSTSGRCh37
Build 36X153,838,278 - 153,838,538RGDNCBI36
CeleraX154,343,823 - 154,344,083RGD
Cytogenetic MapXq28UniSTS
HuRefX142,729,834 - 142,730,094UniSTS
REN91164  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,185,318 - 154,185,572UniSTSGRCh37
Build 36X153,838,512 - 153,838,766RGDNCBI36
CeleraX154,344,057 - 154,344,311RGD
Cytogenetic MapXq28UniSTS
HuRefX142,730,068 - 142,730,322UniSTS
REN91165  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,185,566 - 154,185,826UniSTSGRCh37
Build 36X153,838,760 - 153,839,020RGDNCBI36
CeleraX154,344,305 - 154,344,565RGD
Cytogenetic MapXq28UniSTS
HuRefX142,730,316 - 142,730,576UniSTS
REN91166  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,185,730 - 154,185,958UniSTSGRCh37
Build 36X153,838,924 - 153,839,152RGDNCBI36
CeleraX154,344,469 - 154,344,697RGD
Cytogenetic MapXq28UniSTS
HuRefX142,730,480 - 142,730,708UniSTS
REN91167  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,185,893 - 154,186,117UniSTSGRCh37
Build 36X153,839,087 - 153,839,311RGDNCBI36
CeleraX154,344,632 - 154,344,856RGD
Cytogenetic MapXq28UniSTS
HuRefX142,730,643 - 142,730,867UniSTS
REN91168  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,186,091 - 154,186,330UniSTSGRCh37
Build 36X153,839,285 - 153,839,524RGDNCBI36
CeleraX154,344,830 - 154,345,069RGD
Cytogenetic MapXq28UniSTS
HuRefX142,730,841 - 142,731,080UniSTS
REN91169  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,186,307 - 154,186,556UniSTSGRCh37
Build 36X153,839,501 - 153,839,750RGDNCBI36
CeleraX154,345,046 - 154,345,295RGD
Cytogenetic MapXq28UniSTS
HuRefX142,731,057 - 142,731,306UniSTS
REN91170  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,186,535 - 154,186,781UniSTSGRCh37
Build 36X153,839,729 - 153,839,975RGDNCBI36
CeleraX154,345,274 - 154,345,520RGD
Cytogenetic MapXq28UniSTS
HuRefX142,731,285 - 142,731,532UniSTS
REN91171  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,186,660 - 154,186,902UniSTSGRCh37
Build 36X153,839,854 - 153,840,096RGDNCBI36
CeleraX154,345,399 - 154,345,641RGD
Cytogenetic MapXq28UniSTS
HuRefX142,731,410 - 142,731,653UniSTS
REN91172  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,187,218 - 154,187,485UniSTSGRCh37
Build 36X153,840,412 - 153,840,679RGDNCBI36
CeleraX154,345,957 - 154,346,224RGD
Cytogenetic MapXq28UniSTS
HuRefX142,731,969 - 142,732,236UniSTS
REN91173  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,187,462 - 154,187,723UniSTSGRCh37
Build 36X153,840,656 - 153,840,917RGDNCBI36
CeleraX154,346,201 - 154,346,462RGD
Cytogenetic MapXq28UniSTS
HuRefX142,732,213 - 142,732,474UniSTS
REN91174  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,187,715 - 154,187,949UniSTSGRCh37
Build 36X153,840,909 - 153,841,143RGDNCBI36
CeleraX154,346,454 - 154,346,688RGD
Cytogenetic MapXq28UniSTS
HuRefX142,732,466 - 142,732,700UniSTS
REN91176  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,188,106 - 154,188,336UniSTSGRCh37
Build 36X153,841,300 - 153,841,530RGDNCBI36
CeleraX154,346,845 - 154,347,075RGD
Cytogenetic MapXq28UniSTS
HuRefX142,732,857 - 142,733,087UniSTS
REN91177  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,188,266 - 154,188,495UniSTSGRCh37
Build 36X153,841,460 - 153,841,689RGDNCBI36
CeleraX154,347,005 - 154,347,234RGD
Cytogenetic MapXq28UniSTS
HuRefX142,733,017 - 142,733,246UniSTS
REN91178  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,188,382 - 154,188,634UniSTSGRCh37
Build 36X153,841,576 - 153,841,828RGDNCBI36
CeleraX154,347,121 - 154,347,373RGD
Cytogenetic MapXq28UniSTS
HuRefX142,733,133 - 142,733,385UniSTS
REN91179  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,188,632 - 154,188,879UniSTSGRCh37
Build 36X153,841,826 - 153,842,073RGDNCBI36
CeleraX154,347,371 - 154,347,618RGD
Cytogenetic MapXq28UniSTS
HuRefX142,733,383 - 142,733,630UniSTS
REN91180  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,188,876 - 154,189,119UniSTSGRCh37
Build 36X153,842,070 - 153,842,313RGDNCBI36
CeleraX154,347,615 - 154,347,858RGD
Cytogenetic MapXq28UniSTS
HuRefX142,733,627 - 142,733,870UniSTS
REN91181  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,189,096 - 154,189,356UniSTSGRCh37
Build 36X153,842,290 - 153,842,550RGDNCBI36
CeleraX154,347,835 - 154,348,095RGD
Cytogenetic MapXq28UniSTS
HuRefX142,733,847 - 142,734,107UniSTS
REN91182  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,189,334 - 154,189,585UniSTSGRCh37
Build 36X153,842,528 - 153,842,779RGDNCBI36
CeleraX154,348,073 - 154,348,324RGD
Cytogenetic MapXq28UniSTS
HuRefX142,734,085 - 142,734,336UniSTS
REN91184  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,189,707 - 154,189,970UniSTSGRCh37
Build 36X153,842,901 - 153,843,164RGDNCBI36
CeleraX154,348,446 - 154,348,709RGD
Cytogenetic MapXq28UniSTS
HuRefX142,734,458 - 142,734,652UniSTS
REN91185  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,189,947 - 154,190,197UniSTSGRCh37
Build 36X153,843,141 - 153,843,391RGDNCBI36
CeleraX154,348,686 - 154,348,936RGD
Cytogenetic MapXq28UniSTS
HuRefX142,734,629 - 142,734,879UniSTS
REN91186  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,190,175 - 154,190,429UniSTSGRCh37
Build 36X153,843,369 - 153,843,623RGDNCBI36
CeleraX154,348,914 - 154,349,168RGD
Cytogenetic MapXq28UniSTS
HuRefX142,734,857 - 142,735,111UniSTS
REN91187  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,190,406 - 154,190,656UniSTSGRCh37
Build 36X153,843,600 - 153,843,850RGDNCBI36
CeleraX154,349,145 - 154,349,395RGD
Cytogenetic MapXq28UniSTS
HuRefX142,735,088 - 142,735,338UniSTS
REN91188  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,190,655 - 154,190,880UniSTSGRCh37
Build 36X153,843,849 - 153,844,074RGDNCBI36
CeleraX154,349,394 - 154,349,619RGD
Cytogenetic MapXq28UniSTS
HuRefX142,735,337 - 142,735,562UniSTS
REN91189  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,190,677 - 154,190,939UniSTSGRCh37
Build 36X153,843,871 - 153,844,133RGDNCBI36
CeleraX154,349,416 - 154,349,678RGD
Cytogenetic MapXq28UniSTS
HuRefX142,735,359 - 142,735,621UniSTS
REN91190  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,191,871 - 154,192,095UniSTSGRCh37
Build 36X153,845,065 - 153,845,289RGDNCBI36
CeleraX154,350,610 - 154,350,834RGD
Cytogenetic MapXq28UniSTS
HuRefX142,736,552 - 142,736,776UniSTS
REN91191  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,192,085 - 154,192,336UniSTSGRCh37
Build 36X153,845,279 - 153,845,530RGDNCBI36
CeleraX154,350,824 - 154,351,075RGD
Cytogenetic MapXq28UniSTS
HuRefX142,736,766 - 142,737,017UniSTS
REN91192  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,192,312 - 154,192,553UniSTSGRCh37
Build 36X153,845,506 - 153,845,747RGDNCBI36
CeleraX154,351,051 - 154,351,292RGD
Cytogenetic MapXq28UniSTS
HuRefX142,736,993 - 142,737,234UniSTS
REN91193  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,192,526 - 154,192,789UniSTSGRCh37
Build 36X153,845,720 - 153,845,983RGDNCBI36
CeleraX154,351,265 - 154,351,528RGD
Cytogenetic MapXq28UniSTS
HuRefX142,737,207 - 142,737,470UniSTS
REN91194  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,192,782 - 154,193,056UniSTSGRCh37
Build 36X153,845,976 - 153,846,250RGDNCBI36
CeleraX154,351,521 - 154,351,795RGD
Cytogenetic MapXq28UniSTS
HuRefX142,737,463 - 142,737,737UniSTS
REN91195  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,193,044 - 154,193,315UniSTSGRCh37
Build 36X153,846,238 - 153,846,509RGDNCBI36
CeleraX154,351,783 - 154,352,054RGD
Cytogenetic MapXq28UniSTS
HuRefX142,737,725 - 142,737,996UniSTS
REN91196  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,193,300 - 154,193,553UniSTSGRCh37
Build 36X153,846,494 - 153,846,747RGDNCBI36
CeleraX154,352,039 - 154,352,292RGD
Cytogenetic MapXq28UniSTS
HuRefX142,737,981 - 142,738,234UniSTS
REN91197  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,193,542 - 154,193,803UniSTSGRCh37
Build 36X153,846,736 - 153,846,997RGDNCBI36
CeleraX154,352,281 - 154,352,542RGD
Cytogenetic MapXq28UniSTS
HuRefX142,738,223 - 142,738,937UniSTS
REN91198  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,193,801 - 154,194,054UniSTSGRCh37
Build 36X153,846,995 - 153,847,248RGDNCBI36
CeleraX154,352,540 - 154,352,793RGD
Cytogenetic MapXq28UniSTS
HuRefX142,738,935 - 142,739,188UniSTS
REN91199  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,194,031 - 154,194,280UniSTSGRCh37
Build 36X153,847,225 - 153,847,474RGDNCBI36
CeleraX154,352,770 - 154,353,019RGD
Cytogenetic MapXq28UniSTS
HuRefX142,739,165 - 142,739,414UniSTS
REN91200  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,194,272 - 154,194,524UniSTSGRCh37
Build 36X153,847,466 - 153,847,718RGDNCBI36
CeleraX154,353,011 - 154,353,263RGD
Cytogenetic MapXq28UniSTS
HuRefX142,739,406 - 142,739,658UniSTS
REN91201  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,194,498 - 154,194,752UniSTSGRCh37
Build 36X153,847,692 - 153,847,946RGDNCBI36
CeleraX154,353,237 - 154,353,491RGD
Cytogenetic MapXq28UniSTS
HuRefX142,739,632 - 142,739,886UniSTS
REN91202  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,194,747 - 154,194,992UniSTSGRCh37
Build 36X153,847,941 - 153,848,186RGDNCBI36
CeleraX154,353,486 - 154,353,731RGD
Cytogenetic MapXq28UniSTS
HuRefX142,739,881 - 142,740,126UniSTS
REN91203  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,194,979 - 154,195,236UniSTSGRCh37
Build 36X153,848,173 - 153,848,430RGDNCBI36
CeleraX154,353,718 - 154,353,975RGD
Cytogenetic MapXq28UniSTS
HuRefX142,740,113 - 142,740,370UniSTS
REN91204  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,195,231 - 154,195,474UniSTSGRCh37
Build 36X153,848,425 - 153,848,668RGDNCBI36
CeleraX154,353,970 - 154,354,213RGD
Cytogenetic MapXq28UniSTS
HuRefX142,740,365 - 142,740,608UniSTS
REN91205  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,195,451 - 154,195,725UniSTSGRCh37
Build 36X153,848,645 - 153,848,919RGDNCBI36
CeleraX154,354,190 - 154,354,464RGD
Cytogenetic MapXq28UniSTS
HuRefX142,740,585 - 142,740,859UniSTS
REN91206  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,195,701 - 154,195,942UniSTSGRCh37
Build 36X153,848,895 - 153,849,136RGDNCBI36
CeleraX154,354,440 - 154,354,681RGD
Cytogenetic MapXq28UniSTS
HuRefX142,740,835 - 142,741,076UniSTS
REN91207  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,195,917 - 154,196,155UniSTSGRCh37
Build 36X153,849,111 - 153,849,349RGDNCBI36
CeleraX154,354,656 - 154,354,894RGD
Cytogenetic MapXq28UniSTS
HuRefX142,741,051 - 142,741,289UniSTS
REN91208  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,196,130 - 154,196,371UniSTSGRCh37
Build 36X153,849,324 - 153,849,565RGDNCBI36
CeleraX154,354,869 - 154,355,110RGD
Cytogenetic MapXq28UniSTS
HuRefX142,741,264 - 142,741,505UniSTS
REN91209  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,196,321 - 154,196,571UniSTSGRCh37
Build 36X153,849,515 - 153,849,765RGDNCBI36
CeleraX154,355,060 - 154,355,310RGD
Cytogenetic MapXq28UniSTS
HuRefX142,741,455 - 142,741,705UniSTS
REN91210  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,196,506 - 154,196,749UniSTSGRCh37
Build 36X153,849,700 - 153,849,943RGDNCBI36
CeleraX154,355,245 - 154,355,488RGD
Cytogenetic MapXq28UniSTS
HuRefX142,741,640 - 142,741,883UniSTS
REN91211  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,196,721 - 154,196,981UniSTSGRCh37
Build 36X153,849,915 - 153,850,175RGDNCBI36
CeleraX154,355,460 - 154,355,720RGD
Cytogenetic MapXq28UniSTS
HuRefX142,741,855 - 142,742,115UniSTS
REN91212  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,196,963 - 154,197,225UniSTSGRCh37
Build 36X153,850,157 - 153,850,419RGDNCBI36
CeleraX154,355,702 - 154,355,964RGD
Cytogenetic MapXq28UniSTS
HuRefX142,742,097 - 142,742,359UniSTS
REN91213  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,197,202 - 154,197,465UniSTSGRCh37
Build 36X153,850,396 - 153,850,659RGDNCBI36
CeleraX154,355,941 - 154,356,204RGD
Cytogenetic MapXq28UniSTS
HuRefX142,742,336 - 142,742,599UniSTS
REN91214  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,197,464 - 154,197,703UniSTSGRCh37
Build 36X153,850,658 - 153,850,897RGDNCBI36
CeleraX154,356,203 - 154,356,442RGD
Cytogenetic MapXq28UniSTS
HuRefX142,742,598 - 142,742,837UniSTS
REN91215  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,197,680 - 154,197,913UniSTSGRCh37
Build 36X153,850,874 - 153,851,107RGDNCBI36
CeleraX154,356,419 - 154,356,652RGD
Cytogenetic MapXq28UniSTS
HuRefX142,742,814 - 142,743,047UniSTS
REN91216  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,197,893 - 154,198,165UniSTSGRCh37
Build 36X153,851,087 - 153,851,359RGDNCBI36
CeleraX154,356,632 - 154,356,904RGD
Cytogenetic MapXq28UniSTS
HuRefX142,743,027 - 142,743,299UniSTS
REN91217  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,198,142 - 154,198,391UniSTSGRCh37
Build 36X153,851,336 - 153,851,585RGDNCBI36
CeleraX154,356,881 - 154,357,130RGD
Cytogenetic MapXq28UniSTS
HuRefX142,743,276 - 142,743,525UniSTS
REN91218  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,198,390 - 154,198,636UniSTSGRCh37
Build 36X153,851,584 - 153,851,830RGDNCBI36
CeleraX154,357,129 - 154,357,375RGD
Cytogenetic MapXq28UniSTS
HuRefX142,743,524 - 142,743,770UniSTS
REN91219  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,198,607 - 154,198,854UniSTSGRCh37
Build 36X153,851,801 - 153,852,048RGDNCBI36
CeleraX154,357,346 - 154,357,593RGD
Cytogenetic MapXq28UniSTS
HuRefX142,743,741 - 142,743,988UniSTS
REN91221  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,199,043 - 154,199,303UniSTSGRCh37
Build 36X153,852,237 - 153,852,497RGDNCBI36
CeleraX154,357,782 - 154,358,042RGD
Cytogenetic MapXq28UniSTS
HuRefX142,744,177 - 142,744,437UniSTS
REN91222  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,199,275 - 154,199,509UniSTSGRCh37
Build 36X153,852,469 - 153,852,703RGDNCBI36
CeleraX154,358,014 - 154,358,248RGD
Cytogenetic MapXq28UniSTS
HuRefX142,744,409 - 142,744,643UniSTS
REN91223  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,199,383 - 154,199,616UniSTSGRCh37
Build 36X153,852,577 - 153,852,810RGDNCBI36
CeleraX154,358,122 - 154,358,355RGD
Cytogenetic MapXq28UniSTS
HuRefX142,744,517 - 142,744,750UniSTS
REN91224  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,199,607 - 154,199,834UniSTSGRCh37
Build 36X153,852,801 - 153,853,028RGDNCBI36
CeleraX154,358,346 - 154,358,573RGD
Cytogenetic MapXq28UniSTS
HuRefX142,744,741 - 142,744,968UniSTS
REN91225  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,199,808 - 154,200,056UniSTSGRCh37
Build 36X153,853,002 - 153,853,250RGDNCBI36
CeleraX154,358,547 - 154,358,795RGD
Cytogenetic MapXq28UniSTS
HuRefX142,744,942 - 142,745,190UniSTS
REN91226  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,200,021 - 154,200,267UniSTSGRCh37
Build 36X153,853,215 - 153,853,461RGDNCBI36
CeleraX154,358,760 - 154,359,006RGD
Cytogenetic MapXq28UniSTS
HuRefX142,745,155 - 142,745,401UniSTS
REN91227  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,200,265 - 154,200,518UniSTSGRCh37
Build 36X153,853,459 - 153,853,712RGDNCBI36
CeleraX154,359,004 - 154,359,257RGD
Cytogenetic MapXq28UniSTS
HuRefX142,745,399 - 142,745,652UniSTS
REN91229  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,200,637 - 154,200,871UniSTSGRCh37
Build 36X153,853,831 - 153,854,065RGDNCBI36
CeleraX154,359,376 - 154,359,610RGD
Cytogenetic MapXq28UniSTS
HuRefX142,745,771 - 142,746,005UniSTS
REN91230  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,201,280 - 154,201,523UniSTSGRCh37
Build 36X153,854,474 - 153,854,717RGDNCBI36
CeleraX154,360,017 - 154,360,260RGD
Cytogenetic MapXq28UniSTS
HuRefX142,746,415 - 142,746,658UniSTS
REN91231  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,201,393 - 154,201,643UniSTSGRCh37
Build 36X153,854,587 - 153,854,837RGDNCBI36
CeleraX154,360,130 - 154,360,380RGD
Cytogenetic MapXq28UniSTS
HuRefX142,746,528 - 142,746,778UniSTS
REN91232  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,201,616 - 154,201,854UniSTSGRCh37
Build 36X153,854,810 - 153,855,048RGDNCBI36
CeleraX154,360,353 - 154,360,591RGD
Cytogenetic MapXq28UniSTS
HuRefX142,746,751 - 142,746,989UniSTS
REN91233  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,201,815 - 154,202,040UniSTSGRCh37
Build 36X153,855,009 - 153,855,234RGDNCBI36
CeleraX154,360,552 - 154,360,777RGD
Cytogenetic MapXq28UniSTS
HuRefX142,746,950 - 142,747,175UniSTS
REN91234  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,202,001 - 154,202,251UniSTSGRCh37
Build 36X153,855,195 - 153,855,445RGDNCBI36
CeleraX154,360,738 - 154,360,988RGD
Cytogenetic MapXq28UniSTS
HuRefX142,747,136 - 142,747,386UniSTS
REN91235  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,202,081 - 154,202,331UniSTSGRCh37
Build 36X153,855,275 - 153,855,525RGDNCBI36
CeleraX154,360,818 - 154,361,068RGD
Cytogenetic MapXq28UniSTS
HuRefX142,747,216 - 142,747,466UniSTS
REN91236  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,202,307 - 154,202,562UniSTSGRCh37
Build 36X153,855,501 - 153,855,756RGDNCBI36
CeleraX154,361,044 - 154,361,299RGD
Cytogenetic MapXq28UniSTS
HuRefX142,747,442 - 142,747,697UniSTS
REN91237  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,202,530 - 154,202,782UniSTSGRCh37
Build 36X153,855,724 - 153,855,976RGDNCBI36
CeleraX154,361,267 - 154,361,519RGD
Cytogenetic MapXq28UniSTS
HuRefX142,747,665 - 142,747,917UniSTS
REN91238  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,202,733 - 154,202,998UniSTSGRCh37
Build 36X153,855,927 - 153,856,192RGDNCBI36
CeleraX154,361,470 - 154,361,735RGD
Cytogenetic MapXq28UniSTS
HuRefX142,747,868 - 142,748,133UniSTS
REN91239  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,202,928 - 154,203,152UniSTSGRCh37
Build 36X153,856,122 - 153,856,346RGDNCBI36
CeleraX154,361,665 - 154,361,889RGD
Cytogenetic MapXq28UniSTS
HuRefX142,748,063 - 142,748,287UniSTS
REN91240  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,203,127 - 154,203,383UniSTSGRCh37
Build 36X153,856,321 - 153,856,577RGDNCBI36
CeleraX154,361,864 - 154,362,120RGD
Cytogenetic MapXq28UniSTS
HuRefX142,748,262 - 142,748,518UniSTS
REN91242  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,203,615 - 154,203,867UniSTSGRCh37
Build 36X153,856,809 - 153,857,061RGDNCBI36
CeleraX154,362,352 - 154,362,604RGD
Cytogenetic MapXq28UniSTS
HuRefX142,748,750 - 142,749,002UniSTS
REN91243  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,203,819 - 154,204,059UniSTSGRCh37
Build 36X153,857,013 - 153,857,253RGDNCBI36
CeleraX154,362,556 - 154,362,796RGD
Cytogenetic MapXq28UniSTS
HuRefX142,748,954 - 142,749,194UniSTS
REN91244  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,203,975 - 154,204,210UniSTSGRCh37
Build 36X153,857,169 - 153,857,404RGDNCBI36
CeleraX154,362,712 - 154,362,947RGD
Cytogenetic MapXq28UniSTS
HuRefX142,749,110 - 142,749,345UniSTS
REN91245  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,204,460 - 154,204,684UniSTSGRCh37
Build 36X153,857,654 - 153,857,878RGDNCBI36
CeleraX154,363,197 - 154,363,421RGD
Cytogenetic MapXq28UniSTS
HuRefX142,749,595 - 142,749,819UniSTS
REN91247  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,205,125 - 154,205,376UniSTSGRCh37
Build 36X153,858,319 - 153,858,570RGDNCBI36
CeleraX154,363,862 - 154,364,113RGD
Cytogenetic MapXq28UniSTS
HuRefX142,750,260 - 142,750,511UniSTS
REN91248  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,205,352 - 154,205,606UniSTSGRCh37
Build 36X153,858,546 - 153,858,800RGDNCBI36
CeleraX154,364,089 - 154,364,343RGD
Cytogenetic MapXq28UniSTS
HuRefX142,750,487 - 142,750,741UniSTS
REN91250  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,205,804 - 154,206,071UniSTSGRCh37
Build 36X153,858,998 - 153,859,265RGDNCBI36
CeleraX154,364,541 - 154,364,808RGD
Cytogenetic MapXq28UniSTS
HuRefX142,750,939 - 142,751,206UniSTS
REN91251  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,206,065 - 154,206,308UniSTSGRCh37
Build 36X153,859,259 - 153,859,502RGDNCBI36
CeleraX154,364,802 - 154,365,045RGD
Cytogenetic MapXq28UniSTS
HuRefX142,751,200 - 142,751,443UniSTS
REN91252  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,206,305 - 154,206,565UniSTSGRCh37
Build 36X153,859,499 - 153,859,759RGDNCBI36
CeleraX154,365,042 - 154,365,302RGD
Cytogenetic MapXq28UniSTS
HuRefX142,751,440 - 142,751,700UniSTS
REN91253  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,206,463 - 154,206,712UniSTSGRCh37
Build 36X153,859,657 - 153,859,906RGDNCBI36
CeleraX154,365,200 - 154,365,449RGD
Cytogenetic MapXq28UniSTS
HuRefX142,751,598 - 142,751,847UniSTS
REN91254  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,206,691 - 154,206,932UniSTSGRCh37
Build 36X153,859,885 - 153,860,126RGDNCBI36
CeleraX154,365,428 - 154,365,669RGD
Cytogenetic MapXq28UniSTS
HuRefX142,751,826 - 142,752,067UniSTS
REN91255  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,206,909 - 154,207,160UniSTSGRCh37
Build 36X153,860,103 - 153,860,354RGDNCBI36
CeleraX154,365,646 - 154,365,897RGD
Cytogenetic MapXq28UniSTS
HuRefX142,752,044 - 142,752,295UniSTS
REN91256  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,207,127 - 154,207,373UniSTSGRCh37
Build 36X153,860,321 - 153,860,567RGDNCBI36
CeleraX154,365,864 - 154,366,110RGD
Cytogenetic MapXq28UniSTS
HuRefX142,752,262 - 142,752,508UniSTS
REN91258  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,207,570 - 154,207,820UniSTSGRCh37
Build 36X153,860,764 - 153,861,014RGDNCBI36
CeleraX154,366,307 - 154,366,557RGD
Cytogenetic MapXq28UniSTS
HuRefX142,752,705 - 142,752,955UniSTS
REN91259  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,207,796 - 154,208,047UniSTSGRCh37
Build 36X153,860,990 - 153,861,241RGDNCBI36
CeleraX154,366,533 - 154,366,784RGD
Cytogenetic MapXq28UniSTS
HuRefX142,752,931 - 142,753,182UniSTS
REN91260  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,208,025 - 154,208,281UniSTSGRCh37
Build 36X153,861,219 - 153,861,475RGDNCBI36
CeleraX154,366,762 - 154,367,018RGD
Cytogenetic MapXq28UniSTS
HuRefX142,753,160 - 142,753,416UniSTS
REN91261  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,208,272 - 154,208,529UniSTSGRCh37
Build 36X153,861,466 - 153,861,723RGDNCBI36
CeleraX154,367,009 - 154,367,266RGD
Cytogenetic MapXq28UniSTS
HuRefX142,753,407 - 142,753,664UniSTS
REN91262  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,208,511 - 154,208,761UniSTSGRCh37
Build 36X153,861,705 - 153,861,955RGDNCBI36
CeleraX154,367,248 - 154,367,498RGD
Cytogenetic MapXq28UniSTS
HuRefX142,753,646 - 142,753,896UniSTS
REN91263  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,208,747 - 154,208,997UniSTSGRCh37
Build 36X153,861,941 - 153,862,191RGDNCBI36
CeleraX154,367,484 - 154,367,734RGD
Cytogenetic MapXq28UniSTS
HuRefX142,753,882 - 142,754,132UniSTS
REN91267  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,209,625 - 154,209,885UniSTSGRCh37
Build 36X153,862,819 - 153,863,079RGDNCBI36
CeleraX154,368,362 - 154,368,622RGD
Cytogenetic MapXq28UniSTS
HuRefX142,754,816 - 142,755,076UniSTS
REN91268  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,209,762 - 154,210,003UniSTSGRCh37
Build 36X153,862,956 - 153,863,197RGDNCBI36
CeleraX154,368,499 - 154,368,740RGD
Cytogenetic MapXq28UniSTS
HuRefX142,754,953 - 142,755,194UniSTS
REN91269  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,209,951 - 154,210,186UniSTSGRCh37
Build 36X153,863,145 - 153,863,380RGDNCBI36
CeleraX154,368,688 - 154,368,923RGD
Cytogenetic MapXq28UniSTS
HuRefX142,755,142 - 142,755,377UniSTS
REN91270  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,210,877 - 154,211,102UniSTSGRCh37
Build 36X153,864,071 - 153,864,296RGDNCBI36
CeleraX154,369,612 - 154,369,837RGD
Cytogenetic MapXq28UniSTS
HuRefX142,756,066 - 142,756,287UniSTS
REN91271  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,211,074 - 154,211,299UniSTSGRCh37
Build 36X153,864,268 - 153,864,493RGDNCBI36
CeleraX154,369,809 - 154,370,034RGD
Cytogenetic MapXq28UniSTS
HuRefX142,756,259 - 142,756,484UniSTS
REN91272  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,211,237 - 154,211,482UniSTSGRCh37
Build 36X153,864,431 - 153,864,676RGDNCBI36
CeleraX154,369,972 - 154,370,217RGD
Cytogenetic MapXq28UniSTS
HuRefX142,756,422 - 142,756,667UniSTS
REN91273  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,211,458 - 154,211,689UniSTSGRCh37
Build 36X153,864,652 - 153,864,883RGDNCBI36
CeleraX154,370,193 - 154,370,424RGD
Cytogenetic MapXq28UniSTS
HuRefX142,756,643 - 142,756,874UniSTS
REN91274  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,211,638 - 154,211,885UniSTSGRCh37
Build 36X153,864,832 - 153,865,079RGDNCBI36
CeleraX154,370,373 - 154,370,620RGD
Cytogenetic MapXq28UniSTS
HuRefX142,756,823 - 142,757,070UniSTS
REN91276  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,212,049 - 154,212,295UniSTSGRCh37
Build 36X153,865,243 - 153,865,489RGDNCBI36
CeleraX154,370,784 - 154,371,030RGD
Cytogenetic MapXq28UniSTS
HuRefX142,757,234 - 142,757,480UniSTS
REN91277  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,212,286 - 154,212,524UniSTSGRCh37
Build 36X153,865,480 - 153,865,718RGDNCBI36
CeleraX154,371,021 - 154,371,259RGD
Cytogenetic MapXq28UniSTS
HuRefX142,757,471 - 142,757,709UniSTS
REN91278  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,212,507 - 154,212,770UniSTSGRCh37
Build 36X153,865,701 - 153,865,964RGDNCBI36
CeleraX154,371,242 - 154,371,505RGD
Cytogenetic MapXq28UniSTS
HuRefX142,757,692 - 142,757,955UniSTS
REN91279  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,212,765 - 154,213,007UniSTSGRCh37
Build 36X153,865,959 - 153,866,201RGDNCBI36
CeleraX154,371,500 - 154,371,742RGD
Cytogenetic MapXq28UniSTS
HuRefX142,757,950 - 142,758,192UniSTS
REN91280  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,212,984 - 154,213,228UniSTSGRCh37
Build 36X153,866,178 - 153,866,422RGDNCBI36
CeleraX154,371,719 - 154,371,963RGD
Cytogenetic MapXq28UniSTS
HuRefX142,758,169 - 142,758,413UniSTS
REN91281  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,213,227 - 154,213,474UniSTSGRCh37
Build 36X153,866,421 - 153,866,668RGDNCBI36
CeleraX154,371,962 - 154,372,209RGD
Cytogenetic MapXq28UniSTS
HuRefX142,758,412 - 142,758,659UniSTS
REN91282  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,213,318 - 154,213,574UniSTSGRCh37
Build 36X153,866,512 - 153,866,768RGDNCBI36
CeleraX154,372,053 - 154,372,309RGD
Cytogenetic MapXq28UniSTS
HuRefX142,758,503 - 142,758,759UniSTS
REN91284  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,213,940 - 154,214,185UniSTSGRCh37
Build 36X153,867,134 - 153,867,379RGDNCBI36
CeleraX154,372,675 - 154,372,920RGD
Cytogenetic MapXq28UniSTS
HuRefX142,759,125 - 142,759,370UniSTS
REN91285  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,214,154 - 154,214,399UniSTSGRCh37
Build 36X153,867,348 - 153,867,593RGDNCBI36
CeleraX154,372,889 - 154,373,134RGD
Cytogenetic MapXq28UniSTS
HuRefX142,759,339 - 142,759,584UniSTS
REN91286  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,214,369 - 154,214,608UniSTSGRCh37
Build 36X153,867,563 - 153,867,802RGDNCBI36
CeleraX154,373,104 - 154,373,343RGD
Cytogenetic MapXq28UniSTS
HuRefX142,759,554 - 142,759,793UniSTS
REN91287  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,214,747 - 154,214,983UniSTSGRCh37
Build 36X153,867,941 - 153,868,177RGDNCBI36
CeleraX154,373,482 - 154,373,718RGD
Cytogenetic MapXq28UniSTS
HuRefX142,759,932 - 142,760,168UniSTS
REN91289  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,215,170 - 154,215,418UniSTSGRCh37
Build 36X153,868,364 - 153,868,612RGDNCBI36
CeleraX154,373,905 - 154,374,153RGD
Cytogenetic MapXq28UniSTS
HuRefX142,760,355 - 142,760,603UniSTS
REN91290  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,215,395 - 154,215,654UniSTSGRCh37
Build 36X153,868,589 - 153,868,848RGDNCBI36
CeleraX154,374,130 - 154,374,389RGD
Cytogenetic MapXq28UniSTS
HuRefX142,760,580 - 142,760,839UniSTS
REN91291  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,215,631 - 154,215,882UniSTSGRCh37
Build 36X153,868,825 - 153,869,076RGDNCBI36
CeleraX154,374,366 - 154,374,617RGD
Cytogenetic MapXq28UniSTS
HuRefX142,760,816 - 142,761,066UniSTS
REN91292  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,215,856 - 154,216,123UniSTSGRCh37
Build 36X153,869,050 - 153,869,317RGDNCBI36
CeleraX154,374,591 - 154,374,858RGD
Cytogenetic MapXq28UniSTS
HuRefX142,761,040 - 142,761,307UniSTS
REN91293  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,216,118 - 154,216,377UniSTSGRCh37
Build 36X153,869,312 - 153,869,571RGDNCBI36
CeleraX154,374,853 - 154,375,112RGD
Cytogenetic MapXq28UniSTS
HuRefX142,761,302 - 142,761,561UniSTS
REN91294  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,216,376 - 154,216,618UniSTSGRCh37
Build 36X153,869,570 - 153,869,812RGDNCBI36
CeleraX154,375,111 - 154,375,353RGD
Cytogenetic MapXq28UniSTS
HuRefX142,761,560 - 142,761,802UniSTS
REN91295  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,216,602 - 154,216,854UniSTSGRCh37
Build 36X153,869,796 - 153,870,048RGDNCBI36
CeleraX154,375,337 - 154,375,589RGD
Cytogenetic MapXq28UniSTS
HuRefX142,761,786 - 142,762,038UniSTS
REN91296  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,216,846 - 154,217,089UniSTSGRCh37
Build 36X153,870,040 - 153,870,283RGDNCBI36
CeleraX154,375,581 - 154,375,824RGD
Cytogenetic MapXq28UniSTS
HuRefX142,762,030 - 142,762,273UniSTS
REN91298  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,217,223 - 154,217,452UniSTSGRCh37
Build 36X153,870,417 - 153,870,646RGDNCBI36
CeleraX154,375,958 - 154,376,187RGD
Cytogenetic MapXq28UniSTS
HuRefX142,762,407 - 142,762,636UniSTS
REN91299  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,217,419 - 154,217,665UniSTSGRCh37
Build 36X153,870,613 - 153,870,859RGDNCBI36
CeleraX154,376,154 - 154,376,400RGD
Cytogenetic MapXq28UniSTS
HuRefX142,762,603 - 142,762,844UniSTS
REN91300  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,217,642 - 154,217,876UniSTSGRCh37
Build 36X153,870,836 - 153,871,070RGDNCBI36
CeleraX154,376,377 - 154,376,611RGD
Cytogenetic MapXq28UniSTS
HuRefX142,762,822 - 142,763,056UniSTS
REN91301  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,217,845 - 154,218,072UniSTSGRCh37
Build 36X153,871,039 - 153,871,266RGDNCBI36
CeleraX154,376,580 - 154,376,807RGD
Cytogenetic MapXq28UniSTS
HuRefX142,763,025 - 142,763,252UniSTS
REN91302  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,218,049 - 154,218,317UniSTSGRCh37
Build 36X153,871,243 - 153,871,511RGDNCBI36
CeleraX154,376,784 - 154,377,052RGD
Cytogenetic MapXq28UniSTS
HuRefX142,763,229 - 142,763,497UniSTS
REN91303  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,218,307 - 154,218,552UniSTSGRCh37
Build 36X153,871,501 - 153,871,746RGDNCBI36
CeleraX154,377,042 - 154,377,287RGD
Cytogenetic MapXq28UniSTS
HuRefX142,763,487 - 142,763,732UniSTS
REN91304  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,218,506 - 154,218,763UniSTSGRCh37
Build 36X153,871,700 - 153,871,957RGDNCBI36
CeleraX154,377,241 - 154,377,498RGD
Cytogenetic MapXq28UniSTS
HuRefX142,763,686 - 142,763,943UniSTS
REN91306  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,218,960 - 154,219,210UniSTSGRCh37
Build 36X153,872,154 - 153,872,404RGDNCBI36
CeleraX154,377,695 - 154,377,945RGD
Cytogenetic MapXq28UniSTS
HuRefX142,764,140 - 142,764,390UniSTS
REN91307  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,219,194 - 154,219,435UniSTSGRCh37
Build 36X153,872,388 - 153,872,629RGDNCBI36
CeleraX154,377,929 - 154,378,170RGD
Cytogenetic MapXq28UniSTS
HuRefX142,764,374 - 142,764,615UniSTS
REN91308  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,219,406 - 154,219,631UniSTSGRCh37
Build 36X153,872,600 - 153,872,825RGDNCBI36
CeleraX154,378,141 - 154,378,366RGD
Cytogenetic MapXq28UniSTS
HuRefX142,764,586 - 142,764,811UniSTS
REN91311  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,220,050 - 154,220,299UniSTSGRCh37
Build 36X153,873,244 - 153,873,493RGDNCBI36
CeleraX154,378,785 - 154,379,034RGD
Cytogenetic MapXq28UniSTS
HuRefX142,765,197 - 142,765,446UniSTS
REN91312  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,220,272 - 154,220,497UniSTSGRCh37
Build 36X153,873,466 - 153,873,691RGDNCBI36
CeleraX154,379,007 - 154,379,232RGD
Cytogenetic MapXq28UniSTS
HuRefX142,765,419 - 142,765,644UniSTS
REN91314  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,220,586 - 154,220,834UniSTSGRCh37
Build 36X153,873,780 - 153,874,028RGDNCBI36
CeleraX154,379,321 - 154,379,569RGD
Cytogenetic MapXq28UniSTS
HuRefX142,765,733 - 142,765,981UniSTS
REN91315  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,220,824 - 154,221,086UniSTSGRCh37
Build 36X153,874,018 - 153,874,280RGDNCBI36
CeleraX154,379,559 - 154,379,821RGD
Cytogenetic MapXq28UniSTS
HuRefX142,765,971 - 142,766,233UniSTS
REN91316  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,221,063 - 154,221,305UniSTSGRCh37
Build 36X153,874,257 - 153,874,499RGDNCBI36
CeleraX154,379,798 - 154,380,040RGD
Cytogenetic MapXq28UniSTS
HuRefX142,766,210 - 142,766,452UniSTS
REN91317  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,221,286 - 154,221,535UniSTSGRCh37
Build 36X153,874,480 - 153,874,729RGDNCBI36
CeleraX154,380,021 - 154,380,270RGD
Cytogenetic MapXq28UniSTS
HuRefX142,766,433 - 142,766,682UniSTS
REN91318  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,221,314 - 154,221,551UniSTSGRCh37
Build 36X153,874,508 - 153,874,745RGDNCBI36
CeleraX154,380,049 - 154,380,286RGD
Cytogenetic MapXq28UniSTS
HuRefX142,766,461 - 142,766,698UniSTS
REN91319  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,221,726 - 154,221,965UniSTSGRCh37
Build 36X153,874,920 - 153,875,159RGDNCBI36
CeleraX154,380,461 - 154,380,700RGD
Cytogenetic MapXq28UniSTS
HuRefX142,766,873 - 142,767,112UniSTS
REN91321  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,222,122 - 154,222,380UniSTSGRCh37
Build 36X153,875,316 - 153,875,574RGDNCBI36
CeleraX154,380,857 - 154,381,115RGD
Cytogenetic MapXq28UniSTS
HuRefX142,767,269 - 142,767,527UniSTS
REN91322  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,222,357 - 154,222,621UniSTSGRCh37
Build 36X153,875,551 - 153,875,815RGDNCBI36
CeleraX154,381,092 - 154,381,356RGD
Cytogenetic MapXq28UniSTS
HuRefX142,767,504 - 142,767,768UniSTS
REN91323  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,222,598 - 154,222,838UniSTSGRCh37
Build 36X153,875,792 - 153,876,032RGDNCBI36
CeleraX154,381,333 - 154,381,573RGD
Cytogenetic MapXq28UniSTS
HuRefX142,767,745 - 142,767,985UniSTS
REN91324  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,222,815 - 154,223,052UniSTSGRCh37
Build 36X153,876,009 - 153,876,246RGDNCBI36
CeleraX154,381,550 - 154,381,787RGD
Cytogenetic MapXq28UniSTS
HuRefX142,767,962 - 142,768,199UniSTS
REN91325  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,223,040 - 154,223,295UniSTSGRCh37
Build 36X153,876,234 - 153,876,489RGDNCBI36
CeleraX154,381,775 - 154,382,030RGD
Cytogenetic MapXq28UniSTS
HuRefX142,768,187 - 142,768,442UniSTS
REN91326  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,223,275 - 154,223,537UniSTSGRCh37
Build 36X153,876,469 - 153,876,731RGDNCBI36
CeleraX154,382,010 - 154,382,272RGD
Cytogenetic MapXq28UniSTS
HuRefX142,768,422 - 142,768,684UniSTS
REN91327  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,223,534 - 154,223,791UniSTSGRCh37
Build 36X153,876,728 - 153,876,985RGDNCBI36
CeleraX154,382,269 - 154,382,526RGD
Cytogenetic MapXq28UniSTS
HuRefX142,768,681 - 142,768,938UniSTS
REN91328  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,223,685 - 154,223,919UniSTSGRCh37
Build 36X153,876,879 - 153,877,113RGDNCBI36
CeleraX154,382,420 - 154,382,654RGD
Cytogenetic MapXq28UniSTS
HuRefX142,768,832 - 142,769,066UniSTS
REN91329  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,223,855 - 154,224,103UniSTSGRCh37
Build 36X153,877,049 - 153,877,297RGDNCBI36
CeleraX154,382,590 - 154,382,838RGD
Cytogenetic MapXq28UniSTS
HuRefX142,769,002 - 142,769,250UniSTS
REN91331  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,224,318 - 154,224,562UniSTSGRCh37
Build 36X153,877,512 - 153,877,756RGDNCBI36
CeleraX154,383,053 - 154,383,297RGD
Cytogenetic MapXq28UniSTS
HuRefX142,769,465 - 142,769,709UniSTS
REN91332  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,224,545 - 154,224,789UniSTSGRCh37
Build 36X153,877,739 - 153,877,983RGDNCBI36
CeleraX154,383,280 - 154,383,524RGD
Cytogenetic MapXq28UniSTS
HuRefX142,769,692 - 142,769,936UniSTS
REN91333  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,224,765 - 154,225,021UniSTSGRCh37
Build 36X153,877,959 - 153,878,215RGDNCBI36
CeleraX154,383,500 - 154,383,756RGD
Cytogenetic MapXq28UniSTS
HuRefX142,769,912 - 142,770,168UniSTS
REN91334  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,224,997 - 154,225,236UniSTSGRCh37
Build 36X153,878,191 - 153,878,430RGDNCBI36
CeleraX154,383,732 - 154,383,971RGD
Cytogenetic MapXq28UniSTS
HuRefX142,770,144 - 142,770,383UniSTS
REN91335  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,225,182 - 154,225,438UniSTSGRCh37
Build 36X153,878,376 - 153,878,632RGDNCBI36
CeleraX154,383,917 - 154,384,173RGD
Cytogenetic MapXq28UniSTS
HuRefX142,770,329 - 142,770,585UniSTS
REN91336  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,225,432 - 154,225,659UniSTSGRCh37
Build 36X153,878,626 - 153,878,853RGDNCBI36
CeleraX154,384,167 - 154,384,394RGD
Cytogenetic MapXq28UniSTS
HuRefX142,770,579 - 142,770,806UniSTS
REN91338  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,225,900 - 154,226,130UniSTSGRCh37
Build 36X153,879,094 - 153,879,324RGDNCBI36
CeleraX154,384,635 - 154,384,865RGD
Cytogenetic MapXq28UniSTS
HuRefX142,771,047 - 142,771,277UniSTS
REN91339  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,226,094 - 154,226,363UniSTSGRCh37
Build 36X153,879,288 - 153,879,557RGDNCBI36
CeleraX154,384,829 - 154,385,098RGD
Cytogenetic MapXq28UniSTS
HuRefX142,771,241 - 142,771,510UniSTS
REN91340  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,226,360 - 154,226,607UniSTSGRCh37
Build 36X153,879,554 - 153,879,801RGDNCBI36
CeleraX154,385,095 - 154,385,342RGD
Cytogenetic MapXq28UniSTS
HuRefX142,771,507 - 142,771,754UniSTS
REN91341  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,226,590 - 154,226,821UniSTSGRCh37
Build 36X153,879,784 - 153,880,015RGDNCBI36
CeleraX154,385,325 - 154,385,556RGD
Cytogenetic MapXq28UniSTS
HuRefX142,771,737 - 142,771,968UniSTS
REN91342  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,226,809 - 154,227,060UniSTSGRCh37
Build 36X153,880,003 - 153,880,254RGDNCBI36
CeleraX154,385,544 - 154,385,795RGD
Cytogenetic MapXq28UniSTS
HuRefX142,771,956 - 142,772,207UniSTS
REN91344  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,227,277 - 154,227,502UniSTSGRCh37
Build 36X153,880,471 - 153,880,696RGDNCBI36
CeleraX154,386,012 - 154,386,237RGD
Cytogenetic MapXq28UniSTS
HuRefX142,772,424 - 142,772,649UniSTS
REN91345  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,227,473 - 154,227,738UniSTSGRCh37
Build 36X153,880,667 - 153,880,932RGDNCBI36
CeleraX154,386,208 - 154,386,473RGD
Cytogenetic MapXq28UniSTS
HuRefX142,772,620 - 142,772,885UniSTS
REN91346  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,227,737 - 154,227,987UniSTSGRCh37
Build 36X153,880,931 - 153,881,181RGDNCBI36
CeleraX154,386,472 - 154,386,722RGD
Cytogenetic MapXq28UniSTS
HuRefX142,772,884 - 142,773,134UniSTS
REN91347  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,227,964 - 154,228,207UniSTSGRCh37
Build 36X153,881,158 - 153,881,401RGDNCBI36
CeleraX154,386,699 - 154,386,942RGD
Cytogenetic MapXq28UniSTS
HuRefX142,773,111 - 142,773,354UniSTS
REN91348  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,228,174 - 154,228,398UniSTSGRCh37
Build 36X153,881,368 - 153,881,592RGDNCBI36
CeleraX154,386,909 - 154,387,133RGD
Cytogenetic MapXq28UniSTS
HuRefX142,773,321 - 142,773,545UniSTS
REN91349  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,228,373 - 154,228,645UniSTSGRCh37
Build 36X153,881,567 - 153,881,839RGDNCBI36
CeleraX154,387,108 - 154,387,380RGD
Cytogenetic MapXq28UniSTS
HuRefX142,773,520 - 142,773,792UniSTS
REN91350  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,228,643 - 154,228,914UniSTSGRCh37
Build 36X153,881,837 - 153,882,108RGDNCBI36
CeleraX154,387,378 - 154,387,649RGD
Cytogenetic MapXq28UniSTS
HuRefX142,773,790 - 142,774,061UniSTS
REN91351  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,228,902 - 154,229,167UniSTSGRCh37
Build 36X153,882,096 - 153,882,361RGDNCBI36
CeleraX154,387,637 - 154,387,902RGD
Cytogenetic MapXq28UniSTS
HuRefX142,774,049 - 142,774,314UniSTS
REN91352  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,229,145 - 154,229,396UniSTSGRCh37
Build 36X153,882,339 - 153,882,590RGDNCBI36
CeleraX154,387,880 - 154,388,131RGD
Cytogenetic MapXq28UniSTS
HuRefX142,774,292 - 142,774,543UniSTS
REN91353  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,229,307 - 154,229,537UniSTSGRCh37
Build 36X153,882,501 - 153,882,731RGDNCBI36
CeleraX154,388,042 - 154,388,272RGD
Cytogenetic MapXq28UniSTS
HuRefX142,774,454 - 142,774,684UniSTS
REN91354  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,229,434 - 154,229,662UniSTSGRCh37
Build 36X153,882,628 - 153,882,856RGDNCBI36
CeleraX154,388,169 - 154,388,397RGD
Cytogenetic MapXq28UniSTS
HuRefX142,774,581 - 142,774,809UniSTS
stSG604339  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,130,247 - 154,131,453UniSTSGRCh37
Build 36X153,783,441 - 153,784,647RGDNCBI36
CeleraX154,288,984 - 154,290,190RGD
HuRefX142,674,990 - 142,676,196UniSTS
stSG604340  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,131,434 - 154,132,736UniSTSGRCh37
Build 36X153,784,628 - 153,785,930RGDNCBI36
CeleraX154,290,171 - 154,291,473RGD
HuRefX142,676,177 - 142,677,479UniSTS
stSG604341  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,132,729 - 154,133,766UniSTSGRCh37
Build 36X153,785,923 - 153,786,960RGDNCBI36
CeleraX154,291,466 - 154,292,503RGD
HuRefX142,677,472 - 142,678,509UniSTS
stSG604342  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,133,747 - 154,134,778UniSTSGRCh37
Build 36X153,786,941 - 153,787,972RGDNCBI36
CeleraX154,292,484 - 154,293,515RGD
HuRefX142,678,490 - 142,679,521UniSTS
stSG604343  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,134,761 - 154,136,096UniSTSGRCh37
Build 36X153,787,955 - 153,789,290RGDNCBI36
CeleraX154,293,498 - 154,294,833RGD
HuRefX142,679,504 - 142,680,839UniSTS
stSG604346  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,150,546 - 154,151,579UniSTSGRCh37
Build 36X153,803,740 - 153,804,773RGDNCBI36
CeleraX154,309,284 - 154,310,317RGD
HuRefX142,695,288 - 142,696,321UniSTS
stSG604347  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,155,987 - 154,157,093UniSTSGRCh37
Build 36X153,809,181 - 153,810,287RGDNCBI36
CeleraX154,314,725 - 154,315,831RGD
HuRefX142,700,526 - 142,701,632UniSTS
stSG604350  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,159,624 - 154,160,847UniSTSGRCh37
Build 36X153,812,818 - 153,814,041RGDNCBI36
CeleraX154,318,362 - 154,319,585RGD
HuRefX142,704,163 - 142,705,217UniSTS
stSG604351  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,160,828 - 154,161,852UniSTSGRCh37
Build 36X153,814,022 - 153,815,046RGDNCBI36
CeleraX154,319,566 - 154,320,590RGD
HuRefX142,705,198 - 142,706,222UniSTS
stSG604352  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,161,847 - 154,162,881UniSTSGRCh37
Build 36X153,815,041 - 153,816,075RGDNCBI36
CeleraX154,320,585 - 154,321,619RGD
HuRefX142,706,217 - 142,707,251UniSTS
stSG604355  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,175,851 - 154,176,992UniSTSGRCh37
Build 36X153,829,045 - 153,830,186RGDNCBI36
CeleraX154,334,590 - 154,335,731RGD
HuRefX142,720,602 - 142,721,743UniSTS
stSG604356  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,176,608 - 154,177,686UniSTSGRCh37
Build 36X153,829,802 - 153,830,880RGDNCBI36
CeleraX154,335,347 - 154,336,425RGD
HuRefX142,721,359 - 142,722,437UniSTS
stSG604357  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,177,672 - 154,178,778UniSTSGRCh37
Build 36X153,830,866 - 153,831,972RGDNCBI36
CeleraX154,336,411 - 154,337,517RGD
HuRefX142,722,423 - 142,723,528UniSTS
stSG604358  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,178,759 - 154,180,048UniSTSGRCh37
Build 36X153,831,953 - 153,833,242RGDNCBI36
CeleraX154,337,498 - 154,338,787RGD
HuRefX142,723,509 - 142,724,798UniSTS
stSG604359  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,180,029 - 154,181,282UniSTSGRCh37
Build 36X153,833,223 - 153,834,476RGDNCBI36
CeleraX154,338,768 - 154,340,021RGD
HuRefX142,724,779 - 142,726,032UniSTS
stSG604360  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,181,265 - 154,182,499UniSTSGRCh37
Build 36X153,834,459 - 153,835,693RGDNCBI36
CeleraX154,340,004 - 154,341,238RGD
HuRefX142,726,015 - 142,727,249UniSTS
stSG604361  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,182,385 - 154,183,424UniSTSGRCh37
Build 36X153,835,579 - 153,836,618RGDNCBI36
CeleraX154,341,124 - 154,342,163RGD
HuRefX142,727,135 - 142,728,174UniSTS
stSG604362  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,185,063 - 154,186,271UniSTSGRCh37
Build 36X153,838,257 - 153,839,465RGDNCBI36
CeleraX154,343,802 - 154,345,010RGD
HuRefX142,729,813 - 142,731,021UniSTS
stSG604363  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,186,252 - 154,186,442UniSTSGRCh37
Build 36X153,839,446 - 153,839,636RGDNCBI36
CeleraX154,344,991 - 154,345,181RGD
HuRefX142,731,002 - 142,731,192UniSTS
stSG604364  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,186,482 - 154,187,762UniSTSGRCh37
Build 36X153,839,676 - 153,840,956RGDNCBI36
CeleraX154,345,221 - 154,346,501RGD
HuRefX142,731,232 - 142,732,513UniSTS
stSG604365  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,187,741 - 154,189,050UniSTSGRCh37
Build 36X153,840,935 - 153,842,244RGDNCBI36
CeleraX154,346,480 - 154,347,789RGD
HuRefX142,732,492 - 142,733,801UniSTS
stSG604366  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,188,447 - 154,189,508UniSTSGRCh37
Build 36X153,841,641 - 153,842,702RGDNCBI36
CeleraX154,347,186 - 154,348,247RGD
HuRefX142,733,198 - 142,734,259UniSTS
stSG604367  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,189,488 - 154,190,592UniSTSGRCh37
Build 36X153,842,682 - 153,843,786RGDNCBI36
CeleraX154,348,227 - 154,349,331RGD
HuRefX142,734,239 - 142,735,274UniSTS
stSG604368  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,190,582 - 154,192,042UniSTSGRCh37
Build 36X153,843,776 - 153,845,236RGDNCBI36
CeleraX154,349,321 - 154,350,781RGD
HuRefX142,735,264 - 142,736,723UniSTS
stSG604369  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,192,023 - 154,193,035UniSTSGRCh37
Build 36X153,845,217 - 153,846,229RGDNCBI36
CeleraX154,350,762 - 154,351,774RGD
HuRefX142,736,704 - 142,737,716UniSTS
stSG604371  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,194,380 - 154,195,474UniSTSGRCh37
Build 36X153,847,574 - 153,848,668RGDNCBI36
CeleraX154,353,119 - 154,354,213RGD
HuRefX142,739,514 - 142,740,608UniSTS
stSG604372  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,195,455 - 154,196,843UniSTSGRCh37
Build 36X153,848,649 - 153,850,037RGDNCBI36
CeleraX154,354,194 - 154,355,582RGD
HuRefX142,740,589 - 142,741,977UniSTS
stSG604373  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,196,824 - 154,197,823UniSTSGRCh37
Build 36X153,850,018 - 153,851,017RGDNCBI36
CeleraX154,355,563 - 154,356,562RGD
HuRefX142,741,958 - 142,742,957UniSTS
stSG604374  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,197,813 - 154,198,998UniSTSGRCh37
Build 36X153,851,007 - 153,852,192RGDNCBI36
CeleraX154,356,552 - 154,357,737RGD
HuRefX142,742,947 - 142,744,132UniSTS
stSG604375  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,198,979 - 154,199,340UniSTSGRCh37
Build 36X153,852,173 - 153,852,534RGDNCBI36
CeleraX154,357,718 - 154,358,079RGD
HuRefX142,744,113 - 142,744,474UniSTS
stSG604376  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,208,915 - 154,209,365UniSTSGRCh37
Build 36X153,862,109 - 153,862,559RGDNCBI36
CeleraX154,367,652 - 154,368,102RGD
HuRefX142,754,050 - 142,754,556UniSTS
stSG604377  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,209,366 - 154,209,723UniSTSGRCh37
Build 36X153,862,560 - 153,862,917RGDNCBI36
CeleraX154,368,103 - 154,368,460RGD
HuRefX142,754,557 - 142,754,914UniSTS
stSG604378  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,212,784 - 154,213,873UniSTSGRCh37
Build 36X153,865,978 - 153,867,067RGDNCBI36
CeleraX154,371,519 - 154,372,608RGD
HuRefX142,757,969 - 142,759,058UniSTS
stSG604379  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,213,859 - 154,215,054UniSTSGRCh37
Build 36X153,867,053 - 153,868,248RGDNCBI36
CeleraX154,372,594 - 154,373,789RGD
HuRefX142,759,044 - 142,760,239UniSTS
stSG604380  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,215,035 - 154,216,260UniSTSGRCh37
Build 36X153,868,229 - 153,869,454RGDNCBI36
CeleraX154,373,770 - 154,374,995RGD
HuRefX142,760,220 - 142,761,444UniSTS
stSG604382  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,217,307 - 154,217,703UniSTSGRCh37
Build 36X153,870,501 - 153,870,897RGDNCBI36
CeleraX154,376,042 - 154,376,438RGD
HuRefX142,762,491 - 142,762,883UniSTS
stSG604383  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,220,048 - 154,221,125UniSTSGRCh37
Build 36X153,873,242 - 153,874,319RGDNCBI36
CeleraX154,378,783 - 154,379,860RGD
HuRefX142,765,195 - 142,766,272UniSTS
stSG604384  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,221,114 - 154,222,162UniSTSGRCh37
Build 36X153,874,308 - 153,875,356RGDNCBI36
CeleraX154,379,849 - 154,380,897RGD
HuRefX142,766,261 - 142,767,309UniSTS
stSG604385  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,222,143 - 154,223,301UniSTSGRCh37
Build 36X153,875,337 - 153,876,495RGDNCBI36
CeleraX154,380,878 - 154,382,036RGD
HuRefX142,767,290 - 142,768,448UniSTS
stSG604386  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,223,283 - 154,224,392UniSTSGRCh37
Build 36X153,876,477 - 153,877,586RGDNCBI36
CeleraX154,382,018 - 154,383,127RGD
HuRefX142,768,430 - 142,769,539UniSTS
stSG604388  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,225,524 - 154,226,843UniSTSGRCh37
Build 36X153,878,718 - 153,880,037RGDNCBI36
CeleraX154,384,259 - 154,385,578RGD
HuRefX142,770,671 - 142,771,990UniSTS
stSG604389  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,226,824 - 154,228,104UniSTSGRCh37
Build 36X153,880,018 - 153,881,298RGDNCBI36
CeleraX154,385,559 - 154,386,839RGD
HuRefX142,771,971 - 142,773,251UniSTS
stSG604390  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,228,092 - 154,229,282UniSTSGRCh37
Build 36X153,881,286 - 153,882,476RGDNCBI36
CeleraX154,386,827 - 154,388,017RGD
HuRefX142,773,239 - 142,774,429UniSTS
stSG604391  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,229,263 - 154,229,509UniSTSGRCh37
Build 36X153,882,457 - 153,882,703RGDNCBI36
CeleraX154,387,998 - 154,388,244RGD
HuRefX142,774,410 - 142,774,656UniSTS
stSG604393  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,232,681 - 154,233,697UniSTSGRCh37
Build 36X153,885,875 - 153,886,891RGDNCBI36
CeleraX154,391,415 - 154,392,431RGD
HuRefX142,777,678 - 142,778,694UniSTS
stSG604394  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,233,678 - 154,233,867UniSTSGRCh37
Build 36X153,886,872 - 153,887,061RGDNCBI36
CeleraX154,392,412 - 154,392,601RGD
HuRefX142,778,675 - 142,778,864UniSTS
stSG604395  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,233,868 - 154,235,147UniSTSGRCh37
Build 36X153,887,062 - 153,888,341RGDNCBI36
CeleraX154,392,602 - 154,393,881RGD
HuRefX142,778,865 - 142,780,144UniSTS
stSG604396  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,235,133 - 154,236,174UniSTSGRCh37
Build 36X153,888,327 - 153,889,368RGDNCBI36
CeleraX154,393,867 - 154,394,908RGD
HuRefX142,780,130 - 142,781,171UniSTS
stSG604397  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,236,155 - 154,237,576UniSTSGRCh37
Build 36X153,889,349 - 153,890,770RGDNCBI36
CeleraX154,394,889 - 154,396,310RGD
HuRefX142,781,152 - 142,782,573UniSTS
stSG604398  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,237,557 - 154,238,754UniSTSGRCh37
Build 36X153,890,751 - 153,891,948RGDNCBI36
CeleraX154,396,291 - 154,397,488RGD
HuRefX142,782,554 - 142,783,751UniSTS
stSG604399  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,238,113 - 154,239,120UniSTSGRCh37
Build 36X153,891,307 - 153,892,314RGDNCBI36
CeleraX154,396,847 - 154,397,854RGD
HuRefX142,783,110 - 142,784,117UniSTS
stSG604400  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,239,101 - 154,240,477UniSTSGRCh37
Build 36X153,892,295 - 153,893,671RGDNCBI36
CeleraX154,397,835 - 154,399,211RGD
HuRefX142,784,098 - 142,785,474UniSTS
stSG604401  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,245,188 - 154,246,481UniSTSGRCh37
Build 36X153,898,382 - 153,899,675RGDNCBI36
CeleraX154,403,923 - 154,405,216RGD
HuRefX142,790,189 - 142,791,482UniSTS
stSG604402  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,246,084 - 154,247,428UniSTSGRCh37
Build 36X153,899,278 - 153,900,622RGDNCBI36
CeleraX154,404,819 - 154,406,163RGD
HuRefX142,791,085 - 142,792,429UniSTS
stSG604403  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,249,211 - 154,250,368UniSTSGRCh37
Build 36X153,902,405 - 153,903,562RGDNCBI36
CeleraX154,407,946 - 154,409,103RGD
HuRefX142,794,212 - 142,795,369UniSTS
stSG604404  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,250,349 - 154,251,355UniSTSGRCh37
Build 36X153,903,543 - 153,904,549RGDNCBI36
CeleraX154,409,084 - 154,410,090RGD
HuRefX142,795,350 - 142,796,453UniSTS
stSG604405  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,251,344 - 154,252,473UniSTSGRCh37
Build 36X153,904,538 - 153,905,667RGDNCBI36
CeleraX154,410,079 - 154,411,209RGD
HuRefX142,796,442 - 142,797,571UniSTS
stSG604406  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,252,452 - 154,253,478UniSTSGRCh37
Build 36X153,905,646 - 153,906,672RGDNCBI36
CeleraX154,411,188 - 154,412,214RGD
HuRefX142,797,550 - 142,798,576UniSTS
stSG604407  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,253,545 - 154,254,962UniSTSGRCh37
Build 36X153,906,739 - 153,908,156RGDNCBI36
CeleraX154,412,281 - 154,413,698RGD
HuRefX142,798,643 - 142,799,933UniSTS
stSG604408  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,254,943 - 154,256,296UniSTSGRCh37
Build 36X153,908,137 - 153,909,490RGDNCBI36
CeleraX154,413,679 - 154,415,032RGD
HuRefX142,799,914 - 142,801,268UniSTS
stSG604409  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,255,828 - 154,257,182UniSTSGRCh37
Build 36X153,909,022 - 153,910,376RGDNCBI36
CeleraX154,414,564 - 154,415,920RGD
HuRefX142,800,800 - 142,802,154UniSTS
stSG604410  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,259,943 - 154,261,081UniSTSGRCh37
Build 36X153,913,137 - 153,914,275RGDNCBI36
CeleraX154,418,681 - 154,419,820RGD
HuRefX142,804,977 - 142,806,115UniSTS
stSG604411  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,261,081 - 154,262,454UniSTSGRCh37
Build 36X153,914,275 - 153,915,648RGDNCBI36
CeleraX154,419,820 - 154,421,193RGD
HuRefX142,806,115 - 142,807,489UniSTS
stSG604412  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,262,435 - 154,263,593UniSTSGRCh37
Build 36X153,915,629 - 153,916,787RGDNCBI36
CeleraX154,421,174 - 154,422,332RGD
HuRefX142,807,470 - 142,808,628UniSTS
stSG604413  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,271,901 - 154,272,148UniSTSGRCh37
Build 36X153,925,095 - 153,925,342RGDNCBI36
CeleraX154,430,620 - 154,430,867RGD
HuRefX142,816,468 - 142,816,715UniSTS
stSG604414  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,274,596 - 154,275,610UniSTSGRCh37
Build 36X153,927,790 - 153,928,804RGDNCBI36
CeleraX154,433,312 - 154,434,326RGD
HuRefX142,819,587 - 142,820,601UniSTS
stSG604415  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,275,590 - 154,276,595UniSTSGRCh37
Build 36X153,928,784 - 153,929,789RGDNCBI36
CeleraX154,434,306 - 154,435,311RGD
HuRefX142,820,581 - 142,821,586UniSTS
stSG604416  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,276,574 - 154,277,574UniSTSGRCh37
Build 36X153,929,768 - 153,930,768RGDNCBI36
CeleraX154,435,290 - 154,436,290RGD
HuRefX142,821,565 - 142,822,565UniSTS
stSG604418  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,279,017 - 154,280,339UniSTSGRCh37
Build 36X153,932,211 - 153,933,533RGDNCBI36
CeleraX154,437,733 - 154,439,055RGD
HuRefX142,824,009 - 142,825,330UniSTS
stSG604419  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,280,326 - 154,281,633UniSTSGRCh37
Build 36X153,933,520 - 153,934,827RGDNCBI36
CeleraX154,439,042 - 154,440,349RGD
HuRefX142,825,317 - 142,826,624UniSTS
stSG604420  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,281,614 - 154,283,038UniSTSGRCh37
Build 36X153,934,808 - 153,936,232RGDNCBI36
CeleraX154,440,330 - 154,441,753RGD
HuRefX142,826,605 - 142,828,029UniSTS
stSG604425  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,287,806 - 154,289,301UniSTSGRCh37
Build 36X153,941,000 - 153,942,495RGDNCBI36
CeleraX154,446,521 - 154,448,016RGD
HuRefX142,833,040 - 142,834,535UniSTS
stSG604426  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,289,282 - 154,290,448UniSTSGRCh37
Build 36X153,942,476 - 153,943,642RGDNCBI36
CeleraX154,447,997 - 154,449,165RGD
HuRefX142,834,516 - 142,835,682UniSTS
stSG604439  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,305,437 - 154,306,833UniSTSGRCh37
Build 36X153,958,631 - 153,960,027RGDNCBI36
CeleraX154,464,197 - 154,465,593RGD
HuRefX142,850,154 - 142,851,550UniSTS
stSG604441  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,308,436 - 154,309,699UniSTSGRCh37
Build 36X153,961,630 - 153,962,893RGDNCBI36
CeleraX154,467,196 - 154,468,458RGD
HuRefX142,854,146 - 142,855,409UniSTS
stSG604442  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,309,680 - 154,310,691UniSTSGRCh37
Build 36X153,962,874 - 153,963,885RGDNCBI36
CeleraX154,468,439 - 154,469,450RGD
HuRefX142,855,390 - 142,856,401UniSTS
stSG604443  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,310,691 - 154,312,153UniSTSGRCh37
Build 36X153,963,885 - 153,965,347RGDNCBI36
CeleraX154,469,450 - 154,470,912RGD
HuRefX142,856,401 - 142,857,863UniSTS
stSG604444  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,312,134 - 154,313,450UniSTSGRCh37
Build 36X153,965,328 - 153,966,644RGDNCBI36
CeleraX154,470,893 - 154,472,209RGD
HuRefX142,857,844 - 142,859,169UniSTS
stSG604446  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,314,515 - 154,315,552UniSTSGRCh37
Build 36X153,967,709 - 153,968,746RGDNCBI36
CeleraX154,473,274 - 154,474,311RGD
HuRefX142,860,234 - 142,861,271UniSTS
stSG604447  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,315,533 - 154,316,536UniSTSGRCh37
Build 36X153,968,727 - 153,969,730RGDNCBI36
CeleraX154,474,292 - 154,475,295RGD
HuRefX142,861,252 - 142,862,255UniSTS
stSG604448  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,316,517 - 154,317,579UniSTSGRCh37
Build 36X153,969,711 - 153,970,773RGDNCBI36
CeleraX154,475,276 - 154,476,338RGD
HuRefX142,862,236 - 142,863,298UniSTS
stSG604449  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,317,560 - 154,319,000UniSTSGRCh37
Build 36X153,970,754 - 153,972,194RGDNCBI36
CeleraX154,476,319 - 154,477,759RGD
HuRefX142,863,279 - 142,864,675UniSTS
stSG604450  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,318,981 - 154,320,253UniSTSGRCh37
Build 36X153,972,175 - 153,973,447RGDNCBI36
CeleraX154,477,740 - 154,479,012RGD
HuRefX142,864,656 - 142,865,928UniSTS
stSG604451  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,320,602 - 154,321,637UniSTSGRCh37
Build 36X153,973,796 - 153,974,831RGDNCBI36
CeleraX154,479,361 - 154,480,396RGD
HuRefX142,866,277 - 142,867,312UniSTS
stSG604452  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,321,619 - 154,322,714UniSTSGRCh37
Build 36X153,974,813 - 153,975,908RGDNCBI36
CeleraX154,480,378 - 154,481,474RGD
HuRefX142,867,294 - 142,868,373UniSTS
stSG604453  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,326,712 - 154,328,209UniSTSGRCh37
Build 36X153,979,906 - 153,981,403RGDNCBI36
CeleraX154,485,472 - 154,486,967RGD
HuRefX142,872,371 - 142,873,756UniSTS
stSG604454  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,332,807 - 154,333,838UniSTSGRCh37
Build 36X153,986,001 - 153,987,032RGDNCBI36
CeleraX154,491,565 - 154,492,596RGD
HuRefX142,878,245 - 142,879,276UniSTS
stSG604455  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,333,817 - 154,334,266UniSTSGRCh37
Build 36X153,987,011 - 153,987,460RGDNCBI36
CeleraX154,492,575 - 154,493,024RGD
HuRefX142,879,255 - 142,879,704UniSTS
stSG604457  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,343,423 - 154,344,582UniSTSGRCh37
Build 36X153,996,617 - 153,997,776RGDNCBI36
CeleraX154,502,179 - 154,503,338RGD
HuRefX142,888,658 - 142,889,817UniSTS
stSG604458  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,344,564 - 154,345,825UniSTSGRCh37
Build 36X153,997,758 - 153,999,019RGDNCBI36
CeleraX154,503,320 - 154,504,581RGD
HuRefX142,889,799 - 142,891,060UniSTS
stSG604461  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,347,368 - 154,348,518UniSTSGRCh37
Build 36X154,000,562 - 154,001,712RGDNCBI36
CeleraX154,506,123 - 154,507,273RGD
HuRefX142,892,602 - 142,893,752UniSTS
stSG604462  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,348,477 - 154,349,476UniSTSGRCh37
Build 36X154,001,671 - 154,002,670RGDNCBI36
CeleraX154,507,232 - 154,508,231RGD
HuRefX142,893,711 - 142,894,710UniSTS
stSG604463  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,351,509 - 154,352,810UniSTSGRCh37
Build 36X154,004,703 - 154,006,004RGDNCBI36
CeleraX154,510,264 - 154,511,565RGD
HuRefX142,896,743 - 142,898,045UniSTS
stSG604464  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,352,811 - 154,352,996UniSTSGRCh37
Build 36X154,006,005 - 154,006,190RGDNCBI36
CeleraX154,511,566 - 154,511,751RGD
HuRefX142,898,046 - 142,898,231UniSTS
stSG604465  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,353,587 - 154,354,956UniSTSGRCh37
Build 36X154,006,781 - 154,008,150RGDNCBI36
CeleraX154,512,343 - 154,513,712RGD
HuRefX142,898,822 - 142,900,026UniSTS
stSG604466  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,354,947 - 154,356,071UniSTSGRCh37
Build 36X154,008,141 - 154,009,265RGDNCBI36
CeleraX154,513,703 - 154,514,827RGD
HuRefX142,900,017 - 142,901,141UniSTS
stSG604467  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,356,052 - 154,357,440UniSTSGRCh37
Build 36X154,009,246 - 154,010,634RGDNCBI36
CeleraX154,514,808 - 154,516,196RGD
HuRefX142,901,122 - 142,902,510UniSTS
stSG604468  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,364,797 - 154,366,022UniSTSGRCh37
Build 36X154,017,991 - 154,019,216RGDNCBI36
CeleraX154,523,719 - 154,524,864RGD
HuRefX142,909,867 - 142,911,012UniSTS
stSG604469  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,366,186 - 154,367,410UniSTSGRCh37
Build 36X154,019,380 - 154,020,604RGDNCBI36
CeleraX154,525,028 - 154,526,256RGD
HuRefX142,911,176 - 142,912,384UniSTS
stSG604470  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,367,042 - 154,368,075UniSTSGRCh37
Build 36X154,020,236 - 154,021,269RGDNCBI36
CeleraX154,525,888 - 154,526,921RGD
HuRefX142,912,016 - 142,913,049UniSTS
stSG604471  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,368,056 - 154,369,325UniSTSGRCh37
Build 36X154,021,250 - 154,022,519RGDNCBI36
CeleraX154,526,902 - 154,528,171RGD
HuRefX142,913,030 - 142,914,299UniSTS
stSG604472  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,369,317 - 154,370,390UniSTSGRCh37
Build 36X154,022,511 - 154,023,584RGDNCBI36
CeleraX154,528,163 - 154,529,237RGD
HuRefX142,914,291 - 142,915,365UniSTS
stSG604473  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,370,412 - 154,371,836UniSTSGRCh37
Build 36X154,023,606 - 154,025,030RGDNCBI36
CeleraX154,529,259 - 154,530,683RGD
HuRefX142,915,387 - 142,916,811UniSTS
stSG604474  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,372,173 - 154,373,239UniSTSGRCh37
Build 36X154,025,367 - 154,026,433RGDNCBI36
CeleraX154,531,020 - 154,532,086RGD
HuRefX142,917,148 - 142,918,214UniSTS
stSG604475  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,372,822 - 154,373,906UniSTSGRCh37
Build 36X154,026,016 - 154,027,100RGDNCBI36
CeleraX154,531,669 - 154,532,753RGD
HuRefX142,917,797 - 142,918,881UniSTS
stSG604476  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,373,887 - 154,375,291UniSTSGRCh37
Build 36X154,027,081 - 154,028,485RGDNCBI36
CeleraX154,532,734 - 154,534,138RGD
HuRefX142,918,862 - 142,920,198UniSTS
stSG604477  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,375,272 - 154,375,464UniSTSGRCh37
Build 36X154,028,466 - 154,028,658RGDNCBI36
CeleraX154,534,119 - 154,534,311RGD
HuRefX142,920,179 - 142,920,371UniSTS
stSG604478  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,375,481 - 154,376,542UniSTSGRCh37
Build 36X154,028,675 - 154,029,736RGDNCBI36
CeleraX154,534,328 - 154,535,389RGD
HuRefX142,920,388 - 142,921,449UniSTS
stSG604479  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,376,559 - 154,378,041UniSTSGRCh37
Build 36X154,029,753 - 154,031,235RGDNCBI36
CeleraX154,535,406 - 154,536,888RGD
HuRefX142,921,466 - 142,922,948UniSTS
stSG604480  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,383,812 - 154,384,861UniSTSGRCh37
Build 36X154,037,006 - 154,038,055RGDNCBI36
CeleraX154,542,659 - 154,543,708RGD
HuRefX142,928,719 - 142,929,768UniSTS
stSG604481  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,384,949 - 154,385,313UniSTSGRCh37
Build 36X154,038,143 - 154,038,507RGDNCBI36
CeleraX154,543,796 - 154,544,160RGD
HuRefX142,929,856 - 142,930,220UniSTS
stSG604484  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,394,499 - 154,395,959UniSTSGRCh37
Build 36X154,047,693 - 154,049,153RGDNCBI36
HuRefX142,939,136 - 142,940,596UniSTS
stSG604485  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,395,943 - 154,397,246UniSTSGRCh37
Build 36X154,049,137 - 154,050,440RGDNCBI36
CeleraX154,554,282 - 154,555,585RGD
HuRefX142,940,580 - 142,941,883UniSTS
stSG604486  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,397,240 - 154,398,447UniSTSGRCh37
Build 36X154,050,434 - 154,051,641RGDNCBI36
CeleraX154,555,579 - 154,556,777RGD
HuRefX142,941,877 - 142,943,075UniSTS
stSG604487  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,398,429 - 154,399,928UniSTSGRCh37
Build 36X154,051,623 - 154,053,122RGDNCBI36
CeleraX154,556,759 - 154,558,259RGD
HuRefX142,943,057 - 142,944,556UniSTS
stSG604488  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,399,911 - 154,400,959UniSTSGRCh37
Build 36X154,053,105 - 154,054,153RGDNCBI36
CeleraX154,558,242 - 154,559,295RGD
HuRefX142,944,539 - 142,945,587UniSTS
TMLHE__5099  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,719,609 - 154,720,488UniSTSGRCh37
GRCh37X154,579,733 - 154,580,615UniSTSGRCh37
Build 36X154,232,927 - 154,233,809RGDNCBI36
CeleraX154,738,176 - 154,739,058RGD
HuRefX143,123,496 - 143,124,379UniSTS
A007I18  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,487,565 - 154,487,709UniSTSGRCh37
Build 36X154,140,759 - 154,140,903RGDNCBI36
CeleraX154,646,080 - 154,646,224RGD
Cytogenetic MapXq28UniSTS
HuRefX143,031,418 - 143,031,562UniSTS
GeneMap99-GB4 RH MapX356.07UniSTS
SHGC-32433  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,480,647 - 154,480,796UniSTSGRCh37
Build 36X154,133,841 - 154,133,990RGDNCBI36
CeleraX154,638,956 - 154,639,105RGD
Cytogenetic MapXq28UniSTS
HuRefX143,024,500 - 143,024,649UniSTS
GeneMap99-G3 RH MapX3257.0UniSTS
RH35912  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,466,360 - 154,466,489UniSTSGRCh37
Build 36X154,119,554 - 154,119,683RGDNCBI36
CeleraX154,624,838 - 154,624,967RGD
Cytogenetic MapXq28UniSTS
HuRefX143,010,364 - 143,010,493UniSTS
GeneMap99-GB4 RH MapX356.07UniSTS
UniSTS:57134  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,288,247 - 154,288,369UniSTSGRCh37
Build 36X153,941,441 - 153,941,563RGDNCBI36
CeleraX154,446,962 - 154,447,084RGD
HuRefX142,833,481 - 142,833,603UniSTS
SGC35209  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,716,243 - 154,716,381UniSTSGRCh37
GRCh37X154,583,843 - 154,583,981UniSTSGRCh37
Build 36X154,237,037 - 154,237,175RGDNCBI36
CeleraX154,742,286 - 154,742,424RGD
Cytogenetic MapXq28UniSTS
HuRefX143,127,607 - 143,127,745UniSTS
GeneMap99-GB4 RH MapX356.07UniSTS
Whitehead-RH MapX327.9UniSTS
DXS7532  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,228,426 - 154,228,650UniSTSGRCh37
Build 36X153,881,620 - 153,881,844RGDNCBI36
CeleraX154,387,161 - 154,387,385RGD
Cytogenetic MapXq28UniSTS
HuRefX142,773,573 - 142,773,797UniSTS
WI-13882  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,357,083 - 154,357,209UniSTSGRCh37
Build 36X154,010,277 - 154,010,403RGDNCBI36
CeleraX154,515,839 - 154,515,965RGD
Cytogenetic MapXq28UniSTS
HuRefX142,902,153 - 142,902,279UniSTS
GeneMap99-GB4 RH MapX356.07UniSTS
Whitehead-RH MapX329.6UniSTS
D7S2905  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,289,906 - 154,290,051UniSTSGRCh37
Build 36X153,943,100 - 153,943,245RGDNCBI36
CeleraX154,448,623 - 154,448,768RGD
Cytogenetic MapXq28UniSTS
HuRefX142,835,140 - 142,835,285UniSTS
STS-AA002210  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37572,805,134 - 72,805,419UniSTSGRCh37
GRCh37X154,283,002 - 154,283,263UniSTSGRCh37
Build 36X153,936,196 - 153,936,457RGDNCBI36
CeleraX154,441,717 - 154,441,978RGD
Celera568,700,426 - 68,700,711UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map5q13.2UniSTS
HuRef568,010,641 - 68,010,926UniSTS
HuRefX142,827,993 - 142,828,254UniSTS
GeneMap99-GB4 RH MapX356.07UniSTS
RH78991  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,719,869 - 154,720,017UniSTSGRCh37
GRCh37X154,580,204 - 154,580,353UniSTSGRCh37
Build 36X154,233,398 - 154,233,547RGDNCBI36
CeleraX154,738,647 - 154,738,796RGD
Cytogenetic MapXq28UniSTS
HuRefX143,123,967 - 143,124,116UniSTS
GeneMap99-GB4 RH MapX356.07UniSTS
RH46875  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,721,141 - 154,721,300UniSTSGRCh37
GRCh37X154,578,921 - 154,579,080UniSTSGRCh37
Build 36X154,232,115 - 154,232,274RGDNCBI36
CeleraX154,737,364 - 154,737,523RGD
Cytogenetic MapXq28UniSTS
HuRefX143,122,684 - 143,122,843UniSTS
GeneMap99-GB4 RH MapX356.07UniSTS
MARC_7353-7354:992008374:4  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,292,261 - 154,293,257UniSTSGRCh37
Build 36X153,945,455 - 153,946,451RGDNCBI36
CeleraX154,450,978 - 154,451,974RGD
HuRefX142,837,495 - 142,838,616UniSTS
MTCP1_2941  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,289,768 - 154,290,320UniSTSGRCh37
Build 36X153,942,962 - 153,943,514RGDNCBI36
CeleraX154,448,485 - 154,449,037RGD
HuRefX142,835,002 - 142,835,554UniSTS
VBP1__5062  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,467,483 - 154,468,145UniSTSGRCh37
Build 36X154,120,677 - 154,121,339RGDNCBI36
CeleraX154,625,961 - 154,626,623RGD
HuRefX143,011,487 - 143,012,149UniSTS
WI-12360  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic MapXq28UniSTS
Whitehead-RH MapX329.7UniSTS
DXS522E  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic MapXq28UniSTS
RH171  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic MapXq28UniSTS
GeneMap99-GB4 RH MapX354.15UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:557
Count of miRNA genes:457
Interacting mature miRNAs:469
Transcripts:ENST00000369446
Prediction methods: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


Sequence


Reference Sequences
RefSeq Acc Id: ENST00000610495   ⟹   ENSP00000479624
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,886,349 - 154,888,061 (+)Ensembl
RefSeq Acc Id: NM_012151   ⟹   NP_036283
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,886,355 - 154,888,061 (+)NCBI
GRCh37X154,114,635 - 154,116,336 (+)RGD
Build 36X153,767,829 - 153,769,530 (+)NCBI Archive
CeleraX154,273,254 - 154,274,955 (+)RGD
HuRefX142,658,135 - 143,157,866 (+)RGD
CHM1_1X154,027,043 - 154,027,955 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_036283   ⟸   NM_012151
- UniProtKB: P23610 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000479624   ⟸   ENST00000610495
Protein Domains
F5/8 type C


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 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)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 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 Xq28(chrX:154791149-154931411)x2 copy number gain See cases [RCV000051070] ChrX:154791149..154931411 [GRCh38]
ChrX:153672618..153812880 [NCBI36]
ChrX:Xq28
uncertain significance
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 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: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 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 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:154791149-155996431)x3 copy number gain See cases [RCV000054323] ChrX:154791149..155996431 [GRCh38]
ChrX:153672618..154879290 [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 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: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 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 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 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 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 Xq28(chrX:154836929-155123329)x3 copy number gain See cases [RCV000135629] ChrX:154836929..155123329 [GRCh38]
ChrX:153718398..154004798 [NCBI36]
ChrX:Xq28
likely benign|uncertain significance
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 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 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 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 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: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: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: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: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 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 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 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 Xq21.1-28(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 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 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 Xq28(chrX:154883744-155336409)x2 copy number gain See cases [RCV000141857] ChrX:154883744..155336409 [GRCh38]
ChrX:154112019..154565718 [GRCh37]
ChrX:153765213..154218912 [NCBI36]
ChrX:Xq28
uncertain significance
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 Xq28(chrX:154772625-154971051)x3 copy number gain See cases [RCV000143085] ChrX:154772625..154971051 [GRCh38]
ChrX:153654094..153852520 [NCBI36]
ChrX:Xq28
uncertain significance
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 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)x3 copy number gain See cases [RCV000148141] 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)x1 copy number loss See cases [RCV000148135] ChrX:10679..156022206 [GRCh38]
ChrX:60679..155251871 [GRCh37]
ChrX:679..154905065 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xq28(chrX:154124111-154564398) copy number gain See cases [RCV000169646] ChrX:154124111..154564398 [GRCh37]
ChrX:Xq28
pathogenic
GRCh37/hg19 Xq28(chrX:154124111-154564398) copy number loss See cases [RCV000169647] ChrX:154124111..154564398 [GRCh37]
ChrX:Xq28
pathogenic|likely 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 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:60701-155246271)x3 copy number gain See cases [RCV000239989] ChrX:60701..155246271 [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:71267-155234036)x2 copy number gain See cases [RCV000239874] ChrX:71267..155234036 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xq28(chrX:154115785-154528181)x1 copy number loss See cases [RCV000239872] ChrX:154115785..154528181 [GRCh37]
ChrX:Xq28
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:71267-155255792)x1 copy number loss See cases [RCV000446197] ChrX:71267..155255792 [GRCh37]
ChrX:Xp22.33-q28
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: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 Xq28(chrX:154078083-154115785)x3 copy number gain See cases [RCV000448247] ChrX:154078083..154115785 [GRCh37]
ChrX:Xq28
benign
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 Xq28(chrX:154110363-154565718)x3 copy number gain See cases [RCV000510427] ChrX:154110363..154565718 [GRCh37]
ChrX:Xq28
uncertain significance
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 Xq28(chrX:154110363-154568758)x3 copy number gain See cases [RCV000511866] ChrX:154110363..154568758 [GRCh37]
ChrX:Xq28
uncertain significance
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: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 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 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 Xq26.3-28(chrX:133944147-155233731)x3 copy number gain See cases [RCV000511034] ChrX:133944147..155233731 [GRCh37]
ChrX:Xq26.3-28
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
Single allele deletion not provided [RCV000677993] ChrX:154115785..154528181 [GRCh37]
ChrX:Xq28
likely 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:154110363-154417230)x2 copy number gain not provided [RCV000684417] ChrX:154110363..154417230 [GRCh37]
ChrX:Xq28
likely 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 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 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 Xq28(chrX:154070167-154927199)x1 copy number loss not provided [RCV000753946] ChrX:154070167..154927199 [GRCh37]
ChrX:Xq28
pathogenic
GRCh37/hg19 Xq28(chrX:154038887-154758477)x3 copy number gain not provided [RCV000753944] ChrX:154038887..154758477 [GRCh37]
ChrX:Xq28
benign
GRCh37/hg19 Xq28(chrX:154038887-154921557)x0 copy number loss not provided [RCV000753945] ChrX:154038887..154921557 [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:60262-155245765)x3 copy number gain not provided [RCV000753272] 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
Single allele duplication Autistic disorder of childhood onset [RCV000754365] ChrX:1..156040895 [GRCh38]
ChrX:Xp22.33-q28
pathogenic
GRCh37/hg19 Xp22.33-q28(chrX:60814-155236712)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 Xq25-28(chrX:122757437-155208244)x1 copy number loss Premature ovarian insufficiency [RCV000852349] ChrX:122757437..155208244 [GRCh37]
ChrX:Xq25-28
likely pathogenic
NM_000132.3(F8):c.6429+8606G>C single nucleotide variant Hereditary factor VIII deficiency disease [RCV000991018] ChrX:154887471 [GRCh38]
ChrX:154115746 [GRCh37]
ChrX:Xq28
likely benign
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 Xp22.33-q28(chrX:168546-155233731)x4 copy number gain not provided [RCV000846039] ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-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 Xp11.1-q28(chrX:58455352-155233731)x1 copy number loss not provided [RCV000846274] ChrX:58455352..155233731 [GRCh37]
ChrX:Xp11.1-q28
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 Xq21.1-28(chrX:84387417-155233731)x1 copy number loss not provided [RCV001007322] ChrX:84387417..155233731 [GRCh37]
ChrX:Xq21.1-28
pathogenic
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 Xq28(chrX:153941568-154290231)x2 copy number gain not provided [RCV000846317] ChrX:153941568..154290231 [GRCh37]
ChrX:Xq28
uncertain significance
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 Xq25-28(chrX:122924044-155233731)x1 copy number loss not provided [RCV000849097] ChrX:122924044..155233731 [GRCh37]
ChrX:Xq25-28
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 Xq28(chrX:154112019-154625699)x2 copy number gain not provided [RCV001007369] ChrX:154112019..154625699 [GRCh37]
ChrX:Xq28
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 Xq28(chrX:154051891-155236747)x3 copy number gain See cases [RCV001194554] ChrX:154051891..155236747 [GRCh37]
ChrX:Xq28
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 Xq28(chrX:154078238-154563469)x3 copy number gain not provided [RCV001260057] ChrX:154078238..154563469 [GRCh37]
ChrX:Xq28
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:3547 AgrOrtholog
COSMIC F8A1 COSMIC
Ensembl Genes ENSG00000274791 UniProtKB/Swiss-Prot
  ENSG00000277150 UniProtKB/Swiss-Prot
  ENSG00000277203 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
  ENSG00000288722 Ensembl
Ensembl Protein ENSP00000358518 UniProtKB/Swiss-Prot
  ENSP00000477530 UniProtKB/Swiss-Prot
  ENSP00000479624 ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000369505 UniProtKB/Swiss-Prot
  ENST00000610495 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000622749 UniProtKB/Swiss-Prot
Gene3D-CATH 1.25.40.10 UniProtKB/Swiss-Prot
  2.60.120.260 UniProtKB/TrEMBL
GTEx ENSG00000274791 GTEx
  ENSG00000277150 GTEx
  ENSG00000277203 GTEx
  ENSG00000288722 GTEx
HGNC ID HGNC:3547 ENTREZGENE
Human Proteome Map F8A1 Human Proteome Map
InterPro F8A UniProtKB/Swiss-Prot
  FA58C UniProtKB/TrEMBL
  Galactose-bd-like_sf UniProtKB/TrEMBL
  TPR-like_helical_dom_sf UniProtKB/Swiss-Prot
KEGG Report hsa:474383 UniProtKB/Swiss-Prot
  hsa:474384 UniProtKB/Swiss-Prot
  hsa:8263 UniProtKB/Swiss-Prot
NCBI Gene 8263 ENTREZGENE
OMIM 305423 OMIM
PANTHER PTHR16797 UniProtKB/Swiss-Prot
PharmGKB PA27953 PharmGKB
PROSITE FA58C_2 UniProtKB/TrEMBL
  FA58C_3 UniProtKB/TrEMBL
Superfamily-SCOP SSF48452 UniProtKB/Swiss-Prot
  SSF49785 UniProtKB/TrEMBL
UniProt F8I2_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q0GE96_HUMAN UniProtKB/TrEMBL
UniProt Secondary Q5HY66 UniProtKB/Swiss-Prot
  Q8IXP3 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2017-05-16 F8A1  coagulation factor VIII associated 1    coagulation factor VIII-associated 1  Symbol and/or name change 5135510 APPROVED
2011-09-01 F8A1  coagulation factor VIII-associated 1  F8A1  coagulation factor VIII-associated 1  Symbol and/or name change 5135510 APPROVED
2011-07-27 F8A1  coagulation factor VIII-associated 1  F8A1  coagulation factor VIII-associated (intronic transcript) 1  Symbol and/or name change 5135510 APPROVED