MIR1184-1 (microRNA 1184-1) - Rat Genome Database

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Gene: MIR1184-1 (microRNA 1184-1) Homo sapiens
Analyze
Symbol: MIR1184-1
Name: microRNA 1184-1
RGD ID: 2313001
HGNC Page HGNC
Description: microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]
Type: ncrna
RefSeq Status: PROVISIONAL
Also known as: hsa-mir-1184; hsa-mir-1184-1; MIR1184; MIRN1184
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 EnsemblX154,887,360 - 154,887,458 (-)EnsemblGRCh38hg38GRCh38
GRCh38X154,887,360 - 154,887,458 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X154,115,635 - 154,115,733 (-)NCBIGRCh37GRCh37hg19GRCh37
CeleraX154,274,254 - 154,374,370 (-)NCBI
Cytogenetic MapXq28NCBI
HuRefX143,157,166 - 143,157,263 (-)NCBIHuRef
CHM1_1X154,027,254 - 154,027,352 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
paraquat  (EXP)
radon atom  (EXP)
radon(0)  (EXP)

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:16381832   PMID:17922033   PMID:27265125  


Genomics

Position Markers
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: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
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
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
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
ECD03347  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,159,453 - 154,160,251UniSTSGRCh37
Build 36X153,812,647 - 153,813,445RGDNCBI36
CeleraX154,318,191 - 154,318,989RGD
Cytogenetic MapXq28UniSTS
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
ECD20757  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,209,249 - 154,209,522UniSTSGRCh37
Build 36X153,862,443 - 153,862,716RGDNCBI36
CeleraX154,367,986 - 154,368,259RGD
Cytogenetic MapXq28UniSTS
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
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
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
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
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
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
REN90990  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,131,377 - 154,131,604UniSTSGRCh37
Build 36X153,784,571 - 153,784,798RGDNCBI36
CeleraX154,290,114 - 154,290,341RGD
Cytogenetic MapXq28UniSTS
HuRefX142,676,120 - 142,676,347UniSTS
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
REN90998  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,133,085 - 154,133,317UniSTSGRCh37
Build 36X153,786,279 - 153,786,511RGDNCBI36
CeleraX154,291,822 - 154,292,054RGD
Cytogenetic MapXq28UniSTS
HuRefX142,677,828 - 142,678,060UniSTS
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
REN91005  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,134,456 - 154,134,700UniSTSGRCh37
Build 36X153,787,650 - 153,787,894RGDNCBI36
CeleraX154,293,193 - 154,293,437RGD
Cytogenetic MapXq28UniSTS
HuRefX142,679,199 - 142,679,443UniSTS
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
REN91013  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,136,304 - 154,136,574UniSTSGRCh37
Build 36X153,789,498 - 153,789,768RGDNCBI36
CeleraX154,295,041 - 154,295,311RGD
Cytogenetic MapXq28UniSTS
HuRefX142,681,047 - 142,681,317UniSTS
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
REN91020  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,144,937 - 154,145,162UniSTSGRCh37
Build 36X153,798,131 - 153,798,356RGDNCBI36
CeleraX154,303,674 - 154,303,899RGD
Cytogenetic MapXq28UniSTS
HuRefX142,689,680 - 142,689,905UniSTS
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
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
REN91028  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,146,753 - 154,146,981UniSTSGRCh37
Build 36X153,799,947 - 153,800,175RGDNCBI36
CeleraX154,305,490 - 154,305,718RGD
Cytogenetic MapXq28UniSTS
HuRefX142,691,496 - 142,691,724UniSTS
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
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
REN91037  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,148,704 - 154,148,951UniSTSGRCh37
Build 36X153,801,898 - 153,802,145RGDNCBI36
CeleraX154,307,442 - 154,307,689RGD
Cytogenetic MapXq28UniSTS
HuRefX142,693,446 - 142,693,693UniSTS
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
REN91045  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,151,221 - 154,151,459UniSTSGRCh37
Build 36X153,804,415 - 153,804,653RGDNCBI36
CeleraX154,309,959 - 154,310,197RGD
Cytogenetic MapXq28UniSTS
HuRefX142,695,963 - 142,696,201UniSTS
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
REN91050  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,152,885 - 154,153,115UniSTSGRCh37
Build 36X153,806,079 - 153,806,309RGDNCBI36
CeleraX154,311,623 - 154,311,853RGD
Cytogenetic MapXq28UniSTS
HuRefX142,697,611 - 142,697,841UniSTS
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
REN91052  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,153,217 - 154,153,483UniSTSGRCh37
Build 36X153,806,411 - 153,806,677RGDNCBI36
CeleraX154,311,955 - 154,312,221RGD
Cytogenetic MapXq28UniSTS
REN91053  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,153,492 - 154,153,725UniSTSGRCh37
Build 36X153,806,686 - 153,806,919RGDNCBI36
CeleraX154,312,230 - 154,312,463RGD
Cytogenetic MapXq28UniSTS
REN91054  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,153,695 - 154,153,935UniSTSGRCh37
Build 36X153,806,889 - 153,807,129RGDNCBI36
CeleraX154,312,433 - 154,312,673RGD
Cytogenetic MapXq28UniSTS
REN91055  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,153,892 - 154,154,136UniSTSGRCh37
Build 36X153,807,086 - 153,807,330RGDNCBI36
CeleraX154,312,630 - 154,312,874RGD
Cytogenetic MapXq28UniSTS
REN91056  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,154,103 - 154,154,328UniSTSGRCh37
Build 36X153,807,297 - 153,807,522RGDNCBI36
CeleraX154,312,841 - 154,313,066RGD
Cytogenetic MapXq28UniSTS
REN91057  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,154,379 - 154,154,627UniSTSGRCh37
Build 36X153,807,573 - 153,807,821RGDNCBI36
CeleraX154,313,117 - 154,313,365RGD
Cytogenetic MapXq28UniSTS
REN91058  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,154,626 - 154,154,887UniSTSGRCh37
Build 36X153,807,820 - 153,808,081RGDNCBI36
CeleraX154,313,364 - 154,313,625RGD
Cytogenetic MapXq28UniSTS
REN91059  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,154,871 - 154,155,095UniSTSGRCh37
Build 36X153,808,065 - 153,808,289RGDNCBI36
CeleraX154,313,609 - 154,313,833RGD
Cytogenetic MapXq28UniSTS
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
REN91066  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,156,480 - 154,156,704UniSTSGRCh37
Build 36X153,809,674 - 153,809,898RGDNCBI36
CeleraX154,315,218 - 154,315,442RGD
Cytogenetic MapXq28UniSTS
HuRefX142,701,019 - 142,701,243UniSTS
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
REN91075  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,158,527 - 154,158,793UniSTSGRCh37
Build 36X153,811,721 - 153,811,987RGDNCBI36
CeleraX154,317,265 - 154,317,531RGD
Cytogenetic MapXq28UniSTS
HuRefX142,703,066 - 142,703,332UniSTS
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
REN91082  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,160,118 - 154,160,362UniSTSGRCh37
Build 36X153,813,312 - 153,813,556RGDNCBI36
CeleraX154,318,856 - 154,319,100RGD
Cytogenetic MapXq28UniSTS
REN91083  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,160,333 - 154,160,580UniSTSGRCh37
Build 36X153,813,527 - 153,813,774RGDNCBI36
CeleraX154,319,071 - 154,319,318RGD
Cytogenetic MapXq28UniSTS
REN91084  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,160,571 - 154,160,814UniSTSGRCh37
Build 36X153,813,765 - 153,814,008RGDNCBI36
CeleraX154,319,309 - 154,319,552RGD
Cytogenetic MapXq28UniSTS
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
REN91090  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,161,890 - 154,162,141UniSTSGRCh37
Build 36X153,815,084 - 153,815,335RGDNCBI36
CeleraX154,320,628 - 154,320,879RGD
Cytogenetic MapXq28UniSTS
HuRefX142,706,260 - 142,706,511UniSTS
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
REN91096  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,163,381 - 154,163,624UniSTSGRCh37
Build 36X153,816,575 - 153,816,818RGDNCBI36
CeleraX154,322,119 - 154,322,362RGD
Cytogenetic MapXq28UniSTS
REN91097  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,163,616 - 154,163,868UniSTSGRCh37
Build 36X153,816,810 - 153,817,062RGDNCBI36
CeleraX154,322,354 - 154,322,606RGD
Cytogenetic MapXq28UniSTS
REN91098  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,163,771 - 154,164,012UniSTSGRCh37
Build 36X153,816,965 - 153,817,206RGDNCBI36
CeleraX154,322,509 - 154,322,750RGD
Cytogenetic MapXq28UniSTS
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
REN91106  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,165,398 - 154,165,653UniSTSGRCh37
Build 36X153,818,592 - 153,818,847RGDNCBI36
CeleraX154,324,134 - 154,324,389RGD
Cytogenetic MapXq28UniSTS
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
REN91126  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,176,262 - 154,176,509UniSTSGRCh37
Build 36X153,829,456 - 153,829,703RGDNCBI36
CeleraX154,335,001 - 154,335,248RGD
Cytogenetic MapXq28UniSTS
HuRefX142,721,013 - 142,721,260UniSTS
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
REN91143  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,180,314 - 154,180,560UniSTSGRCh37
Build 36X153,833,508 - 153,833,754RGDNCBI36
CeleraX154,339,053 - 154,339,299RGD
Cytogenetic MapXq28UniSTS
HuRefX142,725,064 - 142,725,310UniSTS
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
REN91175  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,187,903 - 154,188,128UniSTSGRCh37
Build 36X153,841,097 - 153,841,322RGDNCBI36
CeleraX154,346,642 - 154,346,867RGD
Cytogenetic MapXq28UniSTS
HuRefX142,732,654 - 142,732,879UniSTS
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
REN91183  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,189,516 - 154,189,740UniSTSGRCh37
Build 36X153,842,710 - 153,842,934RGDNCBI36
CeleraX154,348,255 - 154,348,479RGD
Cytogenetic MapXq28UniSTS
HuRefX142,734,267 - 142,734,491UniSTS
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
REN91220  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,198,850 - 154,199,086UniSTSGRCh37
Build 36X153,852,044 - 153,852,280RGDNCBI36
CeleraX154,357,589 - 154,357,825RGD
Cytogenetic MapXq28UniSTS
HuRefX142,743,984 - 142,744,220UniSTS
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
REN91228  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,200,447 - 154,200,671UniSTSGRCh37
Build 36X153,853,641 - 153,853,865RGDNCBI36
CeleraX154,359,186 - 154,359,410RGD
Cytogenetic MapXq28UniSTS
HuRefX142,745,581 - 142,745,805UniSTS
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
REN91241  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,203,382 - 154,203,622UniSTSGRCh37
Build 36X153,856,576 - 153,856,816RGDNCBI36
CeleraX154,362,119 - 154,362,359RGD
Cytogenetic MapXq28UniSTS
HuRefX142,748,517 - 142,748,757UniSTS
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
REN91249  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,205,603 - 154,205,828UniSTSGRCh37
Build 36X153,858,797 - 153,859,022RGDNCBI36
CeleraX154,364,340 - 154,364,565RGD
Cytogenetic MapXq28UniSTS
HuRefX142,750,738 - 142,750,963UniSTS
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
REN91257  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,207,364 - 154,207,594UniSTSGRCh37
Build 36X153,860,558 - 153,860,788RGDNCBI36
CeleraX154,366,101 - 154,366,331RGD
Cytogenetic MapXq28UniSTS
HuRefX142,752,499 - 142,752,729UniSTS
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
REN91264  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,208,962 - 154,209,210UniSTSGRCh37
Build 36X153,862,156 - 153,862,404RGDNCBI36
CeleraX154,367,699 - 154,367,947RGD
Cytogenetic MapXq28UniSTS
REN91265  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,209,184 - 154,209,432UniSTSGRCh37
Build 36X153,862,378 - 153,862,626RGDNCBI36
CeleraX154,367,921 - 154,368,169RGD
Cytogenetic MapXq28UniSTS
REN91266  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,209,411 - 154,209,649UniSTSGRCh37
Build 36X153,862,605 - 153,862,843RGDNCBI36
CeleraX154,368,148 - 154,368,386RGD
Cytogenetic MapXq28UniSTS
HuRefX142,754,602 - 142,754,840UniSTS
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
REN91275  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,211,825 - 154,212,072UniSTSGRCh37
GRCh37X154,210,935 - 154,212,072UniSTSGRCh37
Build 36X153,865,019 - 153,865,266RGDNCBI36
CeleraX154,369,670 - 154,370,807UniSTS
CeleraX154,370,560 - 154,370,807RGD
Cytogenetic MapXq28UniSTS
HuRefX142,757,010 - 142,757,257UniSTS
HuRefX142,756,124 - 142,757,257UniSTS
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
REN91283  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,213,764 - 154,213,996UniSTSGRCh37
Build 36X153,866,958 - 153,867,190RGDNCBI36
CeleraX154,372,499 - 154,372,731RGD
Cytogenetic MapXq28UniSTS
HuRefX142,758,949 - 142,759,181UniSTS
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
REN91288  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,214,953 - 154,215,193UniSTSGRCh37
Build 36X153,868,147 - 153,868,387RGDNCBI36
CeleraX154,373,688 - 154,373,928RGD
Cytogenetic MapXq28UniSTS
HuRefX142,760,138 - 142,760,378UniSTS
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
REN91297  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X154,217,059 - 154,217,293UniSTSGRCh37
Build 36X153,870,253 - 153,870,487RGDNCBI36
CeleraX154,375,794 - 154,376,028RGD
Cytogenetic MapXq28UniSTS
HuRefX142,762,243 - 142,762,477UniSTS
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


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system
High
Medium
Low 6 2 2 1 12 1 2 8 5 2 4
Below cutoff 8 2 1 19 3 9 12 14 9 10 16

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000408606
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 EnsemblX154,887,360 - 154,887,458 (-)Ensembl
RefSeq Acc Id: NR_036049
RefSeq Status: PROVISIONAL
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X154,887,360 - 154,887,458 (-)NCBI
GRCh37X154,115,635 - 154,115,733 (-)ENTREZGENE
CeleraX154,274,254 - 154,374,370 (-)RGD
HuRefX143,157,166 - 143,157,263 (-)RGD
CHM1_1X154,027,254 - 154,027,352 (-)NCBI
Sequence:

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
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 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:10679-156013167)x1 copy number loss See cases [RCV000050386] ChrX:10679..156013167 [GRCh38]
ChrX:60679..155242832 [GRCh37]
ChrX:679..154896026 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156013167)x3 copy number gain See cases [RCV000050385] ChrX:10679..156013167 [GRCh38]
ChrX:60679..155242832 [GRCh37]
ChrX:679..154896026 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:14245-155999293)x1 copy number loss See cases [RCV000052982] ChrX:14245..155999293 [GRCh38]
ChrX:64245..155228958 [GRCh37]
ChrX:4245..154882152 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:26102-155996431)x1 copy number loss See cases [RCV000052986] ChrX:26102..155996431 [GRCh38]
ChrX:76102..155226096 [GRCh37]
ChrX:16102..154879290 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:26102-155996431)x3 copy number gain See cases [RCV000052984] ChrX:26102..155996431 [GRCh38]
ChrX:76102..155226096 [GRCh37]
ChrX:16102..154879290 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 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 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 Xp22.33-q28(chrX:10679-156022826)x4 copy number gain See cases [RCV000133654] ChrX:10679..156022826 [GRCh38]
ChrX:60679..155252491 [GRCh37]
ChrX:679..154905685 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX: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 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 Xq11.1-28(chrX:62712230-155978888)x3 copy number gain See cases [RCV000134025] ChrX:62712230..155978888 [GRCh38]
ChrX:61931700..155208553 [GRCh37]
ChrX:61848425..154861747 [NCBI36]
ChrX:Xq11.1-28
pathogenic
GRCh38/hg38 Xp21.1-q28(chrX:37076284-156016920)x1 copy number loss See cases [RCV000135300] ChrX:37076284..156016920 [GRCh38]
ChrX:37094357..155246585 [GRCh37]
ChrX:37004278..154899779 [NCBI36]
ChrX:Xp21.1-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:20297-156026127)x1 copy number loss See cases [RCV000135321] ChrX:20297..156026127 [GRCh38]
ChrX:70297..155255792 [GRCh37]
ChrX:10297..154908986 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq21.31-28(chrX:92222680-156016920)x1 copy number loss See cases [RCV000135307] ChrX:92222680..156016920 [GRCh38]
ChrX:91477679..155246585 [GRCh37]
ChrX:91364335..154899779 [NCBI36]
ChrX:Xq21.31-28
pathogenic
GRCh38/hg38 Xq23-28(chrX:114533139-156022206)x1 copy number loss See cases [RCV000134947] ChrX:114533139..156022206 [GRCh38]
ChrX:113767592..155251871 [GRCh37]
ChrX:113673848..154905065 [NCBI36]
ChrX:Xq23-28
pathogenic
GRCh38/hg38 Xq13.2-28(chrX:74510116-156022206)x1 copy number loss See cases [RCV000134958] ChrX:74510116..156022206 [GRCh38]
ChrX:73729951..155251871 [GRCh37]
ChrX:73646676..154905065 [NCBI36]
ChrX:Xq13.2-28
pathogenic
GRCh38/hg38 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: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 Xp22.33-q28(chrX:10701-156003229)x1 copy number loss See cases [RCV000136097] ChrX:10701..156003229 [GRCh38]
ChrX:60701..155232894 [GRCh37]
ChrX:701..154886088 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq21.33-28(chrX:94462929-156001635)x3 copy number gain See cases [RCV000136552] ChrX:94462929..156001635 [GRCh38]
ChrX:93717928..155231300 [GRCh37]
ChrX:93604584..154884494 [NCBI36]
ChrX:Xq21.33-28
pathogenic
GRCh38/hg38 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 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 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 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 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 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 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 Xq28(chrX:151750863-155522304)x1 copy number loss See cases [RCV000136718] ChrX:151750863..155522304 [GRCh38]
ChrX:150919335..154751965 [GRCh37]
ChrX:150669991..154405159 [NCBI36]
ChrX:Xq28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:2765636-155522304)x3 copy number gain See cases [RCV000136791] ChrX:2765636..155522304 [GRCh38]
ChrX:2683677..154751965 [GRCh37]
ChrX:2693677..154405159 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq28(chrX:153276277-156003242)x3 copy number gain See cases [RCV000137498] ChrX:153276277..156003242 [GRCh38]
ChrX:152465185..155232907 [GRCh37]
ChrX:152118379..154886101 [NCBI36]
ChrX:Xq28
pathogenic
GRCh38/hg38 Xq11.1-28(chrX:62561604-156003242)x3 copy number gain See cases [RCV000137553] ChrX:62561604..156003242 [GRCh38]
ChrX:61781074..155232907 [GRCh37]
ChrX:61697799..154886101 [NCBI36]
ChrX:Xq11.1-28
pathogenic
GRCh38/hg38 Xq22.1-28(chrX:102197284-156003242)x1 copy number loss See cases [RCV000137415] ChrX:102197284..156003242 [GRCh38]
ChrX:101452257..155232907 [GRCh37]
ChrX:101338913..154886101 [NCBI36]
ChrX:Xq22.1-28
pathogenic
GRCh38/hg38 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 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 Xq21.1-28(chrX:82211310-156003229)x1 copy number loss See cases [RCV000139400] ChrX:82211310..156003229 [GRCh38]
ChrX:81466759..155232894 [GRCh37]
ChrX:81353415..154886088 [NCBI36]
ChrX:Xq21.1-28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:1085618-155699644)x1 copy number loss See cases [RCV000139278] ChrX:1085618..155699644 [GRCh38]
ChrX:1118268..154929305 [GRCh37]
ChrX:1038268..154582499 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq21.31-28(chrX:88339926-156003242)x1 copy number loss See cases [RCV000139351] ChrX:88339926..156003242 [GRCh38]
ChrX:87594927..155232907 [GRCh37]
ChrX:87481583..154886101 [NCBI36]
ChrX:Xq21.31-28
pathogenic|likely benign
GRCh38/hg38 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 Xq22.3-28(chrX:106722296-156004066)x1 copy number loss See cases [RCV000142190] ChrX:106722296..156004066 [GRCh38]
ChrX:105965526..155233731 [GRCh37]
ChrX:105852182..154886925 [NCBI36]
ChrX:Xq22.3-28
pathogenic
GRCh38/hg38 Xq24-28(chrX:118856574-156004066)x1 copy number loss See cases [RCV000142137] ChrX:118856574..156004066 [GRCh38]
ChrX:117990537..155233731 [GRCh37]
ChrX:117874565..154886925 [NCBI36]
ChrX:Xq24-28
pathogenic
GRCh38/hg38 Xq21.2-28(chrX:86626431-156004066)x1 copy number loss See cases [RCV000142037] ChrX:86626431..156004066 [GRCh38]
ChrX:85881434..155233731 [GRCh37]
ChrX:85768090..154886925 [NCBI36]
ChrX:Xq21.2-28
pathogenic
GRCh38/hg38 Xq28(chrX:154772625-154971051)x3 copy number gain See cases [RCV000143085] ChrX:154772625..154971051 [GRCh38]
ChrX:153654094..153852520 [NCBI36]
ChrX:Xq28
uncertain significance
GRCh38/hg38 Xq28(chrX:148951460-155434653)x2 copy number gain See cases [RCV000143002] ChrX:148951460..155434653 [GRCh38]
ChrX:148956425..154664314 [GRCh37]
ChrX:147840690..154317508 [NCBI36]
ChrX:Xq28
pathogenic
GRCh38/hg38 Xq23-28(chrX:111050385-156022206)x1 copy number loss See cases [RCV000142577] ChrX:111050385..156022206 [GRCh38]
ChrX:110293613..155251871 [GRCh37]
ChrX:110180269..154905065 [NCBI36]
ChrX:Xq23-28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10701-156003229)x3 copy number gain See cases [RCV000142625] ChrX:10701..156003229 [GRCh38]
ChrX:60701..155232894 [GRCh37]
ChrX:701..154886088 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq13.2-28(chrX:74684615-156004066)x1 copy number loss See cases [RCV000143424] ChrX:74684615..156004066 [GRCh38]
ChrX:73904450..155233731 [GRCh37]
ChrX:73821175..154886925 [NCBI36]
ChrX:Xq13.2-28
pathogenic
GRCh38/hg38 Xp11.22-q28(chrX:53144751-156003242)x1 copy number loss See cases [RCV000143349] ChrX:53144751..156003242 [GRCh38]
ChrX:53321095..155232907 [GRCh37]
ChrX:53190658..154886101 [NCBI36]
ChrX:Xp11.22-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251879-156004066)x1 copy number loss See cases [RCV000143441] ChrX:251879..156004066 [GRCh38]
ChrX:168546..155233731 [GRCh37]
ChrX:108546..154886925 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251879-156004066)x3 copy number gain See cases [RCV000143433] ChrX:251879..156004066 [GRCh38]
ChrX:168546..155233731 [GRCh37]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xq13.3-28(chrX:76557425-156004066)x1 copy number loss See cases [RCV000143132] ChrX:76557425..156004066 [GRCh38]
ChrX:75777833..155233731 [GRCh37]
ChrX:75694237..154886925 [NCBI36]
ChrX:Xq13.3-28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:251880-156004066)x3 copy number gain See cases [RCV000143219] ChrX:251880..156004066 [GRCh38]
ChrX:168547..155233731 [GRCh37]
ChrX:108547..154886925 [NCBI36]
ChrX:Xp22.33-q28
pathogenic
GRCh38/hg38 Xp22.33-q28(chrX:10679-156022206)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
GRCh38/hg38 Xq25-28(chrX:126537861-155996431)x1 copy number loss See cases [RCV000051729] ChrX:126537861..155996431 [GRCh38]
ChrX:125671844..155226096 [GRCh37]
ChrX:125499525..154879290 [NCBI36]
ChrX:Xq25-28
pathogenic
GRCh38/hg38 Xq26.3-28(chrX:136956500-156020993)x1 copy number loss See cases [RCV000051732] ChrX:136956500..156020993 [GRCh38]
ChrX:136038659..155250658 [GRCh37]
ChrX:135866325..154903852 [NCBI36]
ChrX:Xq26.3-28
pathogenic
GRCh38/hg38 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 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 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 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 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 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 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: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:154791149-154931411)x2 copy number gain See cases [RCV000051070] ChrX:154791149..154931411 [GRCh38]
ChrX:153672618..153812880 [NCBI36]
ChrX:Xq28
uncertain significance
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: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: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 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: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 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 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 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:154791149-155996431)x3 copy number gain See cases [RCV000054323] ChrX:154791149..155996431 [GRCh38]
ChrX:153672618..154879290 [NCBI36]
ChrX:Xq28
uncertain significance
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 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
Single allele duplication Autistic disorder of childhood onset [RCV000754365] ChrX:1..156040895 [GRCh38]
ChrX:Xp22.33-q28
pathogenic

Additional Information

Database Acc Id Source(s)
COSMIC MIR1184-1 COSMIC
Ensembl Genes ENSG00000221533 Ensembl, ENTREZGENE
Ensembl Transcript ENST00000408606 ENTREZGENE
GTEx ENSG00000221533 GTEx
HGNC ID HGNC:35265 ENTREZGENE
Human Proteome Map MIR1184-1 Human Proteome Map
miRBase MI0006277 ENTREZGENE
NCBI Gene 100302111 ENTREZGENE
RNAcentral URS000075A55D RNACentral
  URS000075B5BA RNACentral


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2011-09-01 MIR1184-1  microRNA 1184-1  MIR1184-1  microRNA 1184-1  Symbol and/or name change 5135510 APPROVED
2011-07-27 MIR1184-1  microRNA 1184-1  MIR1184  microRNA 1184  Symbol and/or name change 5135510 APPROVED