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Variant : CV162647 (GRCh38/hg38 Xq13.1(chrX:71991402-72276492)x2) Homo sapiens

Symbol: CV162647
Name: GRCh38/hg38 Xq13.1(chrX:71991402-72276492)x2
Condition: See cases [RCV000141397]
Clinical Significance: uncertain significance
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ERCC6L   FLJ44635   NHSL2   PIN4   RPS4X   RTL5  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_71991402)_(72276492_?)dup
NC_000023.10:g.(?_71211252)_(71496342_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X71,991,402 - 72,276,492CLINVAR
GRCh37X71,211,252 - 71,496,342CLINVAR
Build 36X71,127,977 - 71,413,067CLINVAR
Cytogenetic MapXXq13.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9488922
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-17
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.