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Variant : CV161274 (GRCh38/hg38 Xq13.1(chrX:69987949-70082820)x4) Homo sapiens

Symbol: CV161274
Name: GRCh38/hg38 Xq13.1(chrX:69987949-70082820)x4
Condition: See cases [RCV000140232]
Clinical Significance: uncertain significance
Last Evaluated: 09/26/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AWAT2   EDA   MIR676   OTUD6A  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_69987949)_(70082820_?)dup
NC_000023.10:g.(?_69207799)_(69302670_?)dup
NC_000023.9:g.(?_69124524)_(69219395_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X69,987,949 - 70,082,820CLINVAR
GRCh37X69,207,799 - 69,302,670CLINVAR
Build 36X69,124,524 - 69,219,395CLINVAR
Cytogenetic MapXXq13.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487762
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-11-05
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.