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Variant : CV248402 (GRCh37/hg19 Xq12-13.1(chrX:64927267-69276852)x3) Homo sapiens

Symbol: CV248402
Name: GRCh37/hg19 Xq12-13.1(chrX:64927267-69276852)x3
Condition: See cases [RCV000239973]
Clinical Significance: uncertain significance
Last Evaluated: 01/20/2016
Review Status: criteria provided, single submitter
Related Genes: AR   AWAT2   EDA   EDA2R   EFNB1   FAM155B   HEPH   MIR223   MSN   OPHN1   PJA1   STARD8   VSIG4   YIPF6  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X64,927,267 - 69,276,852CLINVAR
Cytogenetic MapXXq12-13.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 11541450
Created: 2016-10-11
Species: Homo sapiens
Last Modified: 2020-03-24
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.