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Variant : CV165212 (GRCh38/hg38 Xq13.1(chrX:71022322-71682982)x2) Homo sapiens

Symbol: CV165212
Name: GRCh38/hg38 Xq13.1(chrX:71022322-71682982)x2
Condition: See cases [RCV000143525]
Clinical Significance: uncertain significance
Last Evaluated: 07/22/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CXCR3   CXorf65   FOXO4   GCNA   GJB1   IL2RG   ITGB1BP2   MED12   NLGN3   NONO   OGT   SNX12   TAF1   ZMYM3  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_71022322)_(71682982_?)dup
Human AssemblyChrPosition (strand)Source
GRCh38X71,022,322 - 71,682,982CLINVAR
GRCh37X70,242,172 - 70,902,832CLINVAR
Build 36X70,158,897 - 70,819,557CLINVAR
Cytogenetic MapXXq13.1CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 9491123
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-10-15
Status: ACTIVE


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