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Variant : CV436560 (GRCh37/hg19 Xq13.1(chrX:70287671-70997047)x2) Homo sapiens

Symbol: CV436560
Name: GRCh37/hg19 Xq13.1(chrX:70287671-70997047)x2
Condition: See cases [RCV000512522]
Clinical Significance: uncertain significance
Last Evaluated: 06/03/2014
Review Status: no assertion criteria provided
Related Genes: CXCR3   CXorf49   CXorf49B   CXorf65   FOXO4   GCNA   GJB1   IL2RG   ITGB1BP2   MED12   NLGN3   NONO   OGT   SNX12   TAF1   ZMYM3  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37X70,287,671 - 70,997,047CLINVAR
Cytogenetic MapXXq13.1CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 13445484
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-03-24
Status: ACTIVE


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