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Variant : CV608290 (GRCh37/hg19 Xq13.1(chrX:70959545-71308921)x2) Homo sapiens

Symbol: CV608290
Name: GRCh37/hg19 Xq13.1(chrX:70959545-71308921)x2
Condition: not provided [RCV000753590]
Clinical Significance: benign
Last Evaluated: 05/22/2012
Review Status: no assertion criteria provided
Related Genes: CXorf49B   NHSL2  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37X70,959,545 - 71,308,921CLINVAR
Cytogenetic MapXXq13.1CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 14350482
Created: 2019-02-12
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.