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Variant : CV608611 (GRCh37/hg19 Xq28(chrX:151307823-151748746)x3) Homo sapiens

Symbol: CV608611
Name: GRCh37/hg19 Xq28(chrX:151307823-151748746)x3
Condition: not provided [RCV000753911]
Clinical Significance: benign
Last Evaluated: 03/18/2013
Review Status: no assertion criteria provided
Related Genes: GABRA3   MIR105-1   MIR105-2  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37X151,307,823 - 151,748,746CLINVAR
Cytogenetic MapXXq28CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 14350814
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-03-31
Status: ACTIVE


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