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Variant : CV608433 (GRCh37/hg19 Xq24(chrX:118053103-119334499)x2) Homo sapiens

Symbol: CV608433
Name: GRCh37/hg19 Xq24(chrX:118053103-119334499)x2
Condition: not provided [RCV000753733]
Clinical Significance: uncertain significance
Last Evaluated: 05/18/2011
Review Status: no assertion criteria provided
Related Genes: AKAP14   CXorf56   KIAA1210   LONRF3   NDUFA1   NKAP   NKRF   PGRMC1   RHOXF1   RHOXF2   RHOXF2B   RNF113A   RPL39   SEPTIN6   SLC25A43   SLC25A5   SOWAHD   UBE2A   UPF3B  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X118,053,103 - 119,334,499CLINVAR
Cytogenetic MapXXq24CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14350628
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-03-17
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.