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Variant : CV556074 (GRCh37/hg19 Xq24(chrX:118749182-119039684)x3) Homo sapiens

Symbol: CV556074
Name: GRCh37/hg19 Xq24(chrX:118749182-119039684)x3
Condition: not provided [RCV000684379]
Clinical Significance: uncertain significance
Last Evaluated: 09/08/2017
Review Status: no assertion criteria provided
Related Genes: AKAP14   NDUFA1   RNF113A   RPL39   SEPTIN6   SOWAHD   UPF3B  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X118,749,182 - 119,039,684CLINVAR
Cytogenetic MapXXq24CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13798615
Created: 2018-10-09
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.