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Variant : CV802961 (GRCh37/hg19 5q32(chr5:148953230-149414017)x3) Homo sapiens

Symbol: CV802961
Name: GRCh37/hg19 5q32(chr5:148953230-149414017)x3
Condition: not provided [RCV001005741]
Clinical Significance: uncertain significance
Last Evaluated: 12/04/2018
Review Status: no assertion criteria provided
Related Genes: ARHGEF37   HMGXB3   MIR378A   PDE6A   PPARGC1B   SLC26A2   TIGD6  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh375148,953,230 - 149,414,017CLINVAR
Cytogenetic Map55q32CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 25319901
Created: 2020-04-07
Species: Homo sapiens
Last Modified: 2020-07-28
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.