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Variant : CV556394 (GRCh37/hg19 1q32.1(chr1:200799541-201011646)x3) Homo sapiens

Symbol: CV556394
Name: GRCh37/hg19 1q32.1(chr1:200799541-201011646)x3
Condition: not provided [RCV000684685]
Clinical Significance: uncertain significance
Last Evaluated: 02/23/2018
Review Status: no assertion criteria provided
Related Genes: CACNA1S   CAMSAP2   GPR25   INAVA   KIF21B  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371200,799,541 - 201,011,646CLINVAR
Cytogenetic Map11q32.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13798927
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-09-29
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.