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Variant : CV592738 (GRCh37/hg19 12q24.11(chr12:111221131-111323418)x3) Homo sapiens

Symbol: CV592738
Name: GRCh37/hg19 12q24.11(chr12:111221131-111323418)x3
Condition: not provided [RCV000738038]
Clinical Significance: benign
Last Evaluated: 01/30/2017
Review Status: no assertion criteria provided
Related Genes: CCDC63  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3712111,221,131 - 111,323,418CLINVAR
Cytogenetic Map1212q24.11CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14353415
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-03-24
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.