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Variant : CV598731 (GRCh37/hg19 4q31.21(chr4:146044393-146056320)x3) Homo sapiens

Symbol: CV598731
Name: GRCh37/hg19 4q31.21(chr4:146044393-146056320)x3
Condition: not provided [RCV000744031]
Clinical Significance: benign
Last Evaluated: 07/21/2011
Review Status: no assertion criteria provided
Related Genes: ABCE1   OTUD4  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh374146,044,393 - 146,056,320CLINVAR
Cytogenetic Map44q31.21CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14359402
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-09-10
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.