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Variant : CV598678 (GRCh37/hg19 4q28.3(chr4:134120109-136354391)x1) Homo sapiens

Symbol: CV598678
Name: GRCh37/hg19 4q28.3(chr4:134120109-136354391)x1
Condition: not provided [RCV000743978]
Clinical Significance: likely benign
Last Evaluated: 04/15/2013
Review Status: no assertion criteria provided
Related Genes: PABPC4L  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh374134,120,109 - 136,354,391CLINVAR
Cytogenetic Map44q28.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14359349
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-08-06
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.