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Variant : CV602663 (GRCh37/hg19 8q24.3(chr8:144771630-144807456)x3) Homo sapiens

Symbol: CV602663
Name: GRCh37/hg19 8q24.3(chr8:144771630-144807456)x3
Condition: not provided [RCV000747963]
Clinical Significance: benign
Last Evaluated: 03/06/2013
Review Status: no assertion criteria provided
Related Genes: CCDC166   FAM83H   MAPK15   ZNF707  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh378144,771,630 - 144,807,456CLINVAR
Cytogenetic Map88q24.3CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 14363308
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-03-17
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.