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Variant : CV602736 (GRCh37/hg19 8q24.3(chr8:145667662-145763152)x3) Homo sapiens

Symbol: CV602736
Name: GRCh37/hg19 8q24.3(chr8:145667662-145763152)x3
Condition: not provided [RCV000748036]
Clinical Significance: benign
Last Evaluated: 03/08/2013
Review Status: no assertion criteria provided
Related Genes: ARHGAP39   C8orf82   CYHR1   FOXH1   GPT   KIFC2   LRRC14   LRRC24   MFSD3   PPP1R16A   RECQL4   TONSL  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh378145,667,662 - 145,763,152CLINVAR
Cytogenetic Map88q24.3CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 14363369
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-03-31
Status: ACTIVE


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