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Variant : CV602724 (GRCh37/hg19 8q24.3(chr8:145638753-145755918)x3) Homo sapiens

Symbol: CV602724
Name: GRCh37/hg19 8q24.3(chr8:145638753-145755918)x3
Condition: not provided [RCV000748024]
Clinical Significance: benign
Last Evaluated: 03/15/2013
Review Status: no assertion criteria provided
Related Genes: ARHGAP39   C8orf82   CYHR1   FOXH1   GPT   KIFC2   LRRC14   LRRC24   MFSD3   PPP1R16A   RECQL4   SLC39A4   TONSL   VPS28  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh378145,638,753 - 145,755,918CLINVAR
Cytogenetic Map88q24.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14351030
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.