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Variant : CV602709 (GRCh37/hg19 8q24.3(chr8:145513753-145753161)x3) Homo sapiens

Symbol: CV602709
Name: GRCh37/hg19 8q24.3(chr8:145513753-145753161)x3
Condition: not provided [RCV000748009]
Clinical Significance: benign
Last Evaluated: 03/14/2013
Review Status: no assertion criteria provided
Related Genes: ADCK5   BOP1   C8orf82   CPSF1   CYHR1   DGAT1   FBXL6   FOXH1   GPT   HSF1   KIFC2   LRRC14   LRRC24   MFSD3   MIR1234   PPP1R16A   RECQL4   SCRT1   SLC39A4   SLC52A2   TMEM249   TONSL   VPS28  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh378145,513,753 - 145,753,161CLINVAR
Cytogenetic Map88q24.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14351022
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-03-17
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.