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Variant : CV602707 (GRCh37/hg19 8q24.3(chr8:145101381-145161823)x3) Homo sapiens

Symbol: CV602707
Name: GRCh37/hg19 8q24.3(chr8:145101381-145161823)x3
Condition: not provided [RCV000748007]
Clinical Significance: benign
Last Evaluated: 02/15/2013
Review Status: no assertion criteria provided
Related Genes: CYC1   EXOSC4   GPAA1   MAF1   OPLAH   SHARPIN   SPATC1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh378145,101,381 - 145,161,823CLINVAR
Cytogenetic Map88q24.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14363352
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.