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Variant : CV673002 (GRCh37/hg19 8q24.3(chr8:142988974-144218537)x3) Homo sapiens

Symbol: CV673002
Name: GRCh37/hg19 8q24.3(chr8:142988974-144218537)x3
Condition: not provided [RCV000846118]
Clinical Significance: uncertain significance
Last Evaluated: 09/11/2017
Review Status: no assertion criteria provided
Related Genes: ADGRB1   ARC   C8orf31   CYP11B1   CYP11B2   GML   JRK   LY6D   LY6E   LY6K   LYNX1   LYPD2   PSCA   SLURP1   THEM6   TSNARE1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh378142,988,974 - 144,218,537CLINVAR
Cytogenetic Map88q24.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14976678
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-05-19
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.