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Variant : CV676556 (GRCh37/hg19 8q24.3(chr8:143786100-143964656)x3) Homo sapiens

Symbol: CV676556
Name: GRCh37/hg19 8q24.3(chr8:143786100-143964656)x3
Condition: not provided [RCV000849655]
Clinical Significance: uncertain significance
Last Evaluated: 10/04/2017
Review Status: no assertion criteria provided
Related Genes: CYP11B1   GML   LY6D   LYNX1   LYPD2   SLURP1   THEM6  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh378143,786,100 - 143,964,656CLINVAR
Cytogenetic Map88q24.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14981158
Created: 2019-10-08
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.