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Variant : CV555017 (GRCh37/hg19 11q24.2(chr11:124296334-124560100)x3) Homo sapiens

Symbol: CV555017
Name: GRCh37/hg19 11q24.2(chr11:124296334-124560100)x3
Condition: not provided [RCV000683322]
Clinical Significance: uncertain significance
Last Evaluated: 10/25/2017
Review Status: no assertion criteria provided
Related Genes: OR8A1   OR8B12   OR8B8   PANX3   SIAE   SPA17   TBRG1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3711124,296,334 - 124,560,100CLINVAR
Cytogenetic Map1111q24.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13796440
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-07-28
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.