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Variant : CV162392 (GRCh38/hg38 11q24.1-24.2(chr11:123543649-124802201)x3) Homo sapiens

Symbol: CV162392
Name: GRCh38/hg38 11q24.1-24.2(chr11:123543649-124802201)x3
Condition: See cases [RCV000141175]
Clinical Significance: uncertain significance
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AP000866.1   AP000866.2   ESAM   GRAMD1B   MSANTD2   NRGN   OR10D3   OR10G4   OR10G6   OR10G7   OR10G8   OR10G9   OR10S1   OR4D5   OR6M1   OR6T1   OR6X1   OR8A1   OR8B12   OR8B2   OR8B3   OR8B4   OR8B8   OR8D1   OR8D2   OR8D4   OR8G1   OR8G2P   OR8G5   PANX3   SCN3B   SIAE   SPA17   TBRG1   TMEM225   VSIG2   VWA5A   ZNF202  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000011.10:g.(?_123543649)_(124802201_?)dup
NC_000011.9:g.(?_123414357)_(124672097_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3811123,543,649 - 124,802,201CLINVAR
GRCh3711123,414,357 - 124,672,097CLINVAR
Build 3611122,919,567 - 124,177,307CLINVAR
Cytogenetic Map1111q24.1-24.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9488702
Created: 2014-09-09
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.