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Variant : CV162391 (GRCh38/hg38 11q13.1(chr11:65520831-65695349)x3) Homo sapiens

Symbol: CV162391
Name: GRCh38/hg38 11q13.1(chr11:65520831-65695349)x3
Condition: See cases [RCV000141174]
Clinical Significance: uncertain significance
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: EHBP1L1   FAM89B   KCNK7   LTBP3   MAP3K11   MIR4489   MIR4690   PCNX3   RELA   RELA-DT   SCYL1   SIPA1   ZNRD2   ZNRD2-AS1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000011.10:g.(?_65520831)_(65695349_?)dup
NC_000011.9:g.(?_65288302)_(65462820_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381165,520,831 - 65,695,349CLINVAR
GRCh371165,288,302 - 65,462,820CLINVAR
Build 361165,044,878 - 65,219,396CLINVAR
Cytogenetic Map1111q13.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9488701
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-11-17
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.