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Variant : CV672921 (GRCh37/hg19 11q13.1(chr11:65529506-65649002)x3) Homo sapiens

Symbol: CV672921
Name: GRCh37/hg19 11q13.1(chr11:65529506-65649002)x3
Condition: not provided [RCV000846037]
Clinical Significance: uncertain significance
Last Evaluated: 03/23/2018
Review Status: no assertion criteria provided
Related Genes: AP5B1   CFL1   CTSW   EFEMP2   MUS81   OVOL1   SNX32  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371165,529,506 - 65,649,002CLINVAR
Cytogenetic Map1111q13.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14976577
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-09-29
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.