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Variant : CV604732 (GRCh37/hg19 11p11.2(chr11:47825128-48601837)x3) Homo sapiens

Symbol: CV604732
Name: GRCh37/hg19 11p11.2(chr11:47825128-48601837)x3
Condition: not provided [RCV000750032]
Clinical Significance: benign
Last Evaluated: 03/21/2012
Review Status: no assertion criteria provided
Related Genes: NUP160   OR4A47   OR4B1   OR4C3   OR4S1   OR4X1   OR4X2   PTPRJ  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371147,825,128 - 48,601,837CLINVAR
Cytogenetic Map1111p11.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14365360
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-02-20
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.