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Variant : CV593116 (GRCh37/hg19 14q11.2(chr14:20005130-20482471)x3) Homo sapiens

Symbol: CV593116
Name: GRCh37/hg19 14q11.2(chr14:20005130-20482471)x3
Condition: not provided [RCV000738416]
Clinical Significance: benign
Last Evaluated: 02/22/2012
Review Status: no assertion criteria provided
Related Genes: OR11H2   OR4K1   OR4K14   OR4K15   OR4K2   OR4K5   OR4M1   OR4N2   OR4Q3   POTEM  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371420,005,130 - 20,482,471CLINVAR
Cytogenetic Map1414q11.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14353796
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-02-11
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.