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Variant : CV596642 (GRCh37/hg19 22q12.3(chr22:36844619-36988654)x3) Homo sapiens

Symbol: CV596642
Name: GRCh37/hg19 22q12.3(chr22:36844619-36988654)x3
Condition: not provided [RCV000741942]
Clinical Significance: benign
Last Evaluated: 06/28/2012
Review Status: no assertion criteria provided
Related Genes: CACNG2   EIF3D   FOXRED2   TXN2  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh372236,844,619 - 36,988,654CLINVAR
Cytogenetic Map2222q12.3CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 14357316
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-01-14
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.