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Variant : CV553697 (GRCh37/hg19 2q37.3(chr2:241611307-241715891)x3) Homo sapiens

Symbol: CV553697
Name: GRCh37/hg19 2q37.3(chr2:241611307-241715891)x3
Condition: not provided [RCV000682002]
Clinical Significance: uncertain significance
Last Evaluated: 06/07/2017
Review Status: no assertion criteria provided
Related Genes: AQP12A   AQP12B   KIF1A  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372241,611,307 - 241,715,891CLINVAR
Cytogenetic Map22q37.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13794696
Created: 2018-10-09
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.