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Variant : CV382432 (GRCh37/hg19 2q37.3(chr2:240982124-241016654)x3) Homo sapiens

Symbol: CV382432
Name: GRCh37/hg19 2q37.3(chr2:240982124-241016654)x3
Condition: See cases [RCV000446381]
Clinical Significance: likely benign
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: OR6B3   PRR21  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh372240,982,124 - 241,016,654CLINVAR
Cytogenetic Map22q37.3CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 12851106
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-02-20
Status: ACTIVE


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