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Variant : CV380975 (GRCh37/hg19 2q37.3(chr2:241626027-241716779)x3) Homo sapiens

Symbol: CV380975
Name: GRCh37/hg19 2q37.3(chr2:241626027-241716779)x3
Condition: See cases [RCV000446440]
Clinical Significance: likely benign
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: AQP12A   KIF1A  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372241,626,027 - 241,716,779CLINVAR
Cytogenetic Map22q37.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12851163
Created: 2017-04-11
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.