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Variant : CV381070 (GRCh37/hg19 2q37.3(chr2:240981290-240987642)x3) Homo sapiens

Symbol: CV381070
Name: GRCh37/hg19 2q37.3(chr2:240981290-240987642)x3
Condition: See cases [RCV000447196]
Clinical Significance: benign
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: OR6B3   PRR21  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372240,981,290 - 240,987,642CLINVAR
Cytogenetic Map22q37.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12851914
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-02-20
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.