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Variant : CV607775 (GRCh37/hg19 2q12.2(chr2:106690493-106700313)x3) Homo sapiens

Symbol: CV607775
Name: GRCh37/hg19 2q12.2(chr2:106690493-106700313)x3
Condition: not provided [RCV000753075]
Clinical Significance: benign
Last Evaluated: 07/06/2011
Review Status: no assertion criteria provided
Related Genes: ECRG4  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372106,690,493 - 106,700,313CLINVAR
Cytogenetic Map22q12.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14349579
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-03-31
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.