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Variant : CV605631 (GRCh37/hg19 13q34(chr13:114585454-114880349)x3) Homo sapiens

Symbol: CV605631
Name: GRCh37/hg19 13q34(chr13:114585454-114880349)x3
Condition: not provided [RCV000750931]
Clinical Significance: benign
Last Evaluated: 07/08/2016
Review Status: no assertion criteria provided
Related Genes: LINC00565   RASA3  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3713114,585,454 - 114,880,349CLINVAR
Cytogenetic Map1313q34CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14366257
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-01-14
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.