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Variant : CV592880 (GRCh37/hg19 13q14.11(chr13:44374981-44511144)x3) Homo sapiens

Symbol: CV592880
Name: GRCh37/hg19 13q14.11(chr13:44374981-44511144)x3
Condition: not provided [RCV000738180]
Clinical Significance: benign
Last Evaluated: 11/08/2012
Review Status: no assertion criteria provided
Related Genes: CCDC122   LACC1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371344,374,981 - 44,511,144CLINVAR
Cytogenetic Map1313q14.11CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14353555
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-12-03
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.