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Variant : CV592884 (GRCh37/hg19 13q14.13(chr13:46513068-47043220)x3) Homo sapiens

Symbol: CV592884
Name: GRCh37/hg19 13q14.13(chr13:46513068-47043220)x3
Condition: not provided [RCV000738184]
Clinical Significance: benign
Last Evaluated: 11/08/2012
Review Status: no assertion criteria provided
Related Genes: CPB2   LCP1   LRRC63   RUBCNL   ZC3H13  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371346,513,068 - 47,043,220CLINVAR
Cytogenetic Map1313q14.13CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14353559
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.