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Variant : CV592904 (GRCh37/hg19 13q14.3(chr13:53420050-53430645)x1) Homo sapiens

Symbol: CV592904
Name: GRCh37/hg19 13q14.3(chr13:53420050-53430645)x1
Condition: not provided [RCV000738204]
Clinical Significance: benign
Last Evaluated: 02/17/2012
Review Status: no assertion criteria provided
Related Genes: PCDH8  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371353,420,050 - 53,430,645CLINVAR
Cytogenetic Map1313q14.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14353579
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.