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Variant : CV675456 (GRCh37/hg19 9q21.13-21.31(chr9:78672613-83349616)x1) Homo sapiens

Symbol: CV675456
Name: GRCh37/hg19 9q21.13-21.31(chr9:78672613-83349616)x1
Condition: not provided [RCV000848555]
Clinical Significance: uncertain significance
Last Evaluated: 09/28/2018
Review Status: no assertion criteria provided
Related Genes: CEP78   FOXB2   GCNT1   GNA14   GNAQ   PCA3   PCSK5   PRUNE2   PSAT1   RFK   TLE4   VPS13A  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37978,672,613 - 83,349,616CLINVAR
Cytogenetic Map99q21.13-21.31CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14980102
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-01-21
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.