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Variant : CV597740 (GRCh37/hg19 3q27.3(chr3:186387299-186420170)x1) Homo sapiens

Symbol: CV597740
Name: GRCh37/hg19 3q27.3(chr3:186387299-186420170)x1
Condition: not provided [RCV000743040]
Clinical Significance: benign
Last Evaluated: 12/19/2012
Review Status: no assertion criteria provided
Related Genes: HRG  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh373186,387,299 - 186,420,170CLINVAR
Cytogenetic Map33q27.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14358411
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.