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Variant : CV597089 (GRCh37/hg19 3p21.31(chr3:46728659-46753976)x1) Homo sapiens

Symbol: CV597089
Name: GRCh37/hg19 3p21.31(chr3:46728659-46753976)x1
Condition: not provided [RCV000742389]
Clinical Significance: benign
Last Evaluated: 07/11/2012
Review Status: no assertion criteria provided
Related Genes: ALS2CL   PRSS50   TMIE  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37346,728,659 - 46,753,976CLINVAR
Cytogenetic Map33p21.31CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14357761
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-02-11
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.