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Variant : CV599096 (GRCh37/hg19 5p15.31(chr5:7394605-7396701)x1) Homo sapiens

Symbol: CV599096
Name: GRCh37/hg19 5p15.31(chr5:7394605-7396701)x1
Condition: not provided [RCV000744396]
Clinical Significance: benign
Last Evaluated: 10/20/2010
Review Status: no assertion criteria provided
Related Genes: ADCY2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3757,394,605 - 7,396,701CLINVAR
Cytogenetic Map55p15.31CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14359765
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-12-03
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.