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Variant : CV603604 (GRCh37/hg19 1p36.21(chr1:12975284-13706571)x1) Homo sapiens

Symbol: CV603604
Name: GRCh37/hg19 1p36.21(chr1:12975284-13706571)x1
Condition: not provided [RCV000748904]
Clinical Significance: benign
Last Evaluated: 09/28/2012
Review Status: no assertion criteria provided
Related Genes: HNRNPCL2   PRAMEF13   PRAMEF15   PRAMEF18   PRAMEF19   PRAMEF22   PRAMEF5   PRAMEF6   PRAMEF7   PRAMEF8   PRAMEF9  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37112,975,284 - 13,706,571CLINVAR
Cytogenetic Map11p36.21CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14364237
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-01-07
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.