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Variant : CV591110 (GRCh37/hg19 1p36.21(chr1:12785494-12998343)x1) Homo sapiens

Symbol: CV591110
Name: GRCh37/hg19 1p36.21(chr1:12785494-12998343)x1
Condition: not provided [RCV000736410]
Clinical Significance: benign
Last Evaluated: 01/23/2014
Review Status: no assertion criteria provided
Related Genes: AADACL3   C1orf158   HNRNPCL1   PRAMEF1   PRAMEF10   PRAMEF11   PRAMEF12   PRAMEF2   PRAMEF4   PRAMEF6   PRAMEF7  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37112,785,494 - 12,998,343CLINVAR
Cytogenetic Map11p36.21CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 14351165
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-01-14
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.