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Variant : CV591109 (GRCh37/hg19 1p36.21(chr1:12741240-15768304)x1) Homo sapiens

Symbol: CV591109
Name: GRCh37/hg19 1p36.21(chr1:12741240-15768304)x1
Condition: not provided [RCV000736409]
Clinical Significance: uncertain significance
Last Evaluated: 09/10/2010
Review Status: no assertion criteria provided
Related Genes: AADACL3   C1orf158   CTRC   EFHD2   FHAD1   HNRNPCL1   HNRNPCL2   KAZN   LRRC38   PDPN   PRAMEF1   PRAMEF10   PRAMEF11   PRAMEF12   PRAMEF13   PRAMEF15   PRAMEF17   PRAMEF18   PRAMEF19   PRAMEF2   PRAMEF20   PRAMEF22   PRAMEF4   PRAMEF5   PRAMEF6   PRAMEF7   PRAMEF8   PRAMEF9   PRDM2   TMEM51  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37112,741,240 - 15,768,304CLINVAR
Cytogenetic Map11p36.21CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14351164
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.