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Variant : CV675842 (GRCh37/hg19 18q21.31(chr18:54583962-55296715)x3) Homo sapiens

Symbol: CV675842
Name: GRCh37/hg19 18q21.31(chr18:54583962-55296715)x3
Condition: not provided [RCV000848941]
Clinical Significance: uncertain significance
Last Evaluated: 10/05/2017
Review Status: no assertion criteria provided
Related Genes: BOD1L2   FECH   LINC-ROR   NARS1   ONECUT2   ST8SIA3   WDR7  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh371854,583,962 - 55,296,715CLINVAR
Cytogenetic Map1818q21.31CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 14980473
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2019-12-03
Status: ACTIVE


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