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Variant : CV676393 (GRCh37/hg19 18q21.31(chr18:55398774-55555371)x3) Homo sapiens

Symbol: CV676393
Name: GRCh37/hg19 18q21.31(chr18:55398774-55555371)x3
Condition: not provided [RCV000849492]
Clinical Significance: uncertain significance
Last Evaluated: 05/15/2017
Review Status: no assertion criteria provided
Related Genes: ATP8B1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371855,398,774 - 55,555,371CLINVAR
Cytogenetic Map1818q21.31CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14981005
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2019-11-12
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.