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Variant : CV160978 (GRCh38/hg38 14q11.2(chr14:20499771-20511908)x3) Homo sapiens

Symbol: CV160978
Name: GRCh38/hg38 14q11.2(chr14:20499771-20511908)x3
Condition: See cases [RCV000139953]
Clinical Significance: benign
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: RNASE10  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000014.9:g.(?_20499771)_(20511908_?)dup
NC_000014.8:g.(?_20967930)_(20980067_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381420,499,771 - 20,511,908CLINVAR
GRCh371420,967,930 - 20,980,067CLINVAR
Build 361420,037,770 - 20,049,907CLINVAR
Cytogenetic Map1414q11.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487483
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-20
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.