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Variant : CV154174 (GRCh38/hg38 20p13(chr20:80106-170967)x3) Homo sapiens

Symbol: CV154174
Name: GRCh38/hg38 20p13(chr20:80106-170967)x3
Condition: See cases [RCV000133905]
Clinical Significance: benign
Last Evaluated: 03/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: DEFB125   DEFB126   DEFB127  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000020.11:g.(?_80106)_(170967_?)dup
NC_000020.10:g.(?_60747)_(151608_?)dup
NC_000020.9:g.(?_8747)_(99608_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh382080,106 - 170,967CLINVAR
GRCh372060,747 - 151,608CLINVAR
Build 36208,747 - 99,608CLINVAR
Cytogenetic Map2020p13CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9481490
Created: 2014-09-09
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.