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Variant : CV154851 (GRCh38/hg38 20p13(chr20:590507-661733)x3) Homo sapiens

Symbol: CV154851
Name: GRCh38/hg38 20p13(chr20:590507-661733)x3
Condition: See cases [RCV000134502]
Clinical Significance: benign
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: SCRT2   SRXN1   TCF15  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000020.11:g.(?_590507)_(661733_?)dup
NC_000020.10:g.(?_571151)_(642377_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3820590,507 - 661,733CLINVAR
GRCh3720571,151 - 642,377CLINVAR
Build 3620519,151 - 590,377CLINVAR
Cytogenetic Map2020p13CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9482082
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-06-23
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.