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Variant : CV161140 (GRCh38/hg38 20p11.1(chr20:25795534-26244487)x3) Homo sapiens

Symbol: CV161140
Name: GRCh38/hg38 20p11.1(chr20:25795534-26244487)x3
Condition: See cases [RCV000140104]
Clinical Significance: benign
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: FAM182A   FAM182B   LINC01733   LOC100134868   LOC101926935   MIR663A   MIR663AHG  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000020.11:g.(?_25795534)_(26244487_?)dup
NC_000020.10:g.(?_25776170)_(26225123_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh382025,795,534 - 26,244,487CLINVAR
GRCh372025,776,170 - 26,225,123CLINVAR
Build 362025,724,170 - 26,173,123CLINVAR
Cytogenetic Map2020p11.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9487634
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-09-22
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.