Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV156266 (GRCh38/hg38 20p13(chr20:89939-1246891)x3) Homo sapiens

Symbol: CV156266
Name: GRCh38/hg38 20p13(chr20:89939-1246891)x3
Condition: See cases [RCV000135794]
Clinical Significance: uncertain significance
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AL110114.1   ANGPT4   C20orf202   C20orf96   CSNK2A1   DEFB125   DEFB126   DEFB127   DEFB128   DEFB129   DEFB132   FAM110A   NRSN2   NRSN2-AS1   PSMF1   RAD21L1   RBCK1   RSPO4   SCRT2   SLC52A3   SOX12   SRXN1   TBC1D20   TCF15   TMEM74B   TRIB3   ZCCHC3  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000020.11:g.(?_89939)_(1246891_?)dup
NC_000020.10:g.(?_70580)_(1227535_?)dup
NC_000020.9:g.(?_18580)_(1175535_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh382089,939 - 1,246,891CLINVAR
GRCh372070,580 - 1,227,535CLINVAR
Build 362018,580 - 1,175,535CLINVAR
Cytogenetic Map2020p13CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9483360
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-06-30
Status: ACTIVE



NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.