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Variant : CV160787 (GRCh38/hg38 20p13(chr20:364204-879317)x3) Homo sapiens

Symbol: CV160787
Name: GRCh38/hg38 20p13(chr20:364204-879317)x3
Condition: See cases [RCV000139812]
Clinical Significance: uncertain significance
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ANGPT4   CSNK2A1   FAM110A   RBCK1   SCRT2   SLC52A3   SRXN1   TBC1D20   TCF15   TRIB3  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000020.11:g.(?_364204)_(879317_?)dup
NC_000020.10:g.(?_344848)_(859960_?)dup
NC_000020.9:g.(?_292848)_(807960_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3820364,204 - 879,317CLINVAR
GRCh3720344,848 - 859,960CLINVAR
Build 3620292,848 - 807,960CLINVAR
Cytogenetic Map2020p13CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9487342
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-06-30
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.