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Variant : CV163977 (GRCh38/hg38 6q13(chr6:70794142-71972780)x3) Homo sapiens

Symbol: CV163977
Name: GRCh38/hg38 6q13(chr6:70794142-71972780)x3
Condition: See cases [RCV000142320]
Clinical Significance: uncertain significance
Last Evaluated: 03/18/2014
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: B3GAT2   LINC00472   LINC01626   MIR30A   MIR30C2   OGFRL1   RIMS1   SMAP1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000006.12:g.(?_70794142)_(71972780_?)dup
NC_000006.11:g.(?_71503845)_(72682483_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38670,794,142 - 71,972,780CLINVAR
GRCh37671,503,845 - 72,682,483CLINVAR
Build 36671,560,566 - 72,739,204CLINVAR
Cytogenetic Map66q13CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9489839
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-07-07
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.