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Variant : CV159976 (GRCh38/hg38 11q14.1(chr11:80281651-82521009)x1) Homo sapiens

Symbol: CV159976
Name: GRCh38/hg38 11q14.1(chr11:80281651-82521009)x1
Condition: See cases [RCV000139112]
Clinical Significance: uncertain significance
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LINC02720   MIR4300   MIR4300HG  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000011.10:g.(?_80281651)_(82521009_?)del
NC_000011.9:g.(?_79992695)_(82232051_?)del
NC_000011.8:g.(?_79670343)_(81909699_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381180,281,651 - 82,521,009CLINVAR
GRCh371179,992,695 - 82,232,051CLINVAR
Build 361179,670,343 - 81,909,699CLINVAR
Cytogenetic Map1111q14.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9486644
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-21
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.