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Variant : CV156020 (GRCh38/hg38 11q14.1(chr11:81686030-82113389)x1) Homo sapiens

Symbol: CV156020
Name: GRCh38/hg38 11q14.1(chr11:81686030-82113389)x1
Condition: See cases [RCV000135576]
Clinical Significance: pathogenic|uncertain significance
Last Evaluated: 01/27/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: MIR4300   MIR4300HG  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000011.10:g.(?_81686030)_(82113389_?)del
NC_000011.9:g.(?_81397072)_(81824431_?)del
NC_000011.8:g.(?_81074720)_(81502079_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381181,686,030 - 82,113,389CLINVAR
GRCh371181,397,072 - 81,824,431CLINVAR
Build 361181,074,720 - 81,502,079CLINVAR
Cytogenetic Map1111q14.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9483148
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-14
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.