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Variant : CV163737 (GRCh38/hg38 12q21.31(chr12:85578345-85815687)x1) Homo sapiens

Symbol: CV163737
Name: GRCh38/hg38 12q21.31(chr12:85578345-85815687)x1
Condition: See cases [RCV000142165]
Clinical Significance: uncertain significance
Last Evaluated: 11/05/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: RASSF9  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000012.12:g.(?_85578345)_(85815687_?)del
NC_000012.11:g.(?_85972123)_(86209465_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381285,578,345 - 85,815,687CLINVAR
GRCh371285,972,123 - 86,209,465CLINVAR
Build 361284,496,254 - 84,733,596CLINVAR
Cytogenetic Map1212q21.31CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9489684
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-05-26
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.