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Variant : CV164941 (GRCh38/hg38 21q21.3(chr21:26244753-28273836)x1) Homo sapiens

Symbol: CV164941
Name: GRCh38/hg38 21q21.3(chr21:26244753-28273836)x1
Condition: See cases [RCV000143254]
Clinical Significance: likely benign|uncertain significance
Last Evaluated: 04/04/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ADAMTS1   ADAMTS5   CYYR1   CYYR1-AS1   LINC00113   LINC00314   LINC01673   LINC01695   LINC01697   LOC110121429   MIR4759  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000021.9:g.(?_26244753)_(28273836_?)del
NC_000021.8:g.(?_27617072)_(29646155_?)del
NC_000021.7:g.(?_26538943)_(28568026_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh382126,244,753 - 28,273,836CLINVAR
GRCh372127,617,072 - 29,646,155CLINVAR
Build 362126,538,943 - 28,568,026CLINVAR
Cytogenetic Map2121q21.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9490852
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-11-17
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.