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Variant : CV158210 (GRCh38/hg38 9p21.1(chr9:28648339-29040540)x1) Homo sapiens

Symbol: CV158210
Name: GRCh38/hg38 9p21.1(chr9:28648339-29040540)x1
Condition: See cases [RCV000137533]
Clinical Significance: likely benign|uncertain significance
Last Evaluated: 05/27/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LINGO2   MIR873   MIR876  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000009.12:g.(?_28648339)_(29040540_?)del
NC_000009.11:g.(?_28648337)_(29040538_?)del
NC_000009.10:g.(?_28638337)_(29030538_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38928,648,339 - 29,040,540CLINVAR
GRCh37928,648,337 - 29,040,538CLINVAR
Build 36928,638,337 - 29,030,538CLINVAR
Cytogenetic Map99p21.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9485088
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-07
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.