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Variant : CV158262 (GRCh38/hg38 11q23.3(chr11:115647670-117581883)x3) Homo sapiens

Symbol: CV158262
Name: GRCh38/hg38 11q23.3(chr11:115647670-117581883)x3
Condition: See cases [RCV000137585]
Clinical Significance: uncertain significance
Last Evaluated: 03/09/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: APOA1   APOA1-AS   APOA4   APOA5   APOC3   BACE1   BACE1-AS   BUD13   CEP164   DSCAML1   LINC00900   LINC02702   LINC02703   PAFAH1B2   PCSK7   RNF214   SIDT2   SIK3   TAGLN   ZPR1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000011.10:g.(?_115647670)_(117581883_?)dup
NC_000011.9:g.(?_115518388)_(117452598_?)dup
NC_000011.8:g.(?_115023598)_(116957808_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3811115,647,670 - 117,581,883CLINVAR
GRCh3711115,518,388 - 117,452,598CLINVAR
Build 3611115,023,598 - 116,957,808CLINVAR
Cytogenetic Map1111q23.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9485139
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-07-28
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.