U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 120

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966263insertion1nstd209human GRCh38 chr10: 28,788,263-28,788,263 , GRCh37.p13 chr10: 29,077,192-29,077,192 LINC00837, LINC01517
    nsv5914382copy number variation1nstd209human GRCh38 chr10: 27,312,316-36,846,398 , GRCh37.p13 chr10: 27,601,245-37,135,326 , RN7SL241P, 160 more genes
    nsv5703311mobile element insertion2nstd211human GRCh38 chr10: 28,788,276-28,788,276 , GRCh37.p13 chr10: 29,077,205-29,077,205 LINC01517, LINC00837
    nsv5643134insertion1nstd207human GRCh38 chr10: 28,788,263-28,788,263 , GRCh37.p13 chr10: 29,077,192-29,077,192 LINC01517, LINC00837
    nsv5137199mobile element insertion1nstd203human GRCh38 chr10: 28,788,268-28,788,276 , GRCh37.p13 chr10: 29,077,197-29,077,205 LINC01517, LINC00837
    nsv5131801mobile element insertion1nstd203human GRCh38 chr10: 28,788,267-28,788,276 , GRCh37.p13 chr10: 29,077,196-29,077,205 LINC00837, LINC01517
    nsv5130662mobile element insertion1nstd203human GRCh38 chr10: 28,788,265-28,788,276 , GRCh37.p13 chr10: 29,077,194-29,077,205 LINC01517, LINC00837
    nsv5127552mobile element insertion1nstd203human GRCh38 chr10: 28,788,264-28,788,276 , GRCh37.p13 chr10: 29,077,193-29,077,205 LINC01517, LINC00837
    nsv5125400mobile element insertion1nstd203human GRCh38 chr10: 28,788,263-28,788,273 , GRCh37.p13 chr10: 29,077,192-29,077,202 LINC00837, LINC01517
    nsv5123827mobile element insertion1nstd203human GRCh38 chr10: 28,788,266-28,788,276 , GRCh37.p13 chr10: 29,077,195-29,077,205 LINC00837, LINC01517
    nsv5123462mobile element insertion1nstd203human GRCh38 chr10: 28,788,251-28,788,263 , GRCh37.p13 chr10: 29,077,180-29,077,192 LINC00837, LINC01517
    nsv4988705copy number variation1nstd200human GRCh38 chr10: 28,757,829-28,831,036 , GRCh37.p13 chr10: 29,046,758-29,119,965 RNU6-270P, LINC01517, 1 more genes
    nsv4841183copy number variation1nstd200human GRCh37 chr10: 29,046,758-29,119,965 , GRCh38.p12 chr10: 28,757,829-28,831,036 LINC00837, RNU6-270P, 1 more genes
    nsv4755652insertion1nstd199human GRCh37 chr10: 29,077,196-29,077,196 , GRCh38.p12 chr10: 28,788,267-28,788,267 LINC00837, LINC01517
    nsv4717154mobile element insertion1nstd186human GRCh37 chr10: 29,077,192-29,077,192 , GRCh38.p12 chr10: 28,788,263-28,788,263 LINC01517, LINC00837
    nsv4691157mobile element insertion1nstd186human GRCh37 chr10: 29,077,205-29,077,205 , GRCh38.p12 chr10: 28,788,276-28,788,276 LINC01517, LINC00837
    nsv4497959mobile element insertion1nstd166human GRCh37.p13 chr10: 29,077,192-29,077,192 , GRCh38.p12 chr10: 28,788,263-28,788,263 LINC00837, LINC01517
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv3921533copy number variation1nstd102humanPathogenic GRCh37 chr10: 28,056,899-30,335,014 , NCBI36 chr10: 28,096,905-30,375,020 , GRCh38 chr10: 27,767,970-30,046,085 ODAD2, LOC107984170, 48 more genes
    nsv3920796copy number variation1nstd102humanPathogenic NCBI36 chr10: 62,842-35,729,127 , GRCh37.p13 chr10: 72,842-35,689,121 , GRCh38.p12 chr10: 26,906-35,400,193 EPC1-AS1, RNU6-452P, 559 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center