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Items: 1 to 20 of 216

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116598mobile element insertion1nstd186human GRCh37 chr18: 53,146,061-53,146,061 , GRCh38.p12 chr18: 55,478,830-55,478,830 TCF4, MIR4529, 1 more genes
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5968113insertion1nstd209human GRCh37.p13 chr18: 53,146,061-53,146,061 , GRCh38 chr18: 55,478,830-55,478,830 TCF4, MIR4529, 1 more genes
    nsv5713469mobile element insertion2nstd211human GRCh38 chr18: 55,478,844-55,478,844 , GRCh37.p13 chr18: 53,146,075-53,146,075 TCF4, MIR4529, 1 more genes
    nsv5645539insertion1nstd207human GRCh38 chr18: 55,478,830-55,478,830 , GRCh37.p13 chr18: 53,146,061-53,146,061 TCF4, MIR4529, 1 more genes
    nsv5415777mobile element insertion1nstd206human GRCh38 chr18: 55,478,830-55,478,830 , GRCh37.p13 chr18: 53,146,061-53,146,061 TCF4, MIR4529, 1 more genes
    nsv5381802copy number variation1nstd102humanPathogenic GRCh37 chr18: 51,925,586-78,010,032 , GRCh38.p12 chr18: 54,399,216-80,252,149 LOC105372200, LOC105372174, 298 more genes
    nsv5159819mobile element insertion1nstd203human GRCh38 chr18: 55,478,802-55,478,830 , GRCh37.p13 chr18: 53,146,033-53,146,061 TCF4, MIR4529, 1 more genes
    nsv5152727mobile element insertion1nstd203human GRCh38 chr18: 55,478,836-55,478,844 , GRCh37.p13 chr18: 53,146,067-53,146,075 TCF4, MIR4529, 1 more genes
    nsv5151541mobile element insertion1nstd203human GRCh38 chr18: 55,478,834-55,478,844 , GRCh37.p13 chr18: 53,146,065-53,146,075 TCF4, MIR4529, 1 more genes
    nsv5148300mobile element insertion1nstd203human GRCh38 chr18: 55,478,837-55,478,844 , GRCh37.p13 chr18: 53,146,068-53,146,075 TCF4, MIR4529, 1 more genes
    nsv5147063mobile element insertion1nstd203human GRCh38 chr18: 55,478,830-55,478,844 , GRCh37.p13 chr18: 53,146,061-53,146,075 TCF4, MIR4529, 1 more genes
    nsv5146665mobile element insertion1nstd203human GRCh38 chr18: 55,478,833-55,478,844 , GRCh37.p13 chr18: 53,146,064-53,146,075 TCF4, MIR4529, 1 more genes
    nsv5144426mobile element insertion1nstd203human GRCh38 chr18: 55,478,832-55,478,844 , GRCh37.p13 chr18: 53,146,063-53,146,075 TCF4, MIR4529, 1 more genes
    nsv5143928mobile element insertion1nstd203human GRCh38 chr18: 55,478,835-55,478,844 , GRCh37.p13 chr18: 53,146,066-53,146,075 TCF4, MIR4529, 1 more genes
    nsv5140935mobile element insertion1nstd203human GRCh38 chr18: 55,478,829-55,478,844 , GRCh37.p13 chr18: 53,146,060-53,146,075 TCF4, MIR4529, 1 more genes
    nsv5140290mobile element insertion1nstd203human GRCh38 chr18: 55,478,844-55,478,844 , GRCh37.p13 chr18: 53,146,075-53,146,075 TCF4, MIR4529, 1 more genes
    nsv4767137insertion1nstd199human GRCh37 chr18: 53,146,073-53,146,073 , GRCh38.p12 chr18: 55,478,842-55,478,842 TCF4, MIR4529, 1 more genes
    nsv4723451insertion1nstd186human GRCh37 chr18: 53,146,061-53,146,061 , GRCh38.p12 chr18: 55,478,830-55,478,830 TCF4, MIR4529, 1 more genes
    nsv4687801mobile element insertion1nstd186human GRCh37 chr18: 53,146,075-53,146,075 , GRCh38.p12 chr18: 55,478,844-55,478,844 TCF4, MIR4529, 1 more genes
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