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Items: 1 to 20 of 389

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5921053copy number variation1nstd209human GRCh38 chr11: 851,944-851,994 , GRCh37.p13 chr11: 851,944-851,994 TSPAN4
    nsv5919783copy number variation1nstd209human GRCh38 chr11: 856,329-856,403 , GRCh37.p13 chr11: 856,329-856,403 TSPAN4
    nsv5918738copy number variation1nstd209human GRCh38 chr11: 736,859-3,895,958 , GRCh37.p13 chr11: 736,859-3,917,188 , TALDO1, 128 more genes
    nsv5917621copy number variation1nstd209human GRCh38 chr11: 844,855-868,189 , GRCh37.p13 chr11: 844,855-868,189 CHID1, TSPAN4
    nsv5915149copy number variation1nstd209human GRCh38 chr11: 857,000-861,674 , GRCh37.p13 chr11: 857,000-861,674 TSPAN4
    nsv5908917copy number variation1nstd209human GRCh38 chr11: 855,233-856,004 , GRCh37.p13 chr11: 855,233-856,004 TSPAN4
    nsv5867547copy number variation2nstd209human GRCh38 chr11: 856,993-861,723 , GRCh37.p13 chr11: 856,993-861,723 TSPAN4
    nsv5862796copy number variation1nstd209human GRCh38 chr11: 859,293-867,434 , GRCh37.p13 chr11: 859,293-867,434 CHID1, TSPAN4
    nsv5861861copy number variation2nstd209human GRCh38 chr11: 854,993-856,192 , GRCh37.p13 chr11: 854,993-856,192 TSPAN4
    nsv5858756copy number variation1nstd209human GRCh38 chr11: 844,832-858,292 , GRCh37.p13 chr11: 844,832-858,292 TSPAN4
    nsv5852855copy number variation2nstd209human GRCh38 chr11: 857,293-859,042 , GRCh37.p13 chr11: 857,293-859,042 TSPAN4
    nsv5852653copy number variation1nstd209human GRCh38 chr11: 843,107-847,894 , GRCh37.p13 chr11: 843,107-847,894 TSPAN4
    nsv5648323insertion1nstd207human GRCh38 chr11: 859,299-859,299 , GRCh37.p13 chr11: 859,299-859,299 TSPAN4
    nsv5646360insertion1nstd207human GRCh38 chr11: 852,367-852,367 , GRCh37.p13 chr11: 852,367-852,367 TSPAN4
    nsv5589942copy number variation1nstd207human GRCh38 chr11: 858,907-859,018 , GRCh37.p13 chr11: 858,907-859,018 TSPAN4
    nsv5586591copy number variation1nstd207human GRCh38 chr11: 859,348-859,397 , GRCh37.p13 chr11: 859,348-859,397 TSPAN4
    nsv5510174copy number variation1nstd206human GRCh38 chr11: 857,000-861,675 , GRCh37.p13 chr11: 857,000-861,675 TSPAN4
    nsv5504575copy number variation1nstd206human GRCh38 chr11: 851,053-1,088,020 , GRCh37.p13 chr11: 851,053-1,075,386 AP2A2, MUC2, 6 more genes
    nsv5500481copy number variation1nstd206human GRCh38 chr11: 844,637-844,819 , GRCh37.p13 chr11: 844,637-844,819 TSPAN4
    nsv5380885copy number variation1nstd102humanUncertain significance GRCh37 chr11: 298,501-4,113,028 , GRCh38.p12 chr11: 298,501-4,091,798 LINC02688, MIR210, 156 more genes
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