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Items: 1 to 20 of 262

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5705093mobile element insertion1nstd211human GRCh38 chr13: 90,926,447-90,926,447 , GRCh37.p13 chr13: 91,578,701-91,578,701 LINC00410
    nsv5703339mobile element insertion1nstd211human GRCh38 chr13: 90,912,086-90,912,086 , GRCh37.p13 chr13: 91,564,340-91,564,340 LINC00410
    nsv5701811mobile element insertion2nstd211human GRCh38 chr13: 90,891,489-90,891,489 , GRCh37.p13 chr13: 91,543,743-91,543,743 LOC105370311, LINC00410
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5561143sequence alteration1nstd206human GRCh38 chr13: 90,841,764-90,916,508 , GRCh37.p13 chr13: 91,494,018-91,568,762 LINC00410, LOC105370311
    nsv5513375copy number variation1nstd206human GRCh38 chr13: 90,874,180-91,050,049 , GRCh37.p13 chr13: 91,526,434-91,702,303 LINC00410, BRK1P2, 1 more genes
    nsv5505707copy number variation1nstd206human GRCh38 chr13: 90,895,660-91,063,591 , GRCh37.p13 chr13: 91,547,914-91,715,845 BRK1P2, LOC105370311, 1 more genes
    nsv5503717copy number variation1nstd206human GRCh38 chr13: 90,902,508-90,902,649 , GRCh37.p13 chr13: 91,554,762-91,554,903 LINC00410
    nsv5422468mobile element insertion1nstd206human GRCh38 chr13: 90,891,489-90,891,540 , GRCh37.p13 chr13: 91,543,743-91,543,794 LINC00410, LOC105370311
    nsv5415649mobile element insertion1nstd206human GRCh38 chr13: 90,912,086-90,912,137 , GRCh37.p13 chr13: 91,564,340-91,564,391 LINC00410
    nsv5415426mobile element insertion1nstd206human GRCh38 chr13: 90,926,447-90,926,498 , GRCh37.p13 chr13: 91,578,701-91,578,752 LINC00410
    nsv5318652copy number variation1nstd204human GRCh38.p13 chr13: 90,895,585-90,895,765 , GRCh37.p13 chr13: 91,547,839-91,548,019 LINC00410, LOC105370311
    nsv5315009copy number variation1nstd204human GRCh37.p13 chr13: 91,430,652-91,672,402 , GRCh38.p13 chr13: 90,778,398-91,020,148 LINC00410, RNU6-75P, 1 more genes
    nsv5276082copy number variation1nstd204human GRCh38.p13 chr13: 90,909,132-90,912,231 , GRCh37.p13 chr13: 91,561,386-91,564,485 LINC00410
    nsv5271419copy number variation1nstd204human GRCh38.p13 chr13: 90,778,401-91,020,200 , GRCh37.p13 chr13: 91,430,655-91,672,454 RNU6-75P, LINC00410, 1 more genes
    nsv5271182copy number variation1nstd204human GRCh38.p13 chr13: 90,911,532-90,952,830 , GRCh37.p13 chr13: 91,563,786-91,605,084 LINC00410
    nsv5155785mobile element insertion1nstd203human GRCh38 chr13: 90,891,480-90,891,489 , GRCh37.p13 chr13: 91,543,734-91,543,743 LINC00410, LOC105370311
    nsv5154230mobile element insertion1nstd203human GRCh38 chr13: 90,891,476-90,891,489 , GRCh37.p13 chr13: 91,543,730-91,543,743 LINC00410, LOC105370311
    nsv5144136mobile element insertion1nstd203human GRCh38 chr13: 90,891,481-90,891,489 , GRCh37.p13 chr13: 91,543,735-91,543,743 LOC105370311, LINC00410
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
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