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Items: 1 to 20 of 438

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5957668insertion1nstd209human GRCh38 chr6: 104,941,463-104,941,463 , GRCh37.p13 chr6: 105,389,338-105,389,338 LIN28B
    nsv5907070copy number variation1nstd209human GRCh38 chr6: 105,050,575-105,051,404 , GRCh37.p13 chr6: 105,498,450-105,499,279 LIN28B
    nsv5714563mobile element insertion1nstd211human GRCh38 chr6: 105,050,634-105,050,634 , GRCh37.p13 chr6: 105,498,509-105,498,509 LIN28B
    nsv5679062mobile element insertion1nstd211human GRCh38 chr6: 105,063,645-105,063,645 , GRCh37.p13 chr6: 105,511,520-105,511,520 LIN28B
    nsv5678520mobile element insertion1nstd211human GRCh38 chr6: 104,989,601-104,989,601 , GRCh37.p13 chr6: 105,437,476-105,437,476 LIN28B
    nsv5641337insertion1nstd207human GRCh38 chr6: 105,023,557-105,023,557 , GRCh37.p13 chr6: 105,471,432-105,471,432 LIN28B
    nsv5636967insertion1nstd207human GRCh38 chr6: 105,023,506-105,023,506 , GRCh37.p13 chr6: 105,471,381-105,471,381 LIN28B
    nsv5634497insertion1nstd207human GRCh38 chr6: 104,941,463-104,941,463 , GRCh37.p13 chr6: 105,389,338-105,389,338 LIN28B
    nsv5634176insertion1nstd207human GRCh38 chr6: 105,023,521-105,023,521 , GRCh37.p13 chr6: 105,471,396-105,471,396 LIN28B
    nsv5546649insertion1nstd206human GRCh38 chr6: 105,039,586-105,039,588 , GRCh37.p13 chr6: 105,487,461-105,487,463 LIN28B
    nsv5543431insertion1nstd206human GRCh38 chr6: 104,941,493-104,941,514 , GRCh37.p13 chr6: 105,389,368-105,389,389 LIN28B
    nsv5469080copy number variation1nstd206human GRCh38 chr6: 104,967,455-104,967,534 , GRCh37.p13 chr6: 105,415,330-105,415,409 LIN28B
    nsv5468340copy number variation1nstd206human GRCh38 chr6: 104,953,149-104,953,232 , GRCh37.p13 chr6: 105,401,024-105,401,107 LIN28B
    nsv5465036copy number variation1nstd206human GRCh38 chr6: 105,023,058-105,023,110 , GRCh37.p13 chr6: 105,470,933-105,470,985 LIN28B
    nsv5464438copy number variation1nstd206human GRCh38 chr6: 105,032,212-105,032,296 , GRCh37.p13 chr6: 105,480,087-105,480,171 LIN28B
    nsv5456507copy number variation1nstd206human GRCh38 chr6: 104,876,708-105,137,844 , GRCh37.p13 chr6: 105,324,583-105,585,719 BVES-AS1, LIN28B-AS1, 3 more genes
    nsv5455620copy number variation1nstd206human GRCh38 chr6: 105,050,212-105,051,405 , GRCh37.p13 chr6: 105,498,087-105,499,280 LIN28B
    nsv5389229copy number variation1nstd186human GRCh37 chr6: 105,498,289-105,499,033 , GRCh38.p12 chr6: 105,050,414-105,051,158 LIN28B
    nsv5387918copy number variation1nstd186human GRCh37 chr6: 105,498,494-105,499,280 , GRCh38.p12 chr6: 105,050,619-105,051,405 LIN28B
    nsv5369565translocation1nstd200human GRCh38 chr6: 105,032,212-105,032,212 , GRCh38 chr6: 105,032,296-105,032,296 , GRCh37.p13 chr6: 105,480,171-105,480,171 , GRCh37.p13 chr6: 105,480,087-105,480,087 LIN28B
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