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Items: 1 to 20 of 606

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5953134insertion1nstd209human GRCh38 chr8: 143,945,022-143,945,022 , GRCh37.p13 chr8|NW_003315923.1: 283,667-283,667 , GRCh37.p13 chr8: 145,019,190-145,019,190 PLEC, MIR661
    nsv5914183copy number variation1nstd209human GRCh38 chr8: 143,931,280-143,931,392 , GRCh37.p13 chr8|NW_003315923.1: 269,925-270,037 , GRCh37.p13 chr8: 145,005,448-145,005,560 PLEC
    nsv5909738copy number variation1nstd209human GRCh38 chr8: 143,942,330-143,942,400 , GRCh37.p13 chr8: 145,016,498-145,016,568 , GRCh37.p13 chr8|NW_003315923.1: 280,975-281,045 PLEC
    nsv5668328inversion1nstd207human GRCh38 chr8: 143,912,249-143,952,547 , GRCh37.p13 chr8: 144,986,417-145,026,715 , GRCh37.p13 chr8|NW_003315923.1: 250,894-291,192 PLEC, MIR661
    nsv5640712insertion2nstd207human GRCh38 chr8: 143,928,664-143,928,664 , GRCh37.p13 chr8|NW_003315923.1: 267,309-267,309 , GRCh37.p13 chr8: 145,002,832-145,002,832 PLEC
    nsv5639711insertion1nstd207human GRCh38 chr8: 143,928,625-143,928,625 , GRCh37.p13 chr8|NW_003315923.1: 267,270-267,270 , GRCh37.p13 chr8: 145,002,793-145,002,793 PLEC
    nsv5638941insertion1nstd207human GRCh38 chr8: 143,931,282-143,931,282 , GRCh37.p13 chr8|NW_003315923.1: 269,927-269,927 , GRCh37.p13 chr8: 145,005,450-145,005,450 PLEC
    nsv5592077copy number variation1nstd207human GRCh38 chr8: 143,931,280-143,931,392 , GRCh37.p13 chr8|NW_003315923.1: 269,925-270,037 , GRCh37.p13 chr8: 145,005,448-145,005,560 PLEC
    nsv5590670copy number variation1nstd207human GRCh38 chr8: 143,928,397-143,928,548 , GRCh37.p13 chr8: 145,002,565-145,002,716 , GRCh37.p13 chr8|NW_003315923.1: 267,042-267,193 PLEC
    nsv5547750insertion1nstd206human GRCh38 chr8: 143,945,047-143,945,073 , GRCh37.p13 chr8|NW_003315923.1: 283,692-283,718 , GRCh37.p13 chr8: 145,019,215-145,019,241 MIR661, PLEC
    nsv5492217copy number variation1nstd206human GRCh38 chr8: 143,939,544-143,940,812 , GRCh37.p13 chr8: 145,013,712-145,014,980 , GRCh37.p13 chr8|NW_003315923.1: 278,189-279,457 PLEC
    nsv5478595copy number variation1nstd206human GRCh38 chr8: 143,942,330-143,942,403 , GRCh37.p13 chr8|NW_003315923.1: 280,975-281,048 , GRCh37.p13 chr8: 145,016,498-145,016,571 PLEC
    nsv5475043copy number variation1nstd206human GRCh38 chr8: 143,949,941-143,950,942 , GRCh37.p13 chr8|NW_003315923.1: 288,586-289,587 , GRCh37.p13 chr8: 145,024,109-145,025,110 PLEC
    nsv5381643copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,047,561-145,701,149 , GRCh38.p12 chr8: 143,973,393-144,475,766 ZFTRAF1, DGAT1, 40 more genes
    nsv5364530translocation1nstd200human GRCh38 chr8: 143,942,403-143,942,403 , GRCh38 chr8: 143,942,330-143,942,330 , GRCh37.p13 chr8: 145,016,498-145,016,498 , GRCh37.p13 chr8|NW_003315923.1: 281,048-281,048 , GRCh37.p13 chr8|NW_003315923.1: 280,975-280,975 , GRCh37.p13 chr8: 145,016,571-145,016,571 PLEC
    nsv5338140translocation1nstd200human GRCh37 chr8: 145,016,498-145,016,498 , GRCh37 chr8: 145,016,571-145,016,571 , GRCh38.p12 chr8: 143,942,403-143,942,403 , GRCh38.p12 chr8: 143,942,330-143,942,330 PLEC
    nsv5324084translocation1nstd204human GRCh38.p13 chr8: 143,942,408-143,942,408 , GRCh38.p13 chr8: 143,942,330-143,942,330 , GRCh37.p13 chr8|NW_003315923.1: 280,975-280,975 , GRCh37.p13 chr8|NW_003315923.1: 281,053-281,053 , GRCh37.p13 chr8: 145,016,498-145,016,498 , GRCh37.p13 chr8: 145,016,576-145,016,576 PLEC
    nsv5318293copy number variation1nstd204human GRCh37.p13 chr8|NW_003315923.1: 282,209-286,815 , GRCh37.p13 chr8: 145,017,732-145,022,338 , GRCh38.p13 chr8: 143,943,564-143,948,170 PLEC, MIR661
    nsv5311555copy number variation1nstd204human GRCh38.p13 chr8: 143,924,990-143,925,294 , GRCh37.p13 chr8: 144,999,158-144,999,462 , GRCh37.p13 chr8|NW_003315923.1: 263,635-263,939 PLEC
    nsv5308443copy number variation1nstd204human GRCh38.p13 chr8: 143,916,562-143,921,172 , GRCh37.p13 chr8|NW_003315923.1: 255,207-259,817 , GRCh37.p13 chr8: 144,990,730-144,995,340 PLEC
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