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Items: 1 to 20 of 304

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5956997insertion1nstd209human GRCh38 chr1: 169,811,813-169,811,813 , GRCh37.p13 chr1: 169,780,954-169,780,954 FIRRM
    nsv5874502copy number variation1nstd209human GRCh38 chr1: 169,811,749-169,811,840 , GRCh37.p13 chr1: 169,780,890-169,780,981 FIRRM
    nsv5692615mobile element insertion1nstd211human GRCh38 chr1: 169,820,199-169,820,199 , GRCh37.p13 chr1: 169,789,340-169,789,340 FIRRM
    nsv5687798mobile element insertion2nstd211human GRCh38 chr1: 169,813,070-169,813,070 , GRCh37.p13 chr1: 169,782,211-169,782,211 FIRRM
    nsv5683496mobile element insertion1nstd211human GRCh38 chr1: 169,851,006-169,851,006 , GRCh37.p13 chr1: 169,820,147-169,820,147 SCYL3, FIRRM
    nsv5683483mobile element insertion1nstd211human GRCh38 chr1: 169,840,873-169,840,873 , GRCh37.p13 chr1: 169,810,014-169,810,014 FIRRM
    nsv5683039mobile element insertion1nstd211human GRCh38 chr1: 169,823,643-169,823,643 , GRCh37.p13 chr1: 169,792,784-169,792,784 FIRRM
    nsv5614011insertion1nstd207human GRCh38 chr1: 169,811,811-169,811,811 , GRCh37.p13 chr1: 169,780,952-169,780,952 FIRRM
    nsv5609223insertion1nstd207human GRCh38 chr1: 169,811,765-169,811,765 , GRCh37.p13 chr1: 169,780,906-169,780,906 FIRRM
    nsv5582748copy number variation1nstd207human GRCh38 chr1: 169,850,982-169,851,044 , GRCh37.p13 chr1: 169,820,123-169,820,185 FIRRM, SCYL3
    nsv5550955insertion1nstd206human GRCh38 chr1: 169,811,861-169,811,877 , GRCh37.p13 chr1: 169,781,002-169,781,018 FIRRM
    nsv5430313copy number variation1nstd206human GRCh38 chr1: 169,850,986-169,851,073 , GRCh37.p13 chr1: 169,820,127-169,820,214 SCYL3, FIRRM
    nsv5427970copy number variation1nstd206human GRCh38 chr1: 169,810,132-169,812,135 , GRCh37.p13 chr1: 169,779,273-169,781,276 FIRRM
    nsv5403337mobile element insertion1nstd206human GRCh38 chr1: 169,823,643-169,823,694 , GRCh37.p13 chr1: 169,792,784-169,792,835 FIRRM
    nsv5403163mobile element insertion1nstd206human GRCh38 chr1: 169,813,070-169,813,121 , GRCh37.p13 chr1: 169,782,211-169,782,262 FIRRM
    nsv5394642mobile element insertion1nstd206human GRCh38 chr1: 169,840,873-169,840,924 , GRCh37.p13 chr1: 169,810,014-169,810,065 FIRRM
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5363987translocation1nstd200human GRCh38 chr1: 169,750,156-169,750,156 , GRCh38 chr1: 169,795,339-169,795,339 , GRCh37.p13 chr1: 169,764,480-169,764,480 , GRCh37.p13 chr1: 169,719,297-169,719,297 METTL18, FIRRM
    nsv5331296translocation1nstd200human GRCh37 chr1: 169,764,480-169,764,480 , GRCh37 chr1: 169,719,297-169,719,297 , GRCh38.p12 chr1: 169,750,156-169,750,156 , GRCh38.p12 chr1: 169,795,339-169,795,339 METTL18, FIRRM
    nsv5213619copy number variation1nstd204human GRCh38.p13 chr1: 169,809,331-169,811,659 , GRCh37.p13 chr1: 169,778,472-169,780,800 FIRRM
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