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Items: 1 to 20 of 965

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137724copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099 PADI1, RPS15AP6, 176 more genes
    nsv5969911inversion1nstd209human GRCh38 chr1: 16,619,297-16,951,954 , GRCh37.p13 chr1: 16,945,792-17,278,449 , RNU1-4, 24 more genes
    nsv5955235insertion1nstd209human GRCh38 chr1: 16,916,183-16,916,183 , GRCh37.p13 chr1: 17,242,678-17,242,678 CROCC
    nsv5882794copy number variation1nstd209human GRCh38 chr1: 16,920,418-16,920,482 , GRCh37.p13 chr1: 17,246,913-17,246,977 CROCC
    nsv5874151copy number variation1nstd209human GRCh38 chr1: 13,714,112-20,623,728 , GRCh37.p13 chr1: 14,040,607-20,950,221 , TRV-CAC11-1, 171 more genes
    nsv5873892copy number variation1nstd209human GRCh38 chr1: 16,934,236-16,934,287 , GRCh37.p13 chr1: 17,260,731-17,260,782 CROCC
    nsv5828720copy number variation2nstd209human GRCh38 chr1: 16,918,779-16,928,154 , GRCh37.p13 chr1: 17,245,274-17,254,649 CROCC
    nsv5828617copy number variation2nstd209human GRCh38 chr1: 16,918,979-16,938,818 , GRCh37.p13 chr1: 17,245,474-17,265,313 CROCC
    nsv5828615copy number variation2nstd209human GRCh38 chr1: 16,904,526-16,918,478 , GRCh37.p13 chr1: 17,231,021-17,244,973 CROCC
    nsv5828404copy number variation2nstd209human GRCh38 chr1: 16,937,419-16,947,103 , GRCh37.p13 chr1: 17,263,914-17,273,598 CROCC
    nsv5669419inversion1nstd207human GRCh38 chr1: 16,761,852-16,946,929 , GRCh37.p13 chr1: 17,088,347-17,273,424 TRE-TTC3-1, CROCC, 12 more genes
    nsv5618871insertion1nstd207human GRCh38 chr1: 16,913,320-16,913,320 , GRCh37.p13 chr1: 17,239,815-17,239,815 CROCC
    nsv5583104copy number variation1nstd207human GRCh38 chr1: 16,915,196-16,915,300 , GRCh37.p13 chr1: 17,241,691-17,241,795 CROCC
    nsv5572686copy number variation1nstd207human GRCh38 chr1: 16,951,884-16,952,141 , GRCh37.p13 chr1: 17,278,379-17,278,636 CROCC
    nsv5568738copy number variation1nstd207human GRCh38 chr1: 16,945,638-16,945,699 , GRCh37.p13 chr1: 17,272,133-17,272,194 CROCC
    nsv5566545copy number variation1nstd207human GRCh38 chr1: 16,950,084-16,950,378 , GRCh37.p13 chr1: 17,276,579-17,276,873 CROCC
    nsv5560911sequence alteration1nstd206human GRCh38 chr1: 16,483,139-16,940,239 , GRCh37.p13 chr1: 16,809,634-17,266,734 , RNU1-4, 35 more genes
    nsv5559248sequence alteration1nstd206human GRCh38 chr1: 16,619,296-16,951,955 , GRCh37.p13 chr1: 16,945,791-17,278,450 , MST1P2, 24 more genes
    nsv5422451copy number variation1nstd206human GRCh38 chr1: 16,851,163-16,949,163 , GRCh37.p13 chr1: 17,177,658-17,275,658 RNU1-5P, LOC112267871, 11 more genes
    nsv5421340copy number variation1nstd206human GRCh38 chr1: 16,934,501-16,935,123 , GRCh37.p13 chr1: 17,260,996-17,261,618 CROCC
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