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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129932insertion1nstd186human GRCh37 chr17: 43,339,871-43,339,878 , GRCh38.p12 chr17: 45,262,504-45,262,511 MAP3K14, SPATA32, 1 more genes
    nsv6113384mobile element insertion1nstd186human GRCh37 chr17: 43,383,714-43,383,765 , GRCh38.p12 chr17: 45,306,348-45,306,399 MAP3K14
    nsv5967861insertion1nstd209human GRCh38 chr17: 45,306,333-45,306,333 , GRCh37.p13 chr17: 43,383,699-43,383,699 MAP3K14
    nsv5706173mobile element insertion2nstd211human GRCh38 chr17: 45,306,348-45,306,348 , GRCh37.p13 chr17: 43,383,714-43,383,714 MAP3K14
    nsv5659109insertion1nstd207human GRCh38 chr17: 45,262,516-45,262,516 , GRCh37.p13 chr17: 43,339,883-43,339,883 MAP3K14, SPATA32, 1 more genes
    nsv5645885insertion1nstd207human GRCh38 chr17: 45,306,333-45,306,333 , GRCh37.p13 chr17: 43,383,699-43,383,699 MAP3K14
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5541911insertion1nstd206human GRCh38 chr17: 45,262,504-45,262,511 , GRCh37.p13 chr17: 43,339,871-43,339,878 MAP3K14, SPATA32, 1 more genes
    nsv5525135copy number variation1nstd206human GRCh38 chr17: 45,281,618-45,282,204 , GRCh37.p13 chr17: 43,358,985-43,359,571 MAP3K14
    nsv5515948copy number variation1nstd206human GRCh38 chr17: 45,279,236-45,280,418 , GRCh37.p13 chr17: 43,356,603-43,357,785 MAP3K14
    nsv5423574mobile element insertion1nstd206human GRCh38 chr17: 45,306,348-45,306,399 , GRCh37.p13 chr17: 43,383,714-43,383,765 MAP3K14
    nsv5151107mobile element insertion1nstd203human GRCh38 chr17: 45,306,340-45,306,348 , GRCh37.p13 chr17: 43,383,706-43,383,714 MAP3K14
    nsv5149181mobile element insertion1nstd203human GRCh38 chr17: 45,306,339-45,306,348 , GRCh37.p13 chr17: 43,383,705-43,383,714 MAP3K14
    nsv5146032mobile element insertion1nstd203human GRCh38 chr17: 45,306,337-45,306,348 , GRCh37.p13 chr17: 43,383,703-43,383,714 MAP3K14
    nsv5144774mobile element insertion1nstd203human GRCh38 chr17: 45,306,338-45,306,347 , GRCh37.p13 chr17: 43,383,704-43,383,713 MAP3K14
    nsv5144503mobile element insertion1nstd203human GRCh38 chr17: 45,306,336-45,306,348 , GRCh37.p13 chr17: 43,383,702-43,383,714 MAP3K14
    nsv5140485mobile element insertion1nstd203human GRCh38 chr17: 45,306,333-45,306,348 , GRCh37.p13 chr17: 43,383,699-43,383,714 MAP3K14
    nsv5016574copy number variation1nstd200human GRCh38 chr17: 45,302,573-45,303,857 , GRCh37.p13 chr17: 43,379,939-43,381,223 MAP3K14
    nsv4867134copy number variation1nstd200human GRCh37 chr17: 43,379,939-43,381,224 , GRCh38.p12 chr17: 45,302,573-45,303,858 MAP3K14
    nsv4717685mobile element insertion1nstd186human GRCh37 chr17: 43,383,699-43,383,699 , GRCh38.p12 chr17: 45,306,333-45,306,333 MAP3K14
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