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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5931453copy number variation1nstd209human GRCh38 chr15: 65,181,027-65,183,288 , GRCh37.p13 chr15: 65,473,365-65,475,626 CLPX
    nsv5855892copy number variation1nstd209human GRCh38 chr15: 65,166,375-65,170,182 , GRCh37.p13 chr15: 65,458,713-65,462,520 CLPX
    nsv5697244mobile element insertion2nstd211human GRCh38 chr15: 65,151,480-65,151,480 , GRCh37.p13 chr15: 65,443,818-65,443,818 CLPX
    nsv5525876copy number variation1nstd206human GRCh38 chr15: 65,169,651-65,171,360 , GRCh37.p13 chr15: 65,461,989-65,463,698 CLPX
    nsv5517360copy number variation1nstd206human GRCh38 chr15: 65,167,761-65,168,260 , GRCh37.p13 chr15: 65,460,099-65,460,598 CLPX
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5155496mobile element insertion1nstd203human GRCh38 chr15: 65,167,461-65,167,482 , GRCh37.p13 chr15: 65,459,799-65,459,820 CLPX
    nsv5152112mobile element insertion1nstd203human GRCh38 chr15: 65,178,642-65,178,656 , GRCh37.p13 chr15: 65,470,980-65,470,994 CLPX
    nsv4992027copy number variation1nstd200human GRCh38 chr15: 65,169,908-65,170,025 , GRCh37.p13 chr15: 65,462,246-65,462,363 CLPX
    nsv4992026copy number variation1nstd200human GRCh38 chr15: 65,169,651-65,171,360 , GRCh37.p13 chr15: 65,461,989-65,463,698 CLPX
    nsv4992025copy number variation1nstd200human GRCh38 chr15: 65,152,133-65,154,405 , GRCh37.p13 chr15: 65,444,471-65,446,743 CLPX
    nsv4849856copy number variation1nstd200human GRCh37 chr15: 65,463,367-65,464,509 , GRCh38.p12 chr15: 65,171,029-65,172,171 CLPX
    nsv4849855copy number variation1nstd200human GRCh37 chr15: 65,462,246-65,462,363 , GRCh38.p12 chr15: 65,169,908-65,170,025 CLPX
    nsv4849854copy number variation1nstd200human GRCh37 chr15: 65,461,989-65,463,698 , GRCh38.p12 chr15: 65,169,651-65,171,360 CLPX
    nsv4849853copy number variation1nstd200human GRCh37 chr15: 65,444,471-65,446,743 , GRCh38.p12 chr15: 65,152,133-65,154,405 CLPX
    nsv4671999copy number variation1nstd186human GRCh37 chr15: 65,461,989-65,463,698 , GRCh38.p12 chr15: 65,169,651-65,171,360 CLPX
    nsv4626198copy number variation1nstd183human GRCh37 chr15: 65,461,989-65,463,698 , GRCh38.p12 chr15: 65,169,651-65,171,360 CLPX
    nsv4513528mobile element insertion1nstd166human GRCh37.p13 chr15: 65,443,117-65,443,117 , GRCh38.p12 chr15: 65,150,779-65,150,779 CLPX
    nsv4456887copy number variation1nstd102humanUncertain significance GRCh37 chr15: 65,258,583-65,742,148 , GRCh38.p12 chr15: 64,966,242-65,449,810 KBTBD13, SLC51B, 16 more genes
    nsv4456541copy number variation1nstd102humanUncertain significance GRCh37 chr15: 65,258,439-65,742,148 , GRCh38.p12 chr15: 64,966,098-65,449,810 CILP, SNORA24B, 16 more genes
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