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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv6112860mobile element insertion1nstd186human GRCh37 chr21: 16,352,947-16,352,998 , GRCh38.p12 chr21: 14,980,626-14,980,677 NRIP1
    nsv5978675insertion1nstd209human GRCh38 chr21: 14,980,613-14,980,613 , GRCh37.p13 chr21: 16,352,934-16,352,934 NRIP1
    nsv5965857copy number variation1nstd209human GRCh38 chr21: 14,377,888-22,678,896 , GRCh37.p13 chr21: 15,750,209-24,051,216 , LOC107985508, 80 more genes
    nsv5956294copy number variation1nstd209human GRCh38 chr21: 15,030,900-15,031,897 , GRCh37.p13 chr21: 16,403,221-16,404,218 NRIP1
    nsv5713099mobile element insertion1nstd211human GRCh38 chr21: 15,040,066-15,040,066 , GRCh37.p13 chr21: 16,412,387-16,412,387 NRIP1
    nsv5711607mobile element insertion1nstd211human GRCh38 chr21: 14,961,301-14,961,301 , GRCh37.p13 chr21: 16,333,622-16,333,622 NRIP1
    nsv5711035mobile element insertion1nstd211human GRCh38 chr21: 15,013,908-15,013,908 , GRCh37.p13 chr21: 16,386,229-16,386,229 NRIP1
    nsv5708837mobile element insertion2nstd211human GRCh38 chr21: 14,980,626-14,980,626 , GRCh37.p13 chr21: 16,352,947-16,352,947 NRIP1
    nsv5699512mobile element insertion2nstd211human GRCh38 chr21: 14,962,843-14,962,843 , GRCh37.p13 chr21: 16,335,164-16,335,164 NRIP1
    nsv5672399insertion1nstd207human GRCh38 chr21: 15,030,864-15,030,864 , GRCh37.p13 chr21: 16,403,185-16,403,185 NRIP1
    nsv5671672insertion1nstd207human GRCh38 chr21: 14,980,613-14,980,613 , GRCh37.p13 chr21: 16,352,934-16,352,934 NRIP1
    nsv5669749insertion1nstd207human GRCh38 chr21: 15,031,026-15,031,026 , GRCh37.p13 chr21: 16,403,347-16,403,347 NRIP1
    nsv5668292insertion1nstd207human GRCh38 chr21: 15,031,398-15,031,398 , GRCh37.p13 chr21: 16,403,719-16,403,719 NRIP1
    nsv5667899insertion1nstd207human GRCh38 chr21: 15,030,991-15,030,991 , GRCh37.p13 chr21: 16,403,312-16,403,312 NRIP1
    nsv5666120insertion1nstd207human GRCh38 chr21: 14,962,829-14,962,829 , GRCh37.p13 chr21: 16,335,150-16,335,150 NRIP1
    nsv5665875insertion3nstd207human GRCh38 chr21: 15,031,103-15,031,103 , GRCh37.p13 chr21: 16,403,424-16,403,424 NRIP1
    nsv5664957insertion1nstd207human GRCh38 chr21: 15,031,348-15,031,348 , GRCh37.p13 chr21: 16,403,669-16,403,669 NRIP1
    nsv5599496copy number variation1nstd207human GRCh38 chr21: 15,030,891-15,030,940 , GRCh37.p13 chr21: 16,403,212-16,403,261 NRIP1
    nsv5592516copy number variation1nstd207human GRCh38 chr21: 15,031,053-15,031,102 , GRCh37.p13 chr21: 16,403,374-16,403,423 NRIP1
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