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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
    nsv5972984inversion1nstd209human GRCh38 chr21: 36,987,387-36,987,604 , GRCh37.p13 chr21: 38,359,687-38,359,904 HLCS
    nsv5969909insertion1nstd209human GRCh38 chr21: 36,868,274-36,868,274 , GRCh37.p13 chr21: 38,240,574-38,240,574 HLCS
    nsv5967366copy number variation1nstd209human GRCh38 chr21: 36,778,971-36,785,478 , GRCh37.p13 chr21: 38,151,272-38,157,779 HLCS
    nsv5966611copy number variation1nstd209human GRCh38 chr21: 36,843,226-36,843,792 , GRCh37.p13 chr21: 38,215,526-38,216,092 HLCS
    nsv5965932copy number variation1nstd209human GRCh38 chr21: 36,959,544-36,962,756 , GRCh37.p13 chr21: 38,331,844-38,335,056 HLCS
    nsv5954882copy number variation1nstd209human GRCh38 chr21: 36,915,723-36,915,787 , GRCh37.p13 chr21: 38,288,023-38,288,087 HLCS
    nsv5954067copy number variation1nstd209human GRCh38 chr21: 36,956,654-36,957,850 , GRCh37.p13 chr21: 38,328,954-38,330,150 HLCS
    nsv5953346copy number variation1nstd209human GRCh38 chr21: 36,987,402-36,989,487 , GRCh37.p13 chr21: 38,359,702-38,361,787 HLCS
    nsv5949967copy number variation1nstd209human GRCh38 chr21: 36,967,775-36,968,074 , GRCh37.p13 chr21: 38,340,075-38,340,374 HLCS
    nsv5881564copy number variation1nstd209human GRCh38 chr21: 36,842,974-36,843,996 , GRCh37.p13 chr21: 38,215,274-38,216,296 HLCS
    nsv5881092copy number variation1nstd209human GRCh38 chr21: 36,987,589-36,989,420 , GRCh37.p13 chr21: 38,359,889-38,361,720 HLCS
    nsv5870517copy number variation1nstd209human GRCh38 chr21: 36,959,569-36,962,568 , GRCh37.p13 chr21: 38,331,869-38,334,868 HLCS
    nsv5695436mobile element insertion1nstd211human GRCh38 chr21: 36,856,257-36,856,257 , GRCh37.p13 chr21: 38,228,557-38,228,557 HLCS
    nsv5673337copy number variation1nstd102humanPathogenic GRCh37 chr21: 38,302,541-38,311,304 , GRCh38.p12 chr21: 36,930,241-36,939,004 HLCS
    nsv5673267copy number variation1nstd102humanPathogenic GRCh37 chr21: 38,269,140-38,311,203 , GRCh38.p12 chr21: 36,896,840-36,938,903 HLCS
    nsv5673266copy number variation1nstd102humanPathogenic GRCh37 chr21: 38,269,140-38,269,451 , GRCh38.p12 chr21: 36,896,840-36,897,151 HLCS
    nsv5673264copy number variation1nstd102humanLikely pathogenic GRCh37 chr21: 38,129,038-38,129,112 , GRCh38 chr21: 36,756,737-36,756,811 HLCS
    nsv5669736insertion1nstd207human GRCh38 chr21: 36,967,548-36,967,548 , GRCh37.p13 chr21: 38,339,848-38,339,848 HLCS
    nsv5603962copy number variation1nstd207human GRCh38 chr21: 36,778,971-36,785,478 , GRCh37.p13 chr21: 38,151,272-38,157,779 HLCS
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