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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3884118copy number variation1nstd102humanLikely pathogenic GRCh38 chr16: 29,824,300-29,826,034 , GRCh37.p13 chr16: 29,835,621-29,837,355 MVP
    nsv7094781copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,825,262-29,830,230 , GRCh38.p12 chr16: 29,813,941-29,818,909 MVP, PAGR1, 1 more genes
    nsv3904555copy number variation2nstd102humanPathogenic GRCh37 chr16: 29,822,338-29,826,328 , GRCh38.p12 chr16: 29,811,017-29,815,007 PAGR1, MVP-DT, 2 more genes
    nsv3894591copy number variation1nstd102humanBenign GRCh37 chr16: 29,797,710-29,818,499 , GRCh38.p12 chr16: 29,786,389-29,807,178 LOC105371167, KIF22, 2 more genes
    nsv3905158copy number variation1nstd102humanUncertain significance GRCh37 chr16: 29,822,122-29,826,328 , GRCh38.p12 chr16: 29,810,801-29,815,007 MAZ, PAGR1, 2 more genes
    nsv3878346copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,824,376-29,916,286 , GRCh38 chr16: 29,813,055-29,904,965 MVP, CDIPT, 6 more genes
    nsv3905855copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,596,299-30,399,167 , GRCh38.p12 chr16: 21,584,978-30,387,846 MVP, LOC107984874, 217 more genes
    nsv3913702copy number variation1nstd102humanPathogenic NCBI36 chr16: 28,311,654-30,239,515 , GRCh37 chr16: 28,404,153-30,332,014 , GRCh38 chr16: 28,392,832-30,320,693 MVP, SPN, 94 more genes
    nsv6637500copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,466,731-30,321,320 , GRCh38.p12 chr16: 28,455,410-30,309,999 MVP, CA5AP1, 92 more genes
    nsv3915125copy number variation1nstd102humanPathogenic GRCh38 chr16: 28,456,967-30,295,107 , GRCh37 chr16: 28,468,288-30,306,428 , NCBI36 chr16: 28,375,789-30,213,929 MVP, SULT1A1, 92 more genes
    nsv3924589copy number variation1nstd102humanPathogenic NCBI36 chr16: 28,310,915-30,104,908 , GRCh37.p13 chr16: 28,403,414-30,197,407 , GRCh38.p12 chr16: 28,392,093-30,186,086 MVP, MIR4517, 86 more genes
    nsv3920951copy number variation1nstd102humanPathogenic NCBI36 chr16: 28,311,654-30,104,842 , GRCh37 chr16: 28,404,153-30,197,341 , GRCh38 chr16: 28,392,832-30,186,020 MVP, TBX6, 86 more genes
    nsv3907632copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,441,538-30,178,406 , GRCh38.p12 chr16: 28,430,217-30,167,085 MVP, LOC102723708, 82 more genes
    nsv4455909copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,466,730-30,191,848 , GRCh38.p12 chr16: 28,455,409-30,180,527 MVP, BOLA2, 82 more genes
    nsv4674913copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,466,730-30,178,406 , GRCh38.p12 chr16: 28,455,409-30,167,085 MVP, ATP2A1, 82 more genes
    nsv4455681copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,466,730-30,177,916 , GRCh38.p12 chr16: 28,455,409-30,166,595 MVP, SMG1P2, 82 more genes
    nsv3898101copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,486,693-30,197,290 , GRCh38.p12 chr16: 28,475,372-30,185,969 MVP, TAOK2, 83 more genes
    nsv3915205copy number variation1nstd102humanPathogenic NCBI36 chr16: 28,406,323-30,104,908 , GRCh37.p13 chr16: 28,498,822-30,197,407 , GRCh38.p12 chr16: 28,487,501-30,186,086 MVP, TMEM219, 83 more genes
    nsv4729918copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,488,319-30,178,406 , GRCh38.p12 chr16: 28,476,998-30,167,085 MVP, SEZ6L2, 81 more genes
    nsv3923420copy number variation1nstd102humanPathogenic NCBI36 chr16: 28,450,605-30,102,254 , GRCh37 chr16: 28,543,104-30,194,753 , GRCh38 chr16: 28,531,783-30,183,432 MVP, KCTD13, 80 more genes
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