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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094607copy number variation1nstd102humanUncertain significance GRCh37 chr16: 8,829,597-11,683,693 , GRCh38.p12 chr16: 8,735,740-11,589,837 LOC400499, NUBP1, 58 more genes
    nsv7076079inversion1nstd229human GRCh38 chr16: 9,015,595-14,846,246 , GRCh37.p13 chr16: 9,109,452-14,940,103 LOC105371093, RNU6-633P, 100 more genes
    nsv7067669inversion1nstd229human GRCh38 chr16: 9,267,619-9,594,862 , GRCh37.p13 chr16: 9,361,476-9,688,719 LINC01195, LOC105371075, 4 more genes
    nsv6977077copy number variation1nstd229human GRCh38 chr16: 9,439,564-9,448,216 , GRCh37.p13 chr16: 9,533,421-9,542,073 LOC101927026, LINC01177, 1 more genes
    nsv6975220copy number variation1nstd229human GRCh38 chr16: 9,437,401-9,440,200 , GRCh37.p13 chr16: 9,531,258-9,534,057 LINC01177, LOC101927026
    nsv6970047copy number variation1nstd229human GRCh38 chr16: 9,438,148-9,441,160 , GRCh37.p13 chr16: 9,532,005-9,535,017 LOC101927026, LINC01177
    nsv6963477copy number variation1nstd229human GRCh38 chr16: 9,430,611-9,442,618 , GRCh37.p13 chr16: 9,524,468-9,536,475 LINC01177, LOC101927026
    nsv6961048copy number variation1nstd229human GRCh38 chr16: 9,394,649-9,445,340 , GRCh37.p13 chr16: 9,488,506-9,539,197 LINC01177, LOC101927026, 2 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    nsv6590142inversion1nstd223human GRCh38 chr16: 9,267,620-9,594,861 , GRCh37.p13 chr16: 9,361,477-9,688,718 LINC02177, LOC101927026, 4 more genes
    nsv6497448copy number variation1nstd223human GRCh38 chr16: 9,437,338-9,440,242 , GRCh37.p13 chr16: 9,531,195-9,534,099 LOC101927026, LINC01177
    nsv6315499copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 5,381,584-10,067,952 , GRCh38.p12 chr16: 5,331,583-9,974,095 ABAT, GRIN2A, 35 more genes
    nsv6309886copy number variation2nstd102humanUncertain significance GRCh37 chr16: 8,829,597-11,650,586 , GRCh38.p12 chr16: 8,735,740-11,556,730 NUBP1, TVP23A, 58 more genes
    nsv6133278copy number variation2nstd213human GRCh37 chr16: 60,000-14,990,001 , GRCh38.p12 chr16: 10,001-14,896,144 , ABAT, 446 more genes
    nsv6031466copy number variation1nstd212human GRCh38 chr16: 9,440,740-9,440,864 , GRCh37.p13 chr16: 9,534,597-9,534,721 LINC01177, LOC101927026
    nsv5516596copy number variation1nstd206human GRCh38 chr16: 9,437,338-9,440,242 , GRCh37.p13 chr16: 9,531,195-9,534,099 LOC101927026, LINC01177
    nsv4992628copy number variation1nstd200human GRCh38 chr16: 9,437,338-9,440,242 , GRCh37.p13 chr16: 9,531,195-9,534,099 LINC01177, LOC101927026
    nsv4992627copy number variation1nstd200human GRCh38 chr16: 9,430,610-9,442,617 , GRCh37.p13 chr16: 9,524,467-9,536,474 LINC01177, LOC101927026
    nsv4850349copy number variation1nstd200human GRCh37 chr16: 9,531,195-9,534,099 , GRCh38.p12 chr16: 9,437,338-9,440,242 LOC101927026, LINC01177
    nsv4850348copy number variation1nstd200human GRCh37 chr16: 9,524,467-9,536,474 , GRCh38.p12 chr16: 9,430,610-9,442,617 LINC01177, LOC101927026
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