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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
    nsv6961537copy number variation1nstd229human GRCh38 chr16: 9,451,264-9,470,825 , GRCh37.p13 chr16: 9,545,121-9,564,682 LINC01195, 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
    nsv6509931copy number variation1nstd223human GRCh38 chr16: 9,446,433-9,451,323 , GRCh37.p13 chr16: 9,540,290-9,545,180 LINC01195, LOC101927026
    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
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 NPIPB9, TMEM219, 597 more genes
    nsv4729614copy number variation1nstd102humanUncertain significance GRCh37 chr16: 8,899,460-10,058,650 , GRCh38.p12 chr16: 8,805,603-9,964,793 CARHSP1, PMM2, 15 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 LOC105371069, PKD1P6-NPIPP1, 654 more genes
    nsv4681568copy number variation2nstd102humanUncertain significance GRCh37 chr16: 8,829,577-10,274,288 , GRCh38.p12 chr16: 8,735,720-10,180,431 LOC105371075, LOC100130283, 20 more genes
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ABAT, ABCA3, 876 more genes
    nsv4350523copy number variation1nstd102humanPathogenic GRCh37 chr16: 8,839,796-9,728,670 , GRCh38.p12 chr16: 8,745,939-9,634,813 LOC105371075, RPL21P119, 15 more genes
    nsv4324333inversion1nstd166human GRCh38.p12 chr16: 9,267,619-9,594,863 , GRCh37.p13 chr16: 9,361,476-9,688,720 LINC02177, LOC101927026, 4 more genes
    nsv4246645copy number variation1nstd166human GRCh37.p13 chr16: 9,488,452-9,539,196 , GRCh38.p12 chr16: 9,394,595-9,445,339 LINC02177, LINC01195, 2 more genes
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