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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112663copy number variation1nstd102humanUncertain significance GRCh38 chr16: 28,812,342-29,035,950 , GRCh37.p13 chr16: 28,823,663-29,047,271 CD19, MIR4517, 12 more genes
    nsv5673078copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,488,827-28,950,294 , GRCh38.p12 chr16: 28,477,506-28,938,973 SH2B1, NUPR1, 21 more genes
    nsv5672755copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 28,668,059-29,001,338 , GRCh38.p12 chr16: 28,656,738-28,990,017 ATP2A1, CD19, 17 more genes
    nsv5516867copy number variation1nstd206human GRCh38 chr16: 28,825,502-28,825,555 , GRCh37.p13 chr16: 28,836,823-28,836,876 ATXN2L
    nsv5279319copy number variation1nstd204human GRCh38.p13 chr16: 28,825,214-28,829,762 , GRCh37.p13 chr16: 28,836,535-28,841,083 ATXN2L
    nsv5274392copy number variation1nstd204human GRCh38.p13 chr16: 28,830,363-28,831,379 , GRCh37.p13 chr16: 28,841,684-28,842,700 ATXN2L
    nsv5270825copy number variation1nstd204human GRCh38.p13 chr16: 28,833,418-28,834,953 , GRCh37.p13 chr16: 28,844,739-28,846,274 ATXN2L
    nsv5269278copy number variation1nstd204human GRCh38.p13 chr16: 28,828,363-28,829,762 , GRCh37.p13 chr16: 28,839,684-28,841,083 ATXN2L
    nsv5264142copy number variation1nstd204human GRCh38.p13 chr16: 28,814,740-28,843,602 , GRCh37.p13 chr16: 28,826,061-28,854,923 TUFM, RPS15AP33, 2 more genes
    nsv5200383copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,615,644-29,042,118 , GRCh38.p12 chr16: 28,604,323-29,030,797 RPS15AP33, ATP2A1-AS1, 19 more genes
    nsv5141345mobile element insertion1nstd203human GRCh38 chr16: 28,822,458-28,822,467 , GRCh37.p13 chr16: 28,833,779-28,833,788 ATXN2L
    nsv4769395copy number variation1nstd102humanUncertain significance GRCh37 chr16: 28,483,631-29,332,591 , GRCh38.p12 chr16: 28,472,310-29,321,270 MIR4517, SULT1A1, 33 more genes
    nsv4730105inversion12nstd198human GRCh38 chr16: 28,339,079-28,822,601 , GRCh37.p13 chr16: 28,350,400-28,833,922 , CLN3, 22 more genes
    nsv4729970copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,819,028-28,988,225 , GRCh38.p12 chr16: 28,807,707-28,976,904 ATXN2L, NFATC2IP, 10 more genes
    nsv4729918copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,488,319-30,178,406 , GRCh38.p12 chr16: 28,476,998-30,167,085 SEZ6L2, C16orf92, 81 more genes
    nsv4729912copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,336,673-29,358,712 , GRCh38.p12 chr16: 28,325,352-29,347,391 ATP2A1-AS1, NPIPB8, 38 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
    nsv4729758copy number variation1nstd102humanUncertain significance GRCh37 chr16: 28,819,028-28,976,572 , GRCh38.p12 chr16: 28,807,707-28,965,251 MIR4517, SH2B1, 9 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
    nsv4685761copy number variation1nstd102humannot provided GRCh37 chr16: 21,312,200-29,646,379 , GRCh38.p12 chr16: 21,300,879-29,635,058 NUPR1, TNRC6A, 176 more genes
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