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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137115copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,467,726-29,044,717 , GRCh38.p12 chr16: 21,456,405-29,033,396 OTOAP1, GGA2, 148 more genes
    nsv7069781inversion1nstd229human GRCh38 chr16: 24,962,563-25,492,782 , GRCh37.p13 chr16: 24,973,884-25,504,103 CYCSP39, ARHGAP17, 13 more genes
    nsv7066307inversion1nstd229human GRCh38 chr16: 25,128,995-25,267,847 , GRCh37.p13 chr16: 25,140,316-25,279,168 AQP8, LCMT1, 3 more genes
    nsv6637633copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,576,803-30,177,240 , GRCh38.p12 chr16: 21,565,482-30,165,919 USP31, CA5AP1, 200 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
    nsv6290289copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,594,997-29,625,302 , GRCh38.p12 chr16: 21,583,676-29,613,981 LOC105371149, SLX1B, 166 more genes
    nsv6289847copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,530,207-29,332,245 , GRCh38.p12 chr16: 21,518,886-29,320,924 GAPDHP35, NSMCE1, 154 more genes
    nsv6133268copy number variation1nstd213human GRCh37 chr16: 22,710,000-32,010,001 , GRCh38.p12 chr16: 22,698,679-31,998,680 ALDOA, AQP8, 269 more genes
    nsv6133267copy number variation1nstd213human GRCh37 chr16: 22,710,000-30,200,001 , GRCh38.p12 chr16: 22,698,679-30,188,680 ALDOA, AQP8, 169 more genes
    nsv6133266copy number variation1nstd213human GRCh37 chr16: 22,710,000-26,360,001 , GRCh38.p12 chr16: 22,698,679-26,348,680 AQP8, NDUFAB1, 54 more genes
    nsv5003274copy number variation1nstd200human GRCh38 chr16: 25,144,704-25,146,666 , GRCh37.p13 chr16: 25,156,025-25,157,987 LCMT1-AS2, LCMT1
    nsv4850804copy number variation1nstd200human GRCh37 chr16: 25,156,025-25,157,987 , GRCh38.p12 chr16: 25,144,704-25,146,666 LCMT1, LCMT1-AS2
    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
    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
    nsv4675970copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,576,802-29,351,826 , GRCh38.p12 chr16: 21,565,481-29,340,505 NSMCE1, LOC105371149, 152 more genes
    nsv4577735mobile element insertion1nstd166human GRCh37.p13 chr16: 25,160,541-25,160,541 , GRCh38.p12 chr16: 25,149,220-25,149,220 LCMT1, LCMT1-AS2
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ABAT, ABCA3, 876 more genes
    nsv4322553inversion1nstd166human GRCh37.p13 chr16: 16,634,964-31,736,102 , GRCh38.p12 chr16: 16,541,107-31,724,781 , ALDOA, 403 more genes
    nsv4252352copy number variation1nstd166human GRCh37.p13 chr16: 25,156,026-25,157,987 , GRCh38.p12 chr16: 25,144,705-25,146,666 LCMT1, LCMT1-AS2
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