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Items: 1 to 20 of 91

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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
    nsv7077002inversion1nstd229human GRCh38 chr16: 11,269,651-11,289,252 , GRCh37.p13 chr16: 11,363,508-11,383,109 PRM1, TNP2, 3 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
    nsv7073432inversion1nstd229human GRCh38 chr16: 11,269,618-11,287,265 , GRCh37.p13 chr16: 11,363,475-11,381,122 LOC105371082, TNP2, 3 more genes
    nsv6970966copy number variation1nstd229human GRCh38 chr16: 11,267,700-11,273,424 , GRCh37.p13 chr16: 11,361,557-11,367,281 PRM3, LOC105371082, 1 more genes
    nsv6967604copy number variation1nstd229human GRCh38 chr16: 11,273,381-11,275,392 , GRCh37.p13 chr16: 11,367,238-11,369,249 PRM2, PRM3, 1 more genes
    nsv6964361copy number variation1nstd229human GRCh38 chr16: 11,273,456-11,273,585 , GRCh37.p13 chr16: 11,367,313-11,367,442 PRM3, LOC105371082
    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
    nsv6637308copy number variation1nstd102humanUncertain significance GRCh37 chr16: 10,423,631-12,176,517 , GRCh38.p12 chr16: 10,329,774-12,082,660 LOC400499, RSL1D1, 46 more genes
    nsv6593519inversion1nstd223human GRCh38 chr16: 11,269,617-11,287,264 , GRCh37.p13 chr16: 11,363,474-11,381,121 PRM1, PRM2, 3 more genes
    nsv6507343copy number variation1nstd223human GRCh38 chr16: 10,144,159-11,379,723 , GRCh37.p13 chr16: 10,238,016-11,473,580 LINC01290, LOC105371078, 35 more genes
    nsv6500831copy number variation1nstd223human GRCh38 chr16: 10,669,159-11,475,479 , GRCh37.p13 chr16: 10,763,016-11,569,335 MTCYBP33, MTND4LP24, 27 more genes
    nsv6313996copy number variation1nstd102humanUncertain significance GRCh37 chr16: 11,364,838-13,592,668 , GRCh38.p12 chr16: 11,270,981-13,498,811 LOC100420951, RSL1D1-DT, 36 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
    nsv6133171copy number variation1nstd213human GRCh37 chr16: 10,820,000-11,690,001 , GRCh38.p12 chr16: 10,726,143-11,596,145 CIITA, NUBP1, 21 more genes
    nsv6132975copy number variation1nstd213human GRCh37 chr16: 11,330,000-11,460,001 , GRCh38.p12 chr16: 11,236,143-11,366,144 PRM1, PRM2, 8 more genes
    nsv5319930copy number variation1nstd204human GRCh37.p13 chr16: 11,367,234-11,369,251 , GRCh38.p13 chr16: 11,273,377-11,275,394 PRM2, PRM3, 1 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
    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
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