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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
    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
    nsv6512130copy number variation1nstd223human GRCh38 chr16: 11,261,523-11,266,053 , GRCh37.p13 chr16: 11,355,380-11,359,910 TNP2, LOC105371082
    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
    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
    nsv5933304copy number variation1nstd209human GRCh38 chr16: 11,261,516-11,266,057 , GRCh37.p13 chr16: 11,355,373-11,359,914 TNP2, LOC105371082
    nsv5885611copy number variation1nstd209human GRCh38 chr16: 11,261,457-11,265,956 , GRCh37.p13 chr16: 11,355,314-11,359,813 TNP2, LOC105371082
    nsv5537655insertion1nstd206human GRCh38 chr16: 11,269,253-11,269,253 , GRCh37.p13 chr16: 11,363,110-11,363,110 LOC105371082, TNP2
    nsv5365516translocation1nstd200human GRCh38 chr16: 11,269,651-11,269,651 , GRCh38 chr16: 11,289,252-11,289,252 , GRCh37.p13 chr16: 11,363,508-11,363,508 , GRCh37.p13 chr16: 11,383,109-11,383,109 TNP2, LOC105371082
    nsv5336166translocation1nstd200human GRCh37 chr16: 11,383,109-11,383,109 , GRCh37 chr16: 11,363,508-11,363,508 , GRCh38.p12 chr16: 11,269,651-11,269,651 , GRCh38.p12 chr16: 11,289,252-11,289,252 LOC105371082, TNP2
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