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Items: 1 to 20 of 110

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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
    nsv6974079copy number variation1nstd229human GRCh38 chr16: 11,341,754-11,345,822 , GRCh37.p13 chr16: 11,435,611-11,439,679 RMI2, LOC105371083, 1 more genes
    nsv6970456copy number variation1nstd229human GRCh38 chr16: 11,340,626-11,346,627 , GRCh37.p13 chr16: 11,434,483-11,440,484 RMI2, LOC105371083, 1 more genes
    nsv6967854copy number variation1nstd229human GRCh38 chr16: 11,337,159-11,397,452 , GRCh37.p13 chr16: 11,431,016-11,491,309 LOC400499, RMI2, 3 more genes
    nsv6964300copy number variation1nstd229human GRCh38 chr16: 11,329,655-11,611,891 , GRCh37.p13 chr16: 11,423,512-11,705,747 LOC400499, LOC100420951, 5 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
    nsv6623312copy number variation1nstd224human GRCh37 chr16: 11,431,919-13,207,154 , GRCh38.p12 chr16: 11,338,062-13,113,297 TNFRSF17, RSL1D1, 29 more genes
    nsv6507863copy number variation1nstd223human GRCh38 chr16: 11,338,312-11,450,114 , GRCh37.p13 chr16: 11,432,169-11,543,970 LOC100420951, LOC400499, 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
    nsv6499508copy number variation1nstd223human GRCh38 chr16: 11,334,717-11,341,295 , GRCh37.p13 chr16: 11,428,574-11,435,152 LOC105371083, LOC105371082
    nsv6496314copy number variation1nstd223human GRCh38 chr16: 11,340,601-11,383,453 , GRCh37.p13 chr16: 11,434,458-11,477,310 LOC105371082, LOC100420951, 3 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
    nsv6132976copy number variation1nstd213human GRCh37 chr16: 11,430,000-11,590,001 , GRCh38.p12 chr16: 11,336,143-11,496,145 RMI2, LOC400499, 4 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
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