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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5884300copy number variation1nstd209human GRCh38 chr16: 85,738,362-85,740,611 , GRCh37.p13 chr16: 85,771,968-85,774,217 C16orf74, MIR1910
    nsv5530601copy number variation1nstd206human GRCh38 chr16: 85,732,492-85,758,503 , GRCh37.p13 chr16: 85,766,098-85,792,109 MIR1910, C16orf74
    nsv5523948copy number variation1nstd206human GRCh38 chr16: 85,740,055-85,740,547 , GRCh37.p13 chr16: 85,773,661-85,774,153 MIR1910, C16orf74
    nsv5292274copy number variation1nstd204human GRCh38.p13 chr16: 85,732,401-85,748,600 , GRCh37.p13 chr16: 85,766,007-85,782,206 MIR1910, C16orf74
    nsv5009971copy number variation1nstd200human GRCh38 chr16: 85,740,527-85,764,300 , GRCh37.p13 chr16: 85,774,133-85,797,906 MIR1910, C16orf74
    nsv5009970copy number variation1nstd200human GRCh38 chr16: 85,739,949-85,743,824 , GRCh37.p13 chr16: 85,773,555-85,777,430 C16orf74, MIR1910
    nsv5009969copy number variation1nstd200human GRCh38 chr16: 85,732,492-85,758,512 , GRCh37.p13 chr16: 85,766,098-85,792,118 C16orf74, MIR1910
    nsv4907300mobile element deletion1nstd200human GRCh38 chr16: 85,739,926-85,740,237 , GRCh37.p13 chr16: 85,773,532-85,773,843 C16orf74, MIR1910
    nsv4850884copy number variation1nstd200human GRCh37 chr16: 85,774,150-85,797,891 , GRCh38.p12 chr16: 85,740,544-85,764,285 MIR1910, C16orf74
    nsv4850883copy number variation1nstd200human GRCh37 chr16: 85,773,555-85,777,431 , GRCh38.p12 chr16: 85,739,949-85,743,825 MIR1910, C16orf74
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4685927copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 83,931,797-86,285,776 , GRCh38.p12 chr16: 83,898,192-86,252,170 COX4I1, IRF8, 57 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4676041copy number variation1nstd102humanUncertain significance GRCh37 chr16: 84,815,936-86,045,285 , GRCh38.p12 chr16: 84,782,330-86,011,679 LINC00311, ZDHHC7, 30 more genes
    nsv4674955copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,872,102-87,678,641 , GRCh38.p12 chr16: 84,838,496-87,645,035 RPL7AP63, LOC105371388, 62 more genes
    nsv4623149copy number variation1nstd183human GRCh37 chr16: 85,728,511-85,805,717 , GRCh38.p12 chr16: 85,694,905-85,772,111 MIR1910, C16orf74
    nsv4457091copy number variation1nstd102humanUncertain significance GRCh37 chr16: 85,038,804-85,876,297 , GRCh38.p12 chr16: 85,005,198-85,842,691 MIR12128, ZDHHC7, 21 more genes
    nsv4455298copy number variation1nstd102humanUncertain significance GRCh37 chr16: 85,746,644-85,847,401 , GRCh38.p12 chr16: 85,713,038-85,813,795 LOC100422319, COX4I1, 5 more genes
    nsv4436581complex substitution1nstd102humanUncertain significance GRCh38.p12 chr16: 56,334,777-90,074,947 , GRCh37 chr16: 56,368,689-90,141,355 AARS1, AP1G1, 662 more genes
    nsv4379629copy number variation1nstd173human GRCh37 chr16: 83,892,715-85,792,443 , GRCh38.p12 chr16: 83,859,110-85,758,837 , MIR1910, 45 more genes
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