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Items: 1 to 20 of 214

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5881195copy number variation1nstd209human GRCh38 chr16: 87,282,769-87,296,424 , GRCh37.p13 chr16: 87,316,375-87,330,030 LOC101928682
    nsv5529243copy number variation1nstd206human GRCh38 chr16: 87,270,753-87,285,988 , GRCh37.p13 chr16: 87,304,359-87,319,594 LOC101928682
    nsv5517301copy number variation1nstd206human GRCh38 chr16: 87,282,559-87,301,087 , GRCh37.p13 chr16: 87,316,165-87,334,693 LOC101928682, C16orf95
    nsv5517295copy number variation1nstd206human GRCh38 chr16: 87,224,799-87,289,634 , GRCh37.p13 chr16: 87,258,405-87,323,240 LOC101928682, RPL39P30, 1 more genes
    nsv5014936copy number variation1nstd200human GRCh38 chr16: 87,282,588-87,301,059 , GRCh37.p13 chr16: 87,316,194-87,334,665 LOC101928682, C16orf95
    nsv5014935copy number variation1nstd200human GRCh38 chr16: 87,282,430-87,309,914 , GRCh37.p13 chr16: 87,316,036-87,343,520 LOC101928682, C16orf95
    nsv5014933copy number variation1nstd200human GRCh38 chr16: 87,254,342-87,277,569 , GRCh37.p13 chr16: 87,287,948-87,311,175 RPL39P30, LOC101928682
    nsv5013533copy number variation1nstd200human GRCh38 chr16: 87,250,972-87,305,156 , GRCh37.p13 chr16: 87,284,578-87,338,762 LOC101928682, C16orf95, 1 more genes
    nsv4850934copy number variation1nstd200human GRCh37 chr16: 87,316,036-87,343,520 , GRCh38.p12 chr16: 87,282,430-87,309,914 C16orf95, LOC101928682
    nsv4850933copy number variation1nstd200human GRCh37 chr16: 87,287,948-87,311,175 , GRCh38.p12 chr16: 87,254,342-87,277,569 LOC101928682, RPL39P30
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729902copy number variation1nstd102humanLikely benign GRCh37 chr16: 87,284,960-87,345,335 , GRCh38.p12 chr16: 87,251,354-87,311,729 RPL39P30, LOC101928682, 1 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
    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
    nsv4508261mobile element insertion1nstd166human GRCh37.p13 chr16: 87,315,685-87,315,685 , GRCh38.p12 chr16: 87,282,079-87,282,079 LOC101928682
    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
    nsv4427594copy number variation1nstd174human GRCh37 chr16: 87,252,185-87,345,335 , GRCh38.p12 chr16: 87,218,579-87,311,729 C16orf95, RPL39P30, 2 more genes
    nsv4388039copy number variation1nstd173human GRCh37 chr16: 87,051,764-87,467,555 , GRCh38.p12 chr16: 87,018,158-87,433,949 , LINC02181, 10 more genes
    nsv4371753copy number variation1nstd173human GRCh37 chr16: 87,284,961-87,340,333 , GRCh38.p12 chr16: 87,251,355-87,306,727 C16orf95, LOC101928682, 1 more genes
    nsv4368066copy number variation1nstd173human GRCh37 chr16: 87,281,025-87,306,895 , GRCh38.p12 chr16: 87,247,419-87,273,289 RPL39P30, LOC101928682
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