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Items: 1 to 20 of 188

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6995012copy number variation1nstd229human GRCh38 chr16: 85,794,601-85,834,000 , GRCh37.p13 chr16: 85,828,207-85,867,606 LOC100422319, RPL10AP12, 2 more genes
    nsv6985285copy number variation1nstd229human GRCh38 chr16: 85,800,038-85,800,081 , GRCh37.p13 chr16: 85,833,644-85,833,687 COX4I1, EMC8
    nsv6979927copy number variation1nstd229human GRCh38 chr16: 85,784,117-85,788,317 , GRCh37.p13 chr16: 85,817,723-85,821,923 EMC8
    nsv6634465copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 71,610,276-90,354,753 , GRCh38.p12 chr16: 71,576,373-90,228,345 AP1G1, AFG3L1P, 349 more genes
    nsv6590742inversion1nstd223human GRCh38 chr16: 83,952,013-85,834,110 , GRCh37.p13 chr16: 83,985,618-85,867,716 LOC101928502, LOC105371382, 47 more genes
    nsv6513909copy number variation1nstd223human GRCh38 chr16: 85,784,117-85,788,320 , GRCh37.p13 chr16: 85,817,723-85,821,926 EMC8
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6290331copy number variation1nstd102humanPathogenic GRCh37 chr16: 80,386,595-90,163,348 , GRCh38.p12 chr16: 80,352,698-90,096,940 GINS2, TCF25, 220 more genes
    nsv6197143copy number variation1nstd214human GRCh38 chr16: 85,795,047-85,795,096 , GRCh37.p13 chr16: 85,828,653-85,828,702 EMC8
    nsv6133286copy number variation1nstd213human GRCh37 chr16: 85,640,000-86,830,001 , GRCh38.p12 chr16: 85,606,394-86,796,395 COX4I1, FOXF1, 32 more genes
    nsv6133284copy number variation1nstd213human GRCh37 chr16: 84,740,000-85,940,001 , GRCh38.p12 chr16: 84,706,394-85,906,395 COX4I1, IRF8, 28 more genes
    nsv6133214copy number variation1nstd213human GRCh37 chr16: 85,100,000-90,290,001 , GRCh38.p12 chr16: 85,066,394-90,223,593 AFG3L1P, APRT, 156 more genes
    nsv6133210copy number variation1nstd213human GRCh37 chr16: 78,970,000-88,180,001 , GRCh38.p12 chr16: 78,936,103-88,146,395 , CA5A, 152 more genes
    nsv5876966copy number variation1nstd209human GRCh38 chr16: 85,774,952-85,776,746 , GRCh37.p13 chr16: 85,808,558-85,810,352 EMC8
    nsv5593150copy number variation1nstd207human GRCh38 chr16: 85,795,047-85,795,096 , GRCh37.p13 chr16: 85,828,653-85,828,702 EMC8
    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
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