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Items: 1 to 20 of 809

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5301051copy number variation1nstd204human GRCh38.p13 chr16: 31,854,272-34,660,717 , GRCh37.p13 chr16: 31,865,593-34,023,151 , BCAP31P2, 80 more genes
    nsv5279555copy number variation1nstd204human GRCh38.p13 chr16: 32,244,001-32,261,400 , GRCh37.p13 chr16: 32,255,322-32,272,721 TP53TG3D
    nsv5279295copy number variation1nstd204human GRCh38.p13 chr16: 32,237,501-32,261,400 , GRCh37.p13 chr16: 32,248,822-32,272,721 TP53TG3D
    nsv5270976copy number variation1nstd204human GRCh38.p13 chr16: 32,241,201-32,262,900 , GRCh37.p13 chr16: 32,252,522-32,274,221 LOC100507221, TP53TG3D
    nsv5263220copy number variation1nstd204human GRCh38.p13 chr16: 32,246,101-32,255,000 , GRCh37.p13 chr16: 32,257,422-32,266,321 TP53TG3D
    nsv5260977copy number variation1nstd204human GRCh38.p13 chr16: 32,248,601-32,258,300 , GRCh37.p13 chr16: 32,259,922-32,269,621 TP53TG3D
    nsv4994635copy number variation1nstd200human GRCh38 chr16: 32,085,579-33,029,092 , GRCh37.p13 chr16: 32,096,900-33,040,413 IGHV2OR16-5, ABHD17AP7, 27 more genes
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 LOC105371069, PKD1P6-NPIPP1, 654 more genes
    nsv4680918copy number variation1nstd189human GRCh37.p13 chr16: 32,058,496-33,631,830 , GRCh38.p12 chr16: 32,047,175-33,829,363 TP53TG3, ABCD1P3, 52 more genes
    nsv4680863copy number variation8nstd189human GRCh37.p13 chr16: 32,146,887-33,631,830 , GRCh38.p12 chr16: 32,135,566-33,829,363 TP53TG3, ABCD1P3, 48 more genes
    nsv4680862copy number variation1nstd189human GRCh37.p13 chr16: 32,124,332-33,612,905 , GRCh38.p12 chr16: 32,113,011-33,810,438 TP53TG3, ABCD1P3, 48 more genes
    nsv4680805copy number variation1nstd189human GRCh37.p13 chr16: 32,124,332-33,681,101 , GRCh38.p12 chr16: 32,113,011-33,878,634 TP53TG3, ABCD1P3, 51 more genes
    nsv4680782copy number variation1nstd189human GRCh37.p13 chr16: 32,033,387-33,631,830 , GRCh38.p12 chr16: 32,022,066-33,829,363 TP53TG3, ABCD1P3, 53 more genes
    nsv4680760copy number variation1nstd189human GRCh37.p13 chr16: 32,113,683-33,864,359 , GRCh38.p12 chr16: 32,102,362-34,061,892 TP53TG3, ABCD1P3, 57 more genes
    nsv4680745copy number variation1nstd189human GRCh37.p13 chr16: 32,244,474-33,776,085 , GRCh38.p12 chr16: 32,233,153-33,973,618 TP53TG3, ABCD1P3, 52 more genes
    nsv4680646copy number variation1nstd189human GRCh37.p13 chr16: 32,146,887-33,667,812 , GRCh38.p12 chr16: 32,135,566-33,865,345 TP53TG3, ABCD1P3, 50 more genes
    nsv4680609copy number variation1nstd189human GRCh37.p13 chr16: 32,146,887-33,681,101 , GRCh38.p12 chr16: 32,135,566-33,878,634 TP53TG3, ABCD1P3, 50 more genes
    nsv4680570copy number variation1nstd189human GRCh37.p13 chr16: 32,080,874-33,631,830 , GRCh38.p12 chr16: 32,069,553-33,829,363 TP53TG3, ABCD1P3, 49 more genes
    nsv4680562copy number variation1nstd189human GRCh37.p13 chr16: 32,058,496-33,776,085 , GRCh38.p12 chr16: 32,047,175-33,973,618 TP53TG3, ABCD1P3, 58 more genes
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