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Items: 1 to 20 of 717

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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
    nsv5279102copy number variation1nstd204human GRCh38.p13 chr16: 32,197,901-32,198,900 , GRCh37.p13 chr16: 32,209,222-32,210,221 ABHD17AP8
    nsv5277849copy number variation1nstd204human GRCh38.p13 chr16: 32,173,001-32,201,700 , GRCh37.p13 chr16: 32,184,322-32,213,021 HERC2P4, ABHD17AP8
    nsv5277669copy number variation1nstd204human GRCh38.p13 chr16: 32,200,701-32,218,100 , GRCh37.p13 chr16: 32,212,022-32,229,421 ABHD17AP8
    nsv5275618copy number variation1nstd204human GRCh38.p13 chr16: 32,203,201-32,207,900 , GRCh37.p13 chr16: 32,214,522-32,219,221 ABHD17AP8
    nsv5271608copy number variation1nstd204human GRCh38.p13 chr16: 32,145,301-32,201,100 , GRCh37.p13 chr16: 32,156,622-32,212,421 HERC2P4, ABHD17AP8
    nsv5268784copy number variation1nstd204human GRCh38.p13 chr16: 32,159,601-32,215,000 , GRCh37.p13 chr16: 32,170,922-32,226,321 HERC2P4, ABHD17AP8
    nsv5266144copy number variation1nstd204human GRCh38.p13 chr16: 32,141,401-32,222,300 , GRCh37.p13 chr16: 32,152,722-32,233,621 HERC2P4, ABHD17AP8
    nsv5263987copy number variation1nstd204human GRCh38.p13 chr16: 32,203,201-32,204,800 , GRCh37.p13 chr16: 32,214,522-32,216,121 ABHD17AP8
    nsv5262209copy number variation1nstd204human GRCh38.p13 chr16: 32,202,301-32,210,000 , GRCh37.p13 chr16: 32,213,622-32,221,321 ABHD17AP8
    nsv5261394copy number variation1nstd204human GRCh38.p13 chr16: 32,202,001-32,216,200 , GRCh37.p13 chr16: 32,213,322-32,227,521 ABHD17AP8
    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
    nsv4703546copy number variation1nstd195human GRCh37 chr16: 32,214,751-32,215,901 , GRCh38.p12 chr16: 32,203,430-32,204,580 ABHD17AP8
    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
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