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Items: 1 to 20 of 123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6856578copy number variation1nstd229human GRCh38 chr8: 70,254,201-70,311,100 , GRCh37.p13 chr8: 71,166,436-71,223,335 NCOA2, BTF3P12
    nsv6854976copy number variation1nstd229human GRCh38 chr8: 70,260,318-70,288,357 , GRCh37.p13 chr8: 71,172,553-71,200,592 BTF3P12, NCOA2
    nsv6852240copy number variation1nstd229human GRCh38 chr8: 70,219,900-70,368,076 , GRCh37.p13 chr8: 71,132,135-71,280,311 NCOA2, RNY3P14, 1 more genes
    nsv6846466copy number variation1nstd229human GRCh38 chr8: 70,246,881-70,271,617 , GRCh37.p13 chr8: 71,159,116-71,183,852 NCOA2, BTF3P12
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6568553inversion1nstd223human GRCh38 chr8: 69,899,793-71,797,262 , GRCh37.p13 chr8: 70,812,028-72,709,497 EYA1, SDCBPP2, 24 more genes
    nsv6432060copy number variation1nstd223human GRCh38 chr8: 70,246,881-70,271,616 , GRCh37.p13 chr8: 71,159,116-71,183,851 BTF3P12, NCOA2
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6291265copy number variation1nstd102humanPathogenic GRCh37 chr8: 69,894,553-72,597,645 , GRCh38.p12 chr8: 68,982,318-71,685,410 LINC01603, LINC03020, 34 more genes
    nsv6136681copy number variation1nstd213human GRCh37 chr8: 46,860,000-86,550,001 , GRCh38.p12 chr8: 45,948,378-85,637,772 CEBPD, EYA1, 519 more genes
    nsv6136594copy number variation1nstd213human GRCh37 chr8: 70,060,000-72,060,001 , GRCh38.p12 chr8: 69,147,765-71,147,766 NCOA2, TRAM1, 26 more genes
    nsv5037389inversion1nstd200human GRCh38 chr8: 70,182,890-71,982,045 , GRCh37.p13 chr8: 71,095,125-72,894,280 LACTB2, RPS18P11, 20 more genes
    nsv4965449copy number variation1nstd200human GRCh38 chr8: 70,246,881-70,271,617 , GRCh37.p13 chr8: 71,159,116-71,183,852 NCOA2, BTF3P12
    nsv4829078copy number variation1nstd200human GRCh37 chr8: 71,159,116-71,183,852 , GRCh38.p12 chr8: 70,246,881-70,271,617 NCOA2, BTF3P12
    nsv4675545copy number variation1nstd102humanUncertain significance GRCh37 chr8: 70,848,713-71,632,067 , GRCh38.p12 chr8: 69,936,478-70,719,832 SDCBPP2, RNY3P14, 16 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4332062inversion1nstd166human GRCh37.p13 chr8: 70,438,609-99,073,700 , GRCh38.p12 chr8: 69,526,374-98,061,472 , FTH1P11, 375 more genes
    nsv4318272inversion1nstd166human GRCh37.p13 chr8: 51,271,211-76,167,888 , GRCh38.p12 chr8: 50,358,651-75,255,653 , ASPH, 341 more genes
    nsv4171339copy number variation1nstd166human GRCh37.p13 chr8: 71,159,116-71,183,858 , GRCh38.p12 chr8: 70,246,881-70,271,623 BTF3P12, NCOA2
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