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Items: 1 to 20 of 136

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6856315copy number variation1nstd229human GRCh38 chr8: 69,716,010-70,222,698 , GRCh37.p13 chr8: 70,628,245-71,134,933 RN7SL675P, RNA5SP270, 10 more genes
    nsv6848139copy number variation1nstd229human GRCh38 chr8: 69,802,665-70,039,383 , GRCh37.p13 chr8: 70,714,900-70,951,618 SUMO2P20, RNA5SP270, 4 more genes
    nsv6847116copy number variation1nstd229human GRCh38 chr8: 68,675,587-70,209,684 , GRCh37.p13 chr8: 69,587,822-71,121,919 LINC01603, SUMO2P20, 20 more genes
    nsv6841175copy number variation1nstd229human GRCh38 chr8: 69,156,248-70,149,472 , GRCh37.p13 chr8: 70,068,483-71,061,707 RN7SL675P, H2AZP2, 14 more genes
    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
    nsv6633104copy number variation1nstd224human GRCh37 chr8: 70,854,206-70,981,780 , GRCh38.p12 chr8: 69,941,971-70,069,545 SDCBPP2, SUMO2P20, 1 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
    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
    nsv5729340mobile element insertion2nstd211human GRCh38 chr8: 69,941,429-69,941,429 , GRCh37.p13 chr8: 70,853,664-70,853,664 SDCBPP2
    nsv5694700mobile element insertion1nstd211human GRCh38 chr8: 69,941,414-69,941,414 , GRCh37.p13 chr8: 70,853,649-70,853,649 SDCBPP2
    nsv5410066mobile element insertion1nstd206human GRCh38 chr8: 69,941,429-69,941,465 , GRCh37.p13 chr8: 70,853,664-70,853,700 SDCBPP2
    nsv5196601mobile element insertion1nstd203human GRCh38 chr8: 69,941,417-69,941,429 , GRCh37.p13 chr8: 70,853,652-70,853,664 SDCBPP2
    nsv5191490mobile element insertion1nstd203human GRCh38 chr8: 69,941,418-69,941,429 , GRCh37.p13 chr8: 70,853,653-70,853,664 SDCBPP2
    nsv5188366mobile element insertion1nstd203human GRCh38 chr8: 69,941,414-69,941,429 , GRCh37.p13 chr8: 70,853,649-70,853,664 SDCBPP2
    nsv4965441copy number variation1nstd200human GRCh38 chr8: 69,802,665-70,039,383 , GRCh37.p13 chr8: 70,714,900-70,951,618 , LOC100288097, 5 more genes
    nsv4829073copy number variation1nstd200human GRCh37 chr8: 70,714,900-70,951,618 , GRCh38.p12 chr8: 69,802,665-70,039,383 , SDCBPP2, 5 more genes
    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
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