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Items: 1 to 20 of 219

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099248copy number variation1nstd231human GRCh38.p12 chr1: 172,685,012-173,856,229 , GRCh37 chr1: 172,654,152-173,825,367 TNFSF4, TNFSF18, 19 more genes
    nsv6644983copy number variation1nstd229human GRCh38 chr1: 173,819,345-173,823,974 , GRCh37.p13 chr1: 173,788,483-173,793,112 CENPL, DARS2
    nsv6644888copy number variation1nstd229human GRCh38 chr1: 173,822,601-173,834,800 , GRCh37.p13 chr1: 173,791,739-173,803,938 CENPL, DARS2
    nsv6644829copy number variation1nstd229human GRCh38 chr1: 173,819,441-173,827,479 , GRCh37.p13 chr1: 173,788,579-173,796,617 CENPL, DARS2
    nsv6644828copy number variation1nstd229human GRCh38 chr1: 173,788,472-173,805,074 , GRCh37.p13 chr1: 173,757,610-173,774,212 CENPL, RN7SKP160
    nsv6644717copy number variation1nstd229human GRCh38 chr1: 172,496,006-174,441,202 , GRCh37.p13 chr1: 172,465,146-174,410,340 RABGAP1L-DT, LOC100506023, 46 more genes
    nsv6547492inversion1nstd223human GRCh38 chr1: 173,819,346-173,819,712 , GRCh37.p13 chr1: 173,788,484-173,788,850 CENPL
    nsv6546844inversion1nstd223human GRCh38 chr1: 173,800,226-173,800,765 , GRCh37.p13 chr1: 173,769,364-173,769,903 CENPL
    nsv6538139inversion1nstd223human GRCh38 chr1: 173,801,982-173,802,377 , GRCh37.p13 chr1: 173,771,120-173,771,515 CENPL
    nsv6313831copy number variation1nstd102humanUncertain significance GRCh37 chr1: 173,750,496-174,538,509 , GRCh38.p12 chr1: 173,781,358-174,569,371 SNORD47, SNORD76, 27 more genes
    nsv6313519copy number variation1nstd102humanPathogenic GRCh37 chr1: 171,881,608-175,899,893 , GRCh38.p12 chr1: 171,912,468-175,930,757 RNU6-693P, PIGC, 73 more genes
    nsv6310765copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr1: 171,605,065-173,962,123 , GRCh38.p12 chr1: 171,635,925-173,992,985 RNU6-157P, SNORD47, 60 more genes
    nsv6289986copy number variation1nstd102humanPathogenic GRCh38 chr1: 173,501,975-175,305,010 , GRCh37.p13 chr1: 173,471,114-175,274,146 GAS5-AS1, ENTR1P2, 44 more genes
    nsv6289891copy number variation1nstd102humanPathogenic GRCh38 chr1: 172,987,296-174,843,232 , GRCh37.p13 chr1: 172,956,436-174,812,370 LOC100302291, SNORD75, 41 more genes
    nsv6289872copy number variation1nstd102humanPathogenic GRCh38 chr1: 173,686,375-176,083,118 , GRCh37.p13 chr1: 173,655,514-176,052,254 ENTR1P2, GAS5-AS1, 49 more genes
    nsv6289861copy number variation1nstd102humanPathogenic GRCh38 chr1: 173,787,361-174,223,422 , GRCh37.p13 chr1: 173,756,499-174,192,560 SNORD76, SNORD75, 24 more genes
    nsv6133933copy number variation1nstd213human GRCh37 chr1: 161,620,000-196,730,001 , GRCh38.p12 chr1: 161,650,210-196,760,871 FASLG, SERPINC1, 510 more genes
    nsv6133749copy number variation1nstd213human GRCh37 chr1: 173,530,000-175,550,001 , GRCh38.p12 chr1: 173,560,861-175,580,865 SERPINC1, KIAA0040, 46 more genes
    nsv6133600copy number variation1nstd213human GRCh37 chr1: 172,520,000-173,820,001 , GRCh38.p12 chr1: 172,550,860-173,850,863 FASLG, GOT2P2, 22 more genes
    nsv6133567copy number variation1nstd213human GRCh37 chr1: 170,760,000-174,730,001 , GRCh38.p12 chr1: 170,790,859-174,760,863 FASLG, SERPINC1, 87 more genes
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