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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6117344copy number variation1nstd186human GRCh37 chr13: 57,714,187-57,747,240 , GRCh38.p12 chr13: 57,140,053-57,173,106 PRR20A, PRR20B, 4 more genes
    nsv5945218copy number variation1nstd209human GRCh38 chr13: 57,119,952-57,261,334 , GRCh37.p13 chr13: 57,694,086-57,835,468 PRR20A, PRR20B, 6 more genes
    nsv5669454inversion1nstd207human GRCh38 chr13: 57,126,708-57,175,448 , GRCh37.p13 chr13: 57,700,842-57,749,582 PRR20A, PRR20B, 4 more genes
    nsv5654388insertion1nstd207human GRCh38 chr13: 57,152,862-57,152,862 , GRCh37.p13 chr13: 57,726,996-57,726,996 PRR20C
    nsv5598647copy number variation1nstd207human GRCh38 chr13: 57,141,375-57,154,520 , GRCh37.p13 chr13: 57,715,509-57,728,654 PRR20A, PRR20B, 1 more genes
    nsv5590310copy number variation1nstd207human GRCh38 chr13: 57,154,301-57,155,754 , GRCh37.p13 chr13: 57,728,435-57,729,888 PRR20C
    nsv5588662copy number variation1nstd207human GRCh38 chr13: 57,153,119-57,153,584 , GRCh37.p13 chr13: 57,727,253-57,727,718 PRR20C
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5504736copy number variation1nstd206human GRCh38 chr13: 57,154,300-57,316,106 , GRCh37.p13 chr13: 57,728,434-57,890,240 PRR20C, PRR20D, 5 more genes
    nsv5496635copy number variation1nstd206human GRCh38 chr13: 56,956,400-57,337,267 , GRCh37.p13 chr13: 57,530,534-57,911,401 PRR20A, PRR20B, 7 more genes
    nsv5428403copy number variation1nstd206human GRCh38 chr13: 57,140,053-57,173,106 , GRCh37.p13 chr13: 57,714,187-57,747,240 PRR20A, PRR20B, 4 more genes
    nsv5308589copy number variation1nstd204human GRCh37.p13 chr13: 57,530,504-57,911,423 , GRCh38.p13 chr13: 56,956,370-57,337,289 PRR20A, PRR20B, 7 more genes
    nsv5280300copy number variation1nstd204human GRCh38.p13 chr13: 57,140,501-57,154,800 , GRCh37.p13 chr13: 57,714,635-57,728,934 PRR20B, PRR20C, 1 more genes
    nsv5278007copy number variation1nstd204human GRCh37.p13 chr13: 57,530,235-57,911,034 , GRCh38.p13 chr13: 56,956,101-57,336,900 PRR20A, PRR20B, 7 more genes
    nsv5277493copy number variation1nstd204human GRCh38.p13 chr13: 57,150,201-57,154,800 , GRCh37.p13 chr13: 57,724,335-57,728,934 PRR20B, PRR20C
    nsv5273429copy number variation1nstd204human GRCh38.p13 chr13: 57,139,301-57,152,900 , GRCh37.p13 chr13: 57,713,435-57,727,034 PRR20B, PRR20A, 1 more genes
    nsv5264076copy number variation1nstd204human GRCh38.p13 chr13: 57,148,701-57,156,700 , GRCh37.p13 chr13: 57,722,835-57,730,834 PRR20B, PRR20C
    nsv5263781copy number variation1nstd204human GRCh38.p13 chr13: 57,140,301-57,157,600 , GRCh37.p13 chr13: 57,714,435-57,731,734 PRR20C, PRR20A, 1 more genes
    nsv5263095copy number variation1nstd204human GRCh38.p13 chr13: 57,149,201-57,153,100 , GRCh37.p13 chr13: 57,723,335-57,727,234 PRR20C, PRR20B
    nsv5262940copy number variation1nstd204human GRCh37.p13 chr13: 57,713,435-57,746,534 , GRCh38.p13 chr13: 57,139,301-57,172,400 PRR20A, PRR20B, 4 more genes
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