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Items: 1 to 20 of 210

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099189copy number variation1nstd231human GRCh38.p12 chr1: 27,937,767-28,509,967 , GRCh37 chr1: 28,264,278-28,836,479 RCC1, EYA3, 17 more genes
    nsv7044103inversion1nstd229human GRCh38 chr1: 26,905,652-33,050,814 , GRCh37.p13 chr1: 27,232,143-33,516,415 ADGRB2, SNORA16A, 169 more genes
    nsv7040604inversion1nstd229human GRCh38 chr1: 28,189,508-28,189,710 , GRCh37.p13 chr1: 28,516,019-28,516,221 PTAFR
    nsv6648284copy number variation1nstd229human GRCh38 chr1: 28,150,401-28,160,500 , GRCh37.p13 chr1: 28,476,912-28,487,011 PTAFR
    nsv6648093copy number variation1nstd229human GRCh38 chr1: 28,188,167-28,228,246 , GRCh37.p13 chr1: 28,514,678-28,554,757 PTAFR, DNAJC8
    nsv6648092copy number variation1nstd229human GRCh38 chr1: 28,158,468-28,165,505 , GRCh37.p13 chr1: 28,484,979-28,492,016 PTAFR
    nsv6551146inversion1nstd223human GRCh38 chr1: 28,154,820-28,155,267 , GRCh37.p13 chr1: 28,481,331-28,481,778 PTAFR
    nsv6546174inversion1nstd223human GRCh38 chr1: 28,157,873-28,158,703 , GRCh37.p13 chr1: 28,484,384-28,485,214 PTAFR
    nsv6539702inversion1nstd223human GRCh38 chr1: 28,189,529-28,189,748 , GRCh37.p13 chr1: 28,516,040-28,516,259 PTAFR
    nsv6335245copy number variation1nstd223human GRCh38 chr1: 28,170,778-28,173,333 , GRCh37.p13 chr1: 28,497,289-28,499,844 PTAFR
    nsv6332071copy number variation1nstd223human GRCh38 chr1: 28,161,408-28,162,026 , GRCh37.p13 chr1: 28,487,919-28,488,537 PTAFR
    nsv6313753copy number variation1nstd102humanUncertain significance GRCh37 chr1: 27,543,877-32,819,121 , GRCh38.p12 chr1: 27,217,386-32,353,520 DCDC2B, SNRNP40, 130 more genes
    nsv6295133copy number variation1nstd186human GRCh37 chr1: 28,481,279-28,485,006 , GRCh38.p12 chr1: 28,154,768-28,158,495 PTAFR
    nsv6290388copy number variation1nstd102humanUncertain significance GRCh37 chr1: 28,493,687-29,242,679 , GRCh38.p12 chr1: 28,167,176-28,916,167 SNORA16A, MED18, 24 more genes
    nsv6241174mobile element insertion1nstd215human GRCh38 chr1: 28,188,963-28,188,963 , GRCh37.p13 chr1: 28,515,474-28,515,474 PTAFR
    nsv6241063mobile element insertion1nstd215human GRCh38 chr1: 28,183,058-28,183,058 , GRCh37.p13 chr1: 28,509,569-28,509,569 PTAFR
    nsv6133648copy number variation1nstd213human GRCh37 chr1: 23,300,000-28,930,001 , GRCh38.p12 chr1: 22,973,507-28,603,489 RUNX3, CD52, 195 more genes
    nsv6050074insertion1nstd212human GRCh38 chr1: 28,158,705-28,158,705 , GRCh37.p13 chr1: 28,485,216-28,485,216 PTAFR
    nsv5680566mobile element insertion2nstd211human GRCh38 chr1: 28,183,058-28,183,058 , GRCh37.p13 chr1: 28,509,569-28,509,569 PTAFR
    nsv5620170insertion1nstd207human GRCh38 chr1: 28,183,042-28,183,042 , GRCh37.p13 chr1: 28,509,553-28,509,553 PTAFR
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