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Items: 1 to 20 of 196

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5881764copy number variation1nstd209human GRCh38 chr1: 160,235,187-160,235,791 , GRCh37.p13 chr1: 160,204,977-160,205,581 DCAF8
    nsv5869805copy number variation1nstd209human GRCh38 chr1: 160,230,812-160,230,932 , GRCh37.p13 chr1: 160,200,602-160,200,722 DCAF8
    nsv5430625copy number variation1nstd206human GRCh38 chr1: 160,230,812-160,230,933 , GRCh37.p13 chr1: 160,200,602-160,200,723 DCAF8
    nsv5415999copy number variation1nstd206human GRCh38 chr1: 160,235,145-160,235,774 , GRCh37.p13 chr1: 160,204,935-160,205,564 DCAF8
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5297692copy number variation1nstd204human GRCh38.p13 chr1: 160,235,258-160,235,783 , GRCh37.p13 chr1: 160,205,048-160,205,573 DCAF8
    nsv5062981mobile element insertion1nstd203human GRCh38 chr1: 160,223,597-160,223,610 , GRCh37.p13 chr1: 160,193,387-160,193,400 DCAF8
    nsv4897730copy number variation1nstd200human GRCh38 chr1: 160,233,293-160,233,442 , GRCh37.p13 chr1: 160,203,083-160,203,232 DCAF8
    nsv4897729copy number variation1nstd200human GRCh38 chr1: 160,227,317-160,229,753 , GRCh37.p13 chr1: 160,197,107-160,199,543 DCAF8
    nsv4897728copy number variation1nstd200human GRCh38 chr1: 160,226,691-160,228,514 , GRCh37.p13 chr1: 160,196,481-160,198,304 DCAF8
    nsv4784440copy number variation1nstd200human GRCh37 chr1: 160,197,107-160,199,543 , GRCh38.p12 chr1: 160,227,317-160,229,753 DCAF8
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4662765copy number variation1nstd186human GRCh37 chr1: 160,204,977-160,205,582 , GRCh38.p12 chr1: 160,235,187-160,235,792 DCAF8
    nsv4594007copy number variation1nstd183human GRCh37 chr1: 160,204,977-160,205,582 , GRCh38.p12 chr1: 160,235,187-160,235,792 DCAF8
    nsv4518016copy number variation1nstd166human GRCh37.p13 chr1: 160,204,388-160,204,442 , GRCh38.p12 chr1: 160,234,598-160,234,652 DCAF8
    nsv4516965copy number variation1nstd166human GRCh37.p13 chr1: 160,204,961-160,205,564 , GRCh38.p12 chr1: 160,235,171-160,235,774 DCAF8
    nsv4459034mobile element insertion1nstd166human GRCh37.p13 chr1: 160,220,530-160,220,530 , GRCh38.p12 chr1: 160,250,740-160,250,740 DCAF8
    nsv4450412copy number variation1nstd102humanPathogenic GRCh37 chr1: 157,321,299-167,391,423 , GRCh38.p12 chr1: 157,351,509-167,422,186 FCGR3B, SLAMF9, 302 more genes
    nsv4450321copy number variation1nstd102humanUncertain significance GRCh37 chr1: 159,808,188-161,011,163 , GRCh38.p12 chr1: 159,838,398-161,041,373 LOC107985216, PPIAP37, 50 more genes
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