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Items: 1 to 20 of 716

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137045copy number variation1nstd102humanPathogenic GRCh37 chr1: 536,777-6,012,896 , GRCh38.p12 chr1: 601,397-5,952,836 MIR200B, LOC105378608, 172 more genes
    nsv7099018copy number variation1nstd102humanPathogenic GRCh37 chr1: 1-2,580,976 , GRCh38.p12 chr1: 10,001-2,649,537 DVL1, LOC100129534, 148 more genes
    nsv7096064copy number variation1nstd102humanUncertain significance GRCh37 chr1: 861,322-948,976 , GRCh38.p12 chr1: 925,942-1,013,596 HES4, PERM1, 6 more genes
    nsv7096007copy number variation1nstd102humanUncertain significance GRCh37 chr1: 874,400-879,533 , GRCh38.p12 chr1: 939,020-944,153 SAMD11, NOC2L
    nsv7095871copy number variation1nstd102humanUncertain significance GRCh37 chr1: 878,613-879,533 , GRCh38.p12 chr1: 943,233-944,153 SAMD11, NOC2L
    nsv7054532inversion1nstd229human GRCh38 chr1: 934,213-953,151 , GRCh37.p13 chr1: 869,593-888,531 SAMD11, NOC2L
    nsv7050861inversion1nstd229human GRCh38 chr1: 950,021-955,189 , GRCh37.p13 chr1: 885,401-890,569 NOC2L
    nsv7044135inversion1nstd229human GRCh38 chr1: 946,586-979,131 , GRCh37.p13 chr1: 881,966-914,511 PLEKHN1, PERM1, 2 more genes
    nsv7043759inversion1nstd229human GRCh38 chr1: 944,758-950,238 , GRCh37.p13 chr1: 880,138-885,618 NOC2L, SAMD11
    nsv6657612copy number variation1nstd229human GRCh38 chr1: 955,047-1,006,777 , GRCh37.p13 chr1: 890,427-942,157 NOC2L, HES4, 4 more genes
    nsv6657603copy number variation1nstd229human GRCh38 chr1: 952,178-954,016 , GRCh37.p13 chr1: 887,558-889,396 NOC2L
    nsv6657581copy number variation1nstd229human GRCh38 chr1: 946,601-972,700 , GRCh37.p13 chr1: 881,981-908,080 PLEKHN1, NOC2L, 1 more genes
    nsv6657411copy number variation1nstd229human GRCh38 chr1: 943,788-962,217 , GRCh37.p13 chr1: 879,168-897,597 KLHL17, NOC2L, 1 more genes
    nsv6657398copy number variation1nstd229human GRCh38 chr1: 940,314-947,968 , GRCh37.p13 chr1: 875,694-883,348 SAMD11, NOC2L
    nsv6657199copy number variation1nstd229human GRCh38 chr1: 926,615-1,239,899 , GRCh37.p13 chr1: 861,995-1,175,279 TTLL10-AS1, MIR200B, 21 more genes
    nsv6657155copy number variation1nstd229human GRCh38 chr1: 917,002-957,005 , GRCh37.p13 chr1: 852,382-892,385 LOC107985728, LINC02593, 2 more genes
    nsv6657115copy number variation1nstd229human GRCh38 chr1: 924,340-942,999 , GRCh37.p13 chr1: 859,720-878,379 LOC107985728, SAMD11, 1 more genes
    nsv6656706copy number variation1nstd229human GRCh38 chr1: 872,115-945,244 , GRCh37.p13 chr1: 807,495-880,624 LINC02593, NOC2L, 5 more genes
    nsv6656705copy number variation1nstd229human GRCh38 chr1: 872,040-1,151,798 , GRCh37.p13 chr1: 807,420-1,087,178 C1orf159, LOC105378948, 17 more genes
    nsv6656432copy number variation1nstd229human GRCh38 chr1: 860,901-1,011,800 , GRCh37.p13 chr1: 796,281-947,180 NOC2L, LOC284600, 12 more genes
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