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Items: 1 to 20 of 414

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5853579copy number variation2nstd209human GRCh38 chr15: 28,655,271-28,656,906 , GRCh37.p13 chr15: 28,900,417-28,902,052 HERC2P9
    nsv5712171mobile element insertion1nstd211human GRCh38 chr15: 28,678,836-28,678,836 , GRCh37.p13 chr15: 28,923,982-28,923,982 LOC100419574, HERC2P9
    nsv5703299mobile element insertion1nstd211human GRCh38 chr15: 28,684,843-28,684,843 , GRCh37.p13 chr15: 28,929,989-28,929,989 HERC2P9
    nsv5672660copy number variation1nstd102humanPathogenic GRCh38 chr15: 22,804,175-30,375,696 , GRCh37.p13 chr15: 23,564,855-30,667,899 TUBBP8, LOC102723564, 218 more genes
    nsv5657500insertion1nstd207human GRCh38 chr15: 28,655,412-28,655,412 , GRCh37.p13 chr15: 28,900,558-28,900,558 HERC2P9
    nsv5593139copy number variation1nstd207human GRCh38 chr15: 28,678,557-28,678,691 , GRCh37.p13 chr15: 28,923,703-28,923,837 HERC2P9, LOC100419574
    nsv5592812copy number variation1nstd207human GRCh38 chr15: 28,678,675-28,678,734 , GRCh37.p13 chr15: 28,923,821-28,923,880 HERC2P9, LOC100419574
    nsv5591489copy number variation1nstd207human GRCh38 chr15: 28,665,696-28,666,455 , GRCh37.p13 chr15: 28,910,842-28,911,601 HERC2P9
    nsv5496896copy number variation1nstd206human GRCh38 chr15: 28,172,874-28,679,000 , GRCh37.p13 chr15: 28,418,020-28,924,146 MIR4509-3, LOC100419574, 18 more genes
    nsv5424295mobile element insertion1nstd206human GRCh38 chr15: 28,684,843-28,684,894 , GRCh37.p13 chr15: 28,929,989-28,930,040 HERC2P9
    nsv5277947copy number variation1nstd204human GRCh38.p13 chr15: 28,653,801-28,654,400 , GRCh37.p13 chr15: 28,898,947-28,899,546 HERC2P9
    nsv5275267copy number variation1nstd204human GRCh38.p13 chr15: 28,683,570-28,684,916 , GRCh37.p13 chr15: 28,928,716-28,930,062 HERC2P9
    nsv5274798copy number variation1nstd204human GRCh38.p13 chr15: 28,655,271-28,656,706 , GRCh37.p13 chr15: 28,900,417-28,901,852 HERC2P9
    nsv5273249copy number variation1nstd204human GRCh38.p13 chr15: 28,683,401-28,684,500 , GRCh37.p13 chr15: 28,928,547-28,929,646 HERC2P9
    nsv5270277copy number variation1nstd204human GRCh38.p13 chr15: 28,665,601-28,668,700 , GRCh37.p13 chr15: 28,910,747-28,913,846 HERC2P9
    nsv5269227copy number variation1nstd204human GRCh38.p13 chr15: 28,670,601-28,679,400 , GRCh37.p13 chr15: 28,915,747-28,924,546 HERC2P9, LOC100419574
    nsv5265998copy number variation1nstd204human GRCh38.p13 chr15: 28,683,101-28,685,600 , GRCh37.p13 chr15: 28,928,247-28,930,746 HERC2P9
    nsv5265914copy number variation1nstd204human GRCh38.p13 chr15: 28,655,201-28,657,500 , GRCh37.p13 chr15: 28,900,347-28,902,646 HERC2P9
    nsv5264117copy number variation1nstd204human GRCh38.p13 chr15: 28,663,001-28,664,600 , GRCh37.p13 chr15: 28,908,147-28,909,746 HERC2P9
    nsv5200367copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,208,842-28,525,460 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,280,314 SNORD115-27, LOC105370747, 246 more genes
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