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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5438036copy number variation1nstd206human GRCh38 chr2: 74,458,121-74,458,198 , GRCh37.p13 chr2: 74,685,248-74,685,325 WBP1, INO80B-WBP1, 1 more genes
    nsv5072183mobile element insertion1nstd203human GRCh38 chr2: 74,454,687-74,454,703 , GRCh37.p13 chr2: 74,681,814-74,681,830 INO80B-WBP1, INO80B
    nsv5066700mobile element insertion1nstd203human GRCh38 chr2: 74,457,008-74,457,018 , GRCh37.p13 chr2: 74,684,135-74,684,145 WBP1, INO80B, 1 more genes
    nsv4908819copy number variation1nstd200human GRCh38 chr2: 74,031,060-74,500,685 , GRCh37.p13 chr2: 74,258,187-74,727,812 LBX2, DCTN1-AS1, 24 more genes
    nsv4781574copy number variation1nstd200human GRCh37 chr2: 74,258,187-74,727,812 , GRCh38.p12 chr2: 74,031,060-74,500,685 MOB1A, SLC4A5, 24 more genes
    nsv4584394copy number variation1nstd183human GRCh37 chr2: 74,679,162-74,686,451 , GRCh38.p12 chr2: 74,452,035-74,459,324 WBP1, INO80B, 2 more genes
    nsv4467778mobile element insertion1nstd166human GRCh37.p13 chr2: 74,684,130-74,684,130 , GRCh38.p12 chr2: 74,457,003-74,457,003 WBP1, INO80B, 1 more genes
    nsv4062821copy number variation1nstd166human GRCh37.p13 chr2: 74,681,000-74,692,000 , GRCh38.p12 chr2: 74,453,873-74,464,873 INO80B, MOGS, 2 more genes
    nsv3965467copy number variation1nstd168human GRCh38 chr2: 74,428,425-74,489,692 , GRCh37.p13 chr2: 74,655,552-74,716,819 RTKN, MOGS, 6 more genes
    nsv3916821copy number variation1nstd102humanPathogenic NCBI36 chr2: 47,701,031-86,783,356 , GRCh37.p13 chr2: 47,847,527-86,929,845 , GRCh38.p12 chr2: 47,620,388-86,702,722 NAGK, NRXN1-DT, 595 more genes
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 DAZAP2P1, RPL36AP16, 2991 more genes
    nsv3909450copy number variation1nstd102humanLikely pathogenic NCBI36 chr2: 74,456,414-75,598,154 , GRCh37 chr2: 74,602,906-75,744,646 , GRCh38 chr2: 74,375,779-75,517,520 AUP1, DCTN1, 39 more genes
    nsv3903805copy number variation1nstd102humanBenign GRCh37 chr2: 7,635,254-88,005,418 , NCBI36 chr2: 7,552,705-87,786,533 , GRCh38 chr2: 7,495,123-87,705,899 LOC101927723, SANBR, 1246 more genes
    nsv3900298copy number variation1nstd102humanPathogenic GRCh37 chr2: 58,506,654-83,814,086 , GRCh38 chr2: 58,279,519-83,586,962 , NCBI36 chr2: 58,360,158-83,667,597 MIR1285-2, SERTAD2, 404 more genes
    nsv3893335copy number variation1nstd102humanUncertain significance GRCh37 chr2: 74,659,196-75,408,753 , GRCh38 chr2: 74,432,069-75,181,627 , NCBI36 chr2: 74,512,704-75,262,261 TTC31, TLX2, 30 more genes
    nsv3886532copy number variation1nstd102humanPathogenic GRCh37 chr2: 74,527,522-89,125,488 , GRCh38.p12 chr2: 74,300,395-88,825,975 RNU6-561P, VAMP5, 249 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 RNU6-674P, KANSL3, 3735 more genes
    nsv3883931copy number variation1nstd102humanPathogenic GRCh37 chr2: 63,671,346-85,698,002 , GRCh38.p12 chr2: 63,444,212-85,470,879 LINC01888, RNU7-64P, 367 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 MTND2P22, LOC112268410, 3724 more genes
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