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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5833717copy number variation1nstd209human GRCh38 chr2: 74,374,521-74,376,811 , GRCh37.p13 chr2: 74,601,648-74,603,938 DCTN1
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5381353copy number variation1nstd102humanUncertain significance GRCh37 chr2: 74,588,271-74,607,174 , GRCh38.p12 chr2: 74,361,144-74,380,047 DCTN1
    nsv5068122mobile element insertion1nstd203human GRCh38 chr2: 74,382,136-74,382,152 , GRCh37.p13 chr2: 74,609,263-74,609,279 DCTN1
    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
    nsv4584392copy number variation1nstd183human GRCh37 chr2: 74,579,636-74,608,147 , GRCh38.p12 chr2: 74,352,509-74,381,020 DCTN1
    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
    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
    nsv3877742copy number variation1nstd102humanPathogenic GRCh37 chr2: 74,365,484-89,129,064 , GRCh38.p12 chr2: 74,138,357-88,829,551 RNU6-561P, M1AP, 253 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 IGKV2OR2-10, LOC105374848, 3737 more genes
    nsv3169185inversion1nstd158human GRCh37 chr2: 33,141,412-240,664,512 , GRCh38.p12 chr2: 32,916,345-239,742,818 , AAMP, 3290 more genes
    nsv3169060copy number variation1nstd158human GRCh38.p12 chr2: 32,916,139-76,194,347 , GRCh37 chr2: 33,141,206-76,421,473 , ACTG2, 703 more genes
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