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Items: 1 to 20 of 97

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098844copy number variation1nstd102humanUncertain significance GRCh37 chr2: 65,296,579-71,305,638 , GRCh38.p12 chr2: 65,069,445-71,078,508 SNRNP27, TEX261, 121 more genes
    nsv7052358inversion1nstd229human GRCh38 chr2: 68,972,696-68,982,310 , GRCh37.p13 chr2: 69,199,828-69,209,442 GKN1
    nsv6677233copy number variation1nstd229human GRCh38 chr2: 68,972,201-68,978,900 , GRCh37.p13 chr2: 69,199,333-69,206,032 GKN1
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6280972insertion2nstd214human GRCh38 chr2: 68,978,302-68,978,302 , GRCh37.p13 chr2: 69,205,434-69,205,434 GKN1
    nsv6134545copy number variation2nstd213human GRCh37 chr2: 47,990,000-75,070,001 , GRCh38.p12 chr2: 47,762,861-74,842,874 ACTG2, ACYP2, 438 more genes
    nsv6134457copy number variation1nstd213human GRCh37 chr2: 38,410,000-75,540,001 , GRCh38.p12 chr2: 38,182,858-75,312,875 , ACTG2, 598 more genes
    nsv6044018insertion1nstd212human GRCh38 chr2: 68,978,271-68,978,271 , GRCh37.p13 chr2: 69,205,403-69,205,403 GKN1
    nsv5948007insertion1nstd209human GRCh38 chr2: 68,978,274-68,978,274 , GRCh37.p13 chr2: 69,205,406-69,205,406 GKN1
    nsv5685793mobile element insertion2nstd211human GRCh38 chr2: 68,974,811-68,974,811 , GRCh37.p13 chr2: 69,201,943-69,201,943 GKN1
    nsv5607310insertion1nstd207human GRCh38 chr2: 68,978,271-68,978,271 , GRCh37.p13 chr2: 69,205,403-69,205,403 GKN1
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5404846mobile element insertion1nstd206human GRCh38 chr2: 68,974,811-68,974,862 , GRCh37.p13 chr2: 69,201,943-69,201,994 GKN1
    nsv4751632insertion1nstd199human GRCh37 chr2: 69,205,349-69,205,349 , GRCh38.p12 chr2: 68,978,217-68,978,217 GKN1
    nsv4467370mobile element insertion1nstd166human GRCh37.p13 chr2: 69,201,929-69,201,929 , GRCh38.p12 chr2: 68,974,797-68,974,797 GKN1
    nsv4347438copy number variation1nstd102humanPathogenic GRCh37 chr2: 67,491,378-69,679,404 , GRCh38.p12 chr2: 67,264,246-69,452,272 LINC02831, ANTXR1, 38 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
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