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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974385inversion1nstd209human GRCh38 chr2: 64,078,330-67,334,176 , GRCh37.p13 chr2: 64,305,464-67,561,308 , MEIS1, 63 more genes
    nsv5960625insertion1nstd209human GRCh38 chr2: 64,989,243-64,989,243 , GRCh37.p13 chr2: 65,216,377-65,216,377 , SLC1A4
    nsv5869567copy number variation1nstd209human GRCh38 chr2: 64,997,839-64,997,970 , GRCh37.p13 chr2: 65,224,973-65,225,104 , SLC1A4
    nsv5869167copy number variation1nstd209human GRCh38 chr2: 64,996,479-64,998,364 , GRCh37.p13 chr2: 65,223,613-65,225,498 , SLC1A4
    nsv5833780copy number variation1nstd209human GRCh38 chr2: 64,996,877-64,998,410 , GRCh37.p13 chr2: 65,224,011-65,225,544 , SLC1A4
    nsv5726546mobile element insertion1nstd211human GRCh38 chr2: 64,997,154-64,997,154 , GRCh37.p13 chr2: 65,224,288-65,224,288 , SLC1A4
    nsv5686284mobile element insertion2nstd211human GRCh38 chr2: 65,010,482-65,010,482 , GRCh37.p13 chr2: 65,237,616-65,237,616 , SLC1A4
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5543328insertion1nstd206human GRCh38 chr2: 64,989,278-64,989,294 , GRCh37.p13 chr2: 65,216,412-65,216,428 , SLC1A4
    nsv5412316mobile element insertion1nstd206human GRCh38 chr2: 65,010,482-65,010,533 , GRCh37.p13 chr2: 65,237,616-65,237,667 , SLC1A4
    nsv5375842translocation1nstd200human GRCh38 chr2: 65,017,088-65,017,088 , GRCh38 chr2: 65,067,735-65,067,735 , GRCh37.p13 chr2: 65,244,222-65,244,222 , GRCh37.p13 chr2: 65,294,869-65,294,869 , SLC1A4, 1 more genes
    nsv5375833translocation1nstd200human GRCh38 chr2: 65,039,833-65,039,833 , GRCh38 chr2: 65,000,823-65,000,823 , GRCh37.p13 chr2: 65,227,957-65,227,957 , GRCh37.p13 chr2: 65,266,967-65,266,967 , SLC1A4, 1 more genes
    nsv5360719translocation1nstd200human GRCh38 chr2: 65,014,710-65,014,710 , GRCh38 chr2: 65,016,582-65,016,582 , GRCh37.p13 chr2: 65,241,844-65,241,844 , GRCh37.p13 chr2: 65,243,716-65,243,716 , SLC1A4
    nsv5167311mobile element insertion1nstd203human GRCh38 chr2: 64,997,137-64,997,154 , GRCh37.p13 chr2: 65,224,271-65,224,288 , SLC1A4
    nsv5079681mobile element insertion1nstd203human GRCh38 chr2: 65,002,570-65,002,595 , GRCh37.p13 chr2: 65,229,704-65,229,729 , SLC1A4
    nsv5067068mobile element insertion1nstd203human GRCh38 chr2: 65,010,475-65,010,482 , GRCh37.p13 chr2: 65,237,609-65,237,616 , SLC1A4
    nsv5063225mobile element insertion1nstd203human GRCh38 chr2: 65,010,471-65,010,482 , GRCh37.p13 chr2: 65,237,605-65,237,616 , SLC1A4
    nsv4908761copy number variation1nstd200human GRCh38 chr2: 64,936,585-65,402,835 , GRCh37.p13 chr2: 65,163,719-65,629,969 , RPL11P1, 9 more genes
    nsv4770474copy number variation1nstd200human GRCh37 chr2: 65,233,576-65,236,381 , GRCh38.p12 chr2: 65,006,442-65,009,247 , SLC1A4
    nsv4535010insertion1nstd166human GRCh37.p13 chr2: 65,216,377-65,216,377 , GRCh38.p12 chr2: 64,989,243-64,989,243 , SLC1A4
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