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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5875418copy number variation1nstd209human GRCh38 chr2: 101,452,978-101,453,149 , GRCh37.p13 chr2: 102,069,440-102,069,611 RFX8
    nsv5722613mobile element insertion1nstd211human GRCh38 chr2: 101,455,031-101,455,031 , GRCh37.p13 chr2: 102,071,493-102,071,493 RFX8
    nsv5722271mobile element insertion1nstd211human GRCh38 chr2: 101,396,688-101,396,688 , GRCh37.p13 chr2: 102,013,150-102,013,150 RFX8
    nsv5611361insertion1nstd207human GRCh38 chr2: 101,469,070-101,469,070 , GRCh37.p13 chr2: 102,085,532-102,085,532 RFX8
    nsv5581589copy number variation1nstd207human GRCh38 chr2: 101,468,991-101,469,040 , GRCh37.p13 chr2: 102,085,453-102,085,502 RFX8
    nsv5571862copy number variation1nstd207human GRCh38 chr2: 101,452,978-101,453,149 , GRCh37.p13 chr2: 102,069,440-102,069,611 RFX8
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5446863copy number variation1nstd206human GRCh38 chr2: 101,403,000-101,531,618 , GRCh37.p13 chr2: 102,019,462-102,148,080 LINC01870, RFX8, 2 more genes
    nsv5436212copy number variation1nstd206human GRCh38 chr2: 101,453,014-101,453,150 , GRCh37.p13 chr2: 102,069,476-102,069,612 RFX8
    nsv5287885copy number variation1nstd204human GRCh38.p13 chr2: 101,453,006-101,453,158 , GRCh37.p13 chr2: 102,069,468-102,069,620 RFX8
    nsv5281322copy number variation1nstd204human GRCh38.p13 chr2: 100,864,060-101,514,976 , GRCh37.p13 chr2: 101,480,522-102,131,438 LINC01870, LOC105373511, 17 more genes
    nsv5217676copy number variation1nstd204human GRCh38.p13 chr2: 100,959,101-101,514,900 , GRCh37.p13 chr2: 101,575,563-102,131,362 RNF149, NPAS2, 17 more genes
    nsv5213726copy number variation1nstd204human GRCh38.p13 chr2: 101,423,991-101,425,075 , GRCh37.p13 chr2: 102,040,453-102,041,537 RFX8
    nsv5210749copy number variation1nstd204human GRCh38.p13 chr2: 101,435,099-101,479,870 , GRCh37.p13 chr2: 102,051,561-102,096,332 RFX8
    nsv5066530mobile element insertion1nstd203human GRCh38 chr2: 101,448,386-101,448,397 , GRCh37.p13 chr2: 102,064,848-102,064,859 RFX8
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4894862copy number variation1nstd200human GRCh38 chr2: 101,472,168-101,488,385 , GRCh37.p13 chr2: 102,088,630-102,104,847 RFX8, LINC01870
    nsv4894861copy number variation1nstd200human GRCh38 chr2: 101,403,569-101,408,371 , GRCh37.p13 chr2: 102,020,031-102,024,833 RFX8
    nsv4894856copy number variation1nstd200human GRCh38 chr2: 100,864,090-101,514,954 , GRCh37.p13 chr2: 101,480,552-102,131,416 CREG2, LOC105373510, 17 more genes
    nsv4892954copy number variation1nstd200human GRCh38 chr2: 101,465,458-101,468,259 , GRCh37.p13 chr2: 102,081,920-102,084,721 RFX8
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