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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
    nsv6126384insertion1nstd186human GRCh37 chr1: 8,929,303-8,929,311 , GRCh38.p12 chr1: 8,869,244-8,869,252 ENO1
    nsv5877304copy number variation1nstd209human GRCh38 chr1: 8,862,945-8,863,233 , GRCh37.p13 chr1: 8,923,004-8,923,292 ENO1
    nsv5875354copy number variation1nstd209human GRCh38 chr1: 8,876,621-8,877,578 , GRCh37.p13 chr1: 8,936,680-8,937,637 ENO1-AS1, ENO1
    nsv5686936mobile element insertion2nstd211human GRCh38 chr1: 8,869,244-8,869,244 , GRCh37.p13 chr1: 8,929,303-8,929,303 ENO1
    nsv5680495mobile element insertion1nstd211human GRCh38 chr1: 8,862,596-8,862,596 , GRCh37.p13 chr1: 8,922,655-8,922,655 ENO1
    nsv5624500insertion1nstd207human GRCh38 chr1: 8,869,228-8,869,228 , GRCh37.p13 chr1: 8,929,287-8,929,287 ENO1
    nsv5605950insertion1nstd207human GRCh38 chr1: 8,871,715-8,871,715 , GRCh37.p13 chr1: 8,931,774-8,931,774 ENO1
    nsv5542070insertion1nstd206human GRCh38 chr1: 8,869,244-8,869,252 , GRCh37.p13 chr1: 8,929,303-8,929,311 ENO1
    nsv5395714mobile element insertion1nstd206human GRCh38 chr1: 8,862,596-8,862,647 , GRCh37.p13 chr1: 8,922,655-8,922,706 ENO1
    nsv5218770copy number variation1nstd204human GRCh38.p13 chr1: 8,841,701-8,876,800 , GRCh37.p13 chr1: 8,901,760-8,936,859 MIR6728, ENO1
    nsv5217844copy number variation1nstd204human GRCh38.p13 chr1: 8,840,772-8,864,673 , GRCh37.p13 chr1: 8,900,831-8,924,732 MIR6728, ENO1
    nsv5201460copy number variation1nstd204human GRCh38.p13 chr1: 8,859,885-8,875,263 , GRCh37.p13 chr1: 8,919,944-8,935,322 MIR6728, ENO1
    nsv5066186mobile element insertion1nstd203human GRCh38 chr1: 8,862,584-8,862,596 , GRCh37.p13 chr1: 8,922,643-8,922,655 ENO1
    nsv5065148mobile element insertion1nstd203human GRCh38 chr1: 8,869,228-8,869,241 , GRCh37.p13 chr1: 8,929,287-8,929,300 ENO1
    nsv5061694mobile element insertion1nstd203human GRCh38 chr1: 8,869,233-8,869,244 , GRCh37.p13 chr1: 8,929,292-8,929,303 ENO1
    nsv5032499inversion1nstd200human GRCh38 chr1: 8,869,421-8,869,606 , GRCh37.p13 chr1: 8,929,480-8,929,665 ENO1
    nsv4894329copy number variation1nstd200human GRCh38 chr1: 8,840,894-8,876,597 , GRCh37.p13 chr1: 8,900,953-8,936,656 ENO1, MIR6728
    nsv4889724copy number variation1nstd200human GRCh38 chr1: 8,871,948-8,876,824 , GRCh37.p13 chr1: 8,932,007-8,936,883 ENO1
    nsv4889723copy number variation1nstd200human GRCh38 chr1: 8,860,165-8,860,265 , GRCh37.p13 chr1: 8,920,224-8,920,324 ENO1
    nsv4728219copy number variation1nstd102humanUncertain significance GRCh37 chr1: 8,869,809-9,115,610 , GRCh38.p12 chr1: 8,809,750-9,055,551 MIR6728, RERE, 10 more genes
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