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Items: 1 to 20 of 169

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5957545insertion1nstd209human GRCh38 chr3: 171,019,095-171,019,095 , GRCh37.p13 chr3: 170,736,884-170,736,884 SLC2A2
    nsv5893573copy number variation1nstd209human GRCh38 chr3: 171,001,779-171,001,846 , GRCh37.p13 chr3: 170,719,568-170,719,635 SLC2A2
    nsv5893518copy number variation1nstd209human GRCh38 chr3: 171,006,248-171,006,307 , GRCh37.p13 chr3: 170,724,037-170,724,096 SLC2A2
    nsv5888003copy number variation1nstd209human GRCh38 chr3: 171,013,719-171,013,886 , GRCh37.p13 chr3: 170,731,508-170,731,675 SLC2A2
    nsv5682161mobile element insertion2nstd211human GRCh38 chr3: 171,013,520-171,013,520 , GRCh37.p13 chr3: 170,731,309-170,731,309 SLC2A2
    nsv5613089insertion1nstd207human GRCh38 chr3: 171,019,129-171,019,129 , GRCh37.p13 chr3: 170,736,918-170,736,918 SLC2A2
    nsv5605006insertion1nstd207human GRCh38 chr3: 171,013,719-171,013,719 , GRCh37.p13 chr3: 170,731,508-170,731,508 SLC2A2
    nsv5569970copy number variation1nstd207human GRCh38 chr3: 171,006,248-171,006,307 , GRCh37.p13 chr3: 170,724,037-170,724,096 SLC2A2
    nsv5548318insertion1nstd206human GRCh38 chr3: 171,019,164-171,019,180 , GRCh37.p13 chr3: 170,736,953-170,736,969 SLC2A2
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5446764copy number variation1nstd206human GRCh38 chr3: 171,013,719-171,013,888 , GRCh37.p13 chr3: 170,731,508-170,731,677 SLC2A2
    nsv5437881copy number variation1nstd206human GRCh38 chr3: 171,007,266-171,008,741 , GRCh37.p13 chr3: 170,725,055-170,726,530 SLC2A2
    nsv5303199copy number variation1nstd204human GRCh38.p13 chr3: 171,013,719-171,013,888 , GRCh37.p13 chr3: 170,731,508-170,731,677 SLC2A2
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4924846copy number variation1nstd200human GRCh38 chr3: 171,013,719-171,013,888 , GRCh37.p13 chr3: 170,731,508-170,731,677 SLC2A2
    nsv4920690copy number variation1nstd200human GRCh38 chr3: 170,987,251-170,995,225 , GRCh37.p13 chr3: 170,705,040-170,713,014 RNU1-70P, SLC2A2
    nsv4804991copy number variation1nstd200human GRCh37 chr3: 170,731,508-170,731,677 , GRCh38.p12 chr3: 171,013,719-171,013,888 SLC2A2
    nsv4674680copy number variation1nstd102humanPathogenic GRCh37 chr3: 169,617,690-190,593,854 , GRCh38.p12 chr3: 169,899,902-190,876,065 RNU6-1120P, LOC105374262, 323 more genes
    nsv4635759copy number variation3nstd186human GRCh37 chr3: 170,731,508-170,731,677 , GRCh38.p12 chr3: 171,013,719-171,013,888 SLC2A2
    nsv4520739copy number variation1nstd166human GRCh37.p13 chr3: 170,731,508-170,731,677 , GRCh38.p12 chr3: 171,013,719-171,013,888 SLC2A2
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