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Items: 1 to 20 of 220

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5436981copy number variation1nstd206human GRCh38 chr3: 170,378,416-170,378,550 , GRCh37.p13 chr3: 170,096,204-170,096,338 SKIL
    nsv5099053mobile element insertion1nstd203human GRCh38 chr3: 170,387,726-170,387,759 , GRCh37.p13 chr3: 170,105,514-170,105,547 SKIL
    nsv5092123mobile element insertion1nstd203human GRCh38 chr3: 170,367,450-170,367,456 , GRCh37.p13 chr3: 170,085,238-170,085,244 SKIL
    nsv5090732mobile element insertion1nstd203human GRCh38 chr3: 170,387,933-170,387,957 , GRCh37.p13 chr3: 170,105,721-170,105,745 SKIL
    nsv5087416mobile element insertion1nstd203human GRCh38 chr3: 170,387,883-170,387,933 , GRCh37.p13 chr3: 170,105,671-170,105,721 SKIL
    nsv5084740mobile element insertion1nstd203human GRCh38 chr3: 170,387,759-170,387,774 , GRCh37.p13 chr3: 170,105,547-170,105,562 SKIL
    nsv5082316mobile element insertion1nstd203human GRCh38 chr3: 170,387,716-170,387,759 , GRCh37.p13 chr3: 170,105,504-170,105,547 SKIL
    nsv5081015mobile element insertion1nstd203human GRCh38 chr3: 170,367,446-170,367,456 , GRCh37.p13 chr3: 170,085,234-170,085,244 SKIL
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4920667copy number variation1nstd200human GRCh38 chr3: 170,386,253-170,389,402 , GRCh37.p13 chr3: 170,104,041-170,107,190 SKIL
    nsv4798533copy number variation1nstd200human GRCh37 chr3: 170,104,041-170,107,314 , GRCh38.p12 chr3: 170,386,253-170,389,526 SKIL
    nsv4714426copy number variation1nstd195human GRCh37 chr3: 170,096,356-170,096,357 , GRCh38.p12 chr3: 170,378,568-170,378,569 SKIL
    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
    nsv4596215copy number variation1nstd183human GRCh37 chr3: 170,075,540-170,075,585 , GRCh38.p12 chr3: 170,357,752-170,357,797 SKIL
    nsv4585578copy number variation1nstd183human GRCh37 chr3: 170,074,085-170,075,315 , GRCh38.p12 chr3: 170,356,297-170,357,527 SKIL
    nsv4390808copy number variation1nstd171human GRCh37 chr3: 170,096,745-170,096,776 , GRCh38.p12 chr3: 170,378,957-170,378,988 SKIL
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4109271copy number variation1nstd166human GRCh37.p13 chr3: 170,109,048-170,110,044 , GRCh38.p12 chr3: 170,391,260-170,392,256 SKIL
    nsv4105789copy number variation1nstd166human GRCh37.p13 chr3: 170,077,496-170,078,108 , GRCh38.p12 chr3: 170,359,708-170,360,320 SKIL
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