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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5958570insertion1nstd209human GRCh38 chr3: 100,436,923-100,436,923 , GRCh37.p13 chr3: 100,155,767-100,155,767 LNP1
    nsv5899642copy number variation1nstd209human GRCh38 chr3: 100,451,741-100,451,797 , GRCh37.p13 chr3: 100,170,585-100,170,641 LNP1
    nsv5683775mobile element insertion1nstd211human GRCh38 chr3: 100,436,935-100,436,935 , GRCh37.p13 chr3: 100,155,779-100,155,779 LNP1
    nsv5615464insertion1nstd207human GRCh38 chr3: 100,436,923-100,436,923 , GRCh37.p13 chr3: 100,155,767-100,155,767 LNP1
    nsv5610268insertion1nstd207human GRCh38 chr3: 100,451,756-100,451,756 , GRCh37.p13 chr3: 100,170,600-100,170,600 LNP1
    nsv5553466insertion1nstd206human GRCh38 chr3: 100,451,798-100,451,807 , GRCh37.p13 chr3: 100,170,642-100,170,651 LNP1
    nsv5346308translocation1nstd200human GRCh38 chr3: 100,420,830-100,420,830 , GRCh38 chr3: 100,417,515-100,417,515 , GRCh37.p13 chr3: 100,139,674-100,139,674 , GRCh37.p13 chr3: 100,136,359-100,136,359 LNP1
    nsv5087176mobile element insertion1nstd203human GRCh38 chr3: 100,432,197-100,432,211 , GRCh37.p13 chr3: 100,151,041-100,151,055 LNP1
    nsv5040665inversion1nstd200human GRCh38 chr3: 94,638,746-100,409,115 , GRCh37.p13 chr3: 94,357,590-100,127,959 , LOC101929278, 82 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5034224inversion1nstd200human GRCh38 chr3: 94,859,289-102,665,887 , GRCh37.p13 chr3: 94,578,133-102,384,731 , LOC105374005, 114 more genes
    nsv4919170copy number variation1nstd200human GRCh38 chr3: 100,452,521-100,454,696 , GRCh37.p13 chr3: 100,171,365-100,173,540 LNP1
    nsv4919169copy number variation1nstd200human GRCh38 chr3: 100,404,836-100,417,541 , GRCh37.p13 chr3: 100,123,680-100,136,385 LNP1
    nsv4914554copy number variation1nstd200human GRCh38 chr3: 100,188,066-100,400,094 , GRCh37.p13 chr3: 99,906,910-100,118,938 TOMM70, NIT2, 5 more genes
    nsv4887622inversion1nstd200human GRCh37 chr3: 94,357,590-100,127,961 , GRCh38.p12 chr3: 94,638,746-100,409,117 , CPOX, 82 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4797688copy number variation1nstd200human GRCh37 chr3: 100,171,365-100,173,540 , GRCh38.p12 chr3: 100,452,521-100,454,696 LNP1
    nsv4797687copy number variation1nstd200human GRCh37 chr3: 100,136,359-100,139,674 , GRCh38.p12 chr3: 100,417,515-100,420,830 LNP1
    nsv4797686copy number variation1nstd200human GRCh37 chr3: 100,123,680-100,136,385 , GRCh38.p12 chr3: 100,404,836-100,417,541 LNP1
    nsv4758374insertion1nstd199human GRCh37 chr3: 100,155,769-100,155,769 , GRCh38.p12 chr3: 100,436,925-100,436,925 LNP1
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