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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959662insertion1nstd209human GRCh38 chr3: 100,393,674-100,393,674 , GRCh37.p13 chr3: 100,112,518-100,112,518 TOMM70
    nsv5951131insertion1nstd209human GRCh38 chr3: 100,376,369-100,376,369 , GRCh37.p13 chr3: 100,095,213-100,095,213 TOMM70
    nsv5906120copy number variation1nstd209human GRCh38 chr3: 100,365,791-100,365,849 , GRCh37.p13 chr3: 100,084,635-100,084,693 TOMM70
    nsv5900715copy number variation1nstd209human GRCh38 chr3: 100,383,018-100,383,087 , GRCh37.p13 chr3: 100,101,862-100,101,931 TOMM70
    nsv5680430mobile element insertion2nstd211human GRCh38 chr3: 100,393,687-100,393,687 , GRCh37.p13 chr3: 100,112,531-100,112,531 TOMM70
    nsv5616871insertion1nstd207human GRCh38 chr3: 100,393,674-100,393,674 , GRCh37.p13 chr3: 100,112,518-100,112,518 TOMM70
    nsv5547673insertion1nstd206human GRCh38 chr3: 100,393,687-100,393,725 , GRCh37.p13 chr3: 100,112,531-100,112,569 TOMM70
    nsv5330729translocation1nstd200human GRCh37 chr3: 100,107,756-100,107,756 , GRCh37 chr3: 100,107,661-100,107,661 , GRCh38.p12 chr3: 100,388,912-100,388,912 , GRCh38.p12 chr3: 100,388,817-100,388,817 TOMM70
    nsv5099842mobile element insertion1nstd203human GRCh38 chr3: 100,376,369-100,376,384 , GRCh37.p13 chr3: 100,095,213-100,095,228 TOMM70
    nsv5096423mobile element insertion1nstd203human GRCh38 chr3: 100,376,343-100,376,384 , GRCh37.p13 chr3: 100,095,187-100,095,228 TOMM70
    nsv5094314mobile element insertion1nstd203human GRCh38 chr3: 100,393,681-100,393,687 , GRCh37.p13 chr3: 100,112,525-100,112,531 TOMM70
    nsv5085518mobile element insertion1nstd203human GRCh38 chr3: 100,393,674-100,393,687 , GRCh37.p13 chr3: 100,112,518-100,112,531 TOMM70
    nsv5085474mobile element insertion1nstd203human GRCh38 chr3: 100,393,673-100,393,687 , GRCh37.p13 chr3: 100,112,517-100,112,531 TOMM70
    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
    nsv4919168copy number variation1nstd200human GRCh38 chr3: 100,388,817-100,388,912 , GRCh37.p13 chr3: 100,107,661-100,107,756 TOMM70
    nsv4919167copy number variation1nstd200human GRCh38 chr3: 100,378,098-100,380,143 , GRCh37.p13 chr3: 100,096,942-100,098,987 TOMM70
    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
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