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Items: 1 to 20 of 1948

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6120400copy number variation1nstd186human GRCh37 chr3: 41,777,492-41,788,992 , GRCh38.p12 chr3: 41,736,000-41,747,500 ULK4
    nsv6113220mobile element insertion1nstd186human GRCh37 chr3: 41,342,790-41,342,841 , GRCh38.p12 chr3: 41,301,299-41,301,350 ULK4
    nsv5975446inversion1nstd209human GRCh38 chr3: 41,320,651-41,321,619 , GRCh37.p13 chr3: 41,362,142-41,363,110 ULK4
    nsv5965330insertion1nstd209human GRCh38 chr3: 41,470,018-41,470,018 , GRCh37.p13 chr3: 41,511,509-41,511,509 ULK4
    nsv5961099insertion1nstd209human GRCh38 chr3: 41,305,733-41,305,733 , GRCh37.p13 chr3: 41,347,224-41,347,224 ULK4
    nsv5959104insertion1nstd209human GRCh38 chr3: 41,506,768-41,506,768 , GRCh37.p13 chr3: 41,548,259-41,548,259 ULK4
    nsv5954998insertion1nstd209human GRCh38 chr3: 41,431,547-41,431,547 , GRCh37.p13 chr3: 41,473,038-41,473,038 ULK4
    nsv5954420insertion1nstd209human GRCh38 chr3: 41,900,236-41,900,236 , GRCh37.p13 chr3: 41,941,728-41,941,728 ULK4
    nsv5951441insertion1nstd209human GRCh38 chr3: 41,306,200-41,306,200 , GRCh37.p13 chr3: 41,347,691-41,347,691 ULK4
    nsv5949186insertion1nstd209human GRCh38 chr3: 41,574,203-41,574,203 , GRCh37.p13 chr3: 41,615,694-41,615,694 ULK4
    nsv5949078insertion1nstd209human GRCh38 chr3: 41,901,479-41,901,479 , GRCh37.p13 chr3: 41,942,971-41,942,971 ULK4
    nsv5906334copy number variation1nstd209human GRCh38 chr3: 41,358,811-41,358,964 , GRCh37.p13 chr3: 41,400,302-41,400,455 ULK4
    nsv5905977copy number variation1nstd209human GRCh38 chr3: 41,898,654-42,136,014 , GRCh37.p13 chr3: 41,940,146-42,177,506 ULK4, GEMIN2P2, 3 more genes
    nsv5905226copy number variation1nstd209human GRCh38 chr3: 41,716,888-41,716,944 , GRCh37.p13 chr3: 41,758,380-41,758,436 ULK4
    nsv5903994copy number variation1nstd209human GRCh38 chr3: 41,363,495-41,364,303 , GRCh37.p13 chr3: 41,404,986-41,405,794 ULK4
    nsv5903821copy number variation1nstd209human GRCh38 chr3: 41,375,269-41,377,009 , GRCh37.p13 chr3: 41,416,760-41,418,500 ULK4
    nsv5901512copy number variation1nstd209human GRCh38 chr3: 41,776,568-41,780,000 , GRCh37.p13 chr3: 41,818,060-41,821,492 ULK4
    nsv5900705copy number variation1nstd209human GRCh38 chr3: 41,432,013-41,433,943 , GRCh37.p13 chr3: 41,473,504-41,475,434 ULK4
    nsv5899885copy number variation1nstd209human GRCh38 chr3: 41,624,405-41,624,658 , GRCh37.p13 chr3: 41,665,896-41,666,149 ULK4
    nsv5898004copy number variation1nstd209human GRCh38 chr3: 41,486,636-41,554,681 , GRCh37.p13 chr3: 41,528,127-41,596,172 ULK4
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