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Items: 1 to 20 of 774

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965829insertion1nstd209human GRCh38 chr3: 74,520,191-74,520,191 , GRCh37.p13 chr3: 74,569,342-74,569,342 CNTN3
    nsv5905286copy number variation1nstd209human GRCh38 chr3: 74,515,789-74,517,191 , GRCh37.p13 chr3: 74,564,940-74,566,342 CNTN3
    nsv5902904copy number variation1nstd209human GRCh38 chr3: 66,803,410-74,489,186 , GRCh37.p13 chr3: 66,853,834-74,538,337 , LOC105377160, 83 more genes
    nsv5899641copy number variation1nstd209human GRCh38 chr3: 74,353,677-74,357,975 , GRCh37.p13 chr3: 74,402,828-74,407,126 CNTN3
    nsv5899505copy number variation1nstd209human GRCh38 chr3: 74,394,674-74,395,312 , GRCh37.p13 chr3: 74,443,825-74,444,463 CNTN3
    nsv5889964copy number variation1nstd209human GRCh38 chr3: 74,516,201-74,516,852 , GRCh37.p13 chr3: 74,565,352-74,566,003 CNTN3
    nsv5836487copy number variation1nstd209human GRCh38 chr3: 74,353,561-74,356,839 , GRCh37.p13 chr3: 74,402,712-74,405,990 CNTN3
    nsv5731036mobile element insertion1nstd211human GRCh38 chr3: 74,606,576-74,606,576 , GRCh37.p13 chr3: 74,655,727-74,655,727 CNTN3
    nsv5730683mobile element insertion1nstd211human GRCh38 chr3: 74,486,859-74,486,859 , GRCh37.p13 chr3: 74,536,010-74,536,010 CNTN3
    nsv5730044mobile element insertion1nstd211human GRCh38 chr3: 74,472,338-74,472,338 , GRCh37.p13 chr3: 74,521,489-74,521,489 CNTN3
    nsv5727835mobile element insertion1nstd211human GRCh38 chr3: 74,492,993-74,492,993 , GRCh37.p13 chr3: 74,542,144-74,542,144 CNTN3
    nsv5724618mobile element insertion1nstd211human GRCh38 chr3: 74,284,798-74,284,798 , GRCh37.p13 chr3: 74,333,949-74,333,949 CNTN3
    nsv5715228mobile element insertion1nstd211human GRCh38 chr3: 74,519,759-74,519,759 , GRCh37.p13 chr3: 74,568,910-74,568,910 CNTN3
    nsv5691310mobile element insertion2nstd211human GRCh38 chr3: 74,520,206-74,520,206 , GRCh37.p13 chr3: 74,569,357-74,569,357 CNTN3
    nsv5687896mobile element insertion2nstd211human GRCh38 chr3: 74,333,711-74,333,711 , GRCh37.p13 chr3: 74,382,862-74,382,862 CNTN3
    nsv5686483mobile element insertion1nstd211human GRCh38 chr3: 74,265,175-74,265,175 , GRCh37.p13 chr3: 74,314,326-74,314,326 CNTN3
    nsv5684306mobile element insertion2nstd211human GRCh38 chr3: 74,405,367-74,405,367 , GRCh37.p13 chr3: 74,454,518-74,454,518 CNTN3
    nsv5677856mobile element insertion2nstd211human GRCh38 chr3: 74,276,580-74,276,580 , GRCh37.p13 chr3: 74,325,731-74,325,731 CNTN3
    nsv5622914insertion1nstd207human GRCh38 chr3: 74,520,191-74,520,191 , GRCh37.p13 chr3: 74,569,342-74,569,342 CNTN3
    nsv5614055insertion1nstd207human GRCh38 chr3: 74,274,599-74,274,599 , GRCh37.p13 chr3: 74,323,750-74,323,750 CNTN3
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