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Items: 1 to 20 of 339

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131127insertion1nstd186human GRCh37 chr12: 86,504,100-86,504,126 , GRCh38.p12 chr12|NW_018654720.1: 16,179-16,205 , GRCh38.p12 chr12: 86,110,322-86,110,348 MGAT4C
    nsv6129693insertion1nstd186human GRCh37 chr12: 86,653,570-86,653,570 , GRCh38.p12 chr12: 86,259,792-86,259,792 , GRCh38.p12 chr12|NW_018654720.1: 165,635-165,635 MGAT4C
    nsv5384452mobile element deletion2nstd186human GRCh37 chr12: 86,523,325-86,523,635 , GRCh38.p12 chr12: 86,129,547-86,129,857 , GRCh38.p12 chr12|NW_018654720.1: 35,404-35,714 MGAT4C
    nsv5337338translocation1nstd200human GRCh37 chr12: 86,586,042-86,586,042 , GRCh37 chr12: 86,586,301-86,586,301 , GRCh38.p12 chr12: 86,192,264-86,192,264 , GRCh38.p12 chr12|NW_018654720.1: 98,121-98,121 , GRCh38.p12 chr12: 86,192,523-86,192,523 , GRCh38.p12 chr12|NW_018654720.1: 98,380-98,380 MGAT4C
    nsv4849147copy number variation1nstd200human GRCh37 chr12: 86,502,100-86,509,781 , GRCh38.p12 chr12: 86,108,322-86,116,003 , GRCh38.p12 chr12|NW_018654720.1: 14,179-21,860 MGAT4C
    nsv4844353copy number variation1nstd200human GRCh37 chr12: 86,605,252-86,606,635 , GRCh38.p12 chr12|NW_018654720.1: 117,331-118,714 , GRCh38.p12 chr12: 86,211,474-86,212,857 MGAT4C
    nsv4843914copy number variation1nstd200human GRCh37 chr12: 86,575,347-86,576,148 , GRCh38.p12 chr12|NW_018654720.1: 87,426-88,227 , GRCh38.p12 chr12: 86,181,569-86,182,370 MGAT4C
    nsv4843426copy number variation1nstd200human GRCh37 chr12: 86,604,677-86,609,244 , GRCh38.p12 chr12|NW_018654720.1: 116,756-121,323 , GRCh38.p12 chr12: 86,210,899-86,215,466 MGAT4C
    nsv4834563copy number variation1nstd200human GRCh37 chr12: 86,613,109-86,613,729 , GRCh38.p12 chr12: 86,219,331-86,219,951 , GRCh38.p12 chr12|NW_018654720.1: 125,188-125,808 MGAT4C
    nsv4834137copy number variation1nstd200human GRCh37 chr12: 86,493,420-86,494,377 , GRCh38.p12 chr12: 86,099,642-86,100,599 , GRCh38.p12 chr12|NW_018654720.1: 5,499-6,456 MGAT4C
    nsv4775119mobile element deletion1nstd200human GRCh37 chr12: 86,523,325-86,523,635 , GRCh38.p12 chr12: 86,129,547-86,129,857 , GRCh38.p12 chr12|NW_018654720.1: 35,404-35,714 MGAT4C
    nsv4759175insertion1nstd199human GRCh37 chr12: 86,504,050-86,504,050 , GRCh38.p12 chr12|NW_018654720.1: 16,129-16,129 , GRCh38.p12 chr12: 86,110,272-86,110,272 MGAT4C
    nsv4752697insertion1nstd199human GRCh37 chr12: 86,653,570-86,653,570 , GRCh38.p12 chr12|NW_018654720.1: 165,635-165,635 , GRCh38.p12 chr12: 86,259,792-86,259,792 MGAT4C
    nsv4731196copy number variation1nstd199human GRCh37 chr12: 86,523,319-86,523,640 , GRCh38.p12 chr12: 86,129,541-86,129,862 , GRCh38.p12 chr12|NW_018654720.1: 35,398-35,719 MGAT4C
    nsv4715029copy number variation4nstd195human GRCh37 chr12: 86,523,315-86,523,316 , GRCh38.p12 chr12: 86,129,537-86,129,538 , GRCh38.p12 chr12|NW_018654720.1: 35,394-35,395 MGAT4C
    nsv4690047mobile element insertion1nstd186human GRCh37 chr12: 86,653,628-86,653,628 , GRCh38.p12 chr12|NW_018654720.1: 172,957-172,957 , GRCh38.p12 chr12: 86,259,850-86,259,850 MGAT4C
    nsv4643412mobile element deletion1nstd186human GRCh37 chr12: 86,523,316-86,523,635 , GRCh38.p12 chr12: 86,129,538-86,129,857 , GRCh38.p12 chr12|NW_018654720.1: 35,395-35,714 MGAT4C
    nsv4642851copy number variation2nstd186human GRCh37 chr12: 86,523,325-86,523,635 , GRCh38.p12 chr12: 86,129,547-86,129,857 , GRCh38.p12 chr12|NW_018654720.1: 35,404-35,714 MGAT4C
    nsv4618292copy number variation1nstd183human GRCh37 chr12: 86,604,717-86,609,023 , GRCh38.p12 chr12|NW_018654720.1: 116,796-121,102 , GRCh38.p12 chr12: 86,210,939-86,215,245 MGAT4C
    nsv4614964copy number variation1nstd183human GRCh37 chr12: 86,501,204-86,510,719 , GRCh38.p12 chr12|NW_018654720.1: 13,283-22,798 , GRCh38.p12 chr12: 86,107,426-86,116,941 MGAT4C
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