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Items: 1 to 20 of 484

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv4009468copy number variation1estd231human GRCh37 chr2: 223,760,178-223,762,671 , GRCh38.p12 chr2: 222,895,460-222,897,953 ACSL3
    esv4009469copy number variation1estd231human GRCh37 chr2: 223,797,358-223,797,675 , GRCh38.p12 chr2: 222,932,640-222,932,957 ACSL3
    nsv6696678copy number variation1nstd229human GRCh38 chr2: 222,895,473-222,897,953 , GRCh37.p13 chr2: 223,760,191-223,762,671 ACSL3
    nsv6678352copy number variation1nstd229human GRCh38 chr2: 222,932,649-222,932,967 , GRCh37.p13 chr2: 223,797,367-223,797,685 ACSL3
    nsv6338000copy number variation1nstd223human GRCh38 chr2: 222,877,829-222,879,915 , GRCh37.p13 chr2: 223,742,547-223,744,633 ACSL3
    nsv6349698copy number variation1nstd223human GRCh38 chr2: 222,937,201-222,938,300 , GRCh37.p13 chr2: 223,801,919-223,803,018 ACSL3
    nsv6347339copy number variation1nstd223human GRCh38 chr2: 222,932,640-222,932,957 , GRCh37.p13 chr2: 223,797,358-223,797,675 ACSL3
    nsv6140025copy number variation1nstd206human GRCh38 chr2: 222,895,453-222,897,973 , GRCh37.p13 chr2: 223,760,171-223,762,691 ACSL3
    nsv6139544copy number variation1nstd206human GRCh38 chr2: 222,932,629-222,932,977 , GRCh37.p13 chr2: 223,797,347-223,797,695 ACSL3
    nsv5393603mobile element deletion1nstd186human GRCh37 chr2: 223,760,191-223,762,671 , GRCh38.p12 chr2: 222,895,473-222,897,953 ACSL3
    nsv4648283copy number variation1nstd186human GRCh37 chr2: 223,760,191-223,762,671 , GRCh38.p12 chr2: 222,895,473-222,897,953 ACSL3
    nsv4653330mobile element deletion1nstd186human GRCh37 chr2: 223,797,359-223,797,675 , GRCh38.p12 chr2: 222,932,641-222,932,957 ACSL3
    nsv5383045mobile element deletion2nstd186human GRCh37 chr2: 223,797,367-223,797,675 , GRCh38.p12 chr2: 222,932,649-222,932,957 ACSL3
    nsv4641427copy number variation1nstd186human GRCh37 chr2: 223,797,367-223,797,675 , GRCh38.p12 chr2: 222,932,649-222,932,957 ACSL3
    nsv5987804copy number variation1nstd212human GRCh38 chr2: 222,895,460-222,897,953 , GRCh37.p13 chr2: 223,760,178-223,762,671 ACSL3
    nsv5988160copy number variation1nstd212human GRCh38 chr2: 222,932,640-222,932,957 , GRCh37.p13 chr2: 223,797,358-223,797,675 ACSL3
    nsv4712963copy number variation3nstd195human GRCh37 chr2: 223,760,178-223,760,179 , GRCh38.p12 chr2: 222,895,460-222,895,461 ACSL3
    nsv4711687copy number variation3nstd195human GRCh37 chr2: 223,797,358-223,797,359 , GRCh38.p12 chr2: 222,932,640-222,932,641 ACSL3
    nsv4736397copy number variation1nstd199human GRCh37 chr2: 223,760,185-223,762,678 , GRCh38.p12 chr2: 222,895,467-222,897,960 ACSL3
    nsv4749956copy number variation1nstd199human GRCh37 chr2: 223,797,361-223,797,678 , GRCh38.p12 chr2: 222,932,643-222,932,960 ACSL3
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