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Items: 1 to 20 of 219

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057443inversion1nstd229human GRCh38 chr2: 28,054-42,021 , GRCh37.p13 chr2: 28,054-42,021 FAM110C
    nsv7040745inversion1nstd229human GRCh38 chr2: 20,610-167,425 , GRCh37.p13 chr2: 20,610-167,425 LOC105373324, FAM110C
    nsv6676313copy number variation1nstd229human GRCh38 chr2: 34,801-37,900 , GRCh37.p13 chr2: 34,801-37,900 FAM110C
    nsv6675801copy number variation1nstd229human GRCh38 chr2: 40,561-52,773 , GRCh37.p13 chr2: 40,561-52,773 FAM110C
    nsv6675348copy number variation1nstd229human GRCh38 chr2: 36,771-49,696 , GRCh37.p13 chr2: 36,771-49,696 FAM110C
    nsv6674491copy number variation1nstd229human GRCh38 chr2: 43,041-53,794 , GRCh37.p13 chr2: 43,041-53,794 FAM110C
    nsv6674029copy number variation1nstd229human GRCh38 chr2: 37,359-118,895 , GRCh37.p13 chr2: 37,359-118,895 FAM110C
    nsv6672860copy number variation1nstd229human GRCh38 chr2: 11,536-251,793 , GRCh37.p13 chr2: 11,536-251,793 SH3YL1, FAM110C, 1 more genes
    nsv6672152copy number variation1nstd229human GRCh38 chr2: 35,340-72,185 , GRCh37.p13 chr2: 35,340-72,185 FAM110C
    nsv6668982copy number variation1nstd229human GRCh38 chr2: 41,321-45,156 , GRCh37.p13 chr2: 41,321-45,156 FAM110C
    nsv6668169copy number variation1nstd229human GRCh38 chr2: 19,041-108,776 , GRCh37.p13 chr2: 19,041-108,776 FAM110C
    nsv6667874copy number variation1nstd229human GRCh38 chr2: 40,133-48,396 , GRCh37.p13 chr2: 40,133-48,396 FAM110C
    nsv6667708copy number variation1nstd229human GRCh38 chr2: 34,194-252,919 , GRCh37.p13 chr2: 34,194-252,919 SH3YL1, FAM110C, 1 more genes
    nsv6667198copy number variation1nstd229human GRCh38 chr2: 40,501-51,100 , GRCh37.p13 chr2: 40,501-51,100 FAM110C
    nsv6666155copy number variation1nstd229human GRCh38 chr2: 20,293-89,303 , GRCh37.p13 chr2: 20,293-89,303 FAM110C
    nsv6664436copy number variation1nstd229human GRCh38 chr2: 26,574-50,525 , GRCh37.p13 chr2: 26,574-50,525 FAM110C
    nsv6664126copy number variation1nstd229human GRCh38 chr2: 1-126,300 , GRCh37.p13 chr2: 10,001-126,300 FAM110C
    nsv6636363copy number variation1nstd102humanPathogenic GRCh37 chr2: 12,771-1,947,832 , GRCh38.p12 chr2: 12,771-1,944,060 LOC105373352, LOC105373346, 26 more genes
    nsv6628104copy number variation1nstd224human GRCh37 chr2: 33,012-55,237 , GRCh38.p12 chr2: 33,012-55,237 FAM110C
    nsv6628103copy number variation1nstd224human GRCh37 chr2: 33,012-193,882 , GRCh38.p12 chr2: 33,012-193,882 FAM110C, LOC105373324
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