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Items: 1 to 20 of 263

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959117insertion1nstd209human GRCh38 chr1: 154,538,854-154,538,854 , GRCh37.p13 chr1: 154,511,330-154,511,330 TDRD10
    nsv5686576mobile element insertion1nstd211human GRCh38 chr1: 154,536,918-154,536,918 , GRCh37.p13 chr1: 154,509,394-154,509,394 TDRD10
    nsv5605745insertion1nstd207human GRCh38 chr1: 154,538,853-154,538,853 , GRCh37.p13 chr1: 154,511,329-154,511,329 TDRD10
    nsv5543111insertion1nstd206human GRCh38 chr1: 154,538,853-154,538,857 , GRCh37.p13 chr1: 154,511,329-154,511,333 TDRD10
    nsv5536736insertion1nstd206human GRCh38 chr1: 154,522,808-154,522,819 , GRCh37.p13 chr1: 154,495,284-154,495,295 TDRD10
    nsv5432440copy number variation1nstd206human GRCh38 chr1: 154,538,286-154,538,591 , GRCh37.p13 chr1: 154,510,762-154,511,067 TDRD10
    nsv5422081copy number variation1nstd206human GRCh38 chr1: 154,502,113-154,502,231 , GRCh37.p13 chr1: 154,474,589-154,474,707 SHE, TDRD10
    nsv5412823mobile element insertion1nstd206human GRCh38 chr1: 154,536,918-154,536,969 , GRCh37.p13 chr1: 154,509,394-154,509,445 TDRD10
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5211686copy number variation1nstd204human GRCh38.p13 chr1: 153,974,901-155,189,600 , GRCh37.p13 chr1: 153,947,377-155,161,231 JTB, PYGO2-AS1, 56 more genes
    nsv5171169mobile element insertion1nstd203human GRCh38 chr1: 154,503,292-154,503,302 , GRCh37.p13 chr1: 154,475,768-154,475,778 TDRD10
    nsv5077796mobile element insertion1nstd203human GRCh38 chr1: 154,530,415-154,530,415 , GRCh37.p13 chr1: 154,502,891-154,502,891 TDRD10
    nsv5076116mobile element insertion1nstd203human GRCh38 chr1: 154,536,899-154,536,914 , GRCh37.p13 chr1: 154,509,375-154,509,390 TDRD10
    nsv5062390mobile element insertion1nstd203human GRCh38 chr1: 154,543,275-154,543,288 , GRCh37.p13 chr1: 154,515,751-154,515,764 TDRD10
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4750822insertion1nstd199human GRCh37 chr1: 154,511,327-154,511,327 , GRCh38.p12 chr1: 154,538,851-154,538,851 TDRD10
    nsv4725532insertion1nstd186human GRCh37 chr1: 154,511,329-154,511,329 , GRCh38.p12 chr1: 154,538,853-154,538,853 TDRD10
    nsv4579472copy number variation2nstd183human GRCh37 chr1: 154,474,148-154,475,093 , GRCh38.p12 chr1: 154,501,672-154,502,617 TDRD10, SHE
    nsv4537882insertion1nstd166human GRCh37.p13 chr1: 154,511,329-154,511,329 , GRCh38.p12 chr1: 154,538,853-154,538,853 TDRD10
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