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Items: 1 to 20 of 374

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6121636copy number variation1nstd186human GRCh37 chr12: 100,474,558-100,474,621 , GRCh38.p12 chr12: 100,080,780-100,080,843 BLTP3B
    nsv5975139insertion1nstd209human GRCh38 chr12: 100,140,720-100,140,720 , GRCh37.p13 chr12: 100,534,498-100,534,498 BLTP3B
    nsv5943089copy number variation1nstd209human GRCh38 chr12: 100,081,015-100,082,150 , GRCh37.p13 chr12: 100,474,793-100,475,928 BLTP3B
    nsv5928486copy number variation1nstd209human GRCh38 chr12: 100,080,780-100,080,840 , GRCh37.p13 chr12: 100,474,558-100,474,618 BLTP3B
    nsv5861064copy number variation1nstd209human GRCh38 chr12: 100,080,976-100,082,175 , GRCh37.p13 chr12: 100,474,754-100,475,953 BLTP3B
    nsv5720105mobile element insertion1nstd211human GRCh38 chr12: 100,114,025-100,114,025 , GRCh37.p13 chr12: 100,507,803-100,507,803 BLTP3B
    nsv5714275mobile element insertion1nstd211human GRCh38 chr12: 100,042,345-100,042,345 , GRCh37.p13 chr12: 100,436,123-100,436,123 BLTP3B
    nsv5711601mobile element insertion1nstd211human GRCh38 chr12: 100,086,129-100,086,129 , GRCh37.p13 chr12: 100,479,907-100,479,907 BLTP3B
    nsv5711064mobile element insertion1nstd211human GRCh38 chr12: 100,132,119-100,132,119 , GRCh37.p13 chr12: 100,525,897-100,525,897 BLTP3B
    nsv5698448mobile element insertion2nstd211human GRCh38 chr12: 100,103,496-100,103,496 , GRCh37.p13 chr12: 100,497,274-100,497,274 BLTP3B
    nsv5598472copy number variation1nstd207human GRCh38 chr12: 100,040,050-100,040,752 , GRCh37.p13 chr12: 100,433,828-100,434,530 BLTP3B
    nsv5585414copy number variation1nstd207human GRCh38 chr12: 100,080,779-100,080,839 , GRCh37.p13 chr12: 100,474,557-100,474,617 BLTP3B
    nsv5558789mobile element insertion1nstd206human GRCh38 chr12: 100,114,038-100,114,076 , GRCh37.p13 chr12: 100,507,816-100,507,854 BLTP3B
    nsv5513502copy number variation1nstd206human GRCh38 chr12: 100,030,654-100,030,961 , GRCh37.p13 chr12: 100,424,432-100,424,739 BLTP3B
    nsv5508241copy number variation1nstd206human GRCh38 chr12: 99,884,143-100,078,827 , GRCh37.p13 chr12: 100,277,921-100,472,605 ANKS1B, BLTP3B, 1 more genes
    nsv5505602copy number variation1nstd206human GRCh38 chr12: 100,105,742-100,107,394 , GRCh37.p13 chr12: 100,499,520-100,501,172 BLTP3B
    nsv5503103copy number variation1nstd206human GRCh38 chr12: 100,080,780-100,080,843 , GRCh37.p13 chr12: 100,474,558-100,474,621 BLTP3B
    nsv5500273copy number variation1nstd206human GRCh38 chr12: 100,081,018-100,082,151 , GRCh37.p13 chr12: 100,474,796-100,475,929 BLTP3B
    nsv5433297mobile element insertion1nstd206human GRCh38 chr12: 100,042,345-100,042,396 , GRCh37.p13 chr12: 100,436,123-100,436,174 BLTP3B
    nsv5431900mobile element insertion1nstd206human GRCh38 chr12: 100,042,558-100,042,609 , GRCh37.p13 chr12: 100,436,336-100,436,387 BLTP3B
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