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Items: 1 to 20 of 198

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146202insertion1nstd232human GRCh37.p13 chr6: 99,860,615-99,860,615 , GRCh38.p12 chr6: 99,412,739-99,412,739 PNISR
    nsv7056770inversion1nstd229human GRCh38 chr6: 99,409,359-99,409,405 , GRCh37.p13 chr6: 99,857,235-99,857,281 PNISR
    nsv6814761copy number variation1nstd229human GRCh38 chr6: 99,369,889-99,413,831 , GRCh37.p13 chr6: 99,817,765-99,861,707 COQ3, PNISR
    nsv6811140copy number variation1nstd229human GRCh38 chr6: 97,373,758-103,907,621 , GRCh37.p13 chr6: 97,821,634-104,355,496 FBXL4, PRDM13, 37 more genes
    nsv6805660copy number variation1nstd229human GRCh38 chr6: 99,417,701-99,420,200 , GRCh37.p13 chr6: 99,865,577-99,868,076 PNISR
    nsv6636789copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 97,904,220-99,964,434 , GRCh38.p12 chr6: 97,456,344-99,516,558 POU3F2, PNISR, 15 more genes
    nsv6636533copy number variation1nstd102humanPathogenic GRCh37 chr6: 96,596,732-105,554,568 , GRCh38.p12 chr6: 96,148,856-105,106,693 MCHR2-AS1, ACTG1P18, 65 more genes
    nsv6636338copy number variation1nstd102humanPathogenic GRCh37 chr6: 96,946,110-106,497,526 , GRCh38.p12 chr6: 96,498,234-106,049,651 BVES-AS1, LIN28B, 74 more genes
    nsv6615289copy number variation1nstd223human GRCh38 chr6: 99,415,865-99,416,327 , GRCh37.p13 chr6: 99,863,741-99,864,203 PNISR
    nsv6614239copy number variation1nstd223human GRCh38 chr6: 99,399,929-99,400,340 , GRCh37.p13 chr6: 99,847,805-99,848,216 PNISR
    nsv6608887copy number variation1nstd223human GRCh38 chr6: 99,417,725-99,418,958 , GRCh37.p13 chr6: 99,865,601-99,866,834 PNISR
    nsv6606696copy number variation1nstd223human GRCh38 chr6: 99,414,864-99,441,267 , GRCh37.p13 chr6: 99,862,740-99,889,143 PNISR, USP45, 2 more genes
    nsv6568400inversion1nstd223human GRCh38 chr6: 99,395,457-99,396,098 , GRCh37.p13 chr6: 99,843,333-99,843,974 PNISR
    nsv6567229inversion1nstd223human GRCh38 chr6: 99,395,169-99,396,374 , GRCh37.p13 chr6: 99,843,045-99,844,250 PNISR
    nsv6566581inversion1nstd223human GRCh38 chr6: 99,419,503-99,420,235 , GRCh37.p13 chr6: 99,867,379-99,868,111 PNISR
    nsv6563737inversion1nstd223human GRCh38 chr6: 99,422,136-99,422,778 , GRCh37.p13 chr6: 99,870,012-99,870,654 PNISR
    nsv6560526inversion1nstd223human GRCh38 chr6: 99,419,566-99,420,185 , GRCh37.p13 chr6: 99,867,442-99,868,061 PNISR
    nsv6559998inversion1nstd223human GRCh38 chr6: 99,405,031-99,405,194 , GRCh37.p13 chr6: 99,852,907-99,853,070 PNISR
    nsv6556895inversion1nstd223human GRCh38 chr6: 99,419,559-99,420,236 , GRCh37.p13 chr6: 99,867,435-99,868,112 PNISR
    nsv6313858copy number variation1nstd102humanPathogenic GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488 RN7SL509P, LAMA4, 311 more genes
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