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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7094785copy number variation1nstd102humanPathogenic GRCh37 chr15: 68,499,209-68,500,605 , GRCh38.p12 chr15: 68,206,871-68,208,267 CLN6
    nsv7094728copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 68,500,468-68,504,211 , GRCh38.p12 chr15: 68,208,130-68,211,873 CLN6
    nsv7069747inversion1nstd229human GRCh38 chr15: 65,994,863-75,247,978 , GRCh37.p13 chr15: 66,287,201-75,540,319 REC114, PARP6, 199 more genes
    nsv7064235inversion1nstd229human GRCh38 chr15: 68,177,132-69,135,262 , GRCh37.p13 chr15: 68,469,470-69,427,601 CORO2B, LOC105370873, 16 more genes
    nsv7063557inversion1nstd229human GRCh38 chr15: 68,148,341-69,105,455 , GRCh37.p13 chr15: 68,440,679-69,397,795 ITGA11, MIR4312, 16 more genes
    nsv7058734inversion1nstd229human GRCh38 chr15: 68,148,356-69,105,454 , GRCh37.p13 chr15: 68,440,694-69,397,794 LOC105370873, CORO2B, 16 more genes
    nsv6978054copy number variation1nstd229human GRCh38 chr15: 68,206,337-68,212,119 , GRCh37.p13 chr15: 68,498,675-68,504,457 CLN6, CALML4
    nsv6968562copy number variation1nstd229human GRCh38 chr15: 68,198,954-68,205,604 , GRCh37.p13 chr15: 68,491,292-68,497,942 CLN6, CALML4
    nsv6967252copy number variation1nstd229human GRCh38 chr15: 68,199,346-68,254,758 , GRCh37.p13 chr15: 68,491,684-68,547,096 CLN6, HMGN2P40, 1 more genes
    nsv6591364inversion1nstd223human GRCh38 chr15: 68,217,610-68,218,481 , GRCh37.p13 chr15: 68,509,948-68,510,819 CLN6
    nsv6577631inversion1nstd223human GRCh38 chr15: 68,226,333-68,226,496 , GRCh37.p13 chr15: 68,518,671-68,518,834 CLN6
    nsv6501519copy number variation1nstd223human GRCh38 chr15: 68,209,891-68,211,037 , GRCh37.p13 chr15: 68,502,229-68,503,375 CLN6
    nsv6309802copy number variation2nstd102humanUncertain significance GRCh37 chr15: 66,161,924-69,018,313 , GRCh38.p12 chr15: 65,869,586-68,725,974 SNORD18B, TRQ-CTG1-4, 50 more genes
    nsv6291815copy number variation1nstd102humanUncertain significance GRCh37 chr15: 68,243,109-68,780,504 , GRCh38.p12 chr15: 67,950,771-68,488,165 PIAS1, ITGA11, 7 more genes
    nsv6201740copy number variation1nstd214human GRCh38 chr15: 68,222,394-68,222,467 , GRCh37.p13 chr15: 68,514,732-68,514,805 CLN6
    nsv6132905copy number variation1nstd213human GRCh37 chr15: 67,010,000-68,680,001 , GRCh38.p12 chr15: 66,717,662-68,387,662 SMAD3, SMAD6, 25 more genes
    nsv6092599insertion1nstd212human GRCh38 chr15: 68,229,772-68,229,772 , GRCh37.p13 chr15: 68,522,110-68,522,110 CLN6
    nsv6092203insertion1nstd212human GRCh38 chr15: 68,221,886-68,221,886 , GRCh37.p13 chr15: 68,514,224-68,514,224 CLN6
    nsv6086542insertion1nstd212human GRCh38 chr15: 68,221,824-68,221,824 , GRCh37.p13 chr15: 68,514,162-68,514,162 CLN6
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