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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5938673copy number variation1nstd209human GRCh38 chr17: 81,663,674-81,664,785 , GRCh37.p13 chr17: 79,630,704-79,631,815 CCDC137, OXLD1
    nsv5533474copy number variation1nstd206human GRCh38 chr17: 81,664,652-81,664,771 , GRCh37.p13 chr17: 79,631,682-79,631,801 CCDC137, OXLD1
    nsv5529550copy number variation1nstd206human GRCh38 chr17: 81,663,633-81,664,816 , GRCh37.p13 chr17: 79,630,663-79,631,846 OXLD1, CCDC137
    nsv5520081copy number variation1nstd206human GRCh38 chr17: 81,663,280-81,664,117 , GRCh37.p13 chr17: 79,630,310-79,631,147 PDE6G, OXLD1
    nsv5298108copy number variation1nstd204human GRCh38.p13 chr17: 80,930,501-82,586,000 , GRCh37.p13 chr17: 78,904,301-80,543,876 , PPP1R27, 89 more genes
    nsv5287926copy number variation1nstd204human GRCh38.p13 chr17: 81,643,901-81,742,500 , GRCh37.p13 chr17: 79,610,927-79,709,049 MRPL12, OXLD1, 8 more genes
    nsv5017060copy number variation1nstd200human GRCh38 chr17: 81,663,532-81,667,398 , GRCh37.p13 chr17: 79,630,562-79,634,428 PDE6G, CCDC137, 1 more genes
    nsv5017044copy number variation1nstd200human GRCh38 chr17: 81,441,456-81,816,579 , GRCh37.p13 chr17: 79,498,418-79,774,455 , LOC105376789, 19 more genes
    nsv4867529copy number variation1nstd200human GRCh37 chr17: 79,630,723-79,631,162 , GRCh38.p12 chr17: 81,663,693-81,664,132 OXLD1
    nsv4634106copy number variation1nstd183human GRCh37 chr17: 79,631,947-79,642,349 , GRCh38.p12 chr17: 81,664,917-81,675,319 CCDC137, OXLD1
    nsv4632300copy number variation1nstd183human GRCh37 chr17: 79,633,501-79,633,644 , GRCh38.p12 chr17: 81,666,471-81,666,614 OXLD1, CCDC137
    nsv4625921copy number variation1nstd183human GRCh37 chr17: 78,632,841-79,703,517 , GRCh38.p12 chr17: 80,659,041-81,736,487 , HGS, 44 more genes
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4457616copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,496,613-79,693,150 , GRCh38.p12 chr17: 81,529,587-81,726,120 MRPL12, ARL16, 10 more genes
    nsv4457483copy number variation1nstd102humanPathogenic GRCh37 chr17: 78,608,912-81,041,938 , GRCh38.p12 chr17: 80,635,112-83,084,062 HEXD, LOC105371929, 94 more genes
    nsv4457456copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,531,886-79,685,043 , GRCh38.p12 chr17: 81,564,860-81,718,013 SLC25A10, MRPL12, 8 more genes
    nsv4432621copy number variation2nstd172human GRCh37.p13 chr17: 79,542,001-79,636,000 , GRCh38.p12 chr17: 81,574,975-81,668,970 PDE6G, NPLOC4, 3 more genes
    nsv4374349copy number variation1nstd173human GRCh37 chr17: 79,330,617-80,189,678 , GRCh38.p12 chr17: 81,356,817-82,231,802 , FAAP100, 49 more genes
    nsv4270519copy number variation1nstd166human GRCh37.p13 chr17: 79,527,172-79,633,826 , GRCh38.p12 chr17: 81,560,146-81,666,796 NPLOC4, OXLD1, 3 more genes
    nsv4268515copy number variation1nstd166human GRCh37.p13 chr17: 79,631,092-79,631,159 , GRCh38.p12 chr17: 81,664,062-81,664,129 OXLD1
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