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Items: 1 to 20 of 234

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935826copy number variation1nstd209human GRCh38 chr17: 81,300,789-81,301,081 , GRCh37.p13 chr17: 79,274,589-79,274,881 LINC00482
    nsv5656995insertion1nstd207human GRCh38 chr17: 81,307,438-81,307,438 , GRCh37.p13 chr17: 79,281,238-79,281,238 LINC00482
    nsv5647677insertion1nstd207human GRCh38 chr17: 81,307,349-81,307,349 , GRCh37.p13 chr17: 79,281,149-79,281,149 LINC00482
    nsv5520262copy number variation1nstd206human GRCh38 chr17: 81,300,000-81,303,547 , GRCh37.p13 chr17: 79,273,800-79,277,347 LINC00482
    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
    nsv5294695copy number variation1nstd204human GRCh38.p13 chr17: 80,930,501-81,587,000 , GRCh37.p13 chr17: 78,904,301-79,554,026 , LOC105371926, 32 more genes
    nsv5017032copy number variation1nstd200human GRCh38 chr17: 81,308,808-81,315,830 , GRCh37.p13 chr17: 79,282,608-79,289,630 TMEM105, LINC00482
    nsv5017031copy number variation1nstd200human GRCh38 chr17: 81,303,134-81,303,811 , GRCh37.p13 chr17: 79,276,934-79,277,611 LINC00482
    nsv5014108copy number variation1nstd200human GRCh38 chr17: 81,203,730-81,483,549 , GRCh37.p13 chr17: 79,177,530-79,319,162 , LINC03048, 13 more genes
    nsv5014106copy number variation1nstd200human GRCh38 chr17: 81,148,551-81,355,635 , GRCh37.p13 chr17: 79,122,351-79,319,162 , LINC00482, 8 more genes
    nsv4867501copy number variation1nstd200human GRCh37 chr17: 79,282,608-79,289,630 , GRCh38.p12 chr17: 81,308,808-81,315,830 LINC00482, TMEM105
    nsv4854440copy number variation1nstd200human GRCh37 chr17: 79,122,351-79,329,435 , GRCh38.p12 chr17: 81,148,551-81,355,635 , TEPSIN, 8 more genes
    nsv4755762insertion1nstd199human GRCh37 chr17: 79,281,182-79,281,182 , GRCh38.p12 chr17: 81,307,382-81,307,382 LINC00482
    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
    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
    nsv4438791insertion1nstd175human GRCh37 chr17: 79,281,238-79,281,238 , GRCh38.p12 chr17: 81,307,438-81,307,438 LINC00482
    nsv4262869copy number variation1nstd166human GRCh37.p13 chr17: 79,260,089-79,398,035 , GRCh38.p12 chr17: 81,286,289-81,424,235 , BAHCC1, 5 more genes
    nsv3965354insertion1nstd168human GRCh38 chr17: 81,184,403-81,452,333 , GRCh37.p13 chr17: 79,158,203-79,319,162 , CEP131, 11 more genes
    nsv3939091insertion1nstd167human GRCh37 chr17: 79,281,238-79,281,238 , GRCh38.p12 chr17: 81,307,438-81,307,438 LINC00482
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