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Items: 1 to 20 of 14455

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 RAB10, MYADML, 326 more genes
    nsv6131469insertion1nstd186human GRCh37 chr19: 15,785,251-15,785,251 , GRCh38.p12 chr19: 15,674,441-15,674,441 CYP4F12
    nsv6130611insertion1nstd186human GRCh37 chr19: 41,386,609-41,386,660 , GRCh38.p12 chr19: 40,880,704-40,880,755 CYP2A7
    nsv6130477insertion1nstd186human GRCh37 chr20: 48,136,480-48,136,521 , GRCh38.p12 chr20: 49,519,943-49,519,984 PTGIS
    nsv6130457insertion1nstd186human GRCh37 chr15: 80,718,429-80,718,451 , GRCh38.p12 chr15: 80,426,087-80,426,109 ARNT2
    nsv6129472insertion1nstd186human GRCh37 chr20: 52,779,081-52,779,103 , GRCh38.p12 chr20: 54,162,542-54,162,564 CYP24A1
    nsv6128326insertion1nstd186human GRCh37 chr2: 24,989,468-24,989,470 , GRCh38.p12 chr2: 24,766,599-24,766,601 NCOA1
    nsv6127404copy number variation1nstd186human GRCh37 chr19: 41,338,779-41,370,779 , GRCh38.p12 chr19: 40,832,874-40,864,874 CYP2A6
    nsv6126930insertion1nstd186human GRCh37 chr4: 69,861,888-114,815,333 , GRCh38.p12 chr4: 68,996,170-113,894,177 DDIT4L-AS1, LOC112267901, 616 more genes
    nsv6126883copy number variation1nstd186human GRCh37 chr19: 15,787,218-15,787,593 , GRCh38.p12 chr19: 15,676,408-15,676,783 CYP4F12
    nsv6126279copy number variation1nstd186human GRCh37 chr19: 15,784,890-15,785,153 , GRCh38.p12 chr19: 15,674,080-15,674,343 CYP4F12
    nsv6126259copy number variation1nstd186human GRCh37 chr19: 16,041,899-16,042,570 , GRCh38.p12 chr19: 15,931,089-15,931,760 CYP4F11
    nsv6125949copy number variation1nstd186human GRCh37 chr19: 16,042,079-16,042,735 , GRCh38.p12 chr19: 15,931,269-15,931,925 CYP4F11
    nsv6125231insertion1nstd186human GRCh37 chr8: 71,071,473-71,071,477 , GRCh38.p12 chr8: 70,159,238-70,159,242 NCOA2
    nsv6124893copy number variation1nstd186human GRCh37 chr19: 15,778,810-15,833,085 , GRCh38.p12 chr19: 15,668,000-15,722,275 CYP4F12
    nsv6124659copy number variation1nstd186human GRCh37 chr19: 41,352,226-41,384,122 , GRCh38.p12 chr19: 40,846,321-40,878,217 CYP2A6, CYP2A7
    nsv6124347insertion1nstd186human GRCh37 chr8: 65,555,595-65,555,647 , GRCh38.p12 chr8: 64,643,038-64,643,090 CYP7B1
    nsv6124104insertion1nstd186human GRCh37 chr8: 65,555,748-65,555,748 , GRCh38.p12 chr8: 64,643,191-64,643,191 CYP7B1
    nsv6124073copy number variation1nstd186human GRCh37 chr19: 16,042,412-16,044,794 , GRCh38.p12 chr19: 15,931,602-15,933,984 CYP4F11
    nsv6123408copy number variation1nstd186human GRCh37 chr19: 41,355,847-41,387,566 , GRCh38.p12 chr19: 40,849,942-40,881,661 CYP2A6, CYP2A7
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