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Items: 1 to 20 of 263

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137216copy number variation1nstd102humanPathogenic GRCh37 chr17: 30,572,862-35,843,988 , GRCh38.p12 chr17: 32,245,843-36,446,544 PSMD11, C17orf50, 117 more genes
    nsv7095147copy number variation1nstd102humanUncertain significance GRCh37 chr17: 33,475,283-34,079,869 , GRCh38.p12 chr17: 35,148,264-35,752,850 SLC35G3, AP2B1, 26 more genes
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv6997564copy number variation1nstd229human GRCh38 chr17: 35,496,113-35,505,226 , GRCh37.p13 chr17: 33,823,132-33,832,245 SLFN12L, TAF5LP1
    nsv6994838copy number variation1nstd229human GRCh38 chr17: 35,170,807-35,536,994 , GRCh37.p13 chr17: 33,497,826-33,864,013 SLFN5, SPICP2, 15 more genes
    nsv6994333copy number variation1nstd229human GRCh38 chr17: 35,507,764-35,509,983 , GRCh37.p13 chr17: 33,834,783-33,837,002 SLFN12L
    nsv6993239copy number variation1nstd229human GRCh38 chr17: 35,167,502-35,536,993 , GRCh37.p13 chr17: 33,494,521-33,864,012 LOC105371932, SLC35G3, 15 more genes
    nsv6993148copy number variation1nstd229human GRCh38 chr17: 35,458,601-35,493,081 , GRCh37.p13 chr17: 33,785,620-33,820,100 SLFN12L, LOC100420061, 1 more genes
    nsv6991806copy number variation1nstd229human GRCh38 chr17: 35,522,959-35,523,182 , GRCh37.p13 chr17: 33,849,978-33,850,201 SLFN12L
    nsv6986391copy number variation1nstd229human GRCh38 chr17: 35,472,225-35,477,613 , GRCh37.p13 chr17: 33,799,244-33,804,632 SLFN12L
    nsv6984998copy number variation1nstd229human GRCh38 chr17: 35,468,672-35,479,105 , GRCh37.p13 chr17: 33,795,691-33,806,124 SLFN12L
    nsv6983316copy number variation1nstd229human GRCh38 chr17: 35,477,852-35,509,671 , GRCh37.p13 chr17: 33,804,871-33,836,690 TAF5LP1, SLFN12L, 1 more genes
    nsv6982202copy number variation1nstd229human GRCh38 chr17: 34,998,758-35,727,529 , GRCh37.p13 chr17: 33,325,777-34,034,851 SLFN11, LOC105371932, 32 more genes
    nsv6979397copy number variation1nstd229human GRCh38 chr17: 35,479,520-35,484,623 , GRCh37.p13 chr17: 33,806,539-33,811,642 SLFN12L
    nsv6634448copy number variation1nstd102humanUncertain significance GRCh37 chr17: 33,756,756-34,005,513 , GRCh38.p12 chr17: 35,429,737-35,678,494 LOC100420062, TAF5LP1, 13 more genes
    nsv6594328inversion1nstd223human GRCh38 chr17: 35,531,651-35,532,435 , GRCh37.p13 chr17: 33,858,670-33,859,454 SLFN12L
    nsv6581189inversion1nstd223human GRCh38 chr17: 35,531,636-35,532,375 , GRCh37.p13 chr17: 33,858,655-33,859,394 SLFN12L
    nsv6580237inversion1nstd223human GRCh38 chr17: 35,534,019-35,535,191 , GRCh37.p13 chr17: 33,861,038-33,862,210 SLFN12L
    nsv6577052inversion1nstd223human GRCh38 chr17: 35,535,378-35,536,750 , GRCh37.p13 chr17: 33,862,397-33,863,769 SLFN12L
    nsv6514114copy number variation1nstd223human GRCh38 chr17: 35,477,846-35,509,674 , GRCh37.p13 chr17: 33,804,865-33,836,693 SLFN12L, TAF5LP1, 1 more genes
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