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Items: 1 to 20 of 415

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147514insertion1nstd232human GRCh37.p13 chr17: 17,179,480-17,179,480 , GRCh38.p12 chr17: 17,276,166-17,276,166 COPS3
    nsv7140827insertion1nstd232human GRCh37.p13 chr17: 17,168,300-17,168,300 , GRCh38.p12 chr17: 17,264,986-17,264,986 COPS3
    nsv7139244insertion1nstd232human GRCh37.p13 chr17: 17,174,322-17,174,322 , GRCh38.p12 chr17: 17,271,008-17,271,008 COPS3
    nsv7137103copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,664,739-20,370,783 , GRCh38.p12 chr17: 16,761,425-20,467,470 NMTRQ-TTG12-1, NOS2P4, 148 more genes
    nsv7098881copy number variation1nstd102humanPathogenic GRCh37 chr17: 17,116,969-20,217,378 , GRCh38.p12 chr17: 17,213,655-20,314,065 LOC105371578, SNORD3B-2, 119 more genes
    nsv7073486inversion1nstd229human GRCh38 chr17: 15,622,817-18,740,940 , GRCh37.p13 chr17: 15,526,131-18,644,253 NCOR1, KRT16P6, 129 more genes
    nsv7073439inversion1nstd229human GRCh38 chr17: 15,962,151-19,146,977 , GRCh37.p13 chr17: 15,865,465-19,050,290 RNU6-767P, KRT17P5, 129 more genes
    nsv7068050inversion1nstd229human GRCh38 chr17: 16,799,901-18,286,035 , GRCh37.p13 chr17: 16,703,215-18,189,349 ATPAF2, TNFRSF13B, 51 more genes
    nsv7067152inversion1nstd229human GRCh38 chr17: 16,993,913-17,832,711 , GRCh37.p13 chr17: 16,897,227-17,736,025 PLD6, TSEN15P1, 21 more genes
    nsv7066862inversion1nstd229human GRCh38 chr17: 15,664,455-18,717,083 , GRCh37.p13 chr17: 15,567,769-18,620,396 KRT16P6, RPLP1P11, 129 more genes
    nsv7063369inversion1nstd229human GRCh38 chr17: 17,251,813-17,332,028 , GRCh37.p13 chr17: 17,155,127-17,235,342 NT5M, COPS3
    nsv7061130inversion1nstd229human GRCh38 chr17: 17,251,926-17,330,861 , GRCh37.p13 chr17: 17,155,240-17,234,175 NT5M, COPS3
    nsv7059177inversion1nstd229human GRCh38 chr17: 15,493,473-18,338,296 , GRCh37.p13 chr17: 15,396,787-18,241,610 TOM1L2, PPIAP53, 107 more genes
    nsv6995851copy number variation1nstd229human GRCh38 chr17: 16,261,589-17,283,740 , GRCh37.p13 chr17: 16,164,903-17,187,054 SRP68P1, SNORD49B, 42 more genes
    nsv6990551copy number variation1nstd229human GRCh38 chr17: 17,277,505-17,277,642 , GRCh37.p13 chr17: 17,180,819-17,180,956 COPS3
    nsv6989605copy number variation1nstd229human GRCh38 chr17: 17,130,501-17,247,600 , GRCh37.p13 chr17: 17,033,815-17,150,914 PLD6, RNU6-767P, 5 more genes
    nsv6986815copy number variation1nstd229human GRCh38 chr17: 17,140,101-17,247,600 , GRCh37.p13 chr17: 17,043,415-17,150,914 PLD6, RNU6-767P, 5 more genes
    nsv6983968copy number variation1nstd229human GRCh38 chr17: 17,281,416-17,286,715 , GRCh37.p13 chr17: 17,184,730-17,190,029 COPS3
    nsv6983372copy number variation1nstd229human GRCh38 chr17: 17,276,163-17,276,395 , GRCh37.p13 chr17: 17,179,477-17,179,709 COPS3
    nsv6637220copy number variation1nstd102humanPathogenic GRCh37 chr17: 17,103,571-19,331,028 , GRCh38.p12 chr17: 17,200,257-19,427,715 PRPSAP2, SNORD3A, 96 more genes
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