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Items: 1 to 20 of 445

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145080copy number variation1nstd232human GRCh37.p13 chr17: 18,182,766-18,182,898 , GRCh38.p12 chr17: 18,279,452-18,279,584 , GRCh38.p12 chr17|NW_017363819.1: 39,826-39,958 TOP3A
    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
    nsv7095078copy number variation1nstd102humanUncertain significance GRCh37 chr17: 18,178,116-18,178,314 , GRCh38.p12 chr17: 18,274,802-18,275,000 , GRCh38.p12 chr17|NW_017363819.1: 35,176-35,374 TOP3A
    nsv7094959copy number variation1nstd102humanUncertain significance GRCh37 chr17: 18,217,893-18,218,092 , GRCh38.p12 chr17: 18,314,579-18,314,778 , GRCh38.p12 chr17|NW_017363819.1: 74,953-75,152 TOP3A, SMCR8
    nsv7077532inversion1nstd229human GRCh38 chr17: 17,907,928-18,966,216 , GRCh37.p13 chr17: 17,811,242-18,869,529 SMCR8, PAIP1P2, 51 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
    nsv7073152inversion1nstd229human GRCh38 chr17: 17,317,750-18,724,343 , GRCh37.p13 chr17: 17,221,064-18,627,656 TOP3A, SMCR8, 60 more genes
    nsv7070575inversion1nstd229human GRCh38 chr17: 18,291,968-18,292,089 , GRCh37.p13 chr17: 18,195,282-18,195,403 TOP3A
    nsv7068050inversion1nstd229human GRCh38 chr17: 16,799,901-18,286,035 , GRCh37.p13 chr17: 16,703,215-18,189,349 ATPAF2, TNFRSF13B, 51 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
    nsv7059177inversion1nstd229human GRCh38 chr17: 15,493,473-18,338,296 , GRCh37.p13 chr17: 15,396,787-18,241,610 TOM1L2, PPIAP53, 107 more genes
    nsv6993663copy number variation1nstd229human GRCh38 chr17: 18,312,187-18,318,318 , GRCh37.p13 chr17: 18,215,501-18,221,632 RPL21P121, SMCR8, 2 more genes
    nsv6991576copy number variation1nstd229human GRCh38 chr17: 18,243,901-18,384,300 , GRCh37.p13 chr17: 18,147,215-18,287,614 TOP3A, LLGL1, 8 more genes
    nsv6980638copy number variation1nstd229human GRCh38 chr17: 18,272,576-18,306,528 , GRCh37.p13 chr17: 18,175,890-18,209,842 TOP3A
    nsv6979362copy number variation1nstd229human GRCh38 chr17: 18,287,659-18,290,157 , GRCh37.p13 chr17: 18,190,973-18,193,471 TOP3A
    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
    nsv6634447copy number variation1nstd102humanUncertain significance GRCh37 chr17: 16,736,709-20,339,460 , GRCh38.p12 chr17: 16,833,395-20,436,147 KCTD9P1, MTCO1P39, 139 more genes
    nsv6624017copy number variation1nstd224human GRCh37 chr17: 18,155,870-18,702,230 , GRCh38.p12 chr17: 18,252,556-18,798,917 SHMT1, SRP68P2, 33 more genes
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