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Items: 1 to 20 of 326

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148268copy number variation1nstd102humanPathogenic GRCh38 chr17: 16,018,139-16,028,011 , GRCh37.p13 chr17: 15,921,453-15,931,325 TTC19, NCOR1
    nsv7142858insertion1nstd232human GRCh37.p13 chr17: 15,932,132-15,932,132 , GRCh38.p12 chr17: 16,028,818-16,028,818 NCOR1, TTC19
    nsv7093244copy number variation1nstd102humanUncertain significance GRCh38 chr17: 16,000,247-16,000,320 , GRCh37 chr17: 15,903,561-15,903,634 TTC19
    nsv7076343inversion1nstd229human GRCh38 chr17: 16,011,388-16,016,979 , GRCh37.p13 chr17: 15,914,702-15,920,293 TTC19
    nsv7076305inversion1nstd229human GRCh38 chr17: 16,008,547-16,011,881 , GRCh37.p13 chr17: 15,911,861-15,915,195 TTC19
    nsv7076244inversion1nstd229human GRCh38 chr17: 16,013,569-16,013,623 , GRCh37.p13 chr17: 15,916,883-15,916,937 TTC19
    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
    nsv7066862inversion1nstd229human GRCh38 chr17: 15,664,455-18,717,083 , GRCh37.p13 chr17: 15,567,769-18,620,396 KRT16P6, RPLP1P11, 129 more genes
    nsv7059660inversion1nstd229human GRCh38 chr17: 16,041,448-17,186,703 , GRCh37.p13 chr17: 15,944,762-17,090,017 SNHG29, ZNF624, 46 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
    nsv6997782copy number variation1nstd229human GRCh38 chr17: 16,028,128-16,031,027 , GRCh37.p13 chr17: 15,931,442-15,934,341 NCOR1, TTC19
    nsv6996605copy number variation1nstd229human GRCh38 chr17: 16,010,126-16,011,157 , GRCh37.p13 chr17: 15,913,440-15,914,471 TTC19
    nsv6995532copy number variation1nstd229human GRCh38 chr17: 15,989,001-16,127,700 , GRCh37.p13 chr17: 15,892,315-16,031,014 RNU6-314P, TTC19, 4 more genes
    nsv6994291copy number variation1nstd229human GRCh38 chr17: 16,007,136-16,013,059 , GRCh37.p13 chr17: 15,910,450-15,916,373 TTC19
    nsv6993167copy number variation1nstd229human GRCh38 chr17: 16,009,015-16,009,048 , GRCh37.p13 chr17: 15,912,329-15,912,362 TTC19
    nsv6992064copy number variation1nstd229human GRCh38 chr17: 15,945,079-16,034,152 , GRCh37.p13 chr17: 15,848,393-15,937,466 TTC19, ZSWIM7, 2 more genes
    nsv6980924copy number variation1nstd229human GRCh38 chr17: 16,033,879-16,033,930 , GRCh37.p13 chr17: 15,937,193-15,937,244 NCOR1, TTC19
    nsv6978375copy number variation1nstd229human GRCh38 chr17: 16,023,431-16,057,572 , GRCh37.p13 chr17: 15,926,745-15,960,886 TTC19, RPLP1P11, 1 more genes
    nsv6978237copy number variation1nstd229human GRCh38 chr17: 16,005,127-16,007,696 , GRCh37.p13 chr17: 15,908,441-15,911,010 TTC19
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