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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066656inversion1nstd229human GRCh38 chr17: 40,822,205-41,582,529 , GRCh37.p13 chr17: 38,978,457-39,738,781 LOC105371777, KRT10, 69 more genes
    nsv6993397copy number variation1nstd229human GRCh38 chr17: 41,557,736-41,568,776 , GRCh37.p13 chr17: 39,713,988-39,725,028 KRT9
    nsv6984984copy number variation1nstd229human GRCh38 chr17: 38,377,708-42,855,253 , GRCh37.p13 chr17: 36,701,616-41,007,270 ZNF385C, AOC2, 248 more genes
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6623853copy number variation1nstd224human GRCh37 chr17: 39,720,391-39,740,012 , GRCh38.p12 chr17: 41,564,139-41,583,760 KRT14, KRT9
    nsv6314661copy number variation1nstd102humanBenign GRCh38 chr17: 41,567,439-41,567,636 , GRCh37 chr17: 39,723,691-39,723,888 KRT9
    nsv6202749copy number variation1nstd214human GRCh38 chr17: 41,567,585-41,567,653 , GRCh37.p13 chr17: 39,723,837-39,723,905 KRT9
    nsv6133056copy number variation1nstd213human GRCh37 chr17: 36,400,000-39,740,001 , GRCh38.p12 chr17: 38,545,381-41,583,749 CACNB1, CDC6, 176 more genes
    nsv6029542copy number variation1nstd212human GRCh38 chr17: 41,567,443-41,567,643 , GRCh37.p13 chr17: 39,723,695-39,723,895 KRT9
    nsv5604130copy number variation1nstd207human GRCh38 chr17: 41,567,438-41,567,635 , GRCh37.p13 chr17: 39,723,690-39,723,887 KRT9
    nsv5564389copy number variation1nstd102humanUncertain significance GRCh37 chr17: 39,723,683-39,723,749 , GRCh38 chr17: 41,567,431-41,567,497 KRT9
    nsv5563145sequence alteration1nstd206human GRCh38 chr17: 41,488,474-41,630,650 , GRCh37.p13 chr17: 39,644,726-39,786,902 KRT13, KRT15, 9 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv4680071copy number variation1nstd189human GRCh37.p13 chr17: 39,432,725-40,293,644 , GRCh38.p12 chr17: 41,276,473-42,141,626 ACLY, CNP, 50 more genes
    nsv4633666copy number variation1nstd183human GRCh37 chr17: 39,679,237-39,744,777 , GRCh38.p12 chr17: 41,522,985-41,588,525 KRT9, LINC00974, 2 more genes
    nsv4428038copy number variation1nstd174human GRCh37 chr17: 39,675,594-39,752,678 , GRCh38.p12 chr17: 41,519,342-41,596,426 KRT14, KRT19, 3 more genes
    nsv4420960copy number variation1nstd174human GRCh37 chr17: 39,644,217-39,786,593 , GRCh38.p12 chr17: 41,487,965-41,630,341 KRT17, LINC00974, 9 more genes
    nsv4341303sequence alteration1nstd166human GRCh37.p13 chr17: 39,644,726-39,786,902 , GRCh38.p12 chr17: 41,488,474-41,630,650 KRT14, KRT19, 9 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4269363copy number variation1nstd166human GRCh37.p13 chr17: 39,713,988-39,725,023 , GRCh38.p12 chr17: 41,557,736-41,568,771 KRT9
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