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Items: 1 to 20 of 224

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6996074copy number variation1nstd229human GRCh38 chr17: 56,867,390-56,869,317 , GRCh37.p13 chr17: 54,944,751-54,946,678 DGKE, RNU6-1158P
    nsv6993834copy number variation1nstd229human GRCh38 chr17: 56,862,944-56,863,615 , GRCh37.p13 chr17: 54,940,305-54,940,976 DGKE
    nsv6589436inversion1nstd223human GRCh38 chr17: 56,839,670-56,840,134 , GRCh37.p13 chr17: 54,917,031-54,917,495 DGKE
    nsv6583954inversion1nstd223human GRCh38 chr17: 56,839,964-56,840,439 , GRCh37.p13 chr17: 54,917,325-54,917,800 DGKE
    nsv6531097copy number variation1nstd223human GRCh38 chr17: 56,849,617-56,851,062 , GRCh37.p13 chr17: 54,926,978-54,928,423 DGKE
    nsv6521360copy number variation1nstd223human GRCh38 chr17: 56,867,390-56,869,315 , GRCh37.p13 chr17: 54,944,751-54,946,676 DGKE, RNU6-1158P
    nsv6310393copy number variation1nstd102humanUncertain significance GRCh37 chr17: 54,671,585-59,938,900 , GRCh38.p12 chr17: 56,594,224-61,861,539 RNF43, LOC107985048, 132 more genes
    nsv6133316copy number variation1nstd213human GRCh37 chr17: 53,930,000-62,410,001 , GRCh38.p12 chr17: 55,852,639-64,332,641 CA4, CD79B, 208 more genes
    nsv6021462copy number variation1nstd212human GRCh38 chr17: 56,859,467-56,859,544 , GRCh37.p13 chr17: 54,936,828-54,936,905 DGKE
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5518022copy number variation1nstd206human GRCh38 chr17: 56,866,942-56,867,044 , GRCh37.p13 chr17: 54,944,303-54,944,405 DGKE
    nsv5358980translocation1nstd200human GRCh38 chr17: 56,832,838-56,832,838 , GRCh38 chr17: 56,832,781-56,832,781 , GRCh37.p13 chr17: 54,910,142-54,910,142 , GRCh37.p13 chr17: 54,910,199-54,910,199 C17orf67, DGKE
    nsv5337925translocation1nstd200human GRCh37 chr17: 54,910,199-54,910,199 , GRCh37 chr17: 54,910,142-54,910,142 , GRCh38.p12 chr17: 56,832,838-56,832,838 , GRCh38.p12 chr17: 56,832,781-56,832,781 DGKE, C17orf67
    nsv5026598copy number variation1nstd200human GRCh38 chr17: 56,841,242-56,841,447 , GRCh37.p13 chr17: 54,918,603-54,918,808 DGKE
    nsv5013841copy number variation1nstd200human GRCh38 chr17: 56,849,480-56,851,113 , GRCh37.p13 chr17: 54,926,841-54,928,474 DGKE
    nsv4670072copy number variation1nstd186human GRCh37 chr17: 54,938,072-54,938,603 , GRCh38.p12 chr17: 56,860,711-56,861,242 DGKE
    nsv4629959copy number variation1nstd183human GRCh37 chr17: 54,938,072-54,938,603 , GRCh38.p12 chr17: 56,860,711-56,861,242 DGKE
    nsv4624482copy number variation1nstd183human GRCh37 chr17: 54,911,181-54,912,516 , GRCh38.p12 chr17: 56,833,820-56,835,155 C17orf67, DGKE
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4266443copy number variation1nstd166human GRCh37.p13 chr17: 54,937,000-54,946,383 , GRCh38.p12 chr17: 56,859,639-56,869,022 DGKE
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