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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137216copy number variation1nstd102humanPathogenic GRCh37 chr17: 30,572,862-35,843,988 , GRCh38.p12 chr17: 32,245,843-36,446,544 PSMD11, C17orf50, 117 more genes
    nsv7058412inversion1nstd229human GRCh38 chr17: 30,021,943-32,643,975 , GRCh37.p13 chr17: 28,348,961-30,970,993 RNU6-990P, LOC105371730, 81 more genes
    nsv6985366copy number variation1nstd229human GRCh38 chr17: 32,217,501-32,374,500 , GRCh37.p13 chr17: 30,544,520-30,701,519 LOC105371731, ZNF207, 6 more genes
    nsv6591023inversion1nstd223human GRCh38 chr17: 32,336,312-32,336,887 , GRCh37.p13 chr17: 30,663,331-30,663,906 C17orf75
    nsv6578264inversion1nstd223human GRCh38 chr17: 32,328,676-32,329,176 , GRCh37.p13 chr17: 30,655,695-30,656,195 C17orf75
    nsv6577273inversion1nstd223human GRCh38 chr17: 32,345,409-32,346,622 , GRCh37.p13 chr17: 30,672,428-30,673,641 C17orf75
    nsv6576677inversion1nstd223human GRCh38 chr17: 32,349,005-32,349,527 , GRCh37.p13 chr17: 30,676,024-30,676,546 ZNF207, C17orf75, 1 more genes
    nsv6133300copy number variation1nstd213human GRCh37 chr17: 30,620,000-31,340,001 , GRCh38.p12 chr17: 32,292,981-33,012,983 ASIC2, MYO1D, 13 more genes
    nsv6133229copy number variation1nstd213human GRCh37 chr17: 25,300,000-32,120,001 , GRCh38.p12 chr17: 26,972,974-33,792,982 BLMH, CPD, 197 more genes
    nsv6133047copy number variation1nstd213human GRCh37 chr17: 30,150,000-30,710,001 , GRCh38.p12 chr17: 31,822,981-32,382,982 SH3GL1P1, ZNF207, 16 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
    nsv5527019copy number variation1nstd206human GRCh38 chr17: 32,339,106-32,339,182 , GRCh37.p13 chr17: 30,666,125-30,666,201 C17orf75
    nsv5155854mobile element insertion1nstd203human GRCh38 chr17: 32,332,472-32,332,488 , GRCh37.p13 chr17: 30,659,491-30,659,507 C17orf75
    nsv5154688mobile element insertion1nstd203human GRCh38 chr17: 32,343,836-32,343,848 , GRCh37.p13 chr17: 30,670,855-30,670,867 C17orf75, OOSP1P2
    nsv5140456mobile element insertion1nstd203human GRCh38 chr17: 32,341,526-32,341,541 , GRCh37.p13 chr17: 30,668,545-30,668,560 C17orf75
    nsv5016049copy number variation1nstd200human GRCh38 chr17: 32,348,114-32,348,836 , GRCh37.p13 chr17: 30,675,133-30,675,855 ZNF207, C17orf75, 1 more genes
    nsv5016048copy number variation1nstd200human GRCh38 chr17: 32,325,785-32,326,669 , GRCh37.p13 chr17: 30,652,804-30,653,688 C17orf75
    nsv4858601copy number variation1nstd200human GRCh37 chr17: 30,666,125-30,666,201 , GRCh38.p12 chr17: 32,339,106-32,339,182 C17orf75
    nsv4858600copy number variation1nstd200human GRCh37 chr17: 30,652,804-30,653,687 , GRCh38.p12 chr17: 32,325,785-32,326,668 C17orf75
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
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