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Items: 1 to 20 of 246

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127234copy number variation1nstd186human GRCh37 chr17: 73,040,299-73,040,599 , GRCh38.p12 chr17: 75,044,204-75,044,504 KCTD2, ATP5PD
    nsv5971172insertion1nstd209human GRCh38 chr17: 75,044,503-75,044,503 , GRCh37.p13 chr17: 73,040,598-73,040,598 KCTD2, ATP5PD
    nsv5940984copy number variation1nstd209human GRCh38 chr17: 75,044,187-75,044,503 , GRCh37.p13 chr17: 73,040,282-73,040,598 ATP5PD, KCTD2
    nsv5940322copy number variation1nstd209human GRCh38 chr17: 75,065,090-75,065,667 , GRCh37.p13 chr17: 73,061,185-73,061,762 KCTD2
    nsv5931204copy number variation1nstd209human GRCh38 chr17: 75,042,897-75,043,235 , GRCh37.p13 chr17: 73,038,992-73,039,330 ATP5PD, KCTD2
    nsv5698259mobile element insertion1nstd211human GRCh38 chr17: 75,053,884-75,053,884 , GRCh37.p13 chr17: 73,049,979-73,049,979 KCTD2
    nsv5596959copy number variation1nstd207human GRCh38 chr17: 75,044,187-75,044,503 , GRCh37.p13 chr17: 73,040,282-73,040,598 KCTD2, ATP5PD
    nsv5532960copy number variation1nstd206human GRCh38 chr17: 75,034,379-75,034,441 , GRCh37.p13 chr17: 73,030,474-73,030,536 KCTD2, TRR-TCG3-1, 2 more genes
    nsv5530079copy number variation1nstd206human GRCh38 chr17: 75,065,092-75,065,668 , GRCh37.p13 chr17: 73,061,187-73,061,763 KCTD2
    nsv5528999copy number variation1nstd206human GRCh38 chr17: 75,055,630-75,067,004 , GRCh37.p13 chr17: 73,051,725-73,063,099 KCTD2
    nsv5524148copy number variation1nstd206human GRCh38 chr17: 75,028,272-75,030,935 , GRCh37.p13 chr17: 73,024,367-73,027,030 RNU6-362P, KCTD2
    nsv5519944copy number variation1nstd206human GRCh38 chr17: 75,044,204-75,044,504 , GRCh37.p13 chr17: 73,040,299-73,040,599 ATP5PD, KCTD2
    nsv5382954mobile element deletion2nstd186human GRCh37 chr17: 73,040,299-73,040,599 , GRCh38.p12 chr17: 75,044,204-75,044,504 ATP5PD, KCTD2
    nsv5349663translocation1nstd200human GRCh38 chr17: 75,065,704-75,065,704 , GRCh38 chr17: 75,065,773-75,065,773 , GRCh37.p13 chr17: 73,061,799-73,061,799 , GRCh37.p13 chr17: 73,061,868-73,061,868 KCTD2
    nsv5349662translocation1nstd200human GRCh38 chr17: 75,065,092-75,065,092 , GRCh38 chr17: 75,065,668-75,065,668 , GRCh37.p13 chr17: 73,061,187-73,061,187 , GRCh37.p13 chr17: 73,061,763-73,061,763 KCTD2
    nsv5330325translocation1nstd200human GRCh37 chr17: 73,061,763-73,061,763 , GRCh37 chr17: 73,061,187-73,061,187 , GRCh38.p12 chr17: 75,065,092-75,065,092 , GRCh38.p12 chr17: 75,065,668-75,065,668 KCTD2
    nsv5324064copy number variation1nstd204human GRCh38.p13 chr17: 75,065,063-75,065,697 , GRCh37.p13 chr17: 73,061,158-73,061,792 KCTD2
    nsv5298973copy number variation1nstd204human GRCh38.p13 chr17: 74,951,501-75,212,200 , GRCh37.p13 chr17: 72,947,596-73,208,295 RNU6-362P, TRR-CCT2-1, 17 more genes
    nsv5293343copy number variation1nstd204human GRCh38.p13 chr17: 74,899,101-76,684,700 , GRCh37.p13 chr17: 72,895,199-74,680,782 , RNU6-24P, 92 more genes
    nsv5217732mobile element deletion1nstd204human GRCh37.p13 chr17: 73,040,025-73,040,827 , GRCh38.p13 chr17: 75,043,930-75,044,732 KCTD2, ATP5PD
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