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Items: 1 to 20 of 222

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978483insertion1nstd209human GRCh38 chr17: 21,033,537-21,033,537 , GRCh37.p13 chr17: 20,936,850-20,936,850 USP22
    nsv5944636copy number variation1nstd209human GRCh38 chr17: 21,027,255-21,027,334 , GRCh37.p13 chr17: 20,930,568-20,930,647 USP22
    nsv5935436copy number variation1nstd209human GRCh38 chr17: 21,016,078-21,016,127 , GRCh37.p13 chr17: 20,919,391-20,919,440 USP22
    nsv5713310mobile element insertion1nstd211human GRCh38 chr17: 21,029,424-21,029,424 , GRCh37.p13 chr17: 20,932,737-20,932,737 USP22
    nsv5670902inversion1nstd207human GRCh37.p13 chr17: 19,143,942-21,250,947 , GRCh38 chr17: 19,240,629-21,558,840 , ALDH3A1, 86 more genes
    nsv5603034copy number variation1nstd207human GRCh38 chr17: 21,027,255-21,027,334 , GRCh37.p13 chr17: 20,930,568-20,930,647 USP22
    nsv5553333insertion1nstd206human GRCh38 chr17: 21,033,537-21,033,537 , GRCh37.p13 chr17: 20,936,850-20,936,850 USP22
    nsv5515253copy number variation1nstd206human GRCh38 chr17: 20,993,552-20,998,383 , GRCh37.p13 chr17: 20,896,865-20,901,696 USP22
    nsv5514153copy number variation1nstd206human GRCh38 chr17: 21,027,257-21,027,335 , GRCh37.p13 chr17: 20,930,570-20,930,648 USP22
    nsv5374844translocation1nstd200human GRCh38 chr17: 20,998,095-20,998,095 , GRCh38 chr17: 20,998,314-20,998,314 , GRCh37.p13 chr17: 20,901,408-20,901,408 , GRCh37.p13 chr17: 20,901,627-20,901,627 USP22
    nsv5358707translocation1nstd200human GRCh38 chr17: 21,027,335-21,027,335 , GRCh38 chr17: 21,027,257-21,027,257 , GRCh37.p13 chr17: 20,930,570-20,930,570 , GRCh37.p13 chr17: 20,930,648-20,930,648 USP22
    nsv5026262copy number variation1nstd200human GRCh38 chr17: 21,039,112-21,039,215 , GRCh37.p13 chr17: 20,942,425-20,942,528 USP22
    nsv4888602inversion1nstd200human GRCh37 chr17: 20,902,149-20,902,256 , GRCh38.p12 chr17: 20,998,836-20,998,943 USP22
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4642578copy number variation1nstd186human GRCh37 chr17: 20,930,570-20,930,648 , GRCh38.p12 chr17: 21,027,257-21,027,335 USP22
    nsv4634084copy number variation1nstd183human GRCh37 chr17: 20,945,133-20,947,213 , GRCh38.p12 chr17: 21,041,820-21,043,900 USP22
    nsv4391738copy number variation1nstd171human GRCh37 chr17: 20,932,263-20,932,293 , GRCh38.p12 chr17: 21,028,950-21,028,980 USP22
    nsv4338141sequence alteration1nstd166human GRCh37.p13 chr17: 20,901,408-20,901,968 , GRCh38.p12 chr17: 20,998,095-20,998,655 USP22
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4243563copy number variation1nstd166human GRCh37.p13 chr17: 20,930,570-20,930,648 , GRCh38.p12 chr17: 21,027,257-21,027,335 USP22
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