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Items: 1 to 20 of 171

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6114611mobile element insertion1nstd186human GRCh37 chr17: 38,550,451-38,550,455 , GRCh38.p12 chr17: 40,394,199-40,394,203 TOP2A
    nsv5703231mobile element insertion2nstd211human GRCh38 chr17: 40,394,199-40,394,199 , GRCh37.p13 chr17: 38,550,451-38,550,451 TOP2A
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5420435mobile element insertion1nstd206human GRCh38 chr17: 40,394,199-40,394,203 , GRCh37.p13 chr17: 38,550,451-38,550,455 TOP2A
    nsv5365768translocation1nstd200human GRCh38 chrX: 79,565,701-79,565,701 , GRCh38 chr17: 40,389,649-40,389,649 , GRCh37.p13 chr17: 38,545,901-38,545,901 , GRCh37.p13 chrX: 78,821,198-78,821,198 TOP2A
    nsv5289915copy number variation1nstd204human GRCh38.p13 chr17: 40,377,801-40,433,500 , GRCh37.p13 chr17: 38,534,053-38,589,752 TOP2A, LOC100421674
    nsv4670853copy number variation1nstd186human GRCh37 chr17: 38,565,393-38,566,364 , GRCh38.p12 chr17: 40,409,141-40,410,112 TOP2A
    nsv4667579copy number variation1nstd186human GRCh37 chr17: 38,567,746-38,567,885 , GRCh38.p12 chr17: 40,411,494-40,411,633 TOP2A
    nsv4631665copy number variation1nstd183human GRCh37 chr17: 38,567,746-38,567,885 , GRCh38.p12 chr17: 40,411,494-40,411,633 TOP2A
    nsv4631249copy number variation1nstd183human GRCh37 chr17: 38,567,549-38,567,619 , GRCh38.p12 chr17: 40,411,297-40,411,367 TOP2A
    nsv4628770copy number variation2nstd183human GRCh37 chr17: 38,565,393-38,566,364 , GRCh38.p12 chr17: 40,409,141-40,410,112 TOP2A
    nsv4625839copy number variation1nstd183human GRCh37 chr17: 38,569,271-38,569,414 , GRCh38.p12 chr17: 40,413,019-40,413,162 TOP2A
    nsv4623624copy number variation1nstd183human GRCh37 chr17: 38,548,509-38,548,686 , GRCh38.p12 chr17: 40,392,257-40,392,434 TOP2A
    nsv4622275copy number variation1nstd183human GRCh37 chr17: 38,548,343-38,548,631 , GRCh38.p12 chr17: 40,392,091-40,392,379 TOP2A
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 more genes
    nsv4334447sequence alteration1nstd166human GRCh37.p13 chr17: 38,428,364-38,577,561 , GRCh38.p12 chr17: 40,272,112-40,421,309 WIPF2, PPIAP54, 8 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
    nsv4260992copy number variation1nstd166human GRCh37.p13 chr17: 38,571,000-38,577,000 , GRCh38.p12 chr17: 40,414,748-40,420,748 TOP2A
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 more genes
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