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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5728573mobile element insertion1nstd211human GRCh38 chr6: 150,377,722-150,377,722 , GRCh37.p13 chr6: 150,698,858-150,698,858 IYD
    nsv5691111mobile element insertion2nstd211human GRCh38 chr6: 150,386,386-150,386,386 , GRCh37.p13 chr6: 150,707,522-150,707,522 IYD
    nsv5640996insertion2nstd207human GRCh38 chr6: 150,372,601-150,372,601 , GRCh37.p13 chr6: 150,693,737-150,693,737 IYD
    nsv5638901insertion1nstd207human GRCh38 chr6: 150,372,324-150,372,324 , GRCh37.p13 chr6: 150,693,460-150,693,460 IYD
    nsv5632161insertion1nstd207human GRCh38 chr6: 150,372,412-150,372,412 , GRCh37.p13 chr6: 150,693,548-150,693,548 IYD
    nsv5582952copy number variation1nstd207human GRCh38 chr6: 150,372,705-150,372,770 , GRCh37.p13 chr6: 150,693,841-150,693,906 IYD
    nsv5577170copy number variation1nstd207human GRCh38 chr6: 150,372,475-150,372,537 , GRCh37.p13 chr6: 150,693,611-150,693,673 IYD
    nsv5576648copy number variation1nstd207human GRCh38 chr6: 150,372,454-150,372,643 , GRCh37.p13 chr6: 150,693,590-150,693,779 IYD
    nsv5463707copy number variation1nstd206human GRCh38 chr6: 150,377,225-150,377,339 , GRCh37.p13 chr6: 150,698,361-150,698,475 IYD
    nsv5462622copy number variation1nstd206human GRCh38 chr6: 150,392,047-150,392,271 , GRCh37.p13 chr6: 150,713,183-150,713,407 IYD
    nsv5408314mobile element insertion1nstd206human GRCh38 chr6: 150,386,386-150,386,437 , GRCh37.p13 chr6: 150,707,522-150,707,573 IYD
    nsv5309860copy number variation1nstd204human GRCh37.p13 chr6: 150,482,738-151,022,419 , GRCh38.p13 chr6: 150,161,602-150,701,283 RNU4-7P, PLEKHG1, 5 more genes
    nsv5228775copy number variation1nstd204human GRCh38.p13 chr6: 150,374,945-150,385,312 , GRCh37.p13 chr6: 150,696,081-150,706,448 SSR1P1, IYD
    nsv5227352copy number variation1nstd204human GRCh38.p13 chr6: 150,342,526-150,370,127 , GRCh37.p13 chr6: 150,663,662-150,691,263 IYD
    nsv5226443copy number variation1nstd204human GRCh37.p13 chr6: 150,482,837-151,022,136 , GRCh38.p13 chr6: 150,161,701-150,701,000 RNU4-7P, PLEKHG1, 5 more genes
    nsv5117623mobile element insertion1nstd203human GRCh38 chr6: 150,386,372-150,386,386 , GRCh37.p13 chr6: 150,707,508-150,707,522 IYD
    nsv4943374copy number variation1nstd200human GRCh38 chr6: 150,404,243-150,412,342 , GRCh37.p13 chr6: 150,725,379-150,733,478 IYD
    nsv4943373copy number variation1nstd200human GRCh38 chr6: 150,383,838-150,385,675 , GRCh37.p13 chr6: 150,704,974-150,706,811 SSR1P1, IYD
    nsv4810896copy number variation1nstd200human GRCh37 chr6: 150,725,379-150,733,478 , GRCh38.p12 chr6: 150,404,243-150,412,342 IYD
    nsv4810895copy number variation1nstd200human GRCh37 chr6: 150,704,974-150,706,811 , GRCh38.p12 chr6: 150,383,838-150,385,675 SSR1P1, IYD
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