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Items: 1 to 20 of 604

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962867insertion1nstd209human GRCh38 chr5: 61,102,844-61,102,844 , GRCh37.p13 chr5: 60,398,671-60,398,671 NDUFAF2
    nsv5949949insertion1nstd209human GRCh38 chr5: 61,147,437-61,147,437 , GRCh37.p13 chr5: 60,443,264-60,443,264 NDUFAF2
    nsv5906306copy number variation1nstd209human GRCh38 chr5: 61,066,499-61,067,764 , GRCh37.p13 chr5: 60,362,326-60,363,591 NDUFAF2
    nsv5902761copy number variation1nstd209human GRCh38 chr5: 61,083,562-61,084,455 , GRCh37.p13 chr5: 60,379,389-60,380,282 NDUFAF2
    nsv5901952copy number variation1nstd209human GRCh38 chr5: 60,825,188-61,041,210 , GRCh37.p13 chr5: 60,121,015-60,337,037 ELOVL7, GNL3LP1, 3 more genes
    nsv5899983copy number variation1nstd209human GRCh38 chr5: 61,105,089-61,108,672 , GRCh37.p13 chr5: 60,400,916-60,404,499 NDUFAF2
    nsv5893162copy number variation1nstd209human GRCh38 chr5: 61,052,100-61,052,185 , GRCh37.p13 chr5: 60,347,927-60,348,012 NDUFAF2
    nsv5891359copy number variation1nstd209human GRCh38 chr5: 61,144,560-61,148,297 , GRCh37.p13 chr5: 60,440,387-60,444,124 NDUFAF2
    nsv5843373copy number variation2nstd209human GRCh38 chr5: 61,066,543-61,067,931 , GRCh37.p13 chr5: 60,362,370-60,363,758 NDUFAF2
    nsv5843372copy number variation2nstd209human GRCh38 chr5: 60,949,867-60,983,882 , GRCh37.p13 chr5: 60,245,694-60,279,709 NDUFAF2
    nsv5843371copy number variation2nstd209human GRCh38 chr5: 60,949,817-60,954,316 , GRCh37.p13 chr5: 60,245,644-60,250,143 NDUFAF2
    nsv5843370copy number variation5nstd209human GRCh38 chr5: 60,949,017-60,950,316 , GRCh37.p13 chr5: 60,244,844-60,246,143 NDUFAF2
    nsv5843131copy number variation1nstd209human GRCh38 chr5: 61,144,551-61,148,050 , GRCh37.p13 chr5: 60,440,378-60,443,877 NDUFAF2
    nsv5843130copy number variation1nstd209human GRCh38 chr5: 61,104,995-61,108,667 , GRCh37.p13 chr5: 60,400,822-60,404,494 NDUFAF2
    nsv5843129copy number variation2nstd209human GRCh38 chr5: 60,949,842-60,956,741 , GRCh37.p13 chr5: 60,245,669-60,252,568 NDUFAF2
    nsv5842798copy number variation2nstd209human GRCh38 chr5: 60,949,818-60,958,751 , GRCh37.p13 chr5: 60,245,645-60,254,578 NDUFAF2
    nsv5842797copy number variation4nstd209human GRCh38 chr5: 60,949,367-60,950,866 , GRCh37.p13 chr5: 60,245,194-60,246,693 NDUFAF2
    nsv5723192mobile element insertion1nstd211human GRCh38 chr5: 61,099,519-61,099,519 , GRCh37.p13 chr5: 60,395,346-60,395,346 NDUFAF2
    nsv5721178mobile element insertion1nstd211human GRCh38 chr5: 61,026,563-61,026,563 , GRCh37.p13 chr5: 60,322,390-60,322,390 NDUFAF2
    nsv5717062mobile element insertion1nstd211human GRCh38 chr5: 61,142,889-61,142,889 , GRCh37.p13 chr5: 60,438,716-60,438,716 NDUFAF2
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