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Items: 1 to 20 of 238

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969885insertion1nstd209human GRCh38 chr10: 114,936,759-114,936,759 , GRCh37.p13 chr10: 116,696,518-116,696,518 TRUB1
    nsv5910929copy number variation1nstd209human GRCh38 chr10: 114,941,264-114,941,403 , GRCh37.p13 chr10: 116,701,023-116,701,162 TRUB1
    nsv5700251mobile element insertion2nstd211human GRCh38 chr10: 114,936,773-114,936,773 , GRCh37.p13 chr10: 116,696,532-116,696,532 TRUB1
    nsv5635152insertion1nstd207human GRCh38 chr10: 114,954,911-114,954,911 , GRCh37.p13 chr10: 116,714,670-116,714,670 TRUB1
    nsv5628468insertion1nstd207human GRCh38 chr10: 114,936,759-114,936,759 , GRCh37.p13 chr10: 116,696,518-116,696,518 TRUB1
    nsv5511223copy number variation1nstd206human GRCh38 chr10: 114,943,441-114,944,655 , GRCh37.p13 chr10: 116,703,200-116,704,414 TRUB1
    nsv5502567copy number variation1nstd206human GRCh38 chr10: 114,959,879-114,971,110 , GRCh37.p13 chr10: 116,719,638-116,730,869 RNU6-1121P, TRUB1
    nsv5500278copy number variation1nstd206human GRCh38 chr10: 114,876,531-115,123,609 , GRCh37.p13 chr10: 116,636,290-116,786,295 ATRNL1, FHIP2A, 6 more genes
    nsv5400238mobile element insertion1nstd206human GRCh38 chr10: 114,936,773-114,936,824 , GRCh37.p13 chr10: 116,696,532-116,696,583 TRUB1
    nsv5327857inversion1nstd204human GRCh37.p13 chr10: 115,288,018-116,786,304 , GRCh38.p13 chr10: 113,528,259-115,723,405 , ADRB1, 31 more genes
    nsv5315881copy number variation1nstd204human GRCh37.p13 chr10: 116,719,614-116,730,892 , GRCh38.p13 chr10: 114,959,855-114,971,133 RNU6-1121P, TRUB1
    nsv5306893copy number variation1nstd204human GRCh38.p13 chr10: 114,929,937-114,937,793 , GRCh37.p13 chr10: 116,689,696-116,697,552 TRUB1
    nsv5257339copy number variation1nstd204human GRCh38.p13 chr10: 114,929,766-114,937,804 , GRCh37.p13 chr10: 116,689,525-116,697,563 TRUB1
    nsv5241212copy number variation1nstd204human GRCh38.p13 chr10: 114,959,901-114,971,100 , GRCh37.p13 chr10: 116,719,660-116,730,859 RNU6-1121P, TRUB1
    nsv5241013copy number variation1nstd204human GRCh38.p13 chr10: 114,959,886-114,968,838 , GRCh37.p13 chr10: 116,719,645-116,728,597 TRUB1, RNU6-1121P
    nsv5137982mobile element insertion1nstd203human GRCh38 chr10: 114,936,761-114,936,773 , GRCh37.p13 chr10: 116,696,520-116,696,532 TRUB1
    nsv5131797mobile element insertion1nstd203human GRCh38 chr10: 114,936,764-114,936,773 , GRCh37.p13 chr10: 116,696,523-116,696,532 TRUB1
    nsv5130173mobile element insertion1nstd203human GRCh38 chr10: 114,936,763-114,936,773 , GRCh37.p13 chr10: 116,696,522-116,696,532 TRUB1
    nsv5126289mobile element insertion1nstd203human GRCh38 chr10: 114,936,759-114,936,773 , GRCh37.p13 chr10: 116,696,518-116,696,532 TRUB1
    nsv5125841mobile element insertion1nstd203human GRCh38 chr10: 114,973,051-114,973,065 , GRCh37.p13 chr10: 116,732,810-116,732,824 TRUB1
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