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Items: 1 to 20 of 296

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977355insertion1nstd209human GRCh38 chr15: 51,839,164-51,839,164 , GRCh37.p13 chr15: 52,131,361-52,131,361 TMOD3
    nsv5968962insertion1nstd209human GRCh38 chr15: 51,832,203-51,832,203 , GRCh37.p13 chr15: 52,124,400-52,124,400 TMOD3
    nsv5930550copy number variation1nstd209human GRCh38 chr15: 51,886,114-51,886,269 , GRCh37.p13 chr15: 52,178,311-52,178,466 TMOD3
    nsv5712015mobile element insertion2nstd211human GRCh38 chr15: 51,891,723-51,891,723 , GRCh37.p13 chr15: 52,183,920-52,183,920 TMOD3
    nsv5711094mobile element insertion2nstd211human GRCh38 chr15: 51,832,679-51,832,679 , GRCh37.p13 chr15: 52,124,876-52,124,876 TMOD3
    nsv5654076insertion1nstd207human GRCh38 chr15: 51,891,711-51,891,711 , GRCh37.p13 chr15: 52,183,908-52,183,908 TMOD3
    nsv5530232copy number variation1nstd206human GRCh38 chr15: 51,851,826-51,851,896 , GRCh37.p13 chr15: 52,144,023-52,144,093 TMOD3
    nsv5526998copy number variation1nstd206human GRCh38 chr15: 51,859,718-51,859,787 , GRCh37.p13 chr15: 52,151,915-52,151,984 TMOD3, LOC100422490
    nsv5429309mobile element insertion1nstd206human GRCh38 chr15: 51,891,711-51,891,711 , GRCh37.p13 chr15: 52,183,908-52,183,908 TMOD3
    nsv5421560mobile element insertion1nstd206human GRCh38 chr15: 51,832,679-51,832,699 , GRCh37.p13 chr15: 52,124,876-52,124,896 TMOD3
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5357925translocation1nstd200human GRCh38 chr15: 51,880,330-51,880,330 , GRCh38 chr15: 51,881,647-51,881,647 , GRCh37.p13 chr15: 52,172,527-52,172,527 , GRCh37.p13 chr15: 52,173,844-52,173,844 TMOD3
    nsv5343345translocation1nstd200human GRCh37 chr15: 52,172,527-52,172,527 , GRCh37 chr15: 52,173,844-52,173,844 , GRCh38.p12 chr15: 51,880,330-51,880,330 , GRCh38.p12 chr15: 51,881,647-51,881,647 TMOD3
    nsv5326307translocation1nstd204human GRCh38.p13 chr15: 51,880,330-51,880,330 , GRCh38.p13 chr15: 51,881,647-51,881,647 , GRCh37.p13 chr15: 52,172,527-52,172,527 , GRCh37.p13 chr15: 52,173,844-52,173,844 TMOD3
    nsv5264437copy number variation1nstd204human GRCh38.p13 chr15: 51,880,301-51,881,700 , GRCh37.p13 chr15: 52,172,498-52,173,897 TMOD3
    nsv5157598mobile element insertion1nstd203human GRCh38 chr15: 51,905,914-51,905,921 , GRCh37.p13 chr15: 52,198,111-52,198,118 RNU6-90P, TMOD3
    nsv5153846mobile element insertion1nstd203human GRCh38 chr15: 51,891,714-51,891,723 , GRCh37.p13 chr15: 52,183,911-52,183,920 TMOD3
    nsv5147865mobile element insertion1nstd203human GRCh38 chr15: 51,832,665-51,832,679 , GRCh37.p13 chr15: 52,124,862-52,124,876 TMOD3
    nsv5144802mobile element insertion1nstd203human GRCh38 chr15: 51,891,716-51,891,723 , GRCh37.p13 chr15: 52,183,913-52,183,920 TMOD3
    nsv5142786mobile element insertion1nstd203human GRCh38 chr15: 51,891,711-51,891,723 , GRCh37.p13 chr15: 52,183,908-52,183,920 TMOD3
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