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Items: 1 to 20 of 314

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5945714copy number variation1nstd209human GRCh38 chr15: 64,434,944-64,435,249 , GRCh37.p13 chr15: 64,727,143-64,727,448 TRIP4
    nsv5941709copy number variation1nstd209human GRCh38 chr15: 64,403,113-64,403,409 , GRCh37.p13 chr15: 64,695,312-64,695,608 TRIP4
    nsv5729337mobile element insertion2nstd211human GRCh38 chr15: 64,401,746-64,401,746 , GRCh37.p13 chr15: 64,693,945-64,693,945 TRIP4
    nsv5713474mobile element insertion1nstd211human GRCh38 chr15: 64,435,907-64,435,907 , GRCh37.p13 chr15: 64,728,106-64,728,106 TRIP4
    nsv5708872mobile element insertion2nstd211human GRCh38 chr15: 64,436,792-64,436,792 , GRCh37.p13 chr15: 64,728,991-64,728,991 TRIP4
    nsv5703484mobile element insertion1nstd211human GRCh38 chr15: 64,435,843-64,435,843 , GRCh37.p13 chr15: 64,728,042-64,728,042 TRIP4
    nsv5646245insertion1nstd207human GRCh38 chr15: 64,431,847-64,431,847 , GRCh37.p13 chr15: 64,724,046-64,724,046 TRIP4
    nsv5560910mobile element insertion1nstd206human GRCh38 chr15: 64,401,746-64,401,797 , GRCh37.p13 chr15: 64,693,945-64,693,996 TRIP4
    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
    nsv5380126translocation1nstd200human GRCh38 chr15: 64,390,788-64,390,788 , GRCh38 chr15: 64,392,848-64,392,848 , GRCh37.p13 chr15: 64,682,987-64,682,987 , GRCh37.p13 chr15: 64,685,047-64,685,047 TRIP4
    nsv5342831translocation1nstd200human GRCh37 chr15: 64,682,987-64,682,987 , GRCh37 chr15: 64,685,047-64,685,047 , GRCh38.p12 chr15: 64,390,788-64,390,788 , GRCh38.p12 chr15: 64,392,848-64,392,848 TRIP4
    nsv5339465translocation1nstd200human GRCh37 chr7: 66,110,097-66,110,097 , GRCh37 chr15: 64,744,122-64,744,122 , GRCh38.p12 chr15: 64,451,923-64,451,923 , GRCh38.p12 chr7: 66,645,110-66,645,110 LOC105370861, TRIP4
    nsv5260923copy number variation1nstd204human GRCh37.p13 chr15: 64,569,600-64,876,599 , GRCh38.p13 chr15: 64,277,401-64,584,400 , TRIP4, 5 more genes
    nsv5187662mobile element insertion1nstd203human GRCh38 chr15: 64,401,734-64,401,746 , GRCh37.p13 chr15: 64,693,933-64,693,945 TRIP4
    nsv5151702mobile element insertion1nstd203human GRCh38 chr15: 64,436,747-64,436,792 , GRCh37.p13 chr15: 64,728,946-64,728,991 TRIP4
    nsv5143702mobile element insertion1nstd203human GRCh38 chr15: 64,436,763-64,436,792 , GRCh37.p13 chr15: 64,728,962-64,728,991 TRIP4
    nsv5143393mobile element insertion1nstd203human GRCh38 chr15: 64,440,585-64,440,601 , GRCh37.p13 chr15: 64,732,784-64,732,800 TRIP4
    nsv4991996copy number variation1nstd200human GRCh38 chr15: 64,408,530-64,411,878 , GRCh37.p13 chr15: 64,700,729-64,704,077 TRIP4
    nsv4991995copy number variation1nstd200human GRCh38 chr15: 64,391,451-64,393,366 , GRCh37.p13 chr15: 64,683,650-64,685,565 TRIP4
    nsv4991994copy number variation1nstd200human GRCh38 chr15: 64,386,616-64,389,958 , GRCh37.p13 chr15: 64,678,815-64,682,157 PCLAF, TRIP4
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