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Items: 1 to 20 of 291

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131437mobile element insertion1nstd186human GRCh37 chr14: 92,619,420-92,619,471 , GRCh38.p12 chr14: 92,153,076-92,153,127 CPSF2
    nsv6130533insertion1nstd186human GRCh37 chr14: 92,586,933-92,586,933 , GRCh38.p12 chr14: 92,120,589-92,120,589 CPSF2, NDUFB1
    nsv5969246insertion1nstd209human GRCh38 chr14: 92,153,061-92,153,061 , GRCh37.p13 chr14: 92,619,405-92,619,405 CPSF2
    nsv5849432copy number variation1nstd209human GRCh38 chr14: 92,154,544-92,155,743 , GRCh37.p13 chr14: 92,620,888-92,622,087 CPSF2
    nsv5729057mobile element insertion1nstd211human GRCh38 chr14: 92,124,183-92,124,183 , GRCh37.p13 chr14: 92,590,527-92,590,527 CPSF2
    nsv5717303mobile element insertion2nstd211human GRCh38 chr14: 92,153,076-92,153,076 , GRCh37.p13 chr14: 92,619,420-92,619,420 CPSF2
    nsv5713598mobile element insertion1nstd211human GRCh38 chr14: 92,163,374-92,163,374 , GRCh37.p13 chr14: 92,629,718-92,629,718 CPSF2
    nsv5655235insertion1nstd207human GRCh38 chr14: 92,120,334-92,120,334 , GRCh37.p13 chr14: 92,586,678-92,586,678 CPSF2, NDUFB1
    nsv5653472insertion1nstd207human GRCh38 chr14: 92,120,589-92,120,589 , GRCh37.p13 chr14: 92,586,933-92,586,933 CPSF2, NDUFB1
    nsv5647219insertion1nstd207human GRCh38 chr14: 92,153,061-92,153,061 , GRCh37.p13 chr14: 92,619,405-92,619,405 CPSF2
    nsv5560696mobile element insertion1nstd206human GRCh38 chr14: 92,124,183-92,124,234 , GRCh37.p13 chr14: 92,590,527-92,590,578 CPSF2
    nsv5555929mobile element insertion1nstd206human GRCh38 chr14: 92,153,076-92,153,127 , GRCh37.p13 chr14: 92,619,420-92,619,471 CPSF2
    nsv5542826insertion1nstd206human GRCh38 chr14: 92,120,589-92,120,589 , GRCh37.p13 chr14: 92,586,933-92,586,933 NDUFB1, CPSF2
    nsv5511354copy number variation1nstd206human GRCh38 chr14: 92,151,976-92,152,202 , GRCh37.p13 chr14: 92,618,320-92,618,546 CPSF2
    nsv5509329copy number variation1nstd206human GRCh38 chr14: 92,160,877-92,161,605 , GRCh37.p13 chr14: 92,627,221-92,627,949 CPSF2
    nsv5500865copy number variation1nstd206human GRCh38 chr14: 92,144,856-92,148,707 , GRCh37.p13 chr14: 92,611,200-92,615,051 CPSF2
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5195844mobile element insertion1nstd203human GRCh38 chr14: 92,153,060-92,153,076 , GRCh37.p13 chr14: 92,619,404-92,619,420 CPSF2
    nsv5193879mobile element insertion1nstd203human GRCh38 chr14: 92,153,067-92,153,076 , GRCh37.p13 chr14: 92,619,411-92,619,420 CPSF2
    nsv5191584mobile element insertion1nstd203human GRCh38 chr14: 92,153,076-92,153,076 , GRCh37.p13 chr14: 92,619,420-92,619,420 CPSF2
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