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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6974110copy number variation1nstd229human GRCh38 chr15: 48,152,996-48,153,044 , GRCh37.p13 chr15: 48,445,193-48,445,241 MYEF2
    nsv6970662copy number variation1nstd229human GRCh38 chr15: 48,152,993-48,153,044 , GRCh37.p13 chr15: 48,445,190-48,445,241 MYEF2
    nsv6966939copy number variation1nstd229human GRCh38 chr15: 48,158,838-48,165,894 , GRCh37.p13 chr15: 48,451,035-48,458,091 MYEF2
    nsv6960158copy number variation1nstd229human GRCh38 chr15: 48,143,072-48,149,029 , GRCh37.p13 chr15: 48,435,269-48,441,226 SLC24A5, MYEF2
    nsv6959741copy number variation1nstd229human GRCh38 chr15: 48,127,034-48,140,358 , GRCh37.p13 chr15: 48,419,231-48,432,555 MYEF2, SLC24A5
    nsv6515012copy number variation1nstd223human GRCh38 chr15: 48,164,673-48,165,100 , GRCh37.p13 chr15: 48,456,870-48,457,297 MYEF2
    nsv6514904copy number variation1nstd223human GRCh38 chr15: 48,156,301-48,157,200 , GRCh37.p13 chr15: 48,448,498-48,449,397 MYEF2
    nsv6512078copy number variation1nstd223human GRCh38 chr15: 48,160,444-48,161,034 , GRCh37.p13 chr15: 48,452,641-48,453,231 MYEF2
    nsv6510747copy number variation1nstd223human GRCh38 chr15: 48,138,043-48,138,715 , GRCh37.p13 chr15: 48,430,240-48,430,912 MYEF2, SLC24A5
    nsv6506416copy number variation1nstd223human GRCh38 chr15: 48,147,501-48,148,300 , GRCh37.p13 chr15: 48,439,698-48,440,497 MYEF2
    nsv6503731copy number variation1nstd223human GRCh38 chr15: 48,139,562-48,140,084 , GRCh37.p13 chr15: 48,431,759-48,432,281 MYEF2, SLC24A5
    nsv6502960copy number variation1nstd223human GRCh38 chr15: 48,159,097-48,159,617 , GRCh37.p13 chr15: 48,451,294-48,451,814 MYEF2
    nsv6497215copy number variation1nstd223human GRCh38 chr15: 48,142,885-48,143,740 , GRCh37.p13 chr15: 48,435,082-48,435,937 MYEF2, SLC24A5
    nsv6496924copy number variation1nstd223human GRCh38 chr15: 48,127,034-48,140,358 , GRCh37.p13 chr15: 48,419,231-48,432,555 MYEF2, SLC24A5
    nsv6496507copy number variation1nstd223human GRCh38 chr15: 48,134,718-48,135,407 , GRCh37.p13 chr15: 48,426,915-48,427,604 SLC24A5, MYEF2
    nsv6495831copy number variation1nstd223human GRCh38 chr15: 48,156,801-48,158,200 , GRCh37.p13 chr15: 48,448,998-48,450,397 MYEF2
    nsv6313917copy number variation1nstd102humanPathogenic GRCh37 chr15: 47,635,238-56,509,908 , GRCh38.p12 chr15: 47,343,041-56,217,710 PYGO1, RNU6-449P, 125 more genes
    nsv6309791copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,426,485-48,730,124 , GRCh38.p12 chr15: 48,134,288-48,437,927 DUT, FBN1, 6 more genes
    nsv6291817copy number variation1nstd102humanUncertain significance GRCh37 chr15: 48,149,321-48,522,259 , GRCh38.p12 chr15: 47,857,124-48,230,062 SLC24A5, LOC102724553, 6 more genes
    nsv6291615copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,179,968-48,727,846 , GRCh38.p12 chr15: 47,887,771-48,435,649 LOC102724553, CTXN2-AS1, 9 more genes
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