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Items: 1 to 20 of 392

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980279insertion1nstd209human GRCh38 chr15: 52,291,731-52,291,731 , GRCh37.p13 chr15: 52,583,928-52,583,928 MYO5C
    nsv5979397insertion1nstd209human GRCh38 chr15: 52,222,610-52,222,610 , GRCh37.p13 chr15: 52,514,807-52,514,807 MYO5C, LOC105370820
    nsv5979216insertion1nstd209human GRCh38 chr15: 52,232,220-52,232,220 , GRCh37.p13 chr15: 52,524,417-52,524,417 MYO5C
    nsv5929322copy number variation1nstd209human GRCh38 chr15: 52,232,986-52,233,318 , GRCh37.p13 chr15: 52,525,183-52,525,515 MYO5C
    nsv5718609mobile element insertion1nstd211human GRCh38 chr15: 52,255,722-52,255,722 , GRCh37.p13 chr15: 52,547,919-52,547,919 MYO5C
    nsv5715389mobile element insertion1nstd211human GRCh38 chr15: 52,255,708-52,255,708 , GRCh37.p13 chr15: 52,547,905-52,547,905 MYO5C
    nsv5706045mobile element insertion1nstd211human GRCh38 chr15: 52,296,068-52,296,068 , GRCh37.p13 chr15: 52,588,265-52,588,265 MYO5C, LOC105370819
    nsv5660509insertion1nstd207human GRCh38 chr15: 52,255,708-52,255,708 , GRCh37.p13 chr15: 52,547,905-52,547,905 MYO5C
    nsv5586238copy number variation1nstd207human GRCh38 chr15: 52,232,986-52,233,318 , GRCh37.p13 chr15: 52,525,183-52,525,515 MYO5C
    nsv5557248mobile element insertion1nstd206human GRCh38 chr15: 52,255,722-52,255,759 , GRCh37.p13 chr15: 52,547,919-52,547,956 MYO5C
    nsv5527026copy number variation1nstd206human GRCh38 chr15: 52,265,756-52,265,907 , GRCh37.p13 chr15: 52,557,953-52,558,104 MYO5C
    nsv5525175copy number variation1nstd206human GRCh38 chr15: 52,232,997-52,233,319 , GRCh37.p13 chr15: 52,525,194-52,525,516 MYO5C
    nsv5523991copy number variation1nstd206human GRCh38 chr15: 52,286,177-52,287,207 , GRCh37.p13 chr15: 52,578,374-52,579,404 MYO5C
    nsv5430854mobile element insertion1nstd206human GRCh38 chr15: 52,296,068-52,296,119 , GRCh37.p13 chr15: 52,588,265-52,588,316 MYO5C, LOC105370819
    nsv5415943mobile element insertion1nstd206human GRCh38 chr15: 52,230,335-52,230,386 , GRCh37.p13 chr15: 52,522,532-52,522,583 MYO5C
    nsv5383598mobile element deletion2nstd186human GRCh37 chr15: 52,525,194-52,525,516 , GRCh38.p12 chr15: 52,232,997-52,233,319 MYO5C
    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
    nsv5357930translocation1nstd200human GRCh38 chr15: 52,240,632-52,240,632 , GRCh38 chr15: 52,240,689-52,240,689 , GRCh37.p13 chr15: 52,532,886-52,532,886 , GRCh37.p13 chr15: 52,532,829-52,532,829 MYO5C
    nsv5277997copy number variation1nstd204human GRCh38.p13 chr15: 52,231,347-52,233,532 , GRCh37.p13 chr15: 52,523,544-52,525,729 MYO5C
    nsv5274811copy number variation1nstd204human GRCh38.p13 chr15: 52,233,001-52,233,200 , GRCh37.p13 chr15: 52,525,198-52,525,397 MYO5C
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