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Items: 1 to 20 of 238

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112688copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,154,188-128,324,987 , GRCh38.p12 chr3: 120,435,341-128,606,144 RNU4-62P, MTCO1P29, 169 more genes
    nsv5903958copy number variation1nstd209human GRCh38 chr3: 122,887,980-122,894,955 , GRCh37.p13 chr3: 122,606,827-122,613,802 SLC49A4, LINC02035
    nsv5892703copy number variation1nstd209human GRCh38 chr3: 122,859,701-122,859,771 , GRCh37.p13 chr3: 122,578,548-122,578,618 SLC49A4
    nsv5834870copy number variation1nstd209human GRCh38 chr3: 122,887,911-122,894,997 , GRCh37.p13 chr3: 122,606,758-122,613,844 SLC49A4, LINC02035
    nsv5679022mobile element insertion2nstd211human GRCh38 chr3: 122,842,144-122,842,144 , GRCh37.p13 chr3: 122,560,991-122,560,991 SLC49A4
    nsv5541518insertion1nstd206human GRCh38 chr3: 122,842,144-122,842,177 , GRCh37.p13 chr3: 122,560,991-122,561,024 SLC49A4
    nsv5445633copy number variation1nstd206human GRCh38 chr3: 122,853,374-122,853,443 , GRCh37.p13 chr3: 122,572,221-122,572,290 SLC49A4
    nsv5440353copy number variation1nstd206human GRCh38 chr3: 122,816,327-122,816,910 , GRCh37.p13 chr3: 122,535,174-122,535,757 SLC49A4
    nsv5346480translocation1nstd200human GRCh38 chr3: 122,853,443-122,853,443 , GRCh38 chr3: 122,853,374-122,853,374 , GRCh37.p13 chr3: 122,572,290-122,572,290 , GRCh37.p13 chr3: 122,572,221-122,572,221 SLC49A4
    nsv5167257mobile element insertion1nstd203human GRCh38 chr3: 122,821,831-122,821,839 , GRCh37.p13 chr3: 122,540,678-122,540,686 SLC49A4
    nsv5098632mobile element insertion1nstd203human GRCh38 chr3: 122,842,126-122,842,144 , GRCh37.p13 chr3: 122,560,973-122,560,991 SLC49A4
    nsv5080818mobile element insertion1nstd203human GRCh38 chr3: 122,846,259-122,846,265 , GRCh37.p13 chr3: 122,565,106-122,565,112 SLC49A4
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5031637inversion1nstd200human GRCh38 chr3: 112,181,184-125,673,487 , GRCh37.p13 chr3: 111,900,031-125,392,331 , ARHGAP31, 218 more genes
    nsv4919869copy number variation1nstd200human GRCh38 chr3: 122,842,832-122,853,857 , GRCh37.p13 chr3: 122,561,679-122,572,704 SLC49A4
    nsv4919868copy number variation1nstd200human GRCh38 chr3: 122,835,220-122,836,136 , GRCh37.p13 chr3: 122,554,067-122,554,983 SLC49A4
    nsv4919867copy number variation1nstd200human GRCh38 chr3: 122,821,812-122,821,904 , GRCh37.p13 chr3: 122,540,659-122,540,751 SLC49A4
    nsv4914706copy number variation1nstd200human GRCh38 chr3: 122,816,327-122,816,910 , GRCh37.p13 chr3: 122,535,174-122,535,757 SLC49A4
    nsv4806995copy number variation1nstd200human GRCh37 chr3: 122,572,221-122,572,290 , GRCh38.p12 chr3: 122,853,374-122,853,443 SLC49A4
    nsv4806994copy number variation1nstd200human GRCh37 chr3: 122,561,679-122,572,704 , GRCh38.p12 chr3: 122,842,832-122,853,857 SLC49A4
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