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Items: 1 to 20 of 522

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5905089copy number variation1nstd209human GRCh38 chr3: 69,833,388-69,833,685 , GRCh37.p13 chr3: 69,882,539-69,882,836 MITF
    nsv5902904copy number variation1nstd209human GRCh38 chr3: 66,803,410-74,489,186 , GRCh37.p13 chr3: 66,853,834-74,538,337 , LOC105377160, 83 more genes
    nsv5901739copy number variation1nstd209human GRCh38 chr3: 69,832,937-69,833,017 , GRCh37.p13 chr3: 69,882,088-69,882,168 MITF
    nsv5897519copy number variation1nstd209human GRCh38 chr3: 69,793,493-69,793,544 , GRCh37.p13 chr3: 69,842,644-69,842,695 MITF
    nsv5895075copy number variation1nstd209human GRCh38 chr3: 69,895,470-69,895,648 , GRCh37.p13 chr3: 69,944,621-69,944,799 MITF
    nsv5887722copy number variation1nstd209human GRCh38 chr3: 69,964,323-69,964,735 , GRCh37.p13 chr3: 70,013,474-70,013,886 MITF
    nsv5887608copy number variation1nstd209human GRCh38 chr3: 69,833,113-69,833,220 , GRCh37.p13 chr3: 69,882,264-69,882,371 MITF
    nsv5690415mobile element insertion1nstd211human GRCh38 chr3: 69,896,463-69,896,463 , GRCh37.p13 chr3: 69,945,614-69,945,614 MITF
    nsv5689688mobile element insertion1nstd211human GRCh38 chr3: 69,904,008-69,904,008 , GRCh37.p13 chr3: 69,953,159-69,953,159 MITF
    nsv5684717mobile element insertion1nstd211human GRCh38 chr3: 69,886,554-69,886,554 , GRCh37.p13 chr3: 69,935,705-69,935,705 MITF
    nsv5683401mobile element insertion1nstd211human GRCh38 chr3: 69,892,250-69,892,250 , GRCh37.p13 chr3: 69,941,401-69,941,401 MITF
    nsv5678330mobile element insertion1nstd211human GRCh38 chr3: 69,813,656-69,813,656 , GRCh37.p13 chr3: 69,862,807-69,862,807 MITF
    nsv5676070mobile element insertion1nstd211human GRCh38 chr3: 69,787,864-69,787,864 , GRCh37.p13 chr3: 69,837,015-69,837,015 MITF
    nsv5614563insertion1nstd207human GRCh38 chr3: 69,793,493-69,793,493 , GRCh37.p13 chr3: 69,842,644-69,842,644 MITF
    nsv5579105copy number variation1nstd207human GRCh38 chr3: 69,832,937-69,833,017 , GRCh37.p13 chr3: 69,882,088-69,882,168 MITF
    nsv5564995copy number variation1nstd207human GRCh38 chr3: 69,964,323-69,964,735 , GRCh37.p13 chr3: 70,013,474-70,013,886 MITF
    nsv5564432copy number variation1nstd102humanPathogenic GRCh37 chr3: 68,939,251-72,700,418 , GRCh38.p12 chr3: 68,890,100-72,651,267 CCDC137P1, LOC105377160, 39 more genes
    nsv5451992copy number variation1nstd206human GRCh38 chr3: 69,964,325-69,964,736 , GRCh37.p13 chr3: 70,013,476-70,013,887 MITF
    nsv5451438copy number variation1nstd206human GRCh38 chr3: 69,833,139-69,833,199 , GRCh37.p13 chr3: 69,882,290-69,882,350 MITF
    nsv5443893copy number variation1nstd206human GRCh38 chr3: 69,838,161-69,838,216 , GRCh37.p13 chr3: 69,887,312-69,887,367 MITF
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