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Items: 1 to 20 of 422

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974720insertion1nstd209human GRCh38 chr20: 47,731,184-47,731,184 , GRCh37.p13 chr20: 46,359,928-46,359,928 SULF2
    nsv5958531copy number variation1nstd209human GRCh38 chr20: 47,657,211-47,657,282 , GRCh37.p13 chr20: 46,285,955-46,286,026 SULF2, NCOA3
    nsv5955574copy number variation1nstd209human GRCh38 chr20: 47,710,212-47,710,699 , GRCh37.p13 chr20: 46,338,956-46,339,443 SULF2
    nsv5949595copy number variation1nstd209human GRCh38 chr20: 47,681,948-47,682,153 , GRCh37.p13 chr20: 46,310,692-46,310,897 SULF2
    nsv5695509mobile element insertion1nstd211human GRCh38 chr20: 47,756,632-47,756,632 , GRCh37.p13 chr20: 46,385,376-46,385,376 SULF2
    nsv5670937insertion1nstd207human GRCh38 chr20: 47,670,707-47,670,707 , GRCh37.p13 chr20: 46,299,451-46,299,451 SULF2
    nsv5670308insertion1nstd207human GRCh38 chr20: 47,666,120-47,666,120 , GRCh37.p13 chr20: 46,294,864-46,294,864 SULF2
    nsv5592494copy number variation1nstd207human GRCh38 chr20: 47,710,212-47,710,699 , GRCh37.p13 chr20: 46,338,956-46,339,443 SULF2
    nsv5530957copy number variation1nstd206human GRCh38 chr20: 47,764,138-47,788,050 , GRCh37.p13 chr20: 46,392,882-46,416,794 SULF2
    nsv5527783copy number variation1nstd206human GRCh38 chr20: 47,681,951-47,682,154 , GRCh37.p13 chr20: 46,310,695-46,310,898 SULF2
    nsv5525080copy number variation1nstd206human GRCh38 chr20: 47,666,754-47,666,871 , GRCh37.p13 chr20: 46,295,498-46,295,615 SULF2
    nsv5520715copy number variation1nstd206human GRCh38 chr20: 47,774,058-47,786,990 , GRCh37.p13 chr20: 46,402,802-46,415,734 SULF2
    nsv5520261copy number variation1nstd206human GRCh38 chr20: 47,748,598-47,750,340 , GRCh37.p13 chr20: 46,377,342-46,379,084 SULF2
    nsv5519335copy number variation1nstd206human GRCh38 chr20: 47,710,214-47,710,700 , GRCh37.p13 chr20: 46,338,958-46,339,444 SULF2
    nsv5392577copy number variation3nstd186human GRCh37 chr20: 46,338,958-46,339,444 , GRCh38.p12 chr20: 47,710,214-47,710,700 SULF2
    nsv5366137translocation1nstd200human GRCh38 chr20: 47,750,582-47,750,582 , GRCh38 chr20: 47,727,868-47,727,868 , GRCh37.p13 chr20: 46,356,612-46,356,612 , GRCh37.p13 chr20: 46,379,326-46,379,326 SULF2
    nsv5350426translocation1nstd200human GRCh38 chr20: 47,705,025-47,705,025 , GRCh38 chr20: 47,704,520-47,704,520 , GRCh37.p13 chr20: 46,333,264-46,333,264 , GRCh37.p13 chr20: 46,333,769-46,333,769 SULF2
    nsv5334908translocation1nstd200human GRCh37 chr20: 46,285,955-46,285,955 , GRCh37 chr20: 46,286,021-46,286,021 , GRCh38.p12 chr20: 47,657,277-47,657,277 , GRCh38.p12 chr20: 47,657,211-47,657,211 NCOA3, SULF2
    nsv5332409translocation1nstd200human GRCh37 chr20: 46,310,898-46,310,898 , GRCh37 chr20: 46,310,695-46,310,695 , GRCh38.p12 chr20: 47,681,951-47,681,951 , GRCh38.p12 chr20: 47,682,154-47,682,154 SULF2
    nsv5328625copy number variation1nstd204human GRCh38.p13 chr20: 47,710,192-47,710,720 , GRCh37.p13 chr20: 46,338,936-46,339,464 SULF2
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