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Items: 1 to 20 of 224

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112740copy number variation1nstd102humanPathogenic GRCh37 chr10: 102,568,846-102,589,718 , GRCh38.p12 chr10: 100,809,089-100,829,961 PAX2
    nsv5917076copy number variation1nstd209human GRCh38 chr10: 100,734,580-100,734,654 , GRCh37.p13 chr10: 102,494,337-102,494,411 PAX2
    nsv5672684copy number variation1nstd102humanPathogenic GRCh37 chr10: 102,566,167-102,566,382 , GRCh38.p12 chr10: 100,806,410-100,806,625 PAX2
    nsv5672683copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 102,510,431-102,510,668 , GRCh38.p12 chr10: 100,750,674-100,750,911 PAX2
    nsv5637288insertion1nstd207human GRCh38 chr10: 100,829,271-100,829,271 , GRCh37.p13 chr10: 102,589,028-102,589,028 PAX2
    nsv5492012copy number variation1nstd206human GRCh38 chr10: 100,748,311-100,748,449 , GRCh37.p13 chr10: 102,508,068-102,508,206 PAX2
    nsv5480447copy number variation1nstd206human GRCh38 chr10: 100,816,607-100,816,689 , GRCh37.p13 chr10: 102,576,364-102,576,446 PAX2
    nsv5477595copy number variation1nstd206human GRCh38 chr10: 100,734,580-100,734,655 , GRCh37.p13 chr10: 102,494,337-102,494,412 PAX2
    nsv5348046translocation1nstd200human GRCh38 chr10: 100,734,580-100,734,580 , GRCh38 chr10: 100,734,655-100,734,655 , GRCh37.p13 chr10: 102,494,337-102,494,337 , GRCh37.p13 chr10: 102,494,412-102,494,412 PAX2
    nsv5203737mobile element deletion1nstd204human GRCh38.p13 chr10: 100,758,118-100,758,464 , GRCh37.p13 chr10: 102,517,875-102,518,221 PAX2
    nsv4970301copy number variation1nstd200human GRCh38 chr10: 100,819,662-100,821,178 , GRCh37.p13 chr10: 102,579,419-102,580,935 PAX2
    nsv4970300copy number variation1nstd200human GRCh38 chr10: 100,793,426-100,793,669 , GRCh37.p13 chr10: 102,553,183-102,553,426 PAX2
    nsv4836749copy number variation1nstd200human GRCh37 chr10: 102,494,337-102,494,412 , GRCh38.p12 chr10: 100,734,580-100,734,655 PAX2
    nsv4774814mobile element deletion1nstd200human GRCh37 chr10: 102,517,901-102,518,196 , GRCh38.p12 chr10: 100,758,144-100,758,439 PAX2
    nsv4747469copy number variation1nstd199human GRCh37 chr10: 102,567,151-102,567,203 , GRCh38.p12 chr10: 100,807,394-100,807,446 PAX2
    nsv4667657copy number variation1nstd186human GRCh37 chr10: 102,504,701-102,509,500 , GRCh38.p12 chr10: 100,744,944-100,749,743 PAX2
    nsv4611493copy number variation1nstd183human GRCh37 chr10: 102,504,701-102,509,500 , GRCh38.p12 chr10: 100,744,944-100,749,743 PAX2
    nsv4561605mobile element insertion1nstd166human GRCh37.p13 chr10: 102,527,562-102,527,562 , GRCh38.p12 chr10: 100,767,805-100,767,805 PAX2
    nsv4379002copy number variation1nstd173human GRCh37 chr10: 102,345,351-102,525,382 , GRCh38.p12 chr10: 100,585,594-100,765,625 PAX2
    nsv4374606copy number variation1nstd173human GRCh37 chr10: 102,345,729-102,516,077 , GRCh38.p12 chr10: 100,585,972-100,756,320 PAX2
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