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Items: 1 to 20 of 223

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5928068copy number variation1nstd209human GRCh38 chr16: 77,661,074-77,727,699 , GRCh37.p13 chr16: 77,694,971-77,761,596 NUDT7
    nsv5544949insertion1nstd206human GRCh38 chr16: 77,724,236-77,724,238 , GRCh37.p13 chr16: 77,758,133-77,758,135 NUDT7
    nsv5533577copy number variation1nstd206human GRCh38 chr16: 77,677,949-78,219,248 , GRCh37.p13 chr16: 77,711,846-78,253,145 CLEC3A, WWOX, 7 more genes
    nsv5529079copy number variation1nstd206human GRCh38 chr16: 77,670,938-77,738,636 , GRCh37.p13 chr16: 77,704,835-77,772,533 NUDT7
    nsv5317490copy number variation1nstd204human GRCh37.p13 chr16: 77,692,319-77,846,170 , GRCh38.p13 chr16: 77,658,422-77,812,273 VAT1L, NUDT7, 1 more genes
    nsv5305011copy number variation1nstd204human GRCh37.p13 chr16: 77,711,836-78,253,149 , GRCh38.p13 chr16: 77,677,939-78,219,252 CLEC3A, WWOX, 7 more genes
    nsv5294337copy number variation1nstd204human GRCh38.p13 chr16: 77,658,324-77,728,740 , GRCh37.p13 chr16: 77,692,221-77,762,637 NUDT7
    nsv5284366copy number variation1nstd204human GRCh38.p13 chr16: 77,720,531-77,722,103 , GRCh37.p13 chr16: 77,754,428-77,756,000 NUDT7
    nsv5283673copy number variation1nstd204human GRCh38.p13 chr16: 77,740,680-77,741,979 , GRCh37.p13 chr16: 77,774,577-77,775,876 LOC107984878, NUDT7
    nsv5148785mobile element insertion1nstd203human GRCh38 chr16: 77,721,687-77,721,705 , GRCh37.p13 chr16: 77,755,584-77,755,602 NUDT7
    nsv5013423copy number variation1nstd200human GRCh38 chr16: 77,727,542-77,775,635 , GRCh37.p13 chr16: 77,761,439-77,809,532 NUDT7, LOC107984878
    nsv5013421copy number variation1nstd200human GRCh38 chr16: 77,705,598-77,737,743 , GRCh37.p13 chr16: 77,739,495-77,771,640 NUDT7
    nsv5013419copy number variation1nstd200human GRCh38 chr16: 77,677,949-78,219,248 , GRCh37.p13 chr16: 77,711,846-78,253,145 CLEC3A, KRT8P22, 7 more genes
    nsv5009433copy number variation1nstd200human GRCh38 chr16: 77,724,850-77,725,036 , GRCh37.p13 chr16: 77,758,747-77,758,933 NUDT7
    nsv5009429copy number variation1nstd200human GRCh38 chr16: 77,658,421-77,812,279 , GRCh37.p13 chr16: 77,692,318-77,846,176 NUDT7, VAT1L, 1 more genes
    nsv4866725copy number variation1nstd200human GRCh37 chr16: 77,692,325-77,846,156 , GRCh38.p12 chr16: 77,658,428-77,812,259 NUDT7, LOC107984878, 1 more genes
    nsv4864282copy number variation1nstd200human GRCh37 chr16: 77,761,381-77,809,608 , GRCh38.p12 chr16: 77,727,484-77,775,711 NUDT7, LOC107984878
    nsv4864279copy number variation1nstd200human GRCh37 chr16: 77,739,495-77,771,640 , GRCh38.p12 chr16: 77,705,598-77,737,743 NUDT7
    nsv4864278copy number variation1nstd200human GRCh37 chr16: 77,711,846-78,253,145 , GRCh38.p12 chr16: 77,677,949-78,219,248 NUDT7, LOC107984878, 7 more genes
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
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