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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5532278copy number variation1nstd206human GRCh38 chr16: 69,677,060-69,924,863 , GRCh37.p13 chr16: 69,710,963-69,958,766 NQO1, NFAT5, 4 more genes
    nsv5519171copy number variation1nstd206human GRCh38 chr16: 69,740,148-69,740,947 , GRCh37.p13 chr16: 69,774,051-69,774,850 NOB1
    nsv5515404copy number variation1nstd206human GRCh38 chr16: 69,747,228-69,747,281 , GRCh37.p13 chr16: 69,781,131-69,781,184 NOB1
    nsv5514258copy number variation1nstd206human GRCh38 chr16: 69,738,102-69,741,108 , GRCh37.p13 chr16: 69,772,005-69,775,011 NOB1
    nsv5368939translocation1nstd200human GRCh38 chr16: 69,753,058-69,753,058 , GRCh38 chr5: 131,365,894-131,365,894 , GRCh37.p13 chr16: 69,786,961-69,786,961 , GRCh37.p13 chr5: 130,701,587-130,701,587 CDC42SE2, NOB1
    nsv5345178translocation1nstd200human GRCh37 chr5: 130,701,587-130,701,587 , GRCh37 chr16: 69,786,961-69,786,961 , GRCh38.p12 chr16: 69,753,058-69,753,058 , GRCh38.p12 chr5: 131,365,894-131,365,894 CDC42SE2, NOB1
    nsv5307624copy number variation1nstd204human GRCh38.p13 chr16: 69,738,121-69,744,124 , GRCh37.p13 chr16: 69,772,024-69,778,027 NOB1
    nsv5270654copy number variation1nstd204human GRCh38.p13 chr16: 69,739,453-69,743,876 , GRCh37.p13 chr16: 69,773,356-69,777,779 NOB1
    nsv5263716copy number variation1nstd204human GRCh37.p13 chr16: 69,700,104-69,946,603 , GRCh38.p13 chr16: 69,666,201-69,912,700 NQO1, NFAT5, 4 more genes
    nsv5149624mobile element insertion1nstd203human GRCh38 chr16: 69,753,524-69,753,540 , GRCh37.p13 chr16: 69,787,427-69,787,443 NOB1, NONOP1
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv4993221copy number variation1nstd200human GRCh38 chr16: 69,749,352-69,749,492 , GRCh37.p13 chr16: 69,783,255-69,783,395 NOB1
    nsv4993220copy number variation1nstd200human GRCh38 chr16: 69,745,011-69,747,956 , GRCh37.p13 chr16: 69,778,914-69,781,859 NOB1
    nsv4993219copy number variation1nstd200human GRCh38 chr16: 69,738,129-69,744,116 , GRCh37.p13 chr16: 69,772,032-69,778,019 NOB1
    nsv4878809inversion1nstd200human GRCh37 chr16: 60,132,255-77,533,939 , GRCh38.p12 chr16: 60,098,351-77,500,042 , ST3GAL2, 313 more genes
    nsv4864216copy number variation1nstd200human GRCh37 chr16: 69,773,799-69,792,262 , GRCh38.p12 chr16: 69,739,896-69,758,359 NOB1, NONOP1
    nsv4857557copy number variation1nstd200human GRCh37 chr16: 69,783,255-69,783,395 , GRCh38.p12 chr16: 69,749,352-69,749,492 NOB1
    nsv4857556copy number variation1nstd200human GRCh37 chr16: 69,772,032-69,778,020 , GRCh38.p12 chr16: 69,738,129-69,744,117 NOB1
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729943copy number variation1nstd102humanUncertain significance GRCh37 chr16: 69,369,131-69,942,990 , GRCh38.p12 chr16: 69,335,228-69,909,087 NIP7, CYB5B, 12 more genes
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