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Items: 1 to 20 of 187

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5939798copy number variation1nstd209human GRCh38 chr19: 19,732,377-19,922,535 , GRCh37.p13 chr19: 19,843,186-20,033,344 , LOC101060187, 10 more genes
    nsv5932571copy number variation1nstd209human GRCh38 chr19: 19,801,683-19,802,096 , GRCh37.p13 chr19: 19,912,492-19,912,905 , ZNF56P, 1 more genes
    nsv5930048copy number variation1nstd209human GRCh38 chr19: 19,751,989-19,799,203 , GRCh37.p13 chr19: 19,862,798-19,910,012 , ZNF56P, 4 more genes
    nsv5876793copy number variation1nstd209human GRCh38 chr19: 19,751,207-19,791,765 , GRCh37.p13 chr19: 19,862,016-19,902,574 , ZNF56P, 4 more genes
    nsv5696583mobile element insertion2nstd211human GRCh38 chr19: 19,792,848-19,792,848 , GRCh37.p13 chr19: 19,903,657-19,903,657 , ZNF56P, 1 more genes
    nsv5651710insertion1nstd207human GRCh38 chr19: 19,792,837-19,792,837 , GRCh37.p13 chr19: 19,903,646-19,903,646 , ZNF56P, 1 more genes
    nsv5532733copy number variation1nstd206human GRCh38 chr19: 19,816,569-19,818,131 , GRCh37.p13 chr19: 19,927,378-19,928,940 ZNF506, ZNF56P
    nsv5524846copy number variation1nstd206human GRCh38 chr19: 19,795,503-19,795,717 , GRCh37.p13 chr19: 19,906,312-19,906,526 , ZNF56P, 1 more genes
    nsv5518611copy number variation1nstd206human GRCh38 chr19: 19,801,548-19,802,088 , GRCh37.p13 chr19: 19,912,357-19,912,897 , ZNF506, 1 more genes
    nsv5429665mobile element insertion1nstd206human GRCh38 chr19: 19,792,848-19,792,899 , GRCh37.p13 chr19: 19,903,657-19,903,708 , ZNF56P, 1 more genes
    nsv5375342translocation1nstd200human GRCh37.p13 chr19|NW_003571053.2: 226,598-226,598 , GRCh38 chr19: 19,795,504-19,795,504 , GRCh38 chr19: 20,309,345-20,309,345 , GRCh37.p13 chr19: 19,906,313-19,906,313 , GRCh37.p13 chr19: 20,420,154-20,420,154 , ZNF56P, 1 more genes
    nsv5328815copy number variation1nstd204human GRCh37.p13 chr19: 19,912,472-19,912,924 , GRCh38.p13 chr19: 19,801,663-19,802,115 , ZNF56P, 1 more genes
    nsv5282760copy number variation1nstd204human GRCh38.p13 chr19: 19,795,201-19,801,900 , GRCh37.p13 chr19: 19,906,010-19,912,709 , ZNF506, 1 more genes
    nsv5176076mobile element insertion1nstd203human GRCh38 chr19: 19,792,842-19,792,848 , GRCh37.p13 chr19: 19,903,651-19,903,657 , ZNF56P, 1 more genes
    nsv5168952mobile element insertion1nstd203human GRCh38 chr19: 19,792,837-19,792,848 , GRCh37.p13 chr19: 19,903,646-19,903,657 , ZNF56P, 1 more genes
    nsv5168379mobile element insertion1nstd203human GRCh38 chr19: 19,817,416-19,817,416 , GRCh37.p13 chr19: 19,928,225-19,928,225 ZNF506, ZNF56P
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5019504copy number variation1nstd200human GRCh38 chr19: 19,816,636-19,817,958 , GRCh37.p13 chr19: 19,927,445-19,928,767 ZNF56P, ZNF506
    nsv5019503copy number variation1nstd200human GRCh38 chr19: 19,805,731-19,805,948 , GRCh37.p13 chr19: 19,916,540-19,916,757 , ZNF506, 1 more genes
    nsv5014667copy number variation1nstd200human GRCh38 chr19: 19,512,643-19,936,068 , GRCh37.p13 chr19: 19,623,452-20,046,877 , GMIP, 20 more genes
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