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Items: 1 to 20 of 234

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6124982copy number variation1nstd186human GRCh37 chr19: 52,849,202-52,849,662 , GRCh38.p12 chr19: 52,345,949-52,346,409 ZNF610
    nsv5974464inversion1nstd209human GRCh38 chr19: 49,769,209-52,432,690 , GRCh37.p13 chr19: 50,272,466-52,935,943 , AP2A1, 172 more genes
    nsv5940219copy number variation1nstd209human GRCh38 chr19: 52,330,084-52,345,861 , GRCh37.p13 chr19: 52,833,337-52,849,114 ZNF610
    nsv5939657copy number variation1nstd209human GRCh38 chr19: 52,335,567-52,336,021 , GRCh37.p13 chr19: 52,838,820-52,839,274 ZNF610
    nsv5935841copy number variation1nstd209human GRCh38 chr19: 52,302,730-52,363,784 , GRCh37.p13 chr19: 52,805,983-52,867,037 ZNF480, ZNF610
    nsv5934462copy number variation1nstd209human GRCh38 chr19: 52,330,202-52,346,441 , GRCh37.p13 chr19: 52,833,455-52,849,694 ZNF610
    nsv5931755copy number variation1nstd209human GRCh38 chr19: 52,359,083-52,360,115 , GRCh37.p13 chr19: 52,862,336-52,863,368 ZNF610
    nsv5929315copy number variation1nstd209human GRCh38 chr19: 52,345,895-52,346,428 , GRCh37.p13 chr19: 52,849,148-52,849,681 ZNF610
    nsv5884223copy number variation1nstd209human GRCh38 chr19: 52,345,579-52,346,590 , GRCh37.p13 chr19: 52,848,832-52,849,843 ZNF610
    nsv5880134copy number variation1nstd209human GRCh38 chr19: 52,347,191-52,348,390 , GRCh37.p13 chr19: 52,850,444-52,851,643 ZNF610
    nsv5877777copy number variation1nstd209human GRCh38 chr19: 52,344,179-52,345,178 , GRCh37.p13 chr19: 52,847,432-52,848,431 ZNF610
    nsv5871688copy number variation2nstd209human GRCh38 chr19: 52,360,094-52,361,493 , GRCh37.p13 chr19: 52,863,347-52,864,746 ZNF610
    nsv5706558mobile element insertion1nstd211human GRCh38 chr19: 52,361,611-52,361,611 , GRCh37.p13 chr19: 52,864,864-52,864,864 ZNF610
    nsv5650670insertion1nstd207human GRCh38 chr19: 52,339,467-52,339,467 , GRCh37.p13 chr19: 52,842,720-52,842,720 ZNF610
    nsv5595007copy number variation1nstd207human GRCh38 chr19: 52,345,947-52,346,405 , GRCh37.p13 chr19: 52,849,200-52,849,658 ZNF610
    nsv5560722sequence alteration1nstd206human GRCh38 chr19: 52,345,862-52,346,409 , GRCh37.p13 chr19: 52,849,115-52,849,662 ZNF610
    nsv5532614copy number variation1nstd206human GRCh38 chr19: 52,340,928-52,342,772 , GRCh37.p13 chr19: 52,844,181-52,846,025 ZNF610
    nsv5524514copy number variation1nstd206human GRCh38 chr19: 52,345,949-52,346,409 , GRCh37.p13 chr19: 52,849,202-52,849,662 ZNF610
    nsv5520548copy number variation1nstd206human GRCh38 chr19: 52,289,775-52,335,073 , GRCh37.p13 chr19: 52,793,028-52,838,326 ZNF610, ZNF766, 1 more genes
    nsv5519099copy number variation1nstd206human GRCh38 chr19: 52,339,467-52,339,523 , GRCh37.p13 chr19: 52,842,720-52,842,776 ZNF610
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