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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5939991copy number variation1nstd209human GRCh38 chr19: 56,187,617-56,188,416 , GRCh37.p13 chr19: 56,698,986-56,699,785 ZSCAN5B
    nsv5935015copy number variation1nstd209human GRCh38 chr19: 56,197,275-56,197,339 , GRCh37.p13 chr19: 56,708,644-56,708,708 ZSCAN5B
    nsv5518646copy number variation1nstd206human GRCh38 chr19: 56,184,073-56,213,951 , GRCh37.p13 chr19: 56,695,442-56,725,320 ZSCAN5B, ZSCAN5C, 1 more genes
    nsv5322586copy number variation1nstd204human GRCh38.p13 chr19: 55,816,789-56,429,675 , GRCh37.p13 chr19: 56,328,155-56,941,044 , ZNF582, 25 more genes
    nsv5298665copy number variation1nstd204human GRCh38.p13 chr19: 56,080,601-56,429,700 , GRCh37.p13 chr19: 56,591,967-56,941,069 , ZSCAN5B, 19 more genes
    nsv5028133copy number variation1nstd200human GRCh38 chr19: 56,191,798-56,215,294 , GRCh37.p13 chr19: 56,703,167-56,726,663 RPL13P13, ZSCAN5B, 1 more genes
    nsv5024987copy number variation1nstd200human GRCh38 chr19: 56,166,406-56,214,122 , GRCh37.p13 chr19: 56,677,775-56,725,491 ZSCAN5B, ZSCAN5C, 1 more genes
    nsv5024977copy number variation1nstd200human GRCh38 chr19: 55,808,607-56,591,629 , GRCh37.p13 chr19: 56,319,973-57,102,997 , VN2R17P, 34 more genes
    nsv4865355copy number variation1nstd200human GRCh37 chr19: 56,319,973-57,102,997 , GRCh38.p12 chr19: 55,808,607-56,591,629 , ZNF583, 34 more genes
    nsv4861453copy number variation1nstd200human GRCh37 chr19: 56,703,167-56,726,662 , GRCh38.p12 chr19: 56,191,798-56,215,293 ZSCAN5B, ZSCAN5C, 1 more genes
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
    nsv4729748copy number variation1nstd102humanUncertain significance GRCh37 chr19: 56,358,060-57,007,128 , GRCh38.p12 chr19: 55,846,694-56,495,759 LOC105372471, LOC646709, 26 more genes
    nsv4679572copy number variation1nstd189human GRCh37.p13 chr19: 56,623,189-57,013,128 , GRCh38.p12 chr19: 56,111,820-56,501,759 , ZNF444, 22 more genes
    nsv4676370copy number variation1nstd102humanUncertain significance GRCh37 chr19: 56,375,683-56,985,884 , GRCh38.p12 chr19: 55,864,317-56,474,515 LOC646709, SLC25A36P1, 24 more genes
    nsv4633764copy number variation1nstd183human GRCh37 chr19: 56,695,414-56,725,285 , GRCh38.p12 chr19: 56,184,045-56,213,916 ZSCAN5B, GALP, 1 more genes
    nsv4628449copy number variation1nstd183human GRCh37 chr19: 56,555,954-56,724,050 , GRCh38.p12 chr19: 56,044,588-56,212,681 ZNF444, GALP, 5 more genes
    nsv4623903copy number variation1nstd183human GRCh37 chr19: 56,709,265-56,741,027 , GRCh38.p12 chr19: 56,197,896-56,229,658 ZSCAN5B, ZSCAN5C, 2 more genes
    nsv4619351copy number variation1nstd183human GRCh37 chr19: 56,679,678-56,723,562 , GRCh38.p12 chr19: 56,168,309-56,212,193 ZSCAN5C, ZSCAN5B, 1 more genes
    nsv4436360complex substitution1nstd102humanUncertain significance GRCh38.p12 chr19: 55,621,933-57,136,909 , GRCh37 chr19: 56,133,299-57,648,277 PEG3, U2AF2, 64 more genes
    nsv4429702copy number variation1nstd174human GRCh37 chr19: 56,695,396-56,736,526 , GRCh38.p12 chr19: 56,184,027-56,225,157 ZSCAN5B, ZSCAN5A, 3 more genes
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