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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5979829insertion1nstd209human GRCh38 chr10: 132,186,856-132,186,856 , GRCh37.p13 chr10: 134,000,360-134,000,360 DPYSL4
    nsv5672526copy number variation1nstd102humanPathogenic GRCh37 chr10: 127,548,166-135,440,251 , GRCh38.p12 chr10: 125,859,597-133,626,747 LINC00601, RPL5P28, 110 more genes
    nsv5643049insertion1nstd207human GRCh38 chr10: 132,186,856-132,186,856 , GRCh37.p13 chr10: 134,000,360-134,000,360 DPYSL4
    nsv5635832insertion1nstd207human GRCh38 chr10: 132,191,932-132,191,932 , GRCh37.p13 chr10: 134,005,436-134,005,436 DPYSL4
    nsv5603377copy number variation1nstd207human GRCh38 chr10: 132,191,518-132,191,846 , GRCh37.p13 chr10: 134,005,022-134,005,350 DPYSL4
    nsv5602759copy number variation1nstd207human GRCh38 chr10: 132,191,103-132,191,157 , GRCh37.p13 chr10: 134,004,607-134,004,661 DPYSL4
    nsv5507934copy number variation1nstd206human GRCh38 chr10: 132,193,834-132,193,903 , GRCh37.p13 chr10: 134,007,338-134,007,407 DPYSL4
    nsv5501883copy number variation1nstd206human GRCh38 chr10: 132,191,391-132,191,917 , GRCh37.p13 chr10: 134,004,895-134,005,421 DPYSL4
    nsv5381769copy number variation1nstd102humanPathogenic GRCh37 chr10: 129,483,682-135,434,178 , GRCh38.p12 chr10: 127,685,418-133,620,674 DPYSL4, LINC02667, 88 more genes
    nsv5354620translocation1nstd200human GRCh38 chr10: 132,195,106-132,195,106 , GRCh38 chr10: 132,195,032-132,195,032 , GRCh37.p13 chr10: 134,008,610-134,008,610 , GRCh37.p13 chr10: 134,008,536-134,008,536 DPYSL4
    nsv4977674copy number variation1nstd200human GRCh38 chr10: 132,194,711-132,196,351 , GRCh37.p13 chr10: 134,008,215-134,009,855 DPYSL4
    nsv4977673copy number variation1nstd200human GRCh38 chr10: 132,184,372-132,184,498 , GRCh37.p13 chr10: 133,997,876-133,998,002 JAKMIP3, JAKMIP3-AS1, 1 more genes
    nsv4746313copy number variation1nstd199human GRCh37 chr10: 134,004,611-134,004,664 , GRCh38.p12 chr10: 132,191,107-132,191,160 DPYSL4
    nsv4729703copy number variation1nstd102humanLikely benign GRCh37 chr10: 133,833,614-134,198,380 , GRCh38.p12 chr10: 132,020,110-132,384,876 JAKMIP3, JAKMIP3-AS1, 3 more genes
    nsv4729670copy number variation1nstd102humanPathogenic GRCh37 chr10: 129,031,265-135,427,143 , GRCh38.p12 chr10: 127,233,001-133,613,639 LOC105378561, LINC01164, 91 more genes
    nsv4675991copy number variation1nstd102humanPathogenic GRCh37 chr10: 119,996,339-135,427,143 , GRCh38.p12 chr10: 118,236,827-133,613,639 STK32C, LOC105378542, 237 more genes
    nsv4675230copy number variation1nstd102humanPathogenic GRCh37 chr10: 129,009,772-135,427,143 , GRCh38.p12 chr10: 127,211,508-133,613,639 EBF3-AS1, LINC02646, 91 more genes
    nsv4674901copy number variation1nstd102humanPathogenic GRCh37 chr10: 129,381,095-135,427,143 , GRCh38.p12 chr10: 127,582,831-133,613,639 LOC100419870, MIR378C, 88 more genes
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