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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
    nsv5926289copy number variation1nstd209human GRCh38 chr10: 133,371,188-133,471,140 , GRCh37.p13 chr10: 135,184,692-135,284,644 , ECHS1, 6 more genes
    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
    nsv5501586copy number variation1nstd206human GRCh38 chr10: 133,401,130-133,457,130 , GRCh37.p13 chr10: 135,214,634-135,270,634 MTG1, SCART1, 2 more genes
    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
    nsv5255637copy number variation1nstd204human GRCh38.p13 chr10: 133,292,501-133,426,700 , GRCh37.p13 chr10: 135,106,005-135,240,204 BANF1P2, FUOM, 9 more genes
    nsv5243523copy number variation1nstd204human GRCh38.p13 chr10: 133,402,919-133,421,717 , GRCh37.p13 chr10: 135,216,423-135,235,221 MTG1, SPRN
    nsv4984081copy number variation1nstd200human GRCh38 chr10: 133,346,604-133,601,248 , GRCh37.p13 chr10: 135,160,108-135,414,752 , OR7M1P, 15 more genes
    nsv4984078copy number variation1nstd200human GRCh38 chr10: 133,339,475-133,432,353 , GRCh37.p13 chr10: 135,152,979-135,245,857 OR6L2P, PRAP1, 7 more genes
    nsv4984060copy number variation1nstd200human GRCh38 chr10: 132,934,989-133,515,554 , GRCh37.p13 chr10: 134,748,493-135,329,058 , SCART1, 33 more genes
    nsv4977745copy number variation1nstd200human GRCh38 chr10: 133,421,099-133,421,962 , GRCh37.p13 chr10: 135,234,603-135,235,466 MTG1, SPRN
    nsv4845271copy number variation1nstd200human GRCh37 chr10: 135,234,603-135,235,466 , GRCh38.p12 chr10: 133,421,099-133,421,962 MTG1, SPRN
    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
    nsv4729448copy number variation1nstd102humanLikely benign GRCh37 chr10: 135,165,733-135,427,143 , GRCh38.p12 chr10: 133,352,229-133,613,639 LOC105378575, OR7M1P, 13 more genes
    nsv4728900copy number variation1nstd102humanLikely benign GRCh37 chr10: 135,204,187-135,408,132 , GRCh38.p12 chr10: 133,390,683-133,594,628 SCART1, LOC105378575, 9 more genes
    nsv4680914copy number variation1nstd189human GRCh37.p13 chr10: 135,234,710-135,534,747 , GRCh38.p12 chr10: 133,421,206-133,787,422 , CYP2E1, 29 more genes
    nsv4680247copy number variation1nstd189human GRCh37.p13 chr10: 135,232,980-135,358,784 , GRCh38.p12 chr10: 133,419,476-133,545,280 , CYP2E1, 7 more genes
    nsv4679370copy number variation1nstd189human GRCh37.p13 chr10: 135,236,018-135,380,340 , GRCh38.p12 chr10: 133,422,514-133,566,836 , CYP2E1, 9 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
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