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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077519inversion1nstd229human GRCh38 chr12: 86,495,718-92,133,299 , GRCh37.p13 chr12: 86,889,495-92,527,075 CEP290, MIR3059, 60 more genes
    nsv7060010inversion1nstd229human GRCh38 chr12: 86,085,575-91,207,469 , GRCh37.p13 chr12: 86,479,353-91,601,246 POC1B, C12orf50, 55 more genes
    nsv6931826copy number variation1nstd229human GRCh38 chr12: 91,170,801-91,264,700 , GRCh37.p13 chr12: 91,564,578-91,658,477 DCN
    nsv6929811copy number variation1nstd229human GRCh38 chr12: 91,171,575-91,171,787 , GRCh37.p13 chr12: 91,565,352-91,565,564 DCN
    nsv6929605copy number variation1nstd229human GRCh38 chr12: 91,140,701-91,142,500 , GRCh37.p13 chr12: 91,534,478-91,536,277 DCN
    nsv6928447copy number variation1nstd229human GRCh38 chr12: 91,155,495-91,155,593 , GRCh37.p13 chr12: 91,549,272-91,549,370 DCN
    nsv6927945copy number variation1nstd229human GRCh38 chr12: 91,167,698-91,173,428 , GRCh37.p13 chr12: 91,561,475-91,567,205 DCN
    nsv6927695copy number variation1nstd229human GRCh38 chr12: 90,167,236-91,253,354 , GRCh37.p13 chr12: 90,561,013-91,647,131 LOC105369895, EPYC, 8 more genes
    nsv6926433copy number variation1nstd229human GRCh38 chr12: 91,170,892-91,171,281 , GRCh37.p13 chr12: 91,564,669-91,565,058 DCN
    nsv6922173copy number variation1nstd229human GRCh38 chr12: 90,850,701-91,231,900 , GRCh37.p13 chr12: 91,244,478-91,625,677 LINC00615, CCER1, 4 more genes
    nsv6921992copy number variation1nstd229human GRCh38 chr12: 91,044,176-91,486,796 , GRCh37.p13 chr12: 91,437,953-91,880,573 DCN, LOC105369896, 4 more genes
    nsv6921136copy number variation1nstd229human GRCh38 chr12: 91,146,251-91,151,651 , GRCh37.p13 chr12: 91,540,028-91,545,428 DCN
    nsv6920877copy number variation1nstd229human GRCh38 chr12: 91,178,587-91,182,652 , GRCh37.p13 chr12: 91,572,364-91,576,429 DCN
    nsv6920532copy number variation1nstd229human GRCh38 chr12: 91,178,622-91,179,372 , GRCh37.p13 chr12: 91,572,399-91,573,149 DCN
    nsv6919849copy number variation1nstd229human GRCh38 chr12: 91,175,338-91,177,390 , GRCh37.p13 chr12: 91,569,115-91,571,167 DCN
    nsv6918810copy number variation1nstd229human GRCh38 chr12: 91,159,915-91,162,933 , GRCh37.p13 chr12: 91,553,692-91,556,710 DCN
    nsv6918597copy number variation1nstd229human GRCh38 chr12: 91,153,191-91,157,077 , GRCh37.p13 chr12: 91,546,968-91,550,854 DCN
    nsv6621897copy number variation1nstd224human GRCh37 chr12: 90,560,078-91,630,155 , GRCh38.p12 chr12: 90,166,301-91,236,378 LINC00615, LINC02822, 8 more genes
    nsv6621758copy number variation1nstd224human GRCh37 chr12: 90,562,017-91,630,155 , GRCh38.p12 chr12: 90,168,240-91,236,378 DCN, EPYC, 8 more genes
    nsv6592657inversion1nstd223human GRCh38 chr12: 91,157,910-91,158,827 , GRCh37.p13 chr12: 91,551,687-91,552,604 DCN
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