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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7071319inversion1nstd229human GRCh38 chr12: 15,736,312-15,736,445 , GRCh37.p13 chr12: 15,889,246-15,889,379 EPS8
    nsv7068800inversion1nstd229human GRCh38 chr12: 15,780,993-15,781,020 , GRCh37.p13 chr12: 15,933,927-15,933,954 EPS8
    nsv7066449inversion1nstd229human GRCh38 chr12: 15,671,304-15,677,813 , GRCh37.p13 chr12: 15,824,238-15,830,747 RNU6-251P, EPS8
    nsv7064011inversion1nstd229human GRCh38 chr12: 11,255,910-17,864,916 , GRCh37.p13 chr12: 11,408,826-18,017,850 MGP, MIR3974, 108 more genes
    nsv6936008copy number variation1nstd229human GRCh38 chr12: 15,748,529-15,748,562 , GRCh37.p13 chr12: 15,901,463-15,901,496 EPS8
    nsv6935765copy number variation1nstd229human GRCh38 chr12: 15,732,981-15,737,704 , GRCh37.p13 chr12: 15,885,915-15,890,638 EPS8
    nsv6933682copy number variation1nstd229human GRCh38 chr12: 15,660,253-15,663,277 , GRCh37.p13 chr12: 15,813,187-15,816,211 EPS8
    nsv6932719copy number variation1nstd229human GRCh38 chr12: 15,774,878-15,775,412 , GRCh37.p13 chr12: 15,927,812-15,928,346 EPS8
    nsv6932718copy number variation1nstd229human GRCh38 chr12: 15,746,364-15,753,564 , GRCh37.p13 chr12: 15,899,298-15,906,498 EPS8
    nsv6931161copy number variation1nstd229human GRCh38 chr12: 15,719,866-15,732,502 , GRCh37.p13 chr12: 15,872,800-15,885,436 EPS8
    nsv6930522copy number variation1nstd229human GRCh38 chr12: 15,745,801-15,753,600 , GRCh37.p13 chr12: 15,898,735-15,906,534 EPS8
    nsv6930317copy number variation1nstd229human GRCh38 chr12: 15,744,501-15,753,500 , GRCh37.p13 chr12: 15,897,435-15,906,434 EPS8
    nsv6929377copy number variation1nstd229human GRCh38 chr12: 15,351,103-15,653,020 , GRCh37.p13 chr12: 15,504,037-15,805,954 PTPRO, EPS8, 2 more genes
    nsv6928498copy number variation1nstd229human GRCh38 chr12: 15,746,601-15,753,600 , GRCh37.p13 chr12: 15,899,535-15,906,534 EPS8
    nsv6925769copy number variation1nstd229human GRCh38 chr12: 15,746,576-15,784,301 , GRCh37.p13 chr12: 15,899,510-15,937,235 EPS8
    nsv6922903copy number variation1nstd229human GRCh38 chr12: 15,747,301-15,753,500 , GRCh37.p13 chr12: 15,900,235-15,906,434 EPS8
    nsv6920627copy number variation1nstd229human GRCh38 chr12: 15,746,401-15,753,500 , GRCh37.p13 chr12: 15,899,335-15,906,434 EPS8
    nsv6919269copy number variation1nstd229human GRCh38 chr12: 15,643,174-15,646,930 , GRCh37.p13 chr12: 15,796,108-15,799,864 EPS8
    nsv6918685copy number variation1nstd229human GRCh38 chr12: 15,702,625-15,702,696 , GRCh37.p13 chr12: 15,855,559-15,855,630 EPS8
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