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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
    nsv6937405copy number variation1nstd229human GRCh38 chr12: 87,957,217-88,286,316 , GRCh37.p13 chr12: 88,350,994-88,680,093 RNA5SP364, LOC107984542, 6 more genes
    nsv6934508copy number variation1nstd229human GRCh38 chr12: 88,007,201-88,020,900 , GRCh37.p13 chr12: 88,400,978-88,414,677 C12orf50
    nsv6932987copy number variation1nstd229human GRCh38 chr12: 87,925,501-88,494,507 , GRCh37.p13 chr12: 88,319,278-88,888,284 LOC107984542, RPS4XP15, 8 more genes
    nsv6931138copy number variation1nstd229human GRCh38 chr12: 88,016,807-88,022,662 , GRCh37.p13 chr12: 88,410,584-88,416,439 C12orf50
    nsv6931119copy number variation1nstd229human GRCh38 chr12: 88,010,370-88,010,442 , GRCh37.p13 chr12: 88,404,147-88,404,219 C12orf50
    nsv6929928copy number variation1nstd229human GRCh38 chr12: 87,978,901-88,153,800 , GRCh37.p13 chr12: 88,372,678-88,547,577 CEP290, C12orf50, 5 more genes
    nsv6928678copy number variation1nstd229human GRCh38 chr12: 88,027,812-88,118,908 , GRCh37.p13 chr12: 88,421,589-88,512,685 RLIG1, LOC100420011, 4 more genes
    nsv6927933copy number variation1nstd229human GRCh38 chr12: 88,006,989-88,039,033 , GRCh37.p13 chr12: 88,400,766-88,432,810 C12orf50, RLIG1, 1 more genes
    nsv6925910copy number variation1nstd229human GRCh38 chr12: 88,000,905-88,010,790 , GRCh37.p13 chr12: 88,394,682-88,404,567 C12orf50
    nsv6920810copy number variation1nstd229human GRCh38 chr12: 86,380,249-87,989,805 , GRCh37.p13 chr12: 86,774,027-88,383,582 LOC107984478, RPL23AP68, 12 more genes
    nsv6919164copy number variation1nstd229human GRCh38 chr12: 88,005,361-88,005,571 , GRCh37.p13 chr12: 88,399,138-88,399,348 C12orf50
    nsv6580037inversion1nstd223human GRCh38 chr12: 87,998,702-88,000,545 , GRCh37.p13 chr12: 88,392,479-88,394,322 C12orf50
    nsv6577940inversion1nstd223human GRCh38 chr12: 87,998,903-88,000,298 , GRCh37.p13 chr12: 88,392,680-88,394,075 C12orf50
    nsv6474738copy number variation1nstd223human GRCh38 chr12: 88,016,763-88,022,659 , GRCh37.p13 chr12: 88,410,540-88,416,436 C12orf50
    nsv6473848copy number variation1nstd223human GRCh38 chr12: 88,000,362-88,000,731 , GRCh37.p13 chr12: 88,394,139-88,394,508 C12orf50
    nsv6472551copy number variation1nstd223human GRCh38 chr12: 87,970,101-87,983,700 , GRCh37.p13 chr12: 88,363,878-88,377,477 C12orf50
    nsv6471385copy number variation1nstd223human GRCh38 chr12: 88,000,935-88,001,506 , GRCh37.p13 chr12: 88,394,712-88,395,283 C12orf50
    nsv6470224copy number variation1nstd223human GRCh38 chr12: 87,988,620-87,989,303 , GRCh37.p13 chr12: 88,382,397-88,383,080 C12orf50
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