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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
    nsv7074287inversion1nstd229human GRCh38 chr12: 91,708,373-92,319,944 , GRCh37.p13 chr12: 92,102,150-92,713,720 LINC01619, LINC02391, 5 more genes
    nsv7072173inversion1nstd229human GRCh38 chr12: 92,142,471-92,142,487 , GRCh37.p13 chr12: 92,536,247-92,536,263 BTG1, LINC01619
    nsv7062138inversion1nstd229human GRCh38 chr12: 91,752,522-94,050,052 , GRCh37.p13 chr12: 92,146,299-94,443,828 , NUDT4, 40 more genes
    nsv6935806copy number variation1nstd229human GRCh38 chr12: 92,071,739-92,072,045 , GRCh37.p13 chr12: 92,465,515-92,465,821 LINC01619
    nsv6932636copy number variation1nstd229human GRCh38 chr12: 92,116,508-92,143,103 , GRCh37.p13 chr12: 92,510,284-92,536,879 BTG1, LINC01619
    nsv6931408copy number variation1nstd229human GRCh38 chr12: 91,949,501-92,023,900 , GRCh37.p13 chr12: 92,343,277-92,417,676 LINC01619, LOC105369901
    nsv6930968copy number variation1nstd229human GRCh38 chr12: 92,083,487-92,140,124 , GRCh37.p13 chr12: 92,477,263-92,533,900 LINC01619, BTG1
    nsv6930490copy number variation1nstd229human GRCh38 chr12: 92,087,918-92,099,722 , GRCh37.p13 chr12: 92,481,694-92,493,498 LINC01619
    nsv6929633copy number variation1nstd229human GRCh38 chr12: 92,119,147-92,122,267 , GRCh37.p13 chr12: 92,512,923-92,516,043 LINC01619
    nsv6929087copy number variation1nstd229human GRCh38 chr12: 92,040,176-92,040,199 , GRCh37.p13 chr12: 92,433,952-92,433,975 LINC01619
    nsv6928363copy number variation1nstd229human GRCh38 chr12: 92,036,234-92,036,457 , GRCh37.p13 chr12: 92,430,010-92,430,233 LINC01619
    nsv6924158copy number variation1nstd229human GRCh38 chr12: 92,103,847-92,104,142 , GRCh37.p13 chr12: 92,497,623-92,497,918 LINC01619
    nsv6923133copy number variation1nstd229human GRCh38 chr12: 91,841,233-92,052,410 , GRCh37.p13 chr12: 92,235,009-92,446,186 LINC01619, LOC105369901, 1 more genes
    nsv6922948copy number variation1nstd229human GRCh38 chr12: 92,080,943-92,123,296 , GRCh37.p13 chr12: 92,474,719-92,517,072 LINC01619
    nsv6922182copy number variation1nstd229human GRCh38 chr12: 92,070,262-92,072,659 , GRCh37.p13 chr12: 92,464,038-92,466,435 LINC01619
    nsv6921925copy number variation1nstd229human GRCh38 chr12: 92,022,240-92,022,321 , GRCh37.p13 chr12: 92,416,016-92,416,097 LINC01619
    nsv6921484copy number variation1nstd229human GRCh38 chr12: 92,104,506-92,109,112 , GRCh37.p13 chr12: 92,498,282-92,502,888 LINC01619
    nsv6920442copy number variation1nstd229human GRCh38 chr12: 92,071,800-92,073,077 , GRCh37.p13 chr12: 92,465,576-92,466,853 LINC01619
    nsv6920253copy number variation1nstd229human GRCh38 chr12: 92,075,695-92,085,936 , GRCh37.p13 chr12: 92,469,471-92,479,712 LINC01619
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