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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148195copy number variation1nstd102humanPathogenic GRCh37 chr18: 63,476,940-77,960,815 , GRCh38.p12 chr18: 65,809,704-80,202,932 LOC105372202, LINC01896, 149 more genes
    nsv7137214copy number variation1nstd102humanPathogenic GRCh37 chr18: 66,057,406-78,014,123 , GRCh38.p12 chr18: 68,390,169-80,256,240 LOC105372228, MIR548AV, 132 more genes
    nsv7137137copy number variation1nstd102humanPathogenic GRCh37 chr18: 71,740,696-78,005,231 , GRCh38.p12 chr18: 74,073,461-80,247,348 LOC339298, LOC105372201, 84 more genes
    nsv7099035copy number variation1nstd102humanPathogenic GRCh37 chr18: 66,434,850-78,075,000 , GRCh38.p12 chr18: 68,767,613-80,259,271 LOC107985151, CD226, 129 more genes
    nsv7017485copy number variation1nstd229human GRCh38 chr18: 75,449,301-75,451,800 , GRCh37.p13 chr18: 73,161,256-73,163,755 SMIM21
    nsv7016539copy number variation1nstd229human GRCh38 chr18: 75,449,864-75,453,240 , GRCh37.p13 chr18: 73,161,819-73,165,195 SMIM21
    nsv7016467copy number variation1nstd229human GRCh38 chr18: 75,375,908-75,432,876 , GRCh37.p13 chr18: 73,087,863-73,144,831 LOC105372200, SMIM21
    nsv7009504copy number variation1nstd229human GRCh38 chr18: 75,456,036-75,460,610 , GRCh37.p13 chr18: 73,167,991-73,172,565 LOC107985177, SMIM21
    nsv7004283copy number variation1nstd229human GRCh38 chr18: 75,406,367-75,427,651 , GRCh37.p13 chr18: 73,118,322-73,139,606 LOC105372200, SMIM21
    nsv7002312copy number variation1nstd229human GRCh38 chr18: 75,421,866-75,422,262 , GRCh37.p13 chr18: 73,133,821-73,134,217 LOC105372200, SMIM21
    nsv7002063copy number variation1nstd229human GRCh38 chr18: 75,223,473-75,507,020 , GRCh37.p13 chr18: 72,935,428-73,218,975 LOC105372200, LOC105372201, 4 more genes
    nsv6638045copy number variation1nstd102humanPathogenic GRCh37 chr18: 66,530,142-78,014,123 , GRCh38.p12 chr18: 68,862,905-80,256,240 LOC105372211, LOC105372188, 128 more genes
    nsv6638004copy number variation1nstd102humanPathogenic GRCh37 chr18: 61,520,071-78,014,123 , GRCh38.p12 chr18: 63,852,837-80,256,240 LOC107985151, CD226, 165 more genes
    nsv6637467copy number variation1nstd102humanPathogenic GRCh37 chr18: 53,624,405-78,014,123 , GRCh38.p12 chr18: 55,957,174-80,256,240 RPL9P31, LOC100422317, 277 more genes
    nsv6634444copy number variation1nstd102humanPathogenic GRCh37 chr18: 72,669,936-77,889,946 , GRCh38.p12 chr18: 74,957,980-80,132,063 LOC105372212, GALR1, 71 more genes
    nsv6535314copy number variation1nstd223human GRCh38 chr18: 75,422,594-75,423,075 , GRCh37.p13 chr18: 73,134,549-73,135,030 SMIM21, LOC105372200
    nsv6533999copy number variation1nstd223human GRCh38 chr18: 75,431,880-75,432,356 , GRCh37.p13 chr18: 73,143,835-73,144,311 SMIM21
    nsv6531572copy number variation1nstd223human GRCh38 chr18: 75,223,473-75,507,020 , GRCh37.p13 chr18: 72,935,428-73,218,975 LOC105372201, TSHZ1, 4 more genes
    nsv6531131copy number variation1nstd223human GRCh38 chr18: 75,455,401-75,456,100 , GRCh37.p13 chr18: 73,167,356-73,168,055 LOC107985177, SMIM21
    nsv6529805copy number variation1nstd223human GRCh38 chr18: 75,449,864-75,453,236 , GRCh37.p13 chr18: 73,161,819-73,165,191 SMIM21
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