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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148271copy number variation1nstd102humanPathogenic GRCh38 chr18: 158,286-14,124,574 , GRCh37.p13 chr18: 158,286-14,124,573 PMM2P2, EIF4A2P1, 225 more genes
    nsv7098917copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-15,400,035 , GRCh38.p12 chr18: 10,001-15,400,036 RNU7-25P, RPL6P27, 275 more genes
    nsv7095454copy number variation1nstd102humanPathogenic GRCh37 chr18: 7,079,954-7,080,476 , GRCh38.p12 chr18: 7,079,955-7,080,477 LAMA1
    nsv7095453copy number variation1nstd102humanPathogenic GRCh37 chr18: 6,999,424-7,000,016 , GRCh38.p12 chr18: 6,999,425-7,000,017 LAMA1
    nsv7095452copy number variation1nstd102humanPathogenic GRCh37 chr18: 6,974,882-6,976,099 , GRCh38.p12 chr18: 6,974,883-6,976,100 LAMA1
    nsv7095451copy number variation1nstd102humanUncertain significance GRCh37 chr18: 6,942,078-7,080,476 , GRCh38.p12 chr18: 6,942,079-7,080,477 LOC101927188, LAMA1
    nsv7095390copy number variation1nstd102humanUncertain significance GRCh37 chr18: 6,942,078-7,050,955 , GRCh38.p12 chr18: 6,942,079-7,050,956 LOC101927188, LAMA1
    nsv7095257copy number variation1nstd102humanPathogenic GRCh37 chr18: 7,013,794-7,015,877 , GRCh38.p12 chr18: 7,013,795-7,015,878 LAMA1
    nsv7075855inversion1nstd229human GRCh38 chr18: 6,609,506-9,295,232 , GRCh37.p13 chr18: 6,609,505-9,295,230 LAMA1, RAB12, 28 more genes
    nsv7075652inversion1nstd229human GRCh38 chr18: 6,609,505-7,953,047 , GRCh37.p13 chr18: 6,609,504-7,953,045 LINC00668, LOC105371975, 14 more genes
    nsv7074863inversion1nstd229human GRCh38 chr18: 7,001,202-7,014,272 , GRCh37.p13 chr18: 7,001,201-7,014,271 LAMA1
    nsv7073615inversion1nstd229human GRCh38 chr18: 6,680,058-7,271,834 , GRCh37.p13 chr18: 6,680,057-7,271,832 LINC00668, ARHGAP28-AS1, 9 more genes
    nsv7070666inversion1nstd229human GRCh38 chr18: 6,394,803-7,542,239 , GRCh37.p13 chr18: 6,394,802-7,542,237 ARHGAP28, LOC107985176, 19 more genes
    nsv7070529inversion1nstd229human GRCh38 chr18: 6,839,499-7,541,337 , GRCh37.p13 chr18: 6,839,498-7,541,335 LOC112577592, SLC25A51P2, 11 more genes
    nsv7068908inversion1nstd229human GRCh38 chr18: 6,679,880-7,275,063 , GRCh37.p13 chr18: 6,679,879-7,275,061 LOC105371973, LAMA1, 9 more genes
    nsv7065817inversion1nstd229human GRCh38 chr18: 6,839,495-9,543,414 , GRCh37.p13 chr18: 6,839,494-9,543,412 ANKRD12, RPS4XP19, 32 more genes
    nsv7065179inversion1nstd229human GRCh38 chr18: 6,976,998-7,018,977 , GRCh37.p13 chr18: 6,976,997-7,018,976 LAMA1
    nsv7064828inversion1nstd229human GRCh38 chr18: 6,351,167-7,375,513 , GRCh37.p13 chr18: 6,351,166-7,375,511 LOC107985176, RNU6-349P, 18 more genes
    nsv7063411inversion1nstd229human GRCh38 chr18: 7,065,613-8,554,097 , GRCh37.p13 chr18: 7,065,612-8,554,095 AKR1B1P6, LOC112577592, 13 more genes
    nsv7017812copy number variation1nstd229human GRCh38 chr18: 6,972,678-6,973,131 , GRCh37.p13 chr18: 6,972,677-6,973,130 LAMA1
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