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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141427insertion1nstd232human GRCh37.p13 chr18: 59,852,898-59,852,898 , GRCh38.p12 chr18: 62,185,665-62,185,665 PIGN, RELCH
    nsv7095448copy number variation1nstd102humanUncertain significance GRCh37 chr18: 59,805,456-60,052,267 , GRCh38.p12 chr18: 62,138,223-62,385,034 PIGN, TNFRSF11A, 1 more genes
    nsv7077367inversion1nstd229human GRCh38 chr18: 62,260,858-62,260,989 , GRCh37.p13 chr18: 59,928,091-59,928,222 RELCH
    nsv7072414inversion1nstd229human GRCh38 chr18: 59,526,812-66,942,199 , GRCh37.p13 chr18: 57,194,044-64,609,436 RPIAP1, LOC105372167, 77 more genes
    nsv7071501inversion1nstd229human GRCh38 chr18: 62,269,541-62,333,423 , GRCh37.p13 chr18: 59,936,774-60,000,656 RELCH, TNFRSF11A
    nsv7069827inversion1nstd229human GRCh38 chr18: 60,254,377-67,312,517 , GRCh37.p13 chr18: 57,921,610-64,979,754 RNU6-142P, TNFRSF11A, 63 more genes
    nsv7066376inversion1nstd229human GRCh38 chr18: 61,808,565-71,004,929 , GRCh37.p13 chr18: 59,475,798-68,672,165 DSEL-AS1, LOC112268209, 84 more genes
    nsv7063421inversion1nstd229human GRCh38 chr18: 62,222,485-62,222,534 , GRCh37.p13 chr18: 59,889,718-59,889,767 RELCH
    nsv7017442copy number variation1nstd229human GRCh38 chr18: 62,205,601-62,208,000 , GRCh37.p13 chr18: 59,872,834-59,875,233 RELCH
    nsv7016738copy number variation1nstd229human GRCh38 chr18: 62,194,406-62,198,072 , GRCh37.p13 chr18: 59,861,639-59,865,305 RELCH
    nsv7016270copy number variation1nstd229human GRCh38 chr18: 62,211,904-62,214,117 , GRCh37.p13 chr18: 59,879,137-59,881,350 RELCH
    nsv7016125copy number variation1nstd229human GRCh38 chr18: 62,234,094-62,243,801 , GRCh37.p13 chr18: 59,901,327-59,911,034 RELCH
    nsv7005351copy number variation1nstd229human GRCh38 chr18: 62,218,538-62,218,580 , GRCh37.p13 chr18: 59,885,771-59,885,813 RELCH
    nsv6998661copy number variation1nstd229human GRCh38 chr18: 62,199,209-62,199,247 , GRCh37.p13 chr18: 59,866,442-59,866,480 RELCH
    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
    nsv6624803copy number variation1nstd224human GRCh37 chr18: 59,941,236-60,000,477 , GRCh38.p12 chr18: 62,274,003-62,333,244 TNFRSF11A, RELCH
    nsv6624409copy number variation1nstd224human GRCh37 chr18: 59,797,153-59,899,595 , GRCh38.p12 chr18: 62,129,920-62,232,362 PIGN, RELCH
    nsv6594929inversion1nstd223human GRCh38 chr18: 62,251,990-62,252,539 , GRCh37.p13 chr18: 59,919,223-59,919,772 RELCH
    nsv6535046copy number variation1nstd223human GRCh38 chr18: 62,297,461-62,298,066 , GRCh37.p13 chr18: 59,964,694-59,965,299 RELCH
    nsv6533468copy number variation1nstd223human GRCh38 chr18: 62,286,701-62,288,900 , GRCh37.p13 chr18: 59,953,934-59,956,133 RELCH
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