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Items: 1 to 20 of 523

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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
    nsv7075676inversion1nstd229human GRCh38 chr18: 79,903,157-80,142,354 , GRCh37.p13 chr18: 77,663,157-77,900,237 SLC66A2, KCNG2, 6 more genes
    nsv7062330inversion1nstd229human GRCh38 chr18: 80,118,957-80,163,259 , GRCh37.p13 chr18: 77,876,840-77,921,142 PARD6G, ADNP2, 1 more genes
    nsv7059531inversion1nstd229human GRCh38 chr18: 80,133,269-80,162,616 , GRCh37.p13 chr18: 77,891,152-77,920,499 PARD6G-AS1, ADNP2, 1 more genes
    nsv7016828copy number variation1nstd229human GRCh38 chr18: 79,790,901-80,154,500 , GRCh37.p13 chr18: 77,550,901-77,912,383 TXNL4A, SLC66A2, 7 more genes
    nsv7016463copy number variation1nstd229human GRCh38 chr18: 79,973,367-80,140,380 , GRCh37.p13 chr18: 77,733,367-77,898,263 ADNP2, RBFADN, 3 more genes
    nsv7014266copy number variation1nstd229human GRCh38 chr18: 80,123,027-80,125,946 , GRCh37.p13 chr18: 77,880,910-77,883,829 ADNP2
    nsv7014263copy number variation1nstd229human GRCh38 chr18: 79,903,487-80,136,645 , GRCh37.p13 chr18: 77,663,487-77,894,528 TXNL4A, SLC25A6P4, 6 more genes
    nsv7009857copy number variation1nstd229human GRCh38 chr18: 80,123,129-80,198,179 , GRCh37.p13 chr18: 77,881,012-77,956,062 PARD6G, ADNP2, 1 more genes
    nsv7008666copy number variation1nstd229human GRCh38 chr18: 79,265,424-80,231,561 , GRCh37.p13 chr18: 77,025,424-77,989,444 CTDP1-DT, SLC66A2, 19 more genes
    nsv7005132copy number variation1nstd229human GRCh38 chr18: 79,986,064-80,141,469 , GRCh37.p13 chr18: 77,746,064-77,899,352 TXNL4A, SLC25A6P4, 3 more genes
    nsv7003872copy number variation1nstd229human GRCh38 chr18: 79,701,238-80,133,958 , GRCh37.p13 chr18: 77,461,238-77,891,841 ADNP2, CTDP1, 7 more genes
    nsv6998749copy number variation1nstd229human GRCh38 chr18: 79,545,818-80,164,173 , GRCh37.p13 chr18: 77,305,818-77,922,056 CTDP1-DT, SLC66A2, 12 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
    nsv6637560copy number variation1nstd102humanPathogenic GRCh37 chr18: 77,685,396-78,014,123 , GRCh38.p12 chr18: 79,925,396-80,256,240 TXNL4A, ADNP2, 7 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
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