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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
    nsv7141741copy number variation1nstd232human GRCh37.p13 chr18: 77,792,972-77,793,023 , GRCh38.p12 chr18: 80,032,972-80,033,023 TXNL4A, RBFA
    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
    nsv7067533inversion1nstd229human GRCh38 chr18: 79,955,283-80,062,390 , GRCh37.p13 chr18: 77,715,283-77,822,390 RBFA, HSBP1L1, 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
    nsv7016192copy number variation1nstd229human GRCh38 chr18: 80,033,784-80,044,453 , GRCh37.p13 chr18: 77,793,784-77,804,453 TXNL4A, RBFA
    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
    nsv7012670copy number variation1nstd229human GRCh38 chr18: 79,955,720-80,043,240 , GRCh37.p13 chr18: 77,715,720-77,803,240 HSBP1L1, TXNL4A, 1 more genes
    nsv7010415copy number variation1nstd229human GRCh38 chr18: 80,006,670-80,051,574 , GRCh37.p13 chr18: 77,766,670-77,811,574 TXNL4A, RBFA
    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
    nsv7006016copy number variation1nstd229human GRCh38 chr18: 80,049,439-80,057,389 , GRCh37.p13 chr18: 77,809,439-77,817,389 RBFA
    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
    nsv7003884copy number variation1nstd229human GRCh38 chr18: 80,032,975-80,033,024 , GRCh37.p13 chr18: 77,792,975-77,793,024 RBFA, TXNL4A
    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
    nsv6999572copy number variation1nstd229human GRCh38 chr18: 80,036,765-80,039,368 , GRCh37.p13 chr18: 77,796,765-77,799,368 RBFA
    nsv6998948copy number variation1nstd229human GRCh38 chr18: 79,770,527-80,078,823 , GRCh37.p13 chr18: 77,530,527-77,836,725 TXNL4A, RBFA, 5 more genes
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