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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112815copy number variation1nstd102humanPathogenic GRCh37 chr18: 54,285,235-77,960,815 , GRCh38.p12 chr18: 56,618,004-80,202,932 RPL31P9, TRG-TCC5-1, 271 more genes
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5936933copy number variation1nstd209human GRCh38 chr18: 80,077,017-80,077,338 , GRCh37.p13 chr18: 77,834,915-77,835,240 RBFADN, SLC25A6P4
    nsv5936067copy number variation1nstd209human GRCh38 chr18: 79,641,572-80,107,313 , GRCh37.p13 chr18: 77,401,572-77,865,197 , KCNG2, 9 more genes
    nsv5883740copy number variation2nstd209human GRCh38 chr18: 80,075,959-80,087,652 , GRCh37.p13 chr18: 77,833,890-77,845,560 RBFADN, SLC25A6P4
    nsv5601903copy number variation1nstd207human GRCh38 chr18: 80,075,650-80,075,724 , GRCh37.p8 chr: NaN-NaN , GRCh37.p13 chr: NaN-NaN RBFADN, SLC25A6P4
    nsv5529792copy number variation1nstd206human GRCh38 chr18: 76,965,528-80,259,528 , GRCh37.p13 chr18: 74,677,484-78,017,154 , KCNG2, 43 more genes
    nsv5526102copy number variation1nstd206human GRCh38 chr18: 79,647,021-80,153,228 , GRCh37.p13 chr18: 77,407,021-77,911,111 , ADNP2, 10 more genes
    nsv5514135copy number variation1nstd206human GRCh38 chr18: 62,909,528-80,261,528 , GRCh37.p13 chr18: 60,576,761-78,017,154 , SMIM21, 190 more genes
    nsv5381802copy number variation1nstd102humanPathogenic GRCh37 chr18: 51,925,586-78,010,032 , GRCh38.p12 chr18: 54,399,216-80,252,149 LOC105372200, LOC105372174, 298 more genes
    nsv5029143copy number variation1nstd200human GRCh38 chr18: 80,068,061-80,085,440 , GRCh37.p13 chr18: 77,828,061-77,843,348 RBFADN, SLC25A6P4
    nsv5029137copy number variation1nstd200human GRCh38 chr18: 79,903,487-80,136,651 , GRCh37.p13 chr18: 77,663,487-77,894,534 SLC25A6P4, KCNG2, 6 more genes
    nsv5018898copy number variation1nstd200human GRCh38 chr18: 80,070,506-80,093,641 , GRCh37.p13 chr18: 77,830,506-77,851,523 SLC25A6P4, RBFADN
    nsv4867999copy number variation1nstd200human GRCh37 chr18: 77,834,918-77,835,241 , GRCh38.p12 chr18: 80,077,020-80,077,339 RBFADN, SLC25A6P4
    nsv4867997copy number variation1nstd200human GRCh37 chr18: 77,830,499-77,851,525 , GRCh38.p12 chr18: 80,070,499-80,093,643 RBFADN, SLC25A6P4
    nsv4854855copy number variation1nstd200human GRCh37 chr18: 77,835,174-77,873,594 , GRCh38.p12 chr18: 80,077,274-80,115,711 SLC25A6P4, RBFADN, 1 more genes
    nsv4854854copy number variation1nstd200human GRCh37 chr18: 77,828,061-77,843,348 , GRCh38.p12 chr18: 80,068,061-80,085,440 SLC25A6P4, RBFADN
    nsv4731623copy number variation1nstd199human GRCh37 chr18: 77,833,430-77,833,809 , GRCh38.p12 chr18: 80,075,532-80,075,911 SLC25A6P4, RBFADN
    nsv4729869copy number variation1nstd102humanLikely pathogenic GRCh37 chr18: 63,747,519-78,014,123 , GRCh38.p12 chr18: 66,080,283-80,256,240 CYB5A, GALR1, 147 more genes
    nsv4729851copy number variation1nstd102humanPathogenic GRCh37 chr18: 70,835,154-78,014,123 , GRCh38.p12 chr18: 73,167,919-80,256,240 ZNF236-DT, LOC339298, 89 more genes
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