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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6123429copy number variation1nstd186human GRCh37 chr18: 23,762,725-23,766,215 , GRCh38.p12 chr18: 26,182,761-26,186,251 PSMA8
    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
    nsv5940391copy number variation1nstd209human GRCh38 chr18: 26,183,007-26,186,163 , GRCh37.p13 chr18: 23,762,971-23,766,127 PSMA8
    nsv5940293copy number variation1nstd209human GRCh38 chr18: 26,167,841-26,171,357 , GRCh37.p13 chr18: 23,747,805-23,751,321 DHFRP1, PSMA8
    nsv5867785copy number variation1nstd209human GRCh38 chr18: 26,182,976-26,185,975 , GRCh37.p13 chr18: 23,762,940-23,765,939 PSMA8
    nsv5646093insertion1nstd207human GRCh38 chr18: 26,163,218-26,163,218 , GRCh37.p13 chr18: 23,743,182-23,743,182 PSMA8
    nsv5596507copy number variation1nstd207human GRCh38 chr18: 26,167,841-26,171,357 , GRCh37.p13 chr18: 23,747,805-23,751,321 PSMA8, DHFRP1
    nsv5596368copy number variation1nstd207human GRCh38 chr18: 26,183,007-26,186,163 , GRCh37.p13 chr18: 23,762,971-23,766,127 PSMA8
    nsv5555775sequence alteration1nstd206human GRCh38 chr18: 26,167,000-26,167,961 , GRCh37.p13 chr18: 23,746,964-23,747,925 PSMA8, DHFRP1
    nsv5550221insertion1nstd206human GRCh38 chr18: 26,167,001-26,167,001 , GRCh37.p13 chr18: 23,746,965-23,746,965 PSMA8, DHFRP1
    nsv5528785copy number variation1nstd206human GRCh38 chr18: 26,167,849-26,171,358 , GRCh37.p13 chr18: 23,747,813-23,751,322 PSMA8, DHFRP1
    nsv5521075copy number variation1nstd206human GRCh38 chr18: 26,182,761-26,186,251 , GRCh37.p13 chr18: 23,762,725-23,766,215 PSMA8
    nsv5519394copy number variation1nstd206human GRCh38 chr18: 26,135,572-26,135,702 , GRCh37.p13 chr18: 23,715,536-23,715,666 PSMA8
    nsv5515147copy number variation1nstd206human GRCh38 chr18: 26,188,197-26,188,260 , GRCh37.p13 chr18: 23,768,161-23,768,224 PSMA8
    nsv5392532copy number variation1nstd186human GRCh37 chr18: 23,762,984-23,766,057 , GRCh38.p12 chr18: 26,183,020-26,186,093 PSMA8
    nsv5389896copy number variation1nstd186human GRCh37 chr18: 23,762,978-23,766,213 , GRCh38.p12 chr18: 26,183,014-26,186,249 PSMA8
    nsv5375136translocation1nstd200human GRCh38 chr18: 26,167,001-26,167,001 , GRCh38 chr18: 26,167,961-26,167,961 , GRCh37.p13 chr18: 23,746,965-23,746,965 , GRCh37.p13 chr18: 23,747,925-23,747,925 DHFRP1, PSMA8
    nsv5328942copy number variation1nstd204human GRCh37.p13 chr18: 23,747,813-23,751,322 , GRCh38.p13 chr18: 26,167,849-26,171,358 PSMA8, DHFRP1
    nsv5322434copy number variation1nstd204human GRCh38.p13 chr18: 26,182,881-26,186,329 , GRCh37.p13 chr18: 23,762,845-23,766,293 PSMA8
    nsv5300121copy number variation1nstd204human GRCh38.p13 chr18: 26,182,001-26,186,100 , GRCh37.p13 chr18: 23,761,965-23,766,064 PSMA8
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