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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5970228inversion1nstd209human GRCh38 chr18: 42,666,448-47,133,105 , GRCh37.p13 chr18: 40,246,413-44,659,476 , ATP5F1A, 50 more genes
    nsv5711405mobile element insertion1nstd211human GRCh38 chr18: 46,009,391-46,009,391 , GRCh37.p13 chr18: 43,589,357-43,589,357 PSTPIP2
    nsv5655865insertion1nstd207human GRCh38 chr18: 45,992,442-45,992,442 , GRCh37.p13 chr18: 43,572,408-43,572,408 PSTPIP2
    nsv5531218copy number variation1nstd206human GRCh38 chr18: 46,017,445-46,017,544 , GRCh37.p13 chr18: 43,597,411-43,597,510 PSTPIP2
    nsv5526907copy number variation1nstd206human GRCh38 chr18: 45,974,919-45,982,519 , GRCh37.p13 chr18: 43,554,885-43,562,485 PSTPIP2
    nsv5525222copy number variation1nstd206human GRCh38 chr18: 45,996,443-46,209,010 , GRCh37.p13 chr18: 43,576,409-43,788,976 ATP5F1A, PSTPIP2, 6 more genes
    nsv5523721copy number variation1nstd206human GRCh38 chr18: 45,979,714-45,993,278 , GRCh37.p13 chr18: 43,559,680-43,573,244 PSTPIP2, RN7SKP26
    nsv5381046copy number variation2nstd102humanUncertain significance GRCh37 chr18: 42,281,312-45,423,127 , GRCh38.p12 chr18: 44,701,347-47,896,756 HDHD2, RNU6-1131P, 45 more genes
    nsv5322304copy number variation1nstd204human GRCh37.p13 chr18: 43,567,899-43,568,176 , GRCh38.p13 chr18: 45,987,933-45,988,210 PSTPIP2, RN7SKP26
    nsv5142028mobile element insertion1nstd203human GRCh38 chr18: 46,055,841-46,055,853 , GRCh37.p13 chr18: 43,635,807-43,635,819 PSTPIP2
    nsv5024169copy number variation1nstd200human GRCh38 chr18: 46,000,516-46,186,861 , GRCh37.p13 chr18: 43,580,482-43,766,827 PSTPIP2, HAUS1, 6 more genes
    nsv5017901copy number variation1nstd200human GRCh38 chr18: 46,059,177-46,068,327 , GRCh37.p13 chr18: 43,639,143-43,648,293 PSTPIP2
    nsv5017900copy number variation1nstd200human GRCh38 chr18: 46,057,919-46,061,229 , GRCh37.p13 chr18: 43,637,885-43,641,195 PSTPIP2
    nsv5017899copy number variation1nstd200human GRCh38 chr18: 46,044,424-46,049,293 , GRCh37.p13 chr18: 43,624,390-43,629,259 PSTPIP2
    nsv5017898copy number variation1nstd200human GRCh38 chr18: 46,029,033-46,029,891 , GRCh37.p13 chr18: 43,608,999-43,609,857 LOC100422497, PSTPIP2
    nsv5017897copy number variation1nstd200human GRCh38 chr18: 45,992,648-45,992,858 , GRCh37.p13 chr18: 43,572,614-43,572,824 PSTPIP2
    nsv4859515copy number variation1nstd200human GRCh37 chr18: 43,608,999-43,609,857 , GRCh38.p12 chr18: 46,029,033-46,029,891 LOC100422497, PSTPIP2
    nsv4859514copy number variation1nstd200human GRCh37 chr18: 43,567,909-43,568,167 , GRCh38.p12 chr18: 45,987,943-45,988,201 PSTPIP2, RN7SKP26
    nsv4732592copy number variation1nstd199human GRCh37 chr18: 43,572,294-43,572,431 , GRCh38.p12 chr18: 45,992,328-45,992,465 PSTPIP2
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