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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095440copy number variation1nstd102humanUncertain significance GRCh37 chr18: 28,647,981-29,648,347 , GRCh38.p12 chr18: 31,068,015-32,068,384 RNU6-167P, LOC390846, 22 more genes
    nsv7093594insertion1nstd102humanUncertain significance GRCh37 chr18: 28,911,832-28,911,832 , GRCh38 chr18: 31,331,869-31,331,869 DSG1
    nsv7074645inversion1nstd229human GRCh38 chr18: 30,537,670-35,063,371 , GRCh37.p13 chr18: 28,117,636-32,643,335 DSC1, RN7SKP44, 46 more genes
    nsv7071421inversion1nstd229human GRCh38 chr18: 31,321,802-32,119,916 , GRCh37.p13 chr18: 28,901,765-29,699,879 TTR, B4GALT6, 20 more genes
    nsv7016199copy number variation1nstd229human GRCh38 chr18: 31,347,868-31,347,897 , GRCh37.p13 chr18: 28,927,831-28,927,860 DSG1, DSG1-AS1
    nsv7013747copy number variation1nstd229human GRCh38 chr18: 31,340,025-31,343,449 , GRCh37.p13 chr18: 28,919,988-28,923,412 DSG1-AS1, RNU6-167P, 1 more genes
    nsv7010105copy number variation1nstd229human GRCh38 chr18: 31,357,036-31,366,145 , GRCh37.p13 chr18: 28,936,999-28,946,108 DSG1-AS1, DSG1
    nsv7008677copy number variation1nstd229human GRCh38 chr18: 31,346,198-31,354,292 , GRCh37.p13 chr18: 28,926,161-28,934,255 DSG1, DSG1-AS1
    nsv7006873copy number variation1nstd229human GRCh38 chr18: 31,259,201-31,318,300 , GRCh37.p13 chr18: 28,839,164-28,898,263 DSG1, LOC105372049
    nsv7006529copy number variation1nstd229human GRCh38 chr18: 31,329,943-31,336,664 , GRCh37.p13 chr18: 28,909,906-28,916,627 DSG1
    nsv7003218copy number variation1nstd229human GRCh38 chr18: 31,282,960-31,322,566 , GRCh37.p13 chr18: 28,862,923-28,902,529 DSG1
    nsv7003055copy number variation1nstd229human GRCh38 chr18: 31,336,616-31,338,312 , GRCh37.p13 chr18: 28,916,579-28,918,275 DSG1
    nsv6624582copy number variation1nstd224human GRCh37 chr18: 28,597,270-29,027,889 , GRCh38.p12 chr18: 31,017,304-31,447,926 DSC1, DSG4, 8 more genes
    nsv6531603copy number variation1nstd223human GRCh38 chr18: 31,330,601-31,332,200 , GRCh37.p13 chr18: 28,910,564-28,912,163 DSG1
    nsv6529876copy number variation1nstd223human GRCh38 chr18: 31,318,501-31,320,100 , GRCh37.p13 chr18: 28,898,464-28,900,063 DSG1
    nsv6523521copy number variation1nstd223human GRCh38 chr18: 31,320,593-31,321,026 , GRCh37.p13 chr18: 28,900,556-28,900,989 DSG1
    nsv6518228copy number variation1nstd223human GRCh38 chr18: 31,356,932-31,358,615 , GRCh37.p13 chr18: 28,936,895-28,938,578 DSG1, DSG1-AS1
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 more genes
    nsv6310419copy number variation1nstd102humanUncertain significance GRCh37 chr18: 28,934,703-28,936,484 , GRCh38.p12 chr18: 31,354,740-31,356,521 DSG1, DSG1-AS1
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