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Items: 1 to 20 of 321

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095014copy number variation1nstd102humanUncertain significance GRCh37 chr18: 47,101,719-47,463,787 , GRCh38.p12 chr18: 49,575,349-49,937,417 SMUG1P1, SNHG22, 6 more genes
    nsv7095013copy number variation1nstd102humanUncertain significance GRCh37 chr18: 47,088,679-47,095,938 , GRCh38.p12 chr18: 49,562,309-49,569,568 LIPG
    nsv7094936copy number variation1nstd102humanUncertain significance GRCh37 chr18: 47,101,719-47,116,892 , GRCh38.p12 chr18: 49,575,349-49,590,522 LIPG
    nsv7076498inversion1nstd229human GRCh38 chr18: 49,503,668-49,593,684 , GRCh37.p13 chr18: 47,030,038-47,120,054 LINC02837, LIPG
    nsv7074210inversion1nstd229human GRCh38 chr18: 45,861,287-52,164,943 , GRCh37.p13 chr18: 43,441,252-49,691,313 LOC105372100, RNA5SP458, 103 more genes
    nsv7064950inversion1nstd229human GRCh38 chr18: 49,426,149-50,066,271 , GRCh37.p13 chr18: 46,952,519-47,592,641 SRP72P1, C18orf32, 19 more genes
    nsv7062073inversion1nstd229human GRCh38 chr18: 42,140,183-50,368,023 , GRCh37.p13 chr18: 39,720,147-47,894,393 ACAA2, MIR4320, 105 more genes
    nsv7058348inversion1nstd229human GRCh38 chr18: 49,550,777-51,013,398 , GRCh37.p13 chr18: 47,077,147-48,539,768 SMUG1P1, CXXC1, 26 more genes
    nsv7015620copy number variation1nstd229human GRCh38 chr18: 48,566,814-53,963,212 , GRCh37.p13 chr18: 46,093,185-51,489,582 LINC02837, RPL29P32, 65 more genes
    nsv7014340copy number variation1nstd229human GRCh38 chr18: 49,565,421-49,567,802 , GRCh37.p13 chr18: 47,091,791-47,094,172 LIPG
    nsv7008134copy number variation1nstd229human GRCh38 chr18: 49,337,146-49,662,979 , GRCh37.p13 chr18: 46,863,516-47,189,349 LIPG, RPL17, 13 more genes
    nsv7006306copy number variation1nstd229human GRCh38 chr18: 49,567,981-49,568,007 , GRCh37.p13 chr18: 47,094,351-47,094,377 LIPG
    nsv6998936copy number variation1nstd229human GRCh38 chr18: 49,574,421-49,939,057 , GRCh37.p13 chr18: 47,100,791-47,465,427 LIPG, LOC105372112, 6 more genes
    nsv6998773copy number variation1nstd229human GRCh38 chr18: 44,716,377-50,773,277 , GRCh37.p13 chr18: 42,296,342-48,299,647 LOC105372101, MTCO2P2, 95 more genes
    nsv6595020inversion1nstd223human GRCh38 chr18: 49,148,101-52,144,680 , GRCh37.p13 chr18: 46,674,471-49,671,050 MYO5B, LIPG, 49 more genes
    nsv6587158inversion1nstd223human GRCh38 chr18: 49,587,318-49,587,976 , GRCh37.p13 chr18: 47,113,688-47,114,346 LIPG
    nsv6530909copy number variation1nstd223human GRCh38 chr18: 49,574,421-49,939,057 , GRCh37.p13 chr18: 47,100,791-47,465,427 SNHG22, LOC105372112, 6 more genes
    nsv6519730copy number variation1nstd223human GRCh38 chr18: 49,570,705-49,572,150 , GRCh37.p13 chr18: 47,097,075-47,098,520 LIPG
    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
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