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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7137196copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072 ECM1P2, LOC105378240, 482 more genes
    nsv7057432inversion1nstd229human GRCh38 chr4: 4,018,387-9,499,063 , GRCh37.p13 chr4: 4,020,114-9,500,707 CPZ, OR7E85P, 127 more genes
    nsv7056696inversion1nstd229human GRCh38 chr4: 8,196,981-8,298,603 , GRCh37.p13 chr4: 8,198,708-8,300,330 SH3TC1, HTRA3, 1 more genes
    nsv7056110inversion1nstd229human GRCh38 chr4: 3,991,106-9,653,685 , GRCh37.p13 chr4: 3,992,833-9,655,309 MAN2B2, SH3TC1, 134 more genes
    nsv7050522inversion1nstd229human GRCh38 chr4: 4,174,346-12,367,773 , GRCh37.p13 chr4: 4,176,073-12,369,397 USP17L29, MIR4274, 165 more genes
    nsv7044696inversion1nstd229human GRCh38 chr4: 3,996,444-9,648,382 , GRCh37.p13 chr4: 3,998,171-9,650,006 EVC, USP17L18, 134 more genes
    nsv7039148inversion1nstd229human GRCh38 chr4: 4,150,240-8,956,846 , GRCh37.p13 chr4: 4,151,967-8,958,572 PPP2R2C, CRMP1, 80 more genes
    nsv7038223inversion1nstd229human GRCh38 chr4: 3,989,150-9,655,696 , GRCh37.p13 chr4: 3,990,877-9,657,320 RNA5SP152, MRFAP1, 134 more genes
    nsv6735189copy number variation1nstd229human GRCh38 chr4: 8,071,057-8,326,595 , GRCh37.p13 chr4: 8,072,784-8,328,322 LINC02517, SH3TC1, 4 more genes
    nsv6733418copy number variation1nstd229human GRCh38 chr4: 8,304,727-8,567,777 , GRCh37.p13 chr4: 8,306,454-8,569,504 ACOX3, LINC02517, 3 more genes
    nsv6732918copy number variation1nstd229human GRCh38 chr4: 8,222,989-8,431,105 , GRCh37.p13 chr4: 8,224,716-8,432,832 ACOX3, LINC02517, 4 more genes
    nsv6732615copy number variation1nstd229human GRCh38 chr4: 8,207,172-8,362,424 , GRCh37.p13 chr4: 8,208,899-8,364,151 LINC02517, SH3TC1, 2 more genes
    nsv6731907copy number variation1nstd229human GRCh38 chr4: 8,243,841-8,277,077 , GRCh37.p13 chr4: 8,245,568-8,278,804 HTRA3, LOC105374373
    nsv6731202copy number variation1nstd229human GRCh38 chr4: 8,275,971-8,276,065 , GRCh37.p13 chr4: 8,277,698-8,277,792 HTRA3
    nsv6730490copy number variation1nstd229human GRCh38 chr4: 8,273,699-8,276,263 , GRCh37.p13 chr4: 8,275,426-8,277,990 HTRA3
    nsv6726867copy number variation1nstd229human GRCh38 chr4: 8,215,957-8,443,600 , GRCh37.p13 chr4: 8,217,684-8,445,327 ACOX3, SH3TC1, 5 more genes
    nsv6724798copy number variation1nstd229human GRCh38 chr4: 8,267,712-8,267,767 , GRCh37.p13 chr4: 8,269,439-8,269,494 LOC105374373, HTRA3
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