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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
    nsv7098818copy number variation1nstd102humanPathogenic GRCh38 chr4: 11,399,082-38,137,335 , GRCh37.p13 chr4: 11,400,706-38,138,956 LOC105374542, PPARGC1A, 232 more genes
    nsv7096981copy number variation1nstd102humanUncertain significance GRCh37 chr4: 13,371,500-13,546,038 , GRCh38.p12 chr4: 13,369,876-13,544,414 LINC01097, LINC01096, 3 more genes
    nsv7039627inversion1nstd229human GRCh38 chr4: 13,469,530-13,469,562 , GRCh37.p13 chr4: 13,471,154-13,471,186 RAB28
    nsv6737904copy number variation1nstd229human GRCh38 chr4: 13,442,562-13,442,750 , GRCh37.p13 chr4: 13,444,186-13,444,374 RAB28
    nsv6737032copy number variation1nstd229human GRCh38 chr4: 13,406,037-13,464,549 , GRCh37.p13 chr4: 13,407,661-13,466,173 RAB28
    nsv6736874copy number variation1nstd229human GRCh38 chr4: 13,434,267-13,445,498 , GRCh37.p13 chr4: 13,435,891-13,447,122 RAB28
    nsv6735775copy number variation1nstd229human GRCh38 chr4: 13,452,571-13,455,240 , GRCh37.p13 chr4: 13,454,195-13,456,864 RAB28
    nsv6735469copy number variation1nstd229human GRCh38 chr4: 13,371,533-13,429,485 , GRCh37.p13 chr4: 13,373,157-13,431,109 RAB28
    nsv6734968copy number variation1nstd229human GRCh38 chr4: 13,389,719-13,394,917 , GRCh37.p13 chr4: 13,391,343-13,396,541 RAB28
    nsv6733420copy number variation1nstd229human GRCh38 chr4: 13,379,644-13,380,457 , GRCh37.p13 chr4: 13,381,268-13,382,081 RAB28
    nsv6733000copy number variation1nstd229human GRCh38 chr4: 13,466,501-13,637,500 , GRCh37.p13 chr4: 13,468,125-13,639,124 LINC01097, MIR5091, 6 more genes
    nsv6732415copy number variation1nstd229human GRCh38 chr4: 13,274,007-13,368,853 , GRCh37.p13 chr4: 13,275,631-13,370,477 HSP90AB2P, RAB28
    nsv6732009copy number variation1nstd229human GRCh38 chr4: 13,174,270-14,155,070 , GRCh37.p13 chr4: 13,175,894-14,156,694 LOC101929048, HSP90AB2P, 14 more genes
    nsv6731857copy number variation1nstd229human GRCh38 chr4: 13,341,201-13,599,300 , GRCh37.p13 chr4: 13,342,825-13,600,924 NKX3-2, LINC01097, 4 more genes
    nsv6730266copy number variation1nstd229human GRCh38 chr4: 11,584,151-13,998,677 , GRCh37.p13 chr4: 11,585,775-14,000,301 LINC02270, LINC02360, 24 more genes
    nsv6729448copy number variation1nstd229human GRCh38 chr4: 13,484,123-13,494,680 , GRCh37.p13 chr4: 13,485,747-13,496,304 LOC105374495, RAB28
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