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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
    nsv7096726copy number variation2nstd102humanUncertain significance GRCh37 chr4: 15,477,557-16,228,080 , GRCh38.p12 chr4: 15,475,933-16,226,457 LOC107986187, CC2D2A, 15 more genes
    nsv6737690copy number variation1nstd229human GRCh38 chr4: 15,744,352-15,744,462 , GRCh37.p13 chr4: 15,745,975-15,746,085 BST1
    nsv6736562copy number variation1nstd229human GRCh38 chr4: 15,689,301-15,792,400 , GRCh37.p13 chr4: 15,690,924-15,794,023 BST1, PFDN1P2, 4 more genes
    nsv6735635copy number variation1nstd229human GRCh38 chr4: 15,755,736-15,756,112 , GRCh37.p13 chr4: 15,757,359-15,757,735 BST1, LOC107986186
    nsv6733754copy number variation1nstd229human GRCh38 chr4: 15,758,763-15,767,209 , GRCh37.p13 chr4: 15,760,386-15,768,832 BST1
    nsv6733381copy number variation1nstd229human GRCh38 chr4: 15,701,601-15,710,100 , GRCh37.p13 chr4: 15,703,224-15,711,723 BST1
    nsv6730370copy number variation1nstd229human GRCh38 chr4: 15,757,701-15,767,100 , GRCh37.p13 chr4: 15,759,324-15,768,723 BST1
    nsv6727695copy number variation1nstd229human GRCh38 chr4: 15,708,235-15,709,135 , GRCh37.p13 chr4: 15,709,858-15,710,758 BST1
    nsv6726434copy number variation1nstd229human GRCh38 chr4: 15,689,201-16,173,800 , GRCh37.p13 chr4: 15,690,824-16,175,423 TAPT1, FAM200B, 11 more genes
    nsv6725829copy number variation1nstd229human GRCh38 chr4: 15,758,801-15,768,700 , GRCh37.p13 chr4: 15,760,424-15,770,323 BST1
    nsv6724116copy number variation1nstd229human GRCh38 chr4: 15,754,233-15,767,846 , GRCh37.p13 chr4: 15,755,856-15,769,469 BST1, LOC107986186
    nsv6723235copy number variation1nstd229human GRCh38 chr4: 15,756,801-15,767,200 , GRCh37.p13 chr4: 15,758,424-15,768,823 LOC107986186, BST1
    nsv6723056copy number variation1nstd229human GRCh38 chr4: 15,640,601-15,745,400 , GRCh37.p13 chr4: 15,642,224-15,747,023 FAM200B, RPL10AP7, 3 more genes
    nsv6720164copy number variation1nstd229human GRCh38 chr4: 15,737,593-15,737,810 , GRCh37.p13 chr4: 15,739,216-15,739,433 BST1
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
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