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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7051444inversion1nstd229human GRCh38 chr4: 70,947,675-74,191,821 , GRCh37.p13 chr4: 71,813,392-75,057,538 , COX18, 44 more genes
    nsv7045939inversion1nstd229human GRCh38 chr4: 69,867,306-75,844,103 , GRCh37.p13 chr4: 70,733,024-76,765,256 , PF4V1, 99 more genes
    nsv7040415inversion1nstd229human GRCh38 chr4: 72,183,424-80,893,316 , GRCh37.p13 chr4: 73,049,141-81,814,470 , KPNA2P1, 148 more genes
    nsv6756948copy number variation1nstd229human GRCh38 chr4: 73,051,181-73,053,084 , GRCh37.p13 chr4: 73,916,898-73,918,801 COX18
    nsv6749244copy number variation1nstd229human GRCh38 chr4: 71,830,854-79,510,197 , GRCh37.p13 chr4: 72,696,571-80,431,351 , COX18, 134 more genes
    nsv6747862copy number variation1nstd229human GRCh38 chr4: 72,931,936-73,155,410 , GRCh37.p13 chr4: 73,797,653-74,021,127 LOC105377273, COX18, 6 more genes
    nsv6746769copy number variation1nstd229human GRCh38 chr4: 69,087,431-73,565,096 , GRCh37.p13 chr4: 69,953,149-74,430,813 LOC642496, CSN2, 76 more genes
    nsv6740221copy number variation1nstd229human GRCh38 chr4: 71,124,425-74,382,728 , GRCh37.p13 chr4: 71,990,142-75,248,445 , ALB, 45 more genes
    nsv6738402copy number variation1nstd229human GRCh38 chr4: 72,878,792-73,201,573 , GRCh37.p13 chr4: 73,744,509-74,067,290 HMGA1P2, RNU6ATAC5P, 6 more genes
    nsv6636298copy number variation1nstd102humanUncertain significance GRCh37 chr4: 73,813,059-74,048,878 , GRCh38.p12 chr4: 72,947,342-73,183,161 LOC107986286, LOC112268467, 6 more genes
    nsv6635476copy number variation1nstd227human GRCh38.p12 chr4: 72,857,260-73,192,689 , GRCh37 chr4: 73,722,977-74,058,406 ANKRD17, HMGA1P2, 6 more genes
    nsv6571895inversion1nstd223human GRCh38 chr4: 73,049,899-73,050,992 , GRCh37.p13 chr4: 73,915,616-73,916,709 COX18
    nsv6560704inversion1nstd223human GRCh38 chr4: 73,057,371-73,057,959 , GRCh37.p13 chr4: 73,923,088-73,923,676 COX18
    nsv6557569inversion1nstd223human GRCh38 chr4: 70,947,674-74,191,820 , GRCh37.p13 chr4: 71,813,391-75,057,537 , HNRNPA1P67, 44 more genes
    nsv6394983copy number variation1nstd223human GRCh38 chr4: 73,066,005-73,067,482 , GRCh37.p13 chr4: 73,931,722-73,933,199 COX18
    nsv6393792copy number variation1nstd223human GRCh38 chr4: 73,051,175-73,053,083 , GRCh37.p13 chr4: 73,916,892-73,918,800 COX18
    nsv6377029copy number variation1nstd223human GRCh38 chr4: 72,948,827-73,184,927 , GRCh37.p13 chr4: 73,814,544-74,050,644 ANKRD17, RNU6ATAC5P, 6 more genes
    nsv6315175copy number variation1nstd102humanUncertain significance GRCh37 chr4: 73,694,233-73,984,429 , GRCh38.p12 chr4: 72,828,516-73,118,712 LOC107986286, LOC105377273, 6 more genes
    nsv6314916copy number variation1nstd102humanPathogenic GRCh38 chr4: 67,833,055-82,716,065 , GRCh37.p13 chr4: 68,698,773-83,637,218 MICOS10P4, SULT1B1, 274 more genes
    nsv6313740copy number variation1nstd102humanPathogenic GRCh37 chr4: 61,867,555-74,711,517 , GRCh38.p12 chr4: 61,001,837-73,845,800 CXCL8, UGT2A1, 175 more genes
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