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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148243copy number variation1nstd102humanPathogenic GRCh38 chr7: 137,463,392-159,345,973 , GRCh37.p13 chr7: 137,148,138-159,128,663 MIR11400, TRBV24-1, 531 more genes
    nsv7148234copy number variation1nstd102humanLikely pathogenic GRCh38 chr7: 138,620,939-159,233,475 , GRCh37.p13 chr7: 138,305,684-159,026,165 AOC1, ALDH7A1P3, 515 more genes
    nsv7138872copy number variation1nstd232human GRCh37.p13 chr7: 139,800,460-139,800,511 , GRCh38.p12 chr7: 140,100,660-140,100,711 KDM7A
    nsv7097864copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,781,014-150,301,047 , GRCh38.p12 chr7: 131,096,255-150,603,959 NOBOX, FAM131B, 466 more genes
    nsv7097607copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr7: 138,391,369-141,759,786 , GRCh38.p12 chr7: 138,706,624-142,059,986 LOC105375535, AGK-DT, 82 more genes
    nsv6832675copy number variation1nstd229human GRCh38 chr7: 140,105,073-140,111,056 , GRCh37.p13 chr7: 139,804,873-139,810,856 KDM7A
    nsv6830776copy number variation1nstd229human GRCh38 chr7: 140,170,159-140,170,187 , GRCh37.p13 chr7: 139,869,959-139,869,987 KDM7A
    nsv6830712copy number variation1nstd229human GRCh38 chr7: 139,834,078-140,145,604 , GRCh37.p13 chr7: 139,533,877-139,845,404 PARP12, LOC105375532, 3 more genes
    nsv6829978copy number variation1nstd229human GRCh38 chr7: 140,016,565-141,119,379 , GRCh37.p13 chr7: 139,716,365-140,819,179 KDM7A, LOC107986854, 29 more genes
    nsv6827353copy number variation1nstd229human GRCh38 chr7: 140,175,743-140,176,621 , GRCh37.p13 chr7: 139,875,543-139,876,421 KDM7A, KDM7A-DT
    nsv6826652copy number variation1nstd229human GRCh38 chr7: 140,173,601-140,177,900 , GRCh37.p13 chr7: 139,873,401-139,877,700 KDM7A, KDM7A-DT
    nsv6636458copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,779,213-149,042,734 , GRCh38.p12 chr7: 132,094,454-149,345,643 TRBD2, TRBV5-2, 403 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6572222inversion1nstd223human GRCh38 chr7: 140,161,540-140,162,339 , GRCh37.p13 chr7: 139,861,340-139,862,139 KDM7A
    nsv6559350inversion1nstd223human GRCh38 chr7: 140,094,614-140,095,260 , GRCh37.p13 chr7: 139,794,414-139,795,060 KDM7A
    nsv6559285inversion1nstd223human GRCh38 chr7: 140,152,624-140,152,936 , GRCh37.p13 chr7: 139,852,424-139,852,736 KDM7A
    nsv6434271copy number variation1nstd223human GRCh38 chr7: 140,172,418-140,173,891 , GRCh37.p13 chr7: 139,872,218-139,873,691 KDM7A
    nsv6429334copy number variation1nstd223human GRCh38 chr7: 140,016,565-141,119,379 , GRCh37.p13 chr7: 139,716,365-140,819,179 LOC105375534, PPP1R2P6, 29 more genes
    nsv6424942copy number variation1nstd223human GRCh38 chr7: 140,175,601-140,180,600 , GRCh37.p13 chr7: 139,875,401-139,880,400 KDM7A-DT, KDM7A
    nsv6424453copy number variation1nstd223human GRCh38 chr7: 140,110,801-140,117,100 , GRCh37.p13 chr7: 139,810,601-139,816,900 KDM7A
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