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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142362insertion1nstd232human GRCh37.p13 chr7: 21,940,005-21,940,005 , GRCh38.p12 chr7: 21,900,387-21,900,387 DNAH11, CDCA7L
    nsv7139414insertion1nstd232human GRCh37.p13 chr7: 21,943,878-21,943,878 , GRCh38.p12 chr7: 21,904,260-21,904,260 CDCA7L
    nsv7097363copy number variation2nstd102humanPathogenic GRCh37 chr7: 20,994,491-23,030,730 , GRCh38.p12 chr7: 20,954,872-22,991,111 STEAP1B-AS1, RNA5SP227, 25 more genes
    nsv7041207inversion1nstd229human GRCh38 chr7: 20,746,775-22,016,045 , GRCh37.p13 chr7: 20,786,398-22,055,663 LINC01162, RPL23P8, 12 more genes
    nsv6817073copy number variation1nstd229human GRCh38 chr7: 21,673,343-22,031,507 , GRCh37.p13 chr7: 21,712,961-22,071,125 DNAH11, LOC107986775, 1 more genes
    nsv6812935copy number variation1nstd229human GRCh38 chr7: 21,914,063-21,914,170 , GRCh37.p13 chr7: 21,953,681-21,953,788 CDCA7L
    nsv6812458copy number variation1nstd229human GRCh38 chr7: 21,889,501-22,010,200 , GRCh37.p13 chr7: 21,929,119-22,049,818 CDCA7L, DNAH11
    nsv6812215copy number variation1nstd229human GRCh38 chr7: 21,944,501-21,946,200 , GRCh37.p13 chr7: 21,984,119-21,985,818 CDCA7L
    nsv6809339copy number variation1nstd229human GRCh38 chr7: 21,935,801-21,942,617 , GRCh37.p13 chr7: 21,975,419-21,982,235 CDCA7L
    nsv6805620copy number variation1nstd229human GRCh38 chr7: 21,846,275-21,900,185 , GRCh37.p13 chr7: 21,885,893-21,939,803 DNAH11, CDCA7L
    nsv6802032copy number variation1nstd229human GRCh38 chr7: 21,784,796-21,947,893 , GRCh37.p13 chr7: 21,824,414-21,987,511 LOC107986775, CDCA7L, 1 more genes
    nsv6801227copy number variation1nstd229human GRCh38 chr7: 21,902,622-21,902,747 , GRCh37.p13 chr7: 21,942,240-21,942,365 CDCA7L
    nsv6799733copy number variation1nstd229human GRCh38 chr7: 21,901,174-21,901,329 , GRCh37.p13 chr7: 21,940,792-21,940,947 CDCA7L, DNAH11
    nsv6636826copy number variation1nstd102humanUncertain significance GRCh37 chr7: 21,713,059-22,067,069 , GRCh38.p12 chr7: 21,673,441-22,027,451 LOC107986775, CDCA7L, 1 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
    nsv6607220copy number variation1nstd223human GRCh38 chr7: 21,872,965-21,944,333 , GRCh37.p13 chr7: 21,912,583-21,983,951 DNAH11, CDCA7L
    nsv6600983copy number variation1nstd223human GRCh38 chr7: 21,937,417-21,937,714 , GRCh37.p13 chr7: 21,977,035-21,977,332 CDCA7L
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313493copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 10,745,750-35,305,167 , GRCh38.p12 chr7: 10,706,123-35,265,556 ADCYAP1R1, AHR, 329 more genes
    nsv6312441copy number variation1nstd102humanUncertain significance GRCh37 chr7: 20,994,491-23,213,917 , GRCh38.p12 chr7: 20,954,872-23,174,298 IL6, LOC105375186, 30 more genes
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