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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137129copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659 VSIG10L2, OR8B6P, 268 more genes
    nsv7077728inversion1nstd229human GRCh38 chr11: 124,239,803-134,089,458 , GRCh37.p13 chr11: 124,110,545-133,959,353 LOC283172, PPP1R10P1, 175 more genes
    nsv6915552copy number variation1nstd229human GRCh38 chr11: 129,850,264-129,862,166 , GRCh37.p13 chr11: 129,720,159-129,732,061 TMEM45B, NFRKB
    nsv6911170copy number variation1nstd229human GRCh38 chr11: 129,824,069-129,833,662 , GRCh37.p13 chr11: 129,693,964-129,703,557 TMEM45B
    nsv6909457copy number variation1nstd229human GRCh38 chr11: 129,805,801-129,814,700 , GRCh37.p13 chr11: 129,675,696-129,684,595 TMEM45B
    nsv6901513copy number variation1nstd229human GRCh38 chr11: 129,838,004-129,842,224 , GRCh37.p13 chr11: 129,707,899-129,712,119 TMEM45B
    nsv6898516copy number variation1nstd229human GRCh38 chr11: 129,835,330-129,885,593 , GRCh37.p13 chr11: 129,705,225-129,755,488 NFRKB, TMEM45B
    nsv6637558copy number variation1nstd102humanPathogenic GRCh37 chr11: 122,975,824-134,938,470 , GRCh38.p12 chr11: 123,105,116-135,068,576 OR8B8, LOC107984373, 234 more genes
    nsv6634467copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 127,074,235-135,006,516 , GRCh38.p12 chr11: 127,204,340-135,076,622 APLP2, BAK1P2, 98 more genes
    nsv6620700copy number variation1nstd224human GRCh37 chr11: 129,719,900-129,743,891 , GRCh38.p12 chr11: 129,850,005-129,873,996 TMEM45B, NFRKB
    nsv6474031copy number variation1nstd223human GRCh38 chr11: 129,850,264-129,862,163 , GRCh37.p13 chr11: 129,720,159-129,732,058 TMEM45B, NFRKB
    nsv6469966copy number variation1nstd223human GRCh38 chr11: 129,832,027-129,832,331 , GRCh37.p13 chr11: 129,701,922-129,702,226 TMEM45B
    nsv6469735copy number variation1nstd223human GRCh38 chr11: 129,838,895-129,839,433 , GRCh37.p13 chr11: 129,708,790-129,709,328 TMEM45B
    nsv6468233copy number variation1nstd223human GRCh38 chr11: 129,826,101-129,828,100 , GRCh37.p13 chr11: 129,695,996-129,697,995 TMEM45B
    nsv6467892copy number variation1nstd223human GRCh38 chr11: 129,813,952-129,816,355 , GRCh37.p13 chr11: 129,683,847-129,686,250 TMEM45B
    nsv6465425copy number variation1nstd223human GRCh38 chr11: 129,841,111-129,841,449 , GRCh37.p13 chr11: 129,711,006-129,711,344 TMEM45B
    nsv6465419copy number variation1nstd223human GRCh38 chr11: 129,819,762-129,823,040 , GRCh37.p13 chr11: 129,689,657-129,692,935 TMEM45B
    nsv6465129copy number variation1nstd223human GRCh38 chr11: 129,745,609-129,826,276 , GRCh37.p13 chr11: 129,615,504-129,696,171 TMEM45B
    nsv6463799copy number variation1nstd223human GRCh38 chr11: 129,816,577-129,817,200 , GRCh37.p13 chr11: 129,686,472-129,687,095 TMEM45B
    nsv6460707copy number variation1nstd223human GRCh38 chr11: 129,846,435-129,848,189 , GRCh37.p13 chr11: 129,716,330-129,718,084 TMEM45B
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