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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073350inversion1nstd229human GRCh38 chr11: 43,844,613-43,846,721 , GRCh37.p13 chr11: 43,866,163-43,868,271 HSD17B12
    nsv7062837inversion1nstd229human GRCh38 chr11: 40,841,838-44,720,409 , GRCh37.p13 chr11: 40,863,388-44,741,959 TTC17, ACCSL, 35 more genes
    nsv6915736copy number variation1nstd229human GRCh38 chr11: 43,829,572-43,837,502 , GRCh37.p13 chr11: 43,851,122-43,859,052 LOC107984328, HSD17B12
    nsv6914655copy number variation1nstd229human GRCh38 chr11: 43,748,801-43,761,100 , GRCh37.p13 chr11: 43,770,351-43,782,650 HSD17B12
    nsv6912720copy number variation1nstd229human GRCh38 chr11: 43,839,318-43,839,689 , GRCh37.p13 chr11: 43,860,868-43,861,239 HSD17B12
    nsv6910860copy number variation1nstd229human GRCh38 chr11: 43,792,722-43,793,498 , GRCh37.p13 chr11: 43,814,272-43,815,048 HSD17B12
    nsv6910482copy number variation1nstd229human GRCh38 chr11: 43,717,093-43,717,494 , GRCh37.p13 chr11: 43,738,643-43,739,044 HSD17B12, RPL23AP63
    nsv6909442copy number variation1nstd229human GRCh38 chr11: 43,720,549-43,727,772 , GRCh37.p13 chr11: 43,742,099-43,749,322 HSD17B12
    nsv6909074copy number variation1nstd229human GRCh38 chr11: 43,710,266-43,953,276 , GRCh37.p13 chr11: 43,731,816-43,974,826 ALKBH3, RPL23AP63, 7 more genes
    nsv6908871copy number variation1nstd229human GRCh38 chr11: 43,596,861-43,597,058 , GRCh37.p13 chr11: 43,618,411-43,618,608 HSD17B12
    nsv6908514copy number variation1nstd229human GRCh38 chr11: 43,808,363-43,810,980 , GRCh37.p13 chr11: 43,829,913-43,832,530 HSD17B12
    nsv6908210copy number variation1nstd229human GRCh38 chr11: 43,594,932-43,595,130 , GRCh37.p13 chr11: 43,616,482-43,616,680 HSD17B12
    nsv6906902copy number variation1nstd229human GRCh38 chr11: 43,738,127-43,738,153 , GRCh37.p13 chr11: 43,759,677-43,759,703 HSD17B12
    nsv6906821copy number variation1nstd229human GRCh38 chr11: 43,680,695-43,688,785 , GRCh37.p13 chr11: 43,702,245-43,710,335 HSD17B12
    nsv6906494copy number variation1nstd229human GRCh38 chr11: 43,608,301-43,615,200 , GRCh37.p13 chr11: 43,629,851-43,636,750 HSD17B12
    nsv6905520copy number variation1nstd229human GRCh38 chr11: 43,723,783-43,743,418 , GRCh37.p13 chr11: 43,745,333-43,764,968 HSD17B12, PHB1P2
    nsv6905171copy number variation1nstd229human GRCh38 chr11: 43,672,397-43,684,691 , GRCh37.p13 chr11: 43,693,947-43,706,241 HSD17B12
    nsv6904441copy number variation1nstd229human GRCh38 chr11: 43,810,509-43,812,981 , GRCh37.p13 chr11: 43,832,059-43,834,531 HSD17B12
    nsv6904433copy number variation1nstd229human GRCh38 chr11: 43,773,678-43,788,155 , GRCh37.p13 chr11: 43,795,228-43,809,705 HSD17B12
    nsv6904327copy number variation1nstd229human GRCh38 chr11: 43,754,009-43,754,327 , GRCh37.p13 chr11: 43,775,559-43,775,877 HSD17B12
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