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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093833copy number variation6nstd102humanUncertain significance GRCh37 chr11: 116,691,583-121,500,272 , GRCh38.p12 chr11: 116,820,867-121,629,563 RN7SL688P, MIR4492, 131 more genes
    nsv7093757copy number variation1nstd102humanUncertain significance GRCh37 chr11: 119,103,138-121,060,609 , GRCh38.p12 chr11: 119,232,428-121,189,900 USP2-AS1, LOC101929208, 41 more genes
    nsv7093753copy number variation1nstd102humanUncertain significance GRCh37 chr11: 117,209,303-120,133,495 , GRCh38.p12 chr11: 117,338,587-120,262,786 TMEM25, HYOU1, 93 more genes
    nsv7074550inversion1nstd229human GRCh38 chr11: 118,332,309-119,477,352 , GRCh37.p13 chr11: 118,203,024-119,348,063 VPS11, LOC100131626, 55 more genes
    nsv7069378inversion1nstd229human GRCh38 chr11: 119,487,613-119,498,962 , GRCh37.p13 chr11: 119,358,325-119,369,673 USP2-AS1
    nsv7064559inversion1nstd229human GRCh38 chr11: 119,404,450-119,404,565 , GRCh37.p13 chr11: 119,275,160-119,275,275 USP2-AS1, LOC100130353
    nsv7062420inversion1nstd229human GRCh38 chr11: 117,681,463-119,526,734 , GRCh37.p13 chr11: 117,552,178-119,397,444 RN7SL688P, MIR4492, 72 more genes
    nsv6917722copy number variation1nstd229human GRCh38 chr11: 119,478,051-119,495,181 , GRCh37.p13 chr11: 119,348,762-119,365,892 USP2-AS1
    nsv6915386copy number variation1nstd229human GRCh38 chr11: 119,422,686-119,503,648 , GRCh37.p13 chr11: 119,293,396-119,374,359 USP2-AS1, DUXAP5, 1 more genes
    nsv6914602copy number variation1nstd229human GRCh38 chr11: 119,292,683-119,545,665 , GRCh37.p13 chr11: 119,163,393-119,416,375 MIR6756, RNF26, 9 more genes
    nsv6914551copy number variation1nstd229human GRCh38 chr11: 119,438,793-119,439,568 , GRCh37.p13 chr11: 119,309,503-119,310,278 USP2-AS1
    nsv6913547copy number variation1nstd229human GRCh38 chr11: 119,449,380-119,451,581 , GRCh37.p13 chr11: 119,320,090-119,322,291 USP2-AS1
    nsv6913193copy number variation1nstd229human GRCh38 chr11: 119,442,880-119,443,166 , GRCh37.p13 chr11: 119,313,590-119,313,876 DUXAP5, USP2-AS1
    nsv6912765copy number variation1nstd229human GRCh38 chr11: 119,476,303-119,479,536 , GRCh37.p13 chr11: 119,347,014-119,350,247 USP2-AS1
    nsv6909633copy number variation1nstd229human GRCh38 chr11: 119,438,827-119,439,644 , GRCh37.p13 chr11: 119,309,537-119,310,354 USP2-AS1
    nsv6909462copy number variation1nstd229human GRCh38 chr11: 119,493,509-119,493,735 , GRCh37.p13 chr11: 119,364,220-119,364,446 USP2-AS1
    nsv6909048copy number variation1nstd229human GRCh38 chr11: 119,462,908-119,466,616 , GRCh37.p13 chr11: 119,333,619-119,337,327 USP2-AS1
    nsv6907555copy number variation1nstd229human GRCh38 chr11: 119,474,401-119,477,300 , GRCh37.p13 chr11: 119,345,112-119,348,011 USP2-AS1
    nsv6905374copy number variation1nstd229human GRCh38 chr11: 119,473,553-119,474,047 , GRCh37.p13 chr11: 119,344,264-119,344,758 USP2-AS1
    nsv6904425copy number variation1nstd229human GRCh38 chr11: 119,392,920-119,393,775 , GRCh37.p13 chr11: 119,263,630-119,264,485 USP2-AS1
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