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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137096copy number variation1nstd102humanLikely benign GRCh37 chr11: 5,094,756-5,785,959 , GRCh38.p12 chr11: 5,073,526-5,764,729 OR51J1, OLFM5P, 52 more genes
    nsv7072693inversion1nstd229human GRCh38 chr11: 5,233,049-5,254,141 , GRCh37.p13 chr11: 5,254,279-5,275,371 HBD, HBG2, 3 more genes
    nsv7063495inversion1nstd229human GRCh38 chr11: 5,016,392-5,387,994 , GRCh37.p13 chr11: 5,037,622-5,409,224 OR51M1, OR52J2P, 29 more genes
    nsv7060711inversion1nstd229human GRCh38 chr11: 5,052,261-5,434,559 , GRCh37.p13 chr11: 5,073,491-5,455,789 HBD, OR52S1P, 29 more genes
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6902995copy number variation1nstd229human GRCh38 chr11: 4,619,101-5,268,938 , GRCh37.p13 chr11: 4,640,331-5,290,168 OR51A9P, OR51F1, 50 more genes
    nsv6900711copy number variation1nstd229human GRCh38 chr11: 5,249,401-5,254,200 , GRCh37.p13 chr11: 5,270,631-5,275,430 HBG1, HBG2
    nsv6899745copy number variation1nstd229human GRCh38 chr11: 5,212,723-5,253,494 , GRCh37.p13 chr11: 5,233,953-5,274,724 HBD, HBB, 4 more genes
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6634327copy number variation1nstd102humanPathogenic GRCh38 chr11: 499,700-5,279,697 , GRCh37.p13 chr11: 499,700-5,300,927 SNORA54, PIDD1, 219 more genes
    nsv6450577copy number variation1nstd223human GRCh38 chr11: 4,619,075-5,268,953 , GRCh37.p13 chr11: 4,640,305-5,290,183 OR52J1P, OR51F2, 50 more genes
    nsv6447227copy number variation1nstd223human GRCh38 chr11: 5,248,884-5,253,857 , GRCh37.p13 chr11: 5,270,114-5,275,087 HBG1, HBG2
    nsv6440498copy number variation1nstd223human GRCh38 chr11: 5,249,601-5,255,200 , GRCh37.p13 chr11: 5,270,831-5,276,430 HBG1, HBG2
    nsv6436512copy number variation1nstd223human GRCh38 chr11: 5,250,314-5,255,480 , GRCh37.p13 chr11: 5,271,544-5,276,710 HBG1, HBG2
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6291427copy number variation1nstd102humannot provided GRCh37 chr11: 230,615-5,525,355 , GRCh38.p12 chr11: 230,615-5,504,125 OR52J1P, IFITM1, 255 more genes
    nsv6132106copy number variation1nstd213human GRCh37 chr11: 4,510,000-5,300,001 , GRCh38.p12 chr11: 4,488,770-5,278,771 HBB, HBBP1, 57 more genes
    nsv6022781copy number variation1nstd212human GRCh38 chr11: 5,252,579-5,252,699 , GRCh37.p13 chr11: 5,273,809-5,273,929 HBG2
    nsv5919692copy number variation1nstd209human GRCh38 chr11: 5,248,961-5,253,943 , GRCh37.p13 chr11: 5,270,191-5,275,173 HBG1, HBG2
    nsv5849474copy number variation2nstd209human GRCh38 chr11: 5,249,309-5,253,941 , GRCh37.p13 chr11: 5,270,539-5,275,171 HBG2, HBG1
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