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Items: 1 to 20 of 21

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 OR10AG1, FAUP4, 2031 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 OR10AG1, LOC105376598, 2842 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 OR10AG1, RTN3, 2833 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 OR10AG1, IGHMBP2, 2829 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 OR10AG1, PYGM, 2125 more genes
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 OR10AG1, TRR-TCT3-2, 494 more genes
    nsv3911150copy number variation1nstd102humanPathogenic GRCh37 chr11: 55,086,995-58,766,250 , NCBI36 chr11: 54,843,571-58,522,826 , GRCh38 chr11: 55,319,519-58,998,777 OR10AG1, OR5BD1P, 197 more genes
    nsv3907587copy number variation1nstd102humanBenign GRCh37 chr11: 55,685,767-55,823,576 , GRCh38.p12 chr11: 55,918,291-56,056,100 OR10AG1, OR5I1, 7 more genes
    nsv3914768copy number variation1nstd102humanBenign NCBI36 chr11: 55,460,312-55,572,888 , GRCh37 chr11: 55,703,736-55,816,312 , GRCh38 chr11: 55,936,260-56,048,836 OR10AG1, OR5I1, 6 more genes
    nsv3924455copy number variation1nstd102humanBenign GRCh38 chr11: 55,445,689-57,114,783 , GRCh37 chr11: 55,213,165-56,882,257 , NCBI36 chr11: 54,969,741-56,638,833 OR10AG1, OR5AL1, 111 more genes
    nsv3896950copy number variation1nstd102humanBenign GRCh37 chr11: 54,697,347-56,021,284 , GRCh38.p12 chr11: 54,929,872-56,253,808 OR10AG1, OR5L1, 66 more genes
    nsv3902541copy number variation1nstd102humanBenign GRCh37 chr11: 54,794,237-56,003,589 , GRCh38.p12 chr11: 55,026,761-56,236,113 OR10AG1, OR5J1P, 65 more genes
    nsv3920198copy number variation1nstd102humanLikely benign NCBI36 chr11: 54,807,338-55,776,171 , GRCh37.p13 chr11: 55,050,762-56,019,595 , GRCh38.p12 chr11: 55,283,286-56,252,119 OR10AG1, OR5F2P, 65 more genes
    nsv3910165copy number variation1nstd102humanBenign GRCh37 chr11: 55,033,261-55,997,702 , GRCh38 chr11: 55,265,785-56,230,226 , NCBI36 chr11: 54,789,837-55,754,278 OR10AG1, OR5D18, 65 more genes
    nsv3902131copy number variation1nstd102humanBenign GRCh37 chr11: 55,029,738-55,980,347 , GRCh38.p12 chr11: 55,262,262-56,212,871 OR10AG1, OR8I2, 64 more genes
    nsv3895805copy number variation1nstd102humanBenign GRCh37 chr11: 55,033,164-55,980,347 , GRCh38.p12 chr11: 55,265,688-56,212,871 OR10AG1, OR5D2P, 64 more genes
    nsv3916926copy number variation2nstd102humanBenign GRCh37 chr11: 55,086,995-55,980,406 , GRCh38 chr11: 55,319,519-56,212,930 , NCBI36 chr11: 54,843,571-55,736,982 OR10AG1, OR4A15, 61 more genes
    nsv3904152copy number variation1nstd102humanUncertain significance GRCh37 chr11: 49,313,405-59,008,426 , GRCh38.p12 chr11: 49,291,853-59,240,953 OR10AG1, FAM111B, 250 more genes
    nsv4453292copy number variation1nstd102humannot provided GRCh37 chr11: 55,033,164-57,518,726 , GRCh38.p12 chr11: 55,265,688-57,751,254 OR10AG1, OR8J3, 150 more genes
    nsv3924646copy number variation1nstd102humanUncertain significance GRCh38 chr11: 55,316,535-57,539,457 , GRCh37 chr11: 55,084,011-57,306,930 , NCBI36 chr11: 54,840,587-57,063,506 OR10AG1, OR5AL1, 134 more genes
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