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Items: 1 to 20 of 187

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5920134copy number variation1nstd209human GRCh38 chr11: 67,992,621-67,992,812 , GRCh37.p13 chr11: 67,760,092-67,760,283 UNC93B1
    nsv5659293insertion1nstd207human GRCh38 chr11: 67,989,353-67,989,353 , GRCh37.p13 chr11: 67,756,824-67,756,824 UNC93B1
    nsv5645814insertion1nstd207human GRCh38 chr11: 68,003,507-68,003,507 , GRCh37.p13 chr11: 67,770,977-67,770,977 UNC93B1
    nsv5503817copy number variation1nstd206human GRCh38 chr11: 68,000,412-68,000,942 , GRCh37.p13 chr11: 67,767,882-67,768,412 UNC93B1
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5325535translocation1nstd204human GRCh37.p13 chr11: 67,766,509-67,766,509 , GRCh37.p13 chr4: 152,365,189-152,365,189 , GRCh38.p13 chr11: 67,999,039-67,999,039 , GRCh38.p13 chr4: 151,444,037-151,444,037 UNC93B1, FHIP1A
    nsv4985096copy number variation1nstd200human GRCh38 chr11: 67,713,718-67,993,805 , GRCh37.p13 chr11: 67,481,189-67,761,276 , RPS3AP40, 15 more genes
    nsv4985094copy number variation1nstd200human GRCh38 chr11: 67,577,565-67,989,543 , GRCh37.p13 chr11: 67,345,036-67,757,014 , RNU6-46P, 24 more genes
    nsv4847858copy number variation1nstd200human GRCh37 chr11: 67,345,007-67,757,088 , GRCh38.p12 chr11: 67,577,536-67,989,617 , LOC105369359, 24 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4715317copy number variation1nstd195human GRCh37 chr11: 67,743,201-68,242,601 , GRCh38.p12 chr11: 67,975,730-68,475,133 ALDH3B1, LRP5, 13 more genes
    nsv4675137copy number variation1nstd102humanUncertain significance GRCh37 chr11: 66,820,585-67,979,510 , GRCh38.p12 chr11: 67,053,114-68,212,043 PPP1CA, RPS3AP40, 58 more genes
    nsv4614889copy number variation1nstd183human GRCh37 chr11: 67,727,839-67,781,569 , GRCh38.p12 chr11: 67,960,368-68,014,099 ALDH3B1, UNC93B1, 1 more genes
    nsv4607860copy number variation2nstd183human GRCh37 chr11: 67,358,348-67,762,604 , GRCh38.p12 chr11: 67,590,877-67,995,133 , OR7E145P, 23 more genes
    nsv4605831copy number variation1nstd183human GRCh37 chr11: 67,771,113-67,771,465 , GRCh38.p12 chr11: 68,003,643-68,003,995 UNC93B1
    nsv4451548copy number variation1nstd102humanUncertain significance GRCh37 chr11: 67,758,997-67,759,348 , GRCh38 chr11: 67,991,526-67,991,877 UNC93B1
    nsv4427714copy number variation1nstd174human GRCh37 chr11: 67,756,642-67,778,389 , GRCh38.p12 chr11: 67,989,171-68,010,919 ALDH3B1, UNC93B1
    nsv4426795copy number variation1nstd174human GRCh37 chr11: 67,474,434-67,757,489 , GRCh38.p12 chr11: 67,706,963-67,990,018 , OR7E145P, 15 more genes
    nsv4419282copy number variation1nstd174human GRCh37 chr11: 67,319,916-67,764,068 , GRCh38.p12 chr11: 67,552,445-67,996,597 , UNC93B1, 24 more genes
    nsv4414985copy number variation1nstd174human GRCh37 chr11: 67,747,160-67,821,610 , GRCh38.p12 chr11: 67,979,689-68,054,143 ALDH3B1, CHKA, 6 more genes
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