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Items: 1 to 20 of 390

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137204copy number variation1nstd102humanPathogenic GRCh37 chr11: 268,586-748,873 , GRCh38.p12 chr11: 268,586-748,873 PKP3, RN7SL838P, 32 more genes
    nsv7137059copy number variation1nstd102humanLikely benign GRCh37 chr11: 530,419-530,474 , GRCh38 chr11: 530,419-530,474 HRAS, LRRC56
    nsv7094089copy number variation2nstd102humanUncertain significance GRCh37 chr11: 532,636-554,276 , GRCh38.p12 chr11: 532,636-554,276 , GRCh38.p12 chr11|NT_187586.1: 62,277-83,916 LRRC56, LMNTD2, 1 more genes
    nsv7093693copy number variation1nstd102humanUncertain significance GRCh37 chr11: 532,636-819,925 , GRCh38.p12 chr11: 532,636-819,925 , GRCh38.p12 chr11|NT_187586.1: 62,277-209,248 HRAS, LRRC56, 25 more genes
    nsv7093222copy number variation1nstd102humanUncertain significance GRCh38 chr11: 533,463-533,464 , GRCh37 chr11: 533,463-533,464 HRAS, LRRC56
    nsv7073154inversion1nstd229human GRCh38 chr11: 516,385-567,173 , GRCh37.p13 chr11: 516,385-567,173 LRRC56, LMNTD2, 5 more genes
    nsv7068392inversion1nstd229human GRCh38 chr11: 260,223-620,051 , GRCh37.p13 chr11: 260,223-620,051 MIR210, LMNTD2-AS1, 25 more genes
    nsv7068164inversion1nstd229human GRCh38 chr11: 525,138-982,890 , GRCh37.p13 chr11: 525,138-982,890 DRD4, LMNTD2-AS1, 32 more genes
    nsv7067944inversion1nstd229human GRCh38 chr11: 288,558-695,861 , GRCh37.p13 chr11: 288,558-695,861 IRF7, TMEM80, 28 more genes
    nsv7058883inversion1nstd229human GRCh38 chr11: 499,565-690,606 , GRCh37.p13 chr11: 499,565-690,606 LOC143666, DEAF1, 13 more genes
    nsv6897071copy number variation1nstd229human GRCh38 chr11: 490,701-585,700 , GRCh37.p13 chr11: 490,701-585,700 MIR210HG, PTDSS2, 9 more genes
    nsv6892374copy number variation1nstd229human GRCh38 chr11: 528,601-530,500 , GRCh37.p13 chr11: 528,601-530,500 HRAS, LRRC56
    nsv6885572copy number variation1nstd229human GRCh38 chr11: 517,256-561,379 , GRCh37.p13 chr11: 517,256-561,379 RASSF7, HRAS, 3 more genes
    nsv6881074copy number variation1nstd229human GRCh38 chr11: 531,701-535,000 , GRCh37.p13 chr11: 531,701-535,000 LRRC56, HRAS
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6637212copy number variation1nstd102humanPathogenic GRCh37 chr11: 461,373-2,157,956 , GRCh38.p12 chr11: 461,373-2,136,726 MIR6744, PTDSS2, 80 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
    nsv6620740copy number variation1nstd224human GRCh37 chr11: 339,943-533,357 , GRCh38.p12 chr11: 339,943-533,357 PKP3, PTDSS2, 8 more genes
    nsv6591624inversion1nstd223human GRCh38 chr11: 428,014-744,559 , GRCh37.p13 chr11: 428,014-744,559 MIR210HG, EPS8L2, 20 more genes
    nsv6588565inversion1nstd223human GRCh38 chr11: 427,925-744,841 , GRCh37.p13 chr11: 427,925-744,841 LOC143666, DEAF1, 20 more genes
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