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Items: 1 to 20 of 511

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925253copy number variation1nstd209human GRCh38 chr11: 5,763,343-5,788,051 , GRCh37.p13 chr11: 5,784,573-5,809,281 OR52N1, OR56B2P, 1 more genes
    nsv5852399copy number variation1nstd209human GRCh38 chr11: 5,763,356-5,788,064 , GRCh37.p13 chr11: 5,784,586-5,809,294 OR56B2P, OR52N1, 1 more genes
    nsv5586681copy number variation1nstd207human GRCh38 chr11: 5,763,345-5,788,053 , GRCh37.p13 chr11: 5,784,575-5,809,283 OR52N1, OR56B2P, 1 more genes
    nsv5512677copy number variation1nstd206human GRCh38 chr11: 5,764,669-5,764,823 , GRCh37.p13 chr11: 5,785,899-5,786,053 OR56B2P
    nsv5508230copy number variation1nstd206human GRCh38 chr11: 5,763,345-5,788,052 , GRCh37.p13 chr11: 5,784,575-5,809,282 OR52N1, OR52N5, 1 more genes
    nsv5391240copy number variation2nstd186human GRCh37 chr11: 5,784,575-5,809,282 , GRCh38.p12 chr11: 5,763,345-5,788,052 OR52N1, OR56B2P, 1 more genes
    nsv5318964copy number variation1nstd204human GRCh37.p13 chr11: 5,784,575-5,809,282 , GRCh38.p13 chr11: 5,763,345-5,788,052 OR52N1, OR56B2P, 1 more genes
    nsv5258962copy number variation1nstd204human GRCh38.p13 chr11: 5,763,301-5,763,900 , GRCh37.p13 chr11: 5,784,531-5,785,130 OR56B2P
    nsv5256761copy number variation1nstd204human GRCh38.p13 chr11: 5,763,301-5,765,800 , GRCh37.p13 chr11: 5,784,531-5,787,030 OR56B2P
    nsv5256229copy number variation1nstd204human GRCh38.p13 chr11: 5,763,300-5,785,900 , GRCh37.p13 chr11: 5,784,530-5,807,130 OR52N5, OR52N1, 1 more genes
    nsv5251369copy number variation1nstd204human GRCh38.p13 chr11: 5,763,301-5,776,800 , GRCh37.p13 chr11: 5,784,531-5,798,030 OR52N5, OR56B2P
    nsv5250734copy number variation1nstd204human GRCh38.p13 chr11: 5,763,301-5,788,000 , GRCh37.p13 chr11: 5,784,531-5,809,230 OR52N1, OR52N5, 1 more genes
    nsv5244276copy number variation1nstd204human GRCh38.p13 chr11: 5,763,301-5,772,400 , GRCh37.p13 chr11: 5,784,531-5,793,630 OR56B2P
    nsv5242018copy number variation1nstd204human GRCh38.p13 chr11: 5,763,301-5,788,900 , GRCh37.p13 chr11: 5,784,531-5,810,130 OR56B2P, OR52N1, 1 more genes
    nsv4978022copy number variation1nstd200human GRCh38 chr11: 5,763,345-5,788,052 , GRCh37.p13 chr11: 5,784,575-5,809,282 OR56B2P, OR52N5, 1 more genes
    nsv4846990copy number variation1nstd200human GRCh37 chr11: 5,784,575-5,809,282 , GRCh38.p12 chr11: 5,763,345-5,788,052 OR56B2P, OR52N1, 1 more genes
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4745670copy number variation1nstd199human GRCh37 chr11: 5,784,575-5,809,283 , GRCh38.p12 chr11: 5,763,345-5,788,053 OR52N1, OR56B2P, 1 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
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