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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5922393copy number variation1nstd209human GRCh38 chr11: 5,602,377-5,602,881 , GRCh37.p13 chr11: 5,623,607-5,624,111 TRIM5, TRIM6, 1 more genes
    nsv5585221copy number variation1nstd207human GRCh38 chr11: 5,602,357-5,602,867 , GRCh37.p13 chr11: 5,623,587-5,624,097 TRIM5, TRIM6, 1 more genes
    nsv5511115copy number variation1nstd206human GRCh38 chr11: 5,612,053-5,635,156 , GRCh37.p13 chr11: 5,633,283-5,656,386 TRIM5, TRIM6, 2 more genes
    nsv5506878copy number variation1nstd206human GRCh38 chr11: 5,464,000-5,676,000 , GRCh37.p13 chr11: 5,485,230-5,697,230 OR52V1P, HNRNPA1P53, 16 more genes
    nsv5505187copy number variation1nstd206human GRCh38 chr11: 5,594,485-5,601,542 , GRCh37.p13 chr11: 5,615,715-5,622,772 TRIM5, TRIM6, 1 more genes
    nsv5391004copy number variation1nstd186human GRCh37 chr11: 5,623,624-5,624,056 , GRCh38.p12 chr11: 5,602,394-5,602,826 TRIM5, TRIM6, 1 more genes
    nsv5317333copy number variation1nstd204human GRCh37.p13 chr11: 5,623,440-5,624,154 , GRCh38.p13 chr11: 5,602,210-5,602,924 TRIM5, TRIM6, 1 more genes
    nsv5251234copy number variation1nstd204human GRCh38.p13 chr11: 5,602,401-5,602,800 , GRCh37.p13 chr11: 5,623,631-5,624,030 TRIM6, TRIM5, 1 more genes
    nsv4984165copy number variation1nstd200human GRCh38 chr11: 5,601,604-5,609,973 , GRCh37.p13 chr11: 5,622,834-5,631,203 TRIM5, TRIM6, 1 more genes
    nsv4984164copy number variation1nstd200human GRCh38 chr11: 5,583,803-5,599,686 , GRCh37.p13 chr11: 5,605,033-5,620,916 TRIM6, TRIM6-TRIM34, 1 more genes
    nsv4978012copy number variation1nstd200human GRCh38 chr11: 5,603,675-5,604,087 , GRCh37.p13 chr11: 5,624,905-5,625,317 TRIM6-TRIM34, TRIM5, 1 more genes
    nsv4848695copy number variation1nstd200human GRCh37 chr11: 5,604,970-5,620,934 , GRCh38.p12 chr11: 5,583,740-5,599,704 TRIM5, TRIM6, 1 more genes
    nsv4836539copy number variation1nstd200human GRCh37 chr11: 5,623,619-5,624,057 , GRCh38.p12 chr11: 5,602,389-5,602,827 TRIM5, TRIM6-TRIM34, 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
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4729242copy number variation1nstd102humanUncertain significance GRCh37 chr11: 5,485,211-5,693,876 , GRCh38.p12 chr11: 5,463,981-5,672,646 OR52D1, OLFM5P, 16 more genes
    nsv4675693copy number variation1nstd102humanLikely benign GRCh37 chr11: 5,505,304-6,199,376 , GRCh38.p12 chr11: 5,484,074-6,178,146 OR52B5P, HNRNPA1P53, 47 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4671188copy number variation1nstd186human GRCh37 chr11: 5,623,565-5,624,080 , GRCh38.p12 chr11: 5,602,335-5,602,850 TRIM5, TRIM6, 1 more genes
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