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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926907copy number variation1nstd209human GRCh38 chr11: 120,129,631-120,131,722 , GRCh37.p13 chr11: 120,000,339-120,002,430 TRIM29, LOC105369529
    nsv5908933copy number variation1nstd209human GRCh38 chr11: 120,121,911-120,121,985 , GRCh37.p13 chr11: 119,992,619-119,992,693 TRIM29
    nsv5860702copy number variation1nstd209human GRCh38 chr11: 120,129,618-120,131,517 , GRCh37.p13 chr11: 120,000,326-120,002,225 TRIM29, LOC105369529
    nsv5853355copy number variation2nstd209human GRCh38 chr11: 120,130,518-120,131,517 , GRCh37.p13 chr11: 120,001,226-120,002,225 LOC105369529, TRIM29
    nsv5602678copy number variation1nstd207human GRCh38 chr11: 120,129,631-120,131,722 , GRCh37.p13 chr11: 120,000,339-120,002,430 LOC105369529, TRIM29
    nsv5507004copy number variation1nstd206human GRCh38 chr11: 120,129,631-120,131,723 , GRCh37.p13 chr11: 120,000,339-120,002,431 TRIM29, LOC105369529
    nsv5497619copy number variation1nstd206human GRCh38 chr11: 120,121,915-120,121,986 , GRCh37.p13 chr11: 119,992,623-119,992,694 TRIM29
    nsv5380954copy number variation1nstd102humanUncertain significance GRCh37 chr11: 119,077,108-120,133,495 , GRCh38.p12 chr11: 119,206,398-120,262,786 NECTIN1-DT, RNU6-262P, 29 more genes
    nsv5348363translocation1nstd200human GRCh38 chr11: 120,129,631-120,129,631 , GRCh38 chr11: 120,131,723-120,131,723 , GRCh37.p13 chr11: 120,002,431-120,002,431 , GRCh37.p13 chr11: 120,000,339-120,000,339 TRIM29, LOC105369529
    nsv5348362translocation1nstd200human GRCh38 chr11: 120,121,915-120,121,915 , GRCh38 chr11: 120,121,986-120,121,986 , GRCh37.p13 chr11: 119,992,623-119,992,623 , GRCh37.p13 chr11: 119,992,694-119,992,694 TRIM29
    nsv5348361translocation1nstd200human GRCh38 chr11: 120,121,803-120,121,803 , GRCh38 chr11: 120,121,746-120,121,746 , GRCh37.p13 chr11: 119,992,454-119,992,454 , GRCh37.p13 chr11: 119,992,511-119,992,511 TRIM29
    nsv5334271translocation1nstd200human GRCh37 chr11: 120,000,338-120,000,338 , GRCh37 chr11: 120,002,430-120,002,430 , GRCh38.p12 chr11: 120,131,722-120,131,722 , GRCh38.p12 chr11: 120,129,630-120,129,630 LOC105369529, TRIM29
    nsv5316051copy number variation1nstd204human GRCh37.p13 chr11: 120,000,309-120,002,460 , GRCh38.p13 chr11: 120,129,601-120,131,752 TRIM29, LOC105369529
    nsv5270370copy number variation1nstd204human GRCh38.p13 chr11: 120,129,601-120,131,700 , GRCh37.p13 chr11: 120,000,309-120,002,408 LOC105369529, TRIM29
    nsv5260680copy number variation1nstd204human GRCh38.p13 chr11: 120,129,568-120,131,767 , GRCh37.p13 chr11: 120,000,276-120,002,475 LOC105369529, TRIM29
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    nsv4674572copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571 ACRV1, APLP2, 382 more genes
    nsv4655712copy number variation1nstd186human GRCh37 chr11: 119,992,623-119,992,694 , GRCh38.p12 chr11: 120,121,915-120,121,986 TRIM29
    nsv4610525copy number variation1nstd183human GRCh37 chr11: 120,000,339-120,002,431 , GRCh38.p12 chr11: 120,129,631-120,131,723 LOC105369529, TRIM29
    nsv4455281copy number variation1nstd102humanPathogenic GRCh37 chr11: 117,830,263-134,938,470 , GRCh38.p12 chr11: 117,959,548-135,068,576 NTM-AS1, LOC403312, 369 more genes
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