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Items: 1 to 20 of 217

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066313inversion1nstd229human GRCh38 chr11: 6,624,146-15,294,249 , GRCh37.p13 chr11: 6,645,377-15,315,795 RNA5SP332, TMEM41B, 163 more genes
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6915731copy number variation1nstd229human GRCh38 chr11: 8,404,910-8,650,143 , GRCh37.p13 chr11: 8,426,457-8,671,690 TRIM66, STK33
    nsv6915289copy number variation1nstd229human GRCh38 chr11: 8,607,381-8,618,529 , GRCh37.p13 chr11: 8,628,928-8,640,076 TRIM66
    nsv6906971copy number variation1nstd229human GRCh38 chr11: 6,634,801-9,831,623 , GRCh37.p13 chr11: 6,656,032-9,853,170 RIC3, LOC644656, 86 more genes
    nsv6906211copy number variation1nstd229human GRCh38 chr11: 8,415,343-8,672,034 , GRCh37.p13 chr11: 8,436,890-8,693,581 STK33, TRIM66
    nsv6901097copy number variation1nstd229human GRCh38 chr11: 8,567,643-8,968,110 , GRCh37.p13 chr11: 8,589,190-8,989,657 SNORA3B, RPL27A, 12 more genes
    nsv6900950copy number variation1nstd229human GRCh38 chr11: 8,665,601-8,670,300 , GRCh37.p13 chr11: 8,687,148-8,691,847 TRIM66
    nsv6899282copy number variation1nstd229human GRCh38 chr11: 8,669,374-8,671,019 , GRCh37.p13 chr11: 8,690,921-8,692,566 TRIM66
    nsv6590466inversion1nstd223human GRCh38 chr11: 8,666,072-8,666,833 , GRCh37.p13 chr11: 8,687,619-8,688,380 TRIM66
    nsv6589133inversion1nstd223human GRCh38 chr11: 8,655,033-8,655,807 , GRCh37.p13 chr11: 8,676,580-8,677,354 TRIM66
    nsv6587253inversion1nstd223human GRCh38 chr11: 8,620,254-8,620,857 , GRCh37.p13 chr11: 8,641,801-8,642,404 TRIM66
    nsv6578417inversion1nstd223human GRCh38 chr11: 7,263,807-16,565,752 , GRCh37.p13 chr11: 7,285,038-16,587,299 TEAD1, IRAG1, 151 more genes
    nsv6442855copy number variation1nstd223human GRCh38 chr11: 6,634,801-9,831,623 , GRCh37.p13 chr11: 6,656,032-9,853,170 LOC105369149, C11orf16, 86 more genes
    nsv6441354copy number variation1nstd223human GRCh38 chr11: 8,619,927-8,620,716 , GRCh37.p13 chr11: 8,641,474-8,642,263 TRIM66
    nsv6437112copy number variation1nstd223human GRCh38 chr11: 8,638,372-8,639,041 , GRCh37.p13 chr11: 8,659,919-8,660,588 TRIM66
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6084452insertion1nstd212human GRCh38 chr11: 8,622,365-8,622,365 , GRCh37.p13 chr11: 8,643,912-8,643,912 TRIM66
    nsv6034881copy number variation1nstd212human GRCh38 chr11: 8,626,940-8,627,405 , GRCh37.p13 chr11: 8,648,487-8,648,952 TRIM66
    nsv5976757insertion1nstd209human GRCh38 chr11: 8,628,636-8,628,636 , GRCh37.p13 chr11: 8,650,183-8,650,183 TRIM66
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