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Items: 1 to 20 of 171

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131683insertion1nstd186human GRCh37 chr14: 90,487,158-90,487,163 , GRCh38.p12 chr14: 90,020,814-90,020,819 TDP1
    nsv5973661insertion1nstd209human GRCh38 chr14: 90,020,374-90,020,374 , GRCh37.p13 chr14: 90,486,718-90,486,718 TDP1
    nsv5969778insertion1nstd209human GRCh38 chr14: 90,020,800-90,020,800 , GRCh37.p13 chr14: 90,487,144-90,487,144 TDP1
    nsv5720379mobile element insertion1nstd211human GRCh38 chr14: 90,031,663-90,031,663 , GRCh37.p13 chr14: 90,498,007-90,498,007 TDP1
    nsv5704458mobile element insertion1nstd211human GRCh38 chr14: 89,975,601-89,975,601 , GRCh37.p13 chr14: 90,441,945-90,441,945 TDP1
    nsv5700973mobile element insertion1nstd211human GRCh38 chr14: 89,954,182-89,954,182 , GRCh37.p13 chr14: 90,420,526-90,420,526 EFCAB11, TDP1
    nsv5699598mobile element insertion1nstd211human GRCh38 chr14: 89,980,726-89,980,726 , GRCh37.p13 chr14: 90,447,070-90,447,070 TDP1
    nsv5657011insertion1nstd207human GRCh38 chr14: 90,020,354-90,020,354 , GRCh37.p13 chr14: 90,486,698-90,486,698 TDP1
    nsv5648684insertion1nstd207human GRCh38 chr14: 90,020,800-90,020,800 , GRCh37.p13 chr14: 90,487,144-90,487,144 TDP1
    nsv5596026copy number variation1nstd207human GRCh38 chr14: 90,020,559-90,020,615 , GRCh37.p13 chr14: 90,486,903-90,486,959 TDP1
    nsv5556708sequence alteration1nstd206human GRCh38 chr14: 89,978,968-89,979,025 , GRCh37.p13 chr14: 90,445,312-90,445,369 TDP1
    nsv5552745insertion1nstd206human GRCh38 chr14: 89,965,322-89,965,371 , GRCh37.p13 chr14: 90,431,666-90,431,715 TDP1
    nsv5548804insertion1nstd206human GRCh38 chr14: 90,020,814-90,020,819 , GRCh37.p13 chr14: 90,487,158-90,487,163 TDP1
    nsv5541831insertion1nstd206human GRCh38 chr14: 89,978,968-89,978,968 , GRCh37.p13 chr14: 90,445,312-90,445,312 TDP1
    nsv5506265copy number variation1nstd206human GRCh38 chr14: 89,963,589-89,963,650 , GRCh37.p13 chr14: 90,429,933-90,429,994 TDP1
    nsv5503911copy number variation1nstd206human GRCh38 chr14: 89,980,328-89,980,399 , GRCh37.p13 chr14: 90,446,672-90,446,743 TDP1
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5431545mobile element insertion1nstd206human GRCh38 chr14: 89,954,182-89,954,233 , GRCh37.p13 chr14: 90,420,526-90,420,577 TDP1, EFCAB11
    nsv5416289mobile element insertion1nstd206human GRCh38 chr14: 89,980,726-89,980,777 , GRCh37.p13 chr14: 90,447,070-90,447,121 TDP1
    nsv5373249translocation1nstd200human GRCh38 chr14: 90,036,546-90,036,546 , GRCh38 chr1: 198,381,980-198,381,980 , GRCh37.p13 chr1: 198,351,110-198,351,110 , GRCh37.p13 chr14: 90,502,890-90,502,890 TDP1
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