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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116857mobile element insertion1nstd186human GRCh37 chr14: 57,744,433-57,744,433 , GRCh38.p12 chr14: 57,277,715-57,277,715 AP5M1
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 ACTN1, ACYP1, 400 more genes
    nsv5979691insertion1nstd209human GRCh38 chr14: 57,277,715-57,277,715 , GRCh37.p13 chr14: 57,744,433-57,744,433 AP5M1
    nsv5938835copy number variation1nstd209human GRCh38 chr14: 50,842,894-59,394,609 , GRCh37.p13 chr14: 51,309,612-59,861,327 , TMX1, 148 more genes
    nsv5929564copy number variation1nstd209human GRCh38 chr14: 57,279,826-57,279,900 , GRCh37.p13 chr14: 57,746,544-57,746,618 AP5M1
    nsv5701802mobile element insertion1nstd211human GRCh38 chr14: 57,293,523-57,293,523 , GRCh37.p13 chr14: 57,760,241-57,760,241 AP5M1
    nsv5694825mobile element insertion2nstd211human GRCh38 chr14: 57,277,732-57,277,732 , GRCh37.p13 chr14: 57,744,450-57,744,450 AP5M1
    nsv5662952insertion1nstd207human GRCh38 chr14: 57,277,715-57,277,715 , GRCh37.p13 chr14: 57,744,433-57,744,433 AP5M1
    nsv5504393copy number variation1nstd206human GRCh38 chr14: 57,279,828-57,279,901 , GRCh37.p13 chr14: 57,746,546-57,746,619 AP5M1
    nsv5503632copy number variation1nstd206human GRCh38 chr14: 57,282,027-57,282,081 , GRCh37.p13 chr14: 57,748,745-57,748,799 AP5M1
    nsv5423973mobile element insertion1nstd206human GRCh38 chr14: 57,293,523-57,293,574 , GRCh37.p13 chr14: 57,760,241-57,760,292 AP5M1
    nsv5416572mobile element insertion1nstd206human GRCh38 chr14: 57,277,715-57,277,715 , GRCh37.p13 chr14: 57,744,433-57,744,433 AP5M1
    nsv5158714mobile element insertion1nstd203human GRCh38 chr14: 57,277,719-57,277,732 , GRCh37.p13 chr14: 57,744,437-57,744,450 AP5M1
    nsv5158432mobile element insertion1nstd203human GRCh38 chr14: 57,277,722-57,277,732 , GRCh37.p13 chr14: 57,744,440-57,744,450 AP5M1
    nsv5153164mobile element insertion1nstd203human GRCh38 chr14: 57,293,514-57,293,523 , GRCh37.p13 chr14: 57,760,232-57,760,241 AP5M1
    nsv5152911mobile element insertion1nstd203human GRCh38 chr14: 57,280,687-57,280,703 , GRCh37.p13 chr14: 57,747,405-57,747,421 AP5M1
    nsv5147352mobile element insertion1nstd203human GRCh38 chr14: 57,277,721-57,277,732 , GRCh37.p13 chr14: 57,744,439-57,744,450 AP5M1
    nsv5146940mobile element insertion1nstd203human GRCh38 chr14: 57,277,715-57,277,732 , GRCh37.p13 chr14: 57,744,433-57,744,450 AP5M1
    nsv5145335mobile element insertion1nstd203human GRCh38 chr14: 57,277,714-57,277,732 , GRCh37.p13 chr14: 57,744,432-57,744,450 AP5M1
    nsv5143754mobile element insertion1nstd203human GRCh38 chr14: 57,277,720-57,277,732 , GRCh37.p13 chr14: 57,744,438-57,744,450 AP5M1
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