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Items: 1 to 20 of 522

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130615insertion1nstd186human GRCh37 chr14: 55,102,056-55,102,061 , GRCh38.p12 chr14: 54,635,338-54,635,343 SAMD4A
    nsv6129762insertion1nstd186human GRCh37 chr14: 55,176,030-55,176,067 , GRCh38.p12 chr14: 54,709,312-54,709,349 SAMD4A
    nsv6129598insertion1nstd186human GRCh37 chr14: 55,102,300-55,102,311 , GRCh38.p12 chr14: 54,635,582-54,635,593 SAMD4A
    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
    nsv5977384insertion1nstd209human GRCh38 chr14: 54,724,012-54,724,012 , GRCh37.p13 chr14: 55,190,730-55,190,730 SAMD4A
    nsv5975184insertion1nstd209human GRCh38 chr14: 54,709,298-54,709,298 , GRCh37.p13 chr14: 55,176,016-55,176,016 SAMD4A
    nsv5969432insertion1nstd209human GRCh38 chr14: 54,678,485-54,678,485 , GRCh37.p13 chr14: 55,145,203-55,145,203 SAMD4A
    nsv5938835copy number variation1nstd209human GRCh38 chr14: 50,842,894-59,394,609 , GRCh37.p13 chr14: 51,309,612-59,861,327 , TMX1, 148 more genes
    nsv5709069mobile element insertion1nstd211human GRCh38 chr14: 54,778,471-54,778,471 , GRCh37.p13 chr14: 55,245,189-55,245,189 SAMD4A
    nsv5703360mobile element insertion2nstd211human GRCh38 chr14: 54,619,101-54,619,101 , GRCh37.p13 chr14: 55,085,819-55,085,819 SAMD4A
    nsv5659879insertion1nstd207human GRCh38 chr14: 54,635,338-54,635,338 , GRCh37.p13 chr14: 55,102,056-55,102,056 SAMD4A
    nsv5657241insertion1nstd207human GRCh38 chr14: 54,635,572-54,635,572 , GRCh37.p13 chr14: 55,102,290-55,102,290 SAMD4A
    nsv5657037insertion1nstd207human GRCh38 chr14: 54,678,492-54,678,492 , GRCh37.p13 chr14: 55,145,210-55,145,210 SAMD4A
    nsv5655979insertion1nstd207human GRCh38 chr14: 54,709,298-54,709,298 , GRCh37.p13 chr14: 55,176,016-55,176,016 SAMD4A
    nsv5553649insertion1nstd206human GRCh38 chr14: 54,635,582-54,635,593 , GRCh37.p13 chr14: 55,102,300-55,102,311 SAMD4A
    nsv5552291insertion1nstd206human GRCh38 chr14: 54,778,471-54,778,503 , GRCh37.p13 chr14: 55,245,189-55,245,221 SAMD4A
    nsv5539478insertion1nstd206human GRCh38 chr14: 54,709,312-54,709,349 , GRCh37.p13 chr14: 55,176,030-55,176,067 SAMD4A
    nsv5536483insertion1nstd206human GRCh38 chr14: 54,635,338-54,635,343 , GRCh37.p13 chr14: 55,102,056-55,102,061 SAMD4A
    nsv5513020copy number variation1nstd206human GRCh38 chr14: 54,782,992-54,787,058 , GRCh37.p13 chr14: 55,249,710-55,253,776 SAMD4A
    nsv5512436copy number variation1nstd206human GRCh38 chr14: 54,579,067-54,579,740 , GRCh37.p13 chr14: 55,045,785-55,046,458 SAMD4A
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