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Items: 1 to 20 of 679

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5949213insertion1nstd209human GRCh38 chr3: 155,491,562-155,491,562 , GRCh37.p13 chr3: 155,209,351-155,209,351 PLCH1
    nsv5902476copy number variation1nstd209human GRCh38 chr3: 155,706,254-155,706,387 , GRCh37.p13 chr3: 155,424,043-155,424,176 PLCH1
    nsv5900278copy number variation1nstd209human GRCh38 chr3: 155,693,168-155,693,492 , GRCh37.p13 chr3: 155,410,957-155,411,281 PLCH1
    nsv5899562copy number variation1nstd209human GRCh38 chr3: 155,566,279-155,566,346 , GRCh37.p13 chr3: 155,284,068-155,284,135 PLCH1
    nsv5720443mobile element insertion1nstd211human GRCh38 chr3: 155,588,433-155,588,433 , GRCh37.p13 chr3: 155,306,222-155,306,222 PLCH1
    nsv5691214mobile element insertion2nstd211human GRCh38 chr3: 155,641,175-155,641,175 , GRCh37.p13 chr3: 155,358,964-155,358,964 PLCH1
    nsv5688576mobile element insertion2nstd211human GRCh38 chr3: 155,665,082-155,665,082 , GRCh37.p13 chr3: 155,382,871-155,382,871 PLCH1
    nsv5620093insertion1nstd207human GRCh38 chr3: 155,458,421-155,458,421 , GRCh37.p13 chr3: 155,176,210-155,176,210 PLCH1
    nsv5613958insertion1nstd207human GRCh38 chr3: 155,667,902-155,667,902 , GRCh37.p13 chr3: 155,385,691-155,385,691 PLCH1
    nsv5612284insertion1nstd207human GRCh38 chr3: 155,745,507-155,745,507 , GRCh37.p13 chr3: 155,463,296-155,463,296 PLCH1
    nsv5609276insertion1nstd207human GRCh38 chr3: 155,665,070-155,665,070 , GRCh37.p13 chr3: 155,382,859-155,382,859 PLCH1
    nsv5577272copy number variation1nstd207human GRCh38 chr3: 155,693,168-155,693,492 , GRCh37.p13 chr3: 155,410,957-155,411,281 PLCH1
    nsv5568656copy number variation1nstd207human GRCh38 chr3: 155,566,148-155,566,207 , GRCh37.p13 chr3: 155,283,937-155,283,996 PLCH1
    nsv5547202insertion1nstd206human GRCh38 chr3: 155,474,953-155,475,003 , GRCh37.p13 chr3: 155,192,742-155,192,792 PLCH1
    nsv5451405copy number variation1nstd206human GRCh38 chr3: 155,667,914-155,668,067 , GRCh37.p13 chr3: 155,385,703-155,385,856 PLCH1
    nsv5445714copy number variation1nstd206human GRCh38 chr3: 154,528,533-156,057,304 , GRCh37.p13 chr3: 154,246,322-155,775,093 LINC01487, MME, 21 more genes
    nsv5442810copy number variation1nstd206human GRCh38 chr3: 155,693,184-155,693,493 , GRCh37.p13 chr3: 155,410,973-155,411,282 PLCH1
    nsv5442186copy number variation1nstd206human GRCh38 chr3: 155,551,402-155,552,664 , GRCh37.p13 chr3: 155,269,191-155,270,453 PLCH1
    nsv5439044copy number variation1nstd206human GRCh38 chr3: 155,692,837-155,693,693 , GRCh37.p13 chr3: 155,410,626-155,411,482 PLCH1
    nsv5438215copy number variation1nstd206human GRCh38 chr3: 155,638,527-155,642,794 , GRCh37.p13 chr3: 155,356,316-155,360,583 PLCH1
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