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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5730588mobile element insertion1nstd211human GRCh38 chr3: 105,886,449-105,886,449 , GRCh37.p13 chr3: 105,605,296-105,605,296
    nsv5678862mobile element insertion1nstd211human GRCh38 chr3: 105,877,467-105,877,467 , GRCh37.p13 chr3: 105,596,311-105,596,311 , LOC105374024
    nsv5563931mobile element insertion1nstd206human GRCh38 chr3: 105,886,449-105,886,449 , GRCh37.p13 chr3: 105,605,296-105,605,296
    nsv5561137sequence alteration1nstd206human GRCh37.p13 chr3: 105,578,270-106,370,032 , GRCh38 chr3: 105,859,426-106,651,185 , CBLB, 6 more genes
    nsv5435086copy number variation1nstd206human GRCh38 chr3: 105,877,872-105,877,926 , GRCh37.p13 chr3: 105,596,716-105,596,770 , LOC105374024
    nsv5094592mobile element insertion1nstd203human GRCh38 chr3: 105,888,727-105,888,740 , GRCh37.p13 chr3: 105,607,574-105,607,587
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4919349copy number variation1nstd200human GRCh38 chr3: 105,890,777-105,895,469 , GRCh37.p13 chr3: 105,609,624-105,614,316
    nsv4919348copy number variation1nstd200human GRCh38 chr3: 105,888,019-105,921,337 , GRCh37.p13 chr3: 105,606,866-105,640,184
    nsv4919347copy number variation1nstd200human GRCh38 chr3: 105,869,495-105,871,085 , GRCh37.p13 chr3: 105,588,339-105,589,929 , LOC105374024, 1 more genes
    nsv4919341copy number variation1nstd200human GRCh38 chr3: 105,669,457-106,330,705 , GRCh37.p13 chr3: 105,388,301-106,049,552 , CBLB, 5 more genes
    nsv4914603copy number variation1nstd200human GRCh38 chr3: 105,870,257-105,884,802 , GRCh37.p13 chr3: 105,589,101-105,603,649 , LOC105374024
    nsv4914601copy number variation1nstd200human GRCh38 chr3: 105,832,301-105,928,703 , GRCh37.p13 chr3: 105,551,145-105,647,550 , LOC105374024, 1 more genes
    nsv4797832copy number variation1nstd200human GRCh37 chr3: 105,609,624-105,614,316 , GRCh38.p12 chr3: 105,890,777-105,895,469
    nsv4797831copy number variation1nstd200human GRCh37 chr3: 105,588,339-105,589,929 , GRCh38.p12 chr3: 105,869,495-105,871,085 , LOC105374024, 1 more genes
    nsv4797826copy number variation1nstd200human GRCh37 chr3: 105,388,301-106,049,552 , GRCh38.p12 chr3: 105,669,457-106,330,705 , CBLB, 5 more genes
    nsv4595933copy number variation1nstd183human GRCh37 chr3: 105,600,836-105,607,929 , GRCh38.p12 chr3: 105,881,992-105,889,082 , LOC105374024
    nsv4584492copy number variation1nstd183human GRCh37 chr3: 105,576,046-105,588,164 , GRCh38.p12 chr3: 105,857,202-105,869,320 , LOC105374024, 1 more genes
    nsv4468504mobile element insertion1nstd166human GRCh37.p13 chr3: 105,596,301-105,596,301 , GRCh38.p12 chr3: 105,877,457-105,877,457 , LOC105374024
    nsv4467891mobile element insertion1nstd166human GRCh37.p13 chr3: 105,607,574-105,607,574 , GRCh38.p12 chr3: 105,888,727-105,888,727
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