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Items: 1 to 20 of 619

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048039inversion1nstd229human GRCh38 chr3: 152,443,283-152,443,295 , GRCh37.p13 chr3: 152,161,072-152,161,084 MBNL1
    nsv7043003inversion1nstd229human GRCh38 chr3: 152,267,064-152,267,175 , GRCh37.p13 chr3: 151,984,853-151,984,964 MBNL1-AS1, MBNL1
    nsv6736871copy number variation1nstd229human GRCh38 chr3: 152,395,701-152,404,500 , GRCh37.p13 chr3: 152,113,490-152,122,289 MBNL1
    nsv6735582copy number variation1nstd229human GRCh38 chr3: 152,311,365-152,313,778 , GRCh37.p13 chr3: 152,029,154-152,031,567 MBNL1
    nsv6735362copy number variation1nstd229human GRCh38 chr3: 152,322,104-152,324,111 , GRCh37.p13 chr3: 152,039,893-152,041,900 MBNL1
    nsv6734363copy number variation1nstd229human GRCh38 chr3: 152,272,458-152,275,228 , GRCh37.p13 chr3: 151,990,247-151,993,017 MBNL1
    nsv6733566copy number variation1nstd229human GRCh38 chr3: 152,428,347-152,440,913 , GRCh37.p13 chr3: 152,146,136-152,158,702 MBNL1
    nsv6730539copy number variation1nstd229human GRCh38 chr3: 152,389,417-152,392,176 , GRCh37.p13 chr3: 152,107,206-152,109,965 MBNL1
    nsv6730151copy number variation1nstd229human GRCh38 chr3: 152,358,959-152,395,830 , GRCh37.p13 chr3: 152,076,748-152,113,619 MBNL1
    nsv6729684copy number variation1nstd229human GRCh38 chr3: 152,376,830-152,381,939 , GRCh37.p13 chr3: 152,094,619-152,099,728 MBNL1
    nsv6728967copy number variation1nstd229human GRCh38 chr3: 152,397,934-152,401,100 , GRCh37.p13 chr3: 152,115,723-152,118,889 MBNL1
    nsv6724223copy number variation1nstd229human GRCh38 chr3: 152,376,854-152,540,724 , GRCh37.p13 chr3: 152,094,643-152,258,513 LOC105374163, MBNL1
    nsv6722076copy number variation1nstd229human GRCh38 chr3: 152,414,123-152,471,661 , GRCh37.p13 chr3: 152,131,912-152,189,450 MBNL1
    nsv6721860copy number variation1nstd229human GRCh38 chr3: 152,414,401-152,470,500 , GRCh37.p13 chr3: 152,132,190-152,188,289 MBNL1
    nsv6719349copy number variation1nstd229human GRCh38 chr3: 152,463,501-152,469,600 , GRCh37.p13 chr3: 152,181,290-152,187,389 MBNL1
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6573510inversion1nstd223human GRCh38 chr3: 152,374,999-152,375,653 , GRCh37.p13 chr3: 152,092,788-152,093,442 MBNL1
    nsv6566828inversion1nstd223human GRCh38 chr3: 152,375,123-152,375,483 , GRCh37.p13 chr3: 152,092,912-152,093,272 MBNL1
    nsv6555836inversion1nstd223human GRCh38 chr3: 152,336,791-152,342,231 , GRCh37.p13 chr3: 152,054,580-152,060,020 MBNL1, TMEM14EP
    nsv6375419copy number variation1nstd223human GRCh38 chr3: 152,418,982-152,419,383 , GRCh37.p13 chr3: 152,136,771-152,137,172 MBNL1
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