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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068024inversion1nstd229human GRCh38 chr17: 45,157,768-45,158,742 , GRCh37.p13 chr17: 43,235,135-43,236,109 HEXIM2, HEXIM2-AS1
    nsv6994989copy number variation1nstd229human GRCh38 chr17: 45,160,533-45,160,740 , GRCh37.p13 chr17: 43,237,900-43,238,107 HEXIM2, HEXIM2-AS1
    nsv6986163copy number variation1nstd229human GRCh38 chr17: 45,132,962-45,253,872 , GRCh37.p13 chr17: 43,210,329-43,331,239 LOC105371795, MAP3K14-AS1, 9 more genes
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6504054copy number variation1nstd223human GRCh38 chr17: 45,132,962-45,253,872 , GRCh37.p13 chr17: 43,210,329-43,331,239 FMNL1-AS1, HEXIM2, 9 more genes
    nsv6038775copy number variation1nstd212human GRCh38 chr17: 45,169,926-45,177,104 , GRCh37.p13 chr17: 43,247,293-43,254,471 HEXIM2, LOC105371795
    nsv6021180copy number variation1nstd212human GRCh38 chr17: 45,168,238-45,168,321 , GRCh37.p13 chr17: 43,245,605-43,245,688 HEXIM2, LOC105371795
    nsv5701466mobile element insertion1nstd211human GRCh38 chr17: 45,165,499-45,165,499 , GRCh37.p13 chr17: 43,242,866-43,242,866 HEXIM2
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5288011copy number variation1nstd204human GRCh37.p13 chr17: 43,129,069-43,257,867 , GRCh38.p13 chr17: 45,051,701-45,180,500 NMT1, HEXIM1, 7 more genes
    nsv5149196mobile element insertion1nstd203human GRCh38 chr17: 45,165,483-45,165,499 , GRCh37.p13 chr17: 43,242,850-43,242,866 HEXIM2
    nsv5144513mobile element insertion1nstd203human GRCh38 chr17: 45,163,021-45,163,034 , GRCh37.p13 chr17: 43,240,388-43,240,401 HEXIM2
    nsv5016563copy number variation1nstd200human GRCh38 chr17: 45,159,722-45,168,244 , GRCh37.p13 chr17: 43,237,089-43,245,611 LOC105371795, HEXIM2-AS1, 1 more genes
    nsv4867122copy number variation1nstd200human GRCh37 chr17: 43,237,089-43,245,611 , GRCh38.p12 chr17: 45,159,722-45,168,244 HEXIM2, LOC105371795, 1 more genes
    nsv4508920mobile element insertion1nstd166human GRCh37.p13 chr17: 43,242,850-43,242,850 , GRCh38.p12 chr17: 45,165,483-45,165,483 HEXIM2
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4265166copy number variation1nstd166human GRCh37.p13 chr17: 43,232,000-43,256,000 , GRCh38.p12 chr17: 45,154,633-45,178,633 HEXIM2-AS1, LOC105371795, 1 more genes
    nsv4264983copy number variation1nstd166human GRCh37.p13 chr17: 43,237,000-43,242,000 , GRCh38.p12 chr17: 45,159,633-45,164,633 HEXIM2, HEXIM2-AS1
    nsv4258933copy number variation1nstd166human GRCh37.p13 chr17: 43,237,090-43,245,611 , GRCh38.p12 chr17: 45,159,723-45,168,244 HEXIM2-AS1, HEXIM2, 1 more genes
    nsv3963477copy number variation1nstd168human GRCh38 chr17: 45,146,461-45,187,791 , GRCh37.p13 chr17: 43,223,828-43,265,158 HEXIM2, HEXIM1, 2 more genes
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