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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099210copy number variation1nstd231human GRCh38.p12 chr1: 66,256,800-84,953,993 , GRCh37 chr1: 66,722,483-85,419,676 ACADM, COX6A1P1, 211 more genes
    nsv7057605inversion1nstd229human GRCh38 chr1: 78,336,704-86,162,072 , GRCh37.p13 chr1: 78,802,388-86,627,755 LINC01712, LOC105378812, 74 more genes
    nsv7057036inversion1nstd229human GRCh38 chr1: 81,424,308-84,666,974 , GRCh37.p13 chr1: 81,889,993-85,132,657 SSX2IP, LINC01361, 29 more genes
    nsv7053103inversion1nstd229human GRCh38 chr1: 81,888,908-86,483,944 , GRCh37.p13 chr1: 82,354,593-86,949,627 C1orf52, DNAI3, 50 more genes
    nsv7050765inversion1nstd229human GRCh38 chr1: 80,818,811-84,572,591 , GRCh37.p13 chr1: 81,284,496-85,038,274 RPF1, LOC105378819, 32 more genes
    nsv7046575inversion1nstd229human GRCh38 chr1: 83,069,893-89,051,563 , GRCh37.p13 chr1: 83,535,576-89,517,246 LOC105378826, RN7SL583P, 87 more genes
    nsv7045562inversion1nstd229human GRCh38 chr1: 82,773,087-84,647,821 , GRCh37.p13 chr1: 83,238,770-85,113,504 LOC107985396, LINC01362, 22 more genes
    nsv7041571inversion1nstd229human GRCh38 chr1: 84,455,419-86,210,703 , GRCh37.p13 chr1: 84,921,102-86,676,386 GNG5, DNAI3, 25 more genes
    nsv6656326copy number variation1nstd229human GRCh38 chr1: 84,458,749-84,493,670 , GRCh37.p13 chr1: 84,924,432-84,959,353 RPF1
    nsv6656160copy number variation1nstd229human GRCh38 chr1: 84,403,990-84,767,957 , GRCh37.p13 chr1: 84,869,673-85,233,640 GNG5, SPATA1, 7 more genes
    nsv6656155copy number variation1nstd229human GRCh38 chr1: 84,297,101-85,026,300 , GRCh37.p13 chr1: 84,762,784-85,491,983 LOC102724892, MCOLN3, 13 more genes
    nsv6536232inversion1nstd223human GRCh38 chr1: 84,485,009-84,486,320 , GRCh37.p13 chr1: 84,950,692-84,952,003 RPF1
    nsv6326244copy number variation1nstd223human GRCh38 chr1: 84,483,347-84,484,766 , GRCh37.p13 chr1: 84,949,030-84,950,449 RPF1
    nsv6313574copy number variation1nstd102humanPathogenic GRCh37 chr1: 68,180,293-92,731,957 , GRCh38.p12 chr1: 67,714,610-92,266,400 RNA5SP51, ADGRL4, 315 more genes
    nsv6051925insertion1nstd212human GRCh38 chr1: 84,486,120-84,486,120 , GRCh37.p13 chr1: 84,951,803-84,951,803 RPF1
    nsv6048971insertion1nstd212human GRCh38 chr1: 84,486,433-84,486,433 , GRCh37.p13 chr1: 84,952,116-84,952,116 RPF1
    nsv5545614insertion1nstd206human GRCh38 chr1: 84,486,440-84,486,461 , GRCh37.p13 chr1: 84,952,123-84,952,144 RPF1
    nsv5191407mobile element insertion1nstd203human GRCh38 chr1: 84,491,328-84,491,328 , GRCh37.p13 chr1: 84,957,011-84,957,011 RPF1
    nsv5073983mobile element insertion1nstd203human GRCh38 chr1: 84,486,423-84,486,440 , GRCh37.p13 chr1: 84,952,106-84,952,123 RPF1
    nsv5064868mobile element insertion1nstd203human GRCh38 chr1: 84,486,121-84,486,134 , GRCh37.p13 chr1: 84,951,804-84,951,817 RPF1
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