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Items: 1 to 20 of 186

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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
    nsv7049591inversion1nstd229human GRCh38 chr1: 78,612,736-84,444,047 , GRCh37.p13 chr1: 79,078,421-84,909,730 RPS20P7, LINC02792, 44 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
    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
    nsv6335205copy number variation1nstd223human GRCh38 chr1: 84,367,210-84,368,311 , GRCh37.p13 chr1: 84,832,893-84,833,994 UOX
    nsv6317154copy number variation1nstd223human GRCh38 chr1: 84,362,418-84,373,248 , GRCh37.p13 chr1: 84,828,101-84,838,931 UOX
    nsv6313647copy number variation1nstd102humanUncertain significance GRCh37 chr1: 84,084,511-84,921,911 , GRCh38.p12 chr1: 83,618,828-84,456,228 LINC01725, TXN2P1, 7 more genes
    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
    nsv6244289mobile element insertion1nstd215human GRCh38 chr1: 84,366,384-84,366,384 , GRCh37.p13 chr1: 84,832,067-84,832,067 UOX
    nsv5985100copy number variation1nstd212human GRCh38 chr1: 84,375,521-84,375,590 , GRCh37.p13 chr1: 84,841,204-84,841,273 UOX
    nsv5721588mobile element insertion2nstd211human GRCh38 chr1: 84,368,306-84,368,306 , GRCh37.p13 chr1: 84,833,989-84,833,989 UOX
    nsv5686124mobile element insertion1nstd211human GRCh38 chr1: 84,363,659-84,363,659 , GRCh37.p13 chr1: 84,829,342-84,829,342 UOX
    nsv5609641insertion1nstd207human GRCh38 chr1: 84,368,292-84,368,292 , GRCh37.p13 chr1: 84,833,975-84,833,975 UOX
    nsv5551973insertion1nstd206human GRCh38 chr1: 84,368,306-84,368,342 , GRCh37.p13 chr1: 84,833,989-84,834,025 UOX
    nsv5433275copy number variation1nstd206human GRCh38 chr1: 84,375,523-84,375,590 , GRCh37.p13 chr1: 84,841,206-84,841,273 UOX
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