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Items: 1 to 20 of 251

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143035copy number variation1nstd232human GRCh37.p13 chr5: 175,815,344-175,815,432 , GRCh38.p12 chr5: 176,388,343-176,388,431 NOP16, HIGD2A, 1 more genes
    nsv7139039insertion1nstd232human GRCh37.p13 chr5: 175,819,946-175,819,946 , GRCh38.p12 chr5: 176,392,945-176,392,945 CLTB, ARL10
    nsv7097267copy number variation3nstd102humanUncertain significance GRCh37 chr5: 175,158,654-179,263,593 , GRCh38.p12 chr5: 175,731,651-179,836,593 LOC112267937, LMAN2, 122 more genes
    nsv7057944inversion1nstd229human GRCh38 chr5: 172,134,356-176,589,266 , GRCh37.p13 chr5: 171,561,360-176,016,267 MIR10523, NIFKP2, 92 more genes
    nsv7055309inversion1nstd229human GRCh38 chr5: 176,251,563-176,434,793 , GRCh37.p13 chr5: 175,678,566-175,861,794 KIAA1191, BRCC3P1, 6 more genes
    nsv7050002inversion1nstd229human GRCh38 chr5: 175,906,338-177,936,522 , GRCh37.p13 chr5: 175,333,341-177,363,523 PRR7, OR1X5P, 60 more genes
    nsv7041901inversion1nstd229human GRCh38 chr5: 175,920,087-179,128,938 , GRCh37.p13 chr5: 175,347,090-178,555,939 LOC100288803, NHP2, 98 more genes
    nsv7040659inversion1nstd229human GRCh38 chr5: 174,927,732-178,443,561 , GRCh37.p13 chr5: 174,354,735-177,870,562 RN7SKP148, FAM193B-DT, 90 more genes
    nsv7038290inversion1nstd229human GRCh38 chr5: 172,489,078-179,485,008 , GRCh37.p13 chr5: 171,916,082-178,912,009 ZFP2, NHP2, 168 more genes
    nsv6797169copy number variation1nstd229human GRCh38 chr5: 176,410,750-176,410,780 , GRCh37.p13 chr5: 175,837,751-175,837,781 ARL10, CLTB
    nsv6795911copy number variation1nstd229human GRCh38 chr5: 176,377,354-176,377,727 , GRCh37.p13 chr5: 175,804,357-175,804,730 ARL10
    nsv6795390copy number variation1nstd229human GRCh38 chr5: 176,377,701-176,385,400 , GRCh37.p13 chr5: 175,804,704-175,812,401 NOP16, ARL10
    nsv6795030copy number variation1nstd229human GRCh38 chr5: 176,384,352-176,401,464 , GRCh37.p13 chr5: 175,811,353-175,828,465 HIGD2A, NOP16, 2 more genes
    nsv6790751copy number variation1nstd229human GRCh38 chr5: 176,370,573-176,375,079 , GRCh37.p13 chr5: 175,797,576-175,802,082 ARL10
    nsv6790389copy number variation1nstd229human GRCh38 chr5: 176,392,946-176,397,605 , GRCh37.p13 chr5: 175,819,947-175,824,606 CLTB, ARL10
    nsv6786854copy number variation1nstd229human GRCh38 chr5: 176,398,048-176,416,176 , GRCh37.p13 chr5: 175,825,049-175,843,177 CLTB, ARL10
    nsv6782450copy number variation1nstd229human GRCh38 chr5: 176,394,583-176,395,901 , GRCh37.p13 chr5: 175,821,584-175,822,902 ARL10, CLTB
    nsv6781612copy number variation1nstd229human GRCh38 chr5: 176,383,767-176,383,876 , GRCh37.p13 chr5: 175,810,770-175,810,879 ARL10, NOP16
    nsv6781033copy number variation1nstd229human GRCh38 chr5: 176,389,462-176,391,836 , GRCh37.p13 chr5: 175,816,463-175,818,837 ARL10, HIGD2A, 1 more genes
    nsv6778711copy number variation1nstd229human GRCh38 chr5: 176,369,757-176,371,350 , GRCh37.p13 chr5: 175,796,760-175,798,353 ARL10
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