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Items: 1 to 20 of 253

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070663inversion1nstd229human GRCh38 chr9: 72,935,575-72,943,987 , GRCh37.p13 chr9: 75,550,491-75,558,903 ALDH1A1
    nsv7065303inversion1nstd229human GRCh38 chr9: 71,473,712-72,923,816 , GRCh37.p13 chr9: 74,088,628-75,538,732 LOC101927234, GDA, 21 more genes
    nsv6876635copy number variation1nstd229human GRCh38 chr9: 72,384,161-74,793,192 , GRCh37.p13 chr9: 74,999,077-77,408,108 LOC101927329, LOC100289351, 27 more genes
    nsv6864359copy number variation1nstd229human GRCh38 chr9: 72,949,410-72,949,609 , GRCh37.p13 chr9: 75,564,326-75,564,525 ALDH1A1
    nsv6863034copy number variation1nstd229human GRCh38 chr9: 72,906,209-73,538,839 , GRCh37.p13 chr9: 75,521,125-76,153,755 DPP3P2, LOC105376084, 7 more genes
    nsv6858263copy number variation1nstd229human GRCh38 chr9: 72,621,927-73,648,904 , GRCh37.p13 chr9: 75,236,843-76,263,820 RPS20P24, LINC01474, 13 more genes
    nsv6637502copy number variation1nstd102humanUncertain significance GRCh37 chr9: 70,966,262-76,901,382 , GRCh38.p12 chr9: 68,351,346-74,286,466 RPS20P24, MAMDC2-AS1, 77 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6574546inversion1nstd223human GRCh38 chr9: 72,908,148-72,909,389 , GRCh37.p13 chr9: 75,523,064-75,524,305 ALDH1A1
    nsv6570283inversion1nstd223human GRCh38 chr9: 72,934,008-72,936,205 , GRCh37.p13 chr9: 75,548,924-75,551,121 ALDH1A1
    nsv6455436copy number variation1nstd223human GRCh38 chr9: 72,931,933-72,932,401 , GRCh37.p13 chr9: 75,546,849-75,547,317 ALDH1A1
    nsv6453716copy number variation1nstd223human GRCh38 chr9: 72,906,209-73,538,841 , GRCh37.p13 chr9: 75,521,125-76,153,757 ANXA1, LOC105376084, 7 more genes
    nsv6453455copy number variation1nstd223human GRCh38 chr9: 72,893,921-72,899,205 , GRCh37.p13 chr9: 75,508,837-75,514,121 ALDH1A1
    nsv6450677copy number variation1nstd223human GRCh38 chr9: 72,905,001-72,906,700 , GRCh37.p13 chr9: 75,519,917-75,521,616 ALDH1A1
    nsv6443898copy number variation1nstd223human GRCh38 chr9: 72,914,301-72,915,600 , GRCh37.p13 chr9: 75,529,217-75,530,516 ALDH1A1
    nsv6441578copy number variation1nstd223human GRCh38 chr9: 72,905,394-72,905,801 , GRCh37.p13 chr9: 75,520,310-75,520,717 ALDH1A1
    nsv6441080copy number variation1nstd223human GRCh38 chr9: 72,942,472-72,942,870 , GRCh37.p13 chr9: 75,557,388-75,557,786 ALDH1A1
    nsv6436033copy number variation1nstd223human GRCh38 chr9: 72,900,201-72,902,200 , GRCh37.p13 chr9: 75,515,117-75,517,116 ALDH1A1
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
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