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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7047569inversion1nstd229human GRCh38 chr3: 152,490,812-161,531,961 , GRCh37.p13 chr3: 152,208,601-161,249,749 RPS2P19, LOC112268450, 128 more genes
    nsv7040587inversion1nstd229human GRCh38 chr3: 160,046,258-160,352,225 , GRCh37.p13 chr3: 159,764,045-160,070,013 C3orf80, TRIM59-IFT80, 4 more genes
    nsv6736360copy number variation1nstd229human GRCh38 chr3: 160,226,163-160,226,619 , GRCh37.p13 chr3: 159,943,950-159,944,406 C3orf80, TRIM59-IFT80
    nsv6730530copy number variation1nstd229human GRCh38 chr3: 160,023,701-160,364,600 , GRCh37.p13 chr3: 159,741,488-160,082,388 BRD7P2, TRIM59-IFT80, 5 more genes
    nsv6725484copy number variation1nstd229human GRCh38 chr3: 160,223,356-160,225,732 , GRCh37.p13 chr3: 159,941,143-159,943,519 TRIM59-IFT80, C3orf80
    nsv6725212copy number variation1nstd229human GRCh38 chr3: 160,180,398-160,232,704 , GRCh37.p13 chr3: 159,898,185-159,950,491 C3orf80, IL12A-AS1, 1 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6562968inversion1nstd223human GRCh38 chr3: 160,046,654-160,345,667 , GRCh37.p13 chr3: 159,764,441-160,063,455 IFT80, C3orf80, 4 more genes
    nsv6368522copy number variation1nstd223human GRCh38 chr3: 160,223,801-160,226,500 , GRCh37.p13 chr3: 159,941,588-159,944,287 TRIM59-IFT80, C3orf80
    nsv6361438copy number variation1nstd223human GRCh38 chr3: 160,225,401-160,227,500 , GRCh37.p13 chr3: 159,943,188-159,945,287 TRIM59-IFT80, C3orf80
    nsv6313678copy number variation1nstd102humanPathogenic GRCh37 chr3: 145,486,960-160,504,834 , GRCh38.p12 chr3: 145,769,173-160,787,046 RNU6-901P, RPL32P8, 229 more genes
    nsv6313664copy number variation1nstd102humanUncertain significance GRCh37 chr3: 156,768,935-160,158,553 , GRCh38.p12 chr3: 157,051,146-160,440,765 LOC105374179, RPL15P6, 49 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 LOC102724145, C3orf80, 273 more genes
    nsv6135000copy number variation1nstd213human GRCh37 chr3: 159,670,000-159,970,001 , GRCh38.p12 chr3: 159,952,212-160,252,214 IL12A, C3orf80, 4 more genes
    nsv6134788copy number variation1nstd213human GRCh37 chr3: 155,010,000-169,630,001 , GRCh38.p12 chr3: 155,292,211-169,912,213 , BCHE, 171 more genes
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4912664copy number variation1nstd200human GRCh38 chr3: 160,200,111-160,248,020 , GRCh37.p13 chr3: 159,917,898-159,965,807 TRIM59-IFT80, IL12A-AS1, 1 more genes
    nsv4798217copy number variation1nstd200human GRCh37 chr3: 159,917,898-159,965,807 , GRCh38.p12 chr3: 160,200,111-160,248,020 C3orf80, IL12A-AS1, 1 more genes
    nsv4684209copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822 MTAPP1, PLS1, 339 more genes
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