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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5301803copy number variation1nstd204human GRCh38.p13 chr3: 145,088,231-147,513,312 , GRCh37.p13 chr3: 144,806,005-147,231,099 LINC02010, ZIC1, 21 more genes
    nsv5035456inversion1nstd200human GRCh37.p13 chr3: 146,894,109-147,607,447 , GRCh38 chr3: 147,176,322-147,889,660 ZIC1, ZIC4, 4 more genes
    nsv5034922inversion1nstd200human GRCh38 chr3: 137,979,992-148,451,901 , GRCh37.p13 chr3: 137,698,834-148,169,688 , LOC105374148, 132 more genes
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4873274inversion1nstd200human GRCh37 chr3: 137,698,834-148,169,688 , GRCh38.p12 chr3: 137,979,992-148,451,901 , PLSCR5, 132 more genes
    nsv4791387copy number variation1nstd200human GRCh37 chr3: 144,806,010-147,231,090 , GRCh38.p12 chr3: 145,088,236-147,513,303 RPL21P71, PLSCR2, 21 more genes
    nsv4707761copy number variation1nstd195human GRCh37 chr3: 147,035,501-147,311,651 , GRCh38.p12 chr3: 147,317,714-147,593,864 ZIC1, ZIC4, 2 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
    nsv4674717copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 144,053,029-150,272,658 , GRCh38.p12 chr3: 144,334,187-150,554,871 AGTR1, CP, 83 more genes
    nsv4673998copy number variation1nstd102humanUncertain significance GRCh37 chr3: 142,909,055-147,190,850 , GRCh38.p12 chr3: 143,190,213-147,473,063 GAPDHP47, RNA5SP144, 32 more genes
    nsv4454501copy number variation1nstd102humanUncertain significance GRCh37 chr3: 146,996,270-148,622,676 , GRCh38.p12 chr3: 147,278,483-148,904,889 CPB1, NPM1P28, 15 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4327115inversion1nstd166human GRCh37.p13 chr3: 131,882,701-162,233,318 , GRCh38.p12 chr3: 132,163,857-162,515,530 , ATP1B3, 446 more genes
    nsv4101285copy number variation1nstd166human GRCh37.p13 chr3: 146,531,191-147,890,638 , GRCh38.p12 chr3: 146,813,404-148,172,851 NPM1P28, LINC02032, 9 more genes
    nsv4095291copy number variation1nstd166human GRCh37.p13 chr3: 147,109,936-147,110,001 , GRCh38.p12 chr3: 147,392,149-147,392,214 ZIC4
    nsv3920790copy number variation1nstd102humanPathogenic GRCh38 chr3: 134,257,180-149,729,538 , NCBI36 chr3: 135,458,712-150,930,015 , GRCh37 chr3: 133,976,022-149,447,325 TFDP2, RPL7L1P7, 203 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 LINC02614, LINC02054, 1469 more genes
    nsv3910200copy number variation1nstd102humanPathogenic GRCh38 chr3: 141,751,960-148,246,189 , GRCh37 chr3: 141,470,802-147,963,976 , NCBI36 chr3: 142,953,492-149,446,666 LNCSRLR, LOC105374143, 70 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
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