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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5694189mobile element insertion2nstd211human GRCh38 chr3: 148,715,276-148,715,276 , GRCh37.p13 chr3: 148,433,063-148,433,063 AGTR1
    nsv5676766mobile element insertion1nstd211human GRCh38 chr3: 148,726,650-148,726,650 , GRCh37.p13 chr3: 148,444,437-148,444,437 AGTR1
    nsv5437560copy number variation1nstd206human GRCh38 chr3: 148,696,328-148,696,546 , GRCh37.p13 chr3: 148,414,115-148,414,333 RPL38P1, AGTR1
    nsv5411034mobile element insertion1nstd206human GRCh38 chr3: 148,715,276-148,715,327 , GRCh37.p13 chr3: 148,433,063-148,433,114 AGTR1
    nsv5410348mobile element insertion1nstd206human GRCh38 chr3: 148,726,650-148,726,701 , GRCh37.p13 chr3: 148,444,437-148,444,488 AGTR1
    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
    nsv5082505mobile element insertion1nstd203human GRCh38 chr3: 148,715,267-148,715,276 , GRCh37.p13 chr3: 148,433,054-148,433,063 AGTR1
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4912301copy number variation1nstd200human GRCh38 chr3: 148,735,268-148,736,234 , GRCh37.p13 chr3: 148,453,055-148,454,021 AGTR1
    nsv4912300copy number variation1nstd200human GRCh38 chr3: 148,700,422-148,708,297 , GRCh37.p13 chr3: 148,418,209-148,426,084 AGTR1
    nsv4707959copy number variation1nstd195human GRCh37 chr3: 148,410,551-148,498,501 , GRCh38.p12 chr3: 148,692,764-148,780,714 AGTR1, RPL38P1
    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
    nsv4469514mobile element insertion1nstd166human GRCh37.p13 chr3: 148,433,054-148,433,054 , GRCh38.p12 chr3: 148,715,267-148,715,267 AGTR1
    nsv4468792mobile element insertion1nstd166human GRCh37.p13 chr3: 148,458,974-148,458,974 , GRCh38.p12 chr3: 148,741,187-148,741,187 AGTR1
    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
    nsv4107825copy number variation1nstd166human GRCh37.p13 chr3: 147,929,985-148,495,809 , GRCh38.p12 chr3: 148,212,198-148,778,022 AGTR1, RPL38P1, 5 more genes
    nsv3958871copy number variation1nstd168human GRCh38 chr3: 148,702,964-148,731,785 , GRCh37.p13 chr3: 148,420,751-148,449,572 AGTR1
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