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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965806insertion1nstd209human GRCh38 chr3: 138,272,408-138,272,408 , GRCh37.p13 chr3: 137,991,250-137,991,250 NME9, ARMC8
    nsv5906122copy number variation1nstd209human GRCh38 chr3: 138,264,758-138,264,812 , GRCh37.p13 chr3: 137,983,600-137,983,654 NME9, ARMC8
    nsv5890216copy number variation1nstd209human GRCh38 chr3: 138,309,589-138,310,427 , GRCh37.p13 chr3: 138,028,431-138,029,269 NME9
    nsv5889866copy number variation1nstd209human GRCh38 chr3: 137,097,814-139,588,879 , GRCh37.p13 chr3: 136,816,656-139,307,721 , LOC105374127, 42 more genes
    nsv5692750mobile element insertion1nstd211human GRCh38 chr3: 138,296,552-138,296,552 , GRCh37.p13 chr3: 138,015,394-138,015,394 NME9, ARMC8
    nsv5687639mobile element insertion2nstd211human GRCh38 chr3: 138,272,419-138,272,419 , GRCh37.p13 chr3: 137,991,261-137,991,261 ARMC8, NME9
    nsv5442118copy number variation1nstd206human GRCh38 chr3: 138,309,646-138,309,724 , GRCh37.p13 chr3: 138,028,488-138,028,566 NME9
    nsv5436421copy number variation1nstd206human GRCh38 chr3: 138,264,758-138,264,824 , GRCh37.p13 chr3: 137,983,600-137,983,666 NME9, ARMC8
    nsv5398422mobile element insertion1nstd206human GRCh38 chr3: 138,272,419-138,272,470 , GRCh37.p13 chr3: 137,991,261-137,991,312 ARMC8, NME9
    nsv5346577translocation1nstd200human GRCh38 chr3: 138,301,066-138,301,066 , GRCh38 chr3: 138,301,143-138,301,143 , GRCh37.p13 chr3: 138,019,985-138,019,985 , GRCh37.p13 chr3: 138,019,908-138,019,908 NME9
    nsv5346576translocation1nstd200human GRCh38 chr3: 138,264,758-138,264,758 , GRCh38 chr3: 138,264,824-138,264,824 , GRCh37.p13 chr3: 137,983,666-137,983,666 , GRCh37.p13 chr3: 137,983,600-137,983,600 ARMC8, NME9
    nsv5174861mobile element insertion1nstd203human GRCh38 chr3: 138,324,230-138,324,232 , GRCh37.p13 chr3: 138,043,072-138,043,074 NME9
    nsv5098687mobile element insertion1nstd203human GRCh38 chr3: 138,280,651-138,280,665 , GRCh37.p13 chr3: 137,999,493-137,999,507 NME9, ARMC8
    nsv5086823mobile element insertion1nstd203human GRCh38 chr3: 138,272,408-138,272,419 , GRCh37.p13 chr3: 137,991,250-137,991,261 NME9, ARMC8
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5034922inversion1nstd200human GRCh38 chr3: 137,979,992-148,451,901 , GRCh37.p13 chr3: 137,698,834-148,169,688 , LOC105374148, 132 more genes
    nsv4928007copy number variation1nstd200human GRCh38 chr3: 138,301,605-138,301,678 , GRCh37.p13 chr3: 138,020,447-138,020,520 NME9
    nsv4914801copy number variation1nstd200human GRCh38 chr3: 137,119,474-138,598,709 , GRCh37.p13 chr3: 136,838,316-138,317,551 , ESYT3, 18 more genes
    nsv4873274inversion1nstd200human GRCh37 chr3: 137,698,834-148,169,688 , GRCh38.p12 chr3: 137,979,992-148,451,901 , PLSCR5, 132 more genes
    nsv4791217copy number variation1nstd200human GRCh37 chr3: 138,044,534-138,045,481 , GRCh38.p12 chr3: 138,325,692-138,326,639 NME9
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