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Items: 1 to 20 of 477

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963801insertion1nstd209human GRCh38 chr6: 55,143,121-55,143,121 , GRCh37.p13 chr6: 55,007,919-55,007,919 HCRTR2
    nsv5961421insertion1nstd209human GRCh38 chr6: 55,241,861-55,241,861 , GRCh37.p13 chr6: 55,106,659-55,106,659 HCRTR2
    nsv5903350copy number variation1nstd209human GRCh38 chr6: 55,153,737-55,165,793 , GRCh37.p13 chr6: 55,018,535-55,030,591 HCRTR2
    nsv5900906copy number variation1nstd209human GRCh38 chr6: 55,129,683-55,129,787 , GRCh37.p13 chr6: 54,994,481-54,994,585 HCRTR2
    nsv5896523copy number variation1nstd209human GRCh38 chr6: 55,142,506-55,143,120 , GRCh37.p13 chr6: 55,007,304-55,007,918 HCRTR2
    nsv5889944copy number variation1nstd209human GRCh38 chr6: 55,147,890-55,148,025 , GRCh37.p13 chr6: 55,012,688-55,012,823 HCRTR2
    nsv5845552copy number variation1nstd209human GRCh38 chr6: 55,154,163-55,164,961 , GRCh37.p13 chr6: 55,018,961-55,029,759 HCRTR2
    nsv5716132mobile element insertion1nstd211human GRCh38 chr6: 55,241,884-55,241,884 , GRCh37.p13 chr6: 55,106,682-55,106,682 HCRTR2
    nsv5689742mobile element insertion1nstd211human GRCh38 chr6: 55,151,186-55,151,186 , GRCh37.p13 chr6: 55,015,984-55,015,984 HCRTR2
    nsv5685101mobile element insertion2nstd211human GRCh38 chr6: 55,143,130-55,143,130 , GRCh37.p13 chr6: 55,007,928-55,007,928 HCRTR2
    nsv5685017mobile element insertion1nstd211human GRCh38 chr6: 55,104,839-55,104,839 , GRCh37.p13 chr6: 54,969,637-54,969,637 HCRTR2
    nsv5684424mobile element insertion1nstd211human GRCh38 chr6: 55,131,629-55,131,629 , GRCh37.p13 chr6: 54,996,427-54,996,427 HCRTR2
    nsv5640266insertion1nstd207human GRCh38 chr6: 55,143,121-55,143,121 , GRCh37.p13 chr6: 55,007,919-55,007,919 HCRTR2
    nsv5626886insertion2nstd207human GRCh38 chr6: 55,274,255-55,274,255 , GRCh37.p13 chr6: 55,139,053-55,139,053 HCRTR2
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5549832insertion1nstd206human GRCh38 chr6: 55,143,121-55,143,121 , GRCh37.p13 chr6: 55,007,919-55,007,919 HCRTR2
    nsv5466898copy number variation1nstd206human GRCh38 chr6: 55,169,974-55,170,047 , GRCh37.p13 chr6: 55,034,772-55,034,845 HCRTR2
    nsv5466754copy number variation1nstd206human GRCh38 chr6: 55,177,912-55,178,094 , GRCh37.p13 chr6: 55,042,710-55,042,892 HCRTR2
    nsv5461225copy number variation1nstd206human GRCh38 chr6: 55,122,142-55,122,412 , GRCh37.p13 chr6: 54,986,940-54,987,210 HCRTR2
    nsv5459265copy number variation1nstd206human GRCh38 chr6: 55,153,697-55,165,837 , GRCh37.p13 chr6: 55,018,495-55,030,635 HCRTR2
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