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Items: 1 to 20 of 221

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146289insertion1nstd232human GRCh37.p13 chr12: 50,399,176-50,399,176 , GRCh38.p12 chr12: 50,005,393-50,005,393 RACGAP1
    nsv7058974inversion1nstd229human GRCh38 chr12: 50,026,609-50,026,896 , GRCh37.p13 chr12: 50,420,392-50,420,679 RACGAP1
    nsv6934588copy number variation1nstd229human GRCh38 chr12: 50,013,048-50,351,036 , GRCh37.p13 chr12: 50,406,831-50,744,819 FAM186A, RACGAP1, 10 more genes
    nsv6932975copy number variation1nstd229human GRCh38 chr12: 50,019,490-50,024,927 , GRCh37.p13 chr12: 50,413,273-50,418,710 RACGAP1
    nsv6930454copy number variation1nstd229human GRCh38 chr12: 50,019,727-50,020,419 , GRCh37.p13 chr12: 50,413,510-50,414,202 RACGAP1
    nsv6926225copy number variation1nstd229human GRCh38 chr12: 49,806,728-50,041,233 , GRCh37.p13 chr12: 50,200,511-50,435,016 RACGAP1, AQP5, 13 more genes
    nsv6926021copy number variation1nstd229human GRCh38 chr12: 50,019,726-50,020,540 , GRCh37.p13 chr12: 50,413,509-50,414,323 RACGAP1
    nsv6924798copy number variation1nstd229human GRCh38 chr12: 50,014,948-50,015,270 , GRCh37.p13 chr12: 50,408,731-50,409,053 RACGAP1
    nsv6921841copy number variation1nstd229human GRCh38 chr12: 49,987,774-49,994,011 , GRCh37.p13 chr12: 50,381,557-50,387,794 RACGAP1
    nsv6634466copy number variation1nstd102humanUncertain significance GRCh37 chr12: 50,331,947-50,439,383 , GRCh38.p12 chr12: 49,938,164-50,045,600 LOC105369763, AQP5-AS1, 5 more genes
    nsv6621706copy number variation1nstd224human GRCh37 chr12: 50,366,997-50,537,839 , GRCh38.p12 chr12: 49,973,214-50,144,056 ASIC1, AQP6, 6 more genes
    nsv6577224inversion1nstd223human GRCh38 chr12: 50,010,359-50,010,899 , GRCh37.p13 chr12: 50,404,142-50,404,682 RACGAP1
    nsv6465747copy number variation1nstd223human GRCh38 chr12: 50,024,062-50,029,217 , GRCh37.p13 chr12: 50,417,845-50,423,000 RACGAP1
    nsv6307893mobile element insertion1nstd186human GRCh37 chr12: 50,401,350-50,401,386 , GRCh38.p12 chr12: 50,007,567-50,007,603 RACGAP1
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132250copy number variation1nstd213human GRCh37 chr12: 49,440,000-51,850,001 , GRCh38.p12 chr12: 49,046,217-51,456,217 DAZAP2, KCNH3, 83 more genes
    nsv6023536copy number variation1nstd212human GRCh38 chr12: 50,030,846-50,030,931 , GRCh37.p13 chr12: 50,424,629-50,424,714 RACGAP1
    nsv5969493inversion1nstd209human GRCh38 chr12: 50,026,611-50,026,899 , GRCh37.p13 chr12: 50,420,394-50,420,682 RACGAP1
    nsv5932051copy number variation1nstd209human GRCh38 chr12: 49,993,633-49,993,928 , GRCh37.p13 chr12: 50,387,416-50,387,711 RACGAP1
    nsv5724709mobile element insertion1nstd211human GRCh38 chr12: 50,007,552-50,007,552 , GRCh37.p13 chr12: 50,401,335-50,401,335 RACGAP1
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