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Items: 1 to 20 of 194

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5720638mobile element insertion1nstd211human GRCh38 chr9: 74,980,907-74,980,907 , GRCh37.p13 chr9: 77,595,823-77,595,823 CARNMT1-AS1, CARNMT1
    nsv5562696mobile element insertion1nstd206human GRCh38 chr9: 74,980,907-74,980,958 , GRCh37.p13 chr9: 77,595,823-77,595,874 CARNMT1-AS1, CARNMT1
    nsv5490858copy number variation1nstd206human GRCh38 chr9: 75,021,522-75,021,590 , GRCh37.p13 chr9: 77,636,438-77,636,506 CARNMT1
    nsv5478533copy number variation1nstd206human GRCh38 chr9: 75,018,269-75,023,443 , GRCh37.p13 chr9: 77,633,185-77,638,359 CARNMT1
    nsv5372598translocation1nstd200human GRCh38 chr22: 40,500,318-40,500,318 , GRCh38 chr9: 75,005,361-75,005,361 , GRCh37.p13 chr9: 77,620,277-77,620,277 , GRCh37.p13 chr22: 40,896,322-40,896,322 CARNMT1, MRTFA
    nsv5372597translocation1nstd200human GRCh38 chr9: 75,003,939-75,003,939 , GRCh38 chr9: 75,004,466-75,004,466 , GRCh37.p13 chr9: 77,619,382-77,619,382 , GRCh37.p13 chr9: 77,618,855-77,618,855 CARNMT1
    nsv5372596translocation1nstd200human GRCh38 chr9: 74,980,837-74,980,837 , GRCh38 chr9: 74,980,946-74,980,946 , GRCh37.p13 chr9: 77,595,753-77,595,753 , GRCh37.p13 chr9: 77,595,862-77,595,862 CARNMT1-AS1, CARNMT1
    nsv5122390mobile element insertion1nstd203human GRCh38 chr9: 74,988,524-74,988,539 , GRCh37.p13 chr9: 77,603,440-77,603,455 CARNMT1, CARNMT1-AS1
    nsv4968433copy number variation1nstd200human GRCh38 chr9: 75,024,929-75,026,497 , GRCh37.p13 chr9: 77,639,845-77,641,413 CARNMT1
    nsv4968432copy number variation1nstd200human GRCh38 chr9: 75,014,218-75,015,412 , GRCh37.p13 chr9: 77,629,134-77,630,328 CARNMT1
    nsv4954843copy number variation1nstd200human GRCh38 chr9: 74,965,822-74,980,291 , GRCh37.p13 chr9: 77,580,738-77,595,207 CARNMT1, CARNMT1-AS1
    nsv4954839copy number variation1nstd200human GRCh38 chr9: 74,637,212-74,987,883 , GRCh37.p13 chr9: 77,252,128-77,602,799 RN7SKP47, C9orf40, 9 more genes
    nsv4814093copy number variation1nstd200human GRCh37 chr9: 77,633,185-77,638,359 , GRCh38.p12 chr9: 75,018,269-75,023,443 CARNMT1
    nsv4751627insertion1nstd199human GRCh37 chr9: 77,616,133-77,616,133 , GRCh38.p12 chr9: 75,001,217-75,001,217 CARNMT1
    nsv4599663copy number variation1nstd183human GRCh37 chr9: 77,624,952-77,628,393 , GRCh38.p12 chr9: 75,010,036-75,013,477 CARNMT1
    nsv4487603mobile element insertion1nstd166human GRCh37.p13 chr9: 77,615,564-77,615,564 , GRCh38.p12 chr9: 75,000,648-75,000,648 CARNMT1
    nsv4487258mobile element insertion1nstd166human GRCh37.p13 chr9: 77,603,440-77,603,440 , GRCh38.p12 chr9: 74,988,524-74,988,524 CARNMT1-AS1, CARNMT1
    nsv4486386mobile element insertion1nstd166human GRCh37.p13 chr9: 77,615,180-77,615,180 , GRCh38.p12 chr9: 75,000,264-75,000,264 CARNMT1
    nsv4479305mobile element insertion1nstd166human GRCh37.p13 chr9: 77,616,128-77,616,128 , GRCh38.p12 chr9: 75,001,212-75,001,212 CARNMT1
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
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