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Items: 1 to 20 of 336

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966583insertion1nstd209human GRCh38 chr2: 157,594,409-157,594,409 , GRCh37.p13 chr2: 158,450,921-158,450,921 ACVR1C
    nsv5960910insertion1nstd209human GRCh38 chr2: 157,554,282-157,554,282 , GRCh37.p13 chr2: 158,410,794-158,410,794 ACVR1C
    nsv5901676copy number variation1nstd209human GRCh38 chr2: 157,576,825-157,577,153 , GRCh37.p13 chr2: 158,433,337-158,433,665 ACVR1C
    nsv5831678copy number variation1nstd209human GRCh38 chr2: 157,615,757-157,617,716 , GRCh37.p13 chr2: 158,472,269-158,474,228 ACVR1C
    nsv5831375copy number variation1nstd209human GRCh38 chr2: 157,604,857-157,608,356 , GRCh37.p13 chr2: 158,461,369-158,464,868 ACVR1C
    nsv5692444mobile element insertion2nstd211human GRCh38 chr2: 157,600,993-157,600,993 , GRCh37.p13 chr2: 158,457,505-158,457,505 ACVR1C
    nsv5675639mobile element insertion2nstd211human GRCh38 chr2: 157,594,424-157,594,424 , GRCh37.p13 chr2: 158,450,936-158,450,936 ACVR1C
    nsv5623700insertion1nstd207human GRCh38 chr2: 157,594,409-157,594,409 , GRCh37.p13 chr2: 158,450,921-158,450,921 ACVR1C
    nsv5614386insertion1nstd207human GRCh38 chr2: 157,554,195-157,554,195 , GRCh37.p13 chr2: 158,410,707-158,410,707 ACVR1C
    nsv5578747copy number variation1nstd207human GRCh38 chr2: 157,576,825-157,577,153 , GRCh37.p13 chr2: 158,433,337-158,433,665 ACVR1C
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5449935copy number variation1nstd206human GRCh38 chr2: 157,628,880-157,628,964 , GRCh37.p13 chr2: 158,485,392-158,485,476 ACVR1C
    nsv5445423copy number variation1nstd206human GRCh38 chr2: 157,586,074-157,586,157 , GRCh37.p13 chr2: 158,442,586-158,442,669 ACVR1C
    nsv5439502copy number variation1nstd206human GRCh38 chr2: 157,576,837-157,577,154 , GRCh37.p13 chr2: 158,433,349-158,433,666 ACVR1C
    nsv5434730copy number variation1nstd206human GRCh38 chr2: 148,693,148-164,933,481 , GRCh37.p13 chr2: 149,450,717-165,789,991 , RBM43, 205 more genes
    nsv5408275mobile element insertion1nstd206human GRCh38 chr2: 157,594,424-157,594,475 , GRCh37.p13 chr2: 158,450,936-158,450,987 ACVR1C
    nsv5397974mobile element insertion1nstd206human GRCh38 chr2: 157,600,993-157,601,044 , GRCh37.p13 chr2: 158,457,505-158,457,556 ACVR1C
    nsv5385066mobile element deletion2nstd186human GRCh37 chr2: 158,433,349-158,433,666 , GRCh38.p12 chr2: 157,576,837-157,577,154 ACVR1C
    nsv5350899translocation1nstd200human GRCh38 chr2: 157,586,157-157,586,157 , GRCh38 chr2: 157,586,074-157,586,074 , GRCh37.p13 chr2: 158,442,586-158,442,586 , GRCh37.p13 chr2: 158,442,669-158,442,669 ACVR1C
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