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Items: 1 to 20 of 116

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5909034copy number variation1nstd209human GRCh38 chr10: 97,440,959-97,483,202 , GRCh37.p13 chr10: 99,200,716-99,242,959 EXOSC1, MMS19, 1 more genes
    nsv5851103copy number variation1nstd209human GRCh38 chr10: 97,441,026-97,459,470 , GRCh37.p13 chr10: 99,200,783-99,219,227 EXOSC1, MMS19, 1 more genes
    nsv5478096copy number variation1nstd206human GRCh38 chr10: 97,437,504-97,437,612 , GRCh37.p13 chr10: 99,197,261-99,197,369 EXOSC1
    nsv5477723copy number variation1nstd206human GRCh38 chr10: 97,428,986-97,444,278 , GRCh37.p13 chr10: 99,188,743-99,204,035 ZDHHC16, PGAM1, 1 more genes
    nsv5365052translocation1nstd200human GRCh38 chr10: 97,437,545-97,437,545 , GRCh38 chr10: 97,437,472-97,437,472 , GRCh37.p13 chr10: 99,197,229-99,197,229 , GRCh37.p13 chr10: 99,197,302-99,197,302 EXOSC1
    nsv5315504copy number variation1nstd204human GRCh38.p13 chr10: 97,439,784-97,441,998 , GRCh37.p13 chr10: 99,199,541-99,201,755 EXOSC1
    nsv5314709copy number variation1nstd204human GRCh37.p13 chr10: 99,177,371-99,269,971 , GRCh38.p13 chr10: 97,417,614-97,510,214 PGAM1, EXOSC1, 4 more genes
    nsv5259980copy number variation1nstd204human GRCh38.p13 chr10: 97,439,226-97,446,524 , GRCh37.p13 chr10: 99,198,983-99,206,281 ZDHHC16, EXOSC1
    nsv5254809copy number variation1nstd204human GRCh37.p13 chr10: 99,177,558-99,269,657 , GRCh38.p13 chr10: 97,417,801-97,509,900 PGAM1, EXOSC1, 4 more genes
    nsv5252284copy number variation1nstd204human GRCh38.p13 chr10: 97,420,016-97,459,857 , GRCh37.p13 chr10: 99,179,773-99,219,614 EXOSC1, PGAM1, 3 more genes
    nsv4986861copy number variation1nstd200human GRCh38 chr10: 97,438,772-97,441,503 , GRCh37.p13 chr10: 99,198,529-99,201,260 EXOSC1
    nsv4973948copy number variation1nstd200human GRCh38 chr10: 97,440,085-97,441,758 , GRCh37.p13 chr10: 99,199,842-99,201,515 EXOSC1
    nsv4973947copy number variation1nstd200human GRCh38 chr10: 97,438,896-97,440,327 , GRCh37.p13 chr10: 99,198,653-99,200,084 EXOSC1
    nsv4831580copy number variation1nstd200human GRCh37 chr10: 99,197,228-99,197,302 , GRCh38.p12 chr10: 97,437,471-97,437,545 EXOSC1
    nsv4618034copy number variation1nstd183human GRCh37 chr10: 99,205,703-99,205,892 , GRCh38.p12 chr10: 97,445,946-97,446,135 EXOSC1, ZDHHC16
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4325673inversion1nstd166human GRCh37.p13 chr10: 92,228,734-107,785,320 , GRCh38.p12 chr10: 90,468,977-106,025,562 , COX15, 323 more genes
    nsv4189712copy number variation1nstd166human GRCh37.p13 chr10: 99,197,261-99,197,369 , GRCh38.p12 chr10: 97,437,504-97,437,612 EXOSC1
    nsv4179147copy number variation1nstd166human GRCh37.p13 chr10: 99,199,922-99,201,488 , GRCh38.p12 chr10: 97,440,165-97,441,731 EXOSC1
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