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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112755copy number variation1nstd102humanPathogenic GRCh37 chr12: 65,251,705-75,263,379 , GRCh38.p12 chr12: 64,857,925-74,869,599 LINC02421, TBC1D15, 144 more genes
    nsv5945054copy number variation1nstd209human GRCh38 chr12: 68,661,013-68,661,196 , GRCh37.p13 chr12: 69,054,793-69,054,976 RAP1B
    nsv5936222copy number variation1nstd209human GRCh38 chr12: 68,612,755-68,612,822 , GRCh37.p13 chr12: 69,006,535-69,006,602 RAP1B
    nsv5936066copy number variation1nstd209human GRCh38 chr12: 68,628,597-68,639,398 , GRCh37.p13 chr12: 69,022,377-69,033,178 RAP1B
    nsv5867158copy number variation2nstd209human GRCh38 chr12: 68,636,087-68,638,746 , GRCh37.p13 chr12: 69,029,867-69,032,526 RAP1B
    nsv5860437copy number variation2nstd209human GRCh38 chr12: 68,628,478-68,633,986 , GRCh37.p13 chr12: 69,022,258-69,027,766 RAP1B
    nsv5855565copy number variation1nstd209human GRCh38 chr12: 68,628,628-68,639,446 , GRCh37.p13 chr12: 69,022,408-69,033,226 RAP1B
    nsv5712485mobile element insertion1nstd211human GRCh38 chr12: 68,643,623-68,643,623 , GRCh37.p13 chr12: 69,037,403-69,037,403 RAP1B
    nsv5556951sequence alteration1nstd206human GRCh38 chr12: 68,612,001-69,442,414 , GRCh37.p13 chr12: 69,005,781-69,836,194 , LYZ, 22 more genes
    nsv5509396copy number variation1nstd206human GRCh38 chr12: 68,655,651-68,655,706 , GRCh37.p13 chr12: 69,049,431-69,049,486 RAP1B
    nsv5505970copy number variation1nstd206human GRCh38 chr12: 68,657,828-68,657,912 , GRCh37.p13 chr12: 69,051,608-69,051,692 RAP1B
    nsv5504945copy number variation1nstd206human GRCh38 chr12: 68,628,598-68,639,399 , GRCh37.p13 chr12: 69,022,378-69,033,179 RAP1B
    nsv5501141copy number variation1nstd206human GRCh38 chr12: 68,657,735-68,657,880 , GRCh37.p13 chr12: 69,051,515-69,051,660 RAP1B
    nsv5499351copy number variation1nstd206human GRCh38 chr12: 68,611,950-68,624,128 , GRCh37.p13 chr12: 69,005,730-69,017,908 RAP1B
    nsv5419173mobile element insertion1nstd206human GRCh38 chr12: 68,643,623-68,643,674 , GRCh37.p13 chr12: 69,037,403-69,037,454 RAP1B
    nsv5365099translocation1nstd200human GRCh38 chr12: 69,442,390-69,442,390 , GRCh38 chr12: 68,623,271-68,623,271 , GRCh37.p13 chr12: 69,017,051-69,017,051 , GRCh37.p13 chr12: 69,836,170-69,836,170 RAP1B
    nsv5365098translocation1nstd200human GRCh38 chr12: 68,612,002-68,612,002 , GRCh38 chr12: 69,442,415-69,442,415 , GRCh37.p13 chr12: 69,836,195-69,836,195 , GRCh37.p13 chr12: 69,005,782-69,005,782 RAP1B
    nsv5356059translocation1nstd200human GRCh38 chr12: 68,628,598-68,628,598 , GRCh38 chr12: 68,639,399-68,639,399 , GRCh37.p13 chr12: 69,033,179-69,033,179 , GRCh37.p13 chr12: 69,022,378-69,022,378 RAP1B
    nsv5356058translocation1nstd200human GRCh38 chr12: 68,625,282-68,625,282 , GRCh38 chr12: 68,625,175-68,625,175 , GRCh37.p13 chr12: 69,019,062-69,019,062 , GRCh37.p13 chr12: 69,018,955-69,018,955 RAP1B, RPL10P12, 1 more genes
    nsv5340620translocation1nstd200human GRCh37 chr12: 69,017,051-69,017,051 , GRCh37 chr12: 69,836,170-69,836,170 , GRCh38.p12 chr12: 69,442,390-69,442,390 , GRCh38.p12 chr12: 68,623,271-68,623,271 RAP1B
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