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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112746copy number variation1nstd102humanPathogenic GRCh37 chr4: 107,092,252-107,092,427 , GRCh38.p12 chr4: 106,171,095-106,171,270 TBCK
    nsv5976348inversion1nstd209human GRCh38 chr4: 103,823,749-108,603,414 , GRCh37.p13 chr4: 104,744,906-109,524,570 , HADH, 54 more genes
    nsv5906482copy number variation1nstd209human GRCh38 chr4: 106,100,046-106,100,147 , GRCh37.p13 chr4: 107,021,203-107,021,304 TBCK
    nsv5902011copy number variation1nstd209human GRCh38 chr4: 106,299,142-106,345,993 , GRCh37.p13 chr4: 107,220,299-107,267,150 AIMP1, TBCK
    nsv5898161copy number variation1nstd209human GRCh38 chr4: 106,055,754-106,055,806 , GRCh37.p13 chr4: 106,976,911-106,976,963 TBCK
    nsv5894484copy number variation1nstd209human GRCh38 chr4: 106,154,582-106,154,712 , GRCh37.p13 chr4: 107,075,739-107,075,869 TBCK
    nsv5892305copy number variation1nstd209human GRCh38 chr4: 106,108,348-106,108,863 , GRCh37.p13 chr4: 107,029,505-107,030,020 TBCK
    nsv5891629copy number variation1nstd209human GRCh38 chr4: 106,179,386-106,179,461 , GRCh37.p13 chr4: 107,100,543-107,100,618 TBCK
    nsv5889648copy number variation1nstd209human GRCh38 chr4: 106,135,421-106,142,204 , GRCh37.p13 chr4: 107,056,578-107,063,361 TBCK
    nsv5837550copy number variation1nstd209human GRCh38 chr4: 106,299,179-106,320,620 , GRCh37.p13 chr4: 107,220,336-107,241,777 TBCK, AIMP1
    nsv5837276copy number variation1nstd209human GRCh38 chr4: 106,135,385-106,142,175 , GRCh37.p13 chr4: 107,056,542-107,063,332 TBCK
    nsv5724194mobile element insertion2nstd211human GRCh38 chr4: 106,173,862-106,173,862 , GRCh37.p13 chr4: 107,095,019-107,095,019 TBCK
    nsv5690148mobile element insertion2nstd211human GRCh38 chr4: 106,227,397-106,227,397 , GRCh37.p13 chr4: 107,148,554-107,148,554 TBCK
    nsv5685707mobile element insertion1nstd211human GRCh38 chr4: 106,195,207-106,195,207 , GRCh37.p13 chr4: 107,116,364-107,116,364 TBCK
    nsv5673738copy number variation1nstd102humanPathogenic GRCh37 chr4: 107,092,232-107,092,447 , GRCh38.p12 chr4: 106,171,075-106,171,290 TBCK
    nsv5623614insertion1nstd207human GRCh38 chr4: 106,227,380-106,227,380 , GRCh37.p13 chr4: 107,148,537-107,148,537 TBCK
    nsv5621584insertion1nstd207human GRCh38 chr4: 106,108,348-106,108,348 , GRCh37.p13 chr4: 107,029,505-107,029,505 TBCK
    nsv5621352insertion1nstd207human GRCh38 chr4: 106,173,846-106,173,846 , GRCh37.p13 chr4: 107,095,003-107,095,003 TBCK
    nsv5568061copy number variation1nstd207human GRCh38 chr4: 106,135,421-106,142,203 , GRCh37.p13 chr4: 107,056,578-107,063,360 TBCK
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
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