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Items: 1 to 20 of 419

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050977inversion1nstd229human GRCh38 chr4: 68,534,027-69,351,113 , GRCh37.p13 chr4: 69,399,745-70,216,831 LOC642496, LOC100422189, 28 more genes
    nsv6757416copy number variation1nstd229human GRCh38 chr4: 68,526,545-69,660,672 , GRCh37.p13 chr4: 69,392,263-70,526,390 UGT2B26P, UGT2B11, 37 more genes
    nsv6755453copy number variation1nstd229human GRCh38 chr4: 68,793,720-69,854,262 , GRCh37.p13 chr4: 69,659,438-70,719,980 SPOPLP1, UGT2B4, 33 more genes
    nsv6750865copy number variation1nstd229human GRCh38 chr4: 68,871,612-69,051,531 , GRCh37.p13 chr4: 69,737,330-69,917,249 UGT2B27P, LOC101930041, 9 more genes
    nsv6750831copy number variation1nstd229human GRCh38 chr4: 69,084,201-69,102,500 , GRCh37.p13 chr4: 69,949,919-69,968,218 UGT2B7
    nsv6749752copy number variation1nstd229human GRCh38 chr4: 68,786,846-69,797,610 , GRCh37.p13 chr4: 69,652,564-70,663,328 UGT2A2, UGT2B10, 33 more genes
    nsv6746832copy number variation1nstd229human GRCh38 chr4: 69,093,393-69,100,850 , GRCh37.p13 chr4: 69,959,111-69,966,568 UGT2B7
    nsv6746769copy number variation1nstd229human GRCh38 chr4: 69,087,431-73,565,096 , GRCh37.p13 chr4: 69,953,149-74,430,813 LOC642496, CSN2, 76 more genes
    nsv6744064copy number variation1nstd229human GRCh38 chr4: 69,017,001-69,058,200 , GRCh37.p13 chr4: 69,882,719-69,923,918 LOC100422020, UGT2B26P, 3 more genes
    nsv6743815copy number variation1nstd229human GRCh38 chr4: 69,048,761-69,049,365 , GRCh37.p13 chr4: 69,914,479-69,915,083 UGT2B7, LOC105377265
    nsv6743415copy number variation1nstd229human GRCh38 chr4: 69,065,952-69,132,094 , GRCh37.p13 chr4: 69,931,670-69,997,812 SPOPLP1, UGT2B7
    nsv6741500copy number variation1nstd229human GRCh38 chr4: 69,006,990-69,113,555 , GRCh37.p13 chr4: 69,872,708-69,979,273 LOC100422020, UGT2B27P, 3 more genes
    nsv6740885copy number variation1nstd229human GRCh38 chr4: 69,096,159-69,106,600 , GRCh37.p13 chr4: 69,961,877-69,972,318 UGT2B7
    nsv6740485copy number variation1nstd229human GRCh38 chr4: 69,086,574-69,090,867 , GRCh37.p13 chr4: 69,952,292-69,956,585 UGT2B7
    nsv6738588copy number variation1nstd229human GRCh38 chr4: 69,091,504-69,094,736 , GRCh37.p13 chr4: 69,957,222-69,960,454 UGT2B7
    nsv6636557copy number variation1nstd102humanUncertain significance GRCh37 chr4: 69,661,413-70,724,847 , GRCh38.p12 chr4: 68,795,695-69,859,129 LOC100422029, LOC100422189, 33 more genes
    nsv6629723copy number variation1nstd224human GRCh37 chr4: 69,681,746-69,974,041 , GRCh38.p12 chr4: 68,816,028-69,108,323 UGT2B26P, UGT2A3, 10 more genes
    nsv6569098inversion1nstd223human GRCh38 chr4: 68,883,875-69,126,466 , GRCh37.p13 chr4: 69,749,593-69,992,184 LOC101927264, UGT2B7, 10 more genes
    nsv6565370inversion1nstd223human GRCh38 chr4: 68,996,961-69,126,451 , GRCh37.p13 chr4: 69,862,679-69,992,169 UGT2B7, UGT2B27P, 5 more genes
    nsv6395077copy number variation1nstd223human GRCh38 chr4: 69,109,497-69,109,993 , GRCh37.p13 chr4: 69,975,215-69,975,711 UGT2B7
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