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Items: 1 to 20 of 232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143068insertion1nstd232human GRCh37.p13 chr17: 79,817,265-79,817,265 , GRCh38.p12 chr17: 81,859,389-81,859,389 P4HB
    nsv7139036insertion1nstd232human GRCh37.p13 chr17: 79,801,968-79,801,968 , GRCh38.p12 chr17: 81,844,092-81,844,092 P4HB
    nsv7098715copy number variation1nstd102humanPathogenic GRCh37 chr17: 79,539,041-81,052,322 , GRCh38.p12 chr17: 81,572,015-83,094,577 LOC105371939, LINC01970, 65 more genes
    nsv7095371copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,618,104-79,894,690 , GRCh38.p12 chr17: 81,651,074-81,936,814 CCDC137, PPP1R27, 21 more genes
    nsv7095370copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,477,716-80,900,339 , GRCh38.p12 chr17: 81,510,690-82,942,463 MIR6787, TBCD, 67 more genes
    nsv7071296inversion1nstd229human GRCh38 chr17: 79,045,634-82,531,412 , GRCh37.p13 chr17: 77,041,716-80,489,288 , ENPP7, 111 more genes
    nsv6995242copy number variation1nstd229human GRCh38 chr17: 81,840,925-81,846,199 , GRCh37.p13 chr17: 79,798,801-79,804,075 P4HB
    nsv6986582copy number variation1nstd229human GRCh38 chr17: 81,847,348-81,859,180 , GRCh37.p13 chr17: 79,805,224-79,817,056 P4HB
    nsv6985626copy number variation1nstd229human GRCh38 chr17: 81,847,342-81,855,141 , GRCh37.p13 chr17: 79,805,218-79,813,017 P4HB
    nsv6983067copy number variation1nstd229human GRCh38 chr17: 81,836,367-81,841,925 , GRCh37.p13 chr17: 79,794,243-79,799,801 P4HB
    nsv6981723copy number variation1nstd229human GRCh38 chr17: 81,855,588-81,859,179 , GRCh37.p13 chr17: 79,813,464-79,817,055 P4HB
    nsv6525507copy number variation1nstd223human GRCh38 chr17: 81,799,201-82,693,800 , GRCh37.p13 chr17: 79,759,050-80,651,676 CENPX, RFNG, 47 more genes
    nsv6315182copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323 DUS1L, PVALEF, 252 more genes
    nsv6310342copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,801,888-79,805,243 , GRCh38.p12 chr17: 81,844,012-81,847,367 P4HB
    nsv6133323copy number variation1nstd213human GRCh37 chr17: 78,760,000-81,195,210 , GRCh38.p12 chr17: 80,786,200-83,247,441 , ACTG1, 100 more genes
    nsv5729324mobile element insertion1nstd211human GRCh38 chr17: 81,848,573-81,848,573 , GRCh37.p13 chr17: 79,806,449-79,806,449 P4HB
    nsv5719653mobile element insertion1nstd211human GRCh38 chr17: 81,848,588-81,848,588 , GRCh37.p13 chr17: 79,806,464-79,806,464 P4HB
    nsv5528091copy number variation1nstd206human GRCh38 chr17: 81,849,376-81,853,454 , GRCh37.p13 chr17: 79,807,252-79,811,330 P4HB
    nsv5320535translocation1nstd204human GRCh38.p13 chr17: 81,841,126-81,841,126 , GRCh38.p13 chr17: 81,841,560-81,841,560 , GRCh37.p13 chr17: 79,799,002-79,799,002 , GRCh37.p13 chr17: 79,799,436-79,799,436 P4HB
    nsv5298108copy number variation1nstd204human GRCh38.p13 chr17: 80,930,501-82,586,000 , GRCh37.p13 chr17: 78,904,301-80,543,876 , PPP1R27, 89 more genes
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