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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978990inversion1nstd209human GRCh38 chr13: 19,387,175-24,442,537 , GRCh37.p13 chr13: 19,961,315-25,016,675 , PARP4, 111 more genes
    nsv5969193inversion1nstd209human GRCh38 chr13: 19,344,229-24,542,503 , GRCh37.p13 chr13: 19,918,369-25,116,641 , PARP4, 117 more genes
    nsv5930119copy number variation1nstd209human GRCh38 chr13: 19,425,704-24,953,999 , GRCh37.p13 chr13: 19,999,844-25,528,137 , LOC105370102, 128 more genes
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5374095translocation1nstd200human GRCh38 chr13: 20,716,591-20,716,591 , GRCh38 chr13: 20,713,114-20,713,114 , GRCh37.p13 chr13: 21,287,253-21,287,253 , GRCh37.p13 chr13: 21,290,730-21,290,730 IL17D
    nsv5374094translocation1nstd200human GRCh38 chr13: 20,710,620-20,710,620 , GRCh38 chr13: 20,716,298-20,716,298 , GRCh37.p13 chr13: 21,290,437-21,290,437 , GRCh37.p13 chr13: 21,284,759-21,284,759 IL17D
    nsv5356631translocation1nstd200human GRCh38 chr13: 20,710,366-20,710,366 , GRCh38 chr13: 20,711,127-20,711,127 , GRCh37.p13 chr13: 21,284,505-21,284,505 , GRCh37.p13 chr13: 21,285,266-21,285,266 IL17D
    nsv5356630translocation1nstd200human GRCh38 chr13: 20,709,962-20,709,962 , GRCh38 chr13: 20,709,861-20,709,861 , GRCh37.p13 chr13: 21,284,101-21,284,101 , GRCh37.p13 chr13: 21,284,000-21,284,000 IL17D
    nsv5334239translocation1nstd200human GRCh37 chr13: 21,284,000-21,284,000 , GRCh37 chr13: 21,284,101-21,284,101 , GRCh38.p12 chr13: 20,709,861-20,709,861 , GRCh38.p12 chr13: 20,709,962-20,709,962 IL17D
    nsv5126130mobile element insertion1nstd203human GRCh38 chr13: 20,708,843-20,708,860 , GRCh37.p13 chr13: 21,282,982-21,282,999 IL17D
    nsv5037324inversion1nstd200human GRCh38 chr13: 20,216,099-22,917,425 , GRCh37.p13 chr13: 20,790,238-23,491,564 , BASP1P1, 56 more genes
    nsv5031336inversion1nstd200human GRCh38 chr13: 20,360,614-20,775,544 , GRCh37.p13 chr13: 20,934,753-21,349,683 IFT88, LOC105370103, 8 more genes
    nsv4996473copy number variation1nstd200human GRCh38 chr13: 20,702,322-20,713,525 , GRCh37.p13 chr13: 21,276,461-21,287,664 IL17D
    nsv4849089copy number variation1nstd200human GRCh37 chr13: 21,284,505-21,285,266 , GRCh38.p12 chr13: 20,710,366-20,711,127 IL17D
    nsv4683415copy number variation1nstd102humanUncertain significance GRCh37 chr13: 20,716,100-21,398,980 , GRCh38.p12 chr13: 20,141,961-20,824,841 GJB6, EEF1AKMT1, 14 more genes
    nsv4675873copy number variation1nstd102humanUncertain significance GRCh37 chr13: 21,034,087-21,404,969 , GRCh38.p12 chr13: 20,459,948-20,830,830 EEF1AKMT1, RANP8, 7 more genes
    nsv4675550copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-24,970,361 , GRCh38.p12 chr13: 18,862,146-24,396,223 MRPL57, TATDN2P3, 129 more genes
    nsv4675255copy number variation1nstd102humanPathogenic GRCh37 chr13: 20,668,070-23,029,230 , GRCh38.p12 chr13: 20,093,931-22,455,091 RPSAP54, SLC35E1P1, 52 more genes
    nsv4457197copy number variation1nstd102humanPathogenic GRCh37 chr13: 20,069,228-27,474,401 , GRCh38.p12 chr13: 19,495,088-26,900,264 ZDHHC20, ANKRD20A10P, 154 more genes
    nsv4456640copy number variation1nstd102humanPathogenic GRCh37 chr13: 20,562,171-22,993,375 , GRCh38.p12 chr13: 19,988,031-22,419,236 RANP8, PPIAP28, 53 more genes
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