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Items: 1 to 20 of 118

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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
    nsv5494375copy number variation1nstd206human GRCh38 chr13: 21,549,535-21,555,795 , GRCh37.p13 chr13: 22,123,674-22,129,934 RNU6-59P, MICU2
    nsv5037324inversion1nstd200human GRCh38 chr13: 20,216,099-22,917,425 , GRCh37.p13 chr13: 20,790,238-23,491,564 , BASP1P1, 56 more genes
    nsv4996506copy number variation1nstd200human GRCh38 chr13: 21,549,450-21,555,795 , GRCh37.p13 chr13: 22,123,589-22,129,934 MICU2, RNU6-59P
    nsv4844431copy number variation1nstd200human GRCh37 chr13: 22,123,589-22,129,934 , GRCh38.p12 chr13: 21,549,450-21,555,795 RNU6-59P, MICU2
    nsv4729551copy number variation1nstd102humanUncertain significance GRCh37 chr13: 21,555,059-22,772,929 , GRCh38.p12 chr13: 20,980,920-22,198,790 LOC105370104, MICU2, 27 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
    nsv4617529copy number variation1nstd183human GRCh37 chr13: 22,123,674-22,129,931 , GRCh38.p12 chr13: 21,549,535-21,555,792 MICU2, RNU6-59P
    nsv4566514inversion1nstd166human GRCh37.p13 chr13: 22,104,164-22,206,952 , GRCh38.p12 chr13: 21,530,025-21,632,813 , FNTAP2, 3 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
    nsv4455063copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-23,274,540 , GRCh38.p12 chr13: 18,862,146-22,700,401 SAP18, LOC105370102, 90 more genes
    nsv4349379copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 19,540,031-22,849,981 , GRCh38.p12 chr13: 18,965,891-22,275,842 FGF9, FNTAP2, 83 more genes
    nsv4231361copy number variation1nstd166human GRCh37.p13 chr13: 22,126,000-22,136,000 , GRCh38.p12 chr13: 21,551,861-21,561,861 MICU2, RNU6-59P
    nsv4220023copy number variation1nstd166human GRCh37.p13 chr13: 22,123,623-22,129,934 , GRCh38.p12 chr13: 21,549,484-21,555,795 MICU2, RNU6-59P
    nsv3924676copy number variation1nstd102humanPathogenic GRCh38 chr13: 18,456,040-114,340,285 , GRCh37 chr13: 19,030,180-115,105,760 , NCBI36 chr13: 17,928,180-114,123,862 GRTP1, FABP5P1, 1334 more genes
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