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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077186inversion1nstd229human GRCh38 chr15: 35,051,912-40,816,689 , GRCh37.p13 chr15: 35,344,113-41,108,887 BUB1B-PAK6, LOC751603, 96 more genes
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv6971544copy number variation1nstd229human GRCh38 chr15: 39,926,172-39,928,987 , GRCh37.p13 chr15: 40,218,373-40,221,188 GPR176-DT
    nsv6964883copy number variation1nstd229human GRCh38 chr15: 39,883,301-41,010,600 , GRCh37.p13 chr15: 40,175,502-41,302,798 SRP14, BUB1B-PAK6, 54 more genes
    nsv6513780copy number variation1nstd223human GRCh38 chr15: 39,915,601-39,938,200 , GRCh37.p13 chr15: 40,207,802-40,230,401 GPR176-DT, GPR176, 1 more genes
    nsv6313915copy number variation1nstd102humanUncertain significance GRCh37 chr15: 40,132,892-40,511,958 , GRCh38.p12 chr15: 39,840,691-40,219,757 LOC107984763, BMF, 11 more genes
    nsv6132806copy number variation1nstd213human GRCh37 chr15: 39,170,000-42,090,001 , GRCh38.p12 chr15: 38,877,799-41,797,803 GCHFR, LTK, 84 more genes
    nsv6021999copy number variation1nstd212human GRCh38 chr15: 39,919,443-39,919,503 , GRCh37.p13 chr15: 40,211,644-40,211,704 GPR176, GPR176-DT
    nsv5939106copy number variation1nstd209human GRCh38 chr15: 38,008,106-40,186,655 , GRCh37.p13 chr15: 38,300,307-40,478,856 , LOC105370784, 36 more genes
    nsv5727724mobile element insertion2nstd211human GRCh38 chr15: 39,925,852-39,925,852 , GRCh37.p13 chr15: 40,218,053-40,218,053 GPR176-DT
    nsv5559454mobile element insertion1nstd206human GRCh38 chr15: 39,925,868-39,925,903 , GRCh37.p13 chr15: 40,218,069-40,218,104 GPR176-DT
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv4436396complex substitution1nstd102humanPathogenic GRCh38.p12 chr15: 34,346,036-41,764,885 , GRCh37 chr15: 34,638,237-42,057,083 ACTC1, BUB1B, 150 more genes
    nsv3923477copy number variation1nstd102humanUncertain significance NCBI36 chr15: 37,790,428-38,374,084 , GRCh37 chr15: 40,003,136-40,586,792 , GRCh38 chr15: 39,710,935-40,294,591 BMF, MTND5P37, 17 more genes
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNRPCP18, SNORD116-30, 1622 more genes
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNORD116-23, UBE2Q2P6, 1622 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 H3P40, EEF1B2P1, 1616 more genes
    nsv3915967copy number variation1nstd102humanPathogenic GRCh38 chr15: 32,635,803-40,233,825 , GRCh37 chr15: 32,928,004-40,526,026 , NCBI36 chr15: 30,715,296-38,313,318 ANP32AP1, FMN1, 112 more genes
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