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Items: 1 to 20 of 116

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5532287copy number variation1nstd206human GRCh38 chr19: 16,023,451-16,023,547 , GRCh37.p13 chr19: 16,134,261-16,134,357 LINC00661
    nsv5525767copy number variation1nstd206human GRCh38 chr19: 16,014,213-16,014,298 , GRCh37.p13 chr19: 16,125,023-16,125,108 LINC00661, LOC105372291
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5014590copy number variation1nstd200human GRCh38 chr19: 15,984,241-16,059,051 , GRCh37.p13 chr19: 16,095,051-16,169,861 OR1AB1P, CYP4F9P, 4 more genes
    nsv5012062copy number variation1nstd200human GRCh38 chr19: 16,025,474-16,028,162 , GRCh37.p13 chr19: 16,136,284-16,138,972 LINC00661
    nsv5012061copy number variation1nstd200human GRCh38 chr19: 16,020,578-16,022,077 , GRCh37.p13 chr19: 16,131,388-16,132,887 LINC00661
    nsv5012060copy number variation1nstd200human GRCh38 chr19: 16,013,143-16,021,621 , GRCh37.p13 chr19: 16,123,953-16,132,431 LINC00661, LOC105372291
    nsv4864961copy number variation1nstd200human GRCh37 chr19: 16,095,051-16,169,861 , GRCh38.p12 chr19: 15,984,241-16,059,051 CYP4F9P, LOC105372291, 4 more genes
    nsv4729750copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,286,624-20,956,753 , GRCh38.p12 chr19: 14,175,812-20,773,947 LOC105372309, RAB8A, 269 more genes
    nsv4628505copy number variation1nstd183human GRCh37 chr19: 15,422,142-16,172,833 , GRCh38.p12 chr19: 15,311,331-16,062,023 , CYP4F8, 36 more genes
    nsv4457713copy number variation1nstd102humanUncertain significance GRCh37 chr19: 15,623,742-16,301,544 , GRCh38.p12 chr19: 15,512,931-16,190,733 CIB3, UCA1-AS1, 34 more genes
    nsv4257241copy number variation1nstd166human GRCh37.p13 chr19: 16,125,023-16,125,108 , GRCh38.p12 chr19: 16,014,213-16,014,298 LOC105372291, LINC00661
    nsv3922457copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,085,489-28,330,584 , GRCh38 chr19: 13,974,677-27,839,676 , NCBI36 chr19: 13,946,489-33,022,424 REX1BD, ZNF92P2, 416 more genes
    nsv3921076copy number variation1nstd102humanPathogenic GRCh38 chr19: 15,133,594-24,193,591 , GRCh37 chr19: 15,244,405-24,376,393 , NCBI36 chr19: 15,105,405-24,168,233 MRPL34, BNIP3P25, 358 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3909889copy number variation1nstd102humanPathogenic NCBI36 chr19: 14,126,774-16,886,123 , GRCh38 chr19: 14,154,962-16,914,313 , GRCh37 chr19: 14,265,774-17,025,123 OR7A1P, SNRPGP15, 108 more genes
    nsv3908579copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,124,666-16,431,349 , GRCh38.p12 chr19: 14,013,854-16,320,538 TMEM167AP2, TEKTL1, 99 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
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