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Items: 1 to 20 of 134

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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
    nsv5287495copy number variation1nstd204human GRCh37.p13 chr19: 15,473,712-15,677,711 , GRCh38.p13 chr19: 15,362,901-15,566,900 AKAP8, AKAP8L, 7 more genes
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 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
    nsv4676112copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,368,330-15,712,368 , GRCh38.p12 chr19: 14,257,518-15,601,557 GIPC1, LOC100422106, 52 more genes
    nsv4667938copy number variation1nstd186human GRCh37 chr19: 15,560,369-15,560,439 , GRCh38.p12 chr19: 15,449,558-15,449,628 WIZ, RASAL3, 1 more genes
    nsv4629201copy number variation1nstd183human GRCh37 chr19: 15,560,330-15,560,439 , GRCh38.p12 chr19: 15,449,519-15,449,628 RASAL3, MIR1470, 1 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
    nsv4625403copy number variation1nstd183human GRCh37 chr19: 15,560,369-15,560,439 , GRCh38.p12 chr19: 15,449,558-15,449,628 WIZ, RASAL3, 1 more genes
    nsv4619364copy number variation1nstd183human GRCh37 chr19: 15,560,336-15,560,677 , GRCh38.p12 chr19: 15,449,525-15,449,866 WIZ, MIR1470, 1 more genes
    nsv4457841copy number variation1nstd102humanUncertain significance GRCh37 chr19: 15,338,105-15,668,026 , GRCh38.p12 chr19: 15,227,294-15,557,215 RASAL3, PGLYRP2, 8 more genes
    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
    nsv3912089copy number variation1nstd102humanUncertain significance GRCh38 chr19: 15,227,306-15,496,644 , NCBI36 chr19: 15,199,117-15,468,455 , GRCh37 chr19: 15,338,117-15,607,455 WIZ, PGLYRP2, 6 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
    nsv3909810copy number variation1nstd102humanBenign GRCh37 chr19: 15,278,099-15,710,360 , GRCh38.p12 chr19: 15,167,288-15,599,549 PGLYRP2, CYP4F23P, 11 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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