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Items: 1 to 20 of 112

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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
    nsv5527650copy number variation1nstd206human GRCh38 chr19: 15,050,284-15,092,143 , GRCh37.p13 chr19: 15,161,095-15,202,954 OR1I1, CASP14
    nsv5283254copy number variation1nstd204human GRCh38.p13 chr19: 15,051,340-15,052,439 , GRCh37.p13 chr19: 15,162,151-15,163,250 CASP14
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5011997copy number variation1nstd200human GRCh38 chr19: 15,033,184-15,054,822 , GRCh37.p13 chr19: 15,143,995-15,165,633 CASP14
    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
    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
    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
    nsv3910918copy number variation1nstd102humanUncertain significance GRCh37 chr19: 14,588,573-15,244,464 , NCBI36 chr19: 14,449,573-15,105,464 , GRCh38 chr19: 14,477,761-15,133,653 GIPC1, TECR, 31 more genes
    nsv3910509copy number variation1nstd102humanPathogenic NCBI36 chr19: 13,505,739-15,342,900 , GRCh37 chr19: 13,644,739-15,481,900 , GRCh38 chr19: 13,533,925-15,371,089 DDX39A, SLC1A6, 76 more genes
    nsv3910299copy number variation1nstd102humanUncertain significance GRCh37 chr19: 14,517,721-15,521,581 , GRCh38 chr19: 14,406,909-15,410,770 , NCBI36 chr19: 14,378,721-15,382,581 EPHX3, SNORA104, 43 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
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3899292copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,883,158-16,788,770 , GRCh38.p12 chr19: 14,772,346-16,677,959 KLF2, ADGRE2, 80 more genes
    nsv3167633copy number variation1nstd151human GRCh37 chr19: 15,164,290-15,198,949 , GRCh38.p12 chr19: 15,053,479-15,088,138 OR1I1, CASP14
    nsv3166482copy number variation1nstd151human GRCh37 chr19: 15,163,060-15,166,090 , GRCh38.p12 chr19: 15,052,249-15,055,279 CASP14
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