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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
    nsv5284321copy number variation1nstd204human GRCh38.p13 chr19: 14,935,395-14,939,972 , GRCh37.p13 chr19: 15,046,207-15,050,784 OR7C2
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5014576copy number variation1nstd200human GRCh38 chr19: 14,844,766-14,943,127 , GRCh37.p13 chr19: 14,955,578-15,053,939 OR7A15P, OR7A11P, 7 more genes
    nsv5011991copy number variation1nstd200human GRCh38 chr19: 14,941,633-14,944,884 , GRCh37.p13 chr19: 15,052,445-15,055,696 OR7C2
    nsv5011990copy number variation1nstd200human GRCh38 chr19: 14,939,536-14,947,103 , GRCh37.p13 chr19: 15,050,348-15,057,915 OR7C2
    nsv4864953copy number variation1nstd200human GRCh37 chr19: 14,955,596-15,053,955 , GRCh38.p12 chr19: 14,844,784-14,943,143 OR7A15P, OR7A11P, 7 more genes
    nsv4860451copy number variation1nstd200human GRCh37 chr19: 15,050,369-15,057,895 , GRCh38.p12 chr19: 14,939,557-14,947,083 OR7C2
    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
    nsv4430649copy number variation1nstd174human GRCh37 chr19: 15,046,091-15,050,633 , GRCh38.p12 chr19: 14,935,279-14,939,821 OR7C2
    nsv4387718copy number variation1nstd173human GRCh37 chr19: 14,921,852-15,061,579 , GRCh38.p12 chr19: 14,811,040-14,950,767 OR7A3P, OR7A1P, 11 more genes
    nsv4264285copy number variation1nstd166human GRCh37.p13 chr19: 15,051,000-15,058,000 , GRCh38.p12 chr19: 14,940,188-14,947,188 OR7C2
    nsv3968400copy number variation1nstd168human GRCh38 chr19: 14,900,606-14,954,569 , GRCh37.p13 chr19: 15,011,418-15,065,381 SLC1A6, OR7C2, 3 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
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