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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
    nsv5941534copy number variation1nstd209human GRCh38 chr19: 33,372,587-33,372,898 , GRCh37.p13 chr19: 33,863,493-33,863,804 CEBPG
    nsv5516662copy number variation1nstd206human GRCh38 chr19: 33,372,601-33,372,899 , GRCh37.p13 chr19: 33,863,507-33,863,805 CEBPG
    nsv5210461mobile element deletion1nstd204human GRCh38.p13 chr19: 33,372,597-33,372,901 , GRCh37.p13 chr19: 33,863,503-33,863,807 CEBPG
    nsv4907534mobile element deletion1nstd200human GRCh38 chr19: 33,372,601-33,372,899 , GRCh37.p13 chr19: 33,863,507-33,863,805 CEBPG
    nsv4769809mobile element deletion1nstd200human GRCh37 chr19: 33,863,507-33,863,805 , GRCh38.p12 chr19: 33,372,601-33,372,899 CEBPG
    nsv4708910copy number variation2nstd195human GRCh37 chr19: 33,863,493-33,863,494 , GRCh38.p12 chr19: 33,372,587-33,372,588 CEBPG
    nsv4630832copy number variation1nstd183human GRCh37 chr19: 33,864,550-33,864,713 , GRCh38.p12 chr19: 33,373,644-33,373,807 CEBPG
    nsv4457819copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,842,279-33,986,911 , GRCh38.p12 chr19: 33,351,373-33,496,005 AKR1B1P7, PEPD, 1 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4270862copy number variation1nstd166human GRCh37.p13 chr19: 33,863,507-33,863,932 , GRCh38.p12 chr19: 33,372,601-33,373,026 CEBPG
    nsv3919618copy number variation1nstd102humanUncertain significance NCBI36 chr19: 32,962,986-39,966,686 , GRCh38 chr19: 27,780,238-34,783,942 , GRCh37 chr19: 28,271,146-35,274,846 LINC00906, TDRD12, 112 more genes
    nsv3919296copy number variation1nstd102humanPathogenic NCBI36 chr19: 34,844,605-43,297,203 , GRCh37 chr19: 30,152,765-38,605,363 , GRCh38 chr19: 29,661,858-38,114,723 UBA2, ZNF529, 241 more genes
    nsv3918197copy number variation1nstd102humanPathogenic GRCh38 chr19: 31,367,353-35,417,098 , NCBI36 chr19: 36,550,099-40,599,840 , GRCh37 chr19: 31,858,259-35,908,000 LINC01531, FXYD5, 110 more genes
    nsv3916007copy number variation1nstd102humanPathogenic GRCh37 chr19: 30,162,231-38,393,630 , NCBI36 chr19: 34,854,071-43,085,470 , GRCh38 chr19: 29,671,324-37,902,990 MAG, RNU6-967P, 238 more genes
    nsv3914228copy number variation1nstd102humanPathogenic NCBI36 chr19: 17,148,576-40,106,894 , GRCh38 chr19: 17,176,767-34,924,150 , GRCh37 chr19: 17,287,576-35,415,054 LOC105372355, SUGP2, 411 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
    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
    nsv3900139copy number variation1nstd102humanPathogenic GRCh37 chr19: 30,735,448-36,120,396 , GRCh38.p12 chr19: 30,244,541-35,629,494 ZNF599, FAM187B2P, 130 more genes
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