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Items: 1 to 20 of 111

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975015inversion1nstd209human GRCh38 chr19: 34,537,657-34,749,386 , GRCh37.p13 chr19: 35,028,562-35,240,291 ZNF302, SCGB2B2, 9 more genes
    nsv5558870inversion1nstd206human GRCh38 chr19: 34,573,445-34,668,770 , GRCh37.p13 chr19: 35,064,350-35,159,675 SCGB2B2, SCGB1B2P, 3 more genes
    nsv5555695sequence alteration1nstd206human GRCh38 chr19: 34,537,631-34,749,387 , GRCh37.p13 chr19: 35,028,536-35,240,292 SCGB2B2, SCGB2B3P, 9 more genes
    nsv5020432copy number variation1nstd200human GRCh38 chr19: 34,640,691-34,644,427 , GRCh37.p13 chr19: 35,131,596-35,135,332 SCGB1B2P, SCGB2B3P
    nsv4868159copy number variation1nstd200human GRCh37 chr19: 35,131,623-35,135,336 , GRCh38.p12 chr19: 34,640,718-34,644,431 SCGB2B3P, SCGB1B2P
    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
    nsv4350190copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,043,556-36,316,644 , GRCh38.p12 chr19: 34,552,651-35,825,742 SCN1B, ETV2, 76 more genes
    nsv4349605copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,111,811-37,744,992 , GRCh38.p12 chr19: 34,620,906-37,254,090 ATP4A, RNY5P10, 129 more genes
    nsv3965243copy number variation1nstd168human GRCh38 chr19: 34,606,405-34,686,919 , GRCh37.p13 chr19: 35,097,310-35,177,824 SCGB1B2P, SCGB2B3P, 3 more genes
    nsv3957780insertion1nstd168human GRCh38 chr19: 34,645,686-34,657,541 , GRCh37.p13 chr19: 35,136,591-35,148,446 SCGB1B2P, SCGB2B3P
    nsv3956827inversion1nstd168human GRCh38 chr19: 34,645,686-34,657,541 , GRCh37.p13 chr19: 35,136,591-35,148,446 SCGB1B2P, SCGB2B3P
    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
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