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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095478copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,167,170-36,643,309 , GRCh38.p12 chr19: 32,676,264-36,152,407 NFKBID, LRP3, 141 more genes
    nsv7074671inversion1nstd229human GRCh38 chr19: 33,126,299-36,006,645 , GRCh37.p13 chr19: 33,617,205-36,497,547 , ZNF30, 120 more genes
    nsv7074279inversion1nstd229human GRCh38 chr19: 33,135,428-36,017,833 , GRCh37.p13 chr19: 33,626,334-36,508,735 , PSENEN, 122 more genes
    nsv7074131inversion1nstd229human GRCh38 chr19: 34,477,873-34,665,876 , GRCh37.p13 chr19: 34,968,778-35,156,781 WTIP, ZNF807P, 7 more genes
    nsv7072782inversion1nstd229human GRCh38 chr19: 34,537,710-34,749,334 , GRCh37.p13 chr19: 35,028,615-35,240,239 SCGB2B2, SCGB2B1P, 9 more genes
    nsv7061035inversion1nstd229human GRCh38 chr19: 34,559,804-34,724,315 , GRCh37.p13 chr19: 35,050,709-35,215,220 LOC100130632, SCGB2B2, 6 more genes
    nsv7060096inversion1nstd229human GRCh38 chr19: 34,537,753-34,746,067 , GRCh37.p13 chr19: 35,028,658-35,236,972 SCGB1B2P, ZNF302, 9 more genes
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7002390copy number variation1nstd229human GRCh38 chr19: 34,589,201-34,597,200 , GRCh37.p13 chr19: 35,080,106-35,088,105 SCGB1B2P, SCGB2B2
    nsv6598844inversion1nstd223human GRCh38 chr19: 34,573,847-34,668,002 , GRCh37.p13 chr19: 35,064,752-35,158,907 SCGB2B2, SCGB1B2P, 3 more genes
    nsv6598572inversion1nstd223human GRCh38 chr19: 34,537,710-34,749,334 , GRCh37.p13 chr19: 35,028,615-35,240,239 ZNF807P, LOC100130632, 9 more genes
    nsv6314074copy number variation1nstd102humanUncertain significance GRCh37 chr19: 32,827,535-35,263,640 , GRCh38.p12 chr19: 32,336,629-34,772,735 LOC100130632, CEP89, 59 more genes
    nsv6291822copy number variation1nstd102humanPathogenic GRCh38 chr19: 34,469,754-34,644,767 , GRCh37.p13 chr19: 34,960,659-35,135,672 UBA2, WTIP, 7 more genes
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv6104002inversion1nstd212human GRCh38 chr19: 34,537,754-34,750,577 , GRCh37.p13 chr19: 35,028,659-35,241,482 ZNF302, SCGB2B2, 9 more genes
    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
    nsv5024554copy number variation1nstd200human GRCh38 chr19: 34,590,489-34,590,693 , GRCh37.p13 chr19: 35,081,394-35,081,598 SCGB1B2P, SCGB2B2
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