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Items: 1 to 20 of 127

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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
    nsv7069250inversion1nstd229human GRCh38 chr19: 35,535,322-35,535,432 , GRCh37.p13 chr19: 36,026,224-36,026,334 GAPDHS
    nsv7011463copy number variation1nstd229human GRCh38 chr19: 35,253,455-35,541,332 , GRCh37.p13 chr19: 35,744,358-36,032,234 CD22, MAG, 18 more genes
    nsv7008200copy number variation1nstd229human GRCh38 chr19: 35,500,961-35,647,974 , GRCh37.p13 chr19: 35,991,863-36,138,876 SBSN, TMEM147-AS1, 10 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
    nsv6998993copy number variation1nstd229human GRCh38 chr19: 35,539,091-35,543,325 , GRCh37.p13 chr19: 36,029,993-36,034,227 TMEM147-AS1, GAPDHS
    nsv6310629copy number variation1nstd102humanUncertain significance GRCh37 chr19: 35,521,725-36,643,309 , GRCh38.p12 chr19: 35,030,821-36,152,407 KRTDAP, WDR62, 78 more genes
    nsv6291710copy number variation1nstd102humanUncertain significance GRCh37 chr19: 36,019,064-36,516,110 , GRCh38.p12 chr19: 35,528,162-36,025,208 NFKBID, APLP1, 38 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
    nsv4674329copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,553,425-36,264,299 , GRCh38.p12 chr19: 35,062,521-35,773,397 LOC105372379, LSR, 50 more genes
    nsv4620651copy number variation1nstd183human GRCh37 chr19: 36,033,210-36,033,428 , GRCh38.p12 chr19: 35,542,308-35,542,526 GAPDHS, TMEM147-AS1
    nsv4574565mobile element insertion1nstd166human GRCh37.p13 chr19: 36,028,815-36,028,815 , GRCh38.p12 chr19: 35,537,913-35,537,913 GAPDHS
    nsv4457800copy number variation1nstd102humanUncertain significance GRCh37 chr19: 35,613,953-36,183,886 , GRCh38.p12 chr19: 35,123,049-35,692,984 SBSN, UPK1A, 38 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
    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
    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
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