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Items: 1 to 20 of 161

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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
    nsv7066069inversion1nstd229human GRCh38 chr19: 35,840,401-35,893,161 , GRCh37.p13 chr19: 36,331,303-36,384,063 NPHS1, NFKBID, 4 more genes
    nsv7012206copy number variation1nstd229human GRCh38 chr19: 35,833,783-36,008,471 , GRCh37.p13 chr19: 36,324,685-36,499,373 TYROBP, SYNE4, 11 more genes
    nsv7009077copy number variation1nstd229human GRCh38 chr19: 35,888,801-35,890,900 , GRCh37.p13 chr19: 36,379,703-36,381,802 NFKBID
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7005456copy number variation1nstd229human GRCh38 chr19: 35,863,391-36,727,332 , GRCh37.p13 chr19: 36,354,293-37,218,234 ZNF146, CLIP3, 39 more genes
    nsv7002690copy number variation1nstd229human GRCh38 chr19: 35,860,444-35,915,414 , GRCh37.p13 chr19: 36,351,346-36,406,316 TYROBP, KIRREL2, 5 more genes
    nsv6532655copy number variation1nstd223human GRCh38 chr19: 35,818,262-36,019,433 , GRCh37.p13 chr19: 36,309,164-36,510,335 TYROBP, LOC101927572, 13 more genes
    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
    nsv6288303insertion1nstd214human GRCh38 chr19: 35,886,747-35,886,747 , GRCh37.p13 chr19: 36,377,649-36,377,649 NFKBID
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv6108580insertion1nstd212human GRCh38 chr19: 35,886,758-35,886,758 , GRCh37.p13 chr19: 36,377,660-36,377,660 NFKBID
    nsv5524344copy number variation1nstd206human GRCh38 chr19: 35,886,725-35,886,791 , GRCh37.p13 chr19: 36,377,627-36,377,693 NFKBID
    nsv5283949copy number variation1nstd204human GRCh38.p13 chr19: 35,897,401-35,905,500 , GRCh37.p13 chr19: 36,388,303-36,396,402 TYROBP, HCST, 1 more genes
    nsv5162370mobile element insertion1nstd203human GRCh38 chr19: 35,886,264-35,886,312 , GRCh37.p13 chr19: 36,377,166-36,377,214 NFKBID
    nsv5027715copy number variation1nstd200human GRCh38 chr19: 35,901,601-35,901,667 , GRCh37.p13 chr19: 36,392,503-36,392,569 HCST, NFKBID
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