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Items: 1 to 20 of 124

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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
    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
    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
    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
    nsv6310478copy number variation1nstd102humanUncertain significance GRCh37 chr19: 36,486,177-36,486,524 , GRCh38.p12 chr19: 35,995,275-35,995,622 SDHAF1
    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
    nsv5024578copy number variation1nstd200human GRCh38 chr19: 35,989,353-36,000,492 , GRCh37.p13 chr19: 36,480,255-36,491,394 SDHAF1
    nsv5024572copy number variation1nstd200human GRCh38 chr19: 35,818,267-36,019,433 , GRCh37.p13 chr19: 36,309,169-36,510,335 SYNE4, LOC107985317, 13 more genes
    nsv5024570copy number variation1nstd200human GRCh38 chr19: 35,722,805-36,225,611 , GRCh37.p13 chr19: 36,213,707-36,716,513 LOC105372385, ALKBH6, 34 more genes
    nsv4865133copy number variation1nstd200human GRCh37 chr19: 36,213,707-36,716,513 , GRCh38.p12 chr19: 35,722,805-36,225,611 KMT2B, PSENEN, 34 more genes
    nsv4536962copy number variation1nstd166human GRCh37.p13 chr19: 36,309,999-36,510,300 , GRCh38.p12 chr19: 35,819,097-36,019,398 KIRREL2, HCST, 13 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
    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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