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Items: 1 to 20 of 160

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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
    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
    nsv6516374copy number variation1nstd223human GRCh38 chr19: 35,520,097-35,521,736 , GRCh37.p13 chr19: 36,010,999-36,012,638 SBSN
    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
    nsv6282850copy number variation1nstd214human GRCh38 chr19: 35,527,739-35,527,792 , GRCh37.p13 chr19: 36,018,641-36,018,694 SBSN
    nsv6220544copy number variation1nstd214human GRCh38 chr19: 35,527,667-35,527,720 , GRCh37.p13 chr19: 36,018,569-36,018,622 SBSN
    nsv6217629copy number variation1nstd214human GRCh38 chr19: 35,526,704-35,526,757 , GRCh37.p13 chr19: 36,017,606-36,017,659 SBSN
    nsv6216226copy number variation1nstd214human GRCh38 chr19: 35,527,655-35,527,708 , GRCh37.p13 chr19: 36,018,557-36,018,610 SBSN
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv6110725insertion1nstd212human GRCh38 chr19: 35,527,492-35,527,492 , GRCh37.p13 chr19: 36,018,394-36,018,394 SBSN
    nsv6110481insertion1nstd212human GRCh38 chr19: 35,527,698-35,527,698 , GRCh37.p13 chr19: 36,018,600-36,018,600 SBSN
    nsv6107047insertion1nstd212human GRCh38 chr19: 35,527,417-35,527,417 , GRCh37.p13 chr19: 36,018,319-36,018,319 SBSN
    nsv6048494copy number variation1nstd212human GRCh38 chr19: 35,527,701-35,527,753 , GRCh37.p13 chr19: 36,018,603-36,018,655 SBSN
    nsv5698986mobile element insertion1nstd211human GRCh38 chr19: 35,522,740-35,522,740 , GRCh37.p13 chr19: 36,013,642-36,013,642 SBSN
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