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Items: 1 to 20 of 146

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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
    nsv7095201copy number variation1nstd102humanPathogenic GRCh37 chr19: 36,398,100-36,399,130 , GRCh38.p12 chr19: 35,907,198-35,908,228 TYROBP
    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
    nsv7011721copy number variation1nstd229human GRCh38 chr19: 35,904,636-35,907,216 , GRCh37.p13 chr19: 36,395,538-36,398,118 HCST, TYROBP
    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
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv5943303copy number variation1nstd209human GRCh38 chr19: 35,905,860-35,911,124 , GRCh37.p13 chr19: 36,396,762-36,402,026 TYROBP
    nsv5885354copy number variation2nstd209human GRCh38 chr19: 35,907,609-35,908,880 , GRCh37.p13 chr19: 36,398,511-36,399,782 TYROBP
    nsv5883197copy number variation1nstd209human GRCh38 chr19: 35,905,909-35,910,380 , GRCh37.p13 chr19: 36,396,811-36,401,282 TYROBP
    nsv5869465copy number variation1nstd209human GRCh38 chr19: 35,906,009-35,907,108 , GRCh37.p13 chr19: 36,396,911-36,398,010 TYROBP
    nsv5672902copy number variation1nstd102humannot provided GRCh37 chr19: 36,396,785-36,402,026 , GRCh38 chr19: 35,905,883-35,911,124 TYROBP
    nsv5293162copy number variation1nstd204human GRCh38.p13 chr19: 35,905,501-35,908,600 , GRCh37.p13 chr19: 36,396,403-36,399,502 TYROBP
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