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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4266319copy number variation1nstd166human GRCh37.p13 chr19: 39,943,231-39,970,150 , GRCh38.p12 chr19: 39,452,591-39,479,510 SNORD175, TIMM50, 1 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3912447copy number variation1nstd102humanPathogenic NCBI36 chr19: 42,502,119-47,934,680 , GRCh37 chr19: 37,810,279-43,242,840 , GRCh38 chr19: 37,319,377-42,738,688 MIR8077, TRI-TAT1-1, 233 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3895066copy number variation1nstd102humanPathogenic GRCh37 chr19: 37,582,250-41,630,908 , GRCh38.p12 chr19: 37,091,348-41,125,003 RNU6-140P, COQ8B, 162 more genes
    nsv3169031copy number variation1nstd158human GRCh38.p12 chr19: 38,412,977-41,901,266 , GRCh37 chr19: 38,903,617-42,405,416 , ACTN4, 162 more genes
    nsv3168446copy number variation1nstd158human GRCh37 chr19: 35,445,908-45,506,757 , GRCh38.p12 chr19: 34,955,004-45,003,499 , ACTN4, 449 more genes
    nsv3167023copy number variation1nstd151human GRCh37 chr19: 39,976,181-39,977,140 , GRCh38.p12 chr19: 39,485,541-39,486,500 TIMM50
    nsv3166128copy number variation2nstd151human GRCh37 chr19: 39,973,522-39,991,317 , GRCh38.p12 chr19: 39,482,882-39,500,677 DLL3, TIMM50
    nsv2757532copy number variation1nstd130human GRCh37 chr19: 266,034-54,723,310 , GRCh38.p12 chr19: 266,034-54,071,460 , BABAM1, 2197 more genes
    nsv2752158copy number variation1nstd130human GRCh37 chr19: 289,244-58,996,454 , GRCh38.p12 chr19: 289,244-58,485,087 , NFKBIB, 2456 more genes
    nsv1958936short tandem repeat3nstd128human GRCh37 chr19: 39,984,917-39,984,928 , GRCh38.p12 chr19: 39,494,277-39,494,288 TIMM50
    nsv1958935short tandem repeat2nstd128human GRCh37 chr19: 39,983,894-39,983,911 , GRCh38.p12 chr19: 39,493,254-39,493,271 TIMM50
    nsv1958934short tandem repeat3nstd128human GRCh37 chr19: 39,981,812-39,981,823 , GRCh38.p12 chr19: 39,491,172-39,491,183 TIMM50
    nsv1958933short tandem repeat2nstd128human GRCh37 chr19: 39,974,487-39,974,511 , GRCh38.p12 chr19: 39,483,847-39,483,871 TIMM50
    nsv1958718short tandem repeat3nstd128human GRCh37 chr19: 39,983,735-39,983,747 , GRCh38.p12 chr19: 39,493,095-39,493,107 TIMM50
    nsv1958717short tandem repeat6nstd128human GRCh37 chr19: 39,973,300-39,973,316 , GRCh38.p12 chr19: 39,482,660-39,482,676 TIMM50
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