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Items: 1 to 20 of 130

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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
    nsv7015462copy number variation1nstd229human GRCh38 chr19: 34,767,521-34,767,903 , GRCh37.p13 chr19: 35,258,426-35,258,808 ZNF599
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7002170copy number variation1nstd229human GRCh38 chr19: 34,757,099-34,757,617 , GRCh37.p13 chr19: 35,248,004-35,248,522 ZNF599
    nsv6527059copy number variation1nstd223human GRCh38 chr19: 34,757,099-34,757,615 , GRCh37.p13 chr19: 35,248,004-35,248,520 ZNF599
    nsv6524770copy number variation1nstd223human GRCh38 chr19: 34,764,301-34,767,000 , GRCh37.p13 chr19: 35,255,206-35,257,905 ZNF599
    nsv6314074copy number variation1nstd102humanUncertain significance GRCh37 chr19: 32,827,535-35,263,640 , GRCh38.p12 chr19: 32,336,629-34,772,735 LOC100130632, CEP89, 59 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
    nsv5528787copy number variation1nstd206human GRCh38 chr19: 34,757,099-34,757,615 , GRCh37.p13 chr19: 35,248,004-35,248,520 ZNF599
    nsv5359742translocation1nstd200human GRCh38 chr19: 34,757,099-34,757,099 , GRCh38 chr19: 34,757,615-34,757,615 , GRCh37.p13 chr19: 35,248,004-35,248,004 , GRCh37.p13 chr19: 35,248,520-35,248,520 ZNF599
    nsv5343263translocation1nstd200human GRCh37 chr19: 35,248,004-35,248,004 , GRCh37 chr19: 35,248,520-35,248,520 , GRCh38.p12 chr19: 34,757,615-34,757,615 , GRCh38.p12 chr19: 34,757,099-34,757,099 ZNF599
    nsv5020438copy number variation1nstd200human GRCh38 chr19: 34,771,120-34,771,269 , GRCh37.p13 chr19: 35,262,025-35,262,174 ZNF599
    nsv4665899copy number variation1nstd186human GRCh37 chr19: 35,248,003-35,248,520 , GRCh38.p12 chr19: 34,757,098-34,757,615 ZNF599
    nsv4628016copy number variation1nstd183human GRCh37 chr19: 35,248,003-35,248,520 , GRCh38.p12 chr19: 34,757,098-34,757,615 ZNF599
    nsv4564280mobile element insertion1nstd166human GRCh37.p13 chr19: 35,261,886-35,261,886 , GRCh38.p12 chr19: 34,770,981-34,770,981 ZNF599
    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
    nsv4421362copy number variation1nstd174human GRCh37 chr19: 35,247,982-35,248,520 , GRCh38.p12 chr19: 34,757,077-34,757,615 ZNF599
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