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Items: 1 to 20 of 246

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5726954mobile element insertion1nstd211human GRCh38 chr15: 66,757,667-66,757,667 , GRCh37.p13 chr15: 67,050,005-67,050,005 SMAD6
    nsv5521116copy number variation1nstd206human GRCh38 chr15: 66,704,197-66,712,155 , GRCh37.p13 chr15: 66,996,535-67,004,493 SMAD6
    nsv5519196copy number variation1nstd206human GRCh38 chr15: 66,739,313-66,765,466 , GRCh37.p13 chr15: 67,031,651-67,057,804 SMAD6
    nsv5518648copy number variation1nstd206human GRCh38 chr15: 66,738,103-66,738,828 , GRCh37.p13 chr15: 67,030,441-67,031,166 SMAD6
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5358026translocation1nstd200human GRCh38 chr15: 66,763,157-66,763,157 , GRCh38 chr15: 66,767,584-66,767,584 , GRCh37.p13 chr15: 67,055,495-67,055,495 , GRCh37.p13 chr15: 67,059,922-67,059,922 SMAD6
    nsv5358025translocation1nstd200human GRCh38 chr15: 66,738,828-66,738,828 , GRCh38 chr15: 66,738,103-66,738,103 , GRCh37.p13 chr15: 67,030,441-67,030,441 , GRCh37.p13 chr15: 67,031,166-67,031,166 SMAD6
    nsv5358024translocation1nstd200human GRCh38 chr15: 66,717,863-66,717,863 , GRCh38 chr15: 66,717,795-66,717,795 , GRCh37.p13 chr15: 67,010,201-67,010,201 , GRCh37.p13 chr15: 67,010,133-67,010,133 SMAD6
    nsv5311175copy number variation1nstd204human GRCh38.p13 chr15: 66,746,251-66,748,371 , GRCh37.p13 chr15: 67,038,589-67,040,709 SMAD6
    nsv5272799copy number variation1nstd204human GRCh38.p13 chr15: 66,746,317-66,748,316 , GRCh37.p13 chr15: 67,038,655-67,040,654 SMAD6
    nsv5267013copy number variation1nstd204human GRCh38.p13 chr15: 66,746,301-66,748,300 , GRCh37.p13 chr15: 67,038,639-67,040,638 SMAD6
    nsv5150303mobile element insertion1nstd203human GRCh38 chr15: 66,778,256-66,778,266 , GRCh37.p13 chr15: 67,070,594-67,070,604 SMAD6
    nsv4992101copy number variation1nstd200human GRCh38 chr15: 66,746,277-66,748,344 , GRCh37.p13 chr15: 67,038,615-67,040,682 SMAD6
    nsv4992100copy number variation1nstd200human GRCh38 chr15: 66,731,697-66,735,354 , GRCh37.p13 chr15: 67,024,035-67,027,692 SMAD6
    nsv4992099copy number variation1nstd200human GRCh38 chr15: 66,721,402-66,725,259 , GRCh37.p13 chr15: 67,013,740-67,017,597 SMAD6
    nsv4849907copy number variation1nstd200human GRCh37 chr15: 67,055,495-67,059,922 , GRCh38.p12 chr15: 66,763,157-66,767,584 SMAD6
    nsv4849906copy number variation1nstd200human GRCh37 chr15: 67,038,589-67,040,707 , GRCh38.p12 chr15: 66,746,251-66,748,369 SMAD6
    nsv4849905copy number variation1nstd200human GRCh37 chr15: 67,030,441-67,031,166 , GRCh38.p12 chr15: 66,738,103-66,738,828 SMAD6
    nsv4849904copy number variation1nstd200human GRCh37 chr15: 67,013,740-67,017,597 , GRCh38.p12 chr15: 66,721,402-66,725,259 SMAD6
    nsv4682879copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,073,325-67,358,708 , GRCh38.p12 chr15: 66,780,987-67,066,370 SMAD3, SMAD6, 6 more genes
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