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Items: 1 to 20 of 102

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098944copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,624,491-10,969,019 , GRCh38.p12 chr19: 10,513,815-10,858,343 DNM2, ILF3-DT, 17 more genes
    nsv7062606inversion1nstd229human GRCh38 chr19: 10,024,335-10,946,724 , GRCh37.p13 chr19: 10,135,011-11,057,400 FDX2, ICAM4, 48 more genes
    nsv7061047inversion1nstd229human GRCh38 chr19: 10,123,796-11,885,300 , GRCh37.p13 chr19: 10,234,472-11,996,115 QTRT1, ZNF653, 82 more genes
    nsv7016581copy number variation1nstd229human GRCh38 chr19: 10,548,401-10,557,000 , GRCh37.p13 chr19: 10,659,077-10,667,676 ATG4D, MIR1238, 2 more genes
    nsv6998289copy number variation1nstd229human GRCh38 chr19: 10,552,459-10,558,098 , GRCh37.p13 chr19: 10,663,135-10,668,774 KRI1, MIR1238, 1 more genes
    nsv6998259copy number variation1nstd229human GRCh38 chr19: 10,046,601-11,033,768 , GRCh37.p13 chr19: 10,157,277-11,144,444 MRPL4, QTRT1, 49 more genes
    nsv6291543copy number variation1nstd102humanUncertain significance GRCh37 chr19: 9,941,033-11,739,567 , GRCh38.p12 chr19: 9,830,357-11,628,752 KRI1, SHFL, 88 more genes
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133479copy number variation1nstd213human GRCh37 chr19: 7,400,000-13,280,001 , GRCh38.p12 chr19: 7,335,095-13,169,187 , ACP5, 299 more genes
    nsv5327274copy number variation1nstd204human GRCh38.p13 chr19: 10,550,920-10,562,660 , GRCh37.p13 chr19: 10,661,596-10,673,336 ATG4D, RNU7-140P, 2 more genes
    nsv5294323copy number variation1nstd204human GRCh38.p13 chr19: 10,550,701-10,562,800 , GRCh37.p13 chr19: 10,661,377-10,673,476 MIR1238, ATG4D, 2 more genes
    nsv5291380copy number variation1nstd204human GRCh38.p13 chr19: 10,335,201-10,670,200 , GRCh37.p13 chr19: 10,445,877-10,780,876 ICAM3, MIR1181, 15 more genes
    nsv5287330copy number variation1nstd204human GRCh38.p13 chr19: 10,335,601-11,755,400 , GRCh37.p13 chr19: 10,446,277-11,866,215 AP1M2, C19orf38, 64 more genes
    nsv5285636copy number variation1nstd204human GRCh38.p13 chr19: 10,550,950-10,563,099 , GRCh37.p13 chr19: 10,661,626-10,673,775 ATG4D, RNU7-140P, 2 more genes
    nsv5283750copy number variation1nstd204human GRCh37.p13 chr19: 10,617,077-10,686,476 , GRCh38.p13 chr19: 10,506,401-10,575,800 CDKN2D, AP1M2, 5 more genes
    nsv4747606copy number variation1nstd199human GRCh38.p12 chr19: 10,550,740-10,557,138 , GRCh37 chr19: 10,661,416-10,667,814 KRI1, ATG4D, 2 more genes
    nsv4685775copy number variation1nstd102humannot provided GRCh37 chr19: 10,642,984-12,810,067 , GRCh38.p12 chr19: 10,532,308-12,699,253 SLC44A2, ZNF833P, 114 more genes
    nsv4676283copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,632,623-11,135,294 , GRCh38.p12 chr19: 10,521,947-11,024,618 ATG4D, RN7SL192P, 21 more genes
    nsv4457721copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,441,330-10,977,962 , GRCh38.p12 chr19: 10,330,654-10,867,286 CDKN2D, QTRT1, 24 more genes
    nsv4451686copy number variation1nstd102humannot provided GRCh37 chr19: 10,642,984-12,810,067 , GRCh38.p12 chr19: 10,532,308-12,699,253 ODAD3, RNA5SP466, 114 more genes
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