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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7061492inversion1nstd229human GRCh38 chr19: 9,327,441-9,333,696 , GRCh37.p13 chr19: 9,438,117-9,444,372 ZNF559-ZNF177, ZNF559
    nsv7014271copy number variation1nstd229human GRCh38 chr19: 9,323,408-9,323,922 , GRCh37.p13 chr19: 9,434,084-9,434,598 ZNF559, ZNF559-ZNF177
    nsv7012105copy number variation1nstd229human GRCh38 chr19: 9,331,383-9,340,540 , GRCh37.p13 chr19: 9,442,059-9,451,216 ZNF559, ZNF559-ZNF177
    nsv7011121copy number variation1nstd229human GRCh38 chr19: 7,159,006-9,938,147 , GRCh37.p13 chr19: 7,159,017-10,048,823 , OR7G1, 117 more genes
    nsv7006998copy number variation1nstd229human GRCh38 chr19: 9,338,401-9,356,000 , GRCh37.p13 chr19: 9,449,077-9,466,676 ZNF559, LOC100128428, 1 more genes
    nsv6525237copy number variation1nstd223human GRCh38 chr19: 9,325,021-9,325,521 , GRCh37.p13 chr19: 9,435,697-9,436,197 ZNF559, ZNF559-ZNF177
    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
    nsv5874600copy number variation1nstd209human GRCh38 chr19: 9,343,199-9,346,048 , GRCh37.p13 chr19: 9,453,875-9,456,724 LOC100128428, ZNF559, 1 more genes
    nsv5532916copy number variation1nstd206human GRCh38 chr19: 9,331,362-9,340,559 , GRCh37.p13 chr19: 9,442,038-9,451,235 ZNF559, ZNF559-ZNF177
    nsv5525473copy number variation1nstd206human GRCh38 chr19: 9,325,172-9,325,520 , GRCh37.p13 chr19: 9,435,848-9,436,196 ZNF559, ZNF559-ZNF177
    nsv5330889translocation1nstd200human GRCh37 chr19: 9,453,164-9,453,164 , GRCh37 chr19: 9,453,095-9,453,095 , GRCh38.p12 chr19: 9,342,488-9,342,488 , GRCh38.p12 chr19: 9,342,419-9,342,419 ZNF559-ZNF177, ZNF559
    nsv5011537copy number variation1nstd200human GRCh38 chr19: 9,338,526-9,338,694 , GRCh37.p13 chr19: 9,449,202-9,449,370 ZNF559-ZNF177, ZNF559
    nsv5011536copy number variation1nstd200human GRCh38 chr19: 9,334,994-9,339,479 , GRCh37.p13 chr19: 9,445,670-9,450,155 ZNF559-ZNF177, ZNF559
    nsv4729955copy number variation1nstd102humanLikely benign GRCh37 chr19: 9,245,167-9,465,565 , GRCh38.p12 chr19: 9,134,491-9,354,889 ZNF699, ZNF559-ZNF177, 14 more genes
    nsv4729799copy number variation1nstd102humanUncertain significance GRCh37 chr19: 8,518,395-10,053,298 , GRCh38.p12 chr19: 8,453,511-9,942,622 ZNF426-DT, ADAMTS10, 61 more genes
    nsv4626879copy number variation1nstd183human GRCh37 chr19: 9,442,033-9,451,193 , GRCh38.p12 chr19: 9,331,357-9,340,517 ZNF559, ZNF559-ZNF177
    nsv4436244complex substitution1nstd102humanUncertain significance GRCh38.p12 chr19: 8,891,157-9,974,378 , GRCh37 chr19: 9,001,833-10,085,054 PIN1, UBE2L4, 51 more genes
    nsv4266894copy number variation1nstd166human GRCh37.p13 chr19: 9,454,812-9,466,625 , GRCh38.p12 chr19: 9,344,136-9,355,949 LOC100128428, ZNF559, 1 more genes
    nsv4264193copy number variation1nstd166human GRCh37.p13 chr19: 9,442,059-9,451,214 , GRCh38.p12 chr19: 9,331,383-9,340,538 ZNF559, ZNF559-ZNF177
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