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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6522268copy number variation1nstd223human GRCh38 chr19: 57,724,720-57,725,518 , GRCh37.p13 chr19: 58,236,088-58,236,886 ZNF671
    nsv3162945copy number variation1nstd151human GRCh37 chr19: 58,231,846-58,234,713 , GRCh38.p12 chr19: 57,720,478-57,723,345 ZNF671
    esv1088460copy number variation1estd22human NCBI36 chr19: 62,927,238-62,927,239 , GRCh37.p13 chr19: 58,235,426-58,235,427 , GRCh38.p12 chr19: 57,724,058-57,724,059 ZNF671
    esv2968018insertion1estd209human GRCh37 chr19: 58,230,003-58,230,003 , GRCh38.p12 chr19: 57,718,635-57,718,635 ZNF671
    esv2302104insertion1estd194human NCBI36 chr19: 62,921,816-62,921,816 , GRCh37.p13 chr19: 58,230,004-58,230,004 , GRCh38.p12 chr19: 57,718,636-57,718,636 ZNF671
    nsv137827insertion1nstd6human NCBI35 chr19: 62,921,816-62,921,816 , GRCh37.p13 chr19: 58,230,004-58,230,004 , GRCh38.p12 chr19: 57,718,636-57,718,636 ZNF671
    nsv6596029inversion1nstd223human GRCh38 chr19: 57,724,042-57,724,527 , GRCh37.p13 chr19: 58,235,410-58,235,895 ZNF671
    nsv1971383short tandem repeat3nstd128human GRCh37 chr19: 58,234,263-58,234,283 , GRCh38.p12 chr19: 57,722,895-57,722,915 ZNF671
    nsv1971257short tandem repeat1nstd128human GRCh37 chr19: 58,237,000-58,237,019 , GRCh38.p12 chr19: 57,725,632-57,725,651 ZNF671
    nsv1972815short tandem repeat6nstd128human GRCh37 chr19: 58,235,896-58,235,912 , GRCh38.p12 chr19: 57,724,528-57,724,544 ZNF671
    nsv1971384short tandem repeat2nstd128human GRCh37 chr19: 58,237,679-58,237,695 , GRCh38.p12 chr19: 57,726,311-57,726,327 ZNF671
    nsv1971256short tandem repeat6nstd128human GRCh37 chr19: 58,235,411-58,235,427 , GRCh38.p12 chr19: 57,724,043-57,724,059 ZNF671
    nsv1972816short tandem repeat3nstd128human GRCh37 chr19: 58,236,523-58,236,536 , GRCh38.p12 chr19: 57,725,155-57,725,168 ZNF671
    nsv5932132copy number variation1nstd209human GRCh38 chr19: 57,708,381-57,725,445 , GRCh37.p13 chr19: 58,219,749-58,236,813 ZNF671, ZNF154
    nsv4262219copy number variation1nstd166human GRCh37.p13 chr19: 58,214,795-58,235,295 , GRCh38.p12 chr19: 57,703,427-57,723,927 ZNF671, ZNF154
    nsv3165848copy number variation1nstd151human GRCh37 chr19: 58,231,846-58,324,793 , GRCh38.p12 chr19: 57,720,478-57,813,425 ZNF671, ZNF776, 2 more genes
    nsv3166518copy number variation1nstd151human GRCh37 chr19: 58,196,627-58,234,713 , GRCh38.p12 chr19: 57,685,259-57,723,345 ZNF671, ZNF154, 1 more genes
    nsv5298876copy number variation1nstd204human GRCh38.p13 chr19: 57,666,473-57,721,827 , GRCh37.p13 chr19: 58,177,841-58,233,195 ZNF671, ZSCAN4, 2 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF671, ZNF321P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 ZNF671, BABAM1, 2426 more genes
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