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Items: 1 to 20 of 259

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5946662copy number variation1nstd209human GRCh38 chr12: 55,770,134-55,770,306 , GRCh37.p13 chr12: 56,163,918-56,164,090 SARNP
    nsv5945619copy number variation1nstd209human GRCh38 chr12: 55,759,679-55,759,975 , GRCh37.p13 chr12: 56,153,463-56,153,759 SARNP
    nsv5930839copy number variation1nstd209human GRCh38 chr12: 55,766,918-55,768,397 , GRCh37.p13 chr12: 56,160,702-56,162,181 SARNP
    nsv5850294copy number variation1nstd209human GRCh38 chr12: 55,766,484-55,768,423 , GRCh37.p13 chr12: 56,160,268-56,162,207 SARNP
    nsv5540111insertion1nstd206human GRCh38 chr12: 55,761,191-55,761,226 , GRCh37.p13 chr12: 56,154,975-56,155,010 SARNP
    nsv5508049copy number variation1nstd206human GRCh38 chr12: 55,770,138-55,770,307 , GRCh37.p13 chr12: 56,163,922-56,164,091 SARNP
    nsv5505576copy number variation1nstd206human GRCh38 chr12: 55,785,342-55,787,364 , GRCh37.p13 chr12: 56,179,126-56,181,148 SARNP
    nsv5494944copy number variation1nstd206human GRCh38 chr12: 55,810,809-55,811,448 , GRCh37.p13 chr12: 56,204,593-56,205,232 SARNP
    nsv5314357copy number variation1nstd204human GRCh38.p13 chr12: 55,770,129-55,770,315 , GRCh37.p13 chr12: 56,163,913-56,164,099 SARNP
    nsv5275584copy number variation1nstd204human GRCh38.p13 chr12: 55,774,573-55,776,640 , GRCh37.p13 chr12: 56,168,357-56,170,424 SARNP
    nsv5193201mobile element insertion1nstd203human GRCh38 chr12: 55,775,657-55,775,666 , GRCh37.p13 chr12: 56,169,441-56,169,450 SARNP
    nsv5184415mobile element insertion1nstd203human GRCh38 chr12: 55,775,653-55,775,666 , GRCh37.p13 chr12: 56,169,437-56,169,450 SARNP
    nsv5136059mobile element insertion1nstd203human GRCh38 chr12: 55,761,174-55,761,191 , GRCh37.p13 chr12: 56,154,958-56,154,975 SARNP
    nsv5124219mobile element insertion1nstd203human GRCh38 chr12: 55,761,175-55,761,191 , GRCh37.p13 chr12: 56,154,959-56,154,975 SARNP
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv4985635copy number variation1nstd200human GRCh38 chr12: 55,793,753-55,794,029 , GRCh37.p13 chr12: 56,187,537-56,187,813 SARNP
    nsv4985634copy number variation1nstd200human GRCh38 chr12: 55,775,310-55,778,891 , GRCh37.p13 chr12: 56,169,094-56,172,675 SARNP
    nsv4972851copy number variation1nstd200human GRCh38 chr12: 55,785,435-55,793,254 , GRCh37.p13 chr12: 56,179,219-56,187,038 SARNP
    nsv4972850copy number variation1nstd200human GRCh38 chr12: 55,785,341-55,787,364 , GRCh37.p13 chr12: 56,179,125-56,181,148 SARNP
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