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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5701512mobile element insertion2nstd211human GRCh38 chr13: 52,172,780-52,172,780 , GRCh37.p13 chr13: 52,746,915-52,746,915 MRPS31P5
    nsv5662782insertion1nstd207human GRCh38 chr13: 52,192,252-52,192,252 , GRCh37.p13 chr13: 52,766,387-52,766,387 MRPS31P5
    nsv5658474insertion1nstd207human GRCh38 chr13: 52,172,767-52,172,767 , GRCh37.p13 chr13: 52,746,902-52,746,902 MRPS31P5
    nsv5656093insertion1nstd207human GRCh38 chr13: 52,187,507-52,187,507 , GRCh37.p13 chr13: 52,761,642-52,761,642 MRPS31P5
    nsv5650125insertion1nstd207human GRCh38 chr13: 52,181,015-52,181,015 , GRCh37.p13 chr13: 52,755,150-52,755,150 MRPS31P5
    nsv5596711copy number variation1nstd207human GRCh38 chr13: 52,182,351-52,182,675 , GRCh37.p13 chr13: 52,756,486-52,756,810 MRPS31P5
    nsv5594257copy number variation1nstd207human GRCh38 chr13: 52,185,011-52,185,327 , GRCh37.p13 chr13: 52,759,146-52,759,462 MRPS31P5
    nsv5593377copy number variation1nstd207human GRCh38 chr13: 52,189,270-52,189,593 , GRCh37.p13 chr13: 52,763,405-52,763,728 MRPS31P5
    nsv5591449copy number variation1nstd207human GRCh38 chr13: 52,190,476-52,190,777 , GRCh37.p13 chr13: 52,764,611-52,764,912 MRPS31P5
    nsv5585440copy number variation1nstd207human GRCh38 chr13: 52,183,598-52,183,928 , GRCh37.p13 chr13: 52,757,733-52,758,063 MRPS31P5
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5356899translocation1nstd200human GRCh38 chr13: 52,376,794-52,376,794 , GRCh38 chr13: 52,167,391-52,167,391 , GRCh37.p13 chr13: 52,741,526-52,741,526 , GRCh37.p13 chr13: 52,950,929-52,950,929 THSD1, THSD1P1, 1 more genes
    nsv5345806translocation1nstd200human GRCh37 chr13: 52,950,929-52,950,929 , GRCh37 chr13: 52,741,526-52,741,526 , GRCh38.p12 chr13: 52,167,391-52,167,391 , GRCh38.p12 chr13: 52,376,794-52,376,794 THSD1, THSD1P1, 1 more genes
    nsv5345262translocation1nstd200human GRCh37 chr13: 53,202,399-53,202,399 , GRCh37 chr13: 52,760,110-52,760,110 , GRCh38.p12 chr13: 52,185,975-52,185,975 , GRCh38.p12 chr13: 52,628,264-52,628,264 HNRNPA1L2, MRPS31P5
    nsv5154118mobile element insertion1nstd203human GRCh38 chr13: 52,172,928-52,172,933 , GRCh37.p13 chr13: 52,747,063-52,747,068 MRPS31P5
    nsv5149976mobile element insertion1nstd203human GRCh38 chr13: 52,172,767-52,172,780 , GRCh37.p13 chr13: 52,746,902-52,746,915 MRPS31P5
    nsv5148835mobile element insertion1nstd203human GRCh38 chr13: 52,172,774-52,172,780 , GRCh37.p13 chr13: 52,746,909-52,746,915 MRPS31P5
    nsv5147907mobile element insertion1nstd203human GRCh38 chr13: 52,173,757-52,173,769 , GRCh37.p13 chr13: 52,747,892-52,747,904 MRPS31P5
    nsv5004602copy number variation1nstd200human GRCh38 chr13: 52,184,606-52,196,680 , GRCh37.p13 chr13: 52,758,741-52,770,815 MRPS31P5
    nsv4997204copy number variation1nstd200human GRCh38 chr13: 43,050,454-56,920,222 , GRCh37.p13 chr13: 43,624,590-57,494,356 , RNY3P2, 222 more genes
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