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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6128015copy number variation1nstd186human GRCh37 chr18: 67,680,605-67,680,666 , GRCh38.p12 chr18: 70,013,369-70,013,430 RTTN
    nsv6112815copy number variation1nstd102humanPathogenic GRCh37 chr18: 54,285,235-77,960,815 , GRCh38.p12 chr18: 56,618,004-80,202,932 RPL31P9, TRG-TCC5-1, 271 more genes
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5978155insertion1nstd209human GRCh38 chr18: 70,152,281-70,152,281 , GRCh37.p13 chr18: 67,819,517-67,819,517 RTTN
    nsv5946528copy number variation1nstd209human GRCh38 chr18: 70,013,369-70,013,420 , GRCh37.p13 chr18: 67,680,605-67,680,656 RTTN
    nsv5722028mobile element insertion1nstd211human GRCh38 chr18: 70,152,298-70,152,298 , GRCh37.p13 chr18: 67,819,534-67,819,534 RTTN
    nsv5718381mobile element insertion1nstd211human GRCh38 chr18: 70,057,975-70,057,975 , GRCh37.p13 chr18: 67,725,211-67,725,211 RTTN
    nsv5712770mobile element insertion1nstd211human GRCh38 chr18: 70,087,029-70,087,029 , GRCh37.p13 chr18: 67,754,265-67,754,265 RTTN
    nsv5710118mobile element insertion1nstd211human GRCh38 chr18: 70,076,953-70,076,953 , GRCh37.p13 chr18: 67,744,189-67,744,189 RTTN
    nsv5707273mobile element insertion1nstd211human GRCh38 chr18: 70,184,717-70,184,717 , GRCh37.p13 chr18: 67,851,953-67,851,953 RTTN
    nsv5703350mobile element insertion1nstd211human GRCh38 chr18: 70,204,694-70,204,694 , GRCh37.p13 chr18: 67,871,930-67,871,930 LOC105372180, RTTN
    nsv5697221mobile element insertion1nstd211human GRCh38 chr18: 70,165,841-70,165,841 , GRCh37.p13 chr18: 67,833,077-67,833,077 RTTN
    nsv5697050mobile element insertion1nstd211human GRCh38 chr18: 70,038,934-70,038,934 , GRCh37.p13 chr18: 67,706,170-67,706,170 RTTN
    nsv5654447insertion1nstd207human GRCh38 chr18: 70,013,369-70,013,369 , GRCh37.p13 chr18: 67,680,605-67,680,605 RTTN
    nsv5533122copy number variation1nstd206human GRCh38 chr18: 70,181,463-70,187,938 , GRCh37.p13 chr18: 67,848,699-67,855,174 RTTN
    nsv5528074copy number variation1nstd206human GRCh38 chr18: 70,100,764-70,107,195 , GRCh37.p13 chr18: 67,768,000-67,774,431 RTTN
    nsv5525048copy number variation1nstd206human GRCh38 chr18: 70,013,369-70,013,430 , GRCh37.p13 chr18: 67,680,605-67,680,666 RTTN
    nsv5514135copy number variation1nstd206human GRCh38 chr18: 62,909,528-80,261,528 , GRCh37.p13 chr18: 60,576,761-78,017,154 , SMIM21, 190 more genes
    nsv5427822mobile element insertion1nstd206human GRCh38 chr18: 70,076,953-70,077,004 , GRCh37.p13 chr18: 67,744,189-67,744,240 RTTN
    nsv5426729mobile element insertion1nstd206human GRCh38 chr18: 70,204,694-70,204,745 , GRCh37.p13 chr18: 67,871,930-67,871,981 LOC105372180, RTTN
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