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Items: 1 to 20 of 322

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112983mobile element insertion1nstd186human GRCh37 chr15: 32,954,696-32,954,747 , GRCh38.p12 chr15: 32,662,495-32,662,546 ARHGAP11A-SCG5, SCG5
    nsv5975020insertion1nstd209human GRCh38 chr15: 32,662,495-32,662,495 , GRCh37.p13 chr15: 32,954,696-32,954,696 SCG5, ARHGAP11A-SCG5
    nsv5970732insertion1nstd209human GRCh38 chr15: 32,657,209-32,657,209 , GRCh37.p13 chr15: 32,949,410-32,949,410 SCG5, ARHGAP11A-SCG5
    nsv5946466copy number variation1nstd209human GRCh38 chr15: 32,645,956-32,648,908 , GRCh37.p13 chr15: 32,938,157-32,941,109 ARHGAP11A-SCG5, SCG5
    nsv5854855copy number variation1nstd209human GRCh38 chr15: 32,645,974-32,648,973 , GRCh37.p13 chr15: 32,938,175-32,941,174 SCG5, ARHGAP11A-SCG5
    nsv5722954mobile element insertion1nstd211human GRCh38 chr15: 32,685,016-32,685,016 , GRCh37.p13 chr15: 32,977,217-32,977,217 SCG5, LOC105370756, 1 more genes
    nsv5710496mobile element insertion2nstd211human GRCh38 chr15: 32,662,495-32,662,495 , GRCh37.p13 chr15: 32,954,696-32,954,696 SCG5, ARHGAP11A-SCG5
    nsv5702933mobile element insertion2nstd211human GRCh38 chr15: 32,692,660-32,692,660 , GRCh37.p13 chr15: 32,984,861-32,984,861 SCG5, ARHGAP11A-SCG5
    nsv5663434insertion1nstd207human GRCh38 chr15: 32,662,486-32,662,486 , GRCh37.p13 chr15: 32,954,687-32,954,687 ARHGAP11A-SCG5, SCG5
    nsv5648982insertion1nstd207human GRCh38 chr15: 32,657,209-32,657,209 , GRCh37.p13 chr15: 32,949,410-32,949,410 SCG5, ARHGAP11A-SCG5
    nsv5564298copy number variation1nstd102humanUncertain significance GRCh37 chr15: 32,964,740-33,002,449 , GRCh38.p12 chr15: 32,672,539-32,710,248 LOC105370756, SCG5-AS1, 2 more genes
    nsv5564217copy number variation1nstd102humanUncertain significance GRCh37 chr15: 32,964,889-33,004,937 , GRCh38.p12 chr15: 32,672,688-32,712,736 SCG5-AS1, ARHGAP11A-SCG5, 2 more genes
    nsv5560628mobile element insertion1nstd206human GRCh38 chr15: 32,685,016-32,685,067 , GRCh37.p13 chr15: 32,977,217-32,977,268 SCG5, LOC105370756, 1 more genes
    nsv5512179copy number variation1nstd206human GRCh38 chr15: 32,640,295-32,640,510 , GRCh37.p13 chr15: 32,932,496-32,932,711 SCG5, ARHGAP11A, 1 more genes
    nsv5428940mobile element insertion1nstd206human GRCh38 chr15: 32,662,495-32,662,546 , GRCh37.p13 chr15: 32,954,696-32,954,747 SCG5, ARHGAP11A-SCG5
    nsv5421387mobile element insertion1nstd206human GRCh38 chr15: 32,692,660-32,692,711 , GRCh37.p13 chr15: 32,984,861-32,984,912 SCG5, ARHGAP11A-SCG5
    nsv5380920copy number variation1nstd102humanUncertain significance GRCh37 chr15: 32,964,889-33,012,502 , GRCh38.p12 chr15: 32,672,688-32,720,301 GREM1-AS1, LOC105370756, 4 more genes
    nsv5380836copy number variation1nstd102humanUncertain significance GRCh37 chr15: 32,964,889-33,010,412 , GRCh38.p12 chr15: 32,672,688-32,718,211 GREM1-AS1, ARHGAP11A-SCG5, 4 more genes
    nsv5380760copy number variation1nstd102humanUncertain significance GRCh37 chr15: 32,964,889-33,010,736 , GRCh38.p12 chr15: 32,672,688-32,718,535 GREM1-AS1, LOC105370756, 4 more genes
    nsv5380759copy number variation1nstd102humanUncertain significance GRCh37 chr15: 32,964,889-32,988,830 , GRCh38.p12 chr15: 32,672,688-32,696,629 SCG5, ARHGAP11A-SCG5, 2 more genes
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