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Items: 1 to 20 of 328

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5884394copy number variation1nstd209human GRCh38 chr1: 94,166,944-94,167,978 , GRCh37.p13 chr1: 94,632,500-94,633,534 ARHGAP29
    nsv5880852copy number variation1nstd209human GRCh38 chr1: 94,205,822-94,207,712 , GRCh37.p13 chr1: 94,671,378-94,673,268 ARHGAP29
    nsv5830850copy number variation1nstd209human GRCh38 chr1: 94,205,720-94,207,830 , GRCh37.p13 chr1: 94,671,276-94,673,386 ARHGAP29
    nsv5689482mobile element insertion1nstd211human GRCh38 chr1: 94,205,439-94,205,439 , GRCh37.p13 chr1: 94,670,995-94,670,995 ARHGAP29
    nsv5673257copy number variation1nstd102humanPathogenic GRCh37 chr1: 94,458,793-95,538,454 , GRCh38.p12 chr1: 93,993,237-95,072,898 ABCD3, KATNBL1P2, 19 more genes
    nsv5415199copy number variation1nstd206human GRCh38 chr1: 94,220,899-94,224,995 , GRCh37.p13 chr1: 94,686,455-94,690,551 ARHGAP29
    nsv5412968mobile element insertion1nstd206human GRCh38 chr1: 94,205,439-94,205,490 , GRCh37.p13 chr1: 94,670,995-94,671,046 ARHGAP29
    nsv5076660mobile element insertion1nstd203human GRCh38 chr1: 94,215,787-94,215,800 , GRCh37.p13 chr1: 94,681,343-94,681,356 ARHGAP29
    nsv5066514mobile element insertion1nstd203human GRCh38 chr1: 94,207,465-94,207,475 , GRCh37.p13 chr1: 94,673,021-94,673,031 ARHGAP29
    nsv5063379mobile element insertion1nstd203human GRCh38 chr1: 94,208,994-94,209,011 , GRCh37.p13 chr1: 94,674,550-94,674,567 ARHGAP29
    nsv4897034copy number variation1nstd200human GRCh38 chr1: 94,265,426-94,267,623 , GRCh37.p13 chr1: 94,730,982-94,733,179 ARHGAP29-AS1, ARHGAP29
    nsv4897033copy number variation1nstd200human GRCh38 chr1: 94,243,289-94,250,114 , GRCh37.p13 chr1: 94,708,845-94,715,670 ARHGAP29-AS1, ARHGAP29
    nsv4897032copy number variation1nstd200human GRCh38 chr1: 94,227,219-94,227,304 , GRCh37.p13 chr1: 94,692,775-94,692,860 ARHGAP29
    nsv4897031copy number variation1nstd200human GRCh38 chr1: 94,224,747-94,229,096 , GRCh37.p13 chr1: 94,690,303-94,694,652 ARHGAP29
    nsv4897030copy number variation1nstd200human GRCh38 chr1: 94,192,392-94,193,384 , GRCh37.p13 chr1: 94,657,948-94,658,940 ARHGAP29
    nsv4788695copy number variation1nstd200human GRCh37 chr1: 94,730,982-94,733,179 , GRCh38.p12 chr1: 94,265,426-94,267,623 ARHGAP29-AS1, ARHGAP29
    nsv4788694copy number variation1nstd200human GRCh37 chr1: 94,708,845-94,715,670 , GRCh38.p12 chr1: 94,243,289-94,250,114 ARHGAP29, ARHGAP29-AS1
    nsv4788693copy number variation1nstd200human GRCh37 chr1: 94,671,378-94,673,269 , GRCh38.p12 chr1: 94,205,822-94,207,713 ARHGAP29
    nsv4788692copy number variation1nstd200human GRCh37 chr1: 94,632,501-94,633,535 , GRCh38.p12 chr1: 94,166,945-94,167,979 ARHGAP29
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
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