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Items: 1 to 20 of 382

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6123849insertion1nstd186human GRCh37 chrX: 24,000,795-24,000,828 , GRCh38.p12 chrX: 23,982,678-23,982,711 KLHL15
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5977788copy number variation1nstd209human GRCh38 chrX: 23,996,395-24,003,221 , GRCh37.p13 chrX: 24,014,512-24,021,338 KLHL15
    nsv5947555insertion1nstd209human GRCh38 chrX: 23,982,660-23,982,660 , GRCh37.p13 chrX: 24,000,777-24,000,777 KLHL15
    nsv5870926copy number variation1nstd209human GRCh38 chrX: 23,997,299-23,997,647 , GRCh37.p13 chrX: 24,015,416-24,015,764 KLHL15
    nsv5868276copy number variation1nstd209human GRCh38 chrX: 23,997,816-24,004,529 , GRCh37.p13 chrX: 24,015,933-24,022,646 KLHL15
    nsv5604532insertion1nstd207human GRCh38 chrX: 23,982,660-23,982,660 , GRCh37.p13 chrX: 24,000,777-24,000,777 KLHL15
    nsv5549033insertion1nstd206human GRCh38 chrX: 23,982,678-23,982,711 , GRCh37.p13 chrX: 24,000,795-24,000,828 KLHL15
    nsv5431305copy number variation1nstd206human GRCh38 chrX: 23,997,811-24,004,522 , GRCh37.p13 chrX: 24,015,928-24,022,639 KLHL15
    nsv5431130copy number variation1nstd206human GRCh38 chrX: 23,990,522-23,990,646 , GRCh37.p13 chrX: 24,008,639-24,008,763 KLHL15
    nsv5427755copy number variation1nstd206human GRCh38 chrX: 23,997,776-24,001,604 , GRCh37.p13 chrX: 24,015,893-24,019,721 KLHL15
    nsv5423688copy number variation1nstd206human GRCh38 chrX: 23,996,171-23,997,856 , GRCh37.p13 chrX: 24,014,288-24,015,973 KLHL15
    nsv5422748copy number variation1nstd206human GRCh38 chrX: 23,990,715-23,990,837 , GRCh37.p13 chrX: 24,008,832-24,008,954 KLHL15
    nsv5422747copy number variation1nstd206human GRCh38 chrX: 23,989,575-23,989,668 , GRCh37.p13 chrX: 24,007,692-24,007,785 KLHL15
    nsv5190985mobile element insertion1nstd203human GRCh38 chrX: 24,002,305-24,002,320 , GRCh37.p13 chrX: 24,020,422-24,020,437 KLHL15
    nsv5185150mobile element insertion1nstd203human GRCh38 chrX: 24,004,269-24,004,269 , GRCh37.p13 chrX: 24,022,386-24,022,386 KLHL15
    nsv5183737mobile element insertion1nstd203human GRCh38 chrX: 23,982,647-23,982,660 , GRCh37.p13 chrX: 24,000,764-24,000,777 KLHL15
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4905274copy number variation1nstd200human GRCh38 chrX: 23,998,324-23,999,073 , GRCh37.p13 chrX: 24,016,441-24,017,190 KLHL15
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