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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6724908copy number variation1nstd229human GRCh38 chr3: 149,033,601-149,033,720 , GRCh37.p13 chr3: 148,751,388-148,751,507 HLTF
    nsv6734724copy number variation1nstd229human GRCh38 chr3: 149,079,466-149,079,517 , GRCh37.p13 chr3: 148,797,253-148,797,304 HLTF
    nsv7137773copy number variation1nstd232human GRCh37.p13 chr3: 148,797,250-148,797,303 , GRCh38.p12 chr3: 149,079,463-149,079,516 HLTF
    nsv6366123copy number variation1nstd223human GRCh38 chr3: 149,078,677-149,082,248 , GRCh37.p13 chr3: 148,796,464-148,800,035 HLTF
    nsv6363563copy number variation1nstd223human GRCh38 chr3: 149,092,060-149,093,664 , GRCh37.p13 chr3: 148,809,847-148,811,451 HLTF-AS1
    nsv6355674copy number variation1nstd223human GRCh38 chr3: 149,063,901-149,065,200 , GRCh37.p13 chr3: 148,781,688-148,782,987 HLTF
    nsv6357197copy number variation1nstd223human GRCh38 chr3: 149,039,301-149,040,400 , GRCh37.p13 chr3: 148,757,088-148,758,187 HLTF
    nsv5450471copy number variation1nstd206human GRCh38 chr3: 149,033,601-149,033,718 , GRCh37.p13 chr3: 148,751,388-148,751,505 HLTF
    nsv5448316copy number variation1nstd206human GRCh38 chr3: 149,067,744-149,067,815 , GRCh37.p13 chr3: 148,785,531-148,785,602 HLTF
    nsv4639011copy number variation1nstd186human GRCh37 chr3: 148,797,152-148,797,304 , GRCh38.p12 chr3: 149,079,365-149,079,517 HLTF
    nsv6161013copy number variation1nstd214human GRCh38 chr3: 149,079,463-149,079,516 , GRCh37.p13 chr3: 148,797,250-148,797,303 HLTF
    nsv5991659copy number variation1nstd212human GRCh38 chr3: 149,067,744-149,067,821 , GRCh37.p13 chr3: 148,785,531-148,785,608 HLTF
    nsv5992075copy number variation1nstd212human GRCh38 chr3: 149,079,463-149,079,516 , GRCh37.p13 chr3: 148,797,250-148,797,303 HLTF
    nsv4739503copy number variation1nstd199human GRCh37 chr3: 148,809,845-148,811,432 , GRCh38.p12 chr3: 149,092,058-149,093,645 HLTF-AS1
    nsv4731825copy number variation1nstd199human GRCh37 chr3: 148,797,248-148,797,302 , GRCh38.p12 chr3: 149,079,461-149,079,515 HLTF
    nsv5571680copy number variation1nstd207human GRCh38 chr3: 149,067,744-149,067,820 , GRCh37.p13 chr3: 148,785,531-148,785,607 HLTF
    nsv5577706copy number variation1nstd207human GRCh38 chr3: 149,079,463-149,079,516 , GRCh37.p13 chr3: 148,797,250-148,797,303 HLTF
    nsv4912308copy number variation1nstd200human GRCh38 chr3: 149,078,675-149,082,250 , GRCh37.p13 chr3: 148,796,462-148,800,037 HLTF
    nsv4791490copy number variation1nstd200human GRCh37 chr3: 148,796,462-148,800,037 , GRCh38.p12 chr3: 149,078,675-149,082,250 HLTF
    nsv4912309copy number variation1nstd200human GRCh38 chr3: 149,092,060-149,093,664 , GRCh37.p13 chr3: 148,809,847-148,811,451 HLTF-AS1
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