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Items: 1 to 20 of 458

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148130copy number variation1nstd102humanPathogenic GRCh37 chr8: 36,763,176-50,929,707 , GRCh38.p12 chr8: 36,905,658-50,017,147 SNTG1, RN7SL806P, 193 more genes
    nsv7147743insertion1nstd232human GRCh37.p13 chr8: 48,777,326-48,777,326 , GRCh38.p12 chr8: 47,864,765-47,864,765 PRKDC
    nsv7147082insertion1nstd232human GRCh37.p13 chr8: 48,734,355-48,734,355 , GRCh38.p12 chr8: 47,821,794-47,821,794 PRKDC
    nsv7144644insertion1nstd232human GRCh37.p13 chr8: 48,713,548-48,713,548 , GRCh38.p12 chr8: 47,800,987-47,800,987 PRKDC
    nsv7143690copy number variation1nstd232human GRCh37.p13 chr8: 48,866,279-48,866,365 , GRCh38.p12 chr8: 47,953,719-47,953,805 PRKDC
    nsv7142319copy number variation1nstd232human GRCh37.p13 chr8: 48,701,609-48,701,709 , GRCh38.p12 chr8: 47,789,048-47,789,148 PRKDC
    nsv7140958insertion1nstd232human GRCh37.p13 chr8: 48,719,888-48,719,888 , GRCh38.p12 chr8: 47,807,327-47,807,327 PRKDC
    nsv7139509insertion1nstd232human GRCh37.p13 chr8: 48,710,960-48,710,960 , GRCh38.p12 chr8: 47,798,399-47,798,399 PRKDC
    nsv7138935insertion1nstd232human GRCh37.p13 chr8: 48,815,356-48,815,356 , GRCh38.p12 chr8: 47,902,796-47,902,796 PRKDC
    nsv7138685insertion1nstd232human GRCh37.p13 chr8: 48,701,800-48,701,800 , GRCh38.p12 chr8: 47,789,239-47,789,239 PRKDC
    nsv7138170copy number variation1nstd232human GRCh37.p13 chr8: 48,761,862-48,761,936 , GRCh38.p12 chr8: 47,849,301-47,849,375 PRKDC
    nsv7137567insertion1nstd232human GRCh37.p13 chr8: 48,686,939-48,686,939 , GRCh38.p12 chr8: 47,774,378-47,774,378 PRKDC
    nsv7097664copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,761,695-48,766,795 , GRCh38.p12 chr8: 47,849,134-47,854,234 PRKDC
    nsv7097663copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,686,734-48,872,686 , GRCh38.p12 chr8: 47,774,173-47,960,126 PRKDC, LOC105375818, 1 more genes
    nsv7064815inversion1nstd229human GRCh38 chr8: 47,739,939-47,800,977 , GRCh37.p13 chr8: 48,652,501-48,713,538 PRKDC
    nsv6856812copy number variation1nstd229human GRCh38 chr8: 47,906,392-47,907,369 , GRCh37.p13 chr8: 48,818,952-48,819,929 PRKDC
    nsv6852681copy number variation1nstd229human GRCh38 chr8: 47,716,464-47,892,923 , GRCh37.p13 chr8: 48,629,026-48,805,484 CEBPD, SPIDR, 1 more genes
    nsv6852156copy number variation1nstd229human GRCh38 chr8: 47,750,935-47,779,806 , GRCh37.p13 chr8: 48,663,497-48,692,367 PRKDC
    nsv6851750copy number variation1nstd229human GRCh38 chr8: 47,809,328-47,813,404 , GRCh37.p13 chr8: 48,721,889-48,725,965 PRKDC
    nsv6850722copy number variation1nstd229human GRCh38 chr8: 47,597,201-48,026,222 , GRCh37.p13 chr8: 48,509,763-48,938,782 CEBPD, RNU6-519P, 7 more genes
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