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Items: 1 to 20 of 26126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6137741copy number variation1nstd102humanBenign GRCh38 chr13: 48,459,928-48,459,979 , GRCh37 chr13: 49,034,064-49,034,115 RB1
    nsv6137727copy number variation2nstd102humanUncertain significance GRCh38 chr3: 12,589,035-12,766,981 , GRCh37.p13 chr3: 12,630,534-12,808,480 RAF1, CRIP1P1, 1 more genes
    nsv6137707copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,565,626-30,221,925 , GRCh38.p12 chr16: 29,554,305-30,210,604 TAOK2, SLC7A5P1, 44 more genes
    nsv6137675copy number variation1nstd102humanLikely benign GRCh37 chr17: 40,489,900-40,489,959 , GRCh38 chr17: 42,337,882-42,337,941 STAT3
    nsv6131202insertion1nstd186human GRCh37 chr19: 54,402,184-54,402,187 , GRCh38.p12 chr19: 53,898,930-53,898,933 PRKCG
    nsv6131079mobile element insertion1nstd186human GRCh37 chr17: 64,637,294-64,637,345 , GRCh38.p12 chr17: 66,641,176-66,641,227 PRKCA
    nsv6130356insertion1nstd186human GRCh37 chr19: 40,734,606-40,734,638 , GRCh38.p12 chr19: 40,228,699-40,228,731 AKT2
    nsv6129919insertion1nstd186human GRCh37 chr13: 49,034,021-49,034,021 , GRCh38.p12 chr13: 48,459,885-48,459,885 RB1
    nsv6129450mobile element insertion1nstd186human GRCh37 chr2: 29,645,166-29,645,217 , GRCh38.p12 chr2: 29,422,300-29,422,351 ALK
    nsv6126556copy number variation1nstd186human GRCh37 chr17: 64,332,752-64,332,805 , GRCh38.p12 chr17: 66,336,634-66,336,687 PRKCA
    nsv6121447copy number variation1nstd186human GRCh37 chr16: 24,070,222-24,070,272 , GRCh38.p12 chr16: 24,058,901-24,058,951 PRKCB
    nsv6118394copy number variation1nstd186human GRCh37 chr3: 25,291,341-25,291,415 , GRCh38.p12 chr3: 25,249,850-25,249,924 , RARB
    nsv6116900copy number variation1nstd186human GRCh37 chr17: 64,794,356-64,795,702 , GRCh38.p12 chr17: 66,798,238-66,799,584 PRKCA
    nsv6115277mobile element insertion1nstd186human GRCh37 chr20: 43,671,538-43,671,589 , GRCh38.p12 chr20: 45,042,897-45,042,948 STK4
    nsv6114990mobile element insertion1nstd186human GRCh37 chr17: 64,419,953-64,420,004 , GRCh38.p12 chr17: 66,423,835-66,423,886 PRKCA
    nsv6114352mobile element insertion1nstd186human GRCh37 chr3: 60,926,052-60,926,103 , GRCh38.p12 chr3: 60,940,380-60,940,431 FHIT
    nsv6113949copy number variation1nstd186human GRCh37 chr16: 2,625,326-2,630,501 , GRCh38.p12 chr16: 2,575,325-2,580,500 PDPK1
    nsv6113585mobile element insertion1nstd186human GRCh37 chr17: 64,334,212-64,334,263 , GRCh38.p12 chr17: 66,338,094-66,338,145 PRKCA
    nsv6112812copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,675,050-30,200,008 , GRCh38.p12 chr16: 29,663,729-30,188,687 INO80E, QPRT, 33 more genes
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