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Items: 1 to 20 of 32

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3892874copy number variation1nstd102humanBenign GRCh37 chr17: 64,513,878-64,557,925 , GRCh38.p12 chr17: 66,517,760-66,561,807 PRKCA
    nsv3908204copy number variation1nstd102humanBenign GRCh37 chr17: 64,457,988-64,458,545 , GRCh38.p12 chr17: 66,461,870-66,462,427 PRKCA
    nsv3903938copy number variation1nstd102humanBenign GRCh37 chr17: 64,410,915-64,482,151 , GRCh38.p12 chr17: 66,414,797-66,486,033 PRKCA, PRKCA-AS1
    nsv3882584copy number variation1nstd102humannot provided GRCh37 chr17: 64,384,076-64,504,644 , GRCh38 chr17: 66,387,958-66,508,526 PRKCA, PRKCA-AS1
    nsv3881437copy number variation1nstd102humannot provided GRCh37 chr17: 64,410,915-64,482,151 , GRCh38 chr17: 66,414,797-66,486,033 PRKCA, PRKCA-AS1
    esv3648838copy number variation1estd216humannot provided GRCh37 chr17: 64,384,076-64,504,644 , GRCh38.p12 chr17: 66,387,958-66,508,526 PRKCA, PRKCA-AS1
    esv3648839copy number variation1estd216humannot provided GRCh37 chr17: 64,410,915-64,482,151 , GRCh38.p12 chr17: 66,414,797-66,486,033 PRKCA, PRKCA-AS1
    nsv3900614copy number variation1nstd102humanBenign GRCh37 chr17: 64,563,520-64,682,078 , GRCh38.p12 chr17: 66,567,402-66,685,960 PRKCA, RNU6-928P, 1 more genes
    nsv3911805copy number variation1nstd102humanUncertain significance NCBI36 chr17: 61,850,758-62,173,017 , GRCh38 chr17: 66,424,178-66,746,437 , GRCh37 chr17: 64,420,296-64,742,555 PRKCA, RNA5SP445, 1 more genes
    nsv3918003copy number variation1nstd102humanUncertain significance NCBI36 chr17: 61,786,042-62,070,721 , GRCh37.p13 chr17: 64,355,580-64,640,259 , GRCh38.p12 chr17: 66,359,462-66,644,141 PRKCA, RNA5SP445, 3 more genes
    nsv4457512copy number variation1nstd102humanUncertain significance GRCh37 chr17: 64,582,010-64,733,650 , GRCh38.p12 chr17: 66,585,892-66,737,532 PRKCA, RNU6-928P, 1 more genes
    nsv4729997copy number variation1nstd102humanUncertain significance GRCh37 chr17: 64,616,234-64,764,945 , GRCh38.p12 chr17: 66,620,116-66,768,827 PRKCA, RNA5SP445, 1 more genes
    nsv6637956copy number variation1nstd102humanUncertain significance GRCh37 chr17: 64,561,748-64,659,111 , GRCh38.p12 chr17: 66,565,630-66,662,993 PRKCA, RNU6-928P, 1 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 PRKCA, PRPSAP1, 1350 more genes
    nsv3914737copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,649,313-65,683,004 , NCBI36 chr17: 60,061,351-63,113,466 , GRCh38 chr17: 64,634,771-67,686,888 PRKCA, AXIN2, 53 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 PRKCA, MIR3185, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 PRKCA, P4HB, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 PRKCA, MIR21, 2366 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 PRKCA, SMURF2, 2366 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 PRKCA, LOC105371922, 1855 more genes
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