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Items: 1 to 20 of 53

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3895034copy number variation1nstd102humanBenign GRCh37 chr7: 679,369-682,932 , GRCh38.p12 chr7: 639,732-643,295 PRKAR1B
    nsv3906381copy number variation1nstd102humanBenign GRCh37 chr7: 682,412-682,932 , GRCh38.p12 chr7: 642,775-643,295 PRKAR1B
    nsv7097639copy number variation1nstd102humanPathogenic GRCh37 chr7: 766,358-825,290 , GRCh38.p12 chr7: 726,721-785,653 PRKAR1B, DNAAF5
    nsv7097638copy number variation1nstd102humanPathogenic GRCh37 chr7: 766,358-769,504 , GRCh38.p12 chr7: 726,721-729,867 PRKAR1B, DNAAF5
    nsv3898129copy number variation1nstd102humanUncertain significance GRCh37 chr7: 704,572-832,973 , GRCh38.p12 chr7: 664,935-793,336 PRKAR1B, DNAAF5
    nsv7098136copy number variation1nstd102humanUncertain significance GRCh37 chr7: 766,358-781,122 , GRCh38.p12 chr7: 726,721-741,485 PRKAR1B, DNAAF5
    nsv3912682copy number variation1nstd102humanUncertain significance NCBI36 chr7: 695,717-861,035 , GRCh38 chr7: 689,554-854,872 , GRCh37 chr7: 729,191-894,509 PRKAR1B, SUN1, 1 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 PRKAR1B, RNU6-438P, 2682 more genes
    nsv3920006copy number variation1nstd102humanPathogenic GRCh37 chr7: 45,130-5,920,006 , GRCh38 chr7: 45,130-5,880,375 , NCBI36 chr7: 140,213-5,886,532 PRKAR1B, RNU6-215P, 120 more genes
    nsv4456136copy number variation1nstd102humanPathogenic GRCh37 chr7: 36,616-4,298,168 , GRCh38.p12 chr7: 36,616-4,258,536 PRKAR1B, LOC442497, 85 more genes
    nsv3898790copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-3,642,604 , GRCh38.p12 chr7: 43,360-3,602,972 PRKAR1B, RPL21P72, 83 more genes
    nsv3911664copy number variation1nstd102humanPathogenic GRCh38 chr7: 54,185-3,324,143 , GRCh37 chr7: 54,185-3,363,775 , NCBI36 chr7: 149,268-3,330,301 PRKAR1B, MIR6836, 81 more genes
    nsv3912605copy number variation1nstd102humanPathogenic GRCh38 chr7: 54,165-3,258,775 , NCBI36 chr7: 149,248-3,264,933 , GRCh37 chr7: 54,165-3,298,407 PRKAR1B, LOC100129603, 80 more genes
    nsv3916297copy number variation2nstd102humanPathogenic GRCh38 chr7: 54,185-1,843,584 , NCBI36 chr7: 149,268-1,849,746 , GRCh37 chr7: 54,185-1,883,220 PRKAR1B, MAD1L1, 51 more genes
    nsv4675871copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-1,750,797 , GRCh38.p12 chr7: 44,935-1,711,161 PRKAR1B, C7orf50, 47 more genes
    nsv4675301copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-1,648,288 , GRCh38.p12 chr7: 43,360-1,608,652 PRKAR1B, LOC112267991, 42 more genes
    nsv3914197copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-1,480,761 , GRCh38 chr7: 54,185-1,441,125 , NCBI36 chr7: 149,268-1,447,287 PRKAR1B, LOC112267991, 34 more genes
    nsv7097362copy number variation1nstd102humanPathogenic GRCh37 chr7: 193,200-1,498,962 , GRCh38.p12 chr7: 193,200-1,459,326 PRKAR1B, ZFAND2A-DT, 28 more genes
    nsv3924345copy number variation1nstd102humanPathogenic NCBI36 chr7: 149,248-731,488 , GRCh38 chr7: 54,165-725,325 , GRCh37 chr7: 54,165-764,962 PRKAR1B, LOC105375114, 19 more genes
    nsv3894780copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842 PRKAR1B, RNU6-565P, 2684 more genes
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