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Items: 1 to 20 of 55

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3892285copy number variation1nstd102humanLikely benign GRCh37 chr10: 53,321,554-53,420,982 , GRCh38.p12 chr10: 51,561,794-51,661,222 PRKG1
    nsv3896603copy number variation1nstd102humanBenign GRCh37 chr10: 53,269,467-53,318,238 , GRCh38.p12 chr10: 51,509,707-51,558,478 PRKG1
    nsv3893304copy number variation1nstd102humanBenign GRCh37 chr10: 54,016,062-54,028,464 , GRCh38.p12 chr10: 52,256,302-52,268,704 PRKG1
    nsv3900884copy number variation1nstd102humanBenign GRCh37 chr10: 53,204,509-53,211,991 , GRCh38.p12 chr10: 51,444,749-51,452,231 PRKG1
    nsv3907055copy number variation1nstd102humanBenign GRCh37 chr10: 54,012,974-54,017,651 , GRCh38.p12 chr10: 52,253,214-52,257,891 PRKG1
    nsv3900234copy number variation1nstd102humanBenign GRCh37 chr10: 54,016,062-54,019,620 , GRCh38.p12 chr10: 52,256,302-52,259,860 PRKG1
    nsv3893854copy number variation1nstd102humanBenign GRCh37 chr10: 54,016,099-54,019,620 , GRCh38.p12 chr10: 52,256,339-52,259,860 PRKG1
    nsv3909143copy number variation1nstd102humanBenign GRCh37 chr10: 53,699,753-53,701,052 , GRCh38.p12 chr10: 51,939,993-51,941,292 PRKG1
    nsv3893527copy number variation1nstd102humanBenign GRCh37 chr10: 53,825,576-53,983,258 , GRCh38.p12 chr10: 52,065,816-52,223,498 PRKG1
    nsv3923112copy number variation1nstd102humanBenign GRCh38 chr10: 52,074,749-52,222,855 , GRCh37 chr10: 53,834,509-53,982,615 , NCBI36 chr10: 53,504,515-53,652,621 PRKG1
    nsv3902341copy number variation1nstd102humanBenign GRCh37 chr10: 54,016,062-54,024,195 , GRCh38.p12 chr10: 52,256,302-52,264,435 PRKG1
    nsv6309148copy number variation1nstd102humanUncertain significance GRCh37 chr10: 53,814,224-54,053,660 , GRCh38.p12 chr10: 52,054,464-52,293,900 PRKG1
    nsv6308913copy number variation1nstd102humanUncertain significance GRCh37 chr10: 53,564,335-53,667,340 , GRCh38.p12 chr10: 51,804,575-51,907,580 PRKG1
    nsv6308914copy number variation1nstd102humanUncertain significance GRCh37 chr10: 53,667,247-53,769,653 , GRCh38.p12 chr10: 51,907,487-52,009,893 PRKG1
    nsv3877857copy number variation1nstd102humannot provided GRCh38 chr10: 51,447,874-51,451,689 , GRCh37 chr10: 53,207,634-53,211,449 PRKG1
    nsv7093790copy number variation1nstd102humanUncertain significance GRCh37 chr10: 54,049,964-54,053,660 , GRCh38.p12 chr10: 52,290,204-52,293,900 PRKG1
    nsv5380789copy number variation1nstd102humanUncertain significance GRCh37 chr10: 53,564,335-53,564,460 , GRCh38.p12 chr10: 51,804,575-51,804,700 PRKG1
    nsv3872948copy number variation1nstd102humanUncertain significance GRCh37 chr10: 53,921,629-53,921,743 , GRCh38 chr10: 52,161,869-52,161,983 PRKG1
    nsv4454039copy number variation1nstd102humanUncertain significance GRCh38 chr10: 52,054,474-52,054,571 , GRCh37 chr10: 53,814,234-53,814,331 PRKG1
    nsv4683451copy number variation1nstd102humanUncertain significance GRCh37 chr10: 53,667,257-53,667,340 , GRCh38.p12 chr10: 51,907,497-51,907,580 PRKG1
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