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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3894769copy number variation1nstd102humanBenign GRCh37 chr18: 55,929,965-55,937,109 , GRCh38.p12 chr18: 58,262,733-58,269,877 NEDD4L
    nsv3901491copy number variation1nstd102humanBenign GRCh37 chr18: 55,931,171-55,937,757 , GRCh38.p12 chr18: 58,263,939-58,270,525 NEDD4L
    nsv3900053copy number variation1nstd102humanBenign GRCh37 chr18: 55,908,826-55,909,242 , GRCh38.p12 chr18: 58,241,594-58,242,010 NEDD4L
    nsv6314639copy number variation1nstd102humanLikely benign GRCh38 chr18: 58,322,501-58,322,572 , GRCh37 chr18: 55,989,733-55,989,804 NEDD4L
    nsv7095174copy number variation1nstd102humanLikely benign GRCh37 chr18: 56,018,203-56,063,501 , GRCh38.p12 chr18: 58,350,971-58,396,269 NEDD4L
    nsv3887157copy number variation1nstd102humannot provided GRCh38 chr18: 58,268,755-58,269,877 , GRCh37 chr18: 55,935,987-55,937,109 NEDD4L
    nsv6310429copy number variation1nstd102humanUncertain significance GRCh37 chr18: 55,996,962-55,997,971 , GRCh38.p12 chr18: 58,329,730-58,330,739 NEDD4L
    nsv5381264copy number variation1nstd102humanUncertain significance GRCh37 chr18: 55,833,010-55,833,103 , GRCh38.p12 chr18: 58,165,778-58,165,871 NEDD4L
    nsv5564230copy number variation1nstd102humanUncertain significance GRCh37 chr18: 55,983,194-56,033,480 , GRCh38.p12 chr18: 58,315,962-58,366,248 NEDD4L
    nsv4454862copy number variation1nstd102humanUncertain significance GRCh38 chr18: 58,350,971-58,396,289 , GRCh37 chr18: 56,018,203-56,063,521 NEDD4L
    nsv5381265copy number variation1nstd102humanUncertain significance GRCh37 chr18: 56,018,213-56,063,501 , GRCh38.p12 chr18: 58,350,981-58,396,269 NEDD4L
    nsv6310428copy number variation2nstd102humanUncertain significance GRCh37 chr18: 55,833,000-55,833,113 , GRCh38.p12 chr18: 58,165,768-58,165,881 NEDD4L
    esv3648855copy number variation1estd216humannot provided GRCh37 chr18: 55,935,987-55,937,109 , GRCh38.p12 chr18: 58,268,755-58,269,877 NEDD4L
    nsv7095173copy number variation1nstd102humanUncertain significance GRCh37 chr18: 55,833,000-56,063,501 , GRCh38.p12 chr18: 58,165,768-58,396,269 NEDD4L, LOC105372143
    nsv7094938copy number variation1nstd102humanUncertain significance GRCh37 chr18: 55,833,000-55,919,306 , GRCh38.p12 chr18: 58,165,768-58,252,074 NEDD4L, LOC105372143
    nsv4457436copy number variation1nstd102humanUncertain significance GRCh37 chr18: 56,018,446-56,119,213 , GRCh38.p12 chr18: 58,351,214-58,451,981 NEDD4L, MIR3591, 1 more genes
    nsv4457536copy number variation1nstd102humanUncertain significance GRCh37 chr18: 56,018,446-56,116,713 , GRCh38.p12 chr18: 58,351,214-58,449,481 NEDD4L, MIR122, 1 more genes
    nsv3902831copy number variation1nstd102humanPathogenic GRCh37 chr18: 46,177,798-78,014,123 , GRCh38.p12 chr18: 48,651,427-80,256,240 NEDD4L, LOC105372180, 370 more genes
    nsv3906152copy number variation1nstd102humanPathogenic GRCh37 chr18: 46,942,427-78,014,123 , GRCh38.p12 chr18: 49,416,057-80,256,240 NEDD4L, RPL17P44, 360 more genes
    nsv3909519copy number variation1nstd102humanPathogenic GRCh37 chr18: 47,656,799-78,014,123 , GRCh38.p12 chr18: 50,130,429-80,256,240 NEDD4L, LOC105372160, 339 more genes
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