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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3893978copy number variation1nstd102humanBenign GRCh37 chr15: 56,132,824-56,162,466 , GRCh38.p12 chr15: 55,840,626-55,870,268 NEDD4
    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 LOC105372143, NEDD4L
    nsv7094938copy number variation1nstd102humanUncertain significance GRCh37 chr18: 55,833,000-55,919,306 , GRCh38.p12 chr18: 58,165,768-58,252,074 LOC105372143, NEDD4L
    nsv4674858copy number variation1nstd102humanUncertain significance GRCh37 chr15: 56,186,664-56,370,552 , GRCh38.p12 chr15: 55,894,466-56,078,354 NEDD4, RN7SL568P, 2 more genes
    nsv4457436copy number variation1nstd102humanUncertain significance GRCh37 chr18: 56,018,446-56,119,213 , GRCh38.p12 chr18: 58,351,214-58,451,981 MIR3591, NEDD4L, 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
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 NEDD4, H3P40, 1616 more genes
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