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Items: 12

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    Number of Variants: 12

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6637818copy number variation1nstd102humanUncertain significance GRCh37 chr19: 4,740,085-4,857,609 , GRCh38.p12 chr19: 4,740,073-4,857,597 PLIN3, FEM1A, 3 more genes
    nsv6291587copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,501,624-5,357,124 , GRCh38.p12 chr19: 3,501,626-5,357,113 PLIN3, RN7SL202P, 67 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 PLIN3, ZNF321P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 PLIN3, BABAM1, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 PLIN3, LENG8, 2408 more genes
    nsv3914351copy number variation1nstd102humanPathogenic NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555 PLIN3, SEMA6B, 299 more genes
    nsv3924102copy number variation1nstd102humanPathogenic GRCh38 chr19: 259,395-6,795,611 , GRCh37 chr19: 259,395-6,795,622 , NCBI36 chr19: 210,395-6,746,622 PLIN3, POLR2E, 283 more genes
    nsv3890584copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,120,160-9,732,820 , GRCh38.p12 chr19: 3,120,162-9,622,144 PLIN3, PCP2, 250 more genes
    nsv3918318copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 3,739,725-5,098,365 , GRCh37 chr19: 3,788,725-5,147,365 , GRCh38 chr19: 3,788,727-5,147,354 PLIN3, DAPK3, 49 more genes
    nsv3910993copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 3,031,619-4,863,634 , GRCh37 chr19: 3,080,619-4,912,634 , GRCh38 chr19: 3,080,621-4,912,622 PLIN3, DAPK3, 74 more genes
    nsv7095297copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777 PLIN3, NCLN, 223 more genes
    nsv3921092copy number variation1nstd102humanUncertain significance GRCh38 chr19: 3,947,934-5,196,676 , GRCh37 chr19: 3,947,932-5,196,687 , NCBI36 chr19: 3,898,932-5,147,687 PLIN3, FEM1A, 43 more genes
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