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Items: 1 to 20 of 3810

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3911019copy number variation1nstd102humanLikely benign NCBI36 chr5: 58,601,048-58,850,131 , GRCh37 chr5: 58,565,291-58,814,374 , GRCh38 chr5: 59,269,465-59,518,548 PDE4D
    nsv3884670copy number variation1nstd102humanLikely benign GRCh37 chr5: 58,673,779-58,786,147 , GRCh38.p12 chr5: 59,377,953-59,490,321 PDE4D
    nsv3889031copy number variation1nstd102humanBenign GRCh37 chr5: 59,178,177-59,261,429 , GRCh38.p12 chr5: 59,882,350-59,965,602 PDE4D
    nsv3882403copy number variation1nstd102humanBenign GRCh37 chr5: 59,481,878-59,496,175 , GRCh38.p12 chr5: 60,186,051-60,200,348 PDE4D
    nsv3888437copy number variation1nstd102humanBenign GRCh37 chr5: 59,490,107-59,502,520 , GRCh38.p12 chr5: 60,194,280-60,206,693 PDE4D
    nsv3884857copy number variation1nstd102humanBenign GRCh37 chr5: 58,365,249-58,594,684 , GRCh38.p12 chr5: 59,069,422-59,298,858 PDE4D
    nsv4455862copy number variation1nstd102humanUncertain significance GRCh37 chr5: 58,635,212-58,718,022 , GRCh38.p12 chr5: 59,339,386-59,422,196 PDE4D
    nsv4729044copy number variation1nstd102humanUncertain significance GRCh37 chr5: 59,193,823-59,267,463 , GRCh38.p12 chr5: 59,897,996-59,971,636 PDE4D
    nsv4729518copy number variation1nstd102humanUncertain significance GRCh37 chr5: 58,202,794-58,274,928 , GRCh38.p12 chr5: 58,906,967-58,979,101 PDE4D
    esv4009836copy number variation1estd231human GRCh37 chr5: 59,489,455-59,496,901 , GRCh38.p12 chr5: 60,193,628-60,201,074 PDE4D
    esv4009835copy number variation1estd231human GRCh37 chr5: 58,772,946-58,774,384 , GRCh38.p12 chr5: 59,477,120-59,478,558 PDE4D
    esv3995397copy number variation1estd218human GRCh37 chr5: 58,893,931-58,940,034 , GRCh38.p12 chr5: 59,598,105-59,644,208 PDE4D
    nsv6770178copy number variation1nstd229human GRCh38 chr5: 59,082,402-59,350,519 , GRCh37.p13 chr5: 58,378,229-58,646,345 PDE4D
    nsv6763093copy number variation1nstd229human GRCh38 chr5: 59,235,445-59,475,725 , GRCh37.p13 chr5: 58,531,271-58,771,551 PDE4D
    nsv6764661copy number variation1nstd229human GRCh38 chr5: 59,250,244-59,403,426 , GRCh37.p13 chr5: 58,546,070-58,699,252 PDE4D
    nsv6765990copy number variation1nstd229human GRCh38 chr5: 59,271,104-59,393,611 , GRCh37.p13 chr5: 58,566,930-58,689,437 PDE4D
    nsv6767617copy number variation1nstd229human GRCh38 chr5: 59,376,342-59,490,812 , GRCh37.p13 chr5: 58,672,168-58,786,638 PDE4D
    nsv6777280copy number variation1nstd229human GRCh38 chr5: 59,303,395-59,402,185 , GRCh37.p13 chr5: 58,599,221-58,698,011 PDE4D
    nsv6767394copy number variation1nstd229human GRCh38 chr5: 59,318,979-59,417,296 , GRCh37.p13 chr5: 58,614,805-58,713,122 PDE4D
    nsv6777363copy number variation1nstd229human GRCh38 chr5: 59,339,498-59,422,197 , GRCh37.p13 chr5: 58,635,324-58,718,023 PDE4D
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