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Items: 1 to 20 of 21

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3913330copy number variation1nstd102humanUncertain significance NCBI36 chr10: 77,703,108-77,852,194 , GRCh37.p13 chr10: 78,033,102-78,182,188 , GRCh38.p12 chr10: 76,273,344-76,422,430 LRMDA, LOC112268057
    nsv3923159copy number variation1nstd102humanUncertain significance GRCh37 chr10: 77,796,106-78,462,249 , GRCh38 chr10: 76,036,348-76,702,491 , NCBI36 chr10: 77,466,112-78,132,255 LRMDA, LOC112268057, 2 more genes
    nsv3895207copy number variation1nstd102humanUncertain significance GRCh37 chr10: 77,158,059-77,272,227 , GRCh38.p12 chr10: 75,398,301-75,512,469 LRMDA, ZNF503-AS2, 3 more genes
    nsv3921858copy number variation1nstd102humanUncertain significance NCBI36 chr10: 77,625,821-77,739,290 , GRCh37.p13 chr10: 77,955,815-78,069,284 , GRCh38.p12 chr10: 76,196,057-76,309,526 LRMDA, RNU6-673P, 2 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 LRMDA, RNU7-12P, 1876 more genes
    nsv6314185copy number variation1nstd102humanPathogenic GRCh37 chr10: 68,735,254-78,885,714 , GRCh38.p12 chr10: 66,975,496-77,125,956 LRMDA, SLC25A16, 204 more genes
    nsv3905190copy number variation1nstd102humanPathogenic GRCh37 chr10: 75,542,067-79,428,995 , GRCh38.p12 chr10: 73,782,309-77,669,237 LRMDA, TIMM9P1, 47 more genes
    nsv3910545copy number variation1nstd102humanPathogenic NCBI36 chr10: 74,150,392-77,042,138 , GRCh38 chr10: 72,720,628-75,612,374 , GRCh37 chr10: 74,480,386-77,372,132 LRMDA, CAMK2G, 73 more genes
    nsv7093731copy number variation1nstd102humanPathogenic GRCh37 chr10: 76,349,020-78,317,046 , GRCh38.p12 chr10: 74,589,262-76,557,288 LRMDA, ADK, 25 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 LRMDA, LOC100419870, 2105 more genes
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 LRMDA, AGAP14P, 2097 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 LRMDA, ANXA11, 2085 more genes
    nsv3891958copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414 LRMDA, TUBB8, 2085 more genes
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 LRMDA, EXOC6, 1906 more genes
    nsv3924859copy number variation1nstd102humanPathogenic NCBI36 chr10: 52,159,133-88,896,941 , GRCh38 chr10: 50,729,367-87,147,204 , GRCh37 chr10: 52,489,127-88,906,961 LRMDA, BMS1P4-AGAP5, 471 more genes
    nsv3891070copy number variation1nstd102humanPathogenic GRCh37 chr10: 69,040,366-93,194,993 , GRCh38.p12 chr10: 67,280,608-91,435,236 LRMDA, NRG3-AS1, 441 more genes
    nsv3917966copy number variation1nstd102humanPathogenic NCBI36 chr10: 68,626,331-80,851,819 , GRCh37 chr10: 68,956,325-81,181,813 , GRCh38 chr10: 67,196,567-79,422,057 LRMDA, LINC02640, 231 more genes
    nsv7093650copy number variation1nstd102humanLikely benign GRCh37 chr10: 76,736,352-77,198,536 , GRCh38.p12 chr10: 74,976,594-75,438,778 LRMDA, VDAC2, 16 more genes
    nsv3907664copy number variation1nstd102humandrug response GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422 LRMDA, SHOC2, 1487 more genes
    nsv3876996copy number variation1nstd102humanUncertain significance NCBI36 chr10: 75,769,258-77,642,312 , GRCh37.p13 chr10: 76,099,252-77,972,306 , GRCh38.p12 chr10: 74,339,494-76,212,548 LRMDA, MIR606, 27 more genes
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