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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3899340copy number variation1nstd102humanBenign GRCh37 chr10: 75,605,636-75,634,662 , GRCh38.p12 chr10: 73,845,878-73,874,904 CAMK2G
    nsv3899208copy number variation1nstd102humanBenign GRCh37 chr10: 75,633,630-75,648,249 , GRCh38.p12 chr10: 73,873,872-73,888,491 CAMK2G
    nsv3897564copy number variation1nstd102humanBenign GRCh37 chr10: 75,633,630-75,647,491 , GRCh38.p12 chr10: 73,873,872-73,887,733 CAMK2G
    nsv3896192copy number variation1nstd102humanBenign GRCh37 chr10: 75,633,630-75,634,662 , GRCh38.p12 chr10: 73,873,872-73,874,904 CAMK2G
    nsv3891344copy number variation1nstd102humanBenign GRCh37 chr10: 75,633,630-75,634,558 , GRCh38.p12 chr10: 73,873,872-73,874,800 CAMK2G
    nsv3896943copy number variation1nstd102humanBenign GRCh37 chr10: 75,633,912-75,634,662 , GRCh38.p12 chr10: 73,874,154-73,874,904 CAMK2G
    nsv7137166copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,585,106-75,634,350 , GRCh38.p12 chr10: 73,825,348-73,874,592 CAMK2G
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 CAMK2G, RNU7-12P, 1876 more genes
    nsv3922335copy number variation1nstd102humanPathogenic GRCh37 chr10: 60,196,226-76,174,974 , GRCh38 chr10: 58,436,466-74,415,216 , NCBI36 chr10: 59,866,232-75,844,980 CAMK2G, UNC5B-AS1, 250 more genes
    nsv3917822copy number variation1nstd102humanPathogenic GRCh38 chr10: 63,402,579-75,296,099 , GRCh37 chr10: 65,162,339-77,055,857 , NCBI36 chr10: 64,832,345-76,725,863 CAMK2G, MYL6P3, 220 more genes
    nsv6314185copy number variation1nstd102humanPathogenic GRCh37 chr10: 68,735,254-78,885,714 , GRCh38.p12 chr10: 66,975,496-77,125,956 CAMK2G, SLC25A16, 204 more genes
    nsv3905190copy number variation1nstd102humanPathogenic GRCh37 chr10: 75,542,067-79,428,995 , GRCh38.p12 chr10: 73,782,309-77,669,237 CAMK2G, 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 CAMK2G, MCU, 73 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 CAMK2G, LOC100419870, 2105 more genes
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 CAMK2G, AGAP14P, 2097 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 CAMK2G, ANXA11, 2085 more genes
    nsv3891958copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414 CAMK2G, TUBB8, 2085 more genes
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 CAMK2G, 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 CAMK2G, 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 CAMK2G, NRG3-AS1, 441 more genes
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