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Items: 1 to 20 of 32

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6314707copy number variation1nstd102humanLikely benign GRCh38 chr10: 74,089,367-74,089,708 , GRCh37 chr10: 75,849,125-75,849,466 VCL
    nsv6313975copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,712,146-75,856,710 , GRCh38.p12 chr10: 73,952,388-74,096,952 VCL
    nsv5564206copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,863,568-75,865,121 , GRCh38.p12 chr10: 74,103,810-74,105,363 VCL
    nsv6634655copy number variation1nstd102humanUncertain significance GRCh38 chr10: 74,102,639-74,103,844 , GRCh37 chr10: 75,862,397-75,863,602 VCL
    nsv7093894copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,842,192-75,843,291 , GRCh38.p12 chr10: 74,082,434-74,083,533 VCL
    nsv4454539copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,757,946-75,758,153 , GRCh38 chr10: 73,998,188-73,998,395 VCL
    nsv4683590copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,757,956-75,758,143 , GRCh38.p12 chr10: 73,998,198-73,998,385 VCL
    nsv6309009copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,757,966-75,843,291 , GRCh38.p12 chr10: 73,998,208-74,083,533 VCL
    nsv7093649copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,757,966-75,758,153 , GRCh38.p12 chr10: 73,998,208-73,998,395 VCL
    nsv3872951copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,802,539-75,896,413 , GRCh38.p12 chr10: 74,042,781-74,136,655 VCL, AP3M1
    nsv7093730copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,802,821-75,877,927 , GRCh38.p12 chr10: 74,043,063-74,118,169 VCL, AP3M1
    nsv4455744copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,832,145-75,885,881 , GRCh38.p12 chr10: 74,072,387-74,126,123 VCL, AP3M1
    nsv7093802copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,830,408-75,877,927 , GRCh38.p12 chr10: 74,070,650-74,118,169 VCL, AP3M1
    nsv4682904copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,873,932-75,877,937 , GRCh38.p12 chr10: 74,114,174-74,118,179 VCL, AP3M1
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 VCL, 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 VCL, 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 VCL, MYL6P3, 220 more genes
    nsv6314185copy number variation1nstd102humanPathogenic GRCh37 chr10: 68,735,254-78,885,714 , GRCh38.p12 chr10: 66,975,496-77,125,956 VCL, SLC25A16, 204 more genes
    nsv3905190copy number variation1nstd102humanPathogenic GRCh37 chr10: 75,542,067-79,428,995 , GRCh38.p12 chr10: 73,782,309-77,669,237 VCL, 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 VCL, CAMK2G, 73 more genes
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