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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3903875copy number variation1nstd102humanLikely benign NCBI36 chrX: 15,874,243-16,115,462 , GRCh37 chrX: 15,964,322-16,205,541 , GRCh38 chrX: 15,946,199-16,187,418 GRPR, MAGEB17
    nsv3900768copy number variation1nstd102humanLikely benign NCBI36 chrX: 15,916,375-16,473,964 , GRCh37 chrX: 16,006,454-16,564,043 , GRCh38 chrX: 15,988,331-16,545,920 GRPR, RPL6P30, 3 more genes
    nsv3902392copy number variation1nstd102humanLikely benign GRCh37 chrX: 15,926,504-16,450,536 , GRCh38 chrX: 15,908,381-16,432,413 , NCBI36 chrX: 15,836,425-16,360,457 GRPR, RNU5F-7P, 3 more genes
    nsv3898053copy number variation1nstd102humanBenign GRCh38 chrX: 16,065,773-16,479,154 , NCBI36 chrX: 15,993,817-16,407,198 , GRCh37 chrX: 16,083,896-16,497,277 GRPR, MAGEB17, 2 more genes
    nsv3898151copy number variation1nstd102humanUncertain significance GRCh37 chrX: 15,950,701-16,541,460 , GRCh38 chrX: 15,932,578-16,523,337 , NCBI36 chrX: 15,860,622-16,451,381 GRPR, RPL6P30, 2 more genes
    nsv3879969copy number variation1nstd102humanUncertain significance GRCh37 chrX: 15,924,814-16,464,876 , GRCh38.p12 chrX: 15,906,691-16,446,753 GRPR, RPL6P30, 3 more genes
    nsv6290518copy number variation1nstd102humanUncertain significance GRCh37 chrX: 15,924,815-16,460,552 , GRCh38.p12 chrX: 15,906,692-16,442,429 GRPR, SETP15, 3 more genes
    nsv3900675copy number variation1nstd102humanUncertain significance GRCh38 chrX: 15,946,117-16,479,154 , NCBI36 chrX: 15,874,161-16,407,198 , GRCh37 chrX: 15,964,240-16,497,277 GRPR, RPL6P30, 2 more genes
    nsv3904162copy number variation1nstd102humanPathogenic GRCh38 chrX: 10,001-156,030,895 , GRCh37 chrX: 60,001-155,260,560 , NCBI36 chrX: 1-154,913,754 GRPR, NANOGNBP3, 2154 more genes
    nsv3913255copy number variation2nstd102humanPathogenic NCBI36 chrX: 701-154,913,754 , GRCh37.p13 chrX: 60,701-155,260,560 , GRCh38.p12 chrX: 10,701-156,030,895 GRPR, NHS-AS1, 2154 more genes
    nsv3907094copy number variation4nstd102humanPathogenic GRCh38 chrX: 10,679-156,022,206 , GRCh37 chrX: 60,679-155,251,871 , NCBI36 chrX: 679-154,905,065 GRPR, GPR119, 2153 more genes
    nsv3878553copy number variation2nstd102humanPathogenic GRCh37 chrX: 60,262-155,245,765 , GRCh38.p12 chrX: 10,262-156,016,100 GRPR, H2AB2, 2152 more genes
    nsv3898149copy number variation1nstd102humanPathogenic GRCh38 chrX: 20,297-156,026,127 , NCBI36 chrX: 10,297-154,908,986 , GRCh37 chrX: 70,297-155,255,792 GRPR, OR3B1P, 2154 more genes
    nsv3877395copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,839 , GRCh38.p12 chrX: 21,267-156,026,174 GRPR, ARMCX2, 2154 more genes
    nsv3884935copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,792 , GRCh38.p12 chrX: 21,267-156,026,127 GRPR, NDUFB11, 2154 more genes
    nsv3903061copy number variation1nstd102humanPathogenic NCBI36 chrX: 679-154,896,026 , GRCh38 chrX: 10,679-156,013,167 , GRCh37 chrX: 60,679-155,242,832 GRPR, SLC38A5, 2152 more genes
    nsv3885865copy number variation1nstd102humanPathogenic GRCh37 chrX: 70,297-155,246,585 , GRCh38.p12 chrX: 20,297-156,016,920 GRPR, MIR1277, 2152 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 GRPR, LOC105373176, 2151 more genes
    nsv3907545copy number variation1nstd102humanPathogenic GRCh37 chrX: 64,245-155,228,958 , NCBI36 chrX: 4,245-154,882,152 , GRCh38 chrX: 14,245-155,999,293 GRPR, TMEM30BP1, 2151 more genes
    nsv3884029copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,224,766 , GRCh38.p12 chrX: 21,267-155,995,101 GRPR, SSX4B, 2150 more genes
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