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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3873768copy number variation1nstd102humanBenign GRCh37 chrX: 34,541,283-34,897,286 , GRCh38.p12 chrX: 34,523,166-34,879,169 TMEM47
    nsv3887860copy number variation1nstd102humanBenign GRCh37 chrX: 34,521,691-34,834,077 , GRCh38.p12 chrX: 34,503,574-34,815,960 TMEM47
    nsv3875454copy number variation1nstd102humanUncertain significance GRCh37 chrX: 34,376,205-34,779,317 , GRCh38.p12 chrX: 34,358,088-34,761,200 TMEM47, SRSF2P1
    nsv3874417copy number variation1nstd102humanLikely benign GRCh37 chrX: 34,310,804-35,457,990 , GRCh38.p12 chrX: 34,292,687-35,439,873 TMEM47, FAM47B, 3 more genes
    nsv4674796copy number variation1nstd102humanLikely benign GRCh37 chrX: 34,645,143-35,206,581 , GRCh38.p12 chrX: 34,627,026-35,188,464 TMEM47, FAM47B, 1 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 TMEM47, 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 TMEM47, 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 TMEM47, GPR119, 2153 more genes
    nsv3878553copy number variation2nstd102humanPathogenic GRCh37 chrX: 60,262-155,245,765 , GRCh38.p12 chrX: 10,262-156,016,100 TMEM47, 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 TMEM47, OR3B1P, 2154 more genes
    nsv3877395copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,839 , GRCh38.p12 chrX: 21,267-156,026,174 TMEM47, ARMCX2, 2154 more genes
    nsv3884935copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,255,792 , GRCh38.p12 chrX: 21,267-156,026,127 TMEM47, 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 TMEM47, SLC38A5, 2152 more genes
    nsv3885865copy number variation1nstd102humanPathogenic GRCh37 chrX: 70,297-155,246,585 , GRCh38.p12 chrX: 20,297-156,016,920 TMEM47, MIR1277, 2152 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 TMEM47, 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 TMEM47, TMEM30BP1, 2151 more genes
    nsv3884029copy number variation1nstd102humanPathogenic GRCh37 chrX: 71,267-155,224,766 , GRCh38.p12 chrX: 21,267-155,995,101 TMEM47, SSX4B, 2150 more genes
    nsv3898185copy number variation2nstd102humanPathogenic GRCh37 chrX: 76,102-155,226,096 , NCBI36 chrX: 16,102-154,879,290 , GRCh38 chrX: 26,102-155,996,431 TMEM47, ANKRD11P2, 2151 more genes
    nsv3891981copy number variation1nstd102humanPathogenic GRCh38 chrX: 10,701-155,978,689 , NCBI36 chrX: 701-154,861,548 , GRCh37 chrX: 60,701-155,208,354 TMEM47, PAICSP7, 2149 more genes
    nsv3892026copy number variation1nstd102humanPathogenic GRCh38 chrX: 40,904-155,998,166 , GRCh37 chrX: 90,904-155,227,831 , NCBI36 chrX: 30,904-154,881,025 TMEM47, MIR934, 2151 more genes
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