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Items: 1 to 20 of 354

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137736copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,263,517-155,260,560 , GRCh38.p12 chrX: 153,998,066-156,030,895 H2AB3, GDI1, 83 more genes
    nsv6137735copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,194,251-153,623,000 , GRCh38.p12 chrX: 153,928,798-154,394,658 EMD, MIR3202-1, 20 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5980455copy number variation1nstd102humanPathogenic GRCh38 chrX: 153,884,414-154,363,935 , GRCh37.p13 chrX|NW_003871103.3: 1,318,396-1,797,914 , GRCh37.p13 chrX: 153,149,868-153,592,303 MIR3202-1, FLNA, 23 more genes
    nsv5672068inversion1nstd207human GRCh37.p13 chrX: 153,576,034-153,612,972 , GRCh38 chrX: 154,347,666-154,384,612 , GRCh37.p13 chrX|NW_003871103.3: 1,781,645-1,818,591 EMD, FLNA, 1 more genes
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv4909288copy number variation1nstd200human GRCh38 chrX: 154,324,390-154,348,187 , GRCh37.p13 chrX|NW_003871103.3: 1,758,369-1,782,166 , GRCh37.p13 chrX: 153,552,736-153,576,555 LOC105373386, FLNA, 1 more genes
    nsv4769250copy number variation1nstd201human GRCh37 chrX: 96,096,220-155,208,244 , GRCh38.p12 chrX: 96,841,221-155,978,579 , AGTR2, 959 more genes
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
    nsv4765964inversion1nstd199human GRCh37 chrX: 153,569,785-153,619,048 , GRCh38.p12 chrX: 154,341,435-154,390,706 EMD, FLNA, 1 more genes
    nsv4764227inversion1nstd199human GRCh37 chrX: 153,570,853-153,617,982 , GRCh38.p12 chrX: 154,342,485-154,389,622 EMD, FLNA, 1 more genes
    nsv4759177inversion1nstd199human GRCh37 chrX: 153,575,614-153,613,223 , GRCh38.p12 chrX: 154,347,246-154,384,863 EMD, FLNA, 1 more genes
    nsv4754021inversion1nstd199human GRCh37 chrX: 153,564,267-153,624,587 , GRCh38.p12 chrX: 154,335,917-154,396,246 EMD, FLNA, 2 more genes
    nsv4730161inversion20nstd198human GRCh37.p13 chrX: 153,565,303-153,644,627 , GRCh38 chrX: 154,336,953-154,416,288 , GRCh37.p13 chrX|NW_003871103.3: 1,770,932-1,850,267 DNASE1L1, EMD, 5 more genes
    nsv4728533copy number variation1nstd102humanPathogenic GRCh37 chrX: 94,264,404-155,233,731 , GRCh38.p12 chrX: 95,009,405-156,004,066 CT45A10, MIR224, 968 more genes
    nsv4728499copy number variation1nstd102humanPathogenic GRCh37 chrX: 55,507,789-155,198,481 , GRCh38.p12 chrX: 55,481,356-155,968,816 GABRE, RN7SL325P, 1371 more genes
    nsv4728292copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,135,257-153,594,096 , GRCh38.p12 chrX: 153,869,802-154,365,728 NAA10, OPN1MW3, 23 more genes
    nsv4728215copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,113,943-153,624,215 , GRCh38.p12 chrX: 153,848,488-154,395,874 ARHGAP4, L1CAM, 24 more genes
    nsv4685620copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 122,132,166-155,097,214 , GRCh38.p12 chrX: 122,998,313-155,867,551 ABCD1, AMD1P2, 560 more genes
    nsv4684397delins1nstd102humanPathogenic GRCh37 chrX: 153,590,180-153,592,124 , GRCh38 chrX: 154,361,812-154,363,756 FLNA
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