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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960786copy number variation1nstd209human GRCh38 chr22: 35,249,171-35,250,145 , GRCh37.p13 chr22: 35,645,164-35,646,138 RNU7-167P, LOC105373017
    nsv5597189copy number variation1nstd207human GRCh38 chr22: 35,249,171-35,250,145 , GRCh37.p13 chr22: 35,645,164-35,646,138 LOC105373017, RNU7-167P
    nsv5537448copy number variation1nstd206human GRCh38 chr22: 35,249,153-35,250,166 , GRCh37.p13 chr22: 35,645,146-35,646,159 RNU7-167P, LOC105373017
    nsv5328208copy number variation1nstd204human GRCh37.p13 chr22: 35,645,166-35,646,139 , GRCh38.p13 chr22: 35,249,173-35,250,146 LOC105373017, RNU7-167P
    nsv5287706copy number variation1nstd204human GRCh38.p13 chr22: 35,249,162-35,250,812 , GRCh37.p13 chr22: 35,645,155-35,646,805 RNU7-167P, LOC105373017
    nsv5029753copy number variation1nstd200human GRCh38 chr22: 35,249,173-35,250,146 , GRCh37.p13 chr22: 35,645,166-35,646,139 LOC105373017, RNU7-167P
    nsv4887696copy number variation1nstd200human GRCh37 chr22: 35,645,166-35,646,139 , GRCh38.p12 chr22: 35,249,173-35,250,146 RNU7-167P, LOC105373017
    nsv4734294copy number variation1nstd199human GRCh37 chr22: 35,645,160-35,646,138 , GRCh38.p12 chr22: 35,249,167-35,250,145 RNU7-167P, LOC105373017
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4710565copy number variation1nstd195human GRCh37 chr22: 35,645,164-35,645,165 , GRCh38.p12 chr22: 35,249,171-35,249,172 LOC105373017, RNU7-167P
    nsv4676292copy number variation1nstd102humanPathogenic GRCh37 chr22: 30,654,764-51,197,838 , GRCh38.p12 chr22: 30,258,775-50,759,410 PDXP-DT, PDGFB, 550 more genes
    nsv4666424copy number variation1nstd186human GRCh37 chr22: 35,645,445-35,646,472 , GRCh38.p12 chr22: 35,249,452-35,250,479 RNU7-167P, LOC105373017
    nsv4645159copy number variation4nstd186human GRCh37 chr22: 35,645,166-35,646,139 , GRCh38.p12 chr22: 35,249,173-35,250,146 LOC105373017, RNU7-167P
    nsv4637225copy number variation1nstd186human GRCh37 chr22: 35,645,163-35,646,142 , GRCh38.p12 chr22: 35,249,170-35,250,149 RNU7-167P, LOC105373017
    nsv4623807copy number variation1nstd183human GRCh37 chr22: 35,645,445-35,646,472 , GRCh38.p12 chr22: 35,249,452-35,250,479 RNU7-167P, LOC105373017
    nsv4623283copy number variation2nstd183human GRCh37 chr22: 35,645,450-35,646,607 , GRCh38.p12 chr22: 35,249,457-35,250,614 LOC105373017, RNU7-167P
    nsv4457771copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410 IGLV3-27, XKR3, 1082 more genes
    nsv4457388copy number variation1nstd102humanUncertain significance GRCh37 chr22: 35,645,948-35,697,504 , GRCh38.p12 chr22: 35,249,955-35,301,511 RNU7-167P, LOC105373017, 2 more genes
    nsv4442041copy number variation1nstd175human GRCh37 chr22: 35,645,164-35,646,139 , GRCh38.p12 chr22: 35,249,171-35,250,146 LOC105373017, RNU7-167P
    nsv4433422copy number variation1nstd172human GRCh37.p13 chr22: 35,645,231-35,646,235 , GRCh38.p12 chr22: 35,249,238-35,250,242 LOC105373017, RNU7-167P
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