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Items: 1 to 20 of 285

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5896777copy number variation1nstd209human GRCh38 chr3: 198,054,813-198,056,716 , GRCh37.p13 chr3: 197,781,684-197,783,587 ANKRD18DP
    nsv5894679copy number variation1nstd209human GRCh38 chr3: 198,072,022-198,072,155 , GRCh37.p13 chr3: 197,798,893-197,799,026 ANKRD18DP
    nsv5892798copy number variation1nstd209human GRCh38 chr3: 198,063,076-198,065,983 , GRCh37.p13 chr3: 197,789,947-197,792,854 ANKRD18DP
    nsv5835820copy number variation2nstd209human GRCh38 chr3: 198,063,046-198,066,745 , GRCh37.p13 chr3: 197,789,917-197,793,616 ANKRD18DP
    nsv5835819copy number variation2nstd209human GRCh38 chr3: 198,056,663-198,057,845 , GRCh37.p13 chr3: 197,783,534-197,784,716 ANKRD18DP
    nsv5835759copy number variation2nstd209human GRCh38 chr3: 198,054,525-198,056,712 , GRCh37.p13 chr3: 197,781,396-197,783,583 ANKRD18DP
    nsv5835209copy number variation1nstd209human GRCh38 chr3: 198,055,975-198,077,609 , GRCh37.p13 chr3: 197,782,846-197,804,480 RNU6-821P, ANKRD18DP
    nsv5726050mobile element insertion1nstd211human GRCh38 chr3: 198,062,019-198,062,019 , GRCh37.p13 chr3: 197,788,890-197,788,890 ANKRD18DP
    nsv5623575insertion1nstd207human GRCh38 chr3: 198,072,040-198,072,040 , GRCh37.p13 chr3: 197,798,911-197,798,911 ANKRD18DP
    nsv5581618copy number variation1nstd207human GRCh38 chr3: 198,077,836-198,077,893 , GRCh37.p13 chr3: 197,804,707-197,804,764 ANKRD18DP
    nsv5573570copy number variation1nstd207human GRCh38 chr3: 198,054,813-198,056,716 , GRCh37.p13 chr3: 197,781,684-197,783,587 ANKRD18DP
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5453460copy number variation1nstd206human GRCh38 chr3: 197,886,861-198,072,114 , GRCh37.p13 chr3: 197,613,732-197,798,985 RPL35A, IQCG, 7 more genes
    nsv5451098copy number variation1nstd206human GRCh38 chr3: 198,073,590-198,073,798 , GRCh37.p13 chr3: 197,800,461-197,800,669 ANKRD18DP
    nsv5451095copy number variation1nstd206human GRCh38 chr3: 198,072,022-198,072,157 , GRCh37.p13 chr3: 197,798,893-197,799,028 ANKRD18DP
    nsv5438691copy number variation1nstd206human GRCh38 chr3: 198,053,673-198,058,569 , GRCh37.p13 chr3: 197,780,544-197,785,440 ANKRD18DP
    nsv5436008copy number variation1nstd206human GRCh38 chr3: 198,068,523-198,070,077 , GRCh37.p13 chr3: 197,795,394-197,796,948 ANKRD18DP, RNU6-821P
    nsv5435397copy number variation1nstd206human GRCh38 chr3: 198,054,146-198,078,973 , GRCh37.p13 chr3: 197,781,017-197,805,844 RNU6-821P, ANKRD18DP
    nsv5435249copy number variation1nstd206human GRCh38 chr3: 198,054,818-198,056,717 , GRCh37.p13 chr3: 197,781,689-197,783,588 ANKRD18DP
    nsv5306583copy number variation1nstd204human GRCh38.p13 chr3: 197,465,734-198,094,188 , GRCh37.p13 chr3: 197,192,605-197,821,059 , FYTTD1, 20 more genes
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