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Items: 1 to 20 of 244

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5955611insertion1nstd209human GRCh38 chr2: 138,707,094-138,707,094 , GRCh37.p13 chr2: 139,464,664-139,464,664 NXPH2
    nsv5725105mobile element insertion1nstd211human GRCh38 chr2: 138,738,290-138,738,290 , GRCh37.p13 chr2: 139,495,860-139,495,860 NXPH2
    nsv5693196mobile element insertion1nstd211human GRCh38 chr2: 138,721,726-138,721,726 , GRCh37.p13 chr2: 139,479,296-139,479,296 NXPH2
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5543854insertion1nstd206human GRCh38 chr2: 138,739,393-138,739,393 , GRCh37.p13 chr2: 139,496,963-139,496,963 NXPH2
    nsv5381338copy number variation1nstd102humanPathogenic GRCh37 chr2: 136,473,383-152,727,396 , GRCh38.p12 chr2: 135,715,813-151,870,882 YY1P2, SPOPL, 156 more genes
    nsv5216994copy number variation1nstd204human GRCh38.p13 chr2: 138,775,001-138,778,900 , GRCh37.p13 chr2: 139,532,571-139,536,470 NXPH2
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv5033955inversion1nstd200human GRCh38 chr2: 103,800,446-187,202,765 , GRCh37.p13 chr2: 104,416,904-188,067,492 , EDDM3CP, 1184 more genes
    nsv4924041copy number variation1nstd200human GRCh38 chr2: 138,755,574-138,760,049 , GRCh37.p13 chr2: 139,513,144-139,517,619 NXPH2
    nsv4909542copy number variation1nstd200human GRCh38 chr2: 138,700,765-138,701,991 , GRCh37.p13 chr2: 139,458,335-139,459,561 NXPH2
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 more genes
    nsv4771080copy number variation1nstd200human GRCh37 chr2: 139,458,335-139,459,561 , GRCh38.p12 chr2: 138,700,765-138,701,991 NXPH2
    nsv4771026copy number variation1nstd200human GRCh37 chr2: 137,223,576-141,429,363 , GRCh38.p12 chr2: 136,466,006-140,671,794 LRP1B, LOC101928273, 35 more genes
    nsv4685664copy number variation1nstd102humanPathogenic GRCh37 chr2: 137,639,637-146,827,604 , GRCh38.p12 chr2: 136,882,067-146,070,036 LOC105373651, MTND6P11, 75 more genes
    nsv4561127mobile element insertion1nstd166human GRCh37.p13 chr2: 139,427,640-139,427,640 , GRCh38.p12 chr2: 138,670,070-138,670,070 NXPH2
    nsv4548707insertion1nstd166human GRCh37.p13 chr2: 139,479,033-139,479,033 , GRCh38.p12 chr2: 138,721,463-138,721,463 NXPH2
    nsv4548403insertion1nstd166human GRCh37.p13 chr2: 139,439,513-139,439,513 , GRCh38.p12 chr2: 138,681,943-138,681,943 NXPH2
    nsv4464021mobile element insertion1nstd166human GRCh37.p13 chr2: 139,511,939-139,511,939 , GRCh38.p12 chr2: 138,754,369-138,754,369 NXPH2
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