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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5452045copy number variation1nstd206human GRCh38 chr2: 136,117,477-136,117,535 , GRCh37.p13 chr2: 136,875,047-136,875,105 CXCR4
    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
    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
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 more genes
    nsv4683675copy number variation1nstd102humanUncertain significance GRCh37 chr2: 136,707,983-136,875,650 , GRCh38.p12 chr2: 135,950,413-136,118,080 DARS1, CXCR4, 1 more genes
    nsv4582456copy number variation1nstd183human GRCh37 chr2: 136,870,501-136,898,155 , GRCh38.p12 chr2: 136,112,931-136,140,585 , CXCR4
    nsv4452826copy number variation1nstd102humanPathogenic GRCh37 chr2: 133,457,177-138,188,195 , GRCh38.p12 chr2: 132,699,604-137,430,625 UBBP1, THSD7B, 42 more genes
    nsv4451808copy number variation1nstd102humanUncertain significance GRCh37 chr2: 135,712,129-137,818,795 , GRCh38.p12 chr2: 134,954,559-137,061,225 MIR128-1, RNU6-512P, 22 more genes
    nsv4450195copy number variation1nstd102humanUncertain significance GRCh37 chr2: 136,707,983-136,875,650 , GRCh38 chr2: 135,950,413-136,118,080 DARS1, DARS1-AS1, 1 more genes
    nsv4433585copy number variation1nstd172human GRCh38.p12 chr2: 136,112,431-136,138,430 , GRCh37.p13 chr2: 136,870,001-136,896,000 , CXCR4
    nsv3924199copy number variation1nstd102humanUncertain significance NCBI36 chr2: 130,861,065-242,751,149 , GRCh37.p13 chr2: 131,144,595-243,102,476 , GRCh38.p12 chr2: 130,387,022-242,160,331 METAP1D, UBE2E3-DT, 1635 more genes
    nsv3923963copy number variation1nstd102humanUncertain significance NCBI36 chr2: 110,190,938-242,751,149 , GRCh37.p13 chr2: 110,833,649-243,102,476 , GRCh38.p12 chr2: 110,076,072-242,160,331 NMTRQ-TTG9-1, MIR6810, 1944 more genes
    nsv3911598copy number variation1nstd102humanUncertain significance NCBI36 chr2: 136,541,486-136,725,313 , GRCh37.p13 chr2: 136,825,016-137,008,843 , GRCh38.p12 chr2: 136,067,446-136,251,273 CXCR4, HNRNPKP2
    nsv3910856copy number variation1nstd102humanPathogenic NCBI36 chr2: 134,449,789-141,806,260 , GRCh37.p13 chr2: 134,733,319-142,089,790 , GRCh38.p12 chr2: 133,975,748-141,332,221 LOC105373643, RPS16P3, 73 more genes
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 DAZAP2P1, RPL36AP16, 2991 more genes
    nsv3902350copy number variation1nstd102humanPathogenic GRCh38 chr2: 136,045,480-142,845,159 , NCBI36 chr2: 136,519,520-143,319,198 , GRCh37 chr2: 136,803,050-143,602,728 LOC101928273, RPL9P13, 48 more genes
    nsv3897428copy number variation1nstd102humanPathogenic GRCh38 chr2: 123,445,762-140,592,538 , NCBI36 chr2: 123,919,808-141,066,577 , GRCh37 chr2: 124,203,338-141,350,107 ARHGAP42P2, LOC647996, 278 more genes
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