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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
    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
    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
    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
    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
    nsv3890186copy number variation1nstd102humanPathogenic GRCh38 chr2: 136,937,358-146,681,810 , GRCh37 chr2: 137,694,928-147,439,378 , NCBI36 chr2: 137,411,398-147,155,848 SPOPL-DT, ARHGAP15-AS1, 80 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 RNU6-674P, KANSL3, 3735 more genes
    nsv3884398copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 138,578,298-144,874,187 , GRCh38.p12 chr2: 137,820,728-144,116,620 HNMT, KYNU, 58 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 MTND2P22, LOC112268410, 3724 more genes
    nsv3876229copy number variation1nstd102humanPathogenic GRCh37 chr2: 120,571,363-141,627,287 , GRCh38.p12 chr2: 119,813,787-140,869,718 MIR9986, KLF2P4, 320 more genes
    nsv3876086copy number variation1nstd102humandrug response GRCh37 chr2: 104,172,062-168,223,828 , GRCh38.p12 chr2: 103,555,604-167,367,318 SLC4A10, NEK2P4, 871 more genes
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