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Items: 1 to 20 of 99

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5899050copy number variation1nstd209human GRCh38 chr2: 112,543,345-112,673,811 , GRCh37.p13 chr2: 113,300,922-113,431,388 SLC20A1, POLR1B, 6 more genes
    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
    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
    nsv4743379copy number variation1nstd199human GRCh37 chr2: 88,481,090-124,440,189 , GRCh38.p12 chr9: 40,649,751-63,450,622 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 88,181,571-123,682,613 , EIF2AK3, 861 more genes
    nsv4678911copy number variation1nstd189human GRCh37.p13 chr2: 113,187,756-113,851,517 , GRCh38.p12 chr2: 112,430,179-113,093,940 IL1A, IL1B, 25 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
    nsv3921207copy number variation1nstd102humanPathogenic NCBI36 chr2: 110,857,227-116,449,787 , GRCh37.p13 chr2: 111,334,455-116,733,317 , GRCh38.p12 chr2: 110,576,878-115,975,741 RABL2A, RPL34P8, 98 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
    nsv3888610copy number variation1nstd102humanPathogenic GRCh37 chr2: 109,556,627-117,570,152 , GRCh38.p12 chr2: 108,940,171-116,812,576 LOC112268438, SOWAHC, 149 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
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 MTND2P22, LOC112268410, 3724 more genes
    nsv3876227copy number variation1nstd102humanPathogenic GRCh37 chr2: 96,353,030-114,045,463 , GRCh38.p12 chr2: 95,687,282-113,287,886 RNU4-8P, RN7SL313P, 346 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
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 IGKV2OR2-10, LOC105374848, 3737 more genes
    nsv3873957copy number variation1nstd102humanPathogenic GRCh37 chr2: 109,798,247-125,658,380 , GRCh38.p12 chr2: 109,181,791-124,900,803 MTND1P28, RPSAP23, 230 more genes
    nsv3872550copy number variation1nstd102humanPathogenic GRCh37 chr2: 106,423,310-115,054,828 , GRCh38.p12 chr2: 105,806,853-114,297,251 SMIM12P1, LIMS4, 189 more genes
    nsv3169185inversion1nstd158human GRCh37 chr2: 33,141,412-240,664,512 , GRCh38.p12 chr2: 32,916,345-239,742,818 , AAMP, 3290 more genes
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