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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5686514mobile element insertion2nstd211human GRCh38 chr2: 155,268,316-155,268,316 , GRCh37.p13 chr2: 156,124,828-156,124,828 LOC105373698, ATP5F1AP2
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 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
    nsv5450895copy number variation1nstd206human GRCh38 chr2: 141,459,078-156,842,302 , GRCh37.p13 chr2: 142,216,647-157,698,814 , LOC105373696, 163 more genes
    nsv5443267copy number variation1nstd206human GRCh38 chr2: 155,215,335-155,274,292 , GRCh37.p13 chr2: 156,071,847-156,130,804 MTCO1P45, ATP5F1AP2, 2 more genes
    nsv5442006copy number variation1nstd206human GRCh38 chr2: 155,263,663-155,269,701 , GRCh37.p13 chr2: 156,120,175-156,126,213 MTND2P20, ATP5F1AP2, 2 more genes
    nsv5434730copy number variation1nstd206human GRCh38 chr2: 148,693,148-164,933,481 , GRCh37.p13 chr2: 149,450,717-165,789,991 , RBM43, 205 more genes
    nsv5410798mobile element insertion1nstd206human GRCh38 chr2: 155,268,316-155,268,319 , GRCh37.p13 chr2: 156,124,828-156,124,831 ATP5F1AP2, LOC105373698
    nsv5350880translocation1nstd200human GRCh38 chr2: 155,269,226-155,269,226 , GRCh38 chr2: 155,269,175-155,269,175 , GRCh37.p13 chr2: 156,125,738-156,125,738 , GRCh37.p13 chr2: 156,125,687-156,125,687 LOC105373698, ATP5F1AP2
    nsv5327227inversion1nstd204human GRCh37.p13 chr2: 151,300,232-168,612,803 , GRCh38.p13 chr2: 150,443,718-167,756,293 , RND3, 198 more genes
    nsv5064453mobile element insertion1nstd203human GRCh38 chr2: 155,268,305-155,268,316 , GRCh37.p13 chr2: 156,124,817-156,124,828 LOC105373698, ATP5F1AP2
    nsv5063913mobile element insertion1nstd203human GRCh38 chr2: 155,268,316-155,268,316 , GRCh37.p13 chr2: 156,124,828-156,124,828 ATP5F1AP2, LOC105373698
    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
    nsv4674226copy number variation1nstd102humanPathogenic GRCh37 chr2: 147,173,792-158,346,266 , GRCh38.p12 chr2: 146,416,224-157,489,754 RBM43, LINC01931, 120 more genes
    nsv4464590mobile element insertion1nstd166human GRCh37.p13 chr2: 156,124,817-156,124,817 , GRCh38.p12 chr2: 155,268,305-155,268,305 LOC105373698, ATP5F1AP2
    nsv4367257copy number variation1nstd173human GRCh37 chr2: 154,683,328-157,754,202 , GRCh38.p12 chr2: 153,826,815-156,897,690 , ATP5F1AP2, 35 more genes
    nsv4072461copy number variation1nstd166human GRCh37.p13 chr2: 156,118,249-156,165,258 , GRCh38.p12 chr2: 155,261,737-155,308,746 ATP5F1AP2, MTND2P20, 2 more genes
    nsv3961464copy number variation1nstd168human GRCh38 chr2: 155,210,047-155,296,550 , GRCh37.p13 chr2: 156,066,559-156,153,062 MTND2P20, MTCO1P45, 3 more genes
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