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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5831879copy number variation1nstd209human GRCh38 chr2: 155,087,253-155,092,546 , GRCh37.p13 chr2: 155,943,765-155,949,058 RNU6-1001P
    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
    nsv5434730copy number variation1nstd206human GRCh38 chr2: 148,693,148-164,933,481 , GRCh37.p13 chr2: 149,450,717-165,789,991 , RBM43, 205 more genes
    nsv5327227inversion1nstd204human GRCh37.p13 chr2: 151,300,232-168,612,803 , GRCh38.p13 chr2: 150,443,718-167,756,293 , RND3, 198 more genes
    nsv5215314copy number variation1nstd204human GRCh38.p13 chr2: 155,084,501-155,092,900 , GRCh37.p13 chr2: 155,941,013-155,949,412 RNU6-1001P
    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
    nsv4924138copy number variation1nstd200human GRCh38 chr2: 155,077,475-155,101,965 , GRCh37.p13 chr2: 155,933,987-155,958,477 RNU6-1001P
    nsv4915890copy number variation1nstd200human GRCh38 chr2: 155,015,166-155,111,418 , GRCh37.p13 chr2: 155,871,678-155,967,930 RNU6-1001P, LOC105373696
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 more genes
    nsv4674696copy number variation1nstd102humanUncertain significance GRCh37 chr2: 155,694,444-155,946,659 , GRCh38.p12 chr2: 154,837,932-155,090,147 RNU6-1001P, CBX3P6, 2 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
    nsv4367257copy number variation1nstd173human GRCh37 chr2: 154,683,328-157,754,202 , GRCh38.p12 chr2: 153,826,815-156,897,690 , ATP5F1AP2, 35 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
    nsv3922653copy number variation1nstd102humanPathogenic NCBI36 chr2: 154,499,404-159,392,834 , GRCh37.p13 chr2: 154,791,158-159,684,588 , GRCh38.p12 chr2: 153,934,645-158,828,076 CCDC148, LINC01876, 59 more genes
    nsv3921316copy number variation1nstd102humanPathogenic NCBI36 chr2: 155,624,215-165,414,901 , GRCh37.p13 chr2: 155,915,969-165,706,655 , GRCh38.p12 chr2: 155,059,457-164,850,145 LOC105373712, MTCO1P45, 121 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
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