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Items: 1 to 20 of 277

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5892782copy number variation1nstd209human GRCh38 chr2: 149,377,943-149,378,017 , GRCh37.p13 chr2: 150,234,457-150,234,531 LYPD6
    nsv5682604mobile element insertion1nstd211human GRCh38 chr2: 149,328,795-149,328,795 , GRCh37.p13 chr2: 150,185,309-150,185,309 LYPD6, MIR9899
    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
    nsv5448359copy number variation1nstd206human GRCh38 chr2: 149,359,177-149,359,239 , GRCh37.p13 chr2: 150,215,691-150,215,753 LYPD6
    nsv5439507copy number variation1nstd206human GRCh38 chr2: 149,418,487-149,418,538 , GRCh37.p13 chr2: 150,275,001-150,275,052 LYPD6
    nsv5438827copy number variation1nstd206human GRCh38 chr2: 149,388,803-149,388,917 , GRCh37.p13 chr2: 150,245,317-150,245,431 LYPD6
    nsv5436055copy number variation1nstd206human GRCh38 chr2: 149,456,459-149,457,845 , GRCh37.p13 chr2: 150,312,973-150,314,359 LYPD6
    nsv5434730copy number variation1nstd206human GRCh38 chr2: 148,693,148-164,933,481 , GRCh37.p13 chr2: 149,450,717-165,789,991 , RBM43, 205 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
    nsv5361613translocation1nstd200human GRCh38 chr2: 149,330,411-149,330,411 , GRCh38 chr2: 149,330,842-149,330,842 , GRCh37.p13 chr2: 150,187,356-150,187,356 , GRCh37.p13 chr2: 150,186,925-150,186,925 LYPD6, MIR9899
    nsv5282693copy number variation1nstd204human GRCh37.p13 chr2: 150,182,936-150,185,096 , GRCh38.p13 chr2: 149,326,422-149,328,582 MIR9899, LYPD6
    nsv5218919copy number variation1nstd204human GRCh38.p13 chr2: 149,460,201-149,464,200 , GRCh37.p13 chr2: 150,316,715-150,320,714 LYPD6
    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
    nsv4924108copy number variation1nstd200human GRCh38 chr2: 149,424,320-149,425,984 , GRCh37.p13 chr2: 150,280,834-150,282,498 LYPD6
    nsv4915689copy number variation1nstd200human GRCh38 chr2: 149,395,559-149,398,144 , GRCh37.p13 chr2: 150,252,073-150,254,658 LYPD6
    nsv4915688copy number variation1nstd200human GRCh38 chr2: 149,350,761-149,355,709 , GRCh37.p13 chr2: 150,207,275-150,212,223 LYPD6
    nsv4915687copy number variation1nstd200human GRCh38 chr2: 149,325,210-149,441,419 , GRCh37.p13 chr2: 150,181,724-150,297,933 LYPD6, RPL17P13, 1 more genes
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 more genes
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