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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7049242inversion1nstd229human GRCh38 chr2: 141,675,999-143,767,674 , GRCh37.p13 chr2: 142,433,568-144,525,243 MTND3P9, LOC101928361, 20 more genes
    nsv6692164copy number variation1nstd229human GRCh38 chr2: 142,173,482-145,423,511 , GRCh37.p13 chr2: 142,931,051-146,181,079 LOC100505498, MTCO2P5, 29 more genes
    nsv6691913copy number variation1nstd229human GRCh38 chr2: 143,011,211-143,666,671 , GRCh37.p13 chr2: 143,768,780-144,424,240 ARHGAP15-AS1, MTND3P9, 11 more genes
    nsv6691605copy number variation1nstd229human GRCh38 chr2: 136,115,914-144,517,285 , GRCh37.p13 chr2: 136,873,484-145,274,852 LOC105373652, LOC105373649, 68 more genes
    nsv6685232copy number variation1nstd229human GRCh38 chr2: 143,565,292-143,597,624 , GRCh37.p13 chr2: 144,322,861-144,355,193 ARHGAP15, LOC101928361
    nsv6536923inversion1nstd223human GRCh38 chr2: 143,604,894-143,606,065 , GRCh37.p13 chr2: 144,362,463-144,363,634 LOC101928361, ARHGAP15
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314748copy number variation1nstd102humanPathogenic GRCh37 chr2: 112,475,655-145,691,999 , GRCh38.p12 chr2: 111,718,078-144,934,432 MED15P9, TMEM37, 474 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6313481copy number variation1nstd102humanPathogenic GRCh37 chr2: 143,258,712-152,867,819 , GRCh38.p12 chr2: 142,501,143-152,011,305 STIP1P1, RNU6-715P, 98 more genes
    nsv6291353copy number variation1nstd102humanPathogenic GRCh37 chr2: 111,484,468-146,333,604 , GRCh38.p12 chr2: 110,726,891-145,576,036 LINC01120, LOC105373585, 490 more genes
    nsv6290982copy number variation1nstd102humanPathogenic GRCh37 chr2: 142,409,401-152,680,804 , GRCh38.p12 chr2: 141,651,832-151,824,290 LOC101928526, MTCO2P5, 101 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
    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
    nsv5068999mobile element insertion1nstd203human GRCh38 chr2: 143,605,858-143,605,875 , GRCh37.p13 chr2: 144,363,427-144,363,444 LOC101928361, ARHGAP15
    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
    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
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