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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7041761inversion1nstd229human GRCh38 chr2: 161,208,254-165,696,625 , GRCh37.p13 chr2: 162,064,765-166,553,135 SCN3A, LOC101929532, 45 more genes
    nsv6691627copy number variation1nstd229human GRCh38 chr2: 161,197,530-161,288,041 , GRCh37.p13 chr2: 162,054,041-162,144,552 LINC01806, TANK, 1 more genes
    nsv6690775copy number variation1nstd229human GRCh38 chr2: 161,208,201-161,275,500 , GRCh37.p13 chr2: 162,064,712-162,132,011 TANK, PSMD14-DT, 1 more genes
    nsv6347105copy number variation1nstd223human GRCh38 chr2: 161,197,530-161,288,036 , GRCh37.p13 chr2: 162,054,041-162,144,547 TANK, LINC01806, 1 more genes
    nsv6338928copy number variation1nstd223human GRCh38 chr2: 161,239,801-161,243,900 , GRCh37.p13 chr2: 162,096,312-162,100,411 PSMD14-DT, LINC01806
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6315160copy number variation1nstd102humanPathogenic GRCh37 chr2: 160,347,642-174,075,851 , GRCh38.p12 chr2: 159,491,131-173,211,123 EIF3EP3, FAP, 158 more genes
    nsv6313780copy number variation1nstd102humanPathogenic GRCh37 chr2: 161,551,326-167,762,790 , GRCh38.p12 chr2: 160,694,815-166,906,280 SCN9A, FIGN, 60 more genes
    nsv6313568copy number variation1nstd102humanPathogenic GRCh37 chr2: 158,950,827-164,456,735 , GRCh38.p12 chr2: 158,094,315-163,600,225 PSMD14-DT, DPP4, 70 more genes
    nsv6134500copy number variation1nstd213human GRCh37 chr2: 149,790,000-179,310,001 , GRCh38.p12 chr2: 148,934,069-178,445,274 , ACVR1, 394 more genes
    nsv6134157copy number variation1nstd213human GRCh37 chr2: 162,050,000-162,150,001 , GRCh38.p12 chr2: 161,193,489-161,293,490 TANK, LINC01806, 1 more genes
    nsv5690979mobile element insertion1nstd211human GRCh38 chr2: 161,249,411-161,249,411 , GRCh37.p13 chr2: 162,105,922-162,105,922 LINC01806, PSMD14-DT
    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
    nsv5434730copy number variation1nstd206human GRCh38 chr2: 148,693,148-164,933,481 , GRCh37.p13 chr2: 149,450,717-165,789,991 , RBM43, 205 more genes
    nsv5402927mobile element insertion1nstd206human GRCh38 chr2: 161,249,411-161,249,417 , GRCh37.p13 chr2: 162,105,922-162,105,928 PSMD14-DT, LINC01806
    nsv5327227inversion1nstd204human GRCh37.p13 chr2: 151,300,232-168,612,803 , GRCh38.p13 chr2: 150,443,718-167,756,293 , RND3, 198 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
    nsv4924144copy number variation1nstd200human GRCh38 chr2: 160,399,608-161,781,141 , GRCh37.p13 chr2: 161,256,119-162,637,651 , LOC100419108, 17 more genes
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