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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5685381mobile element insertion2nstd211human GRCh38 chr2: 162,788,036-162,788,036 , GRCh37.p13 chr2: 163,644,546-163,644,546 KCNH7, KCNH7-AS1
    nsv5682774mobile element insertion1nstd211human GRCh38 chr2: 162,775,239-162,775,239 , GRCh37.p13 chr2: 163,631,749-163,631,749 KCNH7-AS1, KCNH7
    nsv5613585insertion1nstd207human GRCh38 chr2: 162,788,025-162,788,025 , GRCh37.p13 chr2: 163,644,535-163,644,535 KCNH7-AS1, KCNH7
    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
    nsv5412747mobile element insertion1nstd206human GRCh38 chr2: 162,788,036-162,788,087 , GRCh37.p13 chr2: 163,644,546-163,644,597 KCNH7-AS1, KCNH7
    nsv5404732mobile element insertion1nstd206human GRCh38 chr2: 162,775,239-162,775,290 , GRCh37.p13 chr2: 163,631,749-163,631,800 KCNH7, KCNH7-AS1
    nsv5366605translocation1nstd200human GRCh38 chr2: 162,753,030-162,753,030 , GRCh38 chr2: 162,772,302-162,772,302 , GRCh37.p13 chr2: 163,609,540-163,609,540 , GRCh37.p13 chr2: 163,628,812-163,628,812 KCNH7-AS1, KCNH7
    nsv5327227inversion1nstd204human GRCh37.p13 chr2: 151,300,232-168,612,803 , GRCh38.p13 chr2: 150,443,718-167,756,293 , RND3, 198 more genes
    nsv5078801mobile element insertion1nstd203human GRCh38 chr2: 162,788,032-162,788,036 , GRCh37.p13 chr2: 163,644,542-163,644,546 KCNH7, KCNH7-AS1
    nsv5070412mobile element insertion1nstd203human GRCh38 chr2: 162,788,025-162,788,036 , GRCh37.p13 chr2: 163,644,535-163,644,546 KCNH7-AS1, KCNH7
    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
    nsv4768307copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,078,055-182,119,617 , GRCh38.p12 chr2: 162,221,545-181,254,890 RBM45, LOC102724194, 258 more genes
    nsv4728578copy number variation1nstd102humanUncertain significance GRCh37 chr2: 163,418,327-163,811,396 , GRCh38.p12 chr2: 162,561,817-162,954,886 KCNH7-AS1, KCNH7
    nsv4718440mobile element insertion1nstd186human GRCh37 chr2: 163,644,535-163,644,535 , GRCh38.p12 chr2: 162,788,025-162,788,025 KCNH7, KCNH7-AS1
    nsv4690440mobile element insertion1nstd186human GRCh37 chr2: 163,644,546-163,644,546 , GRCh38.p12 chr2: 162,788,036-162,788,036 KCNH7-AS1, KCNH7
    nsv4685668copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 160,075,929-164,666,149 , GRCh38.p12 chr2: 159,219,418-163,809,639 DPP4, FAP, 53 more genes
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