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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6697887copy number variation1nstd229human GRCh38 chr2: 169,689,659-169,708,106 , GRCh37.p13 chr2: 170,546,169-170,564,616 PHOSPHO2, PHOSPHO2-KLHL23, 1 more genes
    nsv6691097copy number variation1nstd229human GRCh38 chr2: 169,695,201-169,698,100 , GRCh37.p13 chr2: 170,551,711-170,554,610 PHOSPHO2-KLHL23, PHOSPHO2
    nsv6687538copy number variation1nstd229human GRCh38 chr2: 169,695,722-169,701,788 , GRCh37.p13 chr2: 170,552,232-170,558,298 PHOSPHO2-KLHL23, PHOSPHO2
    nsv6685937copy number variation1nstd229human GRCh38 chr2: 169,420,757-170,042,345 , GRCh37.p13 chr2: 170,277,267-170,898,855 PHOSPHO2-KLHL23, LOC100421474, 14 more genes
    nsv6682697copy number variation1nstd229human GRCh38 chr2: 169,688,471-169,693,422 , GRCh37.p13 chr2: 170,544,981-170,549,932 CFAP210, PHOSPHO2, 1 more genes
    nsv6678900copy number variation1nstd229human GRCh38 chr2: 168,515,191-170,305,528 , GRCh37.p13 chr2: 169,371,701-171,162,038 METTL5, FASTKD1, 28 more genes
    nsv6351038copy number variation1nstd223human GRCh38 chr2: 169,420,756-170,042,343 , GRCh37.p13 chr2: 170,277,266-170,898,853 LOC100421474, PHOSPHO2-KLHL23, 14 more genes
    nsv6341724copy number variation1nstd223human GRCh38 chr2: 169,652,264-169,783,291 , GRCh37.p13 chr2: 170,508,774-170,639,801 PHOSPHO2-KLHL23, PHOSPHO2, 5 more genes
    nsv6340817copy number variation1nstd223human GRCh38 chr2: 169,692,601-169,698,400 , GRCh37.p13 chr2: 170,549,111-170,554,910 PHOSPHO2, PHOSPHO2-KLHL23, 1 more genes
    nsv6338051copy number variation1nstd223human GRCh38 chr2: 169,695,216-169,698,085 , GRCh37.p13 chr2: 170,551,726-170,554,595 PHOSPHO2-KLHL23, PHOSPHO2
    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
    nsv6243439mobile element insertion1nstd215human GRCh38 chr2: 169,693,909-169,693,909 , GRCh37.p13 chr2: 170,550,419-170,550,419 CFAP210, PHOSPHO2, 1 more genes
    nsv6134632copy number variation1nstd213human GRCh37 chr2: 170,380,000-170,810,001 , GRCh38.p12 chr2: 169,523,490-169,953,491 SSB, PPIG, 13 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
    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
    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
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