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Items: 1 to 20 of 190

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096648copy number variation1nstd102humanUncertain significance GRCh37 chr2: 27,712,462-27,726,506 , GRCh38.p12 chr2: 27,489,595-27,503,639 IFT172, FNDC4, 1 more genes
    nsv7096628copy number variation1nstd102humanUncertain significance GRCh37 chr2: 27,688,258-27,688,405 , GRCh38.p12 chr2: 27,465,391-27,465,538 IFT172
    nsv7096625copy number variation1nstd102humanUncertain significance GRCh37 chr2: 24,443,763-30,143,525 , GRCh38.p12 chr2: 24,220,894-29,920,659 LOC105374381, POMC, 136 more genes
    nsv7096494copy number variation1nstd102humanPathogenic GRCh37 chr2: 27,693,775-27,695,249 , GRCh38.p12 chr2: 27,470,908-27,472,382 IFT172
    nsv7096148copy number variation2nstd102humanUncertain significance GRCh37 chr2: 24,443,763-29,022,169 , GRCh38.p12 chr2: 24,220,894-28,799,303 LOC105374381, SLC35F6, 122 more genes
    nsv7046929inversion1nstd229human GRCh38 chr2: 27,161,080-28,820,407 , GRCh37.p13 chr2: 27,383,948-29,043,273 LOC100422227, PLB1, 54 more genes
    nsv7042984inversion1nstd229human GRCh38 chr2: 26,886,657-32,818,427 , GRCh37.p13 chr2: 27,109,525-33,043,494 CLIP4, LOC102723594, 118 more genes
    nsv6677382copy number variation1nstd229human GRCh38 chr2: 27,453,758-27,528,746 , GRCh37.p13 chr2: 27,676,625-27,751,613 FNDC4, IFT172, 2 more genes
    nsv6673020copy number variation1nstd229human GRCh38 chr2: 27,447,376-27,447,479 , GRCh37.p13 chr2: 27,670,243-27,670,346 IFT172
    nsv6672785copy number variation1nstd229human GRCh38 chr2: 24,384,939-32,866,867 , GRCh37.p13 chr2: 24,607,808-33,091,934 CENPO, TOGARAM2, 170 more genes
    nsv6668803copy number variation1nstd229human GRCh38 chr2: 27,469,773-27,473,746 , GRCh37.p13 chr2: 27,692,640-27,696,613 IFT172, RNU6-986P
    nsv6661650copy number variation1nstd229human GRCh38 chr2: 27,435,327-27,494,660 , GRCh37.p13 chr2: 27,658,194-27,717,527 IFT172, KRTCAP3, 3 more genes
    nsv6658552copy number variation1nstd229human GRCh38 chr2: 27,481,201-27,485,000 , GRCh37.p13 chr2: 27,704,068-27,707,867 IFT172
    nsv6658388copy number variation1nstd229human GRCh38 chr2: 27,464,301-27,470,300 , GRCh37.p13 chr2: 27,687,168-27,693,167 IFT172
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6546927inversion1nstd223human GRCh38 chr2: 26,476,473-32,916,584 , GRCh37.p13 chr2: 26,699,341-33,141,651 LOC105374453, LCLAT1, 129 more genes
    nsv6543735inversion1nstd223human GRCh38 chr2: 24,403,241-32,916,237 , GRCh37.p13 chr2: 24,626,110-33,141,304 LOC105374334, LOC107985861, 172 more genes
    nsv6538559inversion1nstd223human GRCh38 chr2: 25,762,333-32,867,002 , GRCh37.p13 chr2: 25,985,202-33,092,069 MIR558, PCARE, 148 more genes
    nsv6346241copy number variation1nstd223human GRCh38 chr2: 27,448,376-27,448,781 , GRCh37.p13 chr2: 27,671,243-27,671,648 IFT172
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