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Items: 1 to 20 of 286

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098856copy number variation1nstd102humanUncertain significance GRCh37 chr2: 32,466,102-32,466,194 , GRCh38.p12 chr2: 32,241,033-32,241,125 NLRC4
    nsv7096156copy number variation1nstd102humanUncertain significance GRCh37 chr2: 32,461,296-32,466,214 , GRCh38.p12 chr2: 32,236,227-32,241,145 NLRC4
    nsv7047639inversion1nstd229human GRCh38 chr2: 29,857,017-35,800,286 , GRCh37.p13 chr2: 30,079,883-36,025,352 LTBP1, KRT18P52, 67 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
    nsv7040611inversion1nstd229human GRCh38 chr2: 32,238,613-32,243,515 , GRCh37.p13 chr2: 32,463,682-32,468,584 NLRC4
    nsv6677533copy number variation1nstd229human GRCh38 chr2: 32,234,084-32,235,772 , GRCh37.p13 chr2: 32,459,153-32,460,841 NLRC4
    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
    nsv6669003copy number variation1nstd229human GRCh38 chr2: 32,243,715-32,729,758 , GRCh37.p13 chr2: 32,468,784-32,954,825 MIR558, BIRC6-AS2, 5 more genes
    nsv6668302copy number variation1nstd229human GRCh38 chr2: 32,253,732-32,255,223 , GRCh37.p13 chr2: 32,478,801-32,480,292 NLRC4
    nsv6663440copy number variation1nstd229human GRCh38 chr2: 32,215,267-32,395,765 , GRCh37.p13 chr2: 32,440,336-32,620,833 YIPF4, BIRC6, 2 more genes
    nsv6661065copy number variation1nstd229human GRCh38 chr2: 32,258,285-32,258,330 , GRCh37.p13 chr2: 32,483,354-32,483,399 NLRC4
    nsv6660480copy number variation1nstd229human GRCh38 chr2: 32,241,501-32,248,900 , GRCh37.p13 chr2: 32,466,570-32,473,969 NLRC4
    nsv6658754copy number variation1nstd229human GRCh38 chr2: 32,243,816-32,244,186 , GRCh37.p13 chr2: 32,468,885-32,469,255 NLRC4
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6636382copy number variation1nstd102humanUncertain significance GRCh37 chr2: 32,194,952-32,826,745 , GRCh38.p12 chr2: 31,969,883-32,601,678 SPAST, MEMO1, 9 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
    nsv6547131inversion1nstd223human GRCh38 chr2: 32,239,279-32,240,039 , GRCh37.p13 chr2: 32,464,348-32,465,108 NLRC4
    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
    nsv6542846inversion1nstd223human GRCh38 chr2: 32,253,973-32,254,625 , GRCh37.p13 chr2: 32,479,042-32,479,694 NLRC4
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