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Items: 1 to 20 of 559

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7040244inversion1nstd229human GRCh38 chr2: 36,767,443-36,774,745 , GRCh37.p13 chr2: 36,994,586-37,001,888 VIT
    nsv6675507copy number variation1nstd229human GRCh38 chr2: 36,797,897-36,800,819 , GRCh37.p13 chr2: 37,025,040-37,027,962 VIT
    nsv6672125copy number variation1nstd229human GRCh38 chr2: 36,760,019-36,760,207 , GRCh37.p13 chr2: 36,987,162-36,987,350 VIT
    nsv6671913copy number variation1nstd229human GRCh38 chr2: 36,798,071-36,809,344 , GRCh37.p13 chr2: 37,025,214-37,036,487 VIT
    nsv6670828copy number variation1nstd229human GRCh38 chr2: 36,781,528-36,782,062 , GRCh37.p13 chr2: 37,008,671-37,009,205 VIT
    nsv6668531copy number variation1nstd229human GRCh38 chr2: 36,792,001-36,802,800 , GRCh37.p13 chr2: 37,019,144-37,029,943 VIT
    nsv6667868copy number variation1nstd229human GRCh38 chr2: 36,795,926-36,837,923 , GRCh37.p13 chr2: 37,023,069-37,065,066 STRN, VIT
    nsv6667380copy number variation1nstd229human GRCh38 chr2: 36,759,207-36,763,937 , GRCh37.p13 chr2: 36,986,350-36,991,080 VIT
    nsv6666784copy number variation1nstd229human GRCh38 chr2: 36,729,729-36,738,975 , GRCh37.p13 chr2: 36,956,872-36,966,118 VIT
    nsv6666416copy number variation1nstd229human GRCh38 chr2: 36,805,209-36,810,157 , GRCh37.p13 chr2: 37,032,352-37,037,300 VIT
    nsv6665993copy number variation1nstd229human GRCh38 chr2: 36,645,475-36,793,021 , GRCh37.p13 chr2: 36,872,618-37,020,164 RACK1P2, VIT
    nsv6665770copy number variation1nstd229human GRCh38 chr2: 36,622,744-36,740,468 , GRCh37.p13 chr2: 36,849,887-36,967,611 RACK1P2, VIT
    nsv6665375copy number variation1nstd229human GRCh38 chr2: 36,801,678-36,869,460 , GRCh37.p13 chr2: 37,028,821-37,096,603 VIT, STRN, 1 more genes
    nsv6663545copy number variation1nstd229human GRCh38 chr2: 36,719,182-36,721,497 , GRCh37.p13 chr2: 36,946,325-36,948,640 VIT
    nsv6663060copy number variation1nstd229human GRCh38 chr2: 36,708,261-36,711,117 , GRCh37.p13 chr2: 36,935,404-36,938,260 VIT
    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
    nsv6551483inversion1nstd223human GRCh38 chr2: 36,804,570-36,806,841 , GRCh37.p13 chr2: 37,031,713-37,033,984 VIT
    nsv6549542inversion1nstd223human GRCh38 chr2: 32,866,974-37,651,961 , GRCh37.p13 chr2: 33,092,041-37,879,104 QPCT, TYW1P1, 55 more genes
    nsv6548859inversion1nstd223human GRCh38 chr2: 32,866,975-38,526,880 , GRCh37.p13 chr2: 33,092,042-38,754,022 ATP6V0E1P3, ARL14EPP1, 76 more genes
    nsv6548072inversion1nstd223human GRCh38 chr2: 32,866,995-42,468,982 , GRCh37.p13 chr2: 33,092,062-42,696,122 PKDCC, SRSF7, 127 more genes
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