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Items: 1 to 20 of 302

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143163copy number variation1nstd232human GRCh37.p13 chr2: 102,928,351-102,928,494 , GRCh38.p12 chr2: 102,311,891-102,312,034 IL1RL1
    nsv7055923inversion1nstd229human GRCh38 chr2: 102,341,078-102,346,085 , GRCh37.p13 chr2: 102,957,538-102,962,545 IL1RL1
    nsv7051311inversion1nstd229human GRCh38 chr2: 101,647,680-105,928,217 , GRCh37.p13 chr2: 102,264,142-106,544,673 LOC107985929, SLC9A2, 57 more genes
    nsv7043241inversion1nstd229human GRCh38 chr2: 102,333,638-102,346,267 , GRCh37.p13 chr2: 102,950,098-102,962,727 IL1RL1
    nsv6696143copy number variation1nstd229human GRCh38 chr2: 102,339,491-102,339,684 , GRCh37.p13 chr2: 102,955,951-102,956,144 IL1RL1
    nsv6693918copy number variation1nstd229human GRCh38 chr2: 102,313,501-102,316,000 , GRCh37.p13 chr2: 102,929,961-102,932,460 IL1RL1
    nsv6692171copy number variation1nstd229human GRCh38 chr2: 102,211,388-102,443,779 , GRCh37.p13 chr2: 102,827,848-103,060,239 IL18R1, MIR4772, 5 more genes
    nsv6690013copy number variation1nstd229human GRCh38 chr2: 102,314,526-102,314,685 , GRCh37.p13 chr2: 102,930,986-102,931,145 IL1RL1
    nsv6686597copy number variation1nstd229human GRCh38 chr2: 102,314,856-102,320,420 , GRCh37.p13 chr2: 102,931,316-102,936,880 IL1RL1
    nsv6684036copy number variation1nstd229human GRCh38 chr2: 102,342,301-102,349,200 , GRCh37.p13 chr2: 102,958,761-102,965,660 IL1RL1
    nsv6683221copy number variation1nstd229human GRCh38 chr2: 102,318,348-102,318,454 , GRCh37.p13 chr2: 102,934,808-102,934,914 IL1RL1
    nsv6681416copy number variation1nstd229human GRCh38 chr2: 102,350,101-102,350,600 , GRCh37.p13 chr2: 102,966,561-102,967,060 IL1RL1
    nsv6680598copy number variation1nstd229human GRCh38 chr2: 102,165,301-102,311,600 , GRCh37.p13 chr2: 102,781,761-102,928,060 IL1RL1, CFAP144P2, 2 more genes
    nsv6636875copy number variation1nstd102humanUncertain significance GRCh37 chr2: 102,443,532-105,019,078 , GRCh38.p12 chr2: 101,827,070-104,402,620 IL1RL2, LOC107985926, 27 more genes
    nsv6636232copy number variation1nstd102humanUncertain significance GRCh37 chr2: 102,579,520-103,179,707 , GRCh38.p12 chr2: 101,963,058-102,563,248 MIR4772, IL1RL2, 10 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
    nsv6355564copy number variation1nstd223human GRCh38 chr2: 102,318,345-102,318,454 , GRCh37.p13 chr2: 102,934,805-102,934,914 IL1RL1
    nsv6352981copy number variation1nstd223human GRCh38 chr2: 102,127,822-102,717,507 , GRCh37.p13 chr2: 102,744,282-103,333,966 CFAP144P2, SLC9A2, 9 more genes
    nsv6352622copy number variation1nstd223human GRCh38 chr2: 102,350,724-102,352,848 , GRCh37.p13 chr2: 102,967,184-102,969,308 IL1RL1
    nsv6349488copy number variation1nstd223human GRCh38 chr2: 102,314,856-102,320,418 , GRCh37.p13 chr2: 102,931,316-102,936,878 IL1RL1
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