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Items: 1 to 20 of 219

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143350insertion1nstd232human GRCh37.p13 chr2: 103,066,666-103,066,666 , GRCh38.p12 chr2: 102,450,206-102,450,206 IL18RAP
    nsv7051311inversion1nstd229human GRCh38 chr2: 101,647,680-105,928,217 , GRCh37.p13 chr2: 102,264,142-106,544,673 LOC107985929, SLC9A2, 57 more genes
    nsv6695608copy number variation1nstd229human GRCh38 chr2: 102,417,755-102,429,618 , GRCh37.p13 chr2: 103,034,215-103,046,078 IL18RAP
    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
    nsv6689157copy number variation1nstd229human GRCh38 chr2: 102,451,243-102,451,576 , GRCh37.p13 chr2: 103,067,703-103,068,036 IL18RAP
    nsv6685826copy number variation1nstd229human GRCh38 chr2: 102,432,001-102,572,500 , GRCh37.p13 chr2: 103,048,461-103,188,959 IL18RAP, SLC9A4, 1 more genes
    nsv6682688copy number variation1nstd229human GRCh38 chr2: 102,425,519-102,425,806 , GRCh37.p13 chr2: 103,041,979-103,042,266 IL18RAP
    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
    nsv6552259inversion1nstd223human GRCh38 chr2: 102,426,633-102,427,950 , GRCh37.p13 chr2: 103,043,093-103,044,410 IL18RAP
    nsv6354763copy number variation1nstd223human GRCh38 chr2: 102,427,301-102,430,200 , GRCh37.p13 chr2: 103,043,761-103,046,660 IL18RAP
    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
    nsv6350441copy number variation1nstd223human GRCh38 chr2: 102,443,196-102,443,695 , GRCh37.p13 chr2: 103,059,656-103,060,155 IL18RAP
    nsv6349211copy number variation1nstd223human GRCh38 chr2: 102,073,096-102,703,088 , GRCh37.p13 chr2: 102,689,556-103,319,547 SLC9A2, IL1RL2, 8 more genes
    nsv6340493copy number variation1nstd223human GRCh38 chr2: 102,427,601-102,431,200 , GRCh37.p13 chr2: 103,044,061-103,047,660 MIR4772, IL18RAP
    nsv6340045copy number variation1nstd223human GRCh38 chr2: 102,425,519-102,425,806 , GRCh37.p13 chr2: 103,041,979-103,042,266 IL18RAP
    nsv6336856copy number variation1nstd223human GRCh38 chr2: 102,427,552-102,428,187 , GRCh37.p13 chr2: 103,044,012-103,044,647 IL18RAP
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
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