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Items: 1 to 20 of 368

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138891copy number variation1nstd232human GRCh37.p13 chr2: 103,248,560-103,248,613 , GRCh38.p12 chr2: 102,632,101-102,632,154 SLC9A2
    nsv7051311inversion1nstd229human GRCh38 chr2: 101,647,680-105,928,217 , GRCh37.p13 chr2: 102,264,142-106,544,673 LOC107985929, SLC9A2, 57 more genes
    nsv6688510copy number variation1nstd229human GRCh38 chr2: 102,676,901-102,680,700 , GRCh37.p13 chr2: 103,293,360-103,297,159 SLC9A2
    nsv6686127copy number variation1nstd229human GRCh38 chr2: 102,691,563-102,692,038 , GRCh37.p13 chr2: 103,308,022-103,308,497 SLC9A2
    nsv6686101copy number variation1nstd229human GRCh38 chr2: 102,680,918-102,681,254 , GRCh37.p13 chr2: 103,297,377-103,297,713 SLC9A2
    nsv6684009copy number variation1nstd229human GRCh38 chr2: 102,706,037-102,706,359 , GRCh37.p13 chr2: 103,322,496-103,322,818 SLC9A2
    nsv6682229copy number variation1nstd229human GRCh38 chr2: 102,704,859-102,705,279 , GRCh37.p13 chr2: 103,321,318-103,321,738 SLC9A2
    nsv6682107copy number variation1nstd229human GRCh38 chr2: 102,709,092-102,721,595 , GRCh37.p13 chr2: 103,325,551-103,338,054 MFSD9, SLC9A2
    nsv6680460copy number variation1nstd229human GRCh38 chr2: 102,709,372-102,709,425 , GRCh37.p13 chr2: 103,325,831-103,325,884 SLC9A2
    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
    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
    nsv6549259inversion1nstd223human GRCh38 chr2: 102,687,828-102,688,609 , GRCh37.p13 chr2: 103,304,287-103,305,068 SLC9A2
    nsv6540559inversion1nstd223human GRCh38 chr2: 102,665,727-102,666,288 , GRCh37.p13 chr2: 103,282,186-103,282,747 SLC9A2
    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
    nsv6349452copy number variation1nstd223human GRCh38 chr2: 102,653,432-102,655,449 , GRCh37.p13 chr2: 103,269,891-103,271,908 SLC9A2
    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
    nsv6346012copy number variation1nstd223human GRCh38 chr2: 102,706,024-102,706,359 , GRCh37.p13 chr2: 103,322,483-103,322,818 SLC9A2
    nsv6343855copy number variation1nstd223human GRCh38 chr2: 102,680,918-102,681,254 , GRCh37.p13 chr2: 103,297,377-103,297,713 SLC9A2
    nsv6341810copy number variation1nstd223human GRCh38 chr2: 102,625,607-102,631,279 , GRCh37.p13 chr2: 103,242,066-103,247,738 SLC9A2
    nsv6340703copy number variation1nstd223human GRCh38 chr2: 102,702,880-102,703,627 , GRCh37.p13 chr2: 103,319,339-103,320,086 SLC9A2
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