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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096799copy number variation1nstd102humanUncertain significance GRCh37 chr3: 38,180,153-38,618,292 , GRCh38.p12 chr3: 38,138,662-38,576,801 ACVR2B-AS1, SCN5A, 13 more genes
    nsv7056632inversion1nstd229human GRCh38 chr3: 38,288,871-38,294,461 , GRCh37.p13 chr3: 38,330,362-38,335,952 SLC22A14
    nsv7051268inversion1nstd229human GRCh38 chr3: 37,000,362-39,352,689 , GRCh37.p13 chr3: 37,041,853-39,394,180 PLCD1, RNU6-1227P, 59 more genes
    nsv7048850inversion1nstd229human GRCh38 chr3: 37,408,411-39,634,596 , GRCh37.p13 chr3: 37,449,902-39,676,087 OXSR1, ITGA9, 55 more genes
    nsv7045280inversion1nstd229human GRCh38 chr3: 38,291,449-38,299,840 , GRCh37.p13 chr3: 38,332,940-38,341,331 SLC22A14
    nsv7044918inversion1nstd229human GRCh38 chr3: 38,157,316-38,290,534 , GRCh37.p13 chr3: 38,198,807-38,332,025 OXSR1, LOC101928234, 3 more genes
    nsv7042103inversion1nstd229human GRCh38 chr3: 37,827,304-38,566,908 , GRCh37.p13 chr3: 37,868,795-38,608,399 SCN5A, CDC42P7, 22 more genes
    nsv7039010inversion1nstd229human GRCh38 chr3: 37,851,228-39,078,678 , GRCh37.p13 chr3: 37,892,719-39,120,169 CDC42P7, LOC105377033, 28 more genes
    nsv6717419copy number variation1nstd229human GRCh38 chr3: 38,263,993-38,306,550 , GRCh37.p13 chr3: 38,305,484-38,348,041 CDC42P7, SLC22A14, 2 more genes
    nsv6708428copy number variation1nstd229human GRCh38 chr3: 38,308,180-38,308,237 , GRCh37.p13 chr3: 38,349,671-38,349,728 SLC22A14
    nsv6703351copy number variation1nstd229human GRCh38 chr3: 38,269,150-38,436,611 , GRCh37.p13 chr3: 38,310,641-38,478,102 SLC22A14, XYLB, 4 more genes
    nsv6702922copy number variation1nstd229human GRCh38 chr3: 38,298,001-38,302,900 , GRCh37.p13 chr3: 38,339,492-38,344,391 SLC22A14, RNU6-235P
    nsv6702572copy number variation1nstd229human GRCh38 chr3: 38,282,624-38,282,843 , GRCh37.p13 chr3: 38,324,115-38,324,334 SLC22A14
    nsv6701158copy number variation1nstd229human GRCh38 chr3: 38,305,600-38,305,854 , GRCh37.p13 chr3: 38,347,091-38,347,345 SLC22A14
    nsv6628589copy number variation1nstd224human GRCh37 chr3: 38,271,881-38,380,843 , GRCh38.p12 chr3: 38,230,390-38,339,352 SLC22A14, SLC22A13, 4 more genes
    nsv6549620inversion1nstd223human GRCh38 chr3: 38,288,871-38,294,468 , GRCh37.p13 chr3: 38,330,362-38,335,959 SLC22A14
    nsv6545172inversion1nstd223human GRCh38 chr3: 38,285,974-38,286,549 , GRCh37.p13 chr3: 38,327,465-38,328,040 SLC22A14
    nsv6537958inversion1nstd223human GRCh38 chr3: 37,408,438-39,634,613 , GRCh37.p13 chr3: 37,449,929-39,676,104 ITGA9-AS1, MIR26A1, 55 more genes
    nsv6373886copy number variation1nstd223human GRCh38 chr3: 38,290,817-38,292,431 , GRCh37.p13 chr3: 38,332,308-38,333,922 SLC22A14
    nsv6362792copy number variation1nstd223human GRCh38 chr3: 38,263,993-38,306,547 , GRCh37.p13 chr3: 38,305,484-38,348,038 SLC22A14, SLC22A13, 2 more genes
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