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Items: 1 to 20 of 123

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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
    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
    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
    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
    nsv6702587copy number variation1nstd229human GRCh38 chr3: 38,270,397-38,278,773 , GRCh37.p13 chr3: 38,311,888-38,320,264 CDC42P7, SLC22A13
    nsv6700886copy number variation1nstd229human GRCh38 chr3: 38,256,199-38,267,972 , GRCh37.p13 chr3: 38,297,690-38,309,463 SLC22A13, CDC42P7
    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
    nsv6537958inversion1nstd223human GRCh38 chr3: 37,408,438-39,634,613 , GRCh37.p13 chr3: 37,449,929-39,676,104 ITGA9-AS1, MIR26A1, 55 more genes
    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
    nsv6313737copy number variation1nstd102humanUncertain significance GRCh37 chr3: 38,109,534-38,669,316 , GRCh38.p12 chr3: 38,068,043-38,627,825 ACVR2B-AS1, SCN5A, 16 more genes
    nsv6311982copy number variation1nstd102humanUncertain significance GRCh37 chr3: 37,034,542-38,835,501 , GRCh38.p12 chr3: 36,993,051-38,794,010 SCN10A, PPP2R2DP1, 41 more genes
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 LOC102724104, CRIP1P2, 291 more genes
    nsv6134845copy number variation1nstd213human GRCh37 chr3: 37,240,000-38,310,001 , GRCh38.p12 chr3: 37,198,509-38,268,510 ACAA1, GOLGA4, 22 more genes
    nsv6078165insertion1nstd212human GRCh38 chr3: 38,274,364-38,274,364 , GRCh37.p13 chr3: 38,315,855-38,315,855 SLC22A13
    nsv5977843inversion1nstd209human GRCh37.p13 chr3: 38,198,806-38,332,023 , GRCh38 chr3: 38,157,315-38,290,532 SLC22A14, SLC22A13, 3 more genes
    nsv5555820sequence alteration1nstd206human GRCh38 chr3: 38,272,983-38,274,362 , GRCh37.p13 chr3: 38,314,474-38,315,853 SLC22A13
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