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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6716133copy number variation1nstd229human GRCh38 chr3: 87,186,577-87,519,946 , GRCh37.p13 chr3: 87,235,727-87,569,096 MIR4795, POU1F1, 2 more genes
    nsv6715971copy number variation1nstd229human GRCh38 chr3: 87,202,584-87,227,055 , GRCh37.p13 chr3: 87,251,734-87,276,205 MIR4795, CHMP2B
    nsv6698464copy number variation1nstd229human GRCh38 chr3: 87,234,328-87,244,220 , GRCh37.p13 chr3: 87,283,478-87,293,370 CHMP2B
    nsv6698097copy number variation1nstd229human GRCh38 chr3: 87,241,841-87,260,450 , GRCh37.p13 chr3: 87,290,991-87,309,600 POU1F1, CHMP2B
    nsv6636809copy number variation1nstd102humanUncertain significance GRCh37 chr3: 86,841,601-87,862,816 , GRCh38.p12 chr3: 86,792,451-87,813,666 CHMP2B, POU1F1, 12 more genes
    nsv6552187inversion1nstd223human GRCh38 chr3: 87,248,189-87,248,463 , GRCh37.p13 chr3: 87,297,339-87,297,613 CHMP2B
    nsv6373284copy number variation1nstd223human GRCh38 chr3: 87,237,896-87,238,277 , GRCh37.p13 chr3: 87,287,046-87,287,427 CHMP2B
    nsv6370760copy number variation1nstd223human GRCh38 chr3: 87,249,438-87,249,812 , GRCh37.p13 chr3: 87,298,588-87,298,962 CHMP2B
    nsv6368633copy number variation1nstd223human GRCh38 chr3: 87,186,577-87,519,943 , GRCh37.p13 chr3: 87,235,727-87,569,093 POU1F1, MIR4795, 2 more genes
    nsv6368490copy number variation1nstd223human GRCh38 chr3: 87,238,340-87,238,425 , GRCh37.p13 chr3: 87,287,490-87,287,575 CHMP2B
    nsv6359702copy number variation1nstd223human GRCh38 chr3: 87,249,501-87,251,800 , GRCh37.p13 chr3: 87,298,651-87,300,950 CHMP2B
    nsv6357206copy number variation1nstd223human GRCh38 chr3: 87,202,584-87,227,054 , GRCh37.p13 chr3: 87,251,734-87,276,204 CHMP2B, MIR4795
    nsv6355632copy number variation1nstd223human GRCh38 chr3: 87,228,701-87,230,600 , GRCh37.p13 chr3: 87,277,851-87,279,750 CHMP2B
    nsv6314751copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 72,488,757-99,614,758 , GRCh38.p12 chr3: 72,439,606-99,895,914 AKR1B1P2, COL8A1, 231 more genes
    nsv6311804copy number variation1nstd102humanUncertain significance GRCh37 chr3: 87,276,673-87,325,612 , GRCh38.p12 chr3: 87,227,523-87,276,462 POU1F1, CHMP2B
    nsv6290743copy number variation1nstd102humanUncertain significance GRCh37 chr3: 87,158,116-87,306,158 , GRCh38.p12 chr3: 87,108,966-87,257,008 MIR4795, LINC00506, 1 more genes
    nsv6135252copy number variation1nstd213human GRCh37 chr3: 87,020,000-88,110,001 , GRCh38.p12 chr3: 86,970,850-88,060,851 POU1F1, CHMP2B, 14 more genes
    nsv6134705copy number variation1nstd213human GRCh37 chr3: 66,270,000-87,730,001 , GRCh38.p12 chr3: 66,219,846-87,680,851 , AKR1B1P2, 187 more genes
    nsv5994350copy number variation1nstd212human GRCh38 chr3: 87,248,198-87,248,254 , GRCh37.p13 chr3: 87,297,348-87,297,404 CHMP2B
    nsv5888496copy number variation1nstd209human GRCh38 chr3: 87,228,014-87,232,425 , GRCh37.p13 chr3: 87,277,164-87,281,575 CHMP2B
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