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Items: 1 to 20 of 855

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147410copy number variation1nstd232human GRCh37.p13 chr3: 195,413,769-195,413,832 , GRCh38.p12 chr3: 195,686,898-195,686,961 , GRCh38.p12 chr3|NT_187678.1: 109,083-109,146 , GRCh38.p12 chr3|NT_187688.1: 106,001-106,064 , GRCh38.p12 chr3|NT_187689.1: 57,395-57,458 , GRCh38.p12 chr3|NT_187690.1: 106,713-106,776 , GRCh38.p12 chr3|NT_187691.1: 108,150-108,213 , GRCh38.p12 chr3|NT_187532.1: 57,395-57,458 , GRCh38.p12 chr3|NT_187649.1: 105,439-105,502 MIR570HG, SDHAP2
    nsv7143434copy number variation1nstd232human GRCh37.p13 chr3: 195,413,732-195,413,826 , GRCh38.p12 chr3: 195,686,861-195,686,955 , GRCh38.p12 chr3|NT_187678.1: 109,089-109,183 , GRCh38.p12 chr3|NT_187688.1: 106,007-106,101 , GRCh38.p12 chr3|NT_187689.1: 57,358-57,452 , GRCh38.p12 chr3|NT_187690.1: 106,719-106,813 , GRCh38.p12 chr3|NT_187691.1: 108,156-108,250 , GRCh38.p12 chr3|NT_187532.1: 57,358-57,452 , GRCh38.p12 chr3|NT_187649.1: 105,445-105,539 MIR570HG, SDHAP2
    nsv7055557inversion1nstd229human GRCh38 chr3: 195,655,301-197,630,693 , GRCh37.p13 chr3: 195,382,172-197,357,564 MIR570HG, RN7SL434P, 66 more genes
    nsv7053852inversion1nstd229human GRCh38 chr3: 195,653,753-197,300,599 , GRCh37.p13 chr3: 195,380,624-197,027,470 NCBP2-AS1, SMCO1, 59 more genes
    nsv7053446inversion1nstd229human GRCh38 chr3: 195,340,377-197,478,980 , GRCh37.p13 chr3: 195,061,106-197,205,851 CEP19, ACAP2, 73 more genes
    nsv7052049inversion1nstd229human GRCh38 chr3: 195,552,932-195,914,148 , GRCh37.p13 chr3: 195,279,750-195,641,019 MUC20P1, MUC4, 17 more genes
    nsv7050362inversion1nstd229human GRCh38 chr3: 195,649,879-195,938,948 , GRCh37.p13 chr3: 195,376,750-195,665,819 SMBD1P, LINC01983, 15 more genes
    nsv7046059inversion1nstd229human GRCh38 chr3: 195,553,744-195,868,010 , GRCh37.p13 chr3: 195,280,562-195,594,881 TNK2, APOD, 15 more genes
    nsv7044295inversion1nstd229human GRCh38 chr3: 195,547,271-197,153,236 , GRCh37.p13 chr3: 195,274,089-196,880,107 SDHAP1, NCBP2AS2, 64 more genes
    nsv7044261inversion1nstd229human GRCh38 chr3: 195,438,610-197,225,061 , GRCh37.p13 chr3: 195,159,339-196,951,932 MUC4, RPL24P6, 67 more genes
    nsv7044126inversion1nstd229human GRCh38 chr3: 195,494,986-195,706,460 , GRCh37.p13 chr3: 195,221,756-195,433,331 SDHAP2, PPP1R2, 11 more genes
    nsv7043305inversion1nstd229human GRCh38 chr3: 195,684,214-195,830,571 , GRCh37.p13 chr3: 195,411,085-195,557,442 MUC4, MIR570, 4 more genes
    nsv7040982inversion1nstd229human GRCh38 chr3: 193,802,086-196,241,826 , GRCh37.p13 chr3: 193,519,875-195,968,697 CPN2, RNU6ATAC24P, 73 more genes
    nsv7039421inversion1nstd229human GRCh38 chr3: 195,645,059-195,878,873 , GRCh37.p13 chr3: 195,371,930-195,605,744 TNK2, SDHAP2, 11 more genes
    nsv7038287inversion1nstd229human GRCh38 chr3: 195,414,253-196,009,284 , GRCh37.p13 chr3: 195,134,982-195,736,155 LOC105374298, LOC107984010, 24 more genes
    nsv6736382copy number variation1nstd229human GRCh38 chr3: 195,685,867-195,694,489 , GRCh37.p13 chr3: 195,412,738-195,421,360 SDHAP2, MIR570HG
    nsv6719514copy number variation1nstd229human GRCh38 chr3: 195,559,701-195,658,900 , GRCh37.p13 chr3: 195,286,544-195,385,771 LOC105374298, LOC105374297, 4 more genes
    nsv6637050copy number variation1nstd102humanUncertain significance GRCh37 chr3: 195,279,004-195,743,958 , GRCh38.p12 chr3: 195,552,186-196,017,087 LOC100131360, SDHAP2, 22 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6315437copy number variation1nstd102humanPathogenic GRCh37 chr3: 183,498,520-197,851,986 , GRCh38.p12 chr3: 183,780,732-198,125,115 LOC105374291, GP5, 315 more genes
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