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Items: 1 to 20 of 922

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7044486inversion1nstd229human GRCh38 chr3: 195,703,983-196,043,070 , GRCh37.p13 chr3: 195,430,854-195,769,941 SMBD1P, LOC107984010, 13 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
    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
    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
    nsv6636798copy number variation1nstd102humanUncertain significance GRCh37 chr3: 195,456,035-195,678,475 , GRCh38.p12 chr3: 195,729,164-195,951,604 MUC20, MIR6829, 8 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
    nsv6628748copy number variation1nstd224human GRCh37 chr3: 195,453,042-195,475,900 , GRCh38.p12 chr3: 195,726,171-195,749,029 , GRCh38.p12 chr3|NT_187678.1: 47,008-69,873 , GRCh38.p12 chr3|NT_187688.1: 45,707-68,529 , GRCh38.p12 chr3|NT_187689.1: 96,668-119,526 , GRCh38.p12 chr3|NT_187690.1: 45,707-68,538 , GRCh38.p12 chr3|NT_187691.1: 45,707-68,693 , GRCh38.p12 chr3|NT_187532.1: 96,668-119,526 , GRCh38.p12 chr3|NT_187649.1: 45,707-68,529 MUC20, MUC4
    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
    nsv6291320copy number variation1nstd102humanUncertain significance GRCh37 chr3: 195,279,003-195,718,752 , GRCh38.p12 chr3: 195,552,185-195,991,881 SDHAP1, LOC107984010, 20 more genes
    nsv6290259copy number variation1nstd102humanPathogenic GRCh37 chr3: 189,608,636-197,532,175 , GRCh38.p12 chr3: 189,890,847-197,805,304 LINC01972, LINC02026, 174 more genes
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