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Items: 1 to 20 of 1157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6118729copy number variation1nstd186human GRCh37 chr3: 195,413,769-195,414,047 , GRCh38.p12 chr3|NT_187690.1: 106,498-106,776 , GRCh38.p12 chr3|NT_187678.1: 108,868-109,146 , GRCh38.p12 chr3|NT_187688.1: 105,786-106,064 , GRCh38.p12 chr3|NT_187689.1: 57,395-57,673 , GRCh38.p12 chr3|NT_187532.1: 57,395-57,673 , GRCh38.p12 chr3: 195,686,898-195,687,176 , GRCh38.p12 chr3|NT_187691.1: 107,935-108,213 , GRCh38.p12 chr3|NT_187649.1: 105,224-105,502 MIR570HG, SDHAP2
    nsv5971950inversion1nstd209human GRCh38 chr3: 195,691,416-195,957,447 , GRCh37.p13 chr3: 195,418,287-195,684,318 , MUC4, 12 more genes
    nsv5891149copy number variation1nstd209human GRCh38 chr3: 195,710,937-195,711,462 , GRCh37.p13 chr3: 195,437,808-195,438,333 SMBD1P, MIR570HG
    nsv5890611copy number variation1nstd209human GRCh38 chr3: 195,702,638-195,702,755 , GRCh37.p13 chr3: 195,429,509-195,429,626 MIR570HG, SMBD1P
    nsv5667176inversion1nstd207human GRCh37.p13 chr3: 195,347,611-195,707,078 , GRCh38 chr3: 195,620,740-195,980,207 , MUC4, 18 more genes
    nsv5623254insertion1nstd207human GRCh38 chr3: 195,687,249-195,687,249 , GRCh37.p13 chr3: 195,414,120-195,414,120 SDHAP2, MIR570HG
    nsv5623125insertion1nstd207human GRCh38 chr3: 195,694,637-195,694,637 , GRCh37.p13 chr3: 195,421,508-195,421,508 MIR570HG
    nsv5620461insertion1nstd207human GRCh38 chr3: 195,700,006-195,700,006 , GRCh37.p13 chr3: 195,426,877-195,426,877 MIR570HG, SMBD1P
    nsv5617160insertion1nstd207human GRCh38 chr3: 195,711,331-195,711,331 , GRCh37.p13 chr3: 195,438,202-195,438,202 MIR570HG, SMBD1P
    nsv5617103insertion1nstd207human GRCh38 chr3: 195,710,669-195,710,669 , GRCh37.p13 chr3: 195,437,540-195,437,540 MIR570HG, SMBD1P
    nsv5616762insertion1nstd207human GRCh38 chr3: 195,710,544-195,710,544 , GRCh37.p13 chr3: 195,437,415-195,437,415 SMBD1P, MIR570HG
    nsv5613895insertion1nstd207human GRCh38 chr3: 195,710,973-195,710,973 , GRCh37.p13 chr3: 195,437,844-195,437,844 MIR570HG, SMBD1P
    nsv5613806insertion1nstd207human GRCh38 chr3: 195,711,371-195,711,371 , GRCh37.p13 chr3: 195,438,242-195,438,242 MIR570HG, SMBD1P
    nsv5612767insertion1nstd207human GRCh38 chr3: 195,710,953-195,710,953 , GRCh37.p13 chr3: 195,437,824-195,437,824 MIR570HG, SMBD1P
    nsv5609725insertion1nstd207human GRCh38 chr3: 195,710,647-195,710,647 , GRCh37.p13 chr3: 195,437,518-195,437,518 SMBD1P, MIR570HG
    nsv5608969insertion1nstd207human GRCh38 chr3: 195,691,185-195,691,185 , GRCh37.p13 chr3: 195,418,056-195,418,056 MIR570HG
    nsv5607365insertion1nstd207human GRCh38 chr3: 195,702,655-195,702,655 , GRCh37.p13 chr3: 195,429,526-195,429,526 MIR570HG, SMBD1P
    nsv5606948insertion1nstd207human GRCh38 chr3: 195,687,570-195,687,570 , GRCh37.p13 chr3: 195,414,441-195,414,441 MIR570HG, SDHAP2
    nsv5583640copy number variation1nstd207human GRCh38 chr3: 195,699,212-195,699,293 , GRCh37.p13 chr3: 195,426,083-195,426,164 MIR570, MIR570HG
    nsv5582921copy number variation1nstd207human GRCh38 chr3: 195,686,861-195,686,955 , GRCh37.p13 chr3: 195,413,732-195,413,826 MIR570HG, SDHAP2
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