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Items: 1 to 20 of 256

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976546insertion1nstd209human GRCh38 chr17: 38,389,863-38,389,863 , GRCh37.p13 chr17|NW_003315948.2: 173,415-173,415 SOCS7
    nsv5974644insertion1nstd209human GRCh38 chr17: 38,387,610-38,387,610 , GRCh37.p13 chr: NaN-NaN SOCS7
    nsv5941546copy number variation1nstd209human GRCh38 chr17: 38,373,958-38,374,274 , GRCh37.p13 chr17|NW_003315948.2: 157,168-157,485 SOCS7
    nsv5941498copy number variation1nstd209human GRCh38 chr17: 38,379,359-38,388,398 , GRCh37.p13 chr17|NW_003315948.2: 162,570-171,950 SOCS7
    nsv5880618copy number variation1nstd209human GRCh38 chr17: 38,379,389-38,385,115 , GRCh37.p13 chr17|NW_003315948.2: 162,600-168,324 SOCS7
    nsv5664211insertion1nstd207human GRCh38 chr17: 38,387,135-38,387,135 , GRCh37.p13 chr17|NW_003315948.2: 170,347-170,347 SOCS7
    nsv5660596insertion1nstd207human GRCh38 chr17: 38,387,107-38,387,107 , GRCh37.p13 chr17|NW_003315948.2: 170,319-170,319 SOCS7
    nsv5658222insertion1nstd207human GRCh38 chr17: 38,389,863-38,389,863 , GRCh37.p13 chr17|NW_003315948.2: 173,415-173,415 SOCS7
    nsv5652358insertion1nstd207human GRCh38 chr17: 38,387,650-38,387,650 , GRCh37.p13 chr17|NW_003315948.2: 171,203-171,203 SOCS7
    nsv5651615insertion1nstd207human GRCh38 chr17: 38,389,892-38,389,892 , GRCh37.p13 chr17|NW_003315948.2: 173,444-173,444 SOCS7
    nsv5595935copy number variation1nstd207human GRCh38 chr17: 38,371,489-38,371,548 , GRCh37.p13 chr17|NW_003315948.2: 154,760-154,819 SOCS7
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5541804insertion1nstd206human GRCh38 chr17: 38,387,650-38,387,650 , GRCh37.p13 chr17|NW_003315948.2: 171,203-171,203 SOCS7
    nsv5531506copy number variation1nstd206human GRCh38 chr17: 38,379,359-38,388,399 , GRCh37.p13 chr17|NW_003315948.2: 162,570-171,951 SOCS7
    nsv5518768copy number variation1nstd206human GRCh38 chr17: 38,387,578-38,389,883 , GRCh37.p13 chr17|NW_003315948.2: 171,137-173,435 SOCS7
    nsv5374916translocation1nstd200human GRCh38 chr17: 38,379,431-38,379,431 , GRCh38 chr17: 38,388,392-38,388,392 , GRCh37.p13 chr17|NW_003315948.2: 171,944-171,944 , GRCh37.p13 chr17|NW_003315948.2: 162,642-162,642 SOCS7
    nsv5285584copy number variation1nstd204human GRCh38.p13 chr17: 38,350,620-38,351,719 , GRCh37.p13 chr17|NW_003315948.2: 133,887-134,986 SOCS7
    nsv5156743mobile element insertion1nstd203human GRCh38 chr17: 38,394,089-38,394,106 , GRCh37.p13 chr17: 36,550,342-36,550,359 SOCS7
    nsv5145330mobile element insertion1nstd203human GRCh38 chr17: 38,371,549-38,371,549 , GRCh37.p13 chr17|NW_003315948.2: 154,820-154,820 SOCS7
    nsv5016224copy number variation1nstd200human GRCh38 chr17: 38,388,633-38,389,892 , GRCh37.p13 chr17|NW_003315948.2: 172,185-173,444 SOCS7
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