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Items: 1 to 20 of 203

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7060106inversion1nstd229human GRCh38 chr17: 63,466,957-64,030,780 , GRCh37.p13 chr17: 61,544,318-62,108,140 LOC101927898, KCNH6, 30 more genes
    nsv7058709inversion1nstd229human GRCh38 chr17: 63,287,540-63,475,758 , GRCh37.p13 chr17: 61,364,901-61,553,119 TANC2, PPIAP55, 4 more genes
    nsv6994567copy number variation1nstd229human GRCh38 chr17: 63,490,897-63,532,417 , GRCh37.p13 chr17: 61,568,258-61,609,778 ACE3P, ACE, 1 more genes
    nsv6984519copy number variation1nstd229human GRCh38 chr17: 63,483,573-63,488,432 , GRCh37.p13 chr17: 61,560,934-61,565,793 ACE
    nsv6980179copy number variation1nstd229human GRCh38 chr17: 63,476,940-63,479,886 , GRCh37.p13 chr17: 61,554,301-61,557,247 ACE
    nsv6979449copy number variation1nstd229human GRCh38 chr17: 63,497,610-63,502,307 , GRCh37.p13 chr17: 61,574,971-61,579,668 ACE
    nsv6524558copy number variation1nstd223human GRCh38 chr17: 63,490,897-63,532,414 , GRCh37.p13 chr17: 61,568,258-61,609,775 ACE, ACE3P, 1 more genes
    nsv6250944mobile element insertion1nstd215human GRCh38 chr17: 63,488,543-63,488,543 , GRCh37.p13 chr17: 61,565,904-61,565,904 ACE
    nsv6133316copy number variation1nstd213human GRCh37 chr17: 53,930,000-62,410,001 , GRCh38.p12 chr17: 55,852,639-64,332,641 CA4, CD79B, 208 more genes
    nsv6085981insertion1nstd212human GRCh38 chr17: 63,488,529-63,488,529 , GRCh37.p13 chr17: 61,565,890-61,565,890 ACE
    nsv5972136insertion1nstd209human GRCh38 chr17: 63,485,481-63,485,481 , GRCh37.p13 chr17: 61,562,842-61,562,842 ACE
    nsv5970673insertion1nstd209human GRCh38 chr17: 63,488,529-63,488,529 , GRCh37.p13 chr17: 61,565,890-61,565,890 ACE
    nsv5729711mobile element insertion2nstd211human GRCh38 chr17: 63,485,480-63,485,480 , GRCh37.p13 chr17: 61,562,841-61,562,841 ACE
    nsv5694751mobile element insertion2nstd211human GRCh38 chr17: 63,488,543-63,488,543 , GRCh37.p13 chr17: 61,565,904-61,565,904 ACE
    nsv5650105insertion1nstd207human GRCh38 chr17: 63,488,529-63,488,529 , GRCh37.p13 chr17: 61,565,890-61,565,890 ACE
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5545135insertion1nstd206human GRCh38 chr17: 63,485,480-63,485,490 , GRCh37.p13 chr17: 61,562,841-61,562,851 ACE
    nsv5425408mobile element insertion1nstd206human GRCh38 chr17: 63,488,529-63,488,529 , GRCh37.p13 chr17: 61,565,890-61,565,890 ACE
    nsv5323702copy number variation1nstd204human GRCh38.p13 chr17: 63,482,081-63,511,487 , GRCh37.p13 chr17: 61,559,442-61,588,848 ACE3P, ACE
    nsv5291986copy number variation1nstd204human GRCh38.p13 chr17: 63,481,627-63,510,087 , GRCh37.p13 chr17: 61,558,988-61,587,448 ACE3P, ACE
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