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Items: 1 to 20 of 284

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7061007inversion1nstd229human GRCh38 chr17: 63,688,842-63,688,936 , GRCh37.p13 chr17: 61,766,202-61,766,296 MAP3K3, LOC101927898
    nsv7060106inversion1nstd229human GRCh38 chr17: 63,466,957-64,030,780 , GRCh37.p13 chr17: 61,544,318-62,108,140 LOC101927898, KCNH6, 30 more genes
    nsv6992479copy number variation1nstd229human GRCh38 chr17: 63,625,684-63,630,697 , GRCh37.p13 chr17: 61,703,044-61,708,057 MAP3K3
    nsv6989134copy number variation1nstd229human GRCh38 chr17: 63,665,547-63,665,970 , GRCh37.p13 chr17: 61,742,907-61,743,330 MAP3K3
    nsv6985762copy number variation1nstd229human GRCh38 chr17: 63,672,101-63,674,400 , GRCh37.p13 chr17: 61,749,461-61,751,760 MAP3K3
    nsv6985125copy number variation1nstd229human GRCh38 chr17: 63,672,111-63,674,394 , GRCh37.p13 chr17: 61,749,471-61,751,754 MAP3K3
    nsv6984505copy number variation1nstd229human GRCh38 chr17: 63,596,001-63,631,300 , GRCh37.p13 chr17: 61,673,360-61,708,660 FAM136DP, MAP3K3, 1 more genes
    nsv6586595inversion1nstd223human GRCh38 chr17: 63,671,554-63,672,250 , GRCh37.p13 chr17: 61,748,914-61,749,610 MAP3K3
    nsv6586037inversion1nstd223human GRCh38 chr17: 63,661,952-63,662,678 , GRCh37.p13 chr17: 61,739,312-61,740,038 MAP3K3
    nsv6583364inversion1nstd223human GRCh38 chr17: 63,670,443-63,671,545 , GRCh37.p13 chr17: 61,747,803-61,748,905 MAP3K3
    nsv6528443copy number variation1nstd223human GRCh38 chr17: 63,661,920-63,663,970 , GRCh37.p13 chr17: 61,739,280-61,741,330 MAP3K3
    nsv6521161copy number variation1nstd223human GRCh38 chr17: 63,625,684-63,630,693 , GRCh37.p13 chr17: 61,703,044-61,708,053 MAP3K3
    nsv6518786copy number variation1nstd223human GRCh38 chr17: 63,639,579-63,640,043 , GRCh37.p13 chr17: 61,716,939-61,717,403 MAP3K3
    nsv6517132copy number variation1nstd223human GRCh38 chr17: 63,672,117-63,674,376 , GRCh37.p13 chr17: 61,749,477-61,751,736 MAP3K3
    nsv6250945mobile element insertion1nstd215human GRCh38 chr17: 63,654,333-63,654,333 , GRCh37.p13 chr17: 61,731,693-61,731,693 MAP3K3
    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
    nsv6131225insertion1nstd186human GRCh37 chr17: 61,731,675-61,731,675 , GRCh38.p12 chr17: 63,654,315-63,654,315 MAP3K3
    nsv6128909copy number variation1nstd186human GRCh37 chr17: 61,731,528-61,731,675 , GRCh38.p12 chr17: 63,654,168-63,654,315 MAP3K3
    nsv6081145insertion1nstd212human GRCh38 chr17: 63,654,328-63,654,328 , GRCh37.p13 chr17: 61,731,688-61,731,688 MAP3K3
    nsv5978619insertion1nstd209human GRCh38 chr17: 63,654,315-63,654,315 , GRCh37.p13 chr17: 61,731,675-61,731,675 MAP3K3
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