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Items: 1 to 20 of 342

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094921copy number variation1nstd102humanUncertain significance GRCh37 chr17: 76,851,749-78,367,298 , GRCh38.p12 chr17: 78,855,667-80,393,498 RNF213-AS1, EIF4A3, 25 more genes
    nsv7074700inversion1nstd229human GRCh38 chr17: 78,850,618-78,851,783 , GRCh37.p13 chr17: 76,846,700-76,847,865 TIMP2
    nsv7074084inversion1nstd229human GRCh38 chr17: 78,889,349-78,889,464 , GRCh37.p13 chr17: 76,885,431-76,885,546 TIMP2, CEP295NL
    nsv7070319inversion1nstd229human GRCh38 chr17: 78,859,985-78,861,630 , GRCh37.p13 chr17: 76,856,067-76,857,712 TIMP2
    nsv6997635copy number variation1nstd229human GRCh38 chr17: 78,889,423-78,913,191 , GRCh37.p13 chr17: 76,885,505-76,909,273 CEP295NL, TIMP2
    nsv6994435copy number variation1nstd229human GRCh38 chr17: 78,897,224-78,906,707 , GRCh37.p13 chr17: 76,893,306-76,902,789 TIMP2, CEP295NL
    nsv6993964copy number variation1nstd229human GRCh38 chr17: 78,767,102-79,347,128 , GRCh37.p13 chr17: 76,763,184-77,343,210 CYTH1, C1QTNF1-AS1, 9 more genes
    nsv6993667copy number variation1nstd229human GRCh38 chr17: 78,709,580-81,173,842 , GRCh37.p13 chr17: 76,705,662-79,147,642 C1QTNF1-AS1, NPTX1, 47 more genes
    nsv6991516copy number variation1nstd229human GRCh38 chr17: 78,879,309-78,914,805 , GRCh37.p13 chr17: 76,875,391-76,910,887 CEP295NL, TIMP2
    nsv6990720copy number variation1nstd229human GRCh38 chr17: 78,906,294-78,913,819 , GRCh37.p13 chr17: 76,902,376-76,909,901 TIMP2
    nsv6986745copy number variation1nstd229human GRCh38 chr17: 78,916,265-78,919,785 , GRCh37.p13 chr17: 76,912,347-76,915,867 TIMP2
    nsv6983958copy number variation1nstd229human GRCh38 chr17: 78,872,289-78,872,623 , GRCh37.p13 chr17: 76,868,371-76,868,705 TIMP2
    nsv6983296copy number variation1nstd229human GRCh38 chr17: 78,894,601-78,897,800 , GRCh37.p13 chr17: 76,890,683-76,893,882 CEP295NL, TIMP2
    nsv6624116copy number variation1nstd224human GRCh37 chr17: 76,921,790-77,051,253 , GRCh38.p12 chr17: 78,925,708-79,055,171 TIMP2, LGALS3BP, 3 more genes
    nsv6593679inversion1nstd223human GRCh38 chr17: 78,850,618-78,851,783 , GRCh37.p13 chr17: 76,846,700-76,847,865 TIMP2
    nsv6590388inversion1nstd223human GRCh38 chr17: 78,851,731-78,852,144 , GRCh37.p13 chr17: 76,847,813-76,848,226 TIMP2
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6532612copy number variation1nstd223human GRCh38 chr17: 78,897,224-78,906,706 , GRCh37.p13 chr17: 76,893,306-76,902,788 TIMP2, CEP295NL
    nsv6529265copy number variation1nstd223human GRCh38 chr17: 78,919,705-79,477,438 , GRCh37.p13 chr17: 76,915,787-77,412,076 CANT1, C1QTNF1-AS1, 5 more genes
    nsv6527001copy number variation1nstd223human GRCh38 chr17: 78,905,122-78,905,475 , GRCh37.p13 chr17: 76,901,204-76,901,557 TIMP2
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