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Items: 1 to 20 of 184

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076231inversion1nstd229human GRCh38 chr17: 69,015,631-73,552,061 , GRCh37.p13 chr17: 67,011,772-71,548,200 KCNJ2-AS1, ROCR, 52 more genes
    nsv6997430copy number variation1nstd229human GRCh38 chr17: 73,261,665-73,264,202 , GRCh37.p13 chr17: 71,257,804-71,260,341 CPSF4L
    nsv6995575copy number variation1nstd229human GRCh38 chr17: 73,241,567-73,244,517 , GRCh37.p13 chr17: 71,237,706-71,240,656 C17orf80, CPSF4L
    nsv6980922copy number variation1nstd229human GRCh38 chr17: 73,258,401-73,264,800 , GRCh37.p13 chr17: 71,254,540-71,260,939 CPSF4L
    nsv6979456copy number variation1nstd229human GRCh38 chr17: 73,230,688-73,241,450 , GRCh37.p13 chr17: 71,226,827-71,237,589 C17orf80, VCF1, 1 more genes
    nsv6595215inversion1nstd223human GRCh38 chr17: 73,243,701-73,244,338 , GRCh37.p13 chr17: 71,239,840-71,240,477 CPSF4L, C17orf80
    nsv6592038inversion1nstd223human GRCh38 chr17: 73,241,379-73,241,932 , GRCh37.p13 chr17: 71,237,518-71,238,071 CPSF4L, C17orf80
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6529454copy number variation1nstd223human GRCh38 chr17: 73,255,489-73,260,682 , GRCh37.p13 chr17: 71,251,628-71,256,821 CPSF4L
    nsv6524759copy number variation1nstd223human GRCh38 chr17: 73,259,701-73,264,800 , GRCh37.p13 chr17: 71,255,840-71,260,939 CPSF4L
    nsv6519102copy number variation1nstd223human GRCh38 chr17: 73,221,065-73,243,700 , GRCh37.p13 chr17: 71,217,204-71,239,839 C17orf80, VCF1, 1 more genes
    nsv6517913copy number variation1nstd223human GRCh38 chr17: 73,260,577-73,261,414 , GRCh37.p13 chr17: 71,256,716-71,257,553 CPSF4L
    nsv6133070copy number variation1nstd213human GRCh37 chr17: 62,460,000-73,800,001 , GRCh38.p12 chr17: 64,464,645-75,803,920 APOH, CACNG1, 225 more genes
    nsv5708317mobile element insertion2nstd211human GRCh38 chr17: 73,249,716-73,249,716 , GRCh37.p13 chr17: 71,245,855-71,245,855 CPSF4L
    nsv5699161mobile element insertion1nstd211human GRCh38 chr17: 73,257,707-73,257,707 , GRCh37.p13 chr17: 71,253,846-71,253,846 CPSF4L
    nsv5530390copy number variation1nstd206human GRCh38 chr17: 73,260,504-73,261,399 , GRCh37.p13 chr17: 71,256,643-71,257,538 CPSF4L
    nsv5514778copy number variation1nstd206human GRCh38 chr17: 73,257,705-73,258,191 , GRCh37.p13 chr17: 71,253,844-71,254,330 CPSF4L
    nsv5417872mobile element insertion1nstd206human GRCh38 chr17: 73,249,716-73,249,767 , GRCh37.p13 chr17: 71,245,855-71,245,906 CPSF4L
    nsv5151706mobile element insertion1nstd203human GRCh38 chr17: 73,249,699-73,249,716 , GRCh37.p13 chr17: 71,245,838-71,245,855 CPSF4L
    nsv5029562inversion1nstd200human GRCh38 chr17: 64,441,870-75,217,767 , GRCh37.p13 chr17: 62,649,312-73,213,862 , LOC102929163, 207 more genes
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