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Items: 1 to 20 of 181

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138188copy number variation1nstd232human GRCh37.p13 chr17: 76,171,029-76,171,127 , GRCh38.p12 chr17: 78,174,948-78,175,046 TK1
    nsv7074642inversion1nstd229human GRCh38 chr17: 78,138,560-78,604,821 , GRCh37.p13 chr17: 76,134,641-76,600,903 RN7SL454P, DNAH17, 18 more genes
    nsv6997446copy number variation1nstd229human GRCh38 chr17: 78,115,601-78,538,200 , GRCh37.p13 chr17: 76,111,682-76,534,282 BIRC5, PGS1, 19 more genes
    nsv6996134copy number variation1nstd229human GRCh38 chr17: 78,170,920-78,172,600 , GRCh37.p13 chr17: 76,167,001-76,168,681 SYNGR2, TK1
    nsv6994801copy number variation1nstd229human GRCh38 chr17: 78,157,486-78,174,492 , GRCh37.p13 chr17: 76,153,567-76,170,573 TK1, SYNGR2, 2 more genes
    nsv6994461copy number variation1nstd229human GRCh38 chr17: 78,176,213-78,176,290 , GRCh37.p13 chr17: 76,172,294-76,172,371 TK1
    nsv6991963copy number variation1nstd229human GRCh38 chr17: 78,187,257-78,187,317 , GRCh37.p13 chr17: 76,183,338-76,183,398 AFMID, TK1
    nsv6986859copy number variation1nstd229human GRCh38 chr17: 78,182,580-78,185,882 , GRCh37.p13 chr17: 76,178,661-76,181,963 TK1, AFMID
    nsv6984264copy number variation1nstd229human GRCh38 chr17: 74,239,313-78,611,254 , GRCh37.p13 chr17: 72,235,452-76,607,336 SNORD1C, PRCD, 178 more genes
    nsv6982471copy number variation1nstd229human GRCh38 chr17: 78,166,040-78,173,792 , GRCh37.p13 chr17: 76,162,121-76,169,873 TK1, SYNGR2, 1 more genes
    nsv6978863copy number variation1nstd229human GRCh38 chr17: 78,167,157-78,194,983 , GRCh37.p13 chr17: 76,163,238-76,191,064 TK1, SYNGR2, 1 more genes
    nsv6624516copy number variation1nstd224human GRCh37 chr17: 76,179,530-76,202,995 , GRCh38.p12 chr17: 78,183,449-78,206,914 TK1, AFMID
    nsv6624515copy number variation1nstd224human GRCh37 chr17: 76,175,824-76,188,753 , GRCh38.p12 chr17: 78,179,743-78,192,672 TK1, AFMID
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6315182copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323 DUS1L, PVALEF, 252 more genes
    nsv6189178copy number variation1nstd214human GRCh38 chr17: 78,176,215-78,176,289 , GRCh37.p13 chr17: 76,172,296-76,172,370 , TK1
    nsv6097298insertion1nstd212human GRCh38 chr17: 78,175,220-78,175,220 , GRCh37.p13 chr17: 76,171,301-76,171,301 , TK1
    nsv6087229insertion1nstd212human GRCh38 chr17: 78,182,216-78,182,216 , GRCh37.p13 chr17: 76,178,297-76,178,297 , TK1
    nsv5971941insertion1nstd209human GRCh38 chr17: 78,175,213-78,175,213 , GRCh37.p13 chr17: 76,171,294-76,171,294 , TK1
    nsv5927827copy number variation1nstd209human GRCh38 chr17: 78,187,257-78,187,316 , GRCh37.p13 chr17: 76,183,338-76,183,397 TK1, AFMID
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