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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6995824copy number variation1nstd229human GRCh38 chr17: 78,164,380-78,168,026 , GRCh37.p13 chr17: 76,160,461-76,164,107 SYNGR2, C17orf99
    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
    nsv6993404copy number variation1nstd229human GRCh38 chr17: 78,168,717-78,170,815 , GRCh37.p13 chr17: 76,164,798-76,166,896 SYNGR2
    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
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6523113copy number variation1nstd223human GRCh38 chr17: 78,167,017-78,167,834 , GRCh37.p13 chr17: 76,163,098-76,163,915 SYNGR2
    nsv6522158copy number variation1nstd223human GRCh38 chr17: 78,170,417-78,170,701 , GRCh37.p13 chr17: 76,166,498-76,166,782 SYNGR2
    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
    nsv6131053insertion1nstd186human GRCh37 chr17: 76,163,788-76,163,788 , GRCh38.p12 chr17: 78,167,707-78,167,707 SYNGR2
    nsv5979945insertion1nstd209human GRCh38 chr17: 78,167,707-78,167,707 , GRCh37.p13 chr17: 76,163,788-76,163,788 SYNGR2
    nsv5662993insertion1nstd207human GRCh38 chr17: 78,167,707-78,167,707 , GRCh37.p13 chr17: 76,163,788-76,163,788 SYNGR2
    nsv5552677insertion1nstd206human GRCh38 chr17: 78,167,707-78,167,707 , GRCh37.p13 chr17: 76,163,788-76,163,788 SYNGR2
    nsv5530798copy number variation1nstd206human GRCh38 chr17: 78,167,662-78,167,987 , GRCh37.p13 chr17: 76,163,743-76,164,068 SYNGR2
    nsv5526575copy number variation1nstd206human GRCh38 chr17: 78,173,173-78,173,313 , GRCh37.p13 chr17: 76,169,254-76,169,394 , SYNGR2, 1 more genes
    nsv5155861mobile element insertion1nstd203human GRCh38 chr17: 78,167,552-78,167,588 , GRCh37.p13 chr17: 76,163,633-76,163,669 SYNGR2
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