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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7067648inversion1nstd229human GRCh38 chr17: 76,793,091-76,801,617 , GRCh37.p13 chr17: 74,789,173-74,797,699 MFSD11, LINC02080
    nsv7065899inversion1nstd229human GRCh38 chr17: 76,795,251-76,801,032 , GRCh37.p13 chr17: 74,791,333-74,797,114 LINC02080, MFSD11
    nsv6990938copy number variation1nstd229human GRCh38 chr17: 76,794,590-76,897,980 , GRCh37.p13 chr17: 74,790,672-74,894,062 LINC02080, MGAT5B, 3 more genes
    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
    nsv6982239copy number variation1nstd229human GRCh38 chr17: 76,224,241-77,998,670 , GRCh37.p13 chr17: 74,220,322-75,994,751 MFSD11, PRPSAP1, 59 more genes
    nsv6588499inversion1nstd223human GRCh38 chr17: 76,800,077-76,800,804 , GRCh37.p13 chr17: 74,796,159-74,796,886 LINC02080, MFSD11
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6530843copy number variation1nstd223human GRCh38 chr17: 76,735,301-77,145,300 , GRCh37.p13 chr17: 74,731,383-75,141,382 SEC14L1, RNU6-97P, 12 more genes
    nsv6530511copy number variation1nstd223human GRCh38 chr17: 76,792,201-76,799,300 , GRCh37.p13 chr17: 74,788,283-74,795,382 LINC02080, MFSD11
    nsv6529560copy number variation1nstd223human GRCh38 chr17: 76,790,215-76,800,173 , GRCh37.p13 chr17: 74,786,297-74,796,255 LINC02080, MFSD11
    nsv6522632copy number variation1nstd223human GRCh38 chr17: 76,801,724-76,810,434 , GRCh37.p13 chr17: 74,797,806-74,806,516 LINC02080, MFSD11
    nsv6517671copy number variation1nstd223human GRCh38 chr17: 76,781,801-76,823,900 , GRCh37.p13 chr17: 74,777,883-74,819,982 LINC02080, MFSD11, 1 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
    nsv6291780copy number variation1nstd102humanLikely benign GRCh37 chr17: 74,738,014-74,835,074 , GRCh38.p12 chr17: 76,741,932-76,838,992 MFSD11, LINC02080, 2 more genes
    nsv4676341copy number variation1nstd102humanUncertain significance GRCh37 chr17: 74,509,193-75,602,123 , GRCh38.p12 chr17: 76,513,111-77,606,041 CYCSP40, RNU6-97P, 38 more genes
    nsv4676322copy number variation1nstd102humanLikely benign GRCh37 chr17: 74,742,740-74,835,074 , GRCh38.p12 chr17: 76,746,658-76,838,992 RNU6-97P, MFSD11, 2 more genes
    nsv4676104copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963 LLGL2, TSEN54, 165 more genes
    nsv4507316mobile element insertion1nstd166human GRCh37.p13 chr17: 74,800,698-74,800,698 , GRCh38.p12 chr17: 76,804,616-76,804,616 LINC02080
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4254358copy number variation1nstd166human GRCh37.p13 chr17: 74,456,327-75,011,803 , GRCh38.p12 chr17: 76,460,245-77,015,721 RNU6-97P, RHBDF2, 24 more genes
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