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Items: 1 to 20 of 209

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969750insertion1nstd209human GRCh38 chr19: 48,858,627-48,858,627 , GRCh37.p13 chr19: 49,361,884-49,361,884 PLEKHA4
    nsv5969695insertion1nstd209human GRCh38 chr19: 48,856,916-48,856,916 , GRCh37.p13 chr19: 49,360,173-49,360,173 PLEKHA4
    nsv5945269copy number variation1nstd209human GRCh38 chr19: 48,856,312-48,856,447 , GRCh37.p13 chr19: 49,359,569-49,359,704 PLEKHA4
    nsv5943322copy number variation1nstd209human GRCh38 chr19: 48,834,363-48,835,533 , GRCh37.p13 chr19: 49,337,620-49,338,790 PLEKHA4, HSD17B14
    nsv5938285copy number variation1nstd209human GRCh38 chr19: 48,835,626-48,835,698 , GRCh37.p13 chr19: 49,338,883-49,338,955 HSD17B14, PLEKHA4
    nsv5932070copy number variation1nstd209human GRCh38 chr19: 48,844,523-48,844,592 , GRCh37.p13 chr19: 49,347,780-49,347,849 PLEKHA4
    nsv5927584copy number variation1nstd209human GRCh38 chr19: 48,848,754-48,850,162 , GRCh37.p13 chr19: 49,352,011-49,353,419 PLEKHA4
    nsv5882445copy number variation1nstd209human GRCh38 chr19: 48,848,795-48,850,094 , GRCh37.p13 chr19: 49,352,052-49,353,351 PLEKHA4
    nsv5874679copy number variation1nstd209human GRCh38 chr19: 48,860,338-48,862,171 , GRCh37.p13 chr19: 49,363,595-49,365,428 PLEKHA4
    nsv5725793mobile element insertion1nstd211human GRCh38 chr19: 48,858,644-48,858,644 , GRCh37.p13 chr19: 49,361,901-49,361,901 PLEKHA4
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 more genes
    nsv5647175insertion1nstd207human GRCh38 chr19: 48,836,779-48,836,779 , GRCh37.p13 chr19: 49,340,036-49,340,036 PLEKHA4, HSD17B14
    nsv5645587insertion1nstd207human GRCh38 chr19: 48,835,302-48,835,302 , GRCh37.p13 chr19: 49,338,559-49,338,559 HSD17B14, PLEKHA4
    nsv5602395copy number variation1nstd207human GRCh38 chr19: 48,856,312-48,856,447 , GRCh37.p13 chr19: 49,359,569-49,359,704 PLEKHA4
    nsv5598406copy number variation1nstd207human GRCh38 chr19: 48,836,735-48,836,807 , GRCh37.p13 chr19: 49,339,992-49,340,064 HSD17B14, PLEKHA4
    nsv5595815copy number variation1nstd207human GRCh38 chr19: 48,835,081-48,835,301 , GRCh37.p13 chr19: 49,338,338-49,338,558 PLEKHA4, HSD17B14
    nsv5591728copy number variation1nstd207human GRCh38 chr19: 48,835,091-48,835,567 , GRCh37.p13 chr19: 49,338,348-49,338,824 PLEKHA4, HSD17B14
    nsv5585630copy number variation1nstd207human GRCh38 chr19: 48,834,426-48,835,529 , GRCh37.p13 chr19: 49,337,683-49,338,786 HSD17B14, PLEKHA4
    nsv5585456copy number variation1nstd207human GRCh38 chr19: 48,835,265-48,835,338 , GRCh37.p13 chr19: 49,338,522-49,338,595 PLEKHA4, HSD17B14
    nsv5392898copy number variation1nstd186human GRCh37 chr19: 49,337,669-49,338,559 , GRCh38.p12 chr19: 48,834,412-48,835,302 PLEKHA4, HSD17B14
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