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Items: 1 to 20 of 252

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5877747copy number variation1nstd209human GRCh38 chr2: 20,583,358-20,583,435 , GRCh37.p13 chr2: 20,783,118-20,783,195 HS1BP3
    nsv5872973copy number variation1nstd209human GRCh38 chr2: 20,587,139-20,587,311 , GRCh37.p13 chr2: 20,786,899-20,787,071 HS1BP3
    nsv5869256copy number variation1nstd209human GRCh38 chr2: 20,550,880-20,550,941 , GRCh37.p13 chr2: 20,750,640-20,750,701 HS1BP3
    nsv5869151copy number variation1nstd209human GRCh38 chr2: 20,560,775-20,563,964 , GRCh37.p13 chr2: 20,760,535-20,763,724 HS1BP3
    nsv5832378copy number variation1nstd209human GRCh38 chr2: 20,560,731-20,564,173 , GRCh37.p13 chr2: 20,760,491-20,763,933 HS1BP3
    nsv5729345mobile element insertion1nstd211human GRCh38 chr2: 20,601,065-20,601,065 , GRCh37.p13 chr2: 20,800,825-20,800,825 HS1BP3
    nsv5609148insertion1nstd207human GRCh38 chr2: 20,632,464-20,632,464 , GRCh37.p13 chr2: 20,832,224-20,832,224 HS1BP3
    nsv5581739copy number variation1nstd207human GRCh38 chr2: 20,583,295-20,583,372 , GRCh37.p13 chr2: 20,783,055-20,783,132 HS1BP3
    nsv5535064insertion1nstd206human GRCh38 chr2: 20,576,502-20,576,531 , GRCh37.p13 chr2: 20,776,262-20,776,291 HS1BP3
    nsv5449326copy number variation1nstd206human GRCh38 chr2: 20,587,139-20,587,312 , GRCh37.p13 chr2: 20,786,899-20,787,072 HS1BP3
    nsv5435704copy number variation1nstd206human GRCh38 chr2: 20,569,150-20,576,118 , GRCh37.p13 chr2: 20,768,910-20,775,878 HS1BP3
    nsv5358224translocation1nstd200human GRCh38 chr2: 20,651,776-20,651,776 , GRCh38 chr2: 20,651,860-20,651,860 , GRCh37.p13 chr2: 20,851,620-20,851,620 , GRCh37.p13 chr2: 20,851,536-20,851,536 LOC105373466, HS1BP3
    nsv5358216translocation1nstd200human GRCh38 chr2: 20,635,062-20,635,062 , GRCh38 chr2: 20,634,994-20,634,994 , GRCh37.p13 chr2: 20,834,822-20,834,822 , GRCh37.p13 chr2: 20,834,754-20,834,754 HS1BP3
    nsv5358208translocation1nstd200human GRCh38 chr2: 20,562,470-20,562,470 , GRCh38 chr2: 20,562,417-20,562,417 , GRCh37.p13 chr2: 20,762,177-20,762,177 , GRCh37.p13 chr2: 20,762,230-20,762,230 HS1BP3
    nsv4904829copy number variation1nstd200human GRCh38 chr2: 20,591,333-20,633,390 , GRCh37.p13 chr2: 20,791,093-20,833,150 HS1BP3, RPS25P3, 1 more genes
    nsv4900532copy number variation1nstd200human GRCh38 chr2: 20,568,591-20,599,483 , GRCh37.p13 chr2: 20,768,351-20,799,243 HS1BP3, HS1BP3-IT1
    nsv4900531copy number variation1nstd200human GRCh38 chr2: 20,557,184-20,562,440 , GRCh37.p13 chr2: 20,756,944-20,762,200 HS1BP3
    nsv4900530copy number variation1nstd200human GRCh38 chr2: 20,482,526-20,602,603 , GRCh37.p13 chr2: 20,682,287-20,802,363 LOC102724948, NDUFAF2P1, 3 more genes
    nsv4788307copy number variation1nstd200human GRCh37 chr2: 20,786,899-20,787,072 , GRCh38.p12 chr2: 20,587,139-20,587,312 HS1BP3
    nsv4775688copy number variation1nstd200human GRCh37 chr2: 20,768,351-20,799,243 , GRCh38.p12 chr2: 20,568,591-20,599,483 HS1BP3-IT1, HS1BP3
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