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Items: 1 to 20 of 245

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131345mobile element insertion1nstd186human GRCh37 chr2: 36,570,259-36,570,310 , GRCh38.p12 chr2|NW_003315908.1: 20,113-20,146 , GRCh38.p12 chr2: 36,343,116-36,343,167 0
    nsv6114076mobile element insertion1nstd186human GRCh37 chr2: 36,476,684-36,476,684 , GRCh38.p12 chr2: 36,249,541-36,249,541 , GRCh38.p12 chr2|NW_003315908.1: 119,808-119,808 0
    nsv4788376copy number variation1nstd200human GRCh37 chr2: 36,555,882-36,557,738 , GRCh38.p12 chr2|NW_003315908.1: 38,767-40,623 , GRCh38.p12 chr2: 36,328,739-36,330,595 0
    nsv4776145copy number variation1nstd200human GRCh37 chr2: 36,556,560-36,560,331 , GRCh38.p12 chr2|NW_003315908.1: 36,163-39,949 , GRCh38.p12 chr2: 36,329,417-36,333,188 0
    nsv4776144copy number variation1nstd200human GRCh37 chr2: 36,525,534-36,525,989 , GRCh38.p12 chr2: 36,298,391-36,298,846 , GRCh38.p12 chr2|NW_003315908.1: 70,503-70,958 RPL21P36
    nsv4776143copy number variation1nstd200human GRCh37 chr2: 36,521,861-36,522,076 , GRCh38.p12 chr2: 36,294,718-36,294,933 , GRCh38.p12 chr2|NW_003315908.1: 74,416-74,631 0
    nsv4776142copy number variation1nstd200human GRCh37 chr2: 36,492,897-36,493,044 , GRCh38.p12 chr2: 36,265,754-36,265,901 , GRCh38.p12 chr2|NW_003315908.1: 103,448-103,595 0
    nsv4759603insertion1nstd199human GRCh37 chr2: 36,476,689-36,476,689 , GRCh38.p12 chr2: 36,249,546-36,249,546 , GRCh38.p12 chr2|NW_003315908.1: 119,803-119,803 0
    nsv4725054insertion1nstd186human GRCh37 chr2: 36,476,684-36,476,684 , GRCh38.p12 chr2: 36,249,541-36,249,541 , GRCh38.p12 chr2|NW_003315908.1: 119,808-119,808 0
    nsv4721115insertion1nstd186human GRCh37 chr2: 36,517,798-36,517,798 , GRCh38.p12 chr2|NW_003315908.1: 78,694-78,694 , GRCh38.p12 chr2: 36,290,655-36,290,655 0
    nsv4696092mobile element insertion1nstd186human GRCh37 chr2: 36,570,238-36,570,238 , GRCh38.p12 chr2: 36,343,095-36,343,095 , GRCh38.p12 chr2|NW_003315908.1: 26,261-26,261 0
    nsv4690535mobile element insertion1nstd186human GRCh37 chr2: 36,517,812-36,517,812 , GRCh38.p12 chr2|NW_003315908.1: 78,680-78,680 , GRCh38.p12 chr2: 36,290,669-36,290,669 0
    nsv4687138mobile element insertion1nstd186human GRCh37 chr2: 36,476,698-36,476,698 , GRCh38.p12 chr2: 36,249,555-36,249,555 , GRCh38.p12 chr2|NW_003315908.1: 119,794-119,794 0
    nsv4674332copy number variation1nstd102humanLikely benign GRCh37 chr2: 36,521,758-36,589,156 , GRCh38.p12 chr2: 36,294,615-36,362,013 , GRCh38.p12 chr2|NW_003315908.1: 1,303-74,734 CRIM1-DT, RPL21P36, 1 more genes
    nsv4595538copy number variation1nstd183human GRCh37 chr2: 36,353,114-36,569,134 , GRCh38.p12 chr2|NW_003315908.1: 27,367-143,390 , GRCh38.p12 chr2: 36,125,971-36,341,991 RPL21P36
    nsv4583883copy number variation1nstd183human GRCh37 chr2: 36,351,103-36,569,134 , GRCh38.p12 chr2: 36,123,960-36,341,991 , GRCh38.p12 chr2|NW_003315908.1: 27,367-143,390 RPL21P36
    nsv4564811mobile element insertion1nstd166human GRCh37.p13 chr2: 36,559,806-36,559,806 , GRCh38.p12 chr2: 36,332,663-36,332,663 , GRCh38.p12 chr2|NW_003315908.1: 36,703-36,703 0
    nsv4561457mobile element insertion1nstd166human GRCh37.p13 chr2: 36,468,539-36,468,539 , GRCh38.p12 chr2: 36,241,396-36,241,396 , GRCh38.p12 chr2|NW_003315908.1: 127,953-127,953 0
    nsv4537152insertion1nstd166human GRCh37.p13 chr2: 36,459,458-36,459,458 , GRCh38.p12 chr2|NW_003315908.1: 137,034-137,034 , GRCh38.p12 chr2: 36,232,315-36,232,315 0
    nsv4535268insertion1nstd166human GRCh37.p13 chr2: 36,517,798-36,517,798 , GRCh38.p12 chr2: 36,290,655-36,290,655 , GRCh38.p12 chr2|NW_003315908.1: 78,694-78,694 0
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