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Items: 1 to 20 of 317

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6121256copy number variation1nstd186human GRCh37 chr15: 23,270,596-23,277,796 , GRCh38.p12 chr15|NT_187604.1: 239,657-246,846 , GRCh38.p12 chr15: 22,595,300-22,602,500 0
    nsv6115444copy number variation1nstd186human GRCh37 chr15: 20,782,323-20,787,324 , GRCh38.p12 chr15|NT_187604.1: 62,854-67,850 , GRCh38.p12 chr15: 20,577,000-20,582,000 GOLGA8EP
    nsv4762007insertion1nstd199human GRCh37 chr15: 20,795,675-20,795,675 , GRCh38.p12 chr15|NT_187604.1: 54,503-54,503 , GRCh38.p12 chr15: 20,590,351-20,590,351 0
    nsv4747609copy number variation1nstd199human GRCh37 chr15: 20,820,625-20,821,162 , GRCh38.p12 chr15|NT_187604.1: 29,017-29,554 , GRCh38.p12 chr15: 20,615,323-20,615,860 0
    nsv4711122copy number variation1nstd195human GRCh37 chr15: 20,844,901-20,847,351 , GRCh38.p12 chr15: 20,639,597-20,642,050 , GRCh38.p12 chr15|NT_187604.1: 2,830-5,280 IGHV1OR15-6
    nsv4702714copy number variation1nstd195human GRCh37 chr15: 20,817,351-20,818,401 , GRCh38.p12 chr15: 20,612,046-20,613,096 , GRCh38.p12 chr15|NT_187604.1: 31,778-32,828 0
    nsv4673517copy number variation1nstd186human GRCh37 chr15: 20,746,871-20,747,023 , GRCh38.p12 chr15: 20,541,593-20,541,709 , GRCh38.p12 chr15|NT_187604.1: 103,148-103,264 GOLGA6L22, GOLGA6L6
    nsv4673092copy number variation2nstd186human GRCh37 chr15: 20,779,660-20,885,221 , GRCh38.p12 chr15: 20,574,337-20,679,892 , GRCh38.p12 chr15|NT_187604.1: 1-70,513 NBEAP1, IGHV1OR15-6, 6 more genes
    nsv4672165copy number variation1nstd186human GRCh37 chr15: 20,784,650-20,833,669 , GRCh38.p12 chr15: 20,579,327-20,628,366 , GRCh38.p12 chr15|NT_187604.1: 16,514-65,523 LOC401805, LOC441711, 2 more genes
    nsv4672064copy number variation2nstd186human GRCh37 chr15: 23,261,021-23,261,170 , GRCh38.p12 chr15|NT_187604.1: 256,262-256,411 , GRCh38.p12 chr15: 22,611,926-22,612,075 GOLGA8IP
    nsv4667417copy number variation2nstd186human GRCh37 chr15: 20,749,533-20,773,538 , GRCh38.p12 chr15: 20,544,217-20,568,215 , GRCh38.p12 chr15|NT_187604.1: 76,635-100,645 GOLGA8EP, GOLGA8CP, 2 more genes
    nsv4667403copy number variation1nstd186human GRCh37 chr15: 23,267,661-23,301,249 , GRCh38.p12 chr15: 22,571,847-22,605,435 , GRCh38.p12 chr15|NT_187604.1: 216,063-249,771 LOC100419579, HERC2P2
    nsv4655741copy number variation1nstd186human GRCh37 chr15: 20,732,300-20,738,500 , GRCh38.p12 chr15: 20,527,061-20,533,262 , GRCh38.p12 chr15|NT_187604.1: 111,421-117,624 , GOLGA6L22, 2 more genes
    nsv4655194copy number variation2nstd186human GRCh37 chr15: 20,820,627-20,821,162 , GRCh38.p12 chr15|NT_187604.1: 29,017-29,552 , GRCh38.p12 chr15: 20,615,325-20,615,860 0
    nsv4652427copy number variation1nstd186human GRCh37 chr15: 23,339,000-23,346,000 , GRCh38.p12 chr15: 22,527,096-22,534,096 , GRCh38.p12 chr15|NT_187604.1: 171,313-178,314 HERC2P2
    nsv4649993copy number variation4nstd186human GRCh37 chr15: 23,264,500-23,275,050 , GRCh38.p12 chr15: 22,598,046-22,608,596 , GRCh38.p12 chr15|NT_187604.1: 242,400-252,932 GOLGA8IP, LOC101927846, 1 more genes
    nsv4648897copy number variation1nstd186human GRCh37 chr15: 20,781,000-20,811,000 , GRCh38.p12 chr15: 20,575,677-20,605,693 , GRCh38.p12 chr15|NT_187604.1: 39,178-69,173 GOLGA8EP, SPATA31E2P, 2 more genes
    nsv4646511copy number variation1nstd186human GRCh37 chr15: 20,717,000-20,724,000 , GRCh38.p12 chr15: 20,511,757-20,518,757 , GRCh38.p12 chr15|NT_187604.1: 125,940-132,939 , HERC2P7, 1 more genes
    nsv4646011copy number variation1nstd186human GRCh37 chr15: 23,331,850-23,338,750 , GRCh38.p12 chr15: 22,534,346-22,541,246 , GRCh38.p12 chr15|NT_187604.1: 178,564-185,467 HERC2P2
    nsv4645460copy number variation1nstd186human GRCh37 chr15: 20,806,100-20,823,500 , GRCh38.p12 chr15: 20,600,795-20,618,198 , GRCh38.p12 chr15|NT_187604.1: 26,679-44,078 0
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