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Items: 1 to 20 of 181

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5672603copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 119,302,758-124,813,305 , GRCh38.p12 chr10: 117,543,247-123,053,789 ACADSB, DMBT1, 84 more genes
    nsv5598100copy number variation1nstd207human GRCh38 chr10: 119,519,593-119,519,672 , GRCh37.p13 chr10: 121,279,105-121,279,184 RGS10
    nsv5505586copy number variation1nstd206human GRCh38 chr10: 119,522,514-119,522,581 , GRCh37.p13 chr10: 121,282,026-121,282,093 RGS10
    nsv4977198copy number variation1nstd200human GRCh38 chr10: 119,534,637-119,537,149 , GRCh37.p13 chr10: 121,294,149-121,296,661 RGS10
    nsv4977197copy number variation1nstd200human GRCh38 chr10: 119,532,792-119,534,118 , GRCh37.p13 chr10: 121,292,304-121,293,630 RGS10
    nsv4831654copy number variation1nstd200human GRCh37 chr10: 121,294,147-121,296,655 , GRCh38.p12 chr10: 119,534,635-119,537,143 RGS10
    nsv4734740copy number variation1nstd199human GRCh37 chr10: 121,279,115-121,279,193 , GRCh38.p12 chr10: 119,519,603-119,519,681 RGS10
    nsv4675991copy number variation1nstd102humanPathogenic GRCh37 chr10: 119,996,339-135,427,143 , GRCh38.p12 chr10: 118,236,827-133,613,639 STK32C, LOC105378542, 237 more genes
    nsv4578218mobile element insertion1nstd166human GRCh37.p13 chr10: 121,289,310-121,289,310 , GRCh38.p12 chr10: 119,529,798-119,529,798 RGS10
    nsv4456626copy number variation1nstd102humanPathogenic GRCh37 chr10: 114,544,537-135,427,143 , GRCh38.p12 chr10: 112,784,778-133,613,639 LOC105378521, ZRANB1, 317 more genes
    nsv4349508copy number variation1nstd102humanPathogenic GRCh37 chr10: 117,024,753-124,942,806 , GRCh38.p12 chr10: 115,265,276-123,183,290 PRLHR, LOC105378513, 121 more genes
    nsv4348764copy number variation1nstd102humanPathogenic GRCh37 chr10: 110,022,170-135,439,095 , GRCh38.p12 chr10: 108,262,412-133,625,591 LOC105378492, VENTX, 373 more genes
    nsv4327619inversion1nstd166human GRCh37.p13 chr10: 121,264,586-121,264,942 , GRCh38.p12 chr10: 119,505,074-119,505,430 RGS10
    nsv4212223copy number variation1nstd166human GRCh37.p13 chr10: 121,278,842-121,279,189 , GRCh38.p12 chr10: 119,519,330-119,519,677 RGS10
    nsv4205543copy number variation1nstd166human GRCh37.p13 chr10: 121,263,499-121,293,387 , GRCh38.p12 chr10: 119,503,987-119,533,875 RGS10
    nsv4196695copy number variation1nstd166human GRCh37.p13 chr10: 121,283,372-121,296,082 , GRCh38.p12 chr10: 119,523,860-119,536,570 RGS10
    nsv3967881insertion1nstd168human GRCh38 chr10: 119,522,699-119,551,272 , GRCh37.p13 chr10: 121,282,211-121,310,784 RGS10
    nsv3923859copy number variation1nstd102humanPathogenic NCBI36 chr10: 113,062,847-135,284,168 , GRCh37 chr10: 113,072,857-135,434,178 , GRCh38 chr10: 111,313,099-133,620,674 AS-PTPRE, SFXN4, 330 more genes
    nsv3923769copy number variation1nstd102humanPathogenic GRCh38 chr10: 100,194,215-132,432,797 , GRCh37 chr10: 101,953,972-134,246,301 , NCBI36 chr10: 101,943,962-134,096,291 LOC105378493, LINC02627, 477 more genes
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