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Items: 1 to 20 of 102

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5302598copy number variation1nstd204human GRCh38.p13 chr3: 109,643,426-112,176,826 , GRCh37.p13 chr3: 109,362,273-111,895,673 , NECTIN3-AS1, 28 more genes
    nsv5222423copy number variation1nstd204human GRCh38.p13 chr3: 109,643,701-111,524,800 , GRCh37.p13 chr3: 109,362,548-111,243,647 , LOC151760, 11 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4914627copy number variation1nstd200human GRCh38 chr3: 109,643,716-112,176,659 , GRCh37.p13 chr3: 109,362,563-111,895,506 , NECTIN3, 28 more genes
    nsv4914623copy number variation1nstd200human GRCh38 chr3: 109,310,668-113,023,370 , GRCh37.p13 chr3: 109,029,515-112,742,217 , CD200R1, 55 more genes
    nsv4794283copy number variation1nstd200human GRCh37 chr3: 109,362,563-111,895,506 , GRCh38.p12 chr3: 109,643,716-112,176,659 , LOC107984087, 28 more genes
    nsv4674254copy number variation1nstd102humanPathogenic GRCh37 chr3: 101,812,245-112,174,485 , GRCh38.p12 chr3: 102,093,401-112,455,638 IFT57, LINC00636, 111 more genes
    nsv4317801inversion1nstd166human GRCh37.p13 chr3: 106,160,269-123,476,086 , GRCh38.p12 chr3: 106,441,422-123,757,239 , ADPRH, 270 more genes
    nsv4079060copy number variation1nstd166human GRCh37.p13 chr3: 108,352,740-111,211,030 , GRCh38.p12 chr3: 108,633,893-111,492,183 , ATP6V0CP2, 30 more genes
    nsv3966872copy number variation1nstd168human GRCh38 chr3: 111,460,212-111,538,966 , GRCh37.p13 chr3: 111,179,059-111,257,813 ATP6V0CP2, LOC105374039
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 OR7E53P, HSPA8P9, 794 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 LINC02614, LINC02054, 1469 more genes
    nsv3918661copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,088,205-124,418,220 , GRCh37 chr3: 93,605,515-122,935,530 , GRCh38 chr3: 93,886,671-123,216,683 MTCO2P29, GAP43, 401 more genes
    nsv3917160copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,021,157-118,088,593 , GRCh38 chr3: 93,819,623-116,887,056 , GRCh37 chr3: 93,538,467-116,605,903 ATP6V1A, RPS10P4, 297 more genes
    nsv3913319copy number variation1nstd102humanPathogenic NCBI36 chr3: 105,822,754-117,295,421 , GRCh38 chr3: 104,621,220-116,093,884 , GRCh37 chr3: 104,340,064-115,812,731 TAGLN3, LINC00635, 151 more genes
    nsv3913048copy number variation1nstd102humanPathogenic NCBI36 chr3: 109,444,109-117,370,868 , GRCh38 chr3: 108,242,572-116,169,331 , GRCh37 chr3: 107,961,419-115,888,178 RPSAP29, DIMT1P1, 115 more genes
    nsv3911662copy number variation1nstd102humanPathogenic NCBI36 chr3: 102,633,427-117,731,277 , GRCh37.p13 chr3: 101,150,737-116,248,587 , GRCh38.p12 chr3: 101,431,893-116,529,740 SIDT1, PPIAP15, 188 more genes
    nsv3910775copy number variation1nstd102humanPathogenic GRCh37 chr3: 97,514,213-115,382,196 , GRCh38 chr3: 97,795,369-115,663,349 , NCBI36 chr3: 98,996,903-116,864,886 ZBTB11-AS1, RABGGTBP1, 258 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3888585copy number variation1nstd102humanPathogenic GRCh37 chr3: 105,094,834-117,441,953 , GRCh38.p12 chr3: 105,375,990-117,723,106 RFKP2, MTND6P6, 165 more genes
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