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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5887898copy number variation1nstd209human GRCh38 chr6: 71,296,817-71,301,384 , GRCh37.p13 chr6: 72,006,520-72,011,087 OGFRL1
    nsv5845360copy number variation1nstd209human GRCh38 chr6: 71,301,343-71,303,400 , GRCh37.p13 chr6: 72,011,046-72,013,103 OGFRL1
    nsv5460321copy number variation1nstd206human GRCh38 chr6: 71,272,647-71,309,964 , GRCh37.p13 chr6: 71,982,350-72,019,667 OGFRL1
    nsv5191653mobile element insertion1nstd203human GRCh38 chr6: 71,298,554-71,298,569 , GRCh37.p13 chr6: 72,008,257-72,008,272 OGFRL1
    nsv5033711inversion1nstd200human GRCh38 chr6: 66,790,667-77,039,639 , GRCh37.p13 chr6: 67,500,560-77,749,356 , FAM135A-AS1, 116 more genes
    nsv4729236copy number variation1nstd102humanUncertain significance GRCh37 chr6: 71,351,541-72,837,211 , GRCh38.p12 chr6: 70,641,838-72,127,508 LOC105377850, LOC105377853, 17 more genes
    nsv4614780copy number variation1nstd183human GRCh37 chr6: 71,998,452-71,998,675 , GRCh38.p12 chr6: 71,288,749-71,288,972 OGFRL1
    nsv4604820copy number variation1nstd183human GRCh37 chr6: 64,732,117-73,192,183 , GRCh38.p12 chr6: 64,022,224-72,482,481 LOC105377847, LOC105377850, 64 more genes
    nsv4601474copy number variation1nstd183human GRCh37 chr6: 71,998,410-71,999,070 , GRCh38.p12 chr6: 71,288,707-71,289,367 OGFRL1
    nsv4455775copy number variation1nstd102humanPathogenic GRCh37 chr6: 69,481,460-73,185,349 , GRCh38.p12 chr6: 68,771,568-72,475,647 KRT19P1, BECN1P2, 34 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
    nsv4135320copy number variation1nstd166human GRCh37.p13 chr6: 72,002,385-72,002,482 , GRCh38.p12 chr6: 71,292,682-71,292,779 OGFRL1
    nsv3963214insertion1nstd168human GRCh38 chr6: 71,291,636-71,331,381 , GRCh37.p13 chr6: 72,001,339-72,041,084 OGFRL1
    nsv3924180copy number variation1nstd102humanPathogenic NCBI36 chr6: 65,316,269-84,193,229 , GRCh38 chr6: 64,549,655-83,426,791 , GRCh37 chr6: 65,259,548-84,136,510 LOC105377875, KCNQ5-IT1, 188 more genes
    nsv3920009copy number variation1nstd102humanUncertain significance NCBI36 chr6: 71,575,615-72,708,133 , GRCh38 chr6: 70,809,191-71,941,709 , GRCh37 chr6: 71,518,894-72,651,412 SMAP1, MIR30C2, 15 more genes
    nsv3916496copy number variation1nstd102humanUncertain significance GRCh38 chr6: 70,794,142-71,972,780 , GRCh37 chr6: 71,503,845-72,682,483 , NCBI36 chr6: 71,560,566-72,739,204 KRT19P1, BECN1P2, 15 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
    nsv3884980copy number variation1nstd102humanUncertain significance GRCh37 chr6: 71,571,478-72,048,250 , GRCh38.p12 chr6: 70,861,775-71,338,547 SMAP1, LYPLA1P3, 6 more genes
    nsv3882345copy number variation1nstd102humanBenign GRCh37 chr6: 71,998,480-71,998,880 , GRCh38.p12 chr6: 71,288,777-71,289,177 OGFRL1
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