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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906048copy number variation1nstd209human GRCh38 chr6: 65,758,204-65,909,608 , GRCh37.p13 chr6: 66,468,097-66,619,501 SLC25A51P1, ADH5P4
    nsv5898967copy number variation1nstd209human GRCh38 chr6: 65,786,743-65,788,112 , GRCh37.p13 chr6: 66,496,636-66,498,005 SLC25A51P1
    nsv5845927copy number variation1nstd209human GRCh38 chr6: 65,758,165-65,786,305 , GRCh37.p13 chr6: 66,468,058-66,496,198 SLC25A51P1
    nsv5845394copy number variation1nstd209human GRCh38 chr6: 65,786,826-65,789,364 , GRCh37.p13 chr6: 66,496,719-66,499,257 SLC25A51P1
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5457217copy number variation1nstd206human GRCh38 chr6: 65,786,743-65,788,113 , GRCh37.p13 chr6: 66,496,636-66,498,006 SLC25A51P1
    nsv5363113translocation1nstd200human GRCh38 chr6: 65,788,113-65,788,113 , GRCh38 chr6: 65,786,743-65,786,743 , GRCh37.p13 chr6: 66,496,636-66,496,636 , GRCh37.p13 chr6: 66,498,006-66,498,006 SLC25A51P1
    nsv5340816translocation1nstd200human GRCh37 chr6: 66,498,006-66,498,006 , GRCh37 chr6: 66,496,636-66,496,636 , GRCh38.p12 chr6|NT_187555.1: 13,300-13,300 , GRCh38.p12 chr6: 65,786,743-65,786,743 , GRCh38.p12 chr6: 65,788,113-65,788,113 , GRCh38.p12 chr6|NT_187555.1: 11,930-11,930 SLC25A51P1
    nsv5034374inversion1nstd200human GRCh38 chr6: 65,276,237-66,914,065 , GRCh37.p13 chr6: 65,986,130-67,623,958 LOC107986540, LOC105377841, 10 more genes
    nsv4933283copy number variation1nstd200human GRCh38 chr6: 65,680,260-65,799,305 , GRCh37.p13 chr6: 66,390,153-66,509,198 SLC25A51P1, EYS
    nsv4933249copy number variation1nstd200human GRCh38 chr6: 65,047,864-65,807,353 , GRCh37.p13 chr6: 65,757,757-66,517,246 LOC107986607, EYS, 2 more genes
    nsv4660739copy number variation1nstd186human GRCh37 chr6: 66,496,636-66,498,006 , GRCh38.p12 chr6: 65,786,743-65,788,113 , GRCh38.p12 chr6|NT_187555.1: 11,930-13,300 SLC25A51P1
    nsv4618251copy number variation1nstd183human GRCh37 chr6: 66,496,636-66,498,006 , GRCh38.p12 chr6|NT_187555.1: 11,930-13,300 , GRCh38.p12 chr6: 65,786,743-65,788,113 SLC25A51P1
    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
    nsv4456288copy number variation1nstd102humanUncertain significance GRCh37 chr6: 65,348,978-66,754,476 , GRCh38.p12 chr6: 64,639,085-66,044,583 ZC3H11C, LOC107986607, 6 more genes
    nsv4411656copy number variation1nstd174human GRCh37 chr6: 66,393,348-66,503,431 , GRCh38.p12 chr6: 65,683,455-65,793,538 EYS, SLC25A51P1
    nsv4396577copy number variation1nstd174human GRCh37 chr6: 66,496,631-66,498,029 , GRCh38.p12 chr6|NT_187555.1: 11,925-13,323 , GRCh38.p12 chr6: 65,786,738-65,788,136 SLC25A51P1
    nsv4379207copy number variation1nstd173human GRCh37 chr6: 66,465,920-66,622,181 , GRCh38.p12 chr6: 65,756,027-65,912,288 , GRCh38.p12 chr6|NT_187555.1: 1-144,063 ADH5P4, SLC25A51P1
    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
    nsv4146990copy number variation1nstd166human GRCh37.p13 chr6: 66,263,000-66,529,000 , GRCh38.p12 chr6: 65,553,107-65,819,107 SLC25A51P1, EYS
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