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Items: 1 to 20 of 43

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4813824copy number variation1nstd200human GRCh37 chr8: 142,864,981-142,865,441 , GRCh38.p12 chr8|NT_187575.1: 19,988-20,448 , GRCh38.p12 chr8: 141,783,620-141,784,080 0
    nsv4813823copy number variation1nstd200human GRCh37 chr8: 142,851,018-142,856,436 , GRCh38.p12 chr8: 141,769,657-141,775,075 , GRCh38.p12 chr8|NT_187575.1: 2,823-8,241 0
    nsv4813822copy number variation1nstd200human GRCh37 chr8: 142,848,854-142,848,996 , GRCh38.p12 chr8: 141,767,493-141,767,635 , GRCh38.p12 chr8|NT_187575.1: 660-802 0
    nsv4813821copy number variation1nstd200human GRCh37 chr8: 142,847,171-142,852,831 , GRCh38.p12 chr8: 141,765,810-141,771,470 , GRCh38.p12 chr8|NT_187575.1: 1-4,636 0
    nsv4164328copy number variation1nstd166human GRCh37.p13 chr8: 142,861,210-142,862,373 , GRCh38.p12 chr8|NT_187575.1: 16,221-17,384 , GRCh38.p12 chr8: 141,779,849-141,781,012 0
    nsv4158849copy number variation1nstd166human GRCh37.p13 chr8: 142,851,018-142,856,436 , GRCh38.p12 chr8|NT_187575.1: 2,823-8,241 , GRCh38.p12 chr8: 141,769,657-141,775,075 0
    nsv4156719copy number variation1nstd166human GRCh37.p13 chr8: 142,864,883-142,865,441 , GRCh38.p12 chr8: 141,783,522-141,784,080 , GRCh38.p12 chr8|NT_187575.1: 19,890-20,448 0
    nsv3062735insertion1nstd140human GRCh37 chr8: 142,861,034-142,861,034 , GRCh38.p12 chr8: 141,779,673-141,779,673 , GRCh38.p12 chr8|NT_187575.1: 16,045-16,045 0
    esv3855948copy number variation5estd219human GRCh37 chr8: 142,851,025-142,856,601 , GRCh38.p12 chr8|NT_187575.1: 2,830-8,406 , GRCh38.p12 chr8: 141,769,664-141,775,240 0
    esv3855947copy number variation1estd219human GRCh37 chr8: 142,848,436-142,851,536 , GRCh38.p12 chr8|NT_187575.1: 242-3,341 , GRCh38.p12 chr8: 141,767,075-141,770,175 0
    nsv2609389short tandem repeat2nstd128human GRCh37 chr8: 142,880,836-142,880,873 , GRCh38.p12 chr8|NT_187575.1: 35,843-35,880 , GRCh38.p12 chr8: 141,799,475-141,799,512 0
    nsv2606924short tandem repeat1nstd128human GRCh37 chr8: 142,875,303-142,875,339 , GRCh38.p12 chr8: 141,793,942-141,793,978 , GRCh38.p12 chr8|NT_187575.1: 30,310-30,346 0
    nsv2606923short tandem repeat3nstd128human GRCh37 chr8: 142,867,188-142,867,211 , GRCh38.p12 chr8: 141,785,827-141,785,850 , GRCh38.p12 chr8|NT_187575.1: 22,195-22,218 MIR1302-7
    nsv2606922short tandem repeat1nstd128human GRCh37 chr8: 142,852,311-142,852,328 , GRCh38.p12 chr8: 141,770,950-141,770,967 , GRCh38.p12 chr8|NT_187575.1: 4,116-4,133 0
    nsv2606921short tandem repeat1nstd128human GRCh37 chr8: 142,852,205-142,852,219 , GRCh38.p12 chr8|NT_187575.1: 4,010-4,024 , GRCh38.p12 chr8: 141,770,844-141,770,858 0
    nsv2598261short tandem repeat1nstd128human GRCh37 chr8: 142,868,943-142,868,958 , GRCh38.p12 chr8: 141,787,582-141,787,597 , GRCh38.p12 chr8|NT_187575.1: 23,950-23,965 0
    nsv2598260short tandem repeat2nstd128human GRCh37 chr8: 142,863,487-142,863,503 , GRCh38.p12 chr8|NT_187575.1: 18,498-18,514 , GRCh38.p12 chr8: 141,782,126-141,782,142 0
    nsv2598259short tandem repeat1nstd128human GRCh37 chr8: 142,848,509-142,848,527 , GRCh38.p12 chr8|NT_187575.1: 315-333 , GRCh38.p12 chr8: 141,767,148-141,767,166 0
    nsv2577542short tandem repeat18nstd128human GRCh37 chr8: 142,850,888-142,850,925 , GRCh38.p12 chr8|NT_187575.1: 2,694-2,730 , GRCh38.p12 chr8: 141,769,527-141,769,564 0
    esv3678464copy number variation1estd217human GRCh37 chr8: 142,880,708-142,880,872 , GRCh38.p12 chr8: 141,799,347-141,799,511 , GRCh38.p12 chr8|NT_187575.1: 35,715-35,879 0
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