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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974243insertion1nstd209human GRCh37.p13 chr17|NW_003871088.1: 342,790-342,790 , GRCh38 chr17: 68,282,779-68,282,779 , GRCh37.p13 chr17: 66,278,920-66,278,920 SLC16A6, ARSG
    nsv5940346copy number variation1nstd209human GRCh38 chr17: 68,268,536-68,268,666 , GRCh37.p13 chr17: 66,264,677-66,264,807 , GRCh37.p13 chr17|NW_003871088.1: 328,547-328,677 SLC16A6, ARSG
    nsv5938389copy number variation1nstd209human GRCh38 chr17: 68,272,012-68,272,067 , GRCh37.p13 chr17|NW_003871088.1: 332,023-332,078 , GRCh37.p13 chr17: 66,268,153-66,268,208 SLC16A6, ARSG
    nsv5703150mobile element insertion1nstd211human GRCh38 chr17: 68,288,435-68,288,435 , GRCh37.p13 chr17|NW_003871088.1: 348,446-348,446 , GRCh37.p13 chr17: 66,284,576-66,284,576 ARSG, SLC16A6
    nsv5664382insertion1nstd207human GRCh38 chr17: 68,270,661-68,270,661 , GRCh37.p13 chr17|NW_003871088.1: 330,672-330,672 , GRCh37.p13 chr17: 66,266,802-66,266,802 SLC16A6, ARSG
    nsv5533289copy number variation1nstd206human GRCh38 chr17: 68,278,595-68,278,676 , GRCh37.p13 chr17: 66,274,736-66,274,817 , GRCh37.p13 chr17|NW_003871088.1: 338,606-338,687 ARSG, SLC16A6
    nsv5533114copy number variation1nstd206human GRCh38 chr17: 68,272,014-68,272,068 , GRCh37.p13 chr17|NW_003871088.1: 332,025-332,079 , GRCh37.p13 chr17: 66,268,155-66,268,209 SLC16A6, ARSG
    nsv5514649copy number variation1nstd206human GRCh38 chr17: 68,268,536-68,268,690 , GRCh37.p13 chr17: 66,264,677-66,264,831 , GRCh37.p13 chr17|NW_003871088.1: 328,547-328,701 SLC16A6, ARSG
    nsv5298507copy number variation1nstd204human GRCh37.p13 chr17: 66,324,471-66,460,641 , GRCh38.p13 chr17: 68,255,001-68,464,500 PRKAR1A, SLC16A6, 5 more genes
    nsv5290595copy number variation1nstd204human GRCh38.p13 chr17: 68,276,314-68,277,513 , GRCh37.p13 chr17: 66,272,455-66,273,654 , GRCh37.p13 chr17|NW_003871088.1: 336,325-337,524 SLC16A6, ARSG
    nsv5150395mobile element insertion1nstd203human GRCh38 chr17: 68,282,779-68,282,792 , GRCh37.p13 chr17|NW_003871088.1: 342,790-342,803 , GRCh37.p13 chr17: 66,278,920-66,278,933 SLC16A6, ARSG
    nsv5143120mobile element insertion1nstd203human GRCh38 chr17: 68,273,531-68,273,545 , GRCh37.p13 chr17|NW_003871088.1: 333,542-333,556 , GRCh37.p13 chr17: 66,269,672-66,269,686 SLC16A6, ARSG
    nsv5029562inversion1nstd200human GRCh38 chr17: 64,441,870-75,217,767 , GRCh37.p13 chr17: 62,649,312-73,213,862 , LOC102929163, 207 more genes
    nsv5010783copy number variation1nstd200human GRCh38 chr17: 68,279,995-68,281,289 , GRCh37.p13 chr17: 66,276,136-66,277,430 , GRCh37.p13 chr17|NW_003871088.1: 340,006-341,300 ARSG, SLC16A6
    nsv4851775copy number variation1nstd200human GRCh37 chr17: 66,276,136-66,277,430 , GRCh38.p12 chr17: 68,279,995-68,281,289 SLC16A6, ARSG
    nsv4680806copy number variation1nstd189human GRCh37.p13 chr17: 66,175,570-66,359,187 , GRCh38.p12 chr17: 68,179,429-68,363,046 SLC16A6, ARSG, 3 more genes
    nsv4679422copy number variation1nstd189human GRCh37.p13 chr17: 66,166,015-66,345,441 , GRCh38.p12 chr17: 68,169,874-68,349,300 SLC16A6, ARSG, 3 more genes
    nsv4678878copy number variation1nstd189human GRCh37.p13 chr17: 66,175,570-66,348,159 , GRCh38.p12 chr17: 68,179,429-68,352,018 SLC16A6, ARSG, 3 more genes
    nsv4457799copy number variation1nstd102humanPathogenic GRCh37 chr17: 57,869,604-67,078,443 , GRCh38.p12 chr17: 59,792,243-69,082,302 PECAM1, TBX2-AS1, 215 more genes
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
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