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Items: 1 to 20 of 312

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5970228inversion1nstd209human GRCh38 chr18: 42,666,448-47,133,105 , GRCh37.p13 chr18: 40,246,413-44,659,476 , ATP5F1A, 50 more genes
    nsv5941061copy number variation1nstd209human GRCh38 chr18: 46,096,714-46,097,727 , GRCh37.p13 chr18: 43,676,680-43,677,693 ATP5F1A
    nsv5932050copy number variation1nstd209human GRCh38 chr18: 46,082,348-46,082,640 , GRCh37.p13 chr18: 43,662,314-43,662,606 ATP5F1A
    nsv5720069mobile element insertion1nstd211human GRCh38 chr18: 46,085,933-46,085,933 , GRCh37.p13 chr18: 43,665,899-43,665,899 ATP5F1A
    nsv5527449copy number variation1nstd206human GRCh38 chr18: 46,096,715-46,097,728 , GRCh37.p13 chr18: 43,676,681-43,677,694 ATP5F1A
    nsv5526600copy number variation1nstd206human GRCh38 chr18: 46,075,722-46,083,984 , GRCh37.p13 chr18: 43,655,688-43,663,950 RNY4P37, ATP5F1A
    nsv5525222copy number variation1nstd206human GRCh38 chr18: 45,996,443-46,209,010 , GRCh37.p13 chr18: 43,576,409-43,788,976 ATP5F1A, PSTPIP2, 6 more genes
    nsv5381046copy number variation2nstd102humanUncertain significance GRCh37 chr18: 42,281,312-45,423,127 , GRCh38.p12 chr18: 44,701,347-47,896,756 HDHD2, RNU6-1131P, 45 more genes
    nsv5350109translocation1nstd200human GRCh38 chr18: 46,096,715-46,096,715 , GRCh38 chr18: 46,097,728-46,097,728 , GRCh37.p13 chr18: 43,676,681-43,676,681 , GRCh37.p13 chr18: 43,677,694-43,677,694 ATP5F1A
    nsv5331494translocation1nstd200human GRCh37 chr18: 43,676,681-43,676,681 , GRCh37 chr18: 43,677,694-43,677,694 , GRCh38.p12 chr18: 46,097,728-46,097,728 , GRCh38.p12 chr18: 46,096,715-46,096,715 ATP5F1A
    nsv5323565copy number variation1nstd204human GRCh38.p13 chr18: 46,085,280-46,085,601 , GRCh37.p13 chr18: 43,665,246-43,665,567 ATP5F1A
    nsv5323180copy number variation1nstd204human GRCh38.p13 chr18: 46,096,715-46,097,728 , GRCh37.p13 chr18: 43,676,681-43,677,694 ATP5F1A
    nsv5294787copy number variation1nstd204human GRCh38.p13 chr18: 46,081,701-46,113,000 , GRCh37.p13 chr18: 43,661,667-43,692,966 TRK-CTT6-1, HAUS1, 1 more genes
    nsv5282038copy number variation1nstd204human GRCh38.p13 chr18: 46,096,363-46,097,705 , GRCh37.p13 chr18: 43,676,329-43,677,671 ATP5F1A
    nsv5157134mobile element insertion1nstd203human GRCh38 chr18: 46,081,647-46,081,664 , GRCh37.p13 chr18: 43,661,613-43,661,630 ATP5F1A
    nsv5154133mobile element insertion1nstd203human GRCh38 chr18: 46,096,481-46,096,500 , GRCh37.p13 chr18: 43,676,447-43,676,466 ATP5F1A
    nsv5024169copy number variation1nstd200human GRCh38 chr18: 46,000,516-46,186,861 , GRCh37.p13 chr18: 43,580,482-43,766,827 PSTPIP2, HAUS1, 6 more genes
    nsv5017905copy number variation1nstd200human GRCh38 chr18: 46,103,722-46,106,209 , GRCh37.p13 chr18: 43,683,688-43,686,175 HAUS1, ATP5F1A
    nsv5017904copy number variation1nstd200human GRCh38 chr18: 46,096,253-46,096,362 , GRCh37.p13 chr18: 43,676,219-43,676,328 ATP5F1A
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