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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967771inversion1nstd209human GRCh38 chr15: 72,171,325-72,175,177 , GRCh37.p13 chr15: 72,463,666-72,467,518 GRAMD2A
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5928585copy number variation1nstd209human GRCh38 chr15: 72,171,339-72,178,566 , GRCh37.p13 chr15: 72,463,680-72,470,907 GRAMD2A
    nsv5927974copy number variation1nstd209human GRCh38 chr15: 72,172,376-72,172,687 , GRCh37.p13 chr15: 72,464,717-72,465,028 GRAMD2A
    nsv5854555copy number variation1nstd209human GRCh38 chr15: 72,172,734-72,178,321 , GRCh37.p13 chr15: 72,465,075-72,470,662 GRAMD2A
    nsv5698740mobile element insertion1nstd211human GRCh38 chr15: 72,193,979-72,193,979 , GRCh37.p13 chr15: 72,486,320-72,486,320 GRAMD2A
    nsv5558007sequence alteration1nstd206human GRCh38 chr15: 72,171,325-72,178,551 , GRCh37.p13 chr15: 72,463,666-72,470,892 GRAMD2A
    nsv5527602copy number variation1nstd206human GRCh38 chr15: 72,184,658-72,184,722 , GRCh37.p13 chr15: 72,476,999-72,477,063 GRAMD2A
    nsv5520206copy number variation1nstd206human GRCh38 chr15: 72,171,325-72,178,551 , GRCh37.p13 chr15: 72,463,666-72,470,892 GRAMD2A
    nsv5414359mobile element insertion1nstd206human GRCh38 chr15: 72,193,979-72,194,030 , GRCh37.p13 chr15: 72,486,320-72,486,371 GRAMD2A
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5005563copy number variation1nstd200human GRCh38 chr15: 72,156,187-72,159,678 , GRCh37.p13 chr15: 72,448,528-72,452,019 , GRAMD2A
    nsv4992267copy number variation1nstd200human GRCh38 chr15: 72,178,698-72,188,816 , GRCh37.p13 chr15: 72,471,039-72,481,157 GRAMD2A
    nsv4992266copy number variation1nstd200human GRCh38 chr15: 72,171,316-72,178,560 , GRCh37.p13 chr15: 72,463,657-72,470,901 GRAMD2A
    nsv4992265copy number variation1nstd200human GRCh38 chr15: 72,143,124-72,196,404 , GRCh37.p13 chr15: 72,435,465-72,488,745 , GRAMD2A, 1 more genes
    nsv4850036copy number variation1nstd200human GRCh37 chr15: 72,471,068-72,481,161 , GRCh38.p12 chr15: 72,178,727-72,188,820 GRAMD2A
    nsv4728893copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 70,268,937-74,098,081 , GRCh38.p12 chr15: 69,976,598-73,805,740 BBS4, FKBP1AP2, 75 more genes
    nsv4577023mobile element insertion1nstd166human GRCh37.p13 chr15: 72,466,519-72,466,519 , GRCh38.p12 chr15: 72,174,178-72,174,178 GRAMD2A
    nsv4455889copy number variation1nstd102humanUncertain significance GRCh37 chr15: 72,373,639-72,577,870 , GRCh38.p12 chr15: 72,081,298-72,285,529 PARP6, GRAMD2A, 6 more genes
    nsv4245511copy number variation1nstd166human GRCh37.p13 chr15: 72,463,666-72,470,901 , GRCh38.p12 chr15: 72,171,325-72,178,560 GRAMD2A
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