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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5685824mobile element insertion2nstd211human GRCh38 chr5: 131,997,004-131,997,004 , GRCh37.p13 chr5: 131,332,697-131,332,697 ACSL6
    nsv5633006insertion1nstd207human GRCh38 chr5: 131,996,994-131,996,994 , GRCh37.p13 chr5: 131,332,687-131,332,687 ACSL6
    nsv5463471copy number variation1nstd206human GRCh38 chr5: 132,012,290-132,012,416 , GRCh37.p13 chr5: 131,347,983-131,348,109 ACSL6
    nsv5412092mobile element insertion1nstd206human GRCh38 chr5: 131,997,004-131,997,055 , GRCh37.p13 chr5: 131,332,697-131,332,748 ACSL6
    nsv5309294copy number variation1nstd204human GRCh37.p13 chr5: 131,079,220-131,423,874 , GRCh38.p13 chr5: 131,743,527-132,088,181 CSF2, IL3, 5 more genes
    nsv5236964copy number variation1nstd204human GRCh37.p13 chr5: 131,079,294-131,423,893 , GRCh38.p13 chr5: 131,743,601-132,088,200 CSF2, IL3, 5 more genes
    nsv5221341copy number variation1nstd204human GRCh38.p13 chr5: 131,942,310-131,979,886 , GRCh37.p13 chr5: 131,278,003-131,315,579 MEIKIN, ACSL6
    nsv5221199copy number variation1nstd204human GRCh38.p13 chr5: 131,991,444-132,033,430 , GRCh37.p13 chr5: 131,327,137-131,369,123 ACSL6-AS1, ACSL6
    nsv5084690mobile element insertion1nstd203human GRCh38 chr5: 131,996,994-131,997,004 , GRCh37.p13 chr5: 131,332,687-131,332,697 ACSL6
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4945070copy number variation1nstd200human GRCh38 chr5: 131,851,931-132,093,294 , GRCh37.p13 chr5: 131,187,624-131,428,987 CSF2, LOC105379174, 4 more genes
    nsv4938587copy number variation1nstd200human GRCh38 chr5: 131,981,074-131,981,233 , GRCh37.p13 chr5: 131,316,767-131,316,926 ACSL6
    nsv4938586copy number variation1nstd200human GRCh38 chr5: 131,978,771-131,983,329 , GRCh37.p13 chr5: 131,314,464-131,319,022 ACSL6
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4872282inversion1nstd200human GRCh37 chr5: 98,106,197-132,803,784 , GRCh38.p12 chr5: 98,770,493-133,468,092 , LEAP2, 395 more genes
    nsv4805830copy number variation1nstd200human GRCh37 chr5: 131,347,983-131,348,109 , GRCh38.p12 chr5: 132,012,290-132,012,416 ACSL6
    nsv4803980copy number variation1nstd200human GRCh37 chr5: 131,316,767-131,316,926 , GRCh38.p12 chr5: 131,981,074-131,981,233 ACSL6
    nsv4717165mobile element insertion1nstd186human GRCh37 chr5: 131,332,687-131,332,687 , GRCh38.p12 chr5: 131,996,994-131,996,994 ACSL6
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