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Items: 1 to 20 of 882

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137483insertion1nstd232human GRCh37.p13 chr18: 55,380,988-55,380,988 , GRCh38.p12 chr18: 57,713,756-57,713,756 ATP8B1
    nsv7137140copy number variation1nstd102humanPathogenic GRCh37 chr18: 55,020,078-56,892,966 , GRCh38.p12 chr18: 57,352,847-59,225,734 ATP8B1-AS1, ALPK2, 33 more genes
    nsv7095253copy number variation1nstd102humanPathogenic GRCh37 chr18: 55,328,386-55,328,714 , GRCh38.p12 chr18: 57,661,154-57,661,482 ATP8B1-AS1, ATP8B1
    nsv7074298inversion1nstd229human GRCh38 chr18: 57,616,429-58,231,337 , GRCh37.p13 chr18: 55,283,661-55,898,569 LOC105372143, LOC105372140, 11 more genes
    nsv7073526inversion1nstd229human GRCh38 chr18: 53,651,514-59,638,513 , GRCh37.p13 chr18: 51,177,884-57,305,745 MBD2, LOC105372145, 78 more genes
    nsv7066250inversion1nstd229human GRCh38 chr18: 54,862,924-58,506,448 , GRCh37.p13 chr18: 52,530,155-56,173,680 NARS1, FECH, 48 more genes
    nsv7063248inversion1nstd229human GRCh38 chr18: 56,708,701-59,883,923 , GRCh37.p13 chr18: 54,375,932-57,551,155 MRPL37P1, RPS26P54, 49 more genes
    nsv7016882copy number variation1nstd229human GRCh38 chr18: 57,586,677-57,827,641 , GRCh37.p13 chr18: 55,253,909-55,494,873 ATP8B1, RNU6-742P, 7 more genes
    nsv7016682copy number variation1nstd229human GRCh38 chr18: 57,597,222-57,801,271 , GRCh37.p13 chr18: 55,264,454-55,468,503 ATP8B1-AS1, TRG-TCC5-1, 6 more genes
    nsv7015296copy number variation1nstd229human GRCh38 chr18: 57,684,047-57,684,242 , GRCh37.p13 chr18: 55,351,279-55,351,474 ATP8B1
    nsv7014546copy number variation1nstd229human GRCh38 chr18: 57,764,986-57,767,248 , GRCh37.p13 chr18: 55,432,218-55,434,480 ATP8B1
    nsv7013477copy number variation1nstd229human GRCh38 chr18: 57,607,701-57,661,200 , GRCh37.p13 chr18: 55,274,933-55,328,432 ATP8B1, ATP8B1-AS1, 1 more genes
    nsv7013172copy number variation1nstd229human GRCh38 chr18: 57,767,533-57,786,466 , GRCh37.p13 chr18: 55,434,765-55,453,698 ATP8B1
    nsv7012214copy number variation1nstd229human GRCh38 chr18: 57,743,978-57,747,867 , GRCh37.p13 chr18: 55,411,210-55,415,099 ATP8B1
    nsv7009865copy number variation1nstd229human GRCh38 chr18: 57,679,111-57,681,716 , GRCh37.p13 chr18: 55,346,343-55,348,948 TRG-TCC6-1, ATP8B1, 1 more genes
    nsv7009625copy number variation1nstd229human GRCh38 chr18: 57,765,901-57,768,100 , GRCh37.p13 chr18: 55,433,133-55,435,332 ATP8B1
    nsv7008823copy number variation1nstd229human GRCh38 chr18: 57,745,121-57,749,702 , GRCh37.p13 chr18: 55,412,353-55,416,934 ATP8B1
    nsv7007857copy number variation1nstd229human GRCh38 chr18: 57,757,256-57,760,265 , GRCh37.p13 chr18: 55,424,488-55,427,497 ATP8B1
    nsv7005825copy number variation1nstd229human GRCh38 chr18: 57,753,261-57,759,029 , GRCh37.p13 chr18: 55,420,493-55,426,261 RNU6-742P, ATP8B1
    nsv7005536copy number variation1nstd229human GRCh38 chr18: 57,521,249-57,993,718 , GRCh37.p13 chr18: 55,188,481-55,660,950 RNU6-742P, ATP8B1, 9 more genes
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