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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7047799inversion1nstd229human GRCh38 chr5: 118,237,370-118,658,148 , GRCh37.p13 chr5: 117,573,065-117,993,843 LINC02148, LINC02147, 3 more genes
    nsv7040937inversion1nstd229human GRCh38 chr5: 118,256,992-118,628,562 , GRCh37.p13 chr5: 117,592,687-117,964,257 LINC02208, LINC02215, 3 more genes
    nsv6777646copy number variation1nstd229human GRCh38 chr5: 118,272,941-118,284,470 , GRCh37.p13 chr5: 117,608,636-117,620,165 LINC02148
    nsv6776585copy number variation1nstd229human GRCh38 chr5: 117,942,660-118,406,081 , GRCh37.p13 chr5: 117,278,355-117,741,776 LINC02148, LINC02208, 1 more genes
    nsv6776531copy number variation1nstd229human GRCh38 chr5: 117,663,455-118,663,205 , GRCh37.p13 chr5: 116,999,150-117,998,900 LINC02216, LINC02148, 5 more genes
    nsv6770355copy number variation1nstd229human GRCh38 chr5: 117,693,610-118,716,267 , GRCh37.p13 chr5: 117,029,305-118,051,962 LOC100129526, LINC02148, 5 more genes
    nsv6769300copy number variation1nstd229human GRCh38 chr5: 118,160,787-118,281,589 , GRCh37.p13 chr5: 117,496,482-117,617,284 LINC02147, LINC02148
    nsv6766631copy number variation1nstd229human GRCh38 chr5: 118,149,583-118,296,458 , GRCh37.p13 chr5: 117,485,278-117,632,153 LINC02148, LINC02147
    nsv6762380copy number variation1nstd229human GRCh38 chr5: 118,139,395-118,538,475 , GRCh37.p13 chr5: 117,475,090-117,874,170 LINC02148, LINC02147, 1 more genes
    nsv6761623copy number variation1nstd229human GRCh38 chr5: 118,206,626-118,304,463 , GRCh37.p13 chr5: 117,542,321-117,640,158 LINC02148, LINC02147
    nsv6758779copy number variation1nstd229human GRCh38 chr5: 118,282,936-118,282,984 , GRCh37.p13 chr5: 117,618,631-117,618,679 LINC02148
    nsv6637111copy number variation1nstd102humanPathogenic GRCh37 chr5: 112,557,391-128,106,299 , GRCh38.p12 chr5: 113,221,694-128,770,606 SLC12A2, CCDC192, 180 more genes
    nsv6636702copy number variation1nstd102humanUncertain significance GRCh37 chr5: 116,399,071-120,032,310 , GRCh38.p12 chr5: 117,063,375-120,696,615 MIR1244-2, LINC02216, 35 more genes
    nsv6556739inversion1nstd223human GRCh38 chr5: 118,253,355-118,447,457 , GRCh37.p13 chr5: 117,589,050-117,783,152 LINC02148, LINC02208, 1 more genes
    nsv6412867copy number variation1nstd223human GRCh38 chr5: 118,283,574-118,286,386 , GRCh37.p13 chr5: 117,619,269-117,622,081 LINC02148
    nsv6411029copy number variation1nstd223human GRCh38 chr5: 117,693,608-118,716,266 , GRCh37.p13 chr5: 117,029,303-118,051,961 LOC100129526, RPL7L1P4, 5 more genes
    nsv6183114copy number variation1nstd214human GRCh38 chr5: 118,282,841-118,282,934 , GRCh37.p13 chr5: 117,618,536-117,618,629 LINC02148
    nsv6135643copy number variation1nstd213human GRCh37 chr5: 116,750,000-118,790,001 , GRCh38.p12 chr5: 117,414,304-119,454,306 DMXL1, HSD17B4, 23 more genes
    nsv6135639copy number variation1nstd213human GRCh37 chr5: 113,920,000-120,810,001 , GRCh38.p12 chr5: 114,584,303-121,474,306 CDO1, AP3S1, 83 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
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