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Items: 1 to 20 of 534

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146919copy number variation1nstd232human GRCh37.p13 chr4: 177,661,094-177,661,153 , GRCh38.p12 chr4: 176,739,940-176,739,999 VEGFC
    nsv7093619copy number variation1nstd228human GRCh37 chr4: 171,508,974-190,957,473 , GRCh38.p12 chr4: 170,587,823-190,036,318 AGA, SLC25A4, 240 more genes
    nsv7056086inversion1nstd229human GRCh38 chr4: 174,912,619-184,252,538 , GRCh37.p13 chr4: 175,833,770-185,173,691 WDR17, LOC105377580, 84 more genes
    nsv6754761copy number variation1nstd229human GRCh38 chr4: 176,698,757-176,698,894 , GRCh37.p13 chr4: 177,619,911-177,620,048 VEGFC, HAFML
    nsv6754577copy number variation1nstd229human GRCh38 chr4: 176,777,915-176,782,671 , GRCh37.p13 chr4: 177,699,069-177,703,825 VEGFC
    nsv6750923copy number variation1nstd229human GRCh38 chr4: 176,272,550-176,752,778 , GRCh37.p13 chr4: 177,193,701-177,673,932 ASB5, LOC100421630, 3 more genes
    nsv6744245copy number variation1nstd229human GRCh38 chr4: 176,596,014-176,699,084 , GRCh37.p13 chr4: 177,517,165-177,620,238 HAFML, VEGFC, 1 more genes
    nsv6743472copy number variation1nstd229human GRCh38 chr4: 176,688,301-176,698,100 , GRCh37.p13 chr4: 177,609,455-177,619,254 HAFML, VEGFC
    nsv6742298copy number variation1nstd229human GRCh38 chr4: 176,677,801-176,688,300 , GRCh37.p13 chr4: 177,598,952-177,609,454 HAFML, VEGFC
    nsv6740902copy number variation1nstd229human GRCh38 chr4: 176,768,359-176,771,554 , GRCh37.p13 chr4: 177,689,513-177,692,708 VEGFC
    nsv6740127copy number variation1nstd229human GRCh38 chr4: 176,731,456-176,731,550 , GRCh37.p13 chr4: 177,652,610-177,652,704 VEGFC
    nsv6738908copy number variation1nstd229human GRCh38 chr4: 176,752,201-176,800,900 , GRCh37.p13 chr4: 177,673,355-177,722,054 VEGFC
    nsv6738233copy number variation1nstd229human GRCh38 chr4: 176,770,416-176,770,671 , GRCh37.p13 chr4: 177,691,570-177,691,825 VEGFC
    nsv6634364copy number variation1nstd102humanPathogenic GRCh37 chr4: 167,779,888-190,957,473 , GRCh38.p12 chr4: 166,858,737-190,036,318 LOC101928551, LOC107986330, 279 more genes
    nsv6634351copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318 COPS3P1, LOC339975, 363 more genes
    nsv6629390copy number variation1nstd224human GRCh37 chr4: 177,645,549-177,804,746 , GRCh38.p12 chr4: 176,724,395-176,883,592 VEGFC, LINC02509
    nsv6570050inversion1nstd223human GRCh38 chr4: 169,780,525-178,315,900 , GRCh37.p13 chr4: 170,701,676-179,237,054 LOC101928409, LOC100131553, 91 more genes
    nsv6566806inversion1nstd223human GRCh38 chr4: 176,738,922-176,739,288 , GRCh37.p13 chr4: 177,660,076-177,660,442 VEGFC
    nsv6563430inversion1nstd223human GRCh38 chr4: 176,784,096-176,784,759 , GRCh37.p13 chr4: 177,705,250-177,705,913 VEGFC
    nsv6558992inversion1nstd223human GRCh38 chr4: 176,765,663-176,766,346 , GRCh37.p13 chr4: 177,686,817-177,687,500 VEGFC
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