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Items: 1 to 20 of 280

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077587inversion1nstd229human GRCh38 chr20: 49,505,728-49,589,573 , GRCh37.p13 chr20: 48,122,265-48,206,110 LOC101927486, PTGIS
    nsv7075103inversion1nstd229human GRCh38 chr20: 48,844,229-55,780,453 , GRCh37.p13 chr20: 47,460,766-54,355,509 RPL12P4, LOC105372664, 113 more genes
    nsv7065344inversion1nstd229human GRCh38 chr20: 49,128,244-52,291,086 , GRCh37.p13 chr20: 47,744,781-50,907,625 PARD6B, LOC105372657, 77 more genes
    nsv7064075inversion1nstd229human GRCh38 chr20: 49,009,324-55,851,498 , GRCh37.p13 chr20: 47,625,861-54,426,554 DPM1, KCNG1, 115 more genes
    nsv7058418inversion1nstd229human GRCh38 chr20: 49,550,784-49,589,576 , GRCh37.p13 chr20: 48,167,321-48,206,113 LOC101927486, PTGIS
    nsv7034382copy number variation1nstd229human GRCh38 chr20: 49,541,543-49,544,559 , GRCh37.p13 chr20: 48,158,080-48,161,096 PTGIS
    nsv7031799copy number variation1nstd229human GRCh38 chr20: 49,508,557-49,511,693 , GRCh37.p13 chr20: 48,125,094-48,128,230 PTGIS
    nsv7031025copy number variation1nstd229human GRCh38 chr20: 49,405,830-49,759,161 , GRCh37.p13 chr20: 48,022,367-48,375,698 SNRPFP1, B4GALT5, 6 more genes
    nsv7030866copy number variation1nstd229human GRCh38 chr20: 49,517,660-49,518,660 , GRCh37.p13 chr20: 48,134,197-48,135,197 PTGIS
    nsv7028710copy number variation1nstd229human GRCh38 chr20: 49,534,501-49,562,400 , GRCh37.p13 chr20: 48,151,038-48,178,937 PTGIS
    nsv7028228copy number variation1nstd229human GRCh38 chr20: 49,531,301-49,534,600 , GRCh37.p13 chr20: 48,147,838-48,151,137 PTGIS
    nsv7025865copy number variation1nstd229human GRCh38 chr20: 49,529,196-49,619,495 , GRCh37.p13 chr20: 48,145,733-48,236,032 LOC101927486, LOC105372651, 1 more genes
    nsv7024722copy number variation1nstd229human GRCh38 chr20: 49,559,042-49,566,170 , GRCh37.p13 chr20: 48,175,579-48,182,707 LOC101927486, PTGIS
    nsv7024627copy number variation1nstd229human GRCh38 chr20: 49,561,854-49,561,980 , GRCh37.p13 chr20: 48,178,391-48,178,517 PTGIS
    nsv7022918copy number variation1nstd229human GRCh38 chr20: 49,541,384-49,549,899 , GRCh37.p13 chr20: 48,157,921-48,166,436 PTGIS
    nsv7020676copy number variation1nstd229human GRCh38 chr20: 49,534,478-49,562,494 , GRCh37.p13 chr20: 48,151,015-48,179,031 PTGIS
    nsv7020409copy number variation1nstd229human GRCh38 chr20: 49,428,501-51,120,300 , GRCh37.p13 chr20: 48,045,038-49,736,837 LOC100421569, RNU6-147P, 54 more genes
    nsv6635610copy number variation1nstd227human GRCh37 chr20: 48,153,744-48,178,213 , GRCh38.p12 chr20: 49,537,207-49,561,676 PTGIS
    nsv6626787copy number variation1nstd224human GRCh37 chr20: 48,147,756-48,234,349 , GRCh38.p12 chr20: 49,531,219-49,617,812 LOC105372651, LOC101927486, 1 more genes
    nsv6626706copy number variation5nstd224human GRCh37 chr20: 48,156,125-48,166,725 , GRCh38.p12 chr20: 49,539,588-49,550,188 PTGIS
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