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Items: 1 to 20 of 480

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073834inversion1nstd229human GRCh38 chr20: 39,260,815-44,460,004 , GRCh37.p13 chr20: 37,889,458-43,088,644 LOC100128988, LOC100419859, 72 more genes
    nsv7065756inversion1nstd229human GRCh38 chr20: 41,399,093-41,400,192 , GRCh37.p13 chr20: 40,027,733-40,028,832 CHD6
    nsv7062736inversion1nstd229human GRCh38 chr20: 36,955,253-45,585,462 , GRCh37.p13 chr20: 35,583,656-44,214,101 GDAP1L1, PI3, 177 more genes
    nsv7036382copy number variation1nstd229human GRCh38 chr20: 41,548,401-41,550,100 , GRCh37.p13 chr20: 40,177,040-40,178,739 RPL12P11, CHD6
    nsv7035995copy number variation1nstd229human GRCh38 chr20: 41,548,100-41,548,215 , GRCh37.p13 chr20: 40,176,739-40,176,854 RPL12P11, CHD6
    nsv7033848copy number variation1nstd229human GRCh38 chr20: 41,546,801-41,550,300 , GRCh37.p13 chr20: 40,175,440-40,178,939 CHD6, RPL12P11
    nsv7032914copy number variation1nstd229human GRCh38 chr20: 41,545,985-41,550,408 , GRCh37.p13 chr20: 40,174,624-40,179,047 CHD6, RPL12P11
    nsv7032660copy number variation1nstd229human GRCh38 chr20: 41,429,867-42,259,912 , GRCh37.p13 chr20: 40,058,507-40,888,552 PTPRT, LOC643172, 5 more genes
    nsv7031282copy number variation1nstd229human GRCh38 chr20: 41,547,090-41,592,703 , GRCh37.p13 chr20: 40,175,729-40,221,342 RPL12P11, CHD6
    nsv7030884copy number variation1nstd229human GRCh38 chr20: 41,577,475-41,582,202 , GRCh37.p13 chr20: 40,206,114-40,210,841 CHD6
    nsv7030349copy number variation1nstd229human GRCh38 chr20: 41,420,597-41,421,336 , GRCh37.p13 chr20: 40,049,237-40,049,976 CHD6
    nsv7026346copy number variation1nstd229human GRCh38 chr20: 41,535,186-41,539,945 , GRCh37.p13 chr20: 40,163,825-40,168,584 CHD6
    nsv7021198copy number variation1nstd229human GRCh38 chr20: 33,145,032-41,995,765 , GRCh37.p13 chr20: 31,732,838-40,624,405 PXMP4, RPL12P11, 199 more genes
    nsv7020313copy number variation1nstd229human GRCh38 chr20: 41,406,771-41,411,491 , GRCh37.p13 chr20: 40,035,411-40,040,131 CHD6
    nsv7019420copy number variation1nstd229human GRCh38 chr20: 41,452,042-41,452,380 , GRCh37.p13 chr20: 40,080,682-40,081,020 CHD6
    nsv7019146copy number variation1nstd229human GRCh38 chr20: 41,593,071-41,596,146 , GRCh37.p13 chr20: 40,221,710-40,224,785 CHD6
    nsv6637470copy number variation1nstd102humanUncertain significance GRCh37 chr20: 40,135,346-40,399,258 , GRCh38.p12 chr20: 41,506,707-41,770,618 CHD6, RPL12P11, 1 more genes
    nsv6626774copy number variation1nstd224human GRCh37 chr20: 40,130,086-40,408,895 , GRCh38.p12 chr20: 41,501,446-41,780,255 RPL12P11, RNU6-1018P, 1 more genes
    nsv6599606inversion1nstd223human GRCh38 chr20: 41,609,964-41,610,556 , GRCh37.p13 chr20: 40,238,603-40,239,195 CHD6
    nsv6598179inversion1nstd223human GRCh38 chr20: 41,503,917-41,504,370 , GRCh37.p13 chr20: 40,132,556-40,133,009 CHD6
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