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Items: 1 to 20 of 105

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148186copy number variation1nstd102humanUncertain significance GRCh37 chr20: 52,773,668-62,965,020 , GRCh38.p12 chr20: 54,157,129-64,333,667 LOC105372717, CTCFL, 245 more genes
    nsv7139696insertion1nstd232human GRCh37.p13 chr20: 57,570,815-57,570,815 , GRCh38.p12 chr20: 58,995,760-58,995,760 CTSZ
    nsv7037078copy number variation1nstd229human GRCh38 chr20: 54,988,450-63,850,628 , GRCh37.p13 chr20: 53,604,989-62,481,981 , RPL39P, 209 more genes
    nsv7033345copy number variation1nstd229human GRCh38 chr20: 59,003,673-59,026,171 , GRCh37.p13 chr20: 57,578,728-57,601,226 TUBB1, CTSZ, 1 more genes
    nsv7032834copy number variation1nstd229human GRCh38 chr20: 58,901,524-59,002,068 , GRCh37.p13 chr20: 57,476,579-57,577,123 CTSZ, LOC107985382, 3 more genes
    nsv6554032copy number variation1nstd223human GRCh38 chr20: 58,992,788-58,994,422 , GRCh37.p13 chr20: 57,567,843-57,569,477 NELFCD, CTSZ
    nsv6314208copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,835,739-62,915,555 , GRCh38.p12 chr20: 58,260,683-64,284,202 LOC105372698, LOC105372695, 176 more genes
    nsv6314094copy number variation1nstd102humanPathogenic GRCh37 chr20: 55,292,205-57,866,365 , GRCh38.p12 chr20: 56,717,149-59,291,310 PCK1, MIR296, 58 more genes
    nsv6311086copy number variation1nstd102humanUncertain significance GRCh37 chr20: 54,823,900-57,899,514 , GRCh38.p12 chr20: 56,248,844-59,324,459 CTSZ, SPO11, 75 more genes
    nsv6134308copy number variation1nstd213human GRCh37 chr20: 55,660,000-60,880,001 , GRCh38.p12 chr20: 57,084,944-62,304,945 TAF4, OSBPL2, 97 more genes
    nsv6134174copy number variation1nstd213human GRCh37 chr20: 57,120,000-57,640,001 , GRCh38.p12 chr20: 58,544,944-59,064,946 SLMO2-ATP5E, LOC105372695, 19 more genes
    nsv6134040copy number variation1nstd213human GRCh37 chr20: 51,820,000-60,870,001 , GRCh38.p12 chr20: 53,203,461-62,294,945 MC3R, PPP1R3D, 142 more genes
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv6054564copy number variation1nstd212human GRCh38 chr20: 58,999,106-58,999,166 , GRCh37.p13 chr20: 57,574,161-57,574,221 CTSZ
    nsv5524038copy number variation1nstd206human GRCh38 chr20: 59,002,601-59,003,275 , GRCh37.p13 chr20: 57,577,656-57,578,330 CTSZ
    nsv5324622copy number variation1nstd204human GRCh38.p13 chr20: 59,001,083-59,005,653 , GRCh37.p13 chr20: 57,576,138-57,580,708 CTSZ
    nsv5291138copy number variation1nstd204human GRCh38.p13 chr20: 59,000,901-59,005,100 , GRCh37.p13 chr20: 57,575,956-57,580,155 CTSZ
    nsv5289413copy number variation1nstd204human GRCh38.p13 chr20: 59,000,705-59,005,700 , GRCh37.p13 chr20: 57,575,760-57,580,755 CTSZ
    nsv5161599mobile element insertion1nstd203human GRCh38 chr20: 58,999,825-58,999,843 , GRCh37.p13 chr20: 57,574,880-57,574,898 CTSZ
    nsv4777610mobile element deletion1nstd200human GRCh37 chr20: 57,574,850-57,575,136 , GRCh38.p12 chr20: 58,999,795-59,000,081 CTSZ
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