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Items: 1 to 20 of 126

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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
    nsv7072131inversion1nstd229human GRCh38 chr20: 53,548,074-57,294,874 , GRCh37.p13 chr20: 52,164,613-55,869,930 CBLN4, RNU6-1146P, 46 more genes
    nsv7071269inversion1nstd229human GRCh38 chr20: 51,579,374-58,024,568 , GRCh37.p13 chr20: 50,195,913-56,599,624 CBLN4, LOC105372693, 89 more genes
    nsv7063616inversion1nstd229human GRCh38 chr20: 51,911,434-57,961,609 , GRCh37.p13 chr20: 50,527,973-56,536,665 FAM210B, BCAS1, 81 more genes
    nsv7058989inversion1nstd229human GRCh38 chr20: 52,927,440-57,459,107 , GRCh37.p13 chr20: 51,543,979-56,034,163 FAM210B, RPS4XP3, 61 more genes
    nsv7058267inversion1nstd229human GRCh38 chr20: 51,559,821-57,992,303 , GRCh37.p13 chr20: 50,176,360-56,567,359 LOC105372683, MRPS33P4, 89 more genes
    nsv7058201inversion1nstd229human GRCh38 chr20: 51,845,371-57,066,404 , GRCh37.p13 chr20: 50,461,910-55,641,460 RNU6-347P, RPS4XP3, 61 more genes
    nsv7037078copy number variation1nstd229human GRCh38 chr20: 54,988,450-63,850,628 , GRCh37.p13 chr20: 53,604,989-62,481,981 , RPL39P, 209 more genes
    nsv7036177copy number variation1nstd229human GRCh38 chr20: 54,492,617-57,541,251 , GRCh37.p13 chr20: 53,109,156-56,116,307 SPO11, BMP7, 47 more genes
    nsv7030107copy number variation1nstd229human GRCh38 chr20: 56,334,101-56,365,800 , GRCh37.p13 chr20: 54,909,157-54,940,856 FAM210B
    nsv7027878copy number variation1nstd229human GRCh38 chr20: 56,252,646-56,527,506 , GRCh37.p13 chr20: 54,827,702-55,102,562 FAM209A, RPL39P, 7 more genes
    nsv7026150copy number variation1nstd229human GRCh38 chr20: 56,353,201-56,369,800 , GRCh37.p13 chr20: 54,928,257-54,944,856 FAM210B, AURKA
    nsv7022623copy number variation1nstd229human GRCh38 chr20: 56,365,907-56,366,003 , GRCh37.p13 chr20: 54,940,963-54,941,059 FAM210B
    nsv7021126copy number variation1nstd229human GRCh38 chr20: 55,610,437-57,355,505 , GRCh37.p13 chr20: 54,220,678-55,930,561 SPO11, LOC105376989, 35 more genes
    nsv6637604copy number variation1nstd102humanUncertain significance GRCh37 chr20: 52,517,925-55,402,822 , GRCh38.p12 chr20: 53,901,386-56,827,766 DOK5, LOC107984001, 34 more genes
    nsv6547580copy number variation1nstd223human GRCh38 chr20: 56,365,905-56,366,003 , GRCh37.p13 chr20: 54,940,961-54,941,059 FAM210B
    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
    nsv6220176copy number variation1nstd214human GRCh38 chr20: 56,365,905-56,366,002 , GRCh37.p13 chr20: 54,940,961-54,941,058 FAM210B
    nsv6134042copy number variation1nstd213human GRCh37 chr20: 54,510,000-55,170,001 , GRCh38.p12 chr20: 55,934,944-56,594,945 MC3R, AURKA, 13 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
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