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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057713inversion1nstd229human GRCh38 chr6: 56,332,234-57,502,028 , GRCh37.p13 chr6: 56,197,032-57,366,927 OSTCP6, MIR548U, 16 more genes
    nsv6793514copy number variation1nstd229human GRCh38 chr6: 56,979,608-57,010,344 , GRCh37.p13 chr6: 56,844,406-56,875,142 FTH1P15, BEND6
    nsv6792957copy number variation1nstd229human GRCh38 chr6: 57,003,767-57,005,673 , GRCh37.p13 chr6: 56,868,565-56,870,471 BEND6, FTH1P15
    nsv6789580copy number variation1nstd229human GRCh38 chr6: 56,974,142-57,019,102 , GRCh37.p13 chr6: 56,838,940-56,883,900 FTH1P15, BEND6, 1 more genes
    nsv6787499copy number variation1nstd229human GRCh38 chr6: 57,003,901-57,008,800 , GRCh37.p13 chr6: 56,868,699-56,873,598 FTH1P15, BEND6
    nsv6786592copy number variation1nstd229human GRCh38 chr6: 56,982,640-57,007,032 , GRCh37.p13 chr6: 56,847,438-56,871,830 FTH1P15, BEND6
    nsv6781124copy number variation1nstd229human GRCh38 chr6: 57,002,101-57,009,800 , GRCh37.p13 chr6: 56,866,899-56,874,598 FTH1P15, BEND6
    nsv6638066copy number variation1nstd102humanUncertain significance GRCh38 chr6: 53,151,508-58,400,428 , GRCh37.p13 chr6: 53,016,306-58,726,706 NPM1P36, LINC00680-GUSBP4, 73 more genes
    nsv6631428copy number variation1nstd224human GRCh37 chr6: 56,857,324-56,989,605 , GRCh38.p12 chr6: 56,992,526-57,124,807 FTH1P15, ZNF451, 4 more genes
    nsv6631070copy number variation1nstd224human GRCh37 chr6: 54,531,949-57,262,543 , GRCh38.p12 chr6: 54,667,151-57,397,745 DST, BAG2, 28 more genes
    nsv6560587inversion1nstd223human GRCh38 chr6: 56,332,312-57,501,978 , GRCh37.p13 chr6: 56,197,110-57,366,877 RCC2P7, COL21A1, 16 more genes
    nsv6411582copy number variation1nstd223human GRCh38 chr6: 57,003,944-57,008,756 , GRCh37.p13 chr6: 56,868,742-56,873,554 FTH1P15, BEND6
    nsv6401739copy number variation1nstd223human GRCh38 chr6: 56,982,640-57,007,032 , GRCh37.p13 chr6: 56,847,438-56,871,830 FTH1P15, BEND6
    nsv6398302copy number variation1nstd223human GRCh38 chr6: 57,003,767-57,005,671 , GRCh37.p13 chr6: 56,868,565-56,870,469 BEND6, FTH1P15
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 ACTG1P9, CRISP1, 245 more genes
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv4947787copy number variation1nstd200human GRCh38 chr6: 57,003,944-57,008,756 , GRCh37.p13 chr6: 56,868,742-56,873,554 FTH1P15, BEND6
    nsv4947785copy number variation1nstd200human GRCh38 chr6: 56,979,608-57,010,340 , GRCh37.p13 chr6: 56,844,406-56,875,138 FTH1P15, BEND6
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
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