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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5626371insertion1nstd207human GRCh38 chr6: 53,532,440-53,532,440 , GRCh37.p13 chr6: 53,397,238-53,397,238 GCLC
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5471735copy number variation1nstd206human GRCh38 chr6: 53,519,254-53,519,405 , GRCh37.p13 chr6: 53,384,052-53,384,203 GCLC
    nsv5302033copy number variation1nstd204human GRCh38.p13 chr6: 53,519,248-53,519,410 , GRCh37.p13 chr6: 53,384,046-53,384,208 GCLC
    nsv5198987mobile element insertion1nstd203human GRCh38 chr6: 53,534,295-53,534,313 , GRCh37.p13 chr6: 53,399,093-53,399,111 GCLC
    nsv5118401mobile element insertion1nstd203human GRCh38 chr6: 53,514,150-53,514,165 , GRCh37.p13 chr6: 53,378,948-53,378,963 GCLC
    nsv5110352mobile element insertion1nstd203human GRCh38 chr6: 53,506,777-53,506,784 , GRCh37.p13 chr6: 53,371,575-53,371,582 GCLC-AS1, GCLC
    nsv4941476copy number variation1nstd200human GRCh38 chr6: 53,503,941-53,504,672 , GRCh37.p13 chr6: 53,368,739-53,369,470 GCLC-AS1, GCLC
    nsv4816427copy number variation1nstd200human GRCh37 chr6: 53,368,739-53,369,470 , GRCh38.p12 chr6: 53,503,941-53,504,672 GCLC-AS1, GCLC
    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
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4729393copy number variation1nstd102humanUncertain significance GRCh37 chr6: 52,657,712-53,622,715 , GRCh38.p12 chr6: 52,792,914-53,757,917 KILH, GSTA6P, 29 more genes
    nsv4729270copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 48,626,041-55,575,545 , GRCh38.p12 chr6: 48,658,305-55,710,747 CRISP1, SLC25A20P1, 105 more genes
    nsv4715881copy number variation1nstd195human GRCh37 chr6: 53,355,751-53,639,151 , GRCh38.p12 chr6: 53,490,953-53,774,353 GCLC, KLHL31, 3 more genes
    nsv4593654copy number variation1nstd183human GRCh37 chr6: 53,409,614-53,638,635 , GRCh38.p12 chr6: 53,544,816-53,773,837 KILH, LINC01564, 2 more genes
    nsv4490873mobile element insertion1nstd166human GRCh37.p13 chr6: 53,392,925-53,392,925 , GRCh38.p12 chr6: 53,528,127-53,528,127 GCLC
    nsv4456287copy number variation1nstd102humanUncertain significance GRCh37 chr6: 53,113,873-53,385,343 , GRCh38.p12 chr6: 53,249,075-53,520,545 GCLC, RPS16P5, 9 more genes
    nsv4407591copy number variation1nstd174human GRCh37 chr6: 53,090,537-53,487,082 , GRCh38.p12 chr6: 53,225,739-53,622,284 , GCM1, 12 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
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