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Items: 1 to 20 of 155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5949702insertion1nstd209human GRCh38 chr6: 32,391,143-32,391,143 , GRCh37.p13 chr6: 32,358,920-32,358,920 HCG23, TSBP1-AS1
    nsv5626717insertion1nstd207human GRCh38 chr6: 32,391,143-32,391,143 , GRCh37.p13 chr6: 32,358,920-32,358,920 HCG23, TSBP1-AS1
    nsv5233229copy number variation1nstd204human GRCh38.p13 chr6: 32,391,994-32,394,543 , GRCh37.p13 chr6: 32,359,771-32,362,320 TSBP1-AS1, BTNL2, 1 more genes
    nsv5172355mobile element insertion1nstd203human GRCh38 chr6: 32,391,151-32,391,156 , GRCh37.p13 chr6: 32,358,928-32,358,933 HCG23, TSBP1-AS1
    nsv5168097mobile element insertion1nstd203human GRCh38 chr6: 32,391,137-32,391,153 , GRCh37.p13 chr6: 32,358,914-32,358,930 TSBP1-AS1, HCG23
    nsv5164798mobile element insertion1nstd203human GRCh38 chr6: 32,391,144-32,391,156 , GRCh37.p13 chr6: 32,358,921-32,358,933 HCG23, TSBP1-AS1
    nsv5118027mobile element insertion1nstd203human GRCh38 chr6: 32,392,147-32,392,154 , GRCh37.p13 chr6: 32,359,924-32,359,931 BTNL2, HCG23, 1 more genes
    nsv4940717copy number variation1nstd200human GRCh38 chr6: 32,388,854-32,399,911 , GRCh37.p13 chr6: 32,356,631-32,367,688 HCG23, TSBP1-AS1, 1 more genes
    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
    nsv4675941copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 31,036,397-34,088,832 , GRCh38.p12 chr6: 31,068,620-34,121,055 AGER, AIF1, 217 more genes
    nsv4455450copy number variation1nstd102humanUncertain significance GRCh37 chr6: 32,027,371-32,448,599 , GRCh38.p12 chr6: 32,059,594-32,480,822 AGPAT1, HCG23, 23 more genes
    nsv4435955complex substitution1nstd102humanUncertain significance GRCh38.p12 chr6: 32,220,606-32,662,025 , GRCh37 chr6: 32,188,383-32,629,802 HLA-DQA1, HLA-DQB1, 15 more genes
    nsv4393264copy number variation1nstd174human GRCh37 chr6: 32,357,743-32,370,639 , GRCh38.p12 chr6: 32,389,966-32,402,862 TSBP1-AS1, BTNL2, 1 more genes
    nsv4382945copy number variation1nstd173human GRCh37 chr6: 32,315,384-33,052,094 , GRCh38.p12 chr6: 32,347,607-33,084,317 , HLA-DRB1, 35 more genes
    nsv4381819copy number variation1nstd173human GRCh37 chr6: 32,315,654-32,857,364 , GRCh38.p12 chr6: 32,347,877-32,889,587 , LOC102725019, 26 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
    nsv3968975insertion1nstd168human GRCh38 chr6: 32,312,647-32,420,959 , GRCh37.p13 chr6: 32,280,424-32,388,736 TSBP1, BTNL2, 4 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
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