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Items: 1 to 20 of 211

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6117741copy number variation1nstd186human GRCh37 chr6: 32,368,546-32,368,841 , GRCh38.p12 chr6: 32,400,769-32,401,064 TSBP1-AS1, BTNL2
    nsv5565517copy number variation1nstd207human GRCh38 chr6: 32,400,768-32,401,043 , GRCh37.p13 chr6: 32,368,545-32,368,820 BTNL2, TSBP1-AS1
    nsv5470220copy number variation1nstd206human GRCh38 chr6: 32,400,769-32,401,064 , GRCh37.p13 chr6: 32,368,546-32,368,841 BTNL2, TSBP1-AS1
    nsv5386101copy number variation1nstd186human GRCh37 chr6: 32,368,501-32,368,830 , GRCh38.p12 chr6: 32,400,724-32,401,053 TSBP1-AS1, BTNL2
    nsv5300875copy number variation1nstd204human GRCh37.p13 chr6: 32,368,486-32,368,841 , GRCh38.p13 chr6: 32,400,709-32,401,064 TSBP1-AS1, BTNL2
    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
    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
    nsv5115211mobile element insertion1nstd203human GRCh38 chr6: 32,400,912-32,400,926 , GRCh37.p13 chr6: 32,368,689-32,368,703 TSBP1-AS1, BTNL2
    nsv5113130mobile element insertion1nstd203human GRCh38 chr6: 32,400,744-32,400,744 , GRCh37.p13 chr6: 32,368,521-32,368,521 BTNL2, TSBP1-AS1
    nsv5110041mobile element insertion1nstd203human GRCh38 chr6: 32,400,908-32,400,926 , GRCh37.p13 chr6: 32,368,685-32,368,703 TSBP1-AS1, BTNL2
    nsv5108533mobile element insertion1nstd203human GRCh38 chr6: 32,401,224-32,401,235 , GRCh37.p13 chr6: 32,369,001-32,369,012 BTNL2, TSBP1-AS1
    nsv5106235mobile element insertion1nstd203human GRCh38 chr6: 32,400,734-32,400,745 , GRCh37.p13 chr6: 32,368,511-32,368,522 TSBP1-AS1, BTNL2
    nsv5100896mobile element insertion1nstd203human GRCh38 chr6: 32,401,211-32,401,244 , GRCh37.p13 chr6: 32,368,988-32,369,021 BTNL2, TSBP1-AS1
    nsv5100720mobile element insertion1nstd203human GRCh38 chr6: 32,400,745-32,400,763 , GRCh37.p13 chr6: 32,368,522-32,368,540 BTNL2, TSBP1-AS1
    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
    nsv4815875copy number variation1nstd200human GRCh37 chr6: 32,368,471-32,368,860 , GRCh38.p12 chr6: 32,400,694-32,401,083 BTNL2, TSBP1-AS1
    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
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