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Items: 1 to 20 of 174

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057395inversion1nstd229human GRCh38 chr6: 47,292,599-47,292,654 , GRCh37.p13 chr6: 47,260,335-47,260,390 TNFRSF21
    nsv7052971inversion1nstd229human GRCh38 chr6: 47,248,302-47,249,659 , GRCh37.p13 chr6: 47,216,038-47,217,395 TNFRSF21
    nsv7050725inversion1nstd229human GRCh38 chr6: 47,230,859-47,231,279 , GRCh37.p13 chr6: 47,198,595-47,199,015 TNFRSF21
    nsv6792700copy number variation1nstd229human GRCh38 chr6: 47,295,702-47,299,263 , GRCh37.p13 chr6: 47,263,438-47,266,999 TNFRSF21
    nsv6790786copy number variation1nstd229human GRCh38 chr6: 47,209,101-47,245,800 , GRCh37.p13 chr6: 47,176,837-47,213,536 TNFRSF21
    nsv6779157copy number variation1nstd229human GRCh38 chr6: 47,207,401-47,280,300 , GRCh37.p13 chr6: 47,175,137-47,248,036 TNFRSF21
    nsv6555594inversion1nstd223human GRCh38 chr6: 47,255,762-47,256,397 , GRCh37.p13 chr6: 47,223,498-47,224,133 TNFRSF21
    nsv6412078copy number variation1nstd223human GRCh38 chr6: 47,235,686-47,236,616 , GRCh37.p13 chr6: 47,203,422-47,204,352 TNFRSF21
    nsv6411763copy number variation1nstd223human GRCh38 chr6: 46,841,055-48,021,507 , GRCh37.p13 chr6: 46,808,792-47,989,243 RPL27AP7, LOC105375082, 18 more genes
    nsv6411748copy number variation1nstd223human GRCh38 chr6: 47,262,480-47,263,081 , GRCh37.p13 chr6: 47,230,216-47,230,817 TNFRSF21
    nsv6407079copy number variation1nstd223human GRCh38 chr6: 47,279,508-47,281,543 , GRCh37.p13 chr6: 47,247,244-47,249,279 TNFRSF21
    nsv6404113copy number variation1nstd223human GRCh38 chr6: 47,295,702-47,299,259 , GRCh37.p13 chr6: 47,263,438-47,266,995 TNFRSF21
    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
    nsv6277166insertion1nstd214human GRCh38 chr6: 47,287,377-47,287,377 , GRCh37.p13 chr6: 47,255,113-47,255,113 TNFRSF21
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv6006110copy number variation1nstd212human GRCh38 chr6: 47,262,750-47,265,480 , GRCh37.p13 chr6: 47,230,486-47,233,216 TNFRSF21
    nsv5685489mobile element insertion1nstd211human GRCh38 chr6: 47,281,820-47,281,820 , GRCh37.p13 chr6: 47,249,556-47,249,556 TNFRSF21
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5546762insertion1nstd206human GRCh38 chr6: 47,287,333-47,287,377 , GRCh37.p13 chr6: 47,255,069-47,255,113 TNFRSF21
    nsv5465802copy number variation1nstd206human GRCh38 chr6: 47,268,988-47,269,044 , GRCh37.p13 chr6: 47,236,724-47,236,780 TNFRSF21
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