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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
    nsv6792700copy number variation1nstd229human GRCh38 chr6: 47,295,702-47,299,263 , GRCh37.p13 chr6: 47,263,438-47,266,999 TNFRSF21
    nsv6404113copy number variation1nstd223human GRCh38 chr6: 47,295,702-47,299,259 , GRCh37.p13 chr6: 47,263,438-47,266,995 TNFRSF21
    nsv6407079copy number variation1nstd223human GRCh38 chr6: 47,279,508-47,281,543 , GRCh37.p13 chr6: 47,247,244-47,249,279 TNFRSF21
    nsv6412078copy number variation1nstd223human GRCh38 chr6: 47,235,686-47,236,616 , GRCh37.p13 chr6: 47,203,422-47,204,352 TNFRSF21
    nsv6411748copy number variation1nstd223human GRCh38 chr6: 47,262,480-47,263,081 , GRCh37.p13 chr6: 47,230,216-47,230,817 TNFRSF21
    nsv5465802copy number variation1nstd206human GRCh38 chr6: 47,268,988-47,269,044 , GRCh37.p13 chr6: 47,236,724-47,236,780 TNFRSF21
    nsv5464114copy number variation1nstd206human GRCh38 chr6: 47,249,756-47,249,810 , GRCh37.p13 chr6: 47,217,492-47,217,546 TNFRSF21
    nsv4941264copy number variation1nstd200human GRCh38 chr6: 47,235,686-47,236,616 , GRCh37.p13 chr6: 47,203,422-47,204,352 TNFRSF21
    nsv4147159copy number variation1nstd166human GRCh37.p13 chr6: 47,213,595-47,219,804 , GRCh38.p12 chr6: 47,245,859-47,252,068 TNFRSF21
    nsv4133455copy number variation1nstd166human GRCh37.p13 chr6: 47,232,781-47,237,870 , GRCh38.p12 chr6: 47,265,045-47,270,134 TNFRSF21
    nsv4135113copy number variation1nstd166human GRCh37.p13 chr6: 47,263,438-47,266,995 , GRCh38.p12 chr6: 47,295,702-47,299,259 TNFRSF21
    nsv4141137copy number variation1nstd166human GRCh37.p13 chr6: 47,236,580-47,236,662 , GRCh38.p12 chr6: 47,268,844-47,268,926 TNFRSF21
    esv3844634copy number variation1estd219human GRCh37 chr6: 47,236,721-47,236,780 , GRCh38.p12 chr6: 47,268,985-47,269,044 TNFRSF21
    esv3084407copy number variation1estd209human GRCh37 chr6: 47,220,867-47,220,869 , GRCh38.p12 chr6: 47,253,131-47,253,133 TNFRSF21
    esv3448682copy number variation1estd59human NCBI36 chr6: 47,324,166-47,324,565 , GRCh37.p13 chr6: 47,216,207-47,216,606 , GRCh38.p12 chr6: 47,248,471-47,248,870 TNFRSF21
    esv3342508copy number variation8estd59human NCBI36 chr6: 47,383,977-47,386,525 , GRCh37.p13 chr6: 47,276,018-47,278,566 , GRCh38.p12 chr6: 47,308,282-47,310,830 TNFRSF21
    esv2434451copy number variation1estd197human NCBI36 chr6: 47,380,329-47,380,330 , GRCh37.p13 chr6: 47,272,370-47,272,371 , GRCh38.p12 chr6: 47,304,634-47,304,635 TNFRSF21
    esv2146075copy number variation1estd194human NCBI36 chr6: 47,342,788-47,342,790 , GRCh37.p13 chr6: 47,234,829-47,234,831 , GRCh38.p12 chr6: 47,267,093-47,267,095 TNFRSF21
    esv1938153copy number variation1estd194human NCBI36 chr6: 47,380,328-47,380,330 , GRCh37.p13 chr6: 47,272,369-47,272,371 , GRCh38.p12 chr6: 47,304,633-47,304,635 TNFRSF21
    esv2389106copy number variation1estd194human NCBI36 chr6: 47,379,990-47,379,991 , GRCh37.p13 chr6: 47,272,031-47,272,032 , GRCh38.p12 chr6: 47,304,295-47,304,296 TNFRSF21
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