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Items: 1 to 20 of 590

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5924605copy number variation1nstd209human GRCh38 chr7: 38,269,538-38,317,014 , GRCh37.p13 chr7: 38,309,139-38,356,615 , TRG, 9 more genes
    nsv5922463copy number variation1nstd209human GRCh38 chr7: 38,269,541-38,358,508 , GRCh37.p13 chr7: 38,309,142-38,398,109 , TRGJP, 18 more genes
    nsv5919366copy number variation1nstd209human GRCh38 chr7: 38,316,921-38,317,201 , GRCh37.p13 chr7: 38,356,522-38,356,802 TRGV9, TRG
    nsv5846331copy number variation1nstd209human GRCh38 chr7: 38,314,603-38,315,935 , GRCh37.p13 chr7: 38,354,204-38,355,536 TRG, TRGV9
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5485568copy number variation1nstd206human GRCh38 chr7: 38,269,535-38,358,508 , GRCh37.p13 chr7: 38,309,136-38,398,109 , TRGJP1, 18 more genes
    nsv5480054copy number variation1nstd206human GRCh38 chr7: 38,316,921-38,317,203 , GRCh37.p13 chr7: 38,356,522-38,356,804 TRG, TRGV9
    nsv5238490copy number variation1nstd204human GRCh38.p13 chr7: 38,266,601-38,351,800 , GRCh37.p13 chr7: 38,306,202-38,391,401 , TRGJP, 17 more genes
    nsv5226583copy number variation1nstd204human GRCh38.p13 chr7: 38,253,401-38,358,000 , GRCh37.p13 chr7: 38,293,002-38,397,601 , TRGV5, 21 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4966242copy number variation1nstd200human GRCh38 chr7: 38,269,534-38,317,020 , GRCh37.p13 chr7: 38,309,135-38,356,621 , LOC103689914, 9 more genes
    nsv4966236copy number variation1nstd200human GRCh38 chr7: 38,230,213-38,316,242 , GRCh37.p13 chr7: 38,269,814-38,355,843 , STARD3NL, 14 more genes
    nsv4811367copy number variation1nstd200human GRCh37 chr7: 38,309,127-38,398,110 , GRCh38.p12 chr7: 38,269,526-38,358,509 , TRGV5, 18 more genes
    nsv4811366copy number variation1nstd200human GRCh37 chr7: 38,309,135-38,356,621 , GRCh38.p12 chr7: 38,269,534-38,317,020 , TRGV11, 9 more genes
    nsv4729274copy number variation1nstd102humanUncertain significance GRCh37 chr7: 38,357,074-38,481,296 , GRCh38.p12 chr7: 38,317,473-38,441,696 TRGV2, TRGV6, 12 more genes
    nsv4728026copy number variation5nstd197human GRCh38.p12 chr7: 38,249,244-38,354,183 , GRCh37 chr7: 38,288,845-38,393,784 , TRG, 21 more genes
    nsv4706740copy number variation1nstd195human GRCh37 chr7: 38,244,801-39,047,351 , GRCh38.p12 chr7: 38,205,200-39,007,751 , TRGJ1, 32 more genes
    nsv4675078copy number variation1nstd102humanUncertain significance GRCh37 chr7: 37,202,606-39,500,521 , GRCh38.p12 chr7: 37,163,001-39,460,922 TRGV11, SFRP4, 45 more genes
    nsv4618094copy number variation1nstd183human GRCh37 chr7: 38,334,818-38,356,808 , GRCh38.p12 chr7: 38,295,217-38,317,207 TRG, TRGV10, 3 more genes
    nsv4614468copy number variation2nstd183human GRCh37 chr7: 38,293,229-38,364,254 , GRCh38.p12 chr7: 38,253,628-38,324,653 , TRG, 13 more genes
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