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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv2779086copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr6: 156,975-170,919,482 , GRCh38 (hg38) chr6: 156,975-170,610,394 , NCBI36 (hg18) chr6: 101,975-170,761,407 TRA-AGC11-1, LIN28B-AS1, 1429 more genes
    nsv2773711copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr6: 28,735,761-29,585,573 , GRCh38 (hg38) chr6: 28,767,984-29,617,796 , NCBI36 (hg18) chr6: 28,843,740-29,693,552 TRNAL-CAA, TRE-CTC1-6, 43 more genes
    nsv2768223copy-neutral loss of heterozygosity1nstd125human GRCh38.p2 chr: NaN-NaN , GRCh37 (hg19) chr6: 26,097,193-29,353,408 TRA-AGC11-1, TRNAL-CAA, 234 more genes
    esv3844153copy number variation1estd219human GRCh37 (hg19) chr6: 28,777,688-28,788,267 , GRCh38 (hg38) chr6: 28,809,911-28,820,490 TRA-AGC6-1, TRA-TGC5-1
    nsv2731294copy number variation1nstd130human NCBI36 (hg18) chr6: 28,877,254-28,887,907 , GRCh37.p13 chr6|NT_167247.1: 72,676-83,329 , GRCh37.p13 chr6|NT_167248.1: 72,676-83,329 , GRCh37.p13 chr6|NT_167244.1: 72,676-83,329 , GRCh37 (hg19) chr6: 28,769,275-28,779,928 , GRCh37.p13 chr6|NT_167245.1: 72,689-83,338 , GRCh38 (hg38) chr6|NT_167245.2: 67,104-77,753 , GRCh38 (hg38) chr6|NT_167247.2: 67,091-77,744 , GRCh38 (hg38) chr6: 28,801,498-28,812,151 , GRCh38 (hg38) chr6|NT_167249.2: 110,745-121,397 , GRCh38 (hg38) chr6|NT_167246.2: 67,063-77,718 , GRCh38 (hg38) chr6|NT_167244.2: 67,077-77,730 TRA-AGC6-1, TRF-GAA3-1, 1 more genes
    nsv1151707inversion1nstd107human GRCh37 (hg19) chr6: 26,670,798-58,199,550 , GRCh38 (hg38) chr6: 26,709,716-57,800,367 MIR877, TRNAL-CAA, 647 more genes
    nsv1146725copy number variation1nstd107human GRCh37 (hg19) chr6: 26,798,814-58,395,989 , GRCh38 (hg38) chr6: 26,831,035-61,119,912 MIR877, TRNAL-CAA, 633 more genes
    nsv1145096copy number variation1nstd106human GRCh37 (hg19) chr6: 28,594,300-29,686,500 , GRCh38 (hg38) chr6: 28,626,523-29,718,723 TRNAL-CAA, TRE-CTC1-6, 61 more genes
    nsv1133015inversion1nstd106human GRCh37 (hg19) chr6: 26,670,854-58,688,504 , GRCh38 (hg38) chr6: 26,709,716-57,800,367 MIR877, TRNAL-CAA, 647 more genes
    nsv1125315inversion1nstd106human GRCh37 (hg19) chr6: 26,702,686-58,692,232 , GRCh38 (hg38) chr6: 26,709,716-57,800,367 MIR877, TRNAL-CAA, 643 more genes
    nsv1122126copy number variation1nstd106human GRCh37 (hg19) chr6: 28,595,800-31,211,800 , GRCh38 (hg38) chr6: 28,628,023-31,244,023 MIR877, TRNAL-CAA, 119 more genes
    esv3802211tandem duplication1estd192human GRCh37 (hg19) chr6: 7,109,110-35,043,691 , GRCh38 (hg38) chr6: 7,108,877-57,800,367 TRA-AGC11-1, TMEM170B, 815 more genes
    esv3814331tandem duplication2estd192human GRCh37 (hg19) chr6: 28,179,288-33,002,095 , GRCh38 (hg38) chr6: 28,211,510-33,034,318 MIR877, TRNAL-CAA, 245 more genes
    esv3794867tandem duplication1estd192human GRCh37 (hg19) chr6: 5,429,377-37,462,708 , GRCh38 (hg38) chr6: 5,429,144-57,800,367 TRA-AGC11-1, TMEM170B, 822 more genes
    esv3808392tandem duplication1estd192human GRCh37 (hg19) chr6: 5,750,165-157,209,357 , GRCh38 (hg38) chr6: 5,749,932-156,888,223 TRA-AGC11-1, LIN28B-AS1, 1285 more genes
    esv3799303tandem duplication1estd192human GRCh37 (hg19) chr6: 22,604,330-73,841,027 , GRCh38 (hg38) chr6: 22,604,101-73,131,304 TRA-AGC11-1, MIR877, 765 more genes
    esv3798465copy number variation1estd192human GRCh37 (hg19) chr6: 15,711,995-27,268,329 , GRCh38 (hg38) chr6: 15,711,764-57,800,367 TRA-AGC11-1, MIR877, 760 more genes
    esv3802325copy number variation1estd192human GRCh37 (hg19) chr6: 18,470,153-94,001,200 , GRCh38 (hg38) chr6: 18,469,922-93,291,482 TRA-AGC11-1, MIR877, 872 more genes
    esv3800801copy number variation1estd192human GRCh37 (hg19) chr6: 13,388,036-31,387,737 , GRCh38 (hg38) chr6: 13,387,804-57,800,367 TRA-AGC11-1, MIR877, 772 more genes
    esv3805887copy number variation1estd192human GRCh37 (hg19) chr6: 22,240,022-42,552,428 , GRCh38 (hg38) chr6: 22,239,793-57,800,367 TRA-AGC11-1, MIR877, 735 more genes
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