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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, 1408 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, 42 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_167248.1: 72,676-83,329 , GRCh37.p13 chr6|NT_167247.1: 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, 637 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, 625 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, 58 more genes
    nsv1133015inversion1nstd106human GRCh37 (hg19) chr6: 26,670,854-58,688,504 , GRCh38 (hg38) chr6: 26,709,716-57,800,367 MIR877, TRNAL-CAA, 624 more genes
    nsv1125315inversion1nstd106human GRCh37 (hg19) chr6: 26,702,686-58,692,232 , GRCh38 (hg38) chr6: 26,709,716-57,800,367 MIR877, TRNAL-CAA, 624 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, 115 more genes
    nsv1074388copy number variation1nstd99human GRCh37 (hg19) chr6: 28,477,999-29,083,200 , GRCh38 (hg38) chr6: 28,510,222-29,115,423 TRNAL-CAA, TRE-CTC1-6, 51 more genes
    esv3608461copy number variation1estd214human GRCh37 (hg19) chr6: 28,777,688-28,788,267 , GRCh38 (hg38) chr6: 28,809,911-28,820,490 TRA-AGC6-1, TRA-TGC5-1
    nsv1034188copy number variation1nstd100human NCBI36 (hg18) chr6: 128,203-32,252,909 , GRCh37 (hg19) chr6: 183,203-32,144,931 , GRCh38 (hg38) chr6: 183,203-32,177,154 TMEM170B, SCARNA27, 536 more genes
    nsv1028942copy number variation1nstd100human NCBI36 (hg18) chr6: 334,422-31,064,339 , GRCh37 (hg19) chr6: 389,422-30,956,360 , GRCh38 (hg38) chr6: 389,422-30,988,583 TMEM170B, SCARNA27, 450 more genes
    nsv995521copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr6: 156,974-46,757,028 , GRCh38 (hg38) chr6: 156,974-57,800,367 , NCBI36 (hg18) chr6: 101,974-46,864,987 TRA-AGC11-1, TMEM170B, 857 more genes
    nsv995485copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr6: 28,730,964-29,737,605 , GRCh38 (hg38) chr6: 28,763,187-29,769,828 , NCBI36 (hg18) chr6: 28,838,943-29,845,584 TRNAL-CAA, TRE-CTC1-6, 48 more genes
    esv3486939copy number variation2estd59human NCBI36 (hg18) chr6: 28,878,504-28,893,030 , GRCh38 (hg38) chr6|NT_167245.2: 68,354-82,876 , GRCh38 (hg38) chr6|NT_167246.2: 68,313-82,841 , GRCh38 (hg38) chr6|NT_167247.2: 68,341-82,867 , GRCh38 (hg38) chr6|NT_167244.2: 68,327-82,853 , GRCh38 (hg38) chr6|NT_167249.2: 111,995-126,520 , GRCh37.p13 chr6|NT_167244.1: 73,926-88,452 , GRCh37.p13 chr6|NT_167245.1: 73,939-88,461 , GRCh37.p13 chr6|NT_167248.1: 73,926-88,452 , GRCh37.p13 chr6|NT_167247.1: 73,926-88,452 , GRCh37 (hg19) chr6: 28,770,525-28,785,051 , GRCh38 (hg38) chr6: 28,802,748-28,817,274 TRA-AGC6-1, TRA-TGC5-1, 2 more genes
    esv3486940copy number variation1estd59human NCBI36 (hg18) chr6: 28,878,504-28,893,030 , GRCh37.p13 chr6|NT_167247.1: 73,926-88,452 , GRCh37 (hg19) chr6: 28,770,525-28,785,051 , GRCh37.p13 chr6|NT_167248.1: 73,926-88,452 , GRCh37.p13 chr6|NT_167244.1: 73,926-88,452 , GRCh37.p13 chr6|NT_167245.1: 73,939-88,461 , GRCh38 (hg38) chr6|NT_167245.2: 68,354-82,876 , GRCh38 (hg38) chr6|NT_167246.2: 68,313-82,841 , GRCh38 (hg38) chr6|NT_167247.2: 68,341-82,867 , GRCh38 (hg38) chr6: 28,802,748-28,817,274 , GRCh38 (hg38) chr6|NT_167244.2: 68,327-82,853 , GRCh38 (hg38) chr6|NT_167249.2: 111,995-126,520 TRA-AGC6-1, TRA-TGC5-1, 2 more genes
    esv3410540copy number variation4estd59human NCBI36 (hg18) chr6: 28,878,434-28,893,091 , GRCh37.p13 chr6|NT_167248.1: 73,856-88,513 , GRCh37.p13 chr6|NT_167244.1: 73,856-88,513 , GRCh37.p13 chr6|NT_167247.1: 73,856-88,513 , GRCh37.p13 chr6|NT_167245.1: 73,869-88,522 , GRCh37 (hg19) chr6: 28,770,455-28,785,112 , GRCh38 (hg38) chr6|NT_167249.2: 111,925-126,581 , GRCh38 (hg38) chr6|NT_167245.2: 68,284-82,937 , GRCh38 (hg38) chr6|NT_167246.2: 68,243-82,902 , GRCh38 (hg38) chr6|NT_167244.2: 68,257-82,914 , GRCh38 (hg38) chr6|NT_167247.2: 68,271-82,928 , GRCh38 (hg38) chr6: 28,802,678-28,817,335 TRA-AGC6-1, TRA-TGC5-1, 2 more genes
    esv3403106copy number variation1estd59human NCBI36 (hg18) chr6: 28,878,769-28,893,168 , GRCh37.p13 chr6|NT_167248.1: 74,191-88,590 , GRCh37.p13 chr6|NT_167245.1: 74,204-88,599 , GRCh37.p13 chr6|NT_167247.1: 74,191-88,590 , GRCh37.p13 chr6|NT_167244.1: 74,191-88,590 , GRCh37 (hg19) chr6: 28,770,790-28,785,189 , GRCh38 (hg38) chr6|NT_167245.2: 68,619-83,014 , GRCh38 (hg38) chr6: 28,803,013-28,817,412 , GRCh38 (hg38) chr6|NT_167249.2: 112,261-126,658 , GRCh38 (hg38) chr6|NT_167247.2: 68,606-83,005 , GRCh38 (hg38) chr6|NT_167244.2: 68,592-82,991 , GRCh38 (hg38) chr6|NT_167246.2: 68,578-82,979 TRA-AGC6-1, TRA-TGC5-1, 1 more genes
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