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Items: 1 to 20 of 140

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5362794translocation1nstd200human GRCh38 chr6: 27,541,112-27,541,112 , GRCh38 chr6: 75,270,950-75,270,950 , GRCh37.p13 chr6: 27,508,891-27,508,891 , GRCh37.p13 chr6: 75,980,666-75,980,666 TMEM30A, TRS-AGA1-1
    nsv5353752translocation1nstd200human GRCh38 chr6: 75,271,347-75,271,347 , GRCh38 chrX: 93,994,128-93,994,128 , GRCh37.p13 chr6: 75,981,063-75,981,063 , GRCh37.p13 chrX: 93,249,127-93,249,127 TMEM30A
    nsv5344623translocation1nstd200human GRCh37 chr6: 75,980,666-75,980,666 , GRCh37 chr6: 27,508,891-27,508,891 , GRCh38.p12 chr6: 75,270,950-75,270,950 , GRCh38.p12 chr6: 27,541,112-27,541,112 TRS-AGA1-1, TMEM30A
    nsv5340991translocation1nstd200human GRCh37 chr6: 75,981,063-75,981,063 , GRCh37 chrX: 93,249,127-93,249,127 , GRCh38.p12 chr6: 75,271,347-75,271,347 , GRCh38.p12 chrX: 93,994,128-93,994,128 TMEM30A
    nsv5033711inversion1nstd200human GRCh38 chr6: 66,790,667-77,039,639 , GRCh37.p13 chr6: 67,500,560-77,749,356 , FAM135A-AS1, 116 more genes
    nsv4945311copy number variation1nstd200human GRCh38 chr6: 75,136,187-75,394,317 , GRCh37.p13 chr6: 75,845,903-76,104,033 COL12A1, TMEM30A, 5 more genes
    nsv4933675copy number variation1nstd200human GRCh38 chr6: 75,281,721-75,281,850 , GRCh37.p13 chr6: 75,991,437-75,991,566 TMEM30A
    nsv4729340copy number variation1nstd102humanPathogenic GRCh37 chr6: 74,226,559-80,208,037 , GRCh38.p12 chr6: 73,516,836-79,498,320 LOC107986613, LOC101928516, 58 more genes
    nsv4674825copy number variation1nstd102humanUncertain significance GRCh37 chr6: 75,899,299-76,343,518 , GRCh38.p12 chr6: 75,189,583-75,633,802 TMEM30A, TMEM30A-DT, 13 more genes
    nsv4565582mobile element insertion1nstd166human GRCh37.p13 chr6: 75,964,528-75,964,528 , GRCh38.p12 chr6: 75,254,812-75,254,812 TMEM30A
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
    nsv3924180copy number variation1nstd102humanPathogenic NCBI36 chr6: 65,316,269-84,193,229 , GRCh38 chr6: 64,549,655-83,426,791 , GRCh37 chr6: 65,259,548-84,136,510 LOC105377875, KCNQ5-IT1, 188 more genes
    nsv3919111copy number variation1nstd102humanPathogenic GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637 RNU6-770P, MAP3K5-AS2, 810 more genes
    nsv3913604copy number variation1nstd102humanUncertain significance NCBI36 chr6: 74,997,856-77,354,831 , GRCh37.p13 chr6: 74,941,136-77,298,112 , GRCh38.p12 chr6: 74,231,420-76,588,395 RNU6-1016P, IMPG1, 28 more genes
    nsv3889959copy number variation1nstd102humanPathogenic GRCh37 chr6: 73,674,612-84,829,774 , GRCh38.p12 chr6: 72,964,889-84,120,055 MRAP2, LCA5, 125 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 RNU6-411P, LOC107986611, 2910 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 LOC105378061, MIR4640, 2914 more genes
    nsv3872700copy number variation1nstd102humanUncertain significance GRCh37 chr6: 75,889,207-76,522,602 , GRCh38.p12 chr6: 75,179,491-75,812,885 TMEM30A-DT, RNU6-1016P, 17 more genes
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