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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5564276copy number variation1nstd102humanUncertain significance GRCh37 chr6: 121,767,974-121,769,162 , GRCh38.p12 chr6: 121,446,828-121,448,016 GJA1
    nsv5369694translocation1nstd200human GRCh38 chr6: 121,441,351-121,441,351 , GRCh38 chr6: 121,441,558-121,441,558 , GRCh37.p13 chr6: 121,762,497-121,762,497 , GRCh37.p13 chr6: 121,762,704-121,762,704 GJA1
    nsv5107736mobile element insertion1nstd203human GRCh38 chr6: 121,436,872-121,436,881 , GRCh37.p13 chr6: 121,758,018-121,758,027 GJA1
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4933801copy number variation1nstd200human GRCh38 chr6: 121,449,931-121,452,105 , GRCh37.p13 chr6: 121,771,077-121,773,251 GJA1, RNU4-35P
    nsv4768325copy number variation1nstd102humanPathogenic GRCh37 chr6: 116,734,559-123,648,104 , GRCh38.p12 chr6: 116,413,396-123,326,959 GJA1, RNU4-76P, 80 more genes
    nsv4524454copy number variation1nstd166human GRCh37.p13 chr6: 121,568,999-121,977,000 , GRCh38.p12 chr6: 121,247,853-121,655,854 HMGN2P29, LOC260339, 8 more genes
    nsv4456929copy number variation1nstd102humanUncertain significance GRCh37 chr6: 120,694,558-122,064,991 , GRCh38.p12 chr6: 120,373,412-121,743,845 TBC1D32, RPS15AP21, 14 more genes
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
    nsv4139404copy number variation1nstd166human GRCh37.p13 chr6: 121,758,036-121,758,086 , GRCh38.p12 chr6: 121,436,890-121,436,940 GJA1
    nsv3924741copy number variation1nstd102humanPathogenic GRCh37 chr6: 106,951,594-126,102,365 , GRCh38 chr6: 106,503,719-125,781,219 , NCBI36 chr6: 107,058,287-126,144,058 LOC105377979, LOC105377936, 266 more genes
    nsv3924661copy number variation1nstd102humanPathogenic GRCh38 chr6: 115,601,230-128,514,324 , GRCh37 chr6: 115,922,394-128,835,469 , NCBI36 chr6: 116,029,087-128,877,162 MCM9, YWHAZP4, 146 more genes
    nsv3924576copy number variation1nstd102humanPathogenic NCBI36 chr6: 97,164,591-122,524,393 , GRCh38 chr6: 96,609,994-122,161,548 , GRCh37 chr6: 97,057,870-122,482,694 TUBE1, PLN, 318 more genes
    nsv3924512copy number variation1nstd102humanPathogenic NCBI36 chr6: 118,035,003-127,062,818 , GRCh37 chr6: 117,928,310-127,021,125 , GRCh38 chr6: 117,607,147-126,699,980 HSF2, LOC285762, 85 more genes
    nsv3923303copy number variation1nstd102humanUncertain significance NCBI36 chr6: 121,340,227-121,831,554 , GRCh38 chr6: 120,977,382-121,468,709 , GRCh37 chr6: 121,298,528-121,789,855 HMGN2P29, LOC105377977, 5 more genes
    nsv3920683copy number variation1nstd102humanPathogenic NCBI36 chr6: 109,372,795-132,430,553 , GRCh37 chr6: 109,266,102-132,388,860 , GRCh38 chr6: 108,944,899-132,067,720 SSXP10, TRE-CTC1-7, 298 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
    nsv3918326copy number variation1nstd102humanPathogenic NCBI36 chr6: 116,145,074-123,993,898 , GRCh37.p13 chr6: 116,038,381-123,952,199 , GRCh38.p12 chr6: 115,717,217-123,631,054 MCM9, FRK, 93 more genes
    nsv3914300copy number variation1nstd102humanPathogenic NCBI36 chr6: 119,337,879-126,076,146 , GRCh38 chr6: 118,975,015-125,713,307 , GRCh37 chr6: 119,296,180-126,034,453 RNF217-AS1, NKAIN2, 50 more genes
    nsv3913689copy number variation1nstd102humanPathogenic NCBI36 chr6: 121,373,749-146,289,101 , GRCh37.p13 chr6: 121,332,050-146,247,408 , GRCh38.p12 chr6: 121,010,904-145,926,272 TPD52L1, MESTP1, 316 more genes
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