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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5317287copy number variation1nstd204human GRCh38.p13 chr6: 118,909,131-118,911,259 , GRCh37.p13 chr6: 119,230,296-119,232,424 MCM9, ASF1A
    nsv5224373copy number variation1nstd204human GRCh38.p13 chr6: 118,908,621-118,911,161 , GRCh37.p13 chr6: 119,229,786-119,232,326 MCM9, ASF1A
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4945610copy number variation1nstd200human GRCh38 chr6: 118,909,141-118,911,250 , GRCh37.p13 chr6: 119,230,306-119,232,415 ASF1A, MCM9
    nsv4824663copy number variation1nstd200human GRCh37 chr6: 119,230,306-119,232,415 , GRCh38.p12 chr6: 118,909,141-118,911,250 MCM9, ASF1A
    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
    nsv4601468copy number variation1nstd183human GRCh37 chr6: 118,609,435-119,243,377 , GRCh38.p12 chr6: 118,288,272-118,922,212 MCM9, LOC644303, 9 more genes
    nsv4599271copy number variation2nstd183human GRCh37 chr6: 119,228,925-119,230,309 , GRCh38.p12 chr6: 118,907,760-118,909,144 MCM9, ASF1A
    nsv4457007copy number variation1nstd102humanPathogenic GRCh37 chr6: 110,981,075-119,608,396 , GRCh38.p12 chr6: 110,659,872-119,287,231 HDAC2-AS2, NIP7P3, 134 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
    nsv4150766copy number variation1nstd166human GRCh37.p13 chr6: 119,227,024-119,227,230 , GRCh38.p12 chr6: 118,905,859-118,906,065 MCM9, ASF1A
    nsv4133339copy number variation1nstd166human GRCh37.p13 chr6: 119,213,684-119,214,955 , GRCh38.p12 chr6: 118,892,520-118,893,791 ASF1A, MCM9
    nsv3960385copy number variation1nstd168human GRCh38 chr6: 118,861,350-118,937,053 , GRCh37.p13 chr6: 119,182,513-119,258,218 ASF1A, MCM9
    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
    nsv3924281copy number variation1nstd102humanUncertain significance NCBI36 chr6: 119,037,743-119,263,471 , GRCh37.p13 chr6: 118,931,050-119,221,772 , GRCh38.p12 chr6: 118,609,887-118,900,607 MCM9, SELENOKP3, 2 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
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