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Items: 1 to 20 of 124

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5304216copy number variation1nstd204human GRCh38.p13 chr6: 116,238,997-116,254,087 , GRCh37.p13 chr6: 116,560,160-116,575,250 NT5DC1, TSPYL4, 1 more genes
    nsv5234180copy number variation1nstd204human GRCh38.p13 chr6: 116,239,061-116,254,036 , GRCh37.p13 chr6: 116,560,224-116,575,199 TSPYL4, NT5DC1, 1 more genes
    nsv5226654copy number variation1nstd204human GRCh38.p13 chr6: 116,239,001-116,253,400 , GRCh37.p13 chr6: 116,560,164-116,574,563 TSPYL4, DSE, 1 more genes
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4945591copy number variation1nstd200human GRCh38 chr6: 116,239,007-116,254,078 , GRCh37.p13 chr6: 116,560,170-116,575,241 NT5DC1, TSPYL4, 1 more genes
    nsv4824651copy number variation1nstd200human GRCh37 chr6: 116,560,170-116,575,241 , GRCh38.p12 chr6: 116,239,007-116,254,078 DSE, NT5DC1, 1 more genes
    nsv4685989copy number variation1nstd102humanPathogenic GRCh37 chr6: 101,287,058-117,013,245 , GRCh38.p12 chr6: 100,839,182-116,692,082 RPL23AP50, RNU6-960P, 216 more genes
    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
    nsv4312499inversion1nstd166human GRCh37.p13 chr6: 94,532,001-117,422,619 , GRCh38.p12 chr6: 93,822,283-117,101,456 , CRYBG1, 284 more genes
    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
    nsv3924133copy number variation1nstd102humanPathogenic GRCh37 chr6: 115,541,218-117,517,534 , NCBI36 chr6: 115,647,911-117,624,227 , GRCh38 chr6: 115,220,054-117,196,371 FAM162B, RPS5P1, 27 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
    nsv3914719copy number variation1nstd102humanUncertain significance GRCh38 chr6: 115,890,731-116,427,566 , NCBI36 chr6: 116,318,588-116,855,422 , GRCh37 chr6: 116,211,895-116,748,729 NT5DC1, COL10A1, 9 more genes
    nsv3911999copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 115,754,819-118,363,096 , GRCh37 chr6: 115,648,126-118,256,403 , GRCh38 chr6: 115,326,962-117,935,240 COL10A1, FRK, 40 more genes
    nsv3910417copy number variation1nstd102humanPathogenic GRCh38 chr6: 100,054,889-120,488,154 , NCBI36 chr6: 100,609,486-120,850,999 , GRCh37 chr6: 100,502,765-120,809,300 LINC02518, LOC105377937, 266 more genes
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