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Items: 1 to 20 of 159

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5166724mobile element insertion1nstd203human GRCh38 chr6: 116,818,532-116,818,554 , GRCh37.p13 chr6: 117,139,695-117,139,717 GPRC6A
    nsv5119148mobile element insertion1nstd203human GRCh38 chr6: 116,818,532-116,818,576 , GRCh37.p13 chr6: 117,139,695-117,139,739 GPRC6A
    nsv5117523mobile element insertion1nstd203human GRCh38 chr6: 116,799,156-116,799,171 , GRCh37.p13 chr6: 117,120,319-117,120,334 GPRC6A
    nsv5116927mobile element insertion1nstd203human GRCh38 chr6: 116,818,525-116,818,556 , GRCh37.p13 chr6: 117,139,688-117,139,719 GPRC6A
    nsv5113838mobile element insertion1nstd203human GRCh38 chr6: 116,818,499-116,818,532 , GRCh37.p13 chr6: 117,139,662-117,139,695 GPRC6A
    nsv5108872mobile element insertion1nstd203human GRCh38 chr6: 116,818,529-116,818,532 , GRCh37.p13 chr6: 117,139,692-117,139,695 GPRC6A
    nsv5107859mobile element insertion1nstd203human GRCh38 chr6: 116,818,485-116,818,532 , GRCh37.p13 chr6: 117,139,648-117,139,695 GPRC6A
    nsv5101341mobile element insertion1nstd203human GRCh38 chr6: 116,818,488-116,818,532 , GRCh37.p13 chr6: 117,139,651-117,139,695 GPRC6A
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    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
    nsv4729289copy number variation1nstd102humanUncertain significance GRCh37 chr6: 116,978,714-117,537,404 , GRCh38.p12 chr6: 116,657,551-117,216,241 KPNA5, GPRC6A, 6 more genes
    nsv4486789mobile element insertion1nstd166human GRCh37.p13 chr6: 117,118,413-117,118,413 , GRCh38.p12 chr6: 116,797,250-116,797,250 GPRC6A
    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
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