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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5905958copy number variation1nstd209human GRCh38 chr6: 116,668,944-116,669,552 , GRCh37.p13 chr6: 116,990,107-116,990,715 ZUP1
    nsv5363325translocation1nstd200human GRCh38 chr6: 116,646,642-116,646,642 , GRCh38 chr6: 116,659,464-116,659,464 , GRCh37.p13 chr6: 116,980,627-116,980,627 , GRCh37.p13 chr6: 116,967,805-116,967,805 ZUP1
    nsv5226682copy number variation1nstd204human GRCh38.p13 chr6: 116,652,701-116,655,900 , GRCh37.p13 chr6: 116,973,864-116,977,063 ZUP1
    nsv5109822mobile element insertion1nstd203human GRCh38 chr6: 116,655,472-116,655,486 , GRCh37.p13 chr6: 116,976,635-116,976,649 ZUP1
    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
    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
    nsv4479016mobile element insertion1nstd166human GRCh37.p13 chr6: 116,976,635-116,976,635 , GRCh38.p12 chr6: 116,655,472-116,655,472 ZUP1
    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
    nsv4146258copy number variation1nstd166human GRCh37.p13 chr6: 116,927,948-116,957,549 , GRCh38.p12 chr6: 116,606,785-116,636,386 RSPH4A, ZUP1
    nsv3972366copy number variation1nstd102humanUncertain significance GRCh37 chr6: 116,901,182-117,062,990 , GRCh38.p12 chr6: 116,580,019-116,741,827 KPNA5, RWDD1, 2 more genes
    nsv3971351copy number variation1nstd168human GRCh38 chr6: 116,651,411-116,717,085 , GRCh37.p13 chr6: 116,972,574-117,038,248 KPNA5, ZUP1
    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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