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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5904178copy number variation1nstd209human GRCh38 chr6: 116,598,860-116,599,014 , GRCh37.p13 chr6: 116,920,023-116,920,177 RSPH4A
    nsv5110357mobile element insertion1nstd203human GRCh38 chr6: 116,606,838-116,606,846 , GRCh37.p13 chr6: 116,928,001-116,928,009 RSPH4A
    nsv5103775mobile element insertion1nstd203human GRCh38 chr6: 116,626,113-116,626,129 , GRCh37.p13 chr6: 116,947,276-116,947,292 RSPH4A
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4948354copy number variation1nstd200human GRCh38 chr6: 116,609,707-116,610,609 , GRCh37.p13 chr6: 116,930,870-116,931,772 RSPH4A
    nsv4945592copy number variation1nstd200human GRCh38 chr6: 116,586,080-116,597,208 , GRCh37.p13 chr6: 116,907,243-116,918,371 RSPH4A, RWDD1
    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
    nsv4739778copy number variation1nstd199human GRCh37 chr6: 116,929,282-116,929,349 , GRCh38.p12 chr6: 116,608,119-116,608,186 RSPH4A
    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
    nsv4609555copy number variation1nstd183human GRCh37 chr6: 116,947,979-116,948,247 , GRCh38.p12 chr6: 116,626,816-116,627,084 RSPH4A
    nsv4484351mobile element insertion1nstd166human GRCh37.p13 chr6: 116,947,276-116,947,276 , GRCh38.p12 chr6: 116,626,113-116,626,113 RSPH4A
    nsv4479681mobile element insertion1nstd166human GRCh37.p13 chr6: 116,927,994-116,927,994 , GRCh38.p12 chr6: 116,606,831-116,606,831 RSPH4A
    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
    nsv4140092copy number variation1nstd166human GRCh37.p13 chr6: 116,929,657-116,935,936 , GRCh38.p12 chr6: 116,608,494-116,614,773 RSPH4A
    nsv4136274copy number variation1nstd166human GRCh37.p13 chr6: 116,943,809-116,950,415 , GRCh38.p12 chr6: 116,622,646-116,629,252 RSPH4A
    nsv4133304copy number variation1nstd166human GRCh37.p13 chr6: 116,921,652-116,921,822 , GRCh38.p12 chr6: 116,600,489-116,600,659 RSPH4A
    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
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