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Items: 1 to 20 of 116

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5036471inversion1nstd200human GRCh38 chr6: 25,888,426-29,704,316 , GRCh37.p13 chr6: 25,888,654-29,672,093 , OR11A1, 368 more genes
    nsv4879678inversion1nstd200human GRCh37 chr6: 25,888,654-29,672,093 , GRCh38.p12 chr6: 25,888,426-29,704,316 , H1-4, 368 more genes
    nsv4593439copy number variation1nstd183human GRCh37 chr6: 26,017,803-26,061,708 , GRCh38.p12 chr6: 26,017,575-26,061,480 H4C2, H2AC5P, 8 more genes
    nsv4592076copy number variation1nstd183human GRCh37 chr6: 26,020,640-26,033,806 , GRCh38.p12 chr6: 26,020,412-26,033,578 H2AC4, H3C2, 3 more genes
    nsv4456351copy number variation1nstd102humanUncertain significance GRCh37 chr6: 25,896,585-26,287,389 , GRCh38.p12 chr6: 25,896,357-26,287,161 H3P26, H1-6, 44 more genes
    nsv4455820copy number variation1nstd102humanUncertain significance GRCh37 chr6: 25,996,066-26,303,969 , GRCh38.p12 chr6: 25,995,838-26,303,741 H4C6, H4C3, 44 more genes
    nsv4434898copy number variation1nstd172human GRCh38.p12 chr6: 26,019,773-26,056,772 , GRCh37.p13 chr6: 26,020,001-26,057,000 H1-2, H2BC3, 7 more genes
    nsv3961736insertion1nstd168human GRCh38 chr6: 25,986,899-26,062,936 , GRCh37.p13 chr6: 25,987,127-26,063,164 H3C1, H4C2, 10 more genes
    nsv3920564copy number variation1nstd102humanPathogenic GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946 PRELID1P2, RPL7AP7, 785 more genes
    nsv3920471copy number variation1nstd102humanLikely benign GRCh37 chr6: 25,991,630-26,280,921 , NCBI36 chr6: 26,099,609-26,388,900 , GRCh38 chr6: 25,991,402-26,280,693 H2AC8, H2BC8, 41 more genes
    nsv3918212copy number variation1nstd102humanLikely benign GRCh37 chr6: 25,991,619-26,117,057 , GRCh38 chr6: 25,991,391-26,116,829 , NCBI36 chr6: 26,099,598-26,225,036 H2AC4, H4C2, 14 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
    nsv3888702copy number variation1nstd102humanUncertain significance GRCh37 chr6: 25,851,789-26,319,486 , GRCh38.p12 chr6: 25,851,561-26,319,258 TRIM38, TRR-TCG4-1, 54 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 RNU6-411P, LOC107986611, 2910 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 LOC105378061, MIR4640, 2914 more genes
    nsv3872128copy number variation1nstd102humanUncertain significance GRCh37 chr6: 25,839,165-26,536,884 , GRCh38.p12 chr6: 25,838,937-26,536,656 HFE-AS1, H2AC7, 78 more genes
    nsv3225658insertion9nstd152human GRCh38 chr6: 26,022,062-26,056,331 , GRCh37.p13 chr6: 26,022,290-26,056,559 H1-2, H2BC3, 6 more genes
    nsv3169066inversion1nstd158human GRCh37 chr6: 5,923,377-99,717,885 , GRCh38.p12 chr6: 5,923,144-99,270,009 , ABCF1, 1877 more genes
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