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Items: 1 to 20 of 111

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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
    nsv4940477copy number variation1nstd200human GRCh38 chr6: 26,307,190-26,542,987 , GRCh37.p13 chr6: 26,307,418-26,543,215 , BTN1A1P1, 28 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
    nsv4815683copy number variation1nstd200human GRCh37 chr6: 26,307,418-26,543,215 , GRCh38.p12 chr6: 26,307,190-26,542,987 , TRX-CAT1-4, 28 more genes
    nsv4729472copy number variation1nstd102humanUncertain significance GRCh37 chr6: 26,345,595-26,601,092 , GRCh38.p12 chr6: 26,345,367-26,600,864 TRY-GTA6-1, BTN3A2, 26 more genes
    nsv4729341copy number variation1nstd102humanUncertain significance GRCh37 chr6: 26,046,566-26,670,193 , GRCh38.p12 chr6: 26,046,338-26,669,965 H1-4, TRV-CAC1-6, 78 more genes
    nsv4675256copy number variation1nstd102humanUncertain significance GRCh37 chr6: 26,256,525-26,536,884 , GRCh38.p12 chr6: 26,256,297-26,536,656 LOC101928743, TRQ-TTG3-2, 35 more genes
    nsv4593447copy number variation1nstd183human GRCh37 chr6: 26,527,752-26,601,652 , GRCh38.p12 chr6: 26,527,524-26,601,424 TRK-CTT2-4, TRV-CAC1-6, 14 more genes
    nsv4374516copy number variation1nstd173human GRCh37 chr6: 26,128,446-26,856,189 , GRCh38.p12 chr6: 26,128,218-26,888,410 , H3C8, 85 more genes
    nsv4113112copy number variation1nstd166human GRCh37.p13 chr6: 26,511,000-26,532,000 , GRCh38.p12 chr6: 26,510,772-26,531,772 BTN1A1, HCG11, 4 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
    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
    nsv3911053copy number variation1nstd102humanUncertain significance GRCh38 chr6: 26,280,579-28,727,313 , GRCh37 chr6: 26,280,807-28,695,090 , NCBI36 chr6: 26,388,786-28,803,069 GPX5, TRI-AAT9-1, 232 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
    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
    nsv3877826copy number variation1nstd102humanBenign GRCh37 chr6: 26,465,768-26,665,235 , GRCh38.p12 chr6: 26,465,540-26,665,007 TRA-CGC1-1, TRY-GTA8-1, 23 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
    nsv3874196copy number variation1nstd102humanBenign GRCh37 chr6: 26,524,313-26,595,267 , GRCh38.p12 chr6: 26,524,085-26,595,039 TRP-AGG2-2, LOC107986583, 14 more genes
    nsv3872893copy number variation1nstd102humanUncertain significance GRCh37 chr6: 26,178,542-26,670,193 , GRCh38.p12 chr6: 26,178,314-26,669,965 TRX-CAT1-2, TRW-CCA3-1, 67 more genes
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