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Items: 1 to 20 of 113

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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
    nsv4940478copy number variation1nstd200human GRCh38 chr6: 26,322,638-26,327,290 , GRCh37.p13 chr6: 26,322,866-26,327,518 TRR-TCG2-1, H3C9P, 3 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
    nsv4934536copy number variation1nstd200human GRCh38 chr6: 26,150,781-26,331,570 , GRCh37.p13 chr6: 26,151,009-26,331,798 , LARP1P1, 41 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
    nsv4815685copy number variation1nstd200human GRCh37 chr6: 26,322,864-26,327,516 , GRCh38.p12 chr6: 26,322,636-26,327,288 TRR-TCG2-1, LOC101928743, 3 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
    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
    nsv4675352copy number variation1nstd102humanLikely benign GRCh37 chr6: 26,238,509-26,329,714 , GRCh38.p12 chr6: 26,238,281-26,329,486 H3C9P, TRQ-TTG3-2, 22 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
    nsv4598438copy number variation1nstd183human GRCh37 chr6: 26,103,998-26,365,563 , GRCh38.p12 chr6: 26,103,770-26,365,335 , H2AC10P, 46 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
    nsv4129362copy number variation1nstd166human GRCh37.p13 chr6: 26,319,410-26,368,482 , GRCh38.p12 chr6: 26,319,182-26,368,254 , TRX-CAT1-4, 8 more genes
    nsv4128600copy number variation1nstd166human GRCh37.p13 chr6: 26,320,000-26,331,000 , GRCh38.p12 chr6: 26,319,772-26,330,772 , TRX-CAT1-4, 6 more genes
    nsv4115528copy number variation1nstd166human GRCh37.p13 chr6: 26,314,557-26,338,139 , GRCh38.p12 chr6: 26,314,329-26,337,911 , TRX-CAT1-4, 7 more genes
    nsv3960052copy number variation1nstd168human GRCh38 chr6: 26,326,174-26,364,230 , GRCh37.p13 chr6: 26,326,402-26,364,458 , BTN3A2, 5 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
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