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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093698copy number variation1nstd102humanUncertain significance GRCh37 chr11: 6,411,829-6,662,844 , GRCh38.p12 chr11: 6,390,599-6,641,613 SMPD1, HPX, 11 more genes
    nsv7077146inversion1nstd229human GRCh38 chr11: 6,475,304-6,546,520 , GRCh37.p13 chr11: 6,496,534-6,567,750 LOC644169, ARFIP2, 3 more genes
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6908165copy number variation1nstd229human GRCh38 chr11: 6,477,909-6,599,930 , GRCh37.p13 chr11: 6,499,139-6,621,160 LOC644169, ARFIP2, 3 more genes
    nsv6900827copy number variation1nstd229human GRCh38 chr11: 6,191,411-6,542,996 , GRCh37.p13 chr11: 6,212,641-6,564,226 ARFIP2, RRP8, 14 more genes
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6290772copy number variation1nstd102humanUncertain significance GRCh37 chr11: 6,502,523-7,248,333 , GRCh38.p12 chr11: 6,481,293-7,227,102 GVINP2, OR2AG2, 26 more genes
    nsv6132268copy number variation1nstd213human GRCh37 chr11: 6,320,000-6,880,001 , GRCh38.p12 chr11: 6,298,770-6,858,770 APBB1, TPP1, 22 more genes
    nsv5505287copy number variation1nstd206human GRCh38 chr11: 6,477,854-6,488,476 , GRCh37.p13 chr11: 6,499,084-6,509,706 ARFIP2, LOC644169, 1 more genes
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4681173copy number variation2nstd102humanUncertain significance GRCh37 chr11: 5,709,028-6,640,651 , GRCh38.p12 chr11: 5,687,798-6,619,420 OR56B2P, TRIM3, 50 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4613057copy number variation1nstd183human GRCh37 chr11: 6,502,631-6,503,211 , GRCh38.p12 chr11: 6,481,401-6,481,981 ARFIP2, TIMM10B
    nsv4456235copy number variation1nstd102humanUncertain significance GRCh37 chr11: 5,896,551-6,719,852 , GRCh38.p12 chr11: 5,875,321-6,698,621 OR52X1P, LOC112268071, 40 more genes
    nsv4350476copy number variation1nstd102humanPathogenic GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589 KRTAP5-3, OR56A7P, 457 more genes
    nsv4344890sequence alteration1nstd166human GRCh37.p13 chr11: 6,496,346-6,567,751 , GRCh38.p12 chr11: 6,475,116-6,546,521 RRP8, ARFIP2, 3 more genes
    nsv4200885copy number variation1nstd166human GRCh37.p13 chr11: 6,495,000-6,504,000 , GRCh38.p12 chr11: 6,473,770-6,482,770 ARFIP2, TIMM10B, 1 more genes
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