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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5927227copy number variation1nstd209human GRCh38 chr11: 46,386,979-46,387,138 , GRCh37.p13 chr11: 46,408,529-46,408,688 CHRM4
    nsv5563185sequence alteration1nstd206human GRCh38 chr11: 46,388,537-46,391,007 , GRCh37.p13 chr11: 46,410,087-46,412,557 CHRM4
    nsv5508401copy number variation1nstd206human GRCh38 chr11: 46,386,983-46,387,139 , GRCh37.p13 chr11: 46,408,533-46,408,689 CHRM4
    nsv5507746copy number variation1nstd206human GRCh38 chr11: 46,359,908-46,411,705 , GRCh37.p13 chr11: 46,381,458-46,433,255 MIR4688, MDK, 3 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5380725copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 45,827,353-47,804,770 , GRCh38.p12 chr11: 45,805,802-47,783,218 MIR4688, LOC112268075, 58 more genes
    nsv5355058translocation1nstd200human GRCh38 chr11: 46,386,983-46,386,983 , GRCh38 chr11: 46,387,139-46,387,139 , GRCh37.p13 chr11: 46,408,689-46,408,689 , GRCh37.p13 chr11: 46,408,533-46,408,533 CHRM4
    nsv5333628translocation1nstd200human GRCh37 chr11: 46,408,689-46,408,689 , GRCh37 chr11: 46,408,533-46,408,533 , GRCh38.p12 chr11: 46,387,139-46,387,139 , GRCh38.p12 chr11: 46,386,983-46,386,983 CHRM4
    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
    nsv4729454copy number variation1nstd102humanUncertain significance GRCh37 chr11: 46,123,974-46,442,526 , GRCh38.p12 chr11: 46,102,423-46,420,976 CHRM4, MDK, 10 more genes
    nsv4729122copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 45,995,260-46,536,343 , GRCh38.p12 chr11: 45,973,709-46,514,793 CHRM4, MDK, 13 more genes
    nsv4683154copy number variation1nstd102humanUncertain significance GRCh37 chr11: 46,387,807-46,766,127 , GRCh38.p12 chr11: 46,366,257-46,744,577 HARBI1, AMBRA1, 12 more genes
    nsv4646026copy number variation1nstd186human GRCh37 chr11: 46,408,530-46,408,689 , GRCh38.p12 chr11: 46,386,980-46,387,139 CHRM4
    nsv4640309copy number variation1nstd186human GRCh37 chr11: 46,408,533-46,408,689 , GRCh38.p12 chr11: 46,386,983-46,387,139 CHRM4
    nsv4456633copy number variation1nstd102humanUncertain significance GRCh37 chr11: 46,302,171-46,783,079 , GRCh38.p12 chr11: 46,280,620-46,761,529 MIR5582, RPS10P19, 15 more genes
    nsv4428796copy number variation1nstd174human GRCh37 chr11: 46,383,223-46,432,606 , GRCh38.p12 chr11: 46,361,673-46,411,056 CHRM4, MDK, 3 more genes
    nsv4414852copy number variation1nstd174human GRCh37 chr11: 46,408,510-46,408,689 , GRCh38.p12 chr11: 46,386,960-46,387,139 CHRM4
    nsv4200798copy number variation1nstd166human GRCh37.p13 chr11: 46,408,533-46,408,689 , GRCh38.p12 chr11: 46,386,983-46,387,139 CHRM4
    nsv3924778copy number variation1nstd102humanPathogenic GRCh38 chr11: 41,118,322-48,643,003 , GRCh37 chr11: 41,139,872-48,664,555 , NCBI36 chr11: 41,096,448-48,621,131 F2, PSMC3, 140 more genes
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