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Items: 1 to 20 of 115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076407inversion1nstd229human GRCh38 chr11: 46,405,448-49,855,596 , GRCh37.p13 chr11: 46,426,998-49,862,647 KBTBD4, MADD-AS1, 89 more genes
    nsv7061528inversion1nstd229human GRCh38 chr11: 47,146,905-49,892,579 , GRCh37.p13 chr11: 47,168,456-49,862,647 YPEL5P2, MADD, 76 more genes
    nsv6910218copy number variation1nstd229human GRCh38 chr11: 47,410,804-47,427,289 , GRCh37.p13 chr11: 47,432,355-47,448,840 SLC39A13, PSMC3
    nsv6908150copy number variation1nstd229human GRCh38 chr11: 47,095,201-47,553,100 , GRCh37.p13 chr11: 47,116,752-47,574,652 ARFGAP2, MIR6745, 15 more genes
    nsv6900992copy number variation1nstd229human GRCh38 chr11: 47,422,295-47,429,114 , GRCh37.p13 chr11: 47,443,846-47,450,665 PSMC3
    nsv6594498inversion1nstd223human GRCh38 chr11: 47,421,211-47,421,683 , GRCh37.p13 chr11: 47,442,762-47,443,234 PSMC3
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 TRR-TCT3-2, OR4A41P, 494 more genes
    nsv6309366copy number variation1nstd102humanPathogenic GRCh37 chr11: 46,880,534-47,470,516 , GRCh38.p12 chr11: 46,858,983-47,448,964 DDB2, PSMC3, 17 more genes
    nsv6309221copy number variation1nstd102humanUncertain significance GRCh37 chr11: 47,431,646-47,470,726 , GRCh38.p12 chr11: 47,410,095-47,449,174 SLC39A13, PSMC3, 1 more genes
    nsv6132367copy number variation1nstd213human GRCh37 chr11: 46,660,000-47,930,001 , GRCh38.p12 chr11: 46,638,450-47,908,449 ACP2, ARHGAP1, 39 more genes
    nsv6132266copy number variation1nstd213human GRCh37 chr11: 47,180,000-47,890,001 , GRCh38.p12 chr11: 47,158,449-47,868,449 ACP2, DDB2, 28 more genes
    nsv6132180copy number variation1nstd213human GRCh37 chr11: 47,180,000-47,880,001 , GRCh38.p12 chr11: 47,158,449-47,858,449 ACP2, DDB2, 28 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
    nsv4984476copy number variation1nstd200human GRCh38 chr11: 47,422,295-47,429,114 , GRCh37.p13 chr11: 47,443,846-47,450,665 PSMC3
    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
    nsv4209763copy number variation1nstd166human GRCh37.p13 chr11: 47,441,000-47,451,000 , GRCh38.p12 chr11: 47,419,449-47,429,449 PSMC3
    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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