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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6908761copy number variation1nstd229human GRCh38 chr11: 57,236,201-57,248,300 , GRCh37.p13 chr11: 57,003,675-57,015,774 LOC107984364, APLNR
    nsv6906218copy number variation1nstd229human GRCh38 chr11: 57,232,828-57,232,934 , GRCh37.p13 chr11: 57,000,302-57,000,408 APLNR
    nsv6637373copy number variation1nstd102humanUncertain significance GRCh37 chr11: 56,637,024-57,361,915 , GRCh38.p12 chr11: 56,869,548-57,594,442 OR5BQ1P, OR5AK2, 27 more genes
    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
    nsv6101017inversion1nstd212human GRCh38 chr11: 54,578,670-59,501,927 , GRCh37.p13 chr11: 54,711,406-59,269,400 , APLNR, 236 more genes
    nsv5914325copy number variation1nstd209human GRCh38 chr11: 55,273,256-58,053,631 , GRCh37.p13 chr11: 55,040,732-57,821,103 , LOC107984365, 161 more genes
    nsv5513546copy number variation1nstd206human GRCh38 chr11: 57,237,936-57,238,025 , GRCh37.p13 chr11: 57,005,410-57,005,499 APLNR
    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
    nsv5302184copy number variation1nstd204human GRCh38.p13 chr11: 57,237,297-57,237,557 , GRCh37.p13 chr11: 57,004,771-57,005,031 APLNR
    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
    nsv4680588copy number variation1nstd189human GRCh37.p13 chr11: 55,444,212-57,222,540 , GRCh38.p12 chr11: 55,676,736-57,455,067 , APLNR, 109 more genes
    nsv4600938copy number variation1nstd183human GRCh37 chr11: 56,949,439-57,057,074 , GRCh38.p12 chr11: 57,181,965-57,289,600 APLNR, LRRC55, 2 more genes
    nsv4453292copy number variation1nstd102humannot provided GRCh37 chr11: 55,033,164-57,518,726 , GRCh38.p12 chr11: 55,265,688-57,751,254 OR8J3, LINC02735, 150 more genes
    nsv4200747copy number variation1nstd166human GRCh37.p13 chr11: 57,000,302-57,000,411 , GRCh38.p12 chr11: 57,232,828-57,232,937 APLNR
    nsv3924646copy number variation1nstd102humanUncertain significance GRCh38 chr11: 55,316,535-57,539,457 , GRCh37 chr11: 55,084,011-57,306,930 , NCBI36 chr11: 54,840,587-57,063,506 OR5AL1, OR5AK2, 134 more genes
    nsv3918615copy number variation1nstd102humanUncertain significance NCBI36 chr11: 54,789,872-56,896,303 , GRCh37.p13 chr11: 55,033,296-57,139,727 , GRCh38.p12 chr11: 55,265,820-57,372,254 OR8K5, OR5G5P, 127 more genes
    nsv3911150copy number variation1nstd102humanPathogenic GRCh37 chr11: 55,086,995-58,766,250 , NCBI36 chr11: 54,843,571-58,522,826 , GRCh38 chr11: 55,319,519-58,998,777 OR5BD1P, SELENOH, 197 more genes
    nsv3910102copy number variation1nstd102humanLikely benign NCBI36 chr11: 56,571,417-56,896,362 , GRCh37 chr11: 56,814,841-57,139,786 , GRCh38 chr11: 57,047,366-57,372,313 TNKS1BP1, APLNR, 6 more genes
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