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Items: 1 to 20 of 48

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4984972copy number variation1nstd200human GRCh38 chr11: 58,596,469-58,640,354 , GRCh37.p13 chr11: 58,363,942-58,407,827 CNTF, ZFP91, 1 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
    nsv4685714copy number variation1nstd102humannot provided GRCh37 chr11: 58,237,819-58,800,374 , GRCh38.p12 chr11: 58,470,346-59,032,901 GLYATL1, LPXN, 14 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
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3904152copy number variation1nstd102humanUncertain significance GRCh37 chr11: 49,313,405-59,008,426 , GRCh38.p12 chr11: 49,291,853-59,240,953 FAM111B, OR5M1, 250 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
    nsv3168776inversion1nstd158human GRCh37 chr11: 37,074,771-61,357,521 , GRCh38.p12 chr11: 37,053,221-61,590,049 , ACP2, 535 more genes
    nsv3168425copy number variation1nstd158human GRCh37 chr11: 3,543,079-67,662,509 , GRCh38.p12 chr11: 3,521,849-67,895,038 , ACP2, 1535 more genes
    nsv1189028copy number variation1nstd113human NCBI36 chr11: 46,867,445-58,515,771 , GRCh37.p13 chr11: 46,910,869-58,759,195 , GRCh38.p12 chr11: 46,889,318-58,991,722 , ACP2, 313 more genes
    nsv1159883copy number variation1nstd111human GRCh37 chr11: 58,389,319-58,434,191 , GRCh38.p12 chr11: 58,621,846-58,666,718 CNTF, ZFP91, 1 more genes
    nsv1146381inversion1nstd107human GRCh37 chr11: 1,620,499-71,272,308 , GRCh38.p12 chr11: 1,599,269-71,561,262 , ACP2, 1686 more genes
    nsv1132999inversion1nstd106human GRCh37 chr11: 1,620,508-89,079,908 , GRCh38.p12 chr11: 1,599,278-89,346,740 , ACTN3, 2007 more genes
    nsv1125301inversion1nstd106human GRCh37 chr11: 48,489,096-88,979,496 , GRCh38.p12 chr11: 48,467,544-89,246,328 , MRPL49, 1130 more genes
    esv3806158tandem duplication1estd192human GRCh37 chr11: 20,322,957-70,717,303 , GRCh38.p12 chr11: 20,301,411-70,871,198 , LINC02759, 1146 more genes
    esv3799160inversion1estd192human GRCh37 chr11: 57,548,661-62,595,696 , GRCh38.p12 chr11: 57,781,189-62,828,224 , RN7SL435P, 230 more genes
    esv3807849tandem duplication1estd192human GRCh37 chr11: 16,492,879-90,295,791 , GRCh38.p12 chr11: 16,471,332-90,562,623 , LOC107984356, 1605 more genes
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