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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
    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
    nsv4675148copy number variation1nstd102humanUncertain significance GRCh37 chr11: 60,385,382-62,456,278 , GRCh38.p12 chr11: 60,617,909-62,688,806 LOC105369326, MS4A18, 91 more genes
    nsv4195592copy number variation1nstd166human GRCh37.p13 chr11: 61,493,343-61,623,161 , GRCh38.p12 chr11: 61,725,871-61,855,689 MYRF, TMEM258, 7 more genes
    nsv3915850copy number variation1nstd102humanLikely benign GRCh37 chr11: 61,177,001-61,588,631 , GRCh38 chr11: 61,409,529-61,821,159 , NCBI36 chr11: 60,933,577-61,345,207 TMEM258, RN7SL23P, 18 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
    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
    nsv3890886copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 58,935,215-62,177,656 , GRCh38.p12 chr11: 59,167,742-62,410,184 MYRF, TMEM258, 137 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
    nsv1588781short tandem repeat1nstd128human GRCh37 chr11: 61,561,417-61,561,452 , GRCh38.p12 chr11: 61,793,945-61,793,980 FEN1
    nsv1588175short tandem repeat3nstd128human GRCh37 chr11: 61,561,816-61,561,829 , GRCh38.p12 chr11: 61,794,344-61,794,357 FEN1
    nsv1588174short tandem repeat2nstd128human GRCh37 chr11: 61,558,732-61,558,744 , GRCh38.p12 chr11: 61,791,260-61,791,272 MIR611, FEN1, 1 more genes
    nsv1191784copy number variation1nstd113human NCBI36 chr11: 59,621,931-63,918,940 , GRCh37.p13 chr11: 59,865,355-64,162,364 , GRCh38.p12 chr11: 60,097,882-64,394,892 , CD6, 200 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
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