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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5511513copy number variation1nstd206human GRCh38 chr11: 60,501,683-60,501,890 , GRCh37.p13 chr11: 60,269,156-60,269,363 , MS4A12
    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
    nsv5325627inversion1nstd204human GRCh37.p13 chr11: 58,669,453-61,321,541 , GRCh38.p13 chr11: 58,901,980-61,554,069 , CD5, 118 more genes
    nsv4984987copy number variation1nstd200human GRCh38 chr11: 60,502,430-60,510,168 , GRCh37.p13 chr11: 60,269,903-60,277,641 , MS4A12
    nsv4885672inversion1nstd200human GRCh37 chr11: 58,669,461-61,321,541 , GRCh38.p12 chr11: 58,901,988-61,554,069 , MS4A2, 118 more genes
    nsv4831228copy number variation1nstd200human GRCh37 chr11: 60,269,903-60,277,641 , GRCh38.p12 chr11: 60,502,430-60,510,168 , MS4A12
    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
    nsv4199326copy number variation1nstd166human GRCh37.p13 chr11: 60,259,195-60,259,362 , GRCh38.p12 chr11: 60,491,722-60,491,889 MS4A12
    nsv3920536copy number variation1nstd102humanLikely benign GRCh37 chr11: 59,618,746-60,466,753 , NCBI36 chr11: 59,375,322-60,223,329 , GRCh38 chr11: 59,851,273-60,699,280 MS4A3, MS4A2, 23 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
    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
    nsv3157640copy number variation1nstd151human GRCh37 chr11: 59,939,628-60,285,690 , GRCh38.p12 chr11: 60,172,155-60,518,217 , MS4A5, 10 more genes
    nsv3154918copy number variation1nstd151human GRCh37 chr11: 60,264,789-60,274,602 , GRCh38.p12 chr11: 60,497,316-60,507,129 , MS4A12
    nsv3146751copy number variation6nstd151human GRCh37 chr11: 60,215,119-60,296,938 , GRCh38.p12 chr11: 60,447,646-60,529,465 , MS4A5, 3 more genes
    nsv3145502copy number variation1nstd151human GRCh37 chr11: 60,274,198-60,274,602 , GRCh38.p12 chr11: 60,506,725-60,507,129 , MS4A12
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