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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094093copy number variation2nstd102humanUncertain significance GRCh37 chr11: 64,973,914-70,052,579 , GRCh38.p12 chr11: 65,206,443-70,206,473 B4GAT1, CHKA-DT, 208 more genes
    nsv7093406copy number variation1nstd102humanUncertain significance GRCh37 chr11: 66,178,392-66,433,436 , GRCh38.p12 chr11: 66,410,921-66,665,965 MRPL11, NPAS4, 15 more genes
    nsv7068716inversion1nstd229human GRCh38 chr11: 66,546,770-66,568,314 , GRCh37.p13 chr11: 66,314,241-66,335,785 CTSF, ACTN3
    nsv7061947inversion1nstd229human GRCh38 chr11: 66,494,296-66,563,130 , GRCh37.p13 chr11: 66,261,767-66,330,601 CTSF, DPP3, 3 more genes
    nsv6909466copy number variation1nstd229human GRCh38 chr11: 66,552,423-66,562,728 , GRCh37.p13 chr11: 66,319,894-66,330,199 ACTN3, CTSF
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6903249copy number variation1nstd229human GRCh38 chr11: 66,567,193-66,567,342 , GRCh37.p13 chr11: 66,334,664-66,334,813 CTSF
    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
    nsv6314192copy number variation1nstd102humanUncertain significance GRCh37 chr11: 64,935,724-66,405,514 , GRCh38.p12 chr11: 65,168,253-66,638,043 CNIH2, GAL3ST3, 95 more genes
    nsv6314012copy number variation1nstd102humanUncertain significance GRCh37 chr11: 66,188,172-66,402,747 , GRCh38.p12 chr11: 66,420,701-66,635,276 LOC100505524, ZDHHC24, 13 more genes
    nsv6290938copy number variation1nstd102humanUncertain significance GRCh37 chr11: 65,963,737-66,581,485 , GRCh38.p12 chr11: 66,196,266-66,814,014 CCS, RN7SL12P, 38 more genes
    nsv6132271copy number variation1nstd213human GRCh37 chr11: 66,040,000-66,380,001 , GRCh38.p12 chr11: 66,272,529-66,612,530 BBS1, YIF1A, 24 more genes
    nsv6132112copy number variation1nstd213human GRCh37 chr11: 64,220,000-68,010,001 , GRCh38.p12 chr11: 64,452,528-68,242,533 ACTN3, ALDH3B1, 212 more genes
    nsv6024820copy number variation1nstd212human GRCh38 chr11: 66,552,416-66,562,733 , GRCh37.p13 chr11: 66,319,887-66,330,204 CTSF, ACTN3
    nsv5922432copy number variation1nstd209human GRCh38 chr11: 66,552,416-66,562,726 , GRCh37.p13 chr11: 66,319,887-66,330,197 CTSF, ACTN3
    nsv5502731copy number variation1nstd206human GRCh38 chr11: 66,552,416-66,562,727 , GRCh37.p13 chr11: 66,319,887-66,330,198 ACTN3, CTSF
    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
    nsv5305431copy number variation1nstd204human GRCh37.p13 chr11: 66,319,878-66,330,207 , GRCh38.p13 chr11: 66,552,407-66,562,736 ACTN3, CTSF
    nsv5277798copy number variation1nstd204human GRCh38.p13 chr11: 65,676,501-66,823,500 , GRCh37.p13 chr11: 65,443,972-66,590,971 , BBS1, 68 more genes
    nsv5261214copy number variation1nstd204human GRCh38.p13 chr11: 66,552,459-66,562,605 , GRCh37.p13 chr11: 66,319,930-66,330,076 ACTN3, CTSF
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