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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094019copy number variation1nstd102humanUncertain significance GRCh37 chr11: 88,027,174-89,018,142 , GRCh38.p12 chr11: 88,294,006-89,284,974 GRM5, RNU6-16P, 5 more genes
    nsv7069436inversion1nstd229human GRCh38 chr11: 85,936,971-89,461,473 , GRCh37.p13 chr11: 85,648,014-89,194,641 , RNU6-1135P, 45 more genes
    nsv6917254copy number variation1nstd229human GRCh38 chr11: 88,509,271-88,509,323 , GRCh37.p13 chr11: 88,242,439-88,242,491 GRM5, GRM5-AS1
    nsv6915155copy number variation1nstd229human GRCh38 chr11: 88,502,478-88,503,627 , GRCh37.p13 chr11: 88,235,646-88,236,795 GRM5-AS1, GRM5
    nsv6909868copy number variation1nstd229human GRCh38 chr11: 88,469,115-88,505,358 , GRCh37.p13 chr11: 88,202,283-88,238,526 GRM5, GRM5-AS1
    nsv6906961copy number variation1nstd229human GRCh38 chr11: 88,520,526-88,524,264 , GRCh37.p13 chr11: 88,253,694-88,257,432 GRM5-AS1, GRM5
    nsv6901234copy number variation1nstd229human GRCh38 chr11: 88,473,054-88,568,334 , GRCh37.p13 chr11: 88,206,222-88,301,502 GRM5-AS1, GRM5
    nsv6637847copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,562,738-88,663,067 , GRCh38.p12 chr11: 80,851,695-88,929,899 PRSS23, MTCO3P25, 92 more genes
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 LOC107984375, RN7SL222P, 295 more genes
    nsv6593213inversion1nstd223human GRCh38 chr11: 88,458,610-89,118,294 , GRCh37.p13 chr11: 88,191,778-88,851,462 GRM5, RNU6-16P, 1 more genes
    nsv6474540copy number variation1nstd223human GRCh38 chr11: 88,520,526-88,524,260 , GRCh37.p13 chr11: 88,253,694-88,257,428 GRM5-AS1, GRM5
    nsv6464669copy number variation1nstd223human GRCh38 chr11: 88,507,101-88,510,800 , GRCh37.p13 chr11: 88,240,269-88,243,968 GRM5, GRM5-AS1
    nsv6461977copy number variation1nstd223human GRCh38 chr11: 88,436,341-88,775,153 , GRCh37.p13 chr11: 88,169,509-88,508,321 GRM5-AS1, RNU6-16P, 1 more genes
    nsv6455882copy number variation1nstd223human GRCh38 chr11: 88,502,476-88,503,626 , GRCh37.p13 chr11: 88,235,644-88,236,794 GRM5-AS1, GRM5
    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
    nsv6313961copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,855,209-98,002,445 , GRCh38.p12 chr11: 78,144,163-98,131,717 MTND5P38, XIAPP2, 252 more genes
    nsv6290834copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,422,071-118,022,671 , GRCh38.p12 chr11: 85,711,028-118,151,956 CARD17P, RNA5SP350, 480 more genes
    nsv6113792mobile element insertion1nstd186human GRCh37 chr11: 88,240,142-88,240,193 , GRCh38.p12 chr11: 88,506,974-88,507,025 GRM5-AS1, GRM5
    nsv5975328insertion1nstd209human GRCh38 chr11: 88,524,180-88,524,180 , GRCh37.p13 chr11: 88,257,348-88,257,348 GRM5-AS1, GRM5
    nsv5923390copy number variation1nstd209human GRCh38 chr11: 88,502,476-88,503,625 , GRCh37.p13 chr11: 88,235,644-88,236,793 GRM5-AS1, GRM5
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