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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137129copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659 VSIG10L2, OR8B6P, 268 more genes
    nsv7093673copy number variation1nstd102humanUncertain significance GRCh37 chr11: 128,564,154-128,786,626 , GRCh38.p12 chr11: 128,694,259-128,916,731 FLI1, KCNJ1, 4 more genes
    nsv7077728inversion1nstd229human GRCh38 chr11: 124,239,803-134,089,458 , GRCh37.p13 chr11: 124,110,545-133,959,353 LOC283172, PPP1R10P1, 175 more genes
    nsv6916128copy number variation1nstd229human GRCh38 chr11: 128,903,301-128,927,300 , GRCh37.p13 chr11: 128,773,196-128,797,195 KCNJ5-AS1, KCNJ5
    nsv6912205copy number variation1nstd229human GRCh38 chr11: 128,538,001-129,014,800 , GRCh37.p13 chr11: 128,407,896-128,884,695 KCNJ1, KCNJ5-AS1, 11 more genes
    nsv6911733copy number variation1nstd229human GRCh38 chr11: 128,740,649-128,970,889 , GRCh37.p13 chr11: 128,610,544-128,840,784 ARHGAP32, LOC107984409, 5 more genes
    nsv6908501copy number variation1nstd229human GRCh38 chr11: 128,812,462-129,027,216 , GRCh37.p13 chr11: 128,682,357-128,897,111 ARHGAP32, RNU6-876P, 6 more genes
    nsv6906179copy number variation1nstd229human GRCh38 chr11: 128,903,659-128,907,738 , GRCh37.p13 chr11: 128,773,554-128,777,633 KCNJ5-AS1, KCNJ5
    nsv6904808copy number variation1nstd229human GRCh38 chr11: 128,703,944-128,997,953 , GRCh37.p13 chr11: 128,573,839-128,867,848 KCNJ1, LOC107984409, 6 more genes
    nsv6902210copy number variation1nstd229human GRCh38 chr11: 128,878,300-128,978,307 , GRCh37.p13 chr11: 128,748,195-128,848,202 ARHGAP32, KCNJ5-AS1, 2 more genes
    nsv6638048copy number variation1nstd102humanUncertain significance GRCh37 chr11: 128,682,955-128,897,053 , GRCh38.p12 chr11: 128,813,060-129,027,158 RNU6-876P, ARHGAP32, 6 more genes
    nsv6637558copy number variation1nstd102humanPathogenic GRCh37 chr11: 122,975,824-134,938,470 , GRCh38.p12 chr11: 123,105,116-135,068,576 OR8B8, LOC107984373, 234 more genes
    nsv6637508copy number variation1nstd102humanUncertain significance GRCh37 chr11: 128,683,208-128,897,053 , GRCh38.p12 chr11: 128,813,313-129,027,158 KCNJ5, ARHGAP32, 6 more genes
    nsv6637166copy number variation1nstd102humanUncertain significance GRCh37 chr11: 128,683,018-128,897,053 , GRCh38.p12 chr11: 128,813,123-129,027,158 KCNJ5, ARHGAP32, 6 more genes
    nsv6634467copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 127,074,235-135,006,516 , GRCh38.p12 chr11: 127,204,340-135,076,622 APLP2, BAK1P2, 98 more genes
    nsv6620888copy number variation1nstd224human GRCh37 chr11: 128,701,032-128,869,845 , GRCh38.p12 chr11: 128,831,137-128,999,950 KCNJ1, KCNJ5, 5 more genes
    nsv6471155copy number variation1nstd223human GRCh38 chr11: 128,812,462-129,027,216 , GRCh37.p13 chr11: 128,682,357-128,897,111 KCNJ1, KCNJ5, 6 more genes
    nsv6464726copy number variation1nstd223human GRCh38 chr11: 128,905,001-128,906,100 , GRCh37.p13 chr11: 128,774,896-128,775,995 KCNJ5-AS1, KCNJ5
    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
    nsv6315090copy number variation1nstd102humanPathogenic GRCh37 chr11: 128,634,685-134,257,741 , GRCh38.p12 chr11: 128,764,790-134,387,847 BAK1P2, RN7SL167P, 73 more genes
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