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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075540inversion1nstd229human GRCh38 chr11: 67,968,443-71,626,784 , GRCh37.p13 chr11: 67,735,914-71,337,830 S100A11P3, CCND1, 76 more genes
    nsv7065047inversion1nstd229human GRCh38 chr11: 70,831,936-71,057,112 , GRCh37.p13 chr11|NW_004070871.1: 376,149-551,325 , GRCh37.p13 chr11: 70,678,041-70,801,586 MIR3664, SHANK2, 1 more genes
    nsv6906365copy number variation1nstd229human GRCh38 chr11: 70,858,198-70,872,121 , GRCh37.p13 chr11: 70,704,303-70,718,226 , GRCh37.p13 chr11|NW_004070871.1: 402,411-416,334 SHANK2-AS3, MIR3664, 1 more genes
    nsv6904742copy number variation1nstd229human GRCh38 chr11: 70,864,401-70,868,800 , GRCh37.p13 chr11: 70,710,506-70,714,905 , GRCh37.p13 chr11|NW_004070871.1: 408,614-413,013 SHANK2, SHANK2-AS3
    nsv6900931copy number variation1nstd229human GRCh38 chr11: 70,829,302-70,908,624 , GRCh37.p13 chr11|NW_004070871.1: 373,515-452,837 , GRCh37.p13 chr11: 70,675,407-70,754,729 SHANK2, SHANK2-AS3, 1 more genes
    nsv6637432copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 70,517,505-70,807,254 , GRCh38.p12 chr11: 70,671,400-71,096,208 SHANK2, SHANK2-AS3, 1 more genes
    nsv6637191copy number variation1nstd102humanUncertain significance GRCh37 chr11: 70,317,964-70,795,061 , GRCh38.p12 chr11: 70,471,859-70,948,956 SHANK2-AS1, MIR3664, 2 more genes
    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
    nsv6290813copy number variation1nstd102humanPathogenic GRCh37 chr11: 69,214,835-70,821,137 , GRCh38.p12 chr11: 69,400,067-71,110,091 CCND1, LOC101928473, 25 more genes
    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
    nsv4712978copy number variation1nstd195human GRCh37 chr11: 70,142,801-70,877,801 , GRCh38.p12 chr11: 70,296,695-71,166,755 , CTTN, 7 more genes
    nsv4680826copy number variation1nstd189human GRCh37.p13 chr11: 70,407,908-71,069,164 , GRCh38.p12 chr11: 70,561,803-71,358,118 SHANK2, SHANK2-AS3, 2 more genes
    nsv3917463copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 67,555,736-70,982,189 , GRCh37 chr11: 67,799,160-71,304,541 , GRCh38 chr11: 68,031,693-71,593,495 CCND1, CHKA, 71 more genes
    nsv3910316copy number variation1nstd102humanUncertain significance GRCh38 chr11: 70,575,193-70,893,208 , NCBI36 chr11: 70,098,946-70,416,961 , GRCh37 chr11: 70,421,298-70,739,313 MIR3664, SHANK2, 2 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
    nsv3907960copy number variation1nstd102humanLikely benign GRCh37 chr11: 70,557,856-70,819,038 , GRCh38.p12 chr11: 70,711,751-71,107,992 SHANK2, SHANK2-AS3, 1 more genes
    nsv3905300copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 70,390,788-70,807,254 , GRCh38.p12 chr11: 70,544,683-71,096,208 SHANK2, SHANK2-AS3, 2 more genes
    nsv3900284copy number variation1nstd102humanUncertain significance GRCh37 chr11: 70,379,263-70,927,800 , GRCh38.p12 chr11: 70,533,158-71,216,754 SHANK2-AS1, SHANK2-AS3, 2 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
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