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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142993copy number variation1nstd232human GRCh37.p13 chr11: 67,166,323-67,166,405 , GRCh38.p12 chr11: 67,398,852-67,398,934 PPP1CA, RAD9A
    nsv7139690copy number variation1nstd232human GRCh37.p13 chr11: 67,166,116-67,166,191 , GRCh38.p12 chr11: 67,398,645-67,398,720 PPP1CA, RAD9A
    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
    nsv6913713copy number variation1nstd229human GRCh38 chr11: 67,266,401-67,465,100 , GRCh37.p13 chr11: 67,033,872-67,232,571 RNU6-1238P, TMEM134, 16 more genes
    nsv6912757copy number variation1nstd229human GRCh38 chr11: 66,793,001-68,121,500 , GRCh37.p13 chr11: 66,560,472-67,888,967 CHKA-DT, LOC107984341, 66 more genes
    nsv6909452copy number variation1nstd229human GRCh38 chr11: 67,391,601-67,508,800 , GRCh37.p13 chr11: 67,159,072-67,276,271 PPP1CA, TBC1D10C, 14 more genes
    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
    nsv6898634copy number variation1nstd229human GRCh38 chr11: 67,266,601-67,521,900 , GRCh37.p13 chr11: 67,034,072-67,289,371 GRK2, CARNS1, 21 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
    nsv6132373copy number variation1nstd213human GRCh37 chr11: 67,070,000-67,200,001 , GRCh38.p12 chr11: 67,302,529-67,432,530 RPS6KB2, SSH3, 10 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
    nsv6037184copy number variation1nstd212human GRCh38 chr11: 67,401,910-67,401,990 , GRCh37.p13 chr11: 67,169,381-67,169,461 TBC1D10C, PPP1CA
    nsv5503861copy number variation1nstd206human GRCh38 chr11: 67,401,916-67,401,990 , GRCh37.p13 chr11: 67,169,387-67,169,461 PPP1CA, TBC1D10C
    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
    nsv5355313translocation1nstd200human GRCh38 chr11: 67,401,916-67,401,916 , GRCh38 chr11: 67,401,990-67,401,990 , GRCh37.p13 chr11: 67,169,461-67,169,461 , GRCh37.p13 chr11: 67,169,387-67,169,387 TBC1D10C, PPP1CA
    nsv5345380translocation1nstd200human GRCh37 chr11: 67,169,461-67,169,461 , GRCh37 chr11: 67,169,387-67,169,387 , GRCh38.p12 chr11: 67,401,990-67,401,990 , GRCh38.p12 chr11: 67,401,916-67,401,916 TBC1D10C, PPP1CA
    nsv5279549copy number variation1nstd204human GRCh38.p13 chr11: 67,318,601-67,507,600 , GRCh37.p13 chr11: 67,086,072-67,275,071 TMEM134, PTPRCAP, 17 more genes
    nsv5275203copy number variation1nstd204human GRCh38.p13 chr11: 66,946,001-67,700,500 , GRCh37.p13 chr11: 66,713,472-67,467,971 , PC, 38 more genes
    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
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