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Items: 1 to 20 of 164

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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
    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
    nsv6909810copy number variation1nstd229human GRCh38 chr11: 67,414,536-67,423,696 , GRCh37.p13 chr11: 67,182,007-67,191,167 CARNS1
    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
    nsv6902108copy number variation1nstd229human GRCh38 chr11: 67,421,001-67,505,300 , GRCh37.p13 chr11: 67,188,472-67,272,771 PITPNM1, TMEM134, 9 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
    nsv6621196copy number variation1nstd224human GRCh37 chr11: 67,176,572-67,186,613 , GRCh38.p12 chr11: 67,409,101-67,419,142 CARNS1, TBC1D10C
    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
    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
    nsv5373684translocation1nstd200human GRCh38 chr11: 67,418,439-67,418,439 , GRCh38 chr11: 67,420,978-67,420,978 , GRCh37.p13 chr11: 67,188,449-67,188,449 , GRCh37.p13 chr11: 67,185,910-67,185,910 CARNS1
    nsv5373683translocation1nstd200human GRCh38 chr11: 67,418,126-67,418,126 , GRCh38 chr11: 67,416,892-67,416,892 , GRCh37.p13 chr11: 67,184,363-67,184,363 , GRCh37.p13 chr11: 67,185,597-67,185,597 CARNS1
    nsv5345214translocation1nstd200human GRCh37 chr11: 67,188,449-67,188,449 , GRCh37 chr11: 67,185,910-67,185,910 , GRCh38.p12 chr11: 67,418,439-67,418,439 , GRCh38.p12 chr11: 67,420,978-67,420,978 CARNS1
    nsv5343286translocation1nstd200human GRCh37 chr11: 67,184,363-67,184,363 , GRCh37 chr11: 67,185,597-67,185,597 , GRCh38.p12 chr11: 67,416,892-67,416,892 , GRCh38.p12 chr11: 67,418,126-67,418,126 CARNS1
    nsv5315257copy number variation1nstd204human GRCh38.p13 chr11: 67,415,821-67,415,905 , GRCh37.p13 chr11: 67,183,292-67,183,376 CARNS1
    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
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