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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5924538copy number variation1nstd209human GRCh38 chr11: 64,732,255-64,732,530 , GRCh37.p13 chr11: 64,499,727-64,500,002 RASGRP2
    nsv5501284copy number variation1nstd206human GRCh38 chr11: 64,728,657-64,729,626 , GRCh37.p13 chr11: 64,496,129-64,497,098 RASGRP2
    nsv5497595copy number variation1nstd206human GRCh38 chr11: 64,725,136-64,725,343 , GRCh37.p13 chr11: 64,492,608-64,492,815 RASGRP2
    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
    nsv5355286translocation1nstd200human GRCh38 chr11: 64,725,136-64,725,136 , GRCh38 chr11: 64,725,343-64,725,343 , GRCh37.p13 chr11: 64,492,815-64,492,815 , GRCh37.p13 chr11: 64,492,608-64,492,608 RASGRP2
    nsv5267852copy number variation1nstd204human GRCh38.p13 chr11: 64,173,401-65,676,300 , GRCh37.p13 chr11: 63,940,873-65,443,771 , TALAM1, 103 more genes
    nsv5260664copy number variation1nstd204human GRCh37.p13 chr11: 64,363,773-64,544,972 , GRCh38.p13 chr11: 64,596,301-64,777,500 PYGM, SF1, 4 more genes
    nsv5136952mobile element insertion1nstd203human GRCh38 chr11: 64,737,897-64,737,926 , GRCh37.p13 chr11: 64,505,369-64,505,398 RASGRP2
    nsv4979803copy number variation1nstd200human GRCh38 chr11: 64,738,915-64,738,994 , GRCh37.p13 chr11: 64,506,387-64,506,466 RASGRP2
    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
    nsv4679239copy number variation1nstd189human GRCh37.p13 chr11: 64,222,931-65,140,850 , GRCh38.p12 chr11: 64,455,459-65,373,379 ARL2, VPS51, 52 more genes
    nsv4483083mobile element insertion1nstd166human GRCh37.p13 chr11: 64,513,310-64,513,310 , GRCh38.p12 chr11: 64,745,838-64,745,838 PYGM, RASGRP2
    nsv4457218copy number variation1nstd102humanUncertain significance GRCh37 chr11: 64,474,135-64,611,928 , GRCh38.p12 chr11: 64,706,663-64,844,456 CDC42BPG, RASGRP2, 5 more genes
    nsv4456749copy number variation1nstd102humanUncertain significance GRCh37 chr11: 64,396,501-64,883,447 , GRCh38.p12 chr11: 64,629,029-65,115,975 EHD1, TM7SF2, 32 more genes
    nsv4436237copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 63,533,279-65,429,676 , GRCh38.p12 chr11: 63,765,807-65,662,205 ARL2, BAD, 117 more genes
    nsv4197119copy number variation1nstd166human GRCh37.p13 chr11: 64,492,608-64,492,815 , GRCh38.p12 chr11: 64,725,136-64,725,343 RASGRP2
    nsv4196412copy number variation1nstd166human GRCh37.p13 chr11: 64,481,499-64,502,968 , GRCh38.p12 chr11: 64,714,027-64,735,496 NRXN2, RASGRP2
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3902272copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 64,501,919-67,129,258 , GRCh38.p12 chr11: 64,734,447-67,361,787 ACTN3, GRK2, 157 more genes
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