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Items: 1 to 20 of 174

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976130inversion1nstd209human GRCh38 chr11: 89,706,927-90,017,891 , GRCh37.p13 chr11: 89,440,095-89,751,059 TRIM49, UBTFL2, 18 more genes
    nsv5925800copy number variation1nstd209human GRCh38 chr11: 89,495,583-89,923,923 , GRCh37.p13 chr11: 89,228,751-89,657,091 FOLH1B, TRIM49, 16 more genes
    nsv5597415copy number variation1nstd207human GRCh38 chr11: 89,840,713-89,840,803 , GRCh37.p13 chr11: 89,573,881-89,573,971 TRIM53BP
    nsv5513420copy number variation1nstd206human GRCh38 chr11: 89,836,896-90,043,500 , GRCh37.p13 chr11: 89,570,064-89,776,668 ANKRD33BP9, TRIM51BP, 13 more genes
    nsv5507287copy number variation1nstd206human GRCh38 chr11: 89,713,648-89,886,248 , GRCh37.p13 chr11: 89,446,816-89,619,416 TRIM64DP, UBTFL2, 9 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
    nsv5273733copy number variation1nstd204human GRCh38.p13 chr11: 89,851,401-89,859,400 , GRCh37.p13 chr11: 89,584,569-89,592,568 TRIM51BP, TRIM53BP
    nsv5272594copy number variation1nstd204human GRCh38.p13 chr11: 89,834,601-89,840,300 , GRCh37.p13 chr11: 89,567,769-89,573,468 TRIM53BP
    nsv5267606copy number variation1nstd204human GRCh37.p13 chr11: 89,475,969-89,580,268 , GRCh38.p13 chr11: 89,742,801-89,847,100 TRIM49, UBTFL2, 4 more genes
    nsv5265275copy number variation1nstd204human GRCh38.p13 chr11: 89,813,001-89,840,300 , GRCh37.p13 chr11: 89,546,169-89,573,468 LOC642414, TRIM53BP
    nsv5260814copy number variation1nstd204human GRCh38.p13 chr11: 89,850,501-89,851,100 , GRCh37.p13 chr11: 89,583,669-89,584,268 TRIM51BP, TRIM53BP
    nsv4971526copy number variation1nstd200human GRCh38 chr11: 89,816,777-89,922,160 , GRCh37.p13 chr11: 89,549,945-89,655,328 TRIM51BP, TRIM49D1, 7 more genes
    nsv4675846copy number variation1nstd102humanLikely benign GRCh37 chr11: 89,062,443-89,762,600 , GRCh38.p12 chr11: 89,329,275-90,029,432 TRIM64DP, LOC642579, 23 more genes
    nsv4675217copy number variation1nstd102humanPathogenic GRCh37 chr11: 84,830,143-92,029,933 , GRCh38.p12 chr11: 85,119,099-92,296,767 LINC02756, FNTAP1, 98 more genes
    nsv4672562copy number variation1nstd186human GRCh37 chr11: 89,584,330-89,594,855 , GRCh38.p12 chr11: 89,851,162-89,861,687 TRIM53BP, TRIM51BP
    nsv4642637copy number variation1nstd186human GRCh37 chr11: 89,520,078-89,657,031 , GRCh38.p12 chr11: 89,786,910-89,923,863 TRIM51BP, TRIM53BP, 9 more genes
    nsv4616375copy number variation2nstd183human GRCh37 chr11: 89,463,497-89,594,127 , GRCh38.p12 chr11: 89,730,329-89,860,959 TRIM49, UBTFL2, 6 more genes
    nsv4603646copy number variation1nstd183human GRCh37 chr11: 89,584,330-89,594,855 , GRCh38.p12 chr11: 89,851,162-89,861,687 TRIM51BP, TRIM53BP
    nsv4602335copy number variation1nstd183human GRCh37 chr11: 89,505,687-90,005,315 , GRCh38.p12 chr11: 89,772,519-90,272,147 UBTFL1, LOC642414, 23 more genes
    nsv4566414sequence alteration1nstd166human GRCh37.p13 chr11: 89,483,533-89,822,660 , GRCh38.p12 chr11: 89,750,365-90,089,492 TRIM49, TRIM51BP, 21 more genes
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