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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970839inversion1nstd209human GRCh38 chr11: 74,527,352-75,035,369 , GRCh37.p13 chr11: 74,238,397-74,746,414 SPCS2, POLD3, 14 more genes
    nsv5494028copy number variation1nstd206human GRCh38 chr11: 74,225,600-74,828,943 , GRCh37.p13 chr11: 73,936,645-74,539,988 RNF169, MIR4696, 19 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
    nsv5373719translocation1nstd200human GRCh38 chr11: 74,650,211-74,650,211 , GRCh38 chr11: 74,650,875-74,650,875 , GRCh37.p13 chr11: 74,361,256-74,361,256 , GRCh37.p13 chr11: 74,361,920-74,361,920 RANP3, POLD3
    nsv5373718translocation1nstd200human GRCh38 chr11: 74,650,878-74,650,878 , GRCh38 chr11: 74,647,140-74,647,140 , GRCh37.p13 chr11: 74,361,923-74,361,923 , GRCh37.p13 chr11: 74,358,185-74,358,185 POLD3, RANP3
    nsv5342439translocation1nstd200human GRCh37 chr11: 74,358,185-74,358,185 , GRCh37 chr11: 74,361,923-74,361,923 , GRCh38.p12 chr11: 74,647,140-74,647,140 , GRCh38.p12 chr11: 74,650,878-74,650,878 POLD3, RANP3
    nsv4987311copy number variation1nstd200human GRCh38 chr11: 74,651,210-74,653,399 , GRCh37.p13 chr11: 74,362,255-74,364,444 POLD3, RANP3
    nsv4418797copy number variation1nstd174human GRCh37 chr11: 73,936,645-74,539,988 , GRCh38.p12 chr11: 74,225,600-74,828,943 POLD3, CHRDL2, 19 more genes
    nsv4335968sequence alteration1nstd166human GRCh37.p13 chr11: 74,358,184-74,361,945 , GRCh38.p12 chr11: 74,647,139-74,650,900 POLD3, RANP3
    nsv3918639copy number variation1nstd102humanUncertain significance GRCh38 chr11: 74,648,822-74,907,890 , GRCh37 chr11: 74,359,867-74,618,935 , NCBI36 chr11: 74,037,515-74,296,583 RN7SKP297, RANP3, 8 more genes
    nsv3916301copy number variation1nstd102humanPathogenic GRCh38 chr11: 71,928,796-77,064,521 , GRCh37 chr11: 71,639,842-76,751,808 , NCBI36 chr11: 71,317,490-76,453,216 RN7SL786P, LIPT2-AS1, 146 more genes
    nsv3915804copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,680,927-77,943,941 , NCBI36 chr11: 71,358,575-77,621,589 , GRCh38 chr11: 71,969,881-78,232,895 TPBGL, MAP6, 173 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
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3898361copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202 SESN3, LOC107984352, 694 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
    nsv3152203copy number variation1nstd151human GRCh37 chr11: 74,305,103-74,563,130 , GRCh38.p12 chr11: 74,594,058-74,852,085 CHRDL2, RNF169, 8 more genes
    nsv3142081copy number variation1nstd151human GRCh37 chr11: 71,668,270-74,638,536 , GRCh38.p12 chr11: 71,957,224-74,927,491 , RPL36AP38, 92 more genes
    nsv3141404copy number variation1nstd151human GRCh37 chr11: 74,305,103-74,556,319 , GRCh38.p12 chr11: 74,594,058-74,845,274 XRRA1, RN7SKP297, 8 more genes
    esv4009164inversion1estd231human GRCh37 chr11: 74,238,397-74,746,415 , GRCh38.p12 chr11: 74,527,352-75,035,370 SPCS2, POLD3, 14 more genes
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