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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093916copy number variation1nstd102humanPathogenic GRCh37 chr11: 111,657,121-111,922,093 , GRCh38.p12 chr11: 111,786,397-112,051,369 RPL37AP8, DIXDC1, 13 more genes
    nsv7093915copy number variation1nstd102humanPathogenic GRCh37 chr11: 111,171,709-111,958,707 , GRCh38.p12 chr11: 111,300,984-112,087,983 CRYAB, BTG4, 34 more genes
    nsv7093830copy number variation1nstd102humanPathogenic GRCh37 chr11: 111,171,709-111,959,745 , GRCh38.p12 chr11: 111,300,984-112,089,021 LOC100132078, DLAT, 34 more genes
    nsv7093669copy number variation2nstd102humanUncertain significance GRCh37 chr11: 111,171,709-112,104,278 , GRCh38.p12 chr11: 111,300,984-112,233,555 CRYAB, RPS6P16, 43 more genes
    nsv7074145inversion1nstd229human GRCh38 chr11: 104,112,094-113,544,164 , GRCh37.p13 chr11: 103,982,822-113,414,886 COLCA1, LOC105369491, 150 more genes
    nsv7069281inversion1nstd229human GRCh38 chr11: 107,936,485-114,400,629 , GRCh37.p13 chr11: 107,807,211-114,271,351 LRRC37A13P, POU2AF3, 121 more genes
    nsv7065935inversion1nstd229human GRCh38 chr11: 107,044,115-113,544,291 , GRCh37.p13 chr11: 106,914,841-113,415,013 LINC02762, TIMM8B, 112 more genes
    nsv6917646copy number variation1nstd229human GRCh38 chr11: 111,947,121-111,954,451 , GRCh37.p13 chr11|NW_003871080.1: 199,112-206,442 , GRCh37.p13 chr11: 111,817,845-111,825,175 DIXDC1
    nsv6916344copy number variation1nstd229human GRCh38 chr11: 111,909,401-112,149,800 , GRCh37.p13 chr11: 111,780,125-111,945,380 , GRCh37.p13 chr11|NW_003871080.1: 161,392-326,647 SDHD, TIMM8B, 12 more genes
    nsv6915233copy number variation1nstd229human GRCh38 chr11: 112,015,488-112,018,277 , GRCh37.p13 chr11|NW_003871080.1: 267,479-270,268 , GRCh37.p13 chr11: 111,886,212-111,889,001 DIXDC1
    nsv6912378copy number variation1nstd229human GRCh38 chr11: 111,954,075-111,968,024 , GRCh37.p13 chr11: 111,824,799-111,838,748 , GRCh37.p13 chr11|NW_003871080.1: 206,066-220,015 DIXDC1
    nsv6898629copy number variation1nstd229human GRCh38 chr11: 111,807,347-111,971,481 , GRCh37.p13 chr11: 111,678,071-111,842,205 , GRCh37.p13 chr11|NW_003871080.1: 59,339-223,472 RNA5SP351, HSPB2, 9 more genes
    nsv6637811copy number variation1nstd102humanPathogenic GRCh37 chr11: 109,328,787-116,414,966 , GRCh38.p12 chr11: 109,458,061-116,544,249 LOC102723966, NXPE4, 129 more genes
    nsv6620949copy number variation1nstd224human GRCh37 chr11: 111,608,216-111,856,033 , GRCh38.p12 chr11: 111,737,492-111,985,309 PPP2R1B, DIXDC1, 10 more genes
    nsv6592859inversion1nstd223human GRCh38 chr11: 111,952,062-111,952,566 , GRCh37.p13 chr11|NW_003871080.1: 204,053-204,557 , GRCh37.p13 chr11: 111,822,786-111,823,290 DIXDC1
    nsv6586218inversion1nstd223human GRCh38 chr11: 107,936,497-114,408,912 , GRCh37.p13 chr11: 107,807,223-114,279,634 LOC107984390, ATF4P4, 121 more genes
    nsv6582771inversion1nstd223human GRCh38 chr11: 111,989,389-111,990,078 , GRCh37.p13 chr11: 111,860,113-111,860,802 , GRCh37.p13 chr11|NW_003871080.1: 241,380-242,069 DIXDC1
    nsv6470062copy number variation1nstd223human GRCh38 chr11: 111,928,660-111,936,507 , GRCh37.p13 chr11|NW_003871080.1: 180,651-188,498 , GRCh37.p13 chr11: 111,799,384-111,807,231 DIXDC1, RNA5SP351
    nsv6462538copy number variation1nstd223human GRCh38 chr11: 111,969,420-111,973,048 , GRCh37.p13 chr11|NW_003871080.1: 221,411-225,039 , GRCh37.p13 chr11: 111,840,144-111,843,772 DIXDC1
    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
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