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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098787copy number variation1nstd102humanUncertain significance GRCh37 chr6: 32,148,920-36,953,949 , GRCh38.p12 chr6: 32,181,143-36,986,173 CUTA, SYNGAP1, 184 more genes
    nsv7097823copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 35,471,316-35,471,645 , GRCh38.p12 chr6: 35,503,539-35,503,868 TULP1
    nsv7097426copy number variation1nstd102humanUncertain significance GRCh37 chr6: 30,695,893-36,953,949 , GRCh38.p12 chr6: 30,728,116-36,986,173 LEMD2, PSORS1C1, 321 more genes
    nsv7097058copy number variation1nstd102humanUncertain significance GRCh37 chr6: 35,476,966-35,480,635 , GRCh38.p12 chr6: 35,509,189-35,512,858 TULP1
    nsv7093046copy number variation1nstd102humanPathogenic GRCh38 chr6: 35,511,690-35,512,213 , GRCh37 chr6: 35,479,467-35,479,990 TULP1
    nsv7053830inversion1nstd229human GRCh38 chr6: 29,164,448-38,692,657 , GRCh37.p13 chr6: 29,132,225-38,660,433 GTF2H4, RNF8, 472 more genes
    nsv7046831inversion1nstd229human GRCh38 chr6: 35,228,579-36,340,036 , GRCh37.p13 chr6: 35,196,356-36,307,813 MAPK14, TEAD3, 34 more genes
    nsv7045112inversion1nstd229human GRCh38 chr6: 30,561,326-37,907,708 , GRCh37.p13 chr6: 30,529,103-37,875,484 ZBTB22, PNPLA1, 355 more genes
    nsv6792571copy number variation1nstd229human GRCh38 chr6: 35,492,285-35,505,402 , GRCh37.p13 chr6: 35,460,062-35,473,179 TULP1, TEAD3
    nsv6786151copy number variation1nstd229human GRCh38 chr6: 35,501,540-35,501,624 , GRCh37.p13 chr6: 35,469,317-35,469,401 TULP1
    nsv6570358inversion1nstd223human GRCh38 chr6: 32,570,902-37,403,160 , GRCh37.p13 chr6: 32,538,679-37,370,936 RN7SL273P, MKRN6P, 177 more genes
    nsv6565343inversion1nstd223human GRCh38 chr6: 32,527,987-37,402,848 , GRCh37.p13 chr6: 32,495,764-37,370,624 LOC105375022, SNRPC, 180 more genes
    nsv6562119inversion1nstd223human GRCh38 chr6: 32,527,628-37,403,016 , GRCh37.p13 chr6: 32,495,405-37,370,792 HLA-Z, ARMC12, 180 more genes
    nsv6556866inversion1nstd223human GRCh38 chr6: 32,527,208-37,403,016 , GRCh37.p13 chr6: 32,494,985-37,370,792 BAK1, HSD17B8, 180 more genes
    nsv6401356copy number variation1nstd223human GRCh38 chr6: 35,507,944-35,546,005 , GRCh37.p13 chr6: 35,475,721-35,513,782 TULP1, LOC101929309
    nsv6312037copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 35,473,498-35,474,076 , GRCh38.p12 chr6: 35,505,721-35,506,299 TULP1
    nsv6300788copy number variation1nstd186human GRCh37 chr6: 35,475,694-35,513,751 , GRCh38.p12 chr6: 35,507,917-35,545,974 LOC101929309, TULP1
    nsv6265611copy number variation1nstd214human GRCh38 chr6: 35,501,540-35,501,623 , GRCh37.p13 chr6: 35,469,317-35,469,400 TULP1
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv5889578copy number variation1nstd209human GRCh38 chr6: 35,501,540-35,501,623 , GRCh37.p13 chr6: 35,469,317-35,469,400 TULP1
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