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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098720copy number variation1nstd102humanPathogenic GRCh38 chr6: 31,111,325-31,129,674 , GRCh37.p13 chr6: 31,079,102-31,097,451 C6orf15, CDSN, 1 more genes
    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
    nsv7097325copy number variation1nstd102humanUncertain significance GRCh37 chr6: 30,695,893-31,937,492 , GRCh38.p12 chr6: 30,728,116-31,969,715 HCG21, SNORD84, 117 more genes
    nsv7053830inversion1nstd229human GRCh38 chr6: 29,164,448-38,692,657 , GRCh37.p13 chr6: 29,132,225-38,660,433 GTF2H4, RNF8, 472 more genes
    nsv7045629inversion1nstd229human GRCh38 chr6: 30,007,594-31,355,527 , GRCh37.p13 chr6: 29,975,371-31,323,304 USP8P1, LINC02571, 82 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
    nsv6797723copy number variation1nstd229human GRCh38 chr6: 31,087,810-31,117,274 , GRCh37.p13 chr6: 31,055,587-31,085,051 CDSN, C6orf15, 1 more genes
    nsv6795673copy number variation1nstd229human GRCh38 chr6: 30,444,101-31,201,100 , GRCh37.p13 chr6: 30,411,878-31,168,877 POU5F1, DDR1, 51 more genes
    nsv6794381copy number variation1nstd229human GRCh38 chr6: 31,132,409-31,132,465 , GRCh37.p13 chr6: 31,100,186-31,100,242 PSORS1C1
    nsv6794247copy number variation1nstd229human GRCh38 chr6: 30,380,601-31,245,000 , GRCh37.p13 chr6: 30,348,378-31,212,777 MUC22, TMPOP1, 52 more genes
    nsv6790648copy number variation1nstd229human GRCh38 chr6: 31,117,532-31,120,333 , GRCh37.p13 chr6: 31,085,309-31,088,110 CDSN, PSORS1C1
    nsv6778623copy number variation1nstd229human GRCh38 chr6: 31,117,528-31,120,333 , GRCh37.p13 chr6: 31,085,305-31,088,110 CDSN, PSORS1C1
    nsv6562568inversion1nstd223human GRCh38 chr6: 29,766,029-31,471,345 , GRCh37.p13 chr6: 29,733,806-31,439,122 HCG4P9, LINC01149, 126 more genes
    nsv6555679inversion1nstd223human GRCh38 chr6: 31,134,980-31,135,927 , GRCh37.p13 chr6: 31,102,757-31,103,704 PSORS1C1, PSORS1C2
    nsv6397037copy number variation1nstd223human GRCh38 chr6: 31,134,416-31,134,930 , GRCh37.p13 chr6: 31,102,193-31,102,707 PSORS1C1
    nsv6289880copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 28,005,012-31,683,185 , GRCh38.p12 chr6: 28,037,234-31,715,408 ABCF1, AIF1, 313 more genes
    nsv6135918copy number variation1nstd213human GRCh37 chr6: 30,870,000-31,240,001 , GRCh38.p12 chr6: 30,902,223-31,272,224 CDSN, GTF2H4, 19 more genes
    nsv6135917copy number variation1nstd213human GRCh37 chr6: 30,110,000-32,450,001 , GRCh38.p12 chr6: 30,142,223-32,482,224 ABCF1, AGER, 186 more genes
    nsv6008554copy number variation1nstd212human GRCh38 chr6: 31,132,407-31,132,460 , GRCh37.p13 chr6: 31,100,184-31,100,237 PSORS1C1
    nsv5901223copy number variation1nstd209human GRCh38 chr6: 31,132,407-31,132,459 , GRCh37.p13 chr6: 31,100,184-31,100,236 PSORS1C1
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