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Items: 1 to 20 of 136

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098748copy number variation1nstd102humanPathogenic GRCh37 chr13: 32,308,520-32,940,606 , GRCh38.p12 chr13: 31,734,383-32,366,469 BRCA2, FRY, 5 more genes
    nsv7094072copy number variation1nstd102humanUncertain significance GRCh37 chr13: 31,033,232-33,638,323 , GRCh38.p12 chr13: 30,459,095-33,064,186 N4BP2L2, RNY1P4, 37 more genes
    nsv7093387copy number variation1nstd102humannot provided GRCh37 chr13: 31,841,196-36,667,007 , GRCh38.p12 chr13: 31,267,059-36,092,870 VDAC1P12, LOC107984589, 44 more genes
    nsv7075032inversion1nstd229human GRCh38 chr13: 30,791,896-33,130,541 , GRCh37.p13 chr13: 31,366,033-33,704,678 BRCA2, TEX26, 31 more genes
    nsv7069550inversion1nstd229human GRCh38 chr13: 31,196,586-33,130,540 , GRCh37.p13 chr13: 31,770,723-33,704,677 BRCA2, ZAR1L, 21 more genes
    nsv7068176inversion1nstd229human GRCh38 chr13: 30,840,951-32,715,747 , GRCh37.p13 chr13: 31,415,088-33,289,884 MEDAG, N4BP2L1, 25 more genes
    nsv7058180inversion1nstd229human GRCh38 chr13: 29,278,598-37,954,955 , GRCh37.p13 chr13: 29,852,735-38,529,092 ZAR1L, HSPH1, 116 more genes
    nsv6946814copy number variation1nstd229human GRCh38 chr13: 32,028,534-32,030,660 , GRCh37.p13 chr13: 32,602,671-32,604,797 FRY, FRY-AS1
    nsv6938137copy number variation1nstd229human GRCh38 chr13: 32,030,566-32,242,738 , GRCh37.p13 chr13: 32,604,703-32,816,875 FRY, FRY-AS1
    nsv6936097copy number variation1nstd229human GRCh38 chr13: 32,001,190-32,023,210 , GRCh37.p13 chr13: 32,575,327-32,597,347 FRY-AS1
    nsv6926674copy number variation1nstd229human GRCh38 chr13: 31,972,901-32,058,400 , GRCh37.p13 chr13: 32,547,038-32,632,537 FRY, FRY-AS1
    nsv6924346copy number variation1nstd229human GRCh38 chr13: 31,409,618-33,230,882 , GRCh37.p13 chr13: 31,983,755-33,805,019 TOMM22P3, IFIT1P1, 19 more genes
    nsv6918792copy number variation1nstd229human GRCh38 chr13: 31,486,559-32,100,330 , GRCh37.p13 chr13: 32,060,696-32,674,467 LOC105370152, FRY, 3 more genes
    nsv6918690copy number variation1nstd229human GRCh38 chr13: 31,496,428-32,268,695 , GRCh37.p13 chr13: 32,070,565-32,842,832 LOC105370152, FRY, 3 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6622041copy number variation1nstd224human GRCh37 chr13: 32,478,828-32,629,771 , GRCh38.p12 chr13: 31,904,691-32,055,634 FRY, EEF1DP3, 1 more genes
    nsv6491145copy number variation1nstd223human GRCh38 chr13: 32,027,901-32,037,500 , GRCh37.p13 chr13: 32,602,038-32,611,637 FRY-AS1, FRY
    nsv6489286copy number variation1nstd223human GRCh38 chr13: 32,029,501-32,034,200 , GRCh37.p13 chr13: 32,603,638-32,608,337 FRY-AS1, FRY
    nsv6486090copy number variation1nstd223human GRCh38 chr13: 31,496,428-32,268,696 , GRCh37.p13 chr13: 32,070,565-32,842,833 FRY, EEF1DP3, 3 more genes
    nsv6480373copy number variation1nstd223human GRCh38 chr13: 32,001,191-32,023,209 , GRCh37.p13 chr13: 32,575,328-32,597,346 FRY-AS1
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