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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144169insertion1nstd232human GRCh37.p13 chr13: 32,746,033-32,746,033 , GRCh38.p12 chr13: 32,171,896-32,171,896 FRY
    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
    nsv7059737inversion1nstd229human GRCh38 chr13: 32,080,351-32,080,441 , GRCh37.p13 chr13: 32,654,488-32,654,578 FRY
    nsv7058180inversion1nstd229human GRCh38 chr13: 29,278,598-37,954,955 , GRCh37.p13 chr13: 29,852,735-38,529,092 ZAR1L, HSPH1, 116 more genes
    nsv6958042copy number variation1nstd229human GRCh38 chr13: 32,088,242-32,088,588 , GRCh37.p13 chr13: 32,662,379-32,662,725 FRY
    nsv6956438copy number variation1nstd229human GRCh38 chr13: 32,089,434-32,095,862 , GRCh37.p13 chr13: 32,663,571-32,669,999 FRY
    nsv6955470copy number variation1nstd229human GRCh38 chr13: 32,277,593-32,277,757 , GRCh37.p13 chr13: 32,851,730-32,851,894 FRY
    nsv6954896copy number variation1nstd229human GRCh38 chr13: 32,096,901-32,100,600 , GRCh37.p13 chr13: 32,671,038-32,674,737 FRY
    nsv6954001copy number variation1nstd229human GRCh38 chr13: 32,232,591-32,232,693 , GRCh37.p13 chr13: 32,806,728-32,806,830 FRY
    nsv6952690copy number variation1nstd229human GRCh38 chr13: 32,097,619-32,100,581 , GRCh37.p13 chr13: 32,671,756-32,674,718 FRY
    nsv6952381copy number variation1nstd229human GRCh38 chr13: 32,222,962-32,222,993 , GRCh37.p13 chr13: 32,797,099-32,797,130 FRY
    nsv6952342copy number variation1nstd229human GRCh38 chr13: 32,048,574-32,054,073 , GRCh37.p13 chr13: 32,622,711-32,628,210 FRY
    nsv6952008copy number variation1nstd229human GRCh38 chr13: 32,213,862-32,322,754 , GRCh37.p13 chr13: 32,787,999-32,896,891 ZAR1L, BRCA2, 1 more genes
    nsv6949820copy number variation1nstd229human GRCh38 chr13: 32,034,021-32,036,740 , GRCh37.p13 chr13: 32,608,158-32,610,877 FRY
    nsv6946814copy number variation1nstd229human GRCh38 chr13: 32,028,534-32,030,660 , GRCh37.p13 chr13: 32,602,671-32,604,797 FRY, FRY-AS1
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