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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5889540copy number variation1nstd209human GRCh38 chr5: 5,034,369-5,034,441 , GRCh37.p13 chr5: 5,034,482-5,034,554 LINC01020
    nsv5842752copy number variation1nstd209human GRCh38 chr5: 5,050,451-5,051,550 , GRCh37.p13 chr5: 5,050,564-5,051,663 LINC01020
    nsv5469250copy number variation1nstd206human GRCh38 chr5: 5,036,516-5,036,885 , GRCh37.p13 chr5: 5,036,629-5,036,998 LINC01020
    nsv5460754copy number variation1nstd206human GRCh38 chr5: 5,034,369-5,034,442 , GRCh37.p13 chr5: 5,034,482-5,034,555 LINC01020
    nsv5459261copy number variation1nstd206human GRCh38 chr5: 4,951,414-5,428,388 , GRCh37.p13 chr5: 4,951,527-5,428,501 MTCO1P30, LOC105374630, 10 more genes
    nsv5381771copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716 OTULINL, AKTIPP2, 317 more genes
    nsv5377837translocation1nstd200human GRCh38 chr5: 5,034,442-5,034,442 , GRCh38 chr5: 5,034,369-5,034,369 , GRCh37.p13 chr5: 5,034,555-5,034,555 , GRCh37.p13 chr5: 5,034,482-5,034,482 LINC01020
    nsv5345996translocation1nstd200human GRCh37 chr5: 5,034,482-5,034,482 , GRCh37 chr5: 5,034,555-5,034,555 , GRCh38.p12 chr5: 5,034,369-5,034,369 , GRCh38.p12 chr5: 5,034,442-5,034,442 LINC01020
    nsv4946318copy number variation1nstd200human GRCh38 chr5: 5,069,173-5,077,320 , GRCh37.p13 chr5: 5,069,286-5,077,433 LINC01020, LINC02121
    nsv4946317copy number variation1nstd200human GRCh38 chr5: 5,063,156-5,063,978 , GRCh37.p13 chr5: 5,063,269-5,064,091 LINC01020
    nsv4944321copy number variation1nstd200human GRCh38 chr5: 5,049,827-5,071,247 , GRCh37.p13 chr5: 5,049,940-5,071,360 LINC01020, LINC02121
    nsv4944320copy number variation1nstd200human GRCh38 chr5: 4,953,613-5,261,231 , GRCh37.p13 chr5: 4,953,726-5,261,344 LOC101929200, LOC105374630, 5 more genes
    nsv4808601copy number variation1nstd200human GRCh37 chr5: 5,069,286-5,077,433 , GRCh38.p12 chr5: 5,069,173-5,077,320 LINC02121, LINC01020
    nsv4729287copy number variation1nstd102humanUncertain significance GRCh37 chr5: 4,798,963-5,166,195 , GRCh38.p12 chr5: 4,798,850-5,166,082 ADAMTS16, LOC107986400, 6 more genes
    nsv4685752copy number variation1nstd102humanPathogenic GRCh37 chr5: 71,904-22,078,969 , GRCh38.p12 chr5: 71,789-22,078,860 LINC01377, LOC100421308, 277 more genes
    nsv4674705copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-5,657,333 , GRCh38.p12 chr5: 113,461-5,657,220 LOC101929898, MIR4635, 90 more genes
    nsv4674497copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-14,738,180 , GRCh38.p12 chr5: 113,461-14,738,071 LOC101929003, MTCYBP37, 192 more genes
    nsv4674444copy number variation1nstd102humanPathogenic GRCh37 chr5: 1,322,680-10,762,544 , GRCh38.p12 chr5: 1,322,565-10,762,432 LOC100132773, LINC01019, 125 more genes
    nsv4674161copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-23,364,376 , GRCh38.p12 chr5: 113,461-23,364,267 LOC102723561, LOC107986397, 287 more genes
    nsv4674139copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-5,194,484 , GRCh38.p12 chr5: 113,461-5,194,371 BRD9, LOC100310782, 84 more genes
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