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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146876insertion1nstd232human GRCh37.p13 chr5: 38,489,347-38,489,347 , GRCh38.p12 chr5: 38,489,245-38,489,245 LIFR
    nsv7097139copy number variation1nstd102humanUncertain significance GRCh37 chr5: 33,944,753-39,364,566 , GRCh38.p12 chr5: 33,944,648-39,364,464 RNU7-75P, UGT3A1, 77 more genes
    nsv7096774copy number variation1nstd102humanPathogenic GRCh37 chr5: 38,484,867-38,486,092 , GRCh38.p12 chr5: 38,484,765-38,485,990 LIFR
    nsv7055674inversion1nstd229human GRCh38 chr5: 38,533,635-38,541,444 , GRCh37.p13 chr5: 38,533,737-38,541,546 LIFR
    nsv6776604copy number variation1nstd229human GRCh38 chr5: 38,259,807-38,533,091 , GRCh37.p13 chr5: 38,259,909-38,533,193 LIFR, LOC105374732, 3 more genes
    nsv6776581copy number variation1nstd229human GRCh38 chr5: 38,532,019-38,538,502 , GRCh37.p13 chr5: 38,532,121-38,538,604 LIFR
    nsv6775887copy number variation1nstd229human GRCh38 chr5: 38,510,905-38,510,962 , GRCh37.p13 chr5: 38,511,007-38,511,064 LIFR
    nsv6775050copy number variation1nstd229human GRCh38 chr5: 38,597,809-38,803,173 , GRCh37.p13 chr5: 38,597,911-38,803,275 LINC01265, LIFR-AS1, 4 more genes
    nsv6773463copy number variation1nstd229human GRCh38 chr5: 38,235,356-38,548,343 , GRCh37.p13 chr5: 38,235,458-38,548,445 LIFR, EGFLAM-AS2, 3 more genes
    nsv6771552copy number variation1nstd229human GRCh38 chr5: 38,479,212-38,492,191 , GRCh37.p13 chr5: 38,479,314-38,492,293 LIFR
    nsv6770953copy number variation1nstd229human GRCh38 chr5: 38,592,332-38,601,743 , GRCh37.p13 chr5: 38,592,434-38,601,845 LIFR, LIFR-AS1
    nsv6770551copy number variation1nstd229human GRCh38 chr5: 38,472,611-38,472,795 , GRCh37.p13 chr5: 38,472,713-38,472,897 LIFR
    nsv6769429copy number variation1nstd229human GRCh38 chr5: 35,077,787-40,637,192 , GRCh37.p13 chr5: 35,077,889-40,637,294 LINC02110, LOC105374735, 68 more genes
    nsv6768854copy number variation1nstd229human GRCh38 chr5: 38,584,331-38,596,679 , GRCh37.p13 chr5: 38,584,433-38,596,781 LIFR, LIFR-AS1
    nsv6768132copy number variation1nstd229human GRCh38 chr5: 38,386,101-38,519,700 , GRCh37.p13 chr5: 38,386,203-38,519,802 LOC105374732, LIFR, 2 more genes
    nsv6765538copy number variation1nstd229human GRCh38 chr5: 38,505,784-38,515,110 , GRCh37.p13 chr5: 38,505,886-38,515,212 LIFR
    nsv6764301copy number variation1nstd229human GRCh38 chr5: 37,395,324-40,706,253 , GRCh37.p13 chr5: 37,395,426-40,706,355 DAB2, LOC107986414, 39 more genes
    nsv6763625copy number variation1nstd229human GRCh38 chr5: 38,572,515-38,575,777 , GRCh37.p13 chr5: 38,572,617-38,575,879 LIFR-AS1, LOC105374735, 1 more genes
    nsv6763611copy number variation1nstd229human GRCh38 chr5: 38,272,738-38,527,551 , GRCh37.p13 chr5: 38,272,840-38,527,653 EGFLAM-AS4, EGFLAM-AS2, 3 more genes
    nsv6763475copy number variation1nstd229human GRCh38 chr5: 38,506,985-38,510,465 , GRCh37.p13 chr5: 38,507,087-38,510,567 LIFR
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