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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3871099copy number variation1nstd102humanLikely pathogenic GRCh38 chr3: 60,389,119-60,571,624 , GRCh37.p13 chr3: 60,374,852-60,557,357 FHIT
    nsv3880322copy number variation1nstd102humanLikely pathogenic GRCh38 chr3: 60,501,297-60,591,815 , GRCh37.p13 chr3: 60,487,030-60,558,331 FHIT
    nsv5060001copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 60,468,409-60,490,104 , GRCh38 chr3: 60,482,676-60,504,371 FHIT
    nsv3887572copy number variation1nstd102humanBenign GRCh37 chr3: 60,068,730-60,276,722 , GRCh38.p12 chr3: 60,083,004-60,290,993 FHIT
    nsv6291419copy number variation1nstd102humanLikely benign GRCh37 chr3: 60,350,678-60,532,439 , GRCh38.p12 chr3: 60,364,946-60,546,706 FHIT
    nsv3878060copy number variation1nstd102humanBenign GRCh37 chr3: 60,421,119-60,576,769 , GRCh38.p12 chr3: 60,435,386-60,591,036 FHIT
    nsv3916487copy number variation1nstd102humanLikely benign GRCh37 chr3: 60,088,475-60,240,653 , GRCh38 chr3: 60,102,749-60,254,925 , NCBI36 chr3: 60,063,515-60,215,693 FHIT
    nsv3914596copy number variation1nstd102humanBenign GRCh38 chr3: 60,102,627-60,254,729 , GRCh37 chr3: 60,088,353-60,240,457 , NCBI36 chr3: 60,063,393-60,215,497 FHIT
    nsv3917551copy number variation1nstd102humanBenign GRCh37 chr3: 60,089,314-60,237,710 , GRCh38 chr3: 60,103,588-60,251,982 FHIT
    nsv3882478copy number variation1nstd102humanLikely benign GRCh37 chr3: 60,382,706-60,472,496 , GRCh38.p12 chr3: 60,396,973-60,486,763 FHIT
    nsv3884823copy number variation1nstd102humanBenign GRCh37 chr3: 60,333,449-60,423,009 , GRCh38.p12 chr3: 60,347,718-60,437,276 FHIT
    nsv3888191copy number variation1nstd102humanBenign GRCh37 chr3: 60,445,253-60,512,889 , GRCh38.p12 chr3: 60,459,520-60,527,156 FHIT
    nsv3872742copy number variation1nstd102humanBenign GRCh37 chr3: 60,403,658-60,428,024 , GRCh38.p12 chr3: 60,417,925-60,442,291 FHIT
    nsv3881233copy number variation1nstd102humanBenign GRCh37 chr3: 60,441,079-60,465,279 , GRCh38.p12 chr3: 60,455,346-60,479,546 FHIT
    nsv3881812copy number variation1nstd102humanBenign GRCh37 chr3: 60,819,003-60,843,086 , GRCh38.p12 chr3: 60,833,342-60,857,414 FHIT
    nsv3874972copy number variation1nstd102humanBenign GRCh37 chr3: 60,330,356-60,351,746 , GRCh38.p12 chr3: 60,344,625-60,366,014 FHIT
    nsv3880128copy number variation1nstd102humanBenign GRCh37 chr3: 59,946,354-59,961,536 , GRCh38.p12 chr3: 59,960,628-59,975,810 FHIT
    nsv3875978copy number variation1nstd102humanBenign GRCh37 chr3: 61,036,905-61,046,212 , GRCh38.p12 chr3: 61,051,233-61,060,540 FHIT
    nsv3885315copy number variation1nstd102humanBenign GRCh37 chr3: 61,122,318-61,127,981 , GRCh38.p12 chr3: 61,136,645-61,142,308 FHIT
    nsv3874770copy number variation1nstd102humanBenign GRCh37 chr3: 61,127,205-61,132,698 , GRCh38.p12 chr3: 61,141,532-61,147,025 FHIT
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