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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3870510copy number variation1nstd102humanLikely pathogenic GRCh38 chr3: 188,420,063-188,540,464 , GRCh37.p13 chr3: 188,137,851-188,258,252 LPP
    nsv3878782copy number variation1nstd102humanLikely pathogenic GRCh38 chr3: 188,343,948-188,435,451 , GRCh37.p13 chr3: 188,061,736-188,153,239 LPP
    nsv3881074copy number variation1nstd102humanBenign GRCh37 chr3: 188,292,489-188,343,729 , GRCh38.p12 chr3: 188,574,701-188,625,941 LPP
    nsv3876606copy number variation1nstd102humanUncertain significance GRCh37 chr3: 187,984,856-188,266,575 , GRCh38.p12 chr3: 188,267,068-188,548,787 LPP
    nsv3880732copy number variation1nstd102humanUncertain significance GRCh37 chr3: 187,908,490-187,979,733 , GRCh38.p12 chr3: 188,190,702-188,261,945 LPP
    nsv3885147copy number variation1nstd102humanLikely benign GRCh37 chr3: 187,894,262-187,988,945 , GRCh38.p12 chr3: 188,176,474-188,271,157 LPP, FLJ42393
    nsv3915422copy number variation1nstd102humanUncertain significance NCBI36 chr3: 189,691,595-189,871,987 , GRCh37 chr3: 188,208,901-188,389,293 , GRCh38 chr3: 188,491,113-188,671,505 LPP, LPP-AS1
    nsv6291623copy number variation1nstd102humanUncertain significance GRCh38 chr3: 188,671,476-188,811,213 , GRCh37.p13 chr3: 188,389,264-188,529,001 LPP, MIR28
    nsv4728536copy number variation1nstd102humanUncertain significance GRCh37 chr3: 188,298,331-188,428,340 , GRCh38.p12 chr3: 188,580,543-188,710,552 LPP, MIR28
    nsv6636886copy number variation1nstd102humanUncertain significance GRCh37 chr3: 188,199,479-188,298,755 , GRCh38.p12 chr3: 188,481,691-188,580,967 LPP, LPP-AS1
    nsv3924139copy number variation1nstd102humanUncertain significance NCBI36 chr3: 189,879,228-189,914,237 , GRCh37 chr3: 188,396,534-188,431,543 , GRCh38 chr3: 188,678,746-188,713,755 LPP, MIR28
    nsv3922391copy number variation1nstd102humanLikely benign NCBI36 chr3: 189,640,349-189,963,525 , GRCh37 chr3: 188,157,655-188,480,831 , GRCh38 chr3: 188,439,867-188,763,043 LPP, MIR28, 1 more genes
    nsv3888952copy number variation1nstd102humanBenign GRCh37 chr3: 188,584,679-188,781,109 , GRCh38.p12 chr3: 188,866,891-189,063,320 LPP, TPRG1-AS1, 3 more genes
    nsv3875423copy number variation1nstd102humanBenign GRCh37 chr3: 187,865,100-187,979,733 , GRCh38.p12 chr3: 188,147,312-188,261,945 LPP, FLJ42393, 1 more genes
    nsv3915488copy number variation1nstd102humanPathogenic GRCh37 chr3: 185,203,637-197,837,049 , NCBI36 chr3: 186,686,331-199,321,446 , GRCh38 chr3: 185,485,849-198,110,178 LPP, SNAR-I, 260 more genes
    nsv3914166copy number variation1nstd102humanPathogenic GRCh37 chr3: 180,856,452-192,229,812 , GRCh38 chr3: 181,138,664-192,512,023 , NCBI36 chr3: 182,339,146-193,712,506 LPP, SNORA4, 199 more genes
    nsv3920607copy number variation1nstd102humanPathogenic NCBI36 chr3: 187,082,628-197,946,692 , GRCh37.p13 chr3: 185,599,934-196,462,295 , GRCh38.p12 chr3: 185,882,146-196,735,424 LPP, FGF12, 212 more genes
    nsv3882335copy number variation1nstd102humanPathogenic GRCh37 chr3: 182,650,681-191,275,809 , GRCh38.p12 chr3: 182,932,893-191,558,020 LPP, VPS8, 171 more genes
    nsv3918718copy number variation1nstd102humanPathogenic GRCh37 chr3: 186,482,937-194,130,145 , NCBI36 chr3: 187,965,631-195,611,434 , GRCh38 chr3: 186,765,148-194,409,416 LPP, TPRG1-AS1, 114 more genes
    nsv3920718copy number variation1nstd102humanPathogenic NCBI36 chr3: 188,646,713-196,231,151 , GRCh37 chr3: 187,164,019-194,749,862 , GRCh38 chr3: 187,446,231-195,029,133 LPP, LOC105374283, 105 more genes
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