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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3877695copy number variation1nstd102humanBenign GRCh37 chr3: 16,239,634-16,242,101 , GRCh38.p12 chr3: 16,198,127-16,200,594 GALNT15
    nsv3872175copy number variation1nstd102humanUncertain significance GRCh37 chr4: 174,106,348-174,175,781 , GRCh38.p12 chr4: 173,185,197-173,254,630 GALNT7
    nsv3880313copy number variation1nstd102humanBenign GRCh37 chr4: 174,083,622-174,091,110 , GRCh38.p12 chr4: 173,162,471-173,169,959 GALNT7, GALNT7-DT
    nsv3879016copy number variation1nstd102humanBenign GRCh37 chr4: 174,089,080-174,092,791 , GRCh38.p12 chr4: 173,167,929-173,171,640 GALNT7, GALNT7-DT
    nsv3889590copy number variation1nstd102humanBenign GRCh37 chr4: 174,090,107-174,091,110 , GRCh38.p12 chr4: 173,168,956-173,169,959 GALNT7, GALNT7-DT
    nsv4728403copy number variation1nstd102humanLikely benign GRCh37 chr3: 15,822,766-16,235,835 , GRCh38.p12 chr3: 15,781,259-16,194,328 IMPDH1P8, GALNT15, 3 more genes
    nsv3915590copy number variation1nstd102humanLikely benign GRCh38 chr3: 15,806,288-16,201,982 , GRCh37 chr3: 15,847,795-16,243,489 , NCBI36 chr3: 15,822,799-16,218,493 LOC107986064, ANKRD28, 3 more genes
    nsv1398299copy number variation1nstd102humanUncertain significance GRCh37 chr4: 173,873,299-174,090,050 , GRCh38.p12 chr4: 172,952,148-173,168,899 GALNT7, RN7SL253P, 2 more genes
    nsv6634351copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318 GALNT7, COPS3P1, 363 more genes
    nsv4674043copy number variation1nstd102humanPathogenic GRCh37 chr4: 165,010,461-190,957,473 , GRCh38.p12 chr4: 164,089,309-190,036,318 GALNT7, CYP4V2, 319 more genes
    nsv3912039copy number variation1nstd102humanPathogenic GRCh38 chr4: 164,039,530-189,982,708 , GRCh37 chr4: 164,960,682-190,828,225 , NCBI36 chr4: 165,180,132-191,140,857 GALNT7, CYP4V2, 314 more genes
    nsv3916579copy number variation1nstd102humanPathogenic GRCh37 chr4: 166,202,188-190,939,340 , GRCh38 chr4: 165,281,036-190,018,185 , NCBI36 chr4: 166,421,638-191,176,334 GALNT7, LOC105377614, 291 more genes
    nsv4456171copy number variation1nstd102humanPathogenic GRCh37 chr4: 166,623,890-190,957,473 , GRCh38.p12 chr4: 165,702,738-190,036,318 GALNT7, TRIML2, 284 more genes
    nsv3913994copy number variation1nstd102humanPathogenic GRCh38 chr4: 166,317,587-190,095,391 , GRCh37 chr4: 167,238,739-190,828,225 , NCBI36 chr4: 167,458,189-191,250,527 GALNT7, PTGES3P3, 290 more genes
    nsv6634364copy number variation1nstd102humanPathogenic GRCh37 chr4: 167,779,888-190,957,473 , GRCh38.p12 chr4: 166,858,737-190,036,318 GALNT7, LOC101928551, 279 more genes
    nsv3918232copy number variation1nstd102humanPathogenic NCBI36 chr4: 168,531,442-191,194,467 , GRCh37 chr4: 168,294,867-190,957,473 , GRCh38 chr4: 167,373,716-190,036,318 GALNT7, LOC105377560, 277 more genes
    nsv3882557copy number variation1nstd102humanPathogenic GRCh37 chr4: 169,969,014-190,957,473 , GRCh38.p12 chr4: 169,047,863-190,036,318 GALNT7, LOC105377530, 258 more genes
    nsv3921438copy number variation1nstd102humanPathogenic GRCh38 chr4: 169,873,508-190,018,185 , NCBI36 chr4: 171,031,234-191,176,334 , GRCh37 chr4: 170,794,659-190,939,340 GALNT7, FAUP3, 245 more genes
    nsv3886420copy number variation1nstd102humanPathogenic GRCh37 chr4: 162,205,710-182,329,883 , GRCh38.p12 chr4: 161,284,558-181,408,730 GALNT7, RPL35AP12, 187 more genes
    nsv3914938copy number variation1nstd102humanPathogenic GRCh37 chr4: 171,820,275-190,957,473 , NCBI36 chr4: 172,056,850-191,194,467 , GRCh38 chr4: 170,899,124-190,036,318 GALNT7, LOC112268472, 237 more genes
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