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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3870561copy number variation1nstd102humanBenign GRCh37 chr5: 176,273,370-176,289,818 , GRCh38.p12 chr5: 176,846,369-176,862,817 UNC5A
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 UNC5A, MEGF10, 2080 more genes
    nsv1398443copy number variation1nstd102humanPathogenic GRCh37 chr5: 174,397,487-180,686,444 , GRCh38.p12 chr5: 174,970,484-181,259,443 UNC5A, TRV-AAC1-3, 203 more genes
    nsv3920109copy number variation1nstd102humanPathogenic NCBI36 chr5: 174,896,380-180,652,395 , GRCh37 chr5: 174,963,774-180,719,789 , GRCh38 chr5: 175,536,771-181,292,788 UNC5A, LOC100289470, 198 more genes
    nsv3873295copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,570,677-180,719,789 , GRCh38.p12 chr5: 176,143,674-181,292,788 UNC5A, LINC02222, 186 more genes
    nsv3922812copy number variation1nstd102humanPathogenic NCBI36 chr5: 176,059,735-180,629,412 , GRCh38 chr5: 176,700,128-181,269,805 , GRCh37 chr5: 176,127,129-180,696,806 UNC5A, MRPL50P3, 167 more genes
    nsv3913935copy number variation1nstd102humanPathogenic GRCh38 chr5: 176,291,838-178,662,699 , NCBI36 chr5: 175,651,447-178,022,306 , GRCh37 chr5: 175,718,841-178,089,700 UNC5A, DBN1, 74 more genes
    nsv4685982copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,346,695-177,469,711 , GRCh38.p12 chr5: 175,919,692-178,042,710 UNC5A, NOP16, 65 more genes
    nsv3880232copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,346,223-177,423,236 , GRCh38.p12 chr5: 175,919,220-177,996,235 UNC5A, MIR4281, 63 more genes
    nsv3882029copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,438,045-177,481,250 , GRCh38.p12 chr5: 176,011,042-178,054,249 UNC5A, LOC105377752, 64 more genes
    nsv3917273copy number variation1nstd102humanPathogenic GRCh38 chr5: 175,989,092-178,009,412 , NCBI36 chr5: 175,348,701-177,369,019 , GRCh37 chr5: 175,416,095-177,436,413 UNC5A, LOC105377752, 64 more genes
    nsv3875513copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,433,876-177,441,189 , GRCh38.p12 chr5: 176,006,873-178,014,188 UNC5A, RAB24, 64 more genes
    nsv3880220copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,438,045-177,392,885 , GRCh38.p12 chr5: 176,011,042-177,965,884 UNC5A, MIR4281, 59 more genes
    nsv3909885copy number variation1nstd102humanPathogenic NCBI36 chr5: 175,403,085-177,355,366 , GRCh38 chr5: 176,043,476-177,995,759 , GRCh37 chr5: 175,470,479-177,422,760 UNC5A, SNCB, 60 more genes
    nsv3888764copy number variation1nstd102humanPathogenic NCBI36 chr5: 175,492,445-177,359,136 , GRCh37.p13 chr5: 175,559,839-177,426,530 , GRCh38.p12 chr5: 176,132,836-177,999,529 UNC5A, ARL10, 57 more genes
    nsv3889409copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,570,678-177,437,340 , GRCh38.p12 chr5: 176,143,675-178,010,339 UNC5A, MIR4281, 59 more genes
    nsv3924491copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,570,677-177,436,413 , GRCh38 chr5: 176,143,674-178,009,412 , NCBI36 chr5: 175,503,283-177,369,019 UNC5A, CDHR2, 59 more genes
    nsv3883776copy number variation1nstd102humanPathogenic GRCh37 chr5: 175,570,677-177,436,413 , GRCh38.p12 chr5: 176,143,674-178,009,412 UNC5A, MIR1271, 59 more genes
    nsv3914974copy number variation1nstd102humanPathogenic GRCh38 chr5: 176,132,340-177,995,759 , NCBI36 chr5: 175,491,949-177,355,366 , GRCh37 chr5: 175,559,343-177,422,760 UNC5A, RN7SL684P, 57 more genes
    nsv3910181copy number variation1nstd102humanPathogenic NCBI36 chr5: 175,511,682-177,345,820 , GRCh37 chr5: 175,579,076-177,413,214 , GRCh38 chr5: 176,152,073-177,986,213 UNC5A, DBN1, 56 more genes
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