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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3875075copy number variation1nstd102humanBenign GRCh37 chr2: 234,262,974-234,266,842 , GRCh38.p12 chr2|NW_011332690.1: 299,666-303,534 , GRCh38.p12 chr2: 233,354,328-233,358,196 DGKD
    nsv3882017copy number variation1nstd102humanBenign GRCh37 chr2: 234,263,212-234,263,346 , GRCh38.p12 chr2|NW_011332690.1: 299,904-300,038 , GRCh38.p12 chr2: 233,354,566-233,354,700 DGKD
    nsv4681398copy number variation1nstd102humanUncertain significance GRCh37 chr2: 234,171,776-234,299,129 , GRCh38.p12 chr2: 233,263,130-233,390,483 , GRCh38.p12 chr2|NW_011332690.1: 208,468-335,821 DGKD, SAG, 3 more genes
    nsv4454847copy number variation1nstd102humanUncertain significance GRCh37 chr2: 234,162,434-234,275,131 , GRCh38.p12 chr2: 233,253,788-233,366,485 , GRCh38.p12 chr2|NW_011332690.1: 199,126-311,823 DGKD, ATG16L1, 3 more genes
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 DGKD, DAZAP2P1, 2991 more genes
    nsv6313668copy number variation1nstd102humanPathogenic GRCh37 chr2: 219,606,537-239,217,703 , GRCh38.p12 chr2: 218,741,814-238,309,062 DGKD, LOC105373947, 357 more genes
    nsv3898929copy number variation2nstd102humanPathogenic GRCh38 chr2: 231,770,279-242,126,245 , GRCh37 chr2: 232,634,989-243,059,659 , NCBI36 chr2: 232,343,233-242,717,069 DGKD, PDE6D, 227 more genes
    nsv3893827copy number variation1nstd102humanPathogenic NCBI36 chr2: 227,551,089-237,459,981 , GRCh38 chr2: 226,978,129-236,886,599 , GRCh37 chr2: 227,842,845-237,795,242 DGKD, B3GNT7, 193 more genes
    nsv4768328copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,110,452-243,028,452 , GRCh38.p12 chr2: 232,245,742-242,086,301 DGKD, LOC107985836, 217 more genes
    nsv6315436copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,227,837-242,783,384 , GRCh38.p12 chr2: 232,363,127-241,841,232 DGKD, LOC105373929, 204 more genes
    nsv3871027copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,784,243-243,040,217 , GRCh38.p12 chr2: 232,919,533-242,098,066 DGKD, MROH2A, 194 more genes
    nsv3910501copy number variation1nstd102humanPathogenic NCBI36 chr2: 233,599,457-242,717,007 , GRCh37.p13 chr2: 233,891,213-243,068,334 , GRCh38.p12 chr2: 233,026,503-242,126,183 DGKD, UGT1A3, 194 more genes
    nsv3894767copy number variation1nstd102humanPathogenic GRCh38 chr2: 233,420,162-242,086,301 , NCBI36 chr2: 233,704,084-242,677,125 , GRCh37 chr2: 233,995,840-243,028,452 DGKD, LOC112268433, 184 more genes
    nsv3892808copy number variation1nstd102humanPathogenic GRCh37 chr2: 234,362,257-243,041,306 , NCBI36 chr2: 234,026,996-242,689,979 , GRCh38 chr2: 233,453,611-242,099,155 DGKD, RPL3P5, 185 more genes
    nsv3906029copy number variation1nstd102humanPathogenic NCBI36 chr2: 227,916,238-235,912,551 , GRCh38 chr2: 227,343,278-235,339,168 , GRCh37 chr2: 228,207,994-236,247,812 DGKD, SP110, 167 more genes
    nsv6313683copy number variation1nstd102humanPathogenic GRCh37 chr2: 228,807,574-235,475,892 , GRCh38.p12 chr2: 227,942,858-234,567,248 DGKD, RNU7-9P, 143 more genes
    nsv4674274copy number variation1nstd102humanPathogenic GRCh37 chr2: 234,090,049-239,494,702 , GRCh38.p12 chr2: 233,181,403-238,586,061 DGKD, LOC105373933, 105 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 DGKD, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 DGKD, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 DGKD, RNU6-674P, 3735 more genes
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