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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3883640copy number variation1nstd102humanUncertain significance GRCh37 chr2: 233,899,687-233,999,652 , GRCh38.p12 chr2: 233,034,977-233,134,942 , GRCh38.p12 chr2|NW_011332690.1: 1-80,280 INPP5D, NEU2
    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 INPP5D, DAZAP2P1, 2991 more genes
    nsv6313668copy number variation1nstd102humanPathogenic GRCh37 chr2: 219,606,537-239,217,703 , GRCh38.p12 chr2: 218,741,814-238,309,062 INPP5D, 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 INPP5D, 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 INPP5D, B3GNT7, 193 more genes
    nsv4768328copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,110,452-243,028,452 , GRCh38.p12 chr2: 232,245,742-242,086,301 INPP5D, LOC107985836, 217 more genes
    nsv6315436copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,227,837-242,783,384 , GRCh38.p12 chr2: 232,363,127-241,841,232 INPP5D, LOC105373929, 204 more genes
    nsv3871027copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,784,243-243,040,217 , GRCh38.p12 chr2: 232,919,533-242,098,066 INPP5D, 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 INPP5D, UGT1A3, 194 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 INPP5D, SP110, 167 more genes
    nsv6313683copy number variation1nstd102humanPathogenic GRCh37 chr2: 228,807,574-235,475,892 , GRCh38.p12 chr2: 227,942,858-234,567,248 INPP5D, 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 INPP5D, LOC105373933, 105 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 INPP5D, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 INPP5D, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 INPP5D, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 INPP5D, MTND2P22, 3724 more genes
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 INPP5D, LOC105376755, 1013 more genes
    nsv3890898copy number variation1nstd102humanPathogenic GRCh38 chr2: 188,818,195-242,065,208 , NCBI36 chr2: 189,391,166-242,656,032 , GRCh37 chr2: 189,682,921-243,007,359 INPP5D, LOC105373909, 901 more genes
    nsv3896499copy number variation1nstd102humanPathogenic GRCh37 chr2: 190,300,875-242,783,384 , NCBI36 chr2: 190,009,120-242,432,057 , GRCh38 chr2: 189,436,149-241,841,232 INPP5D, RNU6-1206P, 883 more genes
    nsv3908112copy number variation1nstd102humanPathogenic GRCh38 chr2: 190,310,736-241,892,770 , NCBI36 chr2: 190,883,707-242,483,594 , GRCh37 chr2: 191,175,462-242,834,921 INPP5D, LOC101928084, 871 more genes
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