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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137192copy number variation1nstd102humanUncertain significance GRCh37 chr2: 232,520,701-234,168,331 , GRCh38.p12 chr2: 231,655,990-233,259,685 NEU2, MIR562, 38 more genes
    nsv7054895inversion1nstd229human GRCh38 chr2: 229,787,965-232,576,060 , GRCh37.p13 chr2: 230,652,681-233,440,770 GPR55, RN7SL834P, 80 more genes
    nsv6689722copy number variation1nstd229human GRCh38 chr2: 231,850,201-231,995,500 , GRCh37.p13 chr2: 232,714,911-232,860,210 NPPC, DIS3L2, 1 more genes
    nsv6685562copy number variation1nstd229human GRCh38 chr2: 231,902,834-231,920,999 , GRCh37.p13 chr2: 232,767,544-232,785,709 NPPC
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313683copy number variation1nstd102humanPathogenic GRCh37 chr2: 228,807,574-235,475,892 , GRCh38.p12 chr2: 227,942,858-234,567,248 RNU7-9P, SCARNA5, 143 more genes
    nsv6313668copy number variation1nstd102humanPathogenic GRCh37 chr2: 219,606,537-239,217,703 , GRCh38.p12 chr2: 218,741,814-238,309,062 LOC105373947, RN7SL764P, 357 more genes
    nsv6311650copy number variation2nstd102humanUncertain significance GRCh37 chr2: 231,033,840-234,978,657 , GRCh38.p12 chr2: 230,169,124-234,070,013 SP110, LINC00471, 112 more genes
    nsv6134539copy number variation1nstd213human GRCh37 chr2: 231,850,000-233,400,001 , GRCh38.p12 chr2: 230,985,285-232,535,291 ALPI, ALPP, 47 more genes
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4673913copy number variation1nstd102humanPathogenic GRCh37 chr2: 230,814,690-242,783,384 , GRCh38.p12 chr2: 229,949,974-241,841,232 MIR2467, D2HGDH, 270 more genes
    nsv4583441copy number variation1nstd183human GRCh37 chr2: 232,786,607-232,786,850 , GRCh38.p12 chr2: 231,921,897-231,922,140 NPPC
    nsv4436670copy number variation1nstd102humanUncertain significance GRCh37 chr2: 232,550,626-232,968,158 , GRCh38.p12 chr2: 231,685,916-232,103,448 RPL28P2, PDE6D, 8 more genes
    nsv4436121copy number variation1nstd102humanUncertain significance GRCh37 chr2: 232,647,812-232,930,068 , GRCh38.p12 chr2: 231,783,102-232,065,358 RPL28P2, DIS3L2, 4 more genes
    nsv4435891copy number variation1nstd102humanPathogenic GRCh37 chr2: 210,779,657-239,879,183 , GRCh38.p12 chr2: 209,914,933-238,957,487 XRCC5, LINC01173, 494 more genes
    nsv3924332copy number variation1nstd102humanPathogenic NCBI36 chr2: 230,011,029-233,894,271 , GRCh37.p13 chr2: 230,302,785-234,229,532 , GRCh38.p12 chr2: 229,438,069-233,320,886 EIF4E2, LOC107985996, 100 more genes
    nsv3924199copy number variation1nstd102humanUncertain significance NCBI36 chr2: 130,861,065-242,751,149 , GRCh37.p13 chr2: 131,144,595-243,102,476 , GRCh38.p12 chr2: 130,387,022-242,160,331 METAP1D, UBE2E3-DT, 1635 more genes
    nsv3923963copy number variation1nstd102humanUncertain significance NCBI36 chr2: 110,190,938-242,751,149 , GRCh37.p13 chr2: 110,833,649-243,102,476 , GRCh38.p12 chr2: 110,076,072-242,160,331 NMTRQ-TTG9-1, MIR6810, 1944 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 DAZAP2P1, RPL36AP16, 2991 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 LOC101928084, ECEL1P1, 871 more genes
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