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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963102insertion1nstd209human GRCh38 chr2: 240,448,400-240,448,400 , GRCh37.p13 chr2: 241,387,817-241,387,817 GPC1-AS1, GPC1
    nsv5902496copy number variation1nstd209human GRCh38 chr2: 240,453,299-240,453,406 , GRCh37.p13 chr2: 241,392,716-241,392,823 GPC1, GPC1-AS1
    nsv5620117insertion1nstd207human GRCh38 chr2: 240,448,400-240,448,400 , GRCh37.p13 chr2: 241,387,817-241,387,817 GPC1-AS1, GPC1
    nsv5569064copy number variation1nstd207human GRCh38 chr2: 240,453,305-240,453,399 , GRCh37.p13 chr2: 241,392,722-241,392,816 GPC1, GPC1-AS1
    nsv5568760copy number variation1nstd207human GRCh38 chr2: 240,453,350-240,453,403 , GRCh37.p13 chr2: 241,392,767-241,392,820 GPC1, GPC1-AS1
    nsv5539733insertion1nstd206human GRCh38 chr2: 240,448,350-240,448,356 , GRCh37.p13 chr2: 241,387,767-241,387,773 GPC1-AS1, GPC1
    nsv5381323copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,201,756-243,048,760 , GRCh38.p12 chr2: 236,293,113-242,106,609 LRRFIP1, GPR35, 133 more genes
    nsv5366915translocation1nstd200human GRCh38 chr2: 240,454,636-240,454,636 , GRCh38 chr2: 240,457,070-240,457,070 , GRCh37.p13 chr2: 241,394,053-241,394,053 , GRCh37.p13 chr2: 241,396,487-241,396,487 GPC1, MIR149, 1 more genes
    nsv5366914translocation1nstd200human GRCh38 chr2: 240,454,483-240,454,483 , GRCh38 chr2: 240,457,081-240,457,081 , GRCh37.p13 chr2: 241,393,900-241,393,900 , GRCh37.p13 chr2: 241,396,498-241,396,498 GPC1, MIR149, 1 more genes
    nsv5331122translocation1nstd200human GRCh37 chr2: 241,396,487-241,396,487 , GRCh37 chr2: 241,394,053-241,394,053 , GRCh38.p12 chr2: 240,454,636-240,454,636 , GRCh38.p12 chr2: 240,457,070-240,457,070 GPC1, MIR149, 1 more genes
    nsv5217177copy number variation1nstd204human GRCh38.p13 chr2: 240,442,729-240,448,206 , GRCh37.p13 chr2: 241,382,146-241,387,623 GPC1, GPC1-AS1
    nsv4914145copy number variation1nstd200human GRCh38 chr2: 240,173,791-240,447,389 , GRCh37.p13 chr2: 241,113,208-241,386,806 GPC1-AS1, LOC102723825, 3 more genes
    nsv4910429copy number variation1nstd200human GRCh38 chr2: 240,455,911-240,455,973 , GRCh37.p13 chr2: 241,395,328-241,395,390 GPC1-AS1, MIR149, 1 more genes
    nsv4768328copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,110,452-243,028,452 , GRCh38.p12 chr2: 232,245,742-242,086,301 LOC107985836, LOC105373980, 217 more genes
    nsv4734305copy number variation1nstd199human GRCh37 chr2: 241,392,727-241,392,799 , GRCh38.p12 chr2: 240,453,310-240,453,382 GPC1, GPC1-AS1
    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
    nsv4684239copy number variation1nstd102humanUncertain significance GRCh37 chr2: 238,863,455-243,048,760 , GRCh38.p12 chr2: 237,954,813-242,106,609 LOC285191, MTERF4, 103 more genes
    nsv4674624copy number variation1nstd102humanPathogenic GRCh37 chr2: 234,791,927-242,783,384 , GRCh38.p12 chr2: 233,883,281-241,841,232 LOC93463, DUSP28, 151 more genes
    nsv4674620copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,265,271-242,783,384 , GRCh38.p12 chr2: 236,356,628-241,841,232 OR6B2, COPS8, 122 more genes
    nsv4674409copy number variation1nstd102humanPathogenic GRCh37 chr2: 239,914,717-242,783,384 , GRCh38.p12 chr2: 238,993,021-241,841,232 GAL3ST2, UICLM, 68 more genes
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