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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3893698copy number variation1nstd102humanBenign GRCh37 chr19: 409,977-422,238 , GRCh38.p12 chr19: 409,977-422,238 SHC2
    nsv3895558copy number variation1nstd102humanBenign GRCh37 chr19: 409,977-417,714 , GRCh38.p12 chr19: 409,977-417,714 SHC2
    nsv3901374copy number variation1nstd102humanBenign GRCh37 chr19: 409,977-417,556 , GRCh38.p12 chr19: 409,977-417,556 SHC2
    nsv3894124copy number variation1nstd102humanBenign GRCh37 chr19: 410,799-417,556 , GRCh38.p12 chr19: 410,799-417,556 SHC2
    nsv3901936copy number variation1nstd102humanBenign GRCh37 chr19: 423,108-428,608 , GRCh38.p12 chr19: 423,108-428,608 SHC2
    nsv3905905copy number variation1nstd102humanBenign GRCh37 chr19: 423,160-423,625 , GRCh38.p12 chr19: 423,160-423,625 SHC2
    nsv3898993copy number variation1nstd102humanBenign GRCh37 chr19: 399,896-417,714 , GRCh38.p12 chr19: 399,896-417,714 SHC2, C2CD4C
    nsv3896652copy number variation1nstd102humanBenign GRCh37 chr19: 405,501-425,585 , GRCh38.p12 chr19: 405,501-425,585 SHC2, C2CD4C
    nsv3890632copy number variation1nstd102humanBenign GRCh37 chr19: 404,901-423,108 , GRCh38.p12 chr19: 404,901-423,108 SHC2, C2CD4C
    nsv3913456copy number variation1nstd102humanLikely benign GRCh38 chr19: 362,041-471,717 , GRCh37 chr19: 362,041-471,717 , NCBI36 chr19: 313,041-422,717 SHC2, CIMAP1D, 3 more genes
    nsv3898580copy number variation1nstd102humanBenign GRCh37 chr19: 460,883-512,568 , GRCh38.p12 chr19: 460,883-512,568 SHC2, CIMAP1D, 3 more genes
    nsv6315510copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-1,319,319 , GRCh38.p12 chr19: 260,911-1,319,320 SHC2, LOC101928450, 66 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 SHC2, ZNF321P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 SHC2, BABAM1, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 SHC2, LENG8, 2408 more genes
    nsv3924102copy number variation1nstd102humanPathogenic GRCh38 chr19: 259,395-6,795,611 , GRCh37 chr19: 259,395-6,795,622 , NCBI36 chr19: 210,395-6,746,622 SHC2, POLR2E, 283 more genes
    nsv4457776copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-4,788,357 , GRCh38.p12 chr19: 260,911-4,788,345 SHC2, BSG, 217 more genes
    nsv3923561copy number variation1nstd102humanPathogenic NCBI36 chr19: 184,565-4,650,484 , GRCh37 chr19: 233,565-4,699,484 , GRCh38 chr19: 233,565-4,699,472 SHC2, DAPK3, 214 more genes
    nsv4676189copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-4,384,674 , GRCh38.p12 chr19: 260,912-4,384,677 SHC2, MRPL54, 198 more genes
    nsv4676346copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-3,501,271 , GRCh38.p12 chr19: 260,911-3,501,273 SHC2, AZU1, 159 more genes
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