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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3904212copy number variation1nstd102humanBenign GRCh37 chr17: 4,048,081-4,104,311 , GRCh38.p12 chr17: 4,144,787-4,201,016 CYB5D2, ANKFY1, 1 more genes
    nsv3911017copy number variation1nstd102humanUncertain significance GRCh37 chr17: 3,990,675-4,168,935 , GRCh38 chr17: 4,087,381-4,265,640 , NCBI36 chr17: 3,937,424-4,115,684 CYB5D2, LOC100420060, 3 more genes
    nsv3913013copy number variation1nstd102humanPathogenic GRCh38 chr17: 162,016-7,697,012 , GRCh37 chr17: 45,835-7,600,330 , NCBI36 chr17: 11,807-7,541,055 CYB5D2, RPS4XP17, 289 more genes
    nsv3915884copy number variation1nstd102humanPathogenic GRCh37 chr17: 45,835-6,862,369 , GRCh38 chr17: 162,088-6,959,050 , NCBI36 chr17: 11,879-6,803,093 CYB5D2, LOC105371592, 222 more genes
    nsv3922546copy number variation1nstd102humanPathogenic NCBI36 chr17: 525-5,779,421 , GRCh38 chr17: 150,732-5,935,377 , GRCh37 chr17: 525-5,838,697 CYB5D2, CHRNE, 198 more genes
    nsv4674912copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-5,627,408 , GRCh38.p12 chr17: 158,756-5,724,088 CYB5D2, SRR, 196 more genes
    nsv3913795copy number variation1nstd102humanPathogenic NCBI36 chr17: 43,098-5,496,266 , GRCh37 chr17: 45,835-5,555,542 , GRCh38 chr17: 193,307-5,652,222 CYB5D2, BHLHA9, 194 more genes
    nsv3921779copy number variation1nstd102humanPathogenic NCBI36 chr17: 87,039-4,585,577 , GRCh38 chr17: 237,248-4,735,533 , GRCh37 chr17: 396,627-4,638,828 CYB5D2, ARRB2, 146 more genes
    nsv3919819copy number variation1nstd102humanPathogenic GRCh37 chr17: 50,690-4,168,935 , NCBI36 chr17: 48,539-4,115,684 , GRCh38 chr17: 198,748-4,265,640 CYB5D2, LOC105371430, 125 more genes
    nsv3923152copy number variation1nstd102humanPathogenic NCBI36 chr17: 3,451,558-7,022,067 , GRCh38 chr17: 3,601,515-7,178,024 , GRCh37 chr17: 3,504,809-7,081,343 CYB5D2, PSMB6, 133 more genes
    nsv3920795copy number variation1nstd102humanPathogenic GRCh38 chr17: 2,062,380-5,258,340 , NCBI36 chr17: 1,912,424-5,102,359 , GRCh37 chr17: 1,965,674-5,161,635 CYB5D2, LINC01996, 128 more genes
    nsv3892504copy number variation1nstd102humanPathogenic GRCh37 chr17: 2,050,166-4,315,506 , GRCh38.p12 chr17: 2,146,872-4,412,211 CYB5D2, OR3A2, 73 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 CYB5D2, MIR3185, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 CYB5D2, P4HB, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 CYB5D2, MIR21, 2366 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 CYB5D2, SMURF2, 2366 more genes
    nsv3897625copy number variation1nstd102humanPathogenic GRCh37 chr17: 525-15,027,737 , GRCh38.p12 chr17: 150,732-15,124,420 CYB5D2, GP1BA, 439 more genes
    nsv3915354copy number variation1nstd102humanPathogenic GRCh38 chr17: 150,732-14,764,202 , NCBI36 chr17: 525-14,608,244 , GRCh37 chr17: 525-14,667,519 CYB5D2, KIF1C-AS1, 433 more genes
    nsv3917059copy number variation1nstd102humanPathogenic GRCh37 chr17: 45,835-12,247,218 , NCBI36 chr17: 11,807-12,187,943 , GRCh38 chr17: 162,016-12,343,901 CYB5D2, PSMB6, 409 more genes
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 CYB5D2, RFLNB, 401 more genes
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