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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv6112747copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372 GPR78, LOC105374510, 362 more genes
    nsv5906663copy number variation1nstd209human GRCh38 chr4: 2,940,955-2,941,107 , GRCh37.p13 chr4: 2,942,682-2,942,834 NOP14-AS1, NOP14
    nsv5895022copy number variation1nstd209human GRCh38 chr4: 2,961,219-2,961,296 , GRCh37.p13 chr4: 2,962,946-2,963,023 NOP14
    nsv5891672copy number variation1nstd209human GRCh38 chr4: 2,960,853-2,960,952 , GRCh37.p13 chr4: 2,962,580-2,962,679 NOP14
    nsv5673743copy number variation1nstd102humanPathogenic GRCh37 chr4: 2,200,251-5,710,240 , GRCh38.p12 chr4: 2,198,524-5,708,513 ZFYVE28, LINC01587, 81 more genes
    nsv5616346insertion1nstd207human GRCh38 chr4: 2,961,226-2,961,226 , GRCh37.p13 chr4: 2,962,953-2,962,953 NOP14
    nsv5613466insertion1nstd207human GRCh38 chr4: 2,961,198-2,961,198 , GRCh37.p13 chr4: 2,962,925-2,962,925 NOP14
    nsv5609215insertion1nstd207human GRCh38 chr4: 2,960,629-2,960,629 , GRCh37.p13 chr4: 2,962,356-2,962,356 NOP14
    nsv5581505copy number variation1nstd207human GRCh38 chr4: 2,940,955-2,941,107 , GRCh37.p13 chr4: 2,942,682-2,942,834 NOP14, NOP14-AS1
    nsv5580233copy number variation1nstd207human GRCh38 chr4: 2,960,889-2,960,957 , GRCh37.p13 chr4: 2,962,616-2,962,684 NOP14
    nsv5579834copy number variation1nstd207human GRCh38 chr4: 2,945,903-2,945,966 , GRCh37.p13 chr4: 2,947,630-2,947,693 NOP14-AS1, NOP14
    nsv5447941copy number variation1nstd206human GRCh38 chr4: 2,940,424-3,030,121 , GRCh37.p13 chr4: 2,942,151-3,031,848 NOP14-AS1, NOP14, 1 more genes
    nsv5441261copy number variation1nstd206human GRCh38 chr4: 2,940,958-2,941,108 , GRCh37.p13 chr4: 2,942,685-2,942,835 NOP14-AS1, NOP14
    nsv5440612copy number variation1nstd206human GRCh38 chr4: 2,961,219-2,961,301 , GRCh37.p13 chr4: 2,962,946-2,963,028 NOP14
    nsv5439742copy number variation1nstd206human GRCh38 chr4: 2,962,412-2,962,521 , GRCh37.p13 chr4: 2,964,139-2,964,248 GRK4, NOP14
    nsv5435679copy number variation1nstd206human GRCh38 chr4: 2,957,751-3,018,099 , GRCh37.p13 chr4: 2,959,478-3,019,826 NOP14, GRK4
    nsv5381775copy number variation1nstd102humanPathogenic GRCh37 chr4: 388,344-3,872,380 , GRCh38.p12 chr4: 394,555-3,870,653 RN7SL671P, HTT-AS, 96 more genes
    nsv5367324translocation1nstd200human GRCh38 chr12: 16,817,320-16,817,320 , GRCh38 chr4: 2,940,124-2,940,124 , GRCh37.p13 chr12: 16,970,254-16,970,254 , GRCh37.p13 chr4: 2,941,851-2,941,851 NOP14, NOP14-AS1, 1 more genes
    nsv5367323translocation1nstd200human GRCh38 chr12: 16,817,297-16,817,297 , GRCh38 chr4: 2,939,804-2,939,804 , GRCh37.p13 chr12: 16,970,231-16,970,231 , GRCh37.p13 chr4: 2,941,531-2,941,531 NOP14, NOP14-AS1, 1 more genes
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