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Items: 1 to 20 of 691

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 more genes
    nsv7056877inversion1nstd229human GRCh38 chr1: 16,489,319-16,931,765 , GRCh37.p13 chr1: 16,815,814-17,258,260 TRG-CCC5-1, CROCC, 34 more genes
    nsv7054277inversion1nstd229human GRCh38 chr1: 16,622,900-16,948,001 , GRCh37.p13 chr1: 16,949,395-17,274,496 TRV-CAC13-1, EIF1AXP1, 23 more genes
    nsv7052204inversion1nstd229human GRCh38 chr1: 16,525,281-16,882,743 , GRCh37.p13 chr1: 16,851,776-17,209,238 RNU1-4, NBPF1, 26 more genes
    nsv7049927inversion1nstd229human GRCh38 chr1: 12,447,483-21,286,051 , GRCh37.p13 chr1: 12,507,539-21,612,544 SLC25A34, RNA5SP41, 238 more genes
    nsv7047261inversion1nstd229human GRCh38 chr1: 16,519,202-16,887,095 , GRCh37.p13 chr1: 16,845,697-17,213,590 PDE4DIPP9, CROCCP4, 29 more genes
    nsv7046489inversion1nstd229human GRCh38 chr1: 16,494,388-16,927,649 , GRCh37.p13 chr1: 16,820,883-17,254,144 TRV-CAC13-1, PDE4DIPP8, 33 more genes
    nsv7045393inversion1nstd229human GRCh38 chr1: 16,627,549-16,945,109 , GRCh37.p13 chr1: 16,954,044-17,271,604 TRG-CCC1-2, TRG-CCC4-1, 23 more genes
    nsv7043182inversion1nstd229human GRCh38 chr1: 16,510,571-16,892,681 , GRCh37.p13 chr1: 16,837,066-17,219,176 ESPNP, LOC105376805, 31 more genes
    nsv7041202inversion1nstd229human GRCh38 chr1: 16,616,805-16,942,244 , GRCh37.p13 chr1: 16,943,300-17,268,739 ESPNP, TRV-CAC13-1, 23 more genes
    nsv6636785copy number variation1nstd102humanPathogenic GRCh37 chr1: 6,758,933-19,287,770 , GRCh38.p12 chr1: 6,698,873-18,961,276 GPR157, MST1L, 313 more genes
    nsv6625671copy number variation1nstd224human GRCh37 chr1: 16,847,832-17,273,287 , GRCh38.p12 chr1: 16,521,337-16,946,792 TRG-CCC1-1, RNU1-3, 31 more genes
    nsv6290672copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-17,525,065 , GRCh38.p12 chr1: 914,086-17,198,570 RPL9P11, FAM131C2P, 466 more genes
    nsv6290472copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,773,001-20,221,073 , GRCh38.p12 chr1: 16,446,506-19,894,580 MIR1290, RNU6-1099P, 92 more genes
    nsv6137724copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099 PADI1, RPS15AP6, 176 more genes
    nsv5981737copy number variation1nstd212human GRCh38 chr1: 16,758,004-16,758,198 , GRCh37.p13 chr1: 17,084,499-17,084,693 MST1L
    nsv5969911inversion1nstd209human GRCh38 chr1: 16,619,297-16,951,954 , GRCh37.p13 chr1: 16,945,792-17,278,449 , RNU1-4, 24 more genes
    nsv5874151copy number variation1nstd209human GRCh38 chr1: 13,714,112-20,623,728 , GRCh37.p13 chr1: 14,040,607-20,950,221 , TRV-CAC11-1, 171 more genes
    nsv5669419inversion1nstd207human GRCh38 chr1: 16,761,852-16,946,929 , GRCh37.p13 chr1: 17,088,347-17,273,424 TRE-TTC3-1, CROCC, 12 more genes
    nsv5560911sequence alteration1nstd206human GRCh38 chr1: 16,483,139-16,940,239 , GRCh37.p13 chr1: 16,809,634-17,266,734 , RNU1-4, 35 more genes
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