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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4386419copy number variation1nstd173human GRCh37 chr4: 57,402,002-57,789,029 , GRCh38.p12 chr4: 56,535,836-56,922,863 LOC105377666, LOC285453, 10 more genes
    nsv4317585inversion1nstd166human GRCh37.p13 chr4: 57,479,624-69,003,923 , GRCh38.p12 chr4: 56,613,458-68,138,205 CENPC, GNRHR, 98 more genes
    nsv4109315copy number variation1nstd166human GRCh37.p13 chr4: 57,801,878-57,801,939 , GRCh38.p12 chr4: 56,935,712-56,935,773 REST
    nsv4100661copy number variation1nstd166human GRCh37.p13 chr4: 57,787,120-57,819,338 , GRCh38.p12 chr4: 56,920,954-56,953,172 REST
    nsv3919213copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,766,026-60,850,197 , NCBI36 chr4: 52,460,783-60,532,792 , GRCh38 chr4: 51,899,860-59,984,479 LNX1-AS1, RPL7AP31, 106 more genes
    nsv3917232copy number variation1nstd102humanPathogenic NCBI36 chr4: 54,759,525-62,818,428 , GRCh38 chr4: 54,198,601-62,270,115 , GRCh37 chr4: 55,064,768-63,135,833 CLOCK, TMEM165, 84 more genes
    nsv3915769copy number variation1nstd102humanUncertain significance GRCh38 chr4: 56,248,102-57,218,522 , NCBI36 chr4: 56,809,025-57,779,445 , GRCh37 chr4: 57,114,268-58,084,688 GLDCP1, SRP72, 28 more genes
    nsv3914335copy number variation1nstd102humanPathogenic GRCh37 chr4: 44,358,218-63,111,600 , NCBI36 chr4: 44,052,975-62,794,195 , GRCh38 chr4: 44,356,201-62,245,882 RPL22P13, RNA5SP161, 178 more genes
    nsv3913811copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,831,622-97,505,618 , GRCh37 chr4: 52,697,788-98,426,769 , NCBI36 chr4: 52,392,545-98,645,792 LOC105377297, HNRNPA1P56, 582 more genes
    nsv3912235copy number variation1nstd102humanPathogenic GRCh38 chr4: 52,639,018-59,984,479 , GRCh37 chr4: 53,505,185-60,850,197 , NCBI36 chr4: 53,199,942-60,532,792 LOC105377672, PAICS, 97 more genes
    nsv3910089copy number variation1nstd102humanPathogenic NCBI36 chr4: 52,392,545-67,539,802 , GRCh37 chr4: 52,697,788-67,857,207 , GRCh38 chr4: 51,831,622-66,991,489 LINC02260, LINC02928, 154 more genes
    nsv3884499copy number variation1nstd102humanPathogenic GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286 MTND4LP29, RNU6-128P, 2341 more genes
    nsv3883791copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-190,915,650 , GRCh38.p12 chr4: 49,556-189,994,495 LOC105377343, PDGFC, 2341 more genes
    nsv3880085copy number variation2nstd102humanPathogenic GRCh37 chr4: 68,346-190,957,473 , GRCh38.p12 chr4: 68,454-190,036,318 LOC112268460, LINC02435, 2345 more genes
    nsv3877657copy number variation1nstd102humanUncertain significance GRCh37 chr4: 57,759,221-57,795,328 , GRCh38.p12 chr4: 56,893,055-56,929,162 REST
    nsv3876533copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611 LOC100420289, LOC100131038, 2347 more genes
    nsv3873978copy number variation1nstd102humanPathogenic GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724 LOC100422029, H2AZ1, 2358 more genes
    nsv3872797copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-66,440,622 , GRCh38.p12 chr4: 68,453-65,574,904 GNPDA2, HGFAC, 813 more genes
    nsv3168296copy number variation1nstd158human GRCh38.p12 chr4: 45,153,752-66,284,228 , GRCh37 chr4: 45,155,769-67,149,946 , CNGA1, 207 more genes
    nsv3168290copy number variation1nstd158human GRCh37 chr4: 19,079,634-176,998,212 , GRCh38.p12 chr4: 19,078,011-176,077,061 , ADH1A, 1849 more genes
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