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Items: 1 to 20 of 23

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095326copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,451,710-16,532,835 , GRCh38.p12 chr1: 16,125,215-16,206,340 ARHGEF19, EPHA2-AS1, 1 more genes
    nsv6290672copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-17,525,065 , GRCh38.p12 chr1: 914,086-17,198,570 ARHGEF19, RPL9P11, 466 more genes
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 ARHGEF19, LOC107985467, 386 more genes
    nsv3900501copy number variation1nstd102humanPathogenic GRCh38 chr1: 3,006,193-17,688,934 , GRCh37 chr1: 2,922,757-18,015,429 , NCBI36 chr1: 2,912,617-17,888,016 ARHGEF19, MFFP1, 364 more genes
    nsv3900236copy number variation1nstd102humanPathogenic GRCh38 chr1: 5,363,826-18,360,302 , GRCh37 chr1: 5,423,886-18,686,796 , NCBI36 chr1: 5,323,746-18,559,383 ARHGEF19, PDPN, 333 more genes
    nsv6636785copy number variation1nstd102humanPathogenic GRCh37 chr1: 6,758,933-19,287,770 , GRCh38.p12 chr1: 6,698,873-18,961,276 ARHGEF19, GPR157, 313 more genes
    nsv3897535copy number variation1nstd102humanPathogenic NCBI36 chr1: 9,017,317-16,640,547 , GRCh38 chr1: 9,034,671-16,441,465 , GRCh37 chr1: 9,094,730-16,767,960 ARHGEF19, RNU6-771P, 206 more genes
    nsv3892730copy number variation1nstd102humanPathogenic GRCh37 chr1: 10,681,833-16,847,204 , GRCh38 chr1: 10,621,776-16,520,709 , NCBI36 chr1: 10,604,420-16,719,791 ARHGEF19, DHRS3, 170 more genes
    nsv3895493copy number variation1nstd102humanPathogenic NCBI36 chr1: 10,791,683-16,621,582 , GRCh37 chr1: 10,869,096-16,748,995 , GRCh38 chr1: 10,809,039-16,422,500 ARHGEF19, PRAMEF36P, 163 more genes
    nsv3899287copy number variation1nstd102humanPathogenic GRCh37 chr1: 15,711,763-21,306,842 , NCBI36 chr1: 15,584,350-21,179,429 , GRCh38 chr1: 15,385,267-20,980,349 ARHGEF19, EMC1-AS1, 166 more genes
    nsv4728309copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,041,431-21,295,864 , GRCh38.p12 chr1: 15,714,936-20,969,371 ARHGEF19, RNU1-6P, 150 more genes
    nsv3897811copy number variation1nstd102humanPathogenic GRCh37 chr1: 11,181,682-16,650,993 , NCBI36 chr1: 11,104,269-16,523,580 , GRCh38 chr1: 11,121,625-16,324,498 ARHGEF19, DNAJC16, 150 more genes
    nsv3898082copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,008,307-19,988,832 , NCBI36 chr1: 15,880,894-19,861,419 , GRCh38 chr1: 15,681,812-19,662,339 ARHGEF19, ESPNP, 114 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 ARHGEF19, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 ARHGEF19, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 ARHGEF19, RNU1-153P, 4887 more genes
    nsv3909483copy number variation1nstd102humanPathogenic NCBI36 chr1: 13,819,061-18,665,253 , GRCh38 chr1: 13,619,979-18,466,172 , GRCh37 chr1: 13,946,474-18,792,666 ARHGEF19, TMEM51, 117 more genes
    nsv3899259copy number variation1nstd102humanLikely pathogenic NCBI36 chr1: 15,251,130-16,698,955 , GRCh37 chr1: 15,378,543-16,826,368 , GRCh38 chr1: 15,052,047-16,499,873 ARHGEF19, CASP9, 51 more genes
    nsv6315241copy number variation1nstd102humanLikely pathogenic GRCh38 chr1: 10,115,497-16,283,149 , GRCh37.p13 chr1: 10,175,555-16,609,644 ARHGEF19, CASP9, 173 more genes
    nsv4453267copy number variation1nstd102humanUncertain significance GRCh37 chr1: 16,096,742-16,725,355 , GRCh38.p12 chr1: 15,770,247-16,398,860 ARHGEF19, RPL12P14, 21 more genes
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