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Items: 1 to 20 of 168

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973691inversion1nstd209human GRCh38 chr6: 6,312,424-9,433,879 , GRCh37.p13 chr6: 6,312,657-9,434,112 , BMP6, 45 more genes
    nsv5896105copy number variation1nstd209human GRCh38 chr6: 7,548,083-10,446,730 , GRCh37.p13 chr6: 7,548,316-10,446,963 , TFAP2A-AS2, 37 more genes
    nsv4947613copy number variation1nstd200human GRCh38 chr6: 7,598,711-7,598,928 , GRCh37.p13 chr6: 7,598,944-7,599,161 SNRNP48
    nsv4947612copy number variation1nstd200human GRCh38 chr6: 7,593,013-7,593,867 , GRCh37.p13 chr6: 7,593,246-7,594,100 SNRNP48
    nsv4934387copy number variation1nstd200human GRCh38 chr6: 7,366,072-12,459,747 , GRCh37.p13 chr6: 7,366,305-12,459,979 , DSP, 90 more genes
    nsv4809591copy number variation1nstd200human GRCh37 chr6: 7,593,246-7,594,100 , GRCh38.p12 chr6: 7,593,013-7,593,867 SNRNP48
    nsv4729577copy number variation1nstd102humanUncertain significance GRCh37 chr6: 6,495,789-8,070,987 , GRCh38.p12 chr6: 6,495,556-8,070,754 LOC105374904, RPS26P29, 30 more genes
    nsv4679417copy number variation1nstd189human GRCh37.p13 chr6: 7,551,462-7,883,473 , GRCh38.p12 chr6: 7,551,229-7,883,240 , BMP6, 6 more genes
    nsv4679200copy number variation1nstd189human GRCh37.p13 chr6: 7,480,366-7,745,447 , GRCh38.p12 chr6: 7,480,133-7,745,214 , BMP6, 8 more genes
    nsv4675053copy number variation1nstd102humanPathogenic GRCh37 chr6: 5,997,521-8,570,039 , GRCh38.p12 chr6: 5,997,288-8,569,806 BTF3P7, EEF1E1, 42 more genes
    nsv4674928copy number variation1nstd102humanUncertain significance GRCh37 chr6: 6,664,656-7,593,975 , GRCh38.p12 chr6: 6,664,423-7,593,742 LOC101928004, BTF3P7, 19 more genes
    nsv4593700copy number variation1nstd183human GRCh37 chr6: 7,570,253-7,595,126 , GRCh38.p12 chr6: 7,570,020-7,594,893 SNRNP48, DSP
    nsv4592909copy number variation1nstd183human GRCh37 chr6: 7,594,270-7,594,456 , GRCh38.p12 chr6: 7,594,037-7,594,223 SNRNP48
    nsv4592885copy number variation1nstd183human GRCh37 chr6: 7,600,119-7,601,523 , GRCh38.p12 chr6: 7,599,886-7,601,290 SNRNP48
    nsv4523574copy number variation1nstd166human GRCh37.p13 chr6: 7,600,848-7,601,363 , GRCh38.p12 chr6: 7,600,615-7,601,130 SNRNP48
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4456532copy number variation1nstd102humanUncertain significance GRCh37 chr6: 6,846,861-7,759,131 , GRCh38.p12 chr6: 6,846,628-7,758,898 RN7SL554P, RIOK1, 18 more genes
    nsv4131322copy number variation1nstd166human GRCh37.p13 chr6: 7,594,450-7,602,409 , GRCh38.p12 chr6: 7,594,217-7,602,176 SNRNP48
    nsv4126104copy number variation1nstd166human GRCh37.p13 chr6: 7,592,622-7,593,469 , GRCh38.p12 chr6: 7,592,389-7,593,236 SNRNP48
    nsv4125808copy number variation1nstd166human GRCh37.p13 chr6: 7,509,144-7,717,131 , GRCh38.p12 chr6: 7,508,911-7,716,898 DSP, RPL29P1, 4 more genes
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