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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097454copy number variation1nstd102humanUncertain significance GRCh37 chr6: 7,542,149-7,880,576 , GRCh38.p12 chr6: 7,541,916-7,880,343 DSP-AS1, RPL29P1, 6 more genes
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv6796938copy number variation1nstd229human GRCh38 chr6: 7,607,293-7,607,394 , GRCh37.p13 chr6: 7,607,526-7,607,627 SNRNP48
    nsv6796780copy number variation1nstd229human GRCh38 chr6: 7,588,901-7,593,300 , GRCh37.p13 chr6: 7,589,134-7,593,533 SNRNP48
    nsv6409723copy number variation1nstd223human GRCh38 chr6: 7,366,072-12,459,745 , GRCh37.p13 chr6: 7,366,305-12,459,977 EEF1E1, RPS26P29, 82 more genes
    nsv6409276copy number variation1nstd223human GRCh38 chr6: 7,585,101-7,591,500 , GRCh37.p13 chr6: 7,585,334-7,591,733 DSP, SNRNP48
    nsv6398849copy number variation1nstd223human GRCh38 chr6: 7,593,009-7,593,867 , GRCh37.p13 chr6: 7,593,242-7,594,100 SNRNP48
    nsv6398661copy number variation1nstd223human GRCh38 chr6: 7,588,915-7,593,303 , GRCh37.p13 chr6: 7,589,148-7,593,536 SNRNP48
    nsv6136505copy number variation1nstd213human GRCh37 chr6: 380,000-11,010,001 , GRCh38.p12 chr6: 380,000-11,009,768 BMP6, BPHL, 178 more genes
    nsv6135850copy number variation1nstd213human GRCh37 chr6: 7,530,000-7,720,001 , GRCh38.p12 chr6: 7,529,767-7,719,768 DSP, RPL29P1, 3 more genes
    nsv6135513copy number variation1nstd213human GRCh37 chr6: 380,000-10,980,001 , GRCh38.p12 chr6: 380,000-10,979,768 BMP6, BPHL, 178 more genes
    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
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