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Items: 1 to 20 of 579

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098184copy number variation1nstd102humanPathogenic GRCh37 chr8: 87,616,301-87,755,855 , GRCh38.p12 chr8: 86,604,073-86,743,627 CNGB3, UBE2Q2P10, 1 more genes
    nsv7098039copy number variation1nstd102humanUncertain significance GRCh37 chr8: 86,053,597-87,755,855 , GRCh38.p12 chr8: 85,141,362-86,743,627 UBE2Q2P10, LOC107986954, 40 more genes
    nsv7097910copy number variation1nstd102humanPathogenic GRCh37 chr8: 87,666,220-87,683,346 , GRCh38.p12 chr8: 86,653,992-86,671,118 CNGB3, GOLGA2P1, 1 more genes
    nsv7097909copy number variation1nstd102humanPathogenic GRCh37 chr8: 87,616,311-87,641,316 , GRCh38.p12 chr8: 86,604,083-86,629,088 CNGB3
    nsv7097669copy number variation1nstd102humanPathogenic GRCh37 chr8: 87,738,739-87,738,905 , GRCh38.p12 chr8: 86,726,511-86,726,677 CNGB3
    nsv7093138copy number variation1nstd102humanPathogenic GRCh38 chr8: 86,628,909-86,628,959 , GRCh37 chr8: 87,641,137-87,641,187 CNGB3
    nsv7075262inversion1nstd229human GRCh38 chr8: 83,096,825-86,720,422 , GRCh37.p13 chr8: 84,009,060-87,732,650 REXO1L1P, LOC100422614, 54 more genes
    nsv7074480inversion1nstd229human GRCh38 chr8: 86,647,891-86,656,344 , GRCh37.p13 chr8: 87,660,119-87,668,572 CNGB3, GOLGA2P1
    nsv7074158inversion1nstd229human GRCh38 chr8: 86,662,168-86,678,067 , GRCh37.p13 chr8: 87,674,396-87,690,295 UBE2Q2P10, CNGB3
    nsv7071080inversion1nstd229human GRCh38 chr8: 86,412,082-86,645,441 , GRCh37.p13 chr8: 87,424,311-87,657,669 RMDN1, WWP1, 5 more genes
    nsv7067855inversion1nstd229human GRCh38 chr8: 86,645,334-86,866,211 , GRCh37.p13 chr8: 87,657,562-87,878,439 LOC107986895, CNGB3, 3 more genes
    nsv7061888inversion1nstd229human GRCh38 chr8: 86,609,410-86,621,006 , GRCh37.p13 chr8: 87,621,638-87,633,234 CNGB3
    nsv7060805inversion1nstd229human GRCh38 chr8: 86,658,110-86,660,376 , GRCh37.p13 chr8: 87,670,338-87,672,604 CNGB3, GOLGA2P1, 1 more genes
    nsv7060733inversion1nstd229human GRCh38 chr8: 86,664,997-86,665,049 , GRCh37.p13 chr8: 87,677,225-87,677,277 UBE2Q2P10, CNGB3
    nsv6857384copy number variation1nstd229human GRCh38 chr8: 86,596,700-86,601,053 , GRCh37.p13 chr8: 87,608,928-87,613,281 CNGB3
    nsv6854230copy number variation1nstd229human GRCh38 chr8: 86,651,990-86,688,947 , GRCh37.p13 chr8: 87,664,218-87,701,175 UBE2Q2P10, GOLGA2P1, 1 more genes
    nsv6853198copy number variation1nstd229human GRCh38 chr8: 86,614,007-86,617,799 , GRCh37.p13 chr8: 87,626,235-87,630,027 CNGB3
    nsv6852850copy number variation1nstd229human GRCh38 chr8: 86,692,422-86,702,491 , GRCh37.p13 chr8: 87,704,650-87,714,719 CNGB3
    nsv6852215copy number variation1nstd229human GRCh38 chr8: 86,741,850-86,742,156 , GRCh37.p13 chr8: 87,754,078-87,754,384 CNGB3
    nsv6850402copy number variation1nstd229human GRCh38 chr8: 86,729,783-87,299,993 , GRCh37.p13 chr8: 87,742,011-88,312,221 LOC107986895, CNGB3, 1 more genes
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