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Items: 1 to 20 of 274

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142896insertion1nstd232human GRCh37.p13 chr8: 87,541,351-87,541,351 , GRCh38.p12 chr8: 86,529,123-86,529,123 CPNE3
    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
    nsv7075262inversion1nstd229human GRCh38 chr8: 83,096,825-86,720,422 , GRCh37.p13 chr8: 84,009,060-87,732,650 REXO1L1P, LOC100422614, 54 more genes
    nsv7071080inversion1nstd229human GRCh38 chr8: 86,412,082-86,645,441 , GRCh37.p13 chr8: 87,424,311-87,657,669 RMDN1, WWP1, 5 more genes
    nsv6854275copy number variation1nstd229human GRCh38 chr8: 86,192,501-86,533,999 , GRCh37.p13 chr8: 87,204,730-87,546,227 SLC2A3P4, RMDN1, 6 more genes
    nsv6851854copy number variation1nstd229human GRCh38 chr8: 86,519,841-86,528,353 , GRCh37.p13 chr8: 87,532,069-87,540,581 CPNE3
    nsv6846183copy number variation1nstd229human GRCh38 chr8: 86,556,013-86,556,351 , GRCh37.p13 chr8: 87,568,241-87,568,579 CPNE3
    nsv6637803copy number variation1nstd102humanUncertain significance GRCh37 chr8: 87,010,235-91,879,538 , GRCh38.p12 chr8: 85,998,006-90,867,310 LOC105375633, NTAN1P2, 49 more genes
    nsv6637601copy number variation1nstd102humanUncertain significance GRCh37 chr8: 86,841,155-88,126,932 , GRCh38.p12 chr8: 85,828,926-87,114,704 WWP1-AS1, MIOXP1, 18 more genes
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6565741inversion1nstd223human GRCh38 chr8: 86,412,082-86,645,441 , GRCh37.p13 chr8: 87,424,311-87,657,669 CPNE3, WWP1, 5 more genes
    nsv6431127copy number variation1nstd223human GRCh38 chr8: 86,525,025-86,528,074 , GRCh37.p13 chr8: 87,537,253-87,540,302 CPNE3
    nsv6431073copy number variation1nstd223human GRCh38 chr8: 86,523,731-86,524,948 , GRCh37.p13 chr8: 87,535,959-87,537,176 CPNE3
    nsv6429490copy number variation1nstd223human GRCh38 chr8: 86,412,101-86,866,200 , GRCh37.p13 chr8: 87,424,330-87,878,428 RMDN1, MIOXP1, 9 more genes
    nsv6420718copy number variation1nstd223human GRCh38 chr8: 86,520,140-86,520,346 , GRCh37.p13 chr8: 87,532,368-87,532,574 CPNE3
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6313579copy number variation1nstd102humanPathogenic GRCh37 chr8: 77,906,471-88,917,707 , GRCh38.p12 chr8: 76,994,235-87,905,479 LOC105375915, LOC105375918, 143 more genes
    nsv6291319copy number variation1nstd102humanUncertain significance GRCh37 chr8: 87,429,000-87,605,195 , GRCh38.p12 chr8: 86,416,771-86,592,967 CPNE3, SLC2A3P4, 5 more genes
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