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Items: 1 to 20 of 234

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097864copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,781,014-150,301,047 , GRCh38.p12 chr7: 131,096,255-150,603,959 NOBOX, FAM131B, 466 more genes
    nsv7051917inversion1nstd229human GRCh38 chr7: 134,286,289-134,623,481 , GRCh37.p13 chr7: 133,971,041-134,308,233 AKR1B1, AKR1B15, 7 more genes
    nsv7046115inversion1nstd229human GRCh38 chr7: 128,204,685-135,838,306 , GRCh37.p13 chr7: 127,844,738-135,523,054 RPL37P16, BPGM, 155 more genes
    nsv7044624inversion1nstd229human GRCh38 chr7: 134,462,288-134,716,451 , GRCh37.p13 chr7: 134,147,040-134,401,203 BPGM, LOC105375520, 3 more genes
    nsv6837835copy number variation1nstd229human GRCh38 chr7: 128,205,538-135,806,503 , GRCh37.p13 chr7: 127,845,591-135,491,251 RN7SL81P, IMP3P2, 155 more genes
    nsv6834696copy number variation1nstd229human GRCh38 chr7: 134,541,830-134,580,223 , GRCh37.p13 chr7: 134,226,582-134,264,975 AKR1B15, LOC105375520, 1 more genes
    nsv6833796copy number variation1nstd229human GRCh38 chr7: 134,527,880-134,528,092 , GRCh37.p13 chr7: 134,212,632-134,212,844 AKR1B10
    nsv6833007copy number variation1nstd229human GRCh38 chr7: 134,519,133-134,559,687 , GRCh37.p13 chr7: 134,203,885-134,244,439 AKR1B15, LOC105375520, 1 more genes
    nsv6828570copy number variation1nstd229human GRCh38 chr7: 134,250,795-134,763,234 , GRCh37.p13 chr7: 133,935,547-134,447,985 SLC35B4, LINC03060, 10 more genes
    nsv6821153copy number variation1nstd229human GRCh38 chr7: 134,497,728-134,673,957 , GRCh37.p13 chr7: 134,182,480-134,358,709 BPGM, LOC105375520, 2 more genes
    nsv6818805copy number variation1nstd229human GRCh38 chr7: 134,515,728-134,621,473 , GRCh37.p13 chr7: 134,200,480-134,306,225 LOC105375520, AKR1B10, 1 more genes
    nsv6818154copy number variation1nstd229human GRCh38 chr7: 134,512,990-134,539,553 , GRCh37.p13 chr7: 134,197,742-134,224,305 AKR1B10
    nsv6636458copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,779,213-149,042,734 , GRCh38.p12 chr7: 132,094,454-149,345,643 TRBD2, TRBV5-2, 403 more genes
    nsv6635855copy number variation1nstd227human GRCh37 chr7: 134,214,862-134,232,615 , GRCh38.p12 chr7: 134,530,110-134,547,863 AKR1B10, AKR1B15, 1 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6631837copy number variation1nstd224human GRCh37 chr7: 134,215,396-134,227,299 , GRCh38.p12 chr7: 134,530,644-134,542,547 AKR1B10
    nsv6631836copy number variation1nstd224human GRCh37 chr7: 134,203,919-134,223,762 , GRCh38.p12 chr7: 134,519,167-134,539,010 AKR1B10
    nsv6631835copy number variation1nstd224human GRCh37 chr7: 133,915,760-134,298,890 , GRCh38.p12 chr7: 134,231,008-134,614,138 LRGUK, LOC100887077, 8 more genes
    nsv6631565copy number variation1nstd224human GRCh37 chr7: 134,223,009-134,261,169 , GRCh38.p12 chr7: 134,538,257-134,576,417 AKR1B10, LOC105375520, 1 more genes
    nsv6560945inversion1nstd223human GRCh38 chr7: 129,758,099-137,582,370 , GRCh37.p13 chr7: 129,397,939-137,267,116 LOC100506937, SLC35B4, 115 more genes
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