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Items: 1 to 20 of 348

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7040514inversion1nstd229human GRCh38 chr7: 56,030,808-56,035,644 , GRCh37.p13 chr7: 56,098,501-56,103,337 PSPH
    nsv6834298copy number variation1nstd229human GRCh38 chr7: 55,769,234-56,068,384 , GRCh37.p13 chr7: 55,836,927-56,136,077 ZNF713, LOC101409255, 12 more genes
    nsv6832138copy number variation1nstd229human GRCh38 chr7: 56,000,796-56,030,669 , GRCh37.p13 chr7: 56,068,489-56,098,362 PSPH
    nsv6826860copy number variation1nstd229human GRCh38 chr7: 56,023,565-56,026,373 , GRCh37.p13 chr7: 56,091,258-56,094,066 PSPH
    nsv6823794copy number variation1nstd229human GRCh38 chr7: 55,713,901-56,129,100 , GRCh37.p13 chr7: 55,781,594-56,196,793 SEPTIN14, LOC100419984, 23 more genes
    nsv6821860copy number variation1nstd229human GRCh38 chr7: 56,025,438-56,034,677 , GRCh37.p13 chr7: 56,093,131-56,102,370 PSPH
    nsv6636595copy number variation1nstd102humanUncertain significance GRCh37 chr7: 53,991,820-56,148,011 , GRCh38.p12 chr7: 53,924,127-56,080,318 PSPH, SNORA22B, 46 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
    nsv6632158copy number variation1nstd224human GRCh37 chr7: 56,106,397-56,146,310 , GRCh38.p12 chr7: 56,038,704-56,078,617 CCT6A, PHKG1, 4 more genes
    nsv6631902copy number variation1nstd224human GRCh37 chr7: 56,118,293-56,142,388 , GRCh38.p12 chr7: 56,050,600-56,074,695 CCT6A, SNORA22B, 3 more genes
    nsv6619461copy number variation1nstd223human GRCh38 chr7: 56,025,437-56,034,676 , GRCh37.p13 chr7: 56,093,130-56,102,369 PSPH
    nsv6618158copy number variation1nstd223human GRCh38 chr7: 56,020,601-56,021,400 , GRCh37.p13 chr7: 56,088,294-56,089,093 PSPH
    nsv6616362copy number variation1nstd223human GRCh38 chr7: 56,014,561-56,029,021 , GRCh37.p13 chr7: 56,082,254-56,096,714 PSPH
    nsv6609772copy number variation1nstd223human GRCh38 chr7: 56,030,638-56,032,400 , GRCh37.p13 chr7: 56,098,331-56,100,093 PSPH
    nsv6608956copy number variation1nstd223human GRCh38 chr7: 56,037,164-56,039,025 , GRCh37.p13 chr7: 56,104,857-56,106,718 PSPH
    nsv6608468copy number variation1nstd223human GRCh38 chr7: 56,034,988-56,035,871 , GRCh37.p13 chr7: 56,102,681-56,103,564 PSPH
    nsv6575108inversion1nstd223human GRCh38 chr7: 56,027,582-56,028,599 , GRCh37.p13 chr7: 56,095,275-56,096,292 PSPH
    nsv6574726inversion1nstd223human GRCh38 chr7: 56,012,017-56,013,326 , GRCh37.p13 chr7: 56,079,710-56,081,019 PSPH
    nsv6570457inversion1nstd223human GRCh38 chr7: 56,017,791-56,018,271 , GRCh37.p13 chr7: 56,085,484-56,085,964 PSPH
    nsv6570402inversion1nstd223human GRCh38 chr7: 56,047,712-56,048,192 , GRCh37.p13 chr7: 56,115,405-56,115,885 PSPH
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