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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097765copy number variation1nstd102humanUncertain significance GRCh37 chr7: 96,318,236-97,493,828 , GRCh38.p12 chr7: 96,688,924-97,864,516 RN7SKP104, CZ1P-ASNS, 16 more genes
    nsv7052776inversion1nstd229human GRCh38 chr7: 96,709,838-100,726,550 , GRCh37.p13 chr7: 96,339,150-100,324,173 TMEM225B, PILRB, 141 more genes
    nsv7050278inversion1nstd229human GRCh38 chr7: 92,907,694-98,049,952 , GRCh37.p13 chr7: 92,537,008-97,679,264 LOC105375416, RNU6-364P, 88 more genes
    nsv7044481inversion1nstd229human GRCh38 chr7: 96,998,788-97,008,956 , GRCh37.p13 chr7: 96,628,100-96,638,268 DLX6, DLX6-AS1
    nsv6824443copy number variation1nstd229human GRCh38 chr7: 96,985,939-96,995,313 , GRCh37.p13 chr7: 96,615,251-96,624,625 DLX6-AS1
    nsv6823416copy number variation1nstd229human GRCh38 chr7: 96,979,460-96,982,523 , GRCh37.p13 chr7: 96,608,772-96,611,835 DLX6-AS1
    nsv6822063copy number variation1nstd229human GRCh38 chr7: 96,966,697-96,967,192 , GRCh37.p13 chr7: 96,596,009-96,596,504 DLX6-AS1
    nsv6636511copy number variation1nstd102humanPathogenic GRCh37 chr7: 96,264,152-96,860,892 , GRCh38.p12 chr7: 96,634,840-97,231,580 SDHAF3, DLX6, 9 more genes
    nsv6636271copy number variation1nstd102humanPathogenic GRCh37 chr7: 92,721,627-98,311,537 , GRCh38.p12 chr7: 93,092,314-98,682,225 MARK2P10, PON2, 97 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
    nsv6613346copy number variation1nstd223human GRCh38 chr7: 96,979,460-96,982,519 , GRCh37.p13 chr7: 96,608,772-96,611,831 DLX6-AS1
    nsv6609415copy number variation1nstd223human GRCh38 chr7: 96,967,116-96,967,491 , GRCh37.p13 chr7: 96,596,428-96,596,803 DLX6-AS1
    nsv6601851copy number variation1nstd223human GRCh38 chr7: 97,006,001-97,007,400 , GRCh37.p13 chr7: 96,635,313-96,636,712 DLX6, DLX6-AS1
    nsv6601844copy number variation1nstd223human GRCh38 chr7: 96,982,331-96,982,802 , GRCh37.p13 chr7: 96,611,643-96,612,114 DLX6-AS1
    nsv6566907inversion1nstd223human GRCh38 chr7: 97,000,910-97,001,104 , GRCh37.p13 chr7: 96,630,222-96,630,416 DLX6-AS1
    nsv6557884inversion1nstd223human GRCh38 chr7: 97,000,063-97,001,388 , GRCh37.p13 chr7: 96,629,375-96,630,700 DLX6-AS1
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6312877copy number variation1nstd102humanPathogenic GRCh37 chr7: 95,434,042-96,747,209 , GRCh38.p12 chr7: 95,804,730-97,117,897 DYNC1I1, DLX6-AS1, 18 more genes
    nsv6266305copy number variation1nstd214human GRCh38 chr7: 96,996,040-96,996,101 , GRCh37.p13 chr7: 96,625,352-96,625,413 DLX6-AS1
    nsv6137024copy number variation1nstd213human GRCh37 chr7: 93,400,000-97,690,001 , GRCh38.p12 chr7: 93,770,688-98,060,689 , SEM1, 77 more genes
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