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Items: 1 to 20 of 280

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097375copy number variation1nstd102humanUncertain significance GRCh37 chr7: 43,810,758-44,747,598 , GRCh38.p12 chr7: 43,771,159-44,707,999 RASA4CP, OGDH, 31 more genes
    nsv6837797copy number variation1nstd229human GRCh38 chr7: 43,974,601-44,009,100 , GRCh37.p13 chr7: 44,014,200-44,048,699 SPDYE1, POLR2J4
    nsv6825472copy number variation1nstd229human GRCh38 chr7: 44,002,243-44,022,564 , GRCh37.p13 chr7: 44,041,842-44,062,163 SPDYE1, POLR2J4
    nsv6825178copy number variation1nstd229human GRCh38 chr7: 44,006,401-44,163,300 , GRCh37.p13 chr7: 44,046,000-44,202,899 PGAM2, POLR2J4, 14 more genes
    nsv6824378copy number variation1nstd229human GRCh38 chr7: 43,852,301-44,460,500 , GRCh37.p13 chr7: 43,891,900-44,500,099 DBNL, GCK, 23 more genes
    nsv6824175copy number variation1nstd229human GRCh38 chr7: 44,000,801-44,002,500 , GRCh37.p13 chr7: 44,040,400-44,042,099 SPDYE1, POLR2J4
    nsv6819640copy number variation1nstd229human GRCh38 chr7: 44,004,022-44,011,299 , GRCh37.p13 chr7: 44,043,621-44,050,898 POLR2J4, SPDYE1
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6632444copy number variation1nstd224human GRCh37 chr7: 76,134,398-76,432,653 , GRCh38.p12 chr7: 76,505,081-76,803,336 , GRCh38.p12 chr7|NT_187561.1: 4,100-209,586 POMZP3, DTX2, 4 more genes
    nsv6632384copy number variation1nstd224human GRCh37 chr7: 76,134,398-76,452,331 , GRCh38.p12 chr7: 76,505,081-76,823,014 , GRCh38.p12 chr7|NT_187561.1: 4,100-209,586 POMZP3, DTX2, 4 more genes
    nsv6632006copy number variation1nstd224human GRCh37 chr7: 76,131,684-76,209,459 , GRCh38.p12 chr7: 76,502,367-76,580,142 , GRCh38.p12 chr7|NT_187561.1: 1,386-66,977 SPDYE1, UPK3B, 3 more genes
    nsv6614409copy number variation1nstd223human GRCh38 chr7: 44,004,034-44,011,322 , GRCh37.p13 chr7: 44,043,633-44,050,921 SPDYE1, POLR2J4
    nsv6606962copy number variation1nstd223human GRCh38 chr7: 43,996,005-43,998,327 , GRCh37.p13 chr7: 44,035,604-44,037,926 POLR2J4, SPDYE1
    nsv6605422copy number variation1nstd223human GRCh38 chr7: 44,002,101-44,008,000 , GRCh37.p13 chr7: 44,041,700-44,047,599 SPDYE1, POLR2J4
    nsv6605207copy number variation1nstd223human GRCh38 chr7: 44,009,201-44,010,100 , GRCh37.p13 chr7: 44,048,800-44,049,699 POLR2J4, SPDYE1
    nsv6574607inversion1nstd223human GRCh38 chr7: 35,958,610-45,735,691 , GRCh37.p13 chr7: 35,998,220-45,775,290 RPS17P13, LOC105375252, 182 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313509copy number variation1nstd102humanPathogenic GRCh37 chr7: 40,778,439-50,228,656 , GRCh38.p12 chr7: 40,738,840-50,189,060 LINC01447, ABCA13, 142 more genes
    nsv6136995copy number variation1nstd213human GRCh37 chr7: 39,040,000-48,190,001 , GRCh38.p12 chr7: 39,000,400-48,150,404 ADCY1, AEBP1, 161 more genes
    nsv6136183copy number variation1nstd213human GRCh37 chr7: 43,240,000-44,280,001 , GRCh38.p12 chr7: 43,200,401-44,240,402 GCK, YKT6, 31 more genes
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