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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7097256copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr4: 55,124,936-57,368,027 , GRCh38.p12 chr4: 54,258,769-56,501,861 AASDH, EXOC1, 40 more genes
    nsv7043890inversion1nstd229human GRCh38 chr4: 55,335,201-55,508,922 , GRCh37.p13 chr4: 56,201,368-56,375,089 TMEM165, SRD5A3-AS1, 4 more genes
    nsv7042838inversion1nstd229human GRCh38 chr4: 55,519,343-61,509,140 , GRCh37.p13 chr4: 56,385,510-62,374,858 LINC02271, CHAER1, 59 more genes
    nsv6736229copy number variation1nstd229human GRCh38 chr4: 55,501,366-55,501,430 , GRCh37.p13 chr4: 56,367,533-56,367,597 CLOCK
    nsv6732598copy number variation1nstd229human GRCh38 chr4: 55,495,588-55,495,755 , GRCh37.p13 chr4: 56,361,755-56,361,922 CLOCK
    nsv6731995copy number variation1nstd229human GRCh38 chr4: 55,519,549-55,523,059 , GRCh37.p13 chr4: 56,385,716-56,389,226 CLOCK
    nsv6730000copy number variation1nstd229human GRCh38 chr4: 55,445,105-55,445,276 , GRCh37.p13 chr4: 56,311,272-56,311,443 TMEM165, CLOCK
    nsv6729778copy number variation1nstd229human GRCh38 chr4: 55,438,286-55,439,523 , GRCh37.p13 chr4: 56,304,453-56,305,690 CLOCK, TMEM165
    nsv6728590copy number variation1nstd229human GRCh38 chr4: 55,492,931-55,497,732 , GRCh37.p13 chr4: 56,359,098-56,363,899 CLOCK
    nsv6728174copy number variation1nstd229human GRCh38 chr4: 55,519,702-55,530,090 , GRCh37.p13 chr4: 56,385,869-56,396,257 CLOCK
    nsv6727739copy number variation1nstd229human GRCh38 chr4: 55,499,858-55,500,538 , GRCh37.p13 chr4: 56,366,025-56,366,705 CLOCK
    nsv6725591copy number variation1nstd229human GRCh38 chr4: 55,515,301-55,598,400 , GRCh37.p13 chr4: 56,381,468-56,464,567 CLOCK, RN7SKP30, 2 more genes
    nsv6723485copy number variation1nstd229human GRCh38 chr4: 55,332,176-55,534,874 , GRCh37.p13 chr4: 56,198,343-56,401,041 TMEM165, CLOCK, 4 more genes
    nsv6722954copy number variation1nstd229human GRCh38 chr4: 55,532,549-55,535,087 , GRCh37.p13 chr4: 56,398,716-56,401,254 CLOCK
    nsv6721298copy number variation1nstd229human GRCh38 chr4: 55,499,878-55,500,493 , GRCh37.p13 chr4: 56,366,045-56,366,660 CLOCK
    nsv6720857copy number variation1nstd229human GRCh38 chr4: 55,487,273-55,490,372 , GRCh37.p13 chr4: 56,353,440-56,356,539 CLOCK
    nsv6637063copy number variation1nstd102humanUncertain significance GRCh37 chr4: 52,685,980-59,272,025 , GRCh38.p12 chr4: 51,819,814-58,405,859 SPINK2, RN7SL492P, 100 more genes
    nsv6574609inversion1nstd223human GRCh38 chr4: 55,506,715-55,507,216 , GRCh37.p13 chr4: 56,372,882-56,373,383 CLOCK
    nsv6567797inversion1nstd223human GRCh38 chr4: 55,539,588-55,540,023 , GRCh37.p13 chr4: 56,405,755-56,406,190 RN7SKP30, CLOCK
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