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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056430inversion1nstd229human GRCh38 chr7: 4,797,959-5,729,617 , GRCh37.p13 chr7: 4,837,590-5,769,248 RPL22P16, SNORD165, 25 more genes
    nsv7052786inversion1nstd229human GRCh38 chr7: 2,451,109-6,490,439 , GRCh37.p13 chr7: 2,490,744-6,530,070 LOC105375130, DAGLB, 72 more genes
    nsv7046629inversion1nstd229human GRCh38 chr7: 4,803,660-4,922,762 , GRCh37.p13 chr7: 4,843,291-4,962,393 RADIL, PAPOLB, 3 more genes
    nsv7040562inversion1nstd229human GRCh38 chr7: 3,251,541-5,214,703 , GRCh37.p13 chr7: 3,291,173-5,254,334 LOC105375134, RBAK, 24 more genes
    nsv7039347inversion1nstd229human GRCh38 chr7: 4,097,073-5,367,462 , GRCh37.p13 chr7: 4,136,705-5,407,093 SLC29A4, AP5Z1, 23 more genes
    nsv7039273inversion1nstd229human GRCh38 chr7: 4,844,810-5,848,921 , GRCh37.p13 chr7: 4,884,441-5,888,552 RBAK-RBAKDN, ZNF890P, 25 more genes
    nsv6816177copy number variation1nstd229human GRCh38 chr7: 4,791,000-4,871,769 , GRCh37.p13 chr7: 4,830,631-4,911,400 RPL22P16, SNORD165, 3 more genes
    nsv6815979copy number variation1nstd229human GRCh38 chr7: 4,853,190-4,875,408 , GRCh37.p13 chr7: 4,892,821-4,915,039 RADIL, RPL22P16, 1 more genes
    nsv6808383copy number variation1nstd229human GRCh38 chr7: 4,826,200-4,927,496 , GRCh37.p13 chr7: 4,865,831-4,967,127 SNORD165, RPL22P16, 3 more genes
    nsv6807876copy number variation1nstd229human GRCh38 chr7: 4,833,663-4,996,493 , GRCh37.p13 chr7: 4,873,294-5,036,124 RNF216P1, RADIL, 4 more genes
    nsv6807058copy number variation1nstd229human GRCh38 chr7: 4,775,515-4,883,892 , GRCh37.p13 chr7: 4,815,146-4,923,523 RADIL, PAPOLB, 4 more genes
    nsv6801850copy number variation1nstd229human GRCh38 chr7: 4,781,462-4,909,374 , GRCh37.p13 chr7: 4,821,093-4,949,005 MMD2, AP5Z1, 5 more genes
    nsv6800975copy number variation1nstd229human GRCh38 chr7: 4,807,012-4,879,315 , GRCh37.p13 chr7: 4,846,643-4,918,946 SNORD165, RPL22P16, 2 more genes
    nsv6800462copy number variation1nstd229human GRCh38 chr7: 4,785,701-4,879,600 , GRCh37.p13 chr7: 4,825,332-4,919,231 SNORD165, AP5Z1, 4 more genes
    nsv6637140copy number variation1nstd102humanUncertain significance GRCh37 chr7: 4,868,426-5,184,301 , GRCh38.p12 chr7: 4,828,795-5,144,670 SNORD165, OR10AH1P, 11 more genes
    nsv6637083copy number variation1nstd102humanPathogenic GRCh37 chr7: 4,655,928-5,990,874 , GRCh38.p12 chr7: 4,616,297-5,951,243 RN7SL556P, MIR6874, 34 more genes
    nsv6634397copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-19,485,604 , GRCh38.p12 chr7: 43,360-19,445,981 DNAAF5, FSCN1, 277 more genes
    nsv6634339copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-9,649,794 , GRCh38.p12 chr7: 43,360-9,610,164 MRM2, FOXL3, 182 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
    nsv6632153copy number variation1nstd224human GRCh37 chr7: 4,844,843-4,975,010 , GRCh38.p12 chr7: 4,805,212-4,935,379 RADIL, PAPOLB, 3 more genes
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