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Items: 1 to 20 of 205

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7049962inversion1nstd229human GRCh38 chr2: 227,539,172-230,370,061 , GRCh37.p13 chr2: 228,403,888-231,234,776 SPHKAP, TRIP12, 37 more genes
    nsv7047209inversion1nstd229human GRCh38 chr2: 222,803,564-227,992,948 , GRCh37.p13 chr2: 223,668,283-228,857,664 MFF, LOC100289117, 55 more genes
    nsv7045781inversion1nstd229human GRCh38 chr2: 226,619,501-227,899,799 , GRCh37.p13 chr2: 227,484,217-228,764,515 SLC19A3, IRS1, 19 more genes
    nsv7043640inversion1nstd229human GRCh38 chr2: 222,841,128-228,011,478 , GRCh37.p13 chr2: 223,705,846-228,876,194 MFF-DT, LOC105373905, 55 more genes
    nsv6697971copy number variation1nstd229human GRCh38 chr2: 227,871,798-227,882,107 , GRCh37.p13 chr2: 228,736,514-228,746,823 DAW1
    nsv6696711copy number variation1nstd229human GRCh38 chr2: 227,913,838-227,917,576 , GRCh37.p13 chr2: 228,778,554-228,782,292 DAW1
    nsv6695630copy number variation1nstd229human GRCh38 chr2: 227,875,061-227,878,550 , GRCh37.p13 chr2: 228,739,777-228,743,266 DAW1
    nsv6690196copy number variation1nstd229human GRCh38 chr2: 227,908,701-227,914,300 , GRCh37.p13 chr2: 228,773,417-228,779,016 DAW1
    nsv6685985copy number variation1nstd229human GRCh38 chr2: 227,909,401-227,913,900 , GRCh37.p13 chr2: 228,774,117-228,778,616 DAW1
    nsv6684500copy number variation1nstd229human GRCh38 chr2: 227,888,085-227,894,054 , GRCh37.p13 chr2: 228,752,801-228,758,770 DAW1
    nsv6678700copy number variation1nstd229human GRCh38 chr2: 226,880,942-228,292,097 , GRCh37.p13 chr2: 227,745,658-229,156,813 LOC107985993, LOC100533842, 21 more genes
    nsv6546857inversion1nstd223human GRCh38 chr2: 227,892,175-227,893,025 , GRCh37.p13 chr2: 228,756,891-228,757,741 DAW1
    nsv6546353inversion1nstd223human GRCh38 chr2: 227,539,362-230,369,917 , GRCh37.p13 chr2: 228,404,078-231,234,632 FBXO36, LOC729968, 37 more genes
    nsv6541400inversion1nstd223human GRCh38 chr2: 227,539,172-230,370,025 , GRCh37.p13 chr2: 228,403,888-231,234,740 SNRPGP8, DNER, 37 more genes
    nsv6355179copy number variation1nstd223human GRCh38 chr2: 227,908,740-227,914,333 , GRCh37.p13 chr2: 228,773,456-228,779,049 DAW1
    nsv6352942copy number variation1nstd223human GRCh38 chr2: 227,914,495-227,915,105 , GRCh37.p13 chr2: 228,779,211-228,779,821 DAW1
    nsv6352130copy number variation1nstd223human GRCh38 chr2: 227,887,609-227,888,136 , GRCh37.p13 chr2: 228,752,325-228,752,852 DAW1
    nsv6338669copy number variation1nstd223human GRCh38 chr2: 227,888,073-227,894,053 , GRCh37.p13 chr2: 228,752,789-228,758,769 DAW1
    nsv6338332copy number variation1nstd223human GRCh38 chr2: 227,913,836-227,917,575 , GRCh37.p13 chr2: 228,778,552-228,782,291 DAW1
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
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