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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099254copy number variation1nstd231human GRCh38.p12 chr1: 182,376,401-191,898,122 , GRCh37 chr1: 182,345,536-191,867,252 DHX9, GLUL, 99 more genes
    nsv6645920copy number variation1nstd229human GRCh38 chr1: 183,627,201-183,646,000 , GRCh37.p13 chr1: 183,596,336-183,615,135 ARPC5, RGL1, 1 more genes
    nsv6637124copy number variation1nstd102humanPathogenic GRCh37 chr1: 179,727,182-192,260,142 , GRCh38.p12 chr1: 179,758,047-192,291,012 LOC101928933, KIAA1614-AS1, 148 more genes
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 more genes
    nsv6538365inversion1nstd223human GRCh38 chr1: 178,815,320-184,820,865 , GRCh37.p13 chr1: 178,784,455-184,789,999 NPHS2, COLGALT2, 111 more genes
    nsv6330681copy number variation1nstd223human GRCh38 chr1: 183,613,401-183,619,000 , GRCh37.p13 chr1: 183,582,536-183,588,135 ARPC5
    nsv6317339copy number variation1nstd223human GRCh38 chr1: 183,613,101-183,619,900 , GRCh37.p13 chr1: 183,582,236-183,589,035 ARPC5
    nsv6290451copy number variation1nstd102humanPathogenic GRCh37 chr1: 178,522,021-190,322,133 , GRCh38.p12 chr1: 178,552,886-190,353,003 RNU7-13P, LOC105371642, 167 more genes
    nsv6139466copy number variation1nstd206human GRCh38 chr1: 183,612,587-183,619,000 , GRCh37.p13 chr1: 183,581,722-183,588,135 ARPC5
    nsv6133952copy number variation1nstd213human GRCh37 chr1: 182,620,000-185,630,001 , GRCh38.p12 chr1: 182,650,865-185,660,869 DHX9, IVNS1ABP, 54 more genes
    nsv6133950copy number variation1nstd213human GRCh37 chr1: 178,070,000-205,920,001 , GRCh38.p12 chr1: 178,100,865-205,950,873 ADORA1, CACNA1E, 442 more genes
    nsv6133933copy number variation1nstd213human GRCh37 chr1: 161,620,000-196,730,001 , GRCh38.p12 chr1: 161,650,210-196,760,871 FASLG, SERPINC1, 510 more genes
    nsv6133573copy number variation1nstd213human GRCh37 chr1: 173,820,000-189,960,001 , GRCh38.p12 chr1: 173,850,862-189,990,871 ABL2, ASTN1, 235 more genes
    nsv5828572copy number variation1nstd209human GRCh38 chr1: 183,614,636-183,619,597 , GRCh37.p13 chr1: 183,583,771-183,588,732 ARPC5
    nsv5441535copy number variation1nstd206human GRCh38 chr1: 183,613,517-183,619,258 , GRCh37.p13 chr1: 183,582,652-183,588,393 ARPC5
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5218087copy number variation1nstd204human GRCh38.p13 chr1: 183,614,661-183,619,597 , GRCh37.p13 chr1: 183,583,796-183,588,732 ARPC5
    nsv5200818copy number variation1nstd204human GRCh38.p13 chr1: 183,617,887-183,619,397 , GRCh37.p13 chr1: 183,587,022-183,588,532 ARPC5
    nsv4906654copy number variation1nstd200human GRCh38 chr1: 183,613,295-183,619,134 , GRCh37.p13 chr1: 183,582,430-183,588,269 ARPC5
    nsv4904094copy number variation1nstd200human GRCh38 chr1: 183,519,107-183,703,338 , GRCh37.p13 chr1: 183,488,242-183,672,473 , NCF2, 5 more genes
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