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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140497copy number variation1nstd232human GRCh37.p13 chr1: 185,269,474-185,269,566 , GRCh38.p12 chr1: 185,300,342-185,300,434 IVNS1ABP
    nsv7140204copy number variation1nstd232human GRCh37.p13 chr1: 185,269,261-185,269,346 , GRCh38.p12 chr1: 185,300,129-185,300,214 IVNS1ABP
    nsv7137660insertion1nstd232human GRCh37.p13 chr1: 185,274,776-185,274,776 , GRCh38.p12 chr1: 185,305,644-185,305,644 IVNS1ABP
    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
    nsv7053326inversion1nstd229human GRCh38 chr1: 183,856,809-187,909,288 , GRCh37.p13 chr1: 183,825,943-187,878,419 RGL1, TPR, 49 more genes
    nsv6645823copy number variation1nstd229human GRCh38 chr1: 185,310,001-185,326,200 , GRCh37.p13 chr1: 185,279,133-185,295,332 IVNS1ABP, GS1-279B7.1
    nsv6645822copy number variation1nstd229human GRCh38 chr1: 185,296,477-185,300,231 , GRCh37.p13 chr1: 185,265,609-185,269,363 IVNS1ABP
    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
    nsv6548934inversion1nstd223human GRCh38 chr1: 183,856,809-187,909,292 , GRCh37.p13 chr1: 183,825,943-187,878,423 LOC105371649, LINC01633, 49 more genes
    nsv6327952copy number variation1nstd223human GRCh38 chr1: 185,291,306-185,293,219 , GRCh37.p13 chr1: 185,260,438-185,262,351 SWT1, IVNS1ABP
    nsv6327480copy number variation1nstd223human GRCh38 chr1: 185,294,801-185,295,500 , GRCh37.p13 chr1: 185,263,933-185,264,632 IVNS1ABP
    nsv6324104copy number variation1nstd223human GRCh38 chr1: 185,298,552-185,299,035 , GRCh37.p13 chr1: 185,267,684-185,268,167 IVNS1ABP
    nsv6321918copy number variation1nstd223human GRCh38 chr1: 185,296,475-185,300,228 , GRCh37.p13 chr1: 185,265,607-185,269,360 IVNS1ABP
    nsv6319102copy number variation1nstd223human GRCh38 chr1: 185,296,060-185,296,243 , GRCh37.p13 chr1: 185,265,192-185,265,375 IVNS1ABP
    nsv6318082copy number variation1nstd223human GRCh38 chr1: 185,302,701-185,303,600 , GRCh37.p13 chr1: 185,271,833-185,272,732 IVNS1ABP
    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
    nsv6289913copy number variation1nstd102humanPathogenic GRCh37 chr1: 185,276,239-185,287,961 , GRCh38.p12 chr1: 185,307,107-185,318,829 IVNS1ABP
    nsv6257510mobile element insertion1nstd215human GRCh38 chr1: 185,291,312-185,291,312 , GRCh37.p13 chr1: 185,260,444-185,260,444 IVNS1ABP, SWT1
    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
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