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Items: 1 to 20 of 172

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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
    nsv7095494copy number variation1nstd102humanUncertain significance GRCh37 chr1: 185,703,912-186,957,640 , GRCh38.p12 chr1: 185,734,780-186,988,508 RNU6-1240P, PTGS2, 10 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
    nsv7043300inversion1nstd229human GRCh38 chr1: 186,652,644-186,780,688 , GRCh37.p13 chr1: 186,621,776-186,749,820 PACERR, PTGS2
    nsv6646375copy number variation1nstd229human GRCh38 chr1: 186,466,556-187,012,513 , GRCh37.p13 chr1: 186,435,688-186,981,645 PTGS2, LOC100131939, 3 more genes
    nsv6646373copy number variation1nstd229human GRCh38 chr1: 186,411,064-187,073,315 , GRCh37.p13 chr1: 186,380,196-187,042,447 LOC100131939, PTGS2, 5 more genes
    nsv6645841copy number variation1nstd229human GRCh38 chr1: 185,932,287-189,941,246 , GRCh37.p13 chr1: 185,901,419-189,910,376 LINC01036, LOC100131939, 27 more genes
    nsv6637148copy number variation1nstd102humanUncertain significance GRCh37 chr1: 186,137,950-187,028,283 , GRCh38.p12 chr1: 186,168,818-187,059,151 LOC100131939, PTGS2, 10 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
    nsv6554110inversion1nstd223human GRCh38 chr1: 185,994,052-187,137,812 , GRCh37.p13 chr1: 185,963,184-187,106,944 LINC01036, RNU6-1240P, 11 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
    nsv6541191inversion1nstd223human GRCh38 chr1: 186,637,402-189,474,697 , GRCh37.p13 chr1: 186,606,534-189,443,827 CLPTM1LP1, LOC100967224, 16 more genes
    nsv6537463inversion1nstd223human GRCh38 chr1: 186,637,378-189,474,836 , GRCh37.p13 chr1: 186,606,510-189,443,966 LINC01037, RN7SKP156, 16 more genes
    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
    nsv6133954copy number variation1nstd213human GRCh37 chr1: 186,510,000-187,210,001 , GRCh38.p12 chr1: 186,540,868-187,240,869 PLA2G4A, PTGS2, 3 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
    nsv6133837copy number variation1nstd213human GRCh37 chr1: 185,830,000-191,830,001 , GRCh38.p12 chr1: 185,860,868-191,860,871 ODR4, BRINP3, 35 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
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