U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 209

    loading data ...

    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
    nsv6646374copy number variation1nstd229human GRCh38 chr1: 186,437,616-186,452,727 , GRCh37.p13 chr1: 186,406,748-186,421,859 PDC-AS1, PDC
    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
    nsv6646298copy number variation1nstd229human GRCh38 chr1: 186,447,578-186,460,250 , GRCh37.p13 chr1: 186,416,710-186,429,382 PDC, PDC-AS1
    nsv6646297copy number variation1nstd229human GRCh38 chr1: 186,447,322-186,465,558 , GRCh37.p13 chr1: 186,416,454-186,434,690 PDC-AS1, PDC
    nsv6646295copy number variation1nstd229human GRCh38 chr1: 186,435,785-186,474,694 , GRCh37.p13 chr1: 186,404,917-186,443,826 PDC-AS1, PDC
    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
    nsv6325934copy number variation1nstd223human GRCh38 chr1: 186,437,616-186,452,725 , GRCh37.p13 chr1: 186,406,748-186,421,857 PDC-AS1, PDC
    nsv6325548copy number variation1nstd223human GRCh38 chr1: 186,353,351-186,602,074 , GRCh37.p13 chr1: 186,322,483-186,571,206 PDC, PDC-AS1, 3 more genes
    nsv6321076copy number variation1nstd223human GRCh38 chr1: 186,442,842-186,445,251 , GRCh37.p13 chr1: 186,411,974-186,414,383 PDC, PDC-AS1
    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
    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
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center