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Items: 1 to 20 of 174

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097426copy number variation1nstd102humanUncertain significance GRCh37 chr6: 30,695,893-36,953,949 , GRCh38.p12 chr6: 30,728,116-36,986,173 LEMD2, PSORS1C1, 321 more genes
    nsv7097325copy number variation1nstd102humanUncertain significance GRCh37 chr6: 30,695,893-31,937,492 , GRCh38.p12 chr6: 30,728,116-31,969,715 HCG21, SNORD84, 117 more genes
    nsv7053830inversion1nstd229human GRCh38 chr6: 29,164,448-38,692,657 , GRCh37.p13 chr6: 29,132,225-38,660,433 GTF2H4, RNF8, 472 more genes
    nsv7045112inversion1nstd229human GRCh38 chr6: 30,561,326-37,907,708 , GRCh37.p13 chr6: 30,529,103-37,875,484 ZBTB22, PNPLA1, 355 more genes
    nsv6795985copy number variation1nstd229human GRCh38 chr6: 31,835,376-31,840,940 , GRCh37.p13 chr6: 31,803,153-31,808,717 SNHG32, SNORD48, 1 more genes
    nsv6781134copy number variation1nstd229human GRCh38 chr6: 31,832,528-31,839,861 , GRCh37.p13 chr6: 31,800,305-31,807,638 SNORD52, SNHG32, 1 more genes
    nsv6779807copy number variation1nstd229human GRCh38 chr6: 31,800,134-32,311,768 , GRCh37.p13 chr6: 31,767,911-32,279,545 NELFE, CYP21A1P, 43 more genes
    nsv6402801copy number variation1nstd223human GRCh38 chr6: 31,831,130-31,835,700 , GRCh37.p13 chr6: 31,798,907-31,803,477 SNORD48, SNHG32, 1 more genes
    nsv6402266copy number variation1nstd223human GRCh38 chr6: 31,522,086-32,653,908 , GRCh37.p13 chr6: 31,489,863-32,621,685 MIR6833, LY6G5B, 102 more genes
    nsv6400469copy number variation1nstd223human GRCh38 chr6: 31,821,444-31,851,029 , GRCh37.p13 chr6: 31,789,221-31,818,806 HSPA1B, SNORD48, 2 more genes
    nsv6305183copy number variation1nstd186human GRCh37 chr6: 31,794,141-31,807,676 , GRCh38.p12 chr6: 31,826,364-31,839,899 HSPA1B, SNORD52, 2 more genes
    nsv6140608copy number variation1nstd206human GRCh38 chr6: 31,752,000-31,862,000 , GRCh37.p13 chr6: 31,719,777-31,829,777 LSM2, SLC44A4, 14 more genes
    nsv6135917copy number variation1nstd213human GRCh37 chr6: 30,110,000-32,450,001 , GRCh38.p12 chr6: 30,142,223-32,482,224 ABCF1, AGER, 186 more genes
    nsv5466629copy number variation1nstd206human GRCh38 chr6: 31,826,364-31,839,899 , GRCh37.p13 chr6: 31,794,141-31,807,676 SNORD52, SNORD48, 2 more genes
    nsv5301808copy number variation1nstd204human GRCh37.p13 chr6: 31,776,329-31,804,587 , GRCh38.p13 chr6: 31,808,552-31,836,810 HSPA1A, HSPA1B, 4 more genes
    nsv5238432copy number variation1nstd204human GRCh38.p13 chr6: 31,823,901-31,838,400 , GRCh37.p13 chr6: 31,791,678-31,806,177 HSPA1B, SNHG32, 2 more genes
    nsv5235511copy number variation1nstd204human GRCh38.p13 chr6: 31,808,301-31,834,300 , GRCh37.p13 chr6: 31,776,078-31,802,077 HSPA1B, SNORD48, 3 more genes
    nsv5234405copy number variation1nstd204human GRCh38.p13 chr6: 30,240,001-32,313,700 , GRCh37.p13 chr6: 30,207,778-32,281,477 DDAH2, LOC105375018, 175 more genes
    nsv5229879copy number variation1nstd204human GRCh38.p13 chr6: 31,502,001-32,151,900 , GRCh37.p13 chr6: 31,469,778-32,119,677 LTB, PPT2, 80 more genes
    nsv5229526copy number variation1nstd204human GRCh38.p13 chr6: 31,620,501-31,855,300 , GRCh37.p13 chr6: 31,588,278-31,823,077 LOC105375018, DDAH2, 35 more genes
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