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Items: 1 to 20 of 318

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097267copy number variation3nstd102humanUncertain significance GRCh37 chr5: 175,158,654-179,263,593 , GRCh38.p12 chr5: 175,731,651-179,836,593 LOC112267937, LMAN2, 122 more genes
    nsv7096770copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,413,111-179,263,593 , GRCh38.p12 chr5|NW_016107298.1: 1-602,153 , GRCh38.p12 chr5: 178,986,110-179,836,593 HMGB3P22, MAML1, 25 more genes
    nsv7050742inversion1nstd229human GRCh38 chr5: 179,686,454-179,689,257 , GRCh37.p13 chr5: 179,113,455-179,116,258 CANX
    nsv7045128inversion1nstd229human GRCh38 chr5: 179,650,553-179,692,618 , GRCh37.p13 chr5: 179,077,554-179,119,619 CBY3, HMGB3P22, 3 more genes
    nsv6793784copy number variation1nstd229human GRCh38 chr5: 179,673,327-179,687,011 , GRCh37.p13 chr5: 179,100,328-179,114,012 CBY3, CANX, 1 more genes
    nsv6787892copy number variation1nstd229human GRCh38 chr5: 179,677,341-179,688,751 , GRCh37.p13 chr5: 179,104,342-179,115,752 CANX, CBY3
    nsv6787348copy number variation1nstd229human GRCh38 chr5: 179,680,419-179,680,474 , GRCh37.p13 chr5: 179,107,420-179,107,475 CANX, CBY3
    nsv6786644copy number variation1nstd229human GRCh38 chr5: 179,681,901-179,698,400 , GRCh37.p13 chr5: 179,108,902-179,125,401 CANX, HMGB3P22
    nsv6785744copy number variation1nstd229human GRCh38 chr5: 179,693,350-179,693,466 , GRCh37.p13 chr5: 179,120,351-179,120,467 HMGB3P22, CANX
    nsv6784499copy number variation1nstd229human GRCh38 chr5: 179,682,502-179,685,197 , GRCh37.p13 chr5: 179,109,503-179,112,198 CANX
    nsv6782281copy number variation1nstd229human GRCh38 chr5: 179,683,309-179,683,714 , GRCh37.p13 chr5: 179,110,310-179,110,715 CANX
    nsv6781053copy number variation1nstd229human GRCh38 chr5: 179,720,383-179,720,545 , GRCh37.p13 chr5: 179,147,384-179,147,546 CANX
    nsv6636440copy number variation1nstd102humanUncertain significance GRCh37 chr5: 177,746,012-179,975,280 , GRCh38.p12 chr5: 178,319,011-180,548,280 RUFY1-AS1, RPS15AP18, 60 more genes
    nsv6636392copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,947,702-179,645,244 , GRCh38.p12 chr5: 179,520,701-180,218,244 , GRCh38.p12 chr5|NW_016107298.1: 285,253-673,059 LOC646058, LOC100289470, 26 more genes
    nsv6634369copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,350,336-180,719,789 , GRCh38.p12 chr5: 170,923,332-181,292,788 GFPT2, FOXO1B, 287 more genes
    nsv6630512copy number variation1nstd224human GRCh37 chr5: 179,094,108-179,121,263 , GRCh38.p12 chr5: 179,667,107-179,694,262 , GRCh38.p12 chr5|NW_016107298.1: 432,810-459,822 CANX, CBY3, 2 more genes
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6313896copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,860,745-179,534,363 , GRCh38.p12 chr5: 179,433,744-180,107,363 , GRCh38.p12 chr5|NW_016107298.1: 198,326-673,059 RUFY1, HNRNPH1, 27 more genes
    nsv6313755copy number variation1nstd102humanUncertain significance GRCh37 chr5: 177,954,576-180,198,875 , GRCh38.p12 chr5: 178,527,575-180,771,875 MIR340, RASGEF1C, 64 more genes
    nsv6313609copy number variation1nstd102humanUncertain significance GRCh37 chr5: 179,082,801-179,409,280 , GRCh38.p12 chr5|NW_016107298.1: 421,507-673,059 , GRCh38.p12 chr5: 179,655,800-179,982,280 CANX, RN7SKP150, 15 more genes
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