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Items: 1 to 20 of 387

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148111copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,742,396-28,567,325 , GRCh38.p12 chr15: 23,319,714-28,322,179 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 SNORD116-18, PWAR4, 246 more genes
    nsv7137213copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,421-30,386,398 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-30,094,195 TVP23BP1, SNORD115-1, 247 more genes
    nsv7098883copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,406,271-28,566,579 , GRCh38.p12 chr15: 23,319,714-28,321,433 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 LOC105370739, SNORD116-27, 246 more genes
    nsv7093407copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,833,525-28,544,662 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,299,516 UBE2CP4, SERPINE4P, 246 more genes
    nsv7075933inversion1nstd229human GRCh38 chr15: 27,763,634-29,945,003 , GRCh37.p13 chr15: 28,008,780-30,237,206 RN7SL719P, ENTREP2, 39 more genes
    nsv7075173inversion1nstd229human GRCh38 chr15: 28,852,120-29,116,706 , GRCh37.p13 chr15: 29,097,266-29,408,909 APBA2, PDCD6IPP2, 1 more genes
    nsv7074171inversion1nstd229human GRCh38 chr15: 27,576,188-29,433,618 , GRCh37.p13 chr15: 27,821,334-29,725,822 MPHOSPH10P7, RN7SL238P, 34 more genes
    nsv7073515inversion1nstd229human GRCh38 chr15: 28,803,954-28,905,989 , GRCh37.p13 chr15: 29,049,100-29,151,135 LOC100129687, PDCD6IPP2, 3 more genes
    nsv7070433inversion1nstd229human GRCh38 chr15: 28,680,335-30,817,180 , GRCh37.p13 chr15: 28,925,481-31,109,383 RNU6-17P, RN7SL628P, 54 more genes
    nsv7065496inversion1nstd229human GRCh38 chr15: 20,672,644-28,900,286 , GRCh37.p13 chr15: 20,877,973-29,145,432 SNURF, LOC101060118, 290 more genes
    nsv7065294inversion1nstd229human GRCh38 chr15: 27,010,857-29,330,650 , GRCh37.p13 chr15: 27,256,004-29,622,854 GABRG3-AS1, HERC2P1, 40 more genes
    nsv7061220inversion1nstd229human GRCh38 chr15: 28,848,197-32,920,244 , GRCh37.p13 chr15: 29,093,343-33,212,445 LOC105376704, WHAMMP1, 96 more genes
    nsv6974014copy number variation1nstd229human GRCh38 chr15: 28,856,217-28,864,598 , GRCh37.p13 chr15: 29,101,363-29,109,744 FTLP11, PDCD6IPP2
    nsv6971894copy number variation1nstd229human GRCh38 chr15: 28,836,101-28,887,500 , GRCh37.p13 chr15: 29,081,247-29,132,646 APBA2, GOLGA6L7, 2 more genes
    nsv6971426copy number variation1nstd229human GRCh38 chr15: 28,830,358-28,876,073 , GRCh37.p13 chr15: 29,075,504-29,121,219 FTLP11, LOC100129687, 2 more genes
    nsv6965813copy number variation1nstd229human GRCh38 chr15: 28,730,365-28,970,097 , GRCh37.p13 chr15: 28,975,511-29,262,300 LOC100289656, APBA2, 7 more genes
    nsv6637995copy number variation1nstd102humanUncertain significance GRCh37 chr15: 28,934,987-29,688,117 , GRCh38.p12 chr15: 28,689,841-29,395,913 , GRCh38.p12 chr15|NT_187660.1: 965,631-1,671,412 , GRCh38.p12 chr15|NW_011332701.1: 851,845-1,558,928 APBA2, RN7SL719P, 12 more genes
    nsv6637778copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,422-28,545,601 , GRCh38.p12 chr15: 23,319,714-28,300,455 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 LOC107984779, ULK4P1, 246 more genes
    nsv6637612copy number variation1nstd102humanUncertain significance GRCh37 chr15: 28,934,987-30,386,399 , GRCh38.p12 chr15: 28,689,841-30,094,196 , GRCh38.p12 chr15|NW_011332701.1: 851,845-2,266,916 , GRCh38.p12 chr15|NT_187660.1: 965,631-2,379,400 RN7SL719P, LOC100129687, 21 more genes
    nsv6637596copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,290,787-28,560,269 , GRCh38.p12 chr15: 23,319,714-28,315,123 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 SNORD115-23, DEPDC1P1, 246 more genes
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