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Items: 1 to 20 of 220

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050777inversion1nstd229human GRCh38 chr2: 117,420,323-122,585,255 , GRCh37.p13 chr2: 118,177,899-123,342,831 LOC105373578, RPL17P15, 65 more genes
    nsv7044064inversion1nstd229human GRCh38 chr2: 112,019,946-120,004,832 , GRCh37.p13 chr2: 112,777,523-120,762,408 LOC105373563, IL1A, 112 more genes
    nsv6690412copy number variation1nstd229human GRCh38 chr2: 119,252,531-119,258,754 , GRCh37.p13 chr2: 120,010,107-120,016,330 STEAP3
    nsv6686910copy number variation1nstd229human GRCh38 chr2: 119,244,486-119,247,672 , GRCh37.p13 chr2: 120,002,062-120,005,248 STEAP3, STEAP3-AS1
    nsv6683084copy number variation1nstd229human GRCh38 chr2: 119,243,801-119,248,000 , GRCh37.p13 chr2: 120,001,377-120,005,576 STEAP3, STEAP3-AS1
    nsv6678274copy number variation1nstd229human GRCh38 chr2: 119,149,539-119,259,205 , GRCh37.p13 chr2: 119,907,115-120,016,781 LOC107985941, STEAP3, 3 more genes
    nsv6636871copy number variation1nstd102humanPathogenic GRCh37 chr2: 116,761,476-123,897,262 , GRCh38.p12 chr2: 116,003,900-123,139,686 LOC105373578, RPL17P15, 78 more genes
    nsv6553311inversion1nstd223human GRCh38 chr2: 113,382,126-121,687,299 , GRCh37.p13 chr2: 114,139,703-122,444,875 RPSAP23, CCDC93, 98 more genes
    nsv6349537copy number variation1nstd223human GRCh38 chr2: 119,247,614-119,525,129 , GRCh37.p13 chr2: 120,005,190-120,282,705 SCTR, C2orf76, 6 more genes
    nsv6343255copy number variation1nstd223human GRCh38 chr2: 119,228,011-119,229,221 , GRCh37.p13 chr2: 119,985,587-119,986,797 STEAP3
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314748copy number variation1nstd102humanPathogenic GRCh37 chr2: 112,475,655-145,691,999 , GRCh38.p12 chr2: 111,718,078-144,934,432 MED15P9, TMEM37, 474 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6313770copy number variation1nstd102humanPathogenic GRCh37 chr2: 113,188,197-128,144,700 , GRCh38.p12 chr2: 112,430,620-127,387,124 LOC105373575, RPS20P11, 174 more genes
    nsv6291375copy number variation1nstd102humanUncertain significance GRCh37 chr2: 118,991,485-120,025,223 , GRCh38.p12 chr2: 118,233,909-119,267,647 MARCO, LOC107985815, 9 more genes
    nsv6291353copy number variation1nstd102humanPathogenic GRCh37 chr2: 111,484,468-146,333,604 , GRCh38.p12 chr2: 110,726,891-145,576,036 LINC01120, LOC105373585, 490 more genes
    nsv6290805copy number variation1nstd102humanUncertain significance GRCh37 chr2: 119,967,365-121,555,029 , GRCh38.p12 chr2: 119,209,789-120,797,453 LOC101927764, MTND5P28, 29 more genes
    nsv6277759insertion1nstd214human GRCh38 chr2: 119,254,050-119,254,050 , GRCh37.p13 chr2: 120,011,626-120,011,626 STEAP3
    nsv6252918mobile element insertion1nstd215human GRCh38 chr2: 119,260,800-119,260,800 , GRCh37.p13 chr2: 120,018,376-120,018,376 STEAP3
    nsv6162987copy number variation1nstd214human GRCh38 chr2: 119,257,579-119,257,636 , GRCh37.p13 chr2: 120,015,155-120,015,212 STEAP3
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