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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097200copy number variation1nstd102humanUncertain significance GRCh37 chr3: 47,079,136-47,454,675 , GRCh38.p12 chr3: 47,037,646-47,413,185 SETD2, SNORD13P3, 6 more genes
    nsv7096805copy number variation1nstd102humanUncertain significance GRCh37 chr3: 45,435,946-49,137,751 , GRCh38.p12 chr3: 45,394,454-49,100,318 SNORA94, LIMD1-AS1, 120 more genes
    nsv6717613copy number variation1nstd229human GRCh38 chr3: 47,230,954-47,260,715 , GRCh37.p13 chr3: 47,272,444-47,302,205 SNORD13J, KIF9-AS1, 2 more genes
    nsv6715780copy number variation1nstd229human GRCh38 chr3: 47,123,514-47,692,642 , GRCh37.p13 chr3: 47,165,004-47,734,132 SNORD13J, PTPN23, 15 more genes
    nsv6714234copy number variation1nstd229human GRCh38 chr3: 47,246,901-47,286,200 , GRCh37.p13 chr3: 47,288,391-47,327,690 KLHL18, SNORD13P3, 2 more genes
    nsv6714076copy number variation1nstd229human GRCh38 chr3: 47,125,101-47,626,500 , GRCh37.p13 chr3: 47,166,591-47,667,990 LOC105377073, KIF9-AS1, 13 more genes
    nsv6713511copy number variation1nstd229human GRCh38 chr3: 46,395,301-47,630,000 , GRCh37.p13 chr3: 46,436,792-47,671,490 BOLA2P2, LRRC2-AS1, 36 more genes
    nsv6710515copy number variation1nstd229human GRCh38 chr3: 47,248,322-47,402,005 , GRCh37.p13 chr3: 47,289,812-47,443,495 SNORD13P3, SNORD13J, 3 more genes
    nsv6706759copy number variation1nstd229human GRCh38 chr3: 47,123,901-47,954,200 , GRCh37.p13 chr3: 47,165,391-47,995,690 KIF9-AS1, LOC105377073, 18 more genes
    nsv6637062copy number variation1nstd102humanUncertain significance GRCh37 chr3: 47,188,373-47,350,231 , GRCh38.p12 chr3: 47,146,883-47,308,741 KLHL18, SNORD13J, 4 more genes
    nsv6636386copy number variation1nstd102humanUncertain significance GRCh37 chr3: 47,188,373-47,338,349 , GRCh38.p12 chr3: 47,146,883-47,296,859 KIF9, KIF9-AS1, 4 more genes
    nsv6358555copy number variation1nstd223human GRCh38 chr3: 47,223,435-47,451,673 , GRCh37.p13 chr3: 47,264,925-47,493,163 SNORD13P3, KLHL18, 5 more genes
    nsv6357893copy number variation1nstd223human GRCh38 chr3: 47,138,012-47,301,836 , GRCh37.p13 chr3: 47,179,502-47,343,326 SNORD13P3, SNORD13J, 4 more genes
    nsv6315166copy number variation1nstd102humanPathogenic GRCh37 chr3: 44,948,482-49,115,809 , GRCh38.p12 chr3: 44,906,990-49,078,376 TMEM89, TGM4, 129 more genes
    nsv6134694copy number variation1nstd213human GRCh37 chr3: 46,170,000-52,140,001 , GRCh38.p12 chr3: 46,128,508-52,105,985 ACY1, AMT, 210 more genes
    nsv5899296copy number variation1nstd209human GRCh38 chr3: 47,056,814-47,275,173 , GRCh37.p13 chr3: 47,098,304-47,316,663 SNORD13P3, SETD2, 3 more genes
    nsv5888582copy number variation1nstd209human GRCh38 chr3: 46,802,705-48,210,414 , GRCh37.p13 chr3: 46,844,195-48,251,904 SNORD13P3, LOC105377074, 34 more genes
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
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