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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097202copy number variation1nstd102humanUncertain significance GRCh37 chr3: 49,866,536-50,540,854 , GRCh38.p12 chr3: 49,829,103-50,503,423 HYAL2, MON1A, 32 more genes
    nsv6715287copy number variation1nstd229human GRCh38 chr3: 50,246,462-50,249,211 , GRCh37.p13 chr3|NW_003871059.1: 16,310-19,059 , GRCh37.p13 chr3: 50,283,894-50,286,643 GNAI2
    nsv6714122copy number variation1nstd229human GRCh38 chr3: 50,253,184-50,256,191 , GRCh37.p13 chr3|NW_003871059.1: 23,032-26,039 , GRCh37.p13 chr3: 50,290,616-50,293,623 GNAI2
    nsv6701727copy number variation1nstd229human GRCh38 chr3: 50,244,948-50,244,982 , GRCh37.p13 chr3: 50,282,380-50,282,414 , GRCh37.p13 chr3|NW_003871059.1: 14,796-14,830 GNAI2
    nsv6700836copy number variation1nstd229human GRCh38 chr3: 48,056,801-51,204,000 , GRCh37.p13 chr3: 48,098,291-51,241,431 APEH, SLC26A6, 129 more genes
    nsv6699367copy number variation1nstd229human GRCh38 chr3: 50,217,673-50,228,955 , GRCh37.p13 chr3: 50,255,105-50,266,387 SLC38A3, GNAI2, 1 more genes
    nsv6368900copy number variation1nstd223human GRCh38 chr3: 50,236,772-50,288,786 , GRCh37.p13 chr3|NW_003871059.1: 6,620-58,634 , GRCh37.p13 chr3: 50,274,204-50,326,217 IFRD2, SEMA3B, 4 more genes
    nsv6366792copy number variation1nstd223human GRCh38 chr3: 50,225,901-50,228,000 , GRCh37.p13 chr3: 50,263,333-50,265,432 MIR5787, GNAI2
    nsv6311990copy number variation1nstd102humanPathogenic GRCh37 chr3: 49,547,968-50,685,477 , GRCh38.p12 chr3: 49,510,535-50,648,046 APEH, RNA5SP131, 52 more genes
    nsv6253995mobile element insertion1nstd215human GRCh38 chr3: 50,236,888-50,236,888 , GRCh37.p13 chr3|NW_003871059.1: 6,736-6,736 , GRCh37.p13 chr3: 50,274,320-50,274,320 GNAI2
    nsv6135016copy number variation1nstd213human GRCh37 chr3: 48,760,000-52,290,001 , GRCh38.p12 chr3: 48,722,567-52,255,985 ACY1, ALAS1, 128 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
    nsv5891025copy number variation1nstd209human GRCh38 chr3: 49,693,626-52,462,904 , GRCh37.p13 chr3: 49,731,059-52,496,920 , SEMA3G, 106 more genes
    nsv5673729copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,507,870-50,340,407 , GRCh38.p12 chr3: 48,466,471-50,302,976 SEMA3B-AS1, GNAT1, 87 more genes
    nsv5564344copy number variation1nstd102humanUncertain significance GRCh37 chr3: 50,154,507-50,295,122 , GRCh38.p12 chr3: 50,117,074-50,257,690 SEMA3F-AS1, MIR5787, 5 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
    nsv5304956copy number variation1nstd204human GRCh38.p13 chr3: 50,253,584-50,255,878 , GRCh37.p13 chr3|NW_003871059.1: 23,432-25,726 , GRCh37.p13 chr3: 50,291,016-50,293,310 GNAI2
    nsv5210825copy number variation1nstd204human GRCh38.p13 chr3: 50,089,801-50,648,000 , GRCh37.p13 chr3: 50,127,234-50,685,431 C3orf18, GNAI2, 30 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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