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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054901inversion1nstd229human GRCh38 chr5: 86,506,255-87,299,369 , GRCh37.p13 chr5: 85,802,072-86,595,186 RN7SL629P, MIR4280, 12 more genes
    nsv7053596inversion1nstd229human GRCh38 chr5: 85,730,857-88,063,519 , GRCh37.p13 chr5: 85,026,675-87,359,336 LOC100421863, RPL10AP9, 25 more genes
    nsv7050687inversion1nstd229human GRCh38 chr5: 86,603,498-87,299,362 , GRCh37.p13 chr5: 85,899,315-86,595,179 RPL10AP9, LINC01949, 12 more genes
    nsv6774800copy number variation1nstd229human GRCh38 chr5: 86,905,476-87,055,628 , GRCh37.p13 chr5: 86,201,293-86,351,445 LOC645261
    nsv6773611copy number variation1nstd229human GRCh38 chr5: 87,055,100-87,059,120 , GRCh37.p13 chr5: 86,350,917-86,354,937 LOC645261
    nsv6762944copy number variation1nstd229human GRCh38 chr5: 87,046,508-87,930,460 , GRCh37.p13 chr5: 86,342,325-87,226,277 LINC02488, LOC105379065, 13 more genes
    nsv6760025copy number variation1nstd229human GRCh38 chr5: 86,980,801-87,434,400 , GRCh37.p13 chr5: 86,276,618-86,730,217 LOC105379065, RN7SL629P, 11 more genes
    nsv6759572copy number variation1nstd229human GRCh38 chr5: 87,038,775-87,057,735 , GRCh37.p13 chr5: 86,334,592-86,353,552 LOC645261
    nsv6759271copy number variation1nstd229human GRCh38 chr5: 87,047,201-87,061,300 , GRCh37.p13 chr5: 86,343,018-86,357,117 LOC645261
    nsv6758557copy number variation1nstd229human GRCh38 chr5: 87,050,984-87,053,792 , GRCh37.p13 chr5: 86,346,801-86,349,609 LOC645261
    nsv6409521copy number variation1nstd223human GRCh38 chr5: 87,038,770-87,057,727 , GRCh37.p13 chr5: 86,334,587-86,353,544 LOC645261
    nsv6398739copy number variation1nstd223human GRCh38 chr5: 83,701,679-87,055,970 , GRCh37.p13 chr5: 82,997,498-86,351,787 LOC645261, LOC105379061, 28 more genes
    nsv6397941copy number variation1nstd223human GRCh38 chr5: 87,055,103-87,059,120 , GRCh37.p13 chr5: 86,350,920-86,354,937 LOC645261
    nsv6313788copy number variation1nstd102humanPathogenic GRCh37 chr5: 82,185,951-90,110,454 , GRCh38.p12 chr5: 82,890,132-90,814,637 RASA1, HAPLN1, 82 more genes
    nsv6135438copy number variation1nstd213human GRCh37 chr5: 80,920,000-86,370,001 , GRCh38.p12 chr5: 81,624,181-87,074,184 COX7C, HAPLN1, 56 more genes
    nsv6135436copy number variation1nstd213human GRCh37 chr5: 70,260,000-91,630,001 , GRCh38.p12 chr5: 70,964,173-92,334,184 , ARSB, 300 more genes
    nsv6135200copy number variation1nstd213human GRCh37 chr5: 76,540,000-94,260,001 , GRCh38.p12 chr5: 77,244,175-94,924,296 ACTBP2, ARSB, 200 more genes
    nsv5894678copy number variation1nstd209human GRCh38 chr5: 87,038,746-87,057,733 , GRCh37.p13 chr5: 86,334,563-86,353,550 LOC645261
    nsv5843237copy number variation1nstd209human GRCh38 chr5: 87,038,725-87,057,662 , GRCh37.p13 chr5: 86,334,542-86,353,479 LOC645261
    nsv5459904copy number variation1nstd206human GRCh38 chr5: 87,038,771-87,057,709 , GRCh37.p13 chr5: 86,334,588-86,353,526 LOC645261
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