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Items: 1 to 20 of 569

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098989copy number variation1nstd102humanUncertain significance GRCh37 chr5: 126,781,386-126,790,257 , GRCh38.p12 chr5: 127,445,694-127,454,565 MEGF10
    nsv7098958copy number variation1nstd102humanPathogenic GRCh38 chr5: 127,396,532-127,396,778 , GRCh37 chr5: 126,732,224-126,732,470 MEGF10
    nsv7057991inversion1nstd229human GRCh38 chr5: 127,292,060-127,292,178 , GRCh37.p13 chr5: 126,627,752-126,627,870 MEGF10
    nsv7053137inversion1nstd229human GRCh38 chr5: 125,298,532-127,709,938 , GRCh37.p13 chr5: 124,634,225-127,045,630 C5orf63, LINC02039, 31 more genes
    nsv7052452inversion1nstd229human GRCh38 chr5: 127,261,836-127,264,735 , GRCh37.p13 chr5: 126,597,528-126,600,427 LOC105379199, MEGF10
    nsv7050263inversion1nstd229human GRCh38 chr5: 126,655,648-130,498,485 , GRCh37.p13 chr5: 125,991,340-129,834,178 RNA5SP191, LMNB1, 42 more genes
    nsv7050178inversion1nstd229human GRCh38 chr5: 127,268,694-127,274,508 , GRCh37.p13 chr5: 126,604,386-126,610,200 LOC105379199, MEGF10
    nsv7050047inversion1nstd229human GRCh38 chr5: 126,094,727-134,977,523 , GRCh37.p13 chr5: 125,430,420-134,313,213 RNU6-757P, SKP1, 145 more genes
    nsv7049792inversion1nstd229human GRCh38 chr5: 127,416,978-127,417,015 , GRCh37.p13 chr5: 126,752,670-126,752,707 MEGF10
    nsv7047334inversion1nstd229human GRCh38 chr5: 119,494,072-128,765,801 , GRCh37.p13 chr5: 118,829,767-128,101,494 RPL18P3, KRT18P16, 98 more genes
    nsv7044234inversion1nstd229human GRCh38 chr5: 125,118,269-132,850,844 , GRCh37.p13 chr5: 124,453,962-132,186,536 RPLP1P7, IL4, 98 more genes
    nsv7042749inversion1nstd229human GRCh38 chr5: 125,171,898-132,850,836 , GRCh37.p13 chr5: 124,507,591-132,186,528 LOC102723654, LOC105379174, 98 more genes
    nsv7041390inversion1nstd229human GRCh38 chr5: 127,145,025-127,248,685 , GRCh37.p13 chr5: 126,480,717-126,584,377 MEGF10, LOC105379198, 2 more genes
    nsv6797516copy number variation1nstd229human GRCh38 chr5: 127,379,254-127,389,738 , GRCh37.p13 chr5: 126,714,946-126,725,430 MEGF10
    nsv6796977copy number variation1nstd229human GRCh38 chr5: 127,256,473-127,260,696 , GRCh37.p13 chr5: 126,592,165-126,596,388 MEGF10
    nsv6796902copy number variation1nstd229human GRCh38 chr5: 127,436,501-127,440,970 , GRCh37.p13 chr5: 126,772,193-126,776,662 MEGF10
    nsv6794461copy number variation1nstd229human GRCh38 chr5: 127,383,420-127,389,961 , GRCh37.p13 chr5: 126,719,112-126,725,653 MEGF10
    nsv6791325copy number variation1nstd229human GRCh38 chr5: 127,289,647-127,294,860 , GRCh37.p13 chr5: 126,625,339-126,630,552 LOC105379199, MEGF10
    nsv6790020copy number variation1nstd229human GRCh38 chr5: 127,277,183-127,277,374 , GRCh37.p13 chr5: 126,612,875-126,613,066 MEGF10, LOC105379199
    nsv6787667copy number variation1nstd229human GRCh38 chr5: 127,411,803-127,414,604 , GRCh37.p13 chr5: 126,747,495-126,750,296 MEGF10
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