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Items: 1 to 20 of 239

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148238copy number variation1nstd102humanPathogenic GRCh38 chr8: 115,586,904-135,607,135 , GRCh37.p13 chr8: 116,599,131-136,619,378 CCDC26, EFR3A, 238 more genes
    nsv7077533inversion1nstd229human GRCh38 chr8: 125,245,829-133,039,076 , GRCh37.p13 chr8: 126,258,071-134,051,321 PVT1, MTRF1LP2, 76 more genes
    nsv6857318copy number variation1nstd229human GRCh38 chr8: 126,364,525-132,576,581 , GRCh37.p13 chr8: 127,376,770-133,588,829 PRNCR1, MIR1205, 59 more genes
    nsv6855212copy number variation1nstd229human GRCh38 chr8: 130,075,023-130,129,777 , GRCh37.p13 chr8: 131,087,269-131,142,023 ASAP1, ASAP1-IT2
    nsv6848111copy number variation1nstd229human GRCh38 chr8: 129,844,538-130,112,455 , GRCh37.p13 chr8: 130,856,784-131,124,701 ASAP1, RPL15P12, 5 more genes
    nsv6846741copy number variation1nstd229human GRCh38 chr8: 129,895,908-130,615,282 , GRCh37.p13 chr8: 130,908,154-131,627,528 LOC105375758, ASAP1, 6 more genes
    nsv6843746copy number variation1nstd229human GRCh38 chr8: 130,068,464-130,119,717 , GRCh37.p13 chr8: 131,080,710-131,131,963 ASAP1-IT2, RNU6-1255P, 1 more genes
    nsv6637224copy number variation1nstd102humanPathogenic GRCh37 chr8: 112,234,557-133,668,379 , GRCh38.p12 chr8: 111,222,328-132,656,133 RNU4-37P, LOC100420215, 220 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6632315copy number variation1nstd224human GRCh37 chr8: 130,868,363-131,122,500 , GRCh38.p12 chr8: 129,856,117-130,110,254 ASAP1, CYRIB, 5 more genes
    nsv6632252copy number variation1nstd224human GRCh37 chr8: 130,866,512-131,124,559 , GRCh38.p12 chr8: 129,854,266-130,112,313 ASAP1, CYRIB, 5 more genes
    nsv6632251copy number variation2nstd224human GRCh37 chr8: 130,866,512-131,108,193 , GRCh38.p12 chr8: 129,854,266-130,095,947 ASAP1, CYRIB, 5 more genes
    nsv6426624copy number variation1nstd223human GRCh38 chr8: 129,844,538-130,112,455 , GRCh37.p13 chr8: 130,856,784-131,124,701 RPL15P12, RNU7-181P, 5 more genes
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
    nsv6314744copy number variation1nstd102humanPathogenic GRCh37 chr8: 96,496,503-146,295,711 , GRCh38.p12 chr8: 95,484,275-145,070,325 OSR2, LOC392268, 676 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6313487copy number variation1nstd102humanPathogenic GRCh37 chr8: 130,863,093-146,295,771 , GRCh38.p12 chr8: 129,850,847-145,070,385 LOC105375784, CYP11B2, 253 more genes
    nsv6290242copy number variation1nstd102humanUncertain significance GRCh37 chr8: 128,878,931-141,662,233 , GRCh38.p12 chr8: 127,866,685-140,652,134 LINC02055, LOC101927798, 100 more genes
    nsv6136320copy number variation1nstd213human GRCh37 chr8: 131,040,000-132,830,001 , GRCh38.p12 chr8: 130,027,754-131,817,754 LOC105375762, LOC105375758, 10 more genes
    nsv6136319copy number variation1nstd213human GRCh37 chr8: 129,280,000-132,570,001 , GRCh38.p12 chr8: 128,267,754-131,557,754 CYRIB, GSDMC, 21 more genes
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