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Items: 1 to 20 of 164

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5486283copy number variation1nstd206human GRCh38 chr8: 102,655,881-102,655,933 , GRCh37.p13 chr8: 103,668,109-103,668,161 LOC101927245, KLF10
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4674995copy number variation1nstd102humanUncertain significance GRCh37 chr8: 103,560,355-103,697,253 , GRCh38.p12 chr8: 102,548,127-102,685,025 POU5F1P2, LOC105375686, 5 more genes
    nsv4609249copy number variation1nstd183human GRCh37 chr8: 103,664,364-103,667,863 , GRCh38.p12 chr8: 102,652,136-102,655,635 KLF10, LOC101927245
    nsv4608242copy number variation1nstd183human GRCh37 chr8: 103,664,267-103,675,756 , GRCh38.p12 chr8: 102,652,039-102,663,528 LOC101927245, KLF10
    nsv4526407copy number variation1nstd166human GRCh37.p13 chr8: 103,659,953-103,662,276 , GRCh38.p12 chr8: 102,647,725-102,650,048 KLF10
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4318515inversion1nstd166human GRCh37.p13 chr8: 75,861,320-132,789,960 , GRCh38.p12 chr8: 74,949,085-131,777,713 , ANXA13, 716 more genes
    nsv4172268copy number variation1nstd166human GRCh37.p13 chr8: 103,668,109-103,668,161 , GRCh38.p12 chr8: 102,655,881-102,655,933 LOC101927245, KLF10
    nsv4160942copy number variation1nstd166human GRCh37.p13 chr8: 103,665,000-103,670,000 , GRCh38.p12 chr8: 102,652,772-102,657,772 KLF10, LOC101927245
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
    nsv3922470copy number variation1nstd102humanPathogenic GRCh37 chr8: 102,183,491-110,139,893 , GRCh38 chr8: 101,171,263-109,127,664 , NCBI36 chr8: 102,252,667-110,209,069 HMGB1P46, RPS12P15, 109 more genes
    nsv3919996copy number variation1nstd102humanPathogenic GRCh37 chr8: 102,897,047-108,368,371 , GRCh38 chr8: 101,884,819-107,356,143 , NCBI36 chr8: 102,966,223-108,437,547 BAALC-AS1, AZIN1, 79 more genes
    nsv3919841copy number variation1nstd102humanPathogenic GRCh38 chr8: 78,614,077-145,054,634 , GRCh37 chr8: 79,526,312-146,280,020 , NCBI36 chr8: 79,688,867-146,250,824 LY6S-AS1, LOC107984017, 911 more genes
    nsv3919636copy number variation1nstd102humanPathogenic NCBI36 chr8: 101,948,747-146,266,575 , GRCh38 chr8: 100,867,343-145,070,385 , GRCh37 chr8: 101,879,571-146,295,771 RSPO2, MTND2P35, 592 more genes
    nsv3919282copy number variation1nstd102humanPathogenic GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824 MIR4662B, LOC101927845, 2104 more genes
    nsv3919200copy number variation1nstd102humanPathogenic GRCh38 chr8: 241,530-145,049,449 , GRCh37 chr8: 191,530-146,274,835 , NCBI36 chr8: 181,530-146,245,639 LOC112268023, LOC105375925, 2103 more genes
    nsv3916978copy number variation1nstd102humanPathogenic GRCh38 chr8: 86,300,584-137,022,587 , NCBI36 chr8: 87,381,929-138,104,012 , GRCh37 chr8: 87,312,813-138,034,830 MIR5194, TRS-AGA2-5, 601 more genes
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