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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5492556copy number variation1nstd206human GRCh38 chr8: 104,348,322-104,351,255 , GRCh37.p13 chr8: 105,360,550-105,363,483 DCSTAMP
    nsv5482121copy number variation1nstd206human GRCh38 chr8: 104,337,671-104,337,740 , GRCh37.p13 chr8: 105,349,899-105,349,968 DCSTAMP
    nsv5318405copy number variation1nstd204human GRCh38.p13 chr8: 104,033,243-105,151,214 , GRCh37.p13 chr8: 105,045,471-106,163,442 , RPL23P9, 15 more genes
    nsv5248904copy number variation1nstd204human GRCh37.p13 chr8: 105,045,429-105,432,728 , GRCh38.p13 chr8: 104,033,201-104,420,500 DPYS, RIMS2, 4 more genes
    nsv5039005inversion1nstd200human GRCh38 chr8: 102,793,534-107,480,712 , GRCh37.p13 chr8: 103,805,762-108,492,940 , LOC105375693, 58 more genes
    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
    nsv4961665copy number variation1nstd200human GRCh38 chr8: 104,354,036-104,354,091 , GRCh37.p13 chr8: 105,366,264-105,366,319 DCSTAMP
    nsv4874421inversion1nstd200human GRCh37 chr8: 103,805,762-108,492,940 , GRCh38.p12 chr8: 102,793,534-107,480,712 , ZFPM2, 58 more genes
    nsv4572692sequence alteration1nstd166human GRCh37.p13 chr8: 104,115,243-105,852,952 , GRCh38.p12 chr8: 103,103,015-104,840,724 SLC25A32, MIR548A3, 28 more genes
    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
    nsv4456581copy number variation1nstd102humanUncertain significance GRCh37 chr8: 104,878,013-105,555,692 , GRCh38.p12 chr8: 103,865,785-104,543,464 DCSTAMP, LOC107984007, 9 more genes
    nsv4455916copy number variation1nstd102humanUncertain significance GRCh37 chr8: 104,437,051-114,170,843 , GRCh38.p12 chr8: 103,424,823-113,158,614 LOC105375688, DPYS, 82 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
    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
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