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Items: 1 to 20 of 85

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5730323mobile element insertion1nstd211human GRCh38 chr6: 144,214,952-144,214,952 , GRCh37.p13 chr6: 144,536,089-144,536,089 TRL-TAA1-1
    nsv5555374mobile element insertion1nstd206human GRCh38 chr6: 144,214,967-144,215,003 , GRCh37.p13 chr6: 144,536,104-144,536,140 TRL-TAA1-1
    nsv5197887mobile element insertion1nstd203human GRCh38 chr6: 144,214,956-144,214,956 , GRCh37.p13 chr6: 144,536,093-144,536,093 TRL-TAA1-1
    nsv5186755mobile element insertion1nstd203human GRCh38 chr6: 144,214,952-144,214,967 , GRCh37.p13 chr6: 144,536,089-144,536,104 TRL-TAA1-1
    nsv4675434copy number variation1nstd102humanUncertain significance GRCh37 chr6: 144,285,958-144,758,765 , GRCh38.p12 chr6: 143,964,821-144,437,629 LOC105378036, LOC100131041, 10 more genes
    nsv4562083mobile element insertion1nstd166human GRCh37.p13 chr6: 144,536,089-144,536,089 , GRCh38.p12 chr6: 144,214,952-144,214,952 TRL-TAA1-1
    nsv4350212copy number variation1nstd102humanPathogenic GRCh37 chr6: 135,239,633-146,997,510 , GRCh38.p12 chr6: 134,918,495-146,676,374 LOC100131041, ADGB-DT, 146 more genes
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
    nsv3969692copy number variation1nstd168human GRCh38 chr6: 144,211,684-144,251,104 , GRCh37.p13 chr6: 144,532,821-144,572,240 TRL-TAA1-1
    nsv3921844copy number variation1nstd102humanPathogenic GRCh37 chr6: 143,940,111-144,734,319 , GRCh38 chr6: 143,618,974-144,413,183 , NCBI36 chr6: 143,981,804-144,776,012 ZC2HC1B, LOC100420214, 13 more genes
    nsv3920975copy number variation1nstd102humanPathogenic GRCh37 chr6: 141,454,127-169,739,666 , GRCh38 chr6: 141,132,990-169,339,571 , NCBI36 chr6: 141,495,820-169,481,591 UST-AS2, LOC729681, 394 more genes
    nsv3916499copy number variation1nstd102humanPathogenic NCBI36 chr6: 136,359,437-146,708,473 , GRCh37.p13 chr6: 136,317,744-146,666,780 , GRCh38.p12 chr6: 135,996,606-146,345,644 SLC35D3, SHPRH, 127 more genes
    nsv3915150copy number variation1nstd102humanPathogenic NCBI36 chr6: 124,322,082-156,156,864 , GRCh37.p13 chr6: 124,280,383-156,115,172 , GRCh38.p12 chr6: 123,959,238-155,794,038 KATNA1, RNF217-AS1, 422 more genes
    nsv3913689copy number variation1nstd102humanPathogenic NCBI36 chr6: 121,373,749-146,289,101 , GRCh37.p13 chr6: 121,332,050-146,247,408 , GRCh38.p12 chr6: 121,010,904-145,926,272 TPD52L1, MESTP1, 316 more genes
    nsv3912178copy number variation1nstd102humanPathogenic NCBI36 chr6: 142,070,748-145,748,578 , GRCh37.p13 chr6: 142,029,055-145,706,885 , GRCh38.p12 chr6: 141,707,918-145,385,749 GJE1, LOC105378030, 40 more genes
    nsv3911993copy number variation1nstd102humanPathogenic NCBI36 chr6: 133,900,102-166,209,023 , GRCh38 chr6: 133,537,271-165,875,545 , GRCh37 chr6: 133,858,409-166,289,033 LOC105369171, SHPRH, 418 more genes
    nsv3911164copy number variation1nstd102humanPathogenic NCBI36 chr6: 135,720,981-155,817,943 , GRCh37 chr6: 135,679,288-155,776,251 , GRCh38 chr6: 135,358,150-155,455,117 HYMAI, SMIM28, 263 more genes
    nsv3891146copy number variation1nstd102humanPathogenic GRCh37 chr6: 139,513,020-150,389,231 , GRCh38.p12 chr6: 139,191,883-150,068,095 UST, RAET1K, 131 more genes
    nsv3890752copy number variation1nstd102humanPathogenic GRCh37 chr6: 144,075,695-152,337,005 , GRCh38.p12 chr6: 143,754,558-152,015,870 LOC105378052, RNU6-302P, 109 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
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