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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4729446copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 151,472,860-154,839,846 , GRCh38.p12 chr6: 151,151,725-154,518,712 ESR1, OPRM1, 45 more genes
    nsv4675234copy number variation1nstd102humanPathogenic GRCh37 chr6: 149,431,322-154,120,064 , GRCh38.p12 chr6: 149,110,186-153,798,929 RNU7-3P, HSPD1P16, 86 more genes
    nsv4608654copy number variation1nstd183human GRCh37 chr6: 153,319,788-153,320,231 , GRCh38.p12 chr6: 152,998,653-152,999,096 MTRF1L
    nsv4487353mobile element insertion1nstd166human GRCh37.p13 chr6: 153,320,021-153,320,021 , GRCh38.p12 chr6: 152,998,886-152,998,886 MTRF1L
    nsv4484378mobile element insertion1nstd166human GRCh37.p13 chr6: 153,314,963-153,314,963 , GRCh38.p12 chr6: 152,993,828-152,993,828 MTRF1L
    nsv4456488copy number variation1nstd102humanPathogenic GRCh37 chr6: 148,195,086-160,127,254 , GRCh38.p12 chr6: 147,873,950-159,706,222 PDCL3P5, SYTL3, 176 more genes
    nsv4436131complex substitution1nstd102humanPathogenic GRCh38.p12 chr6: 151,122,197-170,745,979 , GRCh37 chr6: 151,443,333-171,115,067 ACAT2, CCR6, 303 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
    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
    nsv3920651copy number variation1nstd102humanPathogenic GRCh38 chr6: 144,932,561-152,985,364 , NCBI36 chr6: 145,295,390-153,348,192 , GRCh37 chr6: 145,253,697-153,306,499 PPP1R14C, RAET1K, 107 more genes
    nsv3916405copy number variation1nstd102humanPathogenic NCBI36 chr6: 150,744,068-159,894,974 , GRCh38 chr6: 150,381,239-159,553,952 , GRCh37 chr6: 150,702,375-159,974,984 LOC112267968, ARMT1, 126 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
    nsv3913037copy number variation1nstd102humanPathogenic GRCh37 chr6: 152,697,473-170,921,089 , GRCh38 chr6: 152,376,338-170,612,001 , NCBI36 chr6: 152,739,166-170,763,014 KRT8P44, TULP4, 283 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
    nsv3911475copy number variation1nstd102humanPathogenic GRCh38 chr6: 152,793,402-170,610,394 , GRCh37 chr6: 153,114,537-170,919,482 , NCBI36 chr6: 153,156,230-170,761,407 SNORA116, PRR18, 275 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
    nsv3908882copy number variation1nstd102humanBenign GRCh37 chr6: 153,285,650-153,330,704 , GRCh38.p12 chr6: 152,964,515-153,009,569 MTRF1L, FBXO5, 1 more genes
    nsv3908622copy number variation1nstd102humanPathogenic GRCh37 chr6: 150,284,435-170,919,470 , GRCh38.p12 chr6: 149,963,299-170,610,382 LOC105378120, LOC107986661, 319 more genes
    nsv3908080copy number variation1nstd102humanBenign GRCh37 chr6: 153,285,650-153,344,133 , GRCh38.p12 chr6: 152,964,515-153,022,998 FBXO5, RGS17, 1 more genes
    nsv3907401copy number variation1nstd102humanBenign GRCh37 chr6: 153,291,923-153,333,328 , GRCh38.p12 chr6: 152,970,788-153,012,193 FBXO5, RGS17, 1 more genes
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