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Items: 1 to 20 of 216

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098787copy number variation1nstd102humanUncertain significance GRCh37 chr6: 32,148,920-36,953,949 , GRCh38.p12 chr6: 32,181,143-36,986,173 CUTA, SYNGAP1, 184 more genes
    nsv7097426copy number variation1nstd102humanUncertain significance GRCh37 chr6: 30,695,893-36,953,949 , GRCh38.p12 chr6: 30,728,116-36,986,173 LEMD2, PSORS1C1, 321 more genes
    nsv7053830inversion1nstd229human GRCh38 chr6: 29,164,448-38,692,657 , GRCh37.p13 chr6: 29,132,225-38,660,433 GTF2H4, RNF8, 472 more genes
    nsv7046831inversion1nstd229human GRCh38 chr6: 35,228,579-36,340,036 , GRCh37.p13 chr6: 35,196,356-36,307,813 MAPK14, TEAD3, 34 more genes
    nsv7045112inversion1nstd229human GRCh38 chr6: 30,561,326-37,907,708 , GRCh37.p13 chr6: 30,529,103-37,875,484 ZBTB22, PNPLA1, 355 more genes
    nsv6796446copy number variation1nstd229human GRCh38 chr6: 35,472,651-35,472,834 , GRCh37.p13 chr6: 35,440,428-35,440,611 TEAD3
    nsv6792571copy number variation1nstd229human GRCh38 chr6: 35,492,285-35,505,402 , GRCh37.p13 chr6: 35,460,062-35,473,179 TULP1, TEAD3
    nsv6781970copy number variation1nstd229human GRCh38 chr6: 35,490,738-35,492,546 , GRCh37.p13 chr6: 35,458,515-35,460,323 TEAD3
    nsv6781631copy number variation1nstd229human GRCh38 chr6: 35,448,889-35,493,578 , GRCh37.p13 chr6: 35,416,666-35,461,355 RPL10A, FANCE, 3 more genes
    nsv6570358inversion1nstd223human GRCh38 chr6: 32,570,902-37,403,160 , GRCh37.p13 chr6: 32,538,679-37,370,936 RN7SL273P, MKRN6P, 177 more genes
    nsv6565343inversion1nstd223human GRCh38 chr6: 32,527,987-37,402,848 , GRCh37.p13 chr6: 32,495,764-37,370,624 LOC105375022, SNRPC, 180 more genes
    nsv6562119inversion1nstd223human GRCh38 chr6: 32,527,628-37,403,016 , GRCh37.p13 chr6: 32,495,405-37,370,792 HLA-Z, ARMC12, 180 more genes
    nsv6556866inversion1nstd223human GRCh38 chr6: 32,527,208-37,403,016 , GRCh37.p13 chr6: 32,494,985-37,370,792 BAK1, HSD17B8, 180 more genes
    nsv6404563copy number variation1nstd223human GRCh38 chr6: 35,448,889-35,493,573 , GRCh37.p13 chr6: 35,416,666-35,461,350 MKRN6P, FANCE, 3 more genes
    nsv6396158copy number variation1nstd223human GRCh38 chr6: 35,460,351-35,473,073 , GRCh37.p13 chr6: 35,428,128-35,440,850 TEAD3, MIR7111, 2 more genes
    nsv6281503insertion1nstd214human GRCh38 chr6: 35,475,159-35,475,159 , GRCh37.p13 chr6: 35,442,936-35,442,936 TEAD3
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv5200371copy number variation1nstd102humanPathogenic GRCh37 chr6: 34,401,304-38,435,497 , GRCh38.p12 chr6: 34,433,527-38,467,721 RPS15AP19, FKBP5, 95 more genes
    nsv5031134inversion1nstd200human GRCh38 chr6: 35,178,266-40,407,996 , GRCh37.p13 chr6: 35,146,043-40,375,735 , LOC105375040, 114 more genes
    nsv4940861copy number variation1nstd200human GRCh38 chr6: 35,472,654-35,472,834 , GRCh37.p13 chr6: 35,440,431-35,440,611 TEAD3
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