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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
    nsv7045112inversion1nstd229human GRCh38 chr6: 30,561,326-37,907,708 , GRCh37.p13 chr6: 30,529,103-37,875,484 ZBTB22, PNPLA1, 355 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
    nsv6313582copy number variation1nstd102humanUncertain significance GRCh37 chr6: 33,069,892-33,751,391 , GRCh38.p12 chr6: 33,102,115-33,783,614 LOC107986537, MYL12BP3, 46 more genes
    nsv6136500copy number variation1nstd213human GRCh37 chr6: 33,150,000-33,430,001 , GRCh38.p12 chr6: 33,182,223-33,462,224 COL11A2, RXRB, 30 more genes
    nsv5240227copy number variation1nstd204human GRCh38.p13 chr6: 33,206,553-33,209,338 , GRCh37.p13 chr6: 33,174,330-33,177,115 RING1, MIR219A1, 1 more genes
    nsv5231786copy number variation1nstd204human GRCh38.p13 chr6: 33,016,601-33,499,100 , GRCh37.p13 chr6: 32,984,378-33,466,877 COL11A2, RXRB, 39 more genes
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4682849copy number variation1nstd102humanUncertain significance GRCh37 chr6: 33,141,458-33,419,703 , GRCh38.p12 chr6: 33,173,681-33,451,926 RPL35AP4, RGL2, 29 more genes
    nsv4675941copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 31,036,397-34,088,832 , GRCh38.p12 chr6: 31,068,620-34,121,055 AGER, AIF1, 217 more genes
    nsv4451881copy number variation1nstd102humanUncertain significance GRCh37 chr6: 33,131,435-33,419,703 , GRCh38 chr6: 33,163,658-33,451,926 COL11A2, HSD17B8, 29 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
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