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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097899copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,654,526-145,669,797 , GRCh38.p12 chr8: 144,431,464-144,444,414 MIR6893, TONSL-AS1, 1 more genes
    nsv7097789copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 145,664,016-145,668,209 , GRCh38.p12 chr8: 144,438,633-144,442,826 TONSL, TONSL-AS1
    nsv7072209inversion1nstd229human GRCh38 chr8: 144,433,363-144,843,412 , GRCh37.p13 chr8: 145,659,902-146,068,797 ZNF517, RN7SL395P, 26 more genes
    nsv7058715inversion1nstd229human GRCh38 chr8: 144,335,004-144,510,116 , GRCh37.p13 chr8|NW_003315924.1: 104,263-203,777 , GRCh37.p13 chr8: 145,558,666-145,659,901 MIR10400, MIR939, 22 more genes
    nsv6875883copy number variation1nstd229human GRCh38 chr8: 144,225,852-144,741,098 , GRCh37.p13 chr8: 145,280,755-145,966,483 FBXL6, MIR6848, 36 more genes
    nsv6875796copy number variation1nstd229human GRCh38 chr8: 144,439,629-144,458,952 , GRCh37.p13 chr8: 145,665,012-145,684,335 TONSL-AS1, ZFTRAF1, 1 more genes
    nsv6874599copy number variation1nstd229human GRCh38 chr8: 144,386,401-144,547,900 , GRCh37.p13 chr8: 145,659,902-145,773,284 MIR1234, LOC101928953, 21 more genes
    nsv6873776copy number variation1nstd229human GRCh38 chr8: 143,662,901-144,626,400 , GRCh37.p13 chr8: 145,146,063-145,851,785 LRRC14, SCX, 67 more genes
    nsv6873542copy number variation1nstd229human GRCh38 chr8: 144,315,680-144,852,644 , GRCh37.p13 chr8: 145,659,902-146,078,029 FBXL6, MIR6848, 40 more genes
    nsv6872003copy number variation1nstd229human GRCh38 chr8: 144,397,201-144,547,500 , GRCh37.p13 chr8: 145,659,902-145,772,884 ZFTRAF1, C8orf82, 19 more genes
    nsv6870283copy number variation1nstd229human GRCh38 chr8: 144,432,080-144,435,540 , GRCh37.p13 chr8: 145,657,463-145,659,901 , GRCh37.p13 chr8|NW_003315924.1: 201,339-203,777 MIR6893, TONSL-AS1, 1 more genes
    nsv6868966copy number variation1nstd229human GRCh38 chr8: 144,394,595-144,450,728 , GRCh37.p13 chr8|NW_003315924.1: 163,854-203,777 , GRCh37.p13 chr8: 145,619,810-145,659,901 TONSL-AS1, MIR6893, 8 more genes
    nsv6868929copy number variation1nstd229human GRCh38 chr8: 144,423,852-144,451,086 , GRCh37.p13 chr8: 145,659,902-145,676,469 TONSL, VPS28, 3 more genes
    nsv6867293copy number variation1nstd229human GRCh38 chr8: 144,414,857-144,451,245 , GRCh37.p13 chr8: 145,640,241-145,659,901 , GRCh37.p13 chr8|NW_003315924.1: 184,116-203,777 SLC39A4, TONSL, 4 more genes
    nsv6866250copy number variation1nstd229human GRCh38 chr8: 143,771,901-144,562,100 , GRCh37.p13 chr8: 145,146,063-145,787,484 MIR939, MIR10400, 58 more genes
    nsv6861677copy number variation1nstd229human GRCh38 chr8: 144,430,121-144,437,194 , GRCh37.p13 chr8|NW_003315924.1: 199,380-203,777 , GRCh37.p13 chr8: 145,655,504-145,659,901 MIR6893, TONSL-AS1, 1 more genes
    nsv6635631copy number variation1nstd227human GRCh38.p12 chr8: 144,351,265-144,509,999 , GRCh37 chr8: 145,574,930-145,735,382 , GRCh38.p12 chr8|NW_018654716.1: 81,868-165,120 GPT, TONSL, 21 more genes
    nsv6635626copy number variation1nstd227human GRCh38.p12 chr8: 144,351,265-144,539,160 , GRCh37 chr8: 145,574,930-145,764,544 GPT, TONSL, 25 more genes
    nsv6635574copy number variation1nstd227human GRCh38.p12 chr8: 144,354,636-144,539,160 , GRCh37 chr8: 145,578,296-145,764,544 GPT, TONSL, 25 more genes
    nsv6635554copy number variation1nstd227human GRCh38.p12 chr8: 144,351,265-144,621,185 , GRCh37 chr8: 145,574,930-145,846,570 GPT, TONSL, 25 more genes
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