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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    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
    nsv6865554copy number variation1nstd229human GRCh38 chr8: 144,495,158-144,500,882 , GRCh37.p13 chr8: 145,720,541-145,726,265 GPT, LOC101928953, 1 more genes
    nsv6863121copy number variation1nstd229human GRCh38 chr8: 144,504,241-144,504,365 , GRCh37.p13 chr8: 145,729,624-145,729,748 GPT, LOC101928953
    nsv6860937copy number variation1nstd229human GRCh38 chr8: 144,472,734-144,576,131 , GRCh37.p13 chr8: 145,698,117-145,801,515 C8orf82, RECQL4, 9 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
    nsv6635136copy number variation1nstd227human GRCh38.p12 chr8: 144,373,823-144,560,767 , GRCh37 chr8: 145,597,512-145,786,151 GPT, TONSL, 21 more genes
    nsv6635070copy number variation1nstd227human GRCh38.p12 chr8: 144,354,636-144,515,746 , GRCh37 chr8: 145,578,296-145,741,130 GPT, TONSL, 21 more genes
    nsv6634880copy number variation1nstd227human GRCh38.p12 chr8: 144,351,265-144,515,746 , GRCh37 chr8: 145,574,930-145,741,130 , GRCh38.p12 chr8|NW_018654716.1: 81,868-165,120 GPT, TONSL, 21 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6632693copy number variation1nstd224human GRCh37 chr8: 145,698,599-145,758,635 , GRCh38.p12 chr8: 144,473,216-144,533,251 GPT, RECQL4, 9 more genes
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