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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7058053inversion1nstd229human GRCh38 chr6: 12,061,960-18,307,388 , GRCh37.p13 chr6: 12,062,193-18,307,619 RNU7-133P, CAP2, 87 more genes
    nsv7053453inversion1nstd229human GRCh38 chr6: 17,383,243-17,712,215 , GRCh37.p13 chr6: 17,383,474-17,712,446 RNU6-190P, RPL7P26, 7 more genes
    nsv7052698inversion1nstd229human GRCh38 chr6: 17,404,230-18,326,837 , GRCh37.p13 chr6: 17,404,461-18,327,068 LOC101928491, RPL7P26, 16 more genes
    nsv7052430inversion1nstd229human GRCh38 chr6: 17,595,120-17,758,544 , GRCh37.p13 chr6: 17,595,351-17,758,775 KIF13A, RNA5SP204, 5 more genes
    nsv7041680inversion1nstd229human GRCh38 chr6: 17,485,402-17,679,014 , GRCh37.p13 chr6: 17,485,633-17,679,245 RNU6-190P, NUP153, 6 more genes
    nsv7040300inversion1nstd229human GRCh38 chr6: 17,593,898-17,802,294 , GRCh37.p13 chr6: 17,594,129-17,802,525 NUP153, FAM8A1, 5 more genes
    nsv6795646copy number variation1nstd229human GRCh38 chr6: 17,594,101-17,607,200 , GRCh37.p13 chr6: 17,594,332-17,607,431 LOC102724591, FAM8A1
    nsv6793946copy number variation1nstd229human GRCh38 chr6: 17,383,201-17,658,900 , GRCh37.p13 chr6: 17,383,432-17,659,131 NUP153, RPL7P26, 6 more genes
    nsv6792420copy number variation1nstd229human GRCh38 chr6: 17,415,966-17,641,151 , GRCh37.p13 chr6: 17,416,197-17,641,382 RPL7P26, LOC101928491, 6 more genes
    nsv6790565copy number variation1nstd229human GRCh38 chr6: 16,741,614-19,141,206 , GRCh37.p13 chr6: 16,741,845-19,141,437 LOC105374951, RNU6-263P, 34 more genes
    nsv6789725copy number variation1nstd229human GRCh38 chr6: 17,397,428-17,994,514 , GRCh37.p13 chr6: 17,397,659-17,994,745 RNA5SP204, NUP153-AS1, 11 more genes
    nsv6788108copy number variation1nstd229human GRCh38 chr6: 17,455,729-17,633,191 , GRCh37.p13 chr6: 17,455,960-17,633,422 NUP153, LOC102724591, 6 more genes
    nsv6786009copy number variation1nstd229human GRCh38 chr6: 17,450,856-17,961,065 , GRCh37.p13 chr6: 17,451,087-17,961,296 NUP153, LOC102724591, 11 more genes
    nsv6785447copy number variation1nstd229human GRCh38 chr6: 17,412,598-17,880,550 , GRCh37.p13 chr6: 17,412,829-17,880,781 NUP153-AS1, LOC101928491, 10 more genes
    nsv6784484copy number variation1nstd229human GRCh38 chr6: 17,401,572-17,631,100 , GRCh37.p13 chr6: 17,401,803-17,631,331 RPL7P26, CAP2, 6 more genes
    nsv6783150copy number variation1nstd229human GRCh38 chr6: 17,475,316-17,721,034 , GRCh37.p13 chr6: 17,475,547-17,721,265 CAP2, SUMO2P13, 8 more genes
    nsv6781528copy number variation1nstd229human GRCh38 chr6: 17,556,721-17,828,989 , GRCh37.p13 chr6: 17,556,952-17,829,220 SUMO2P13, CAP2, 7 more genes
    nsv6778948copy number variation1nstd229human GRCh38 chr6: 17,426,142-17,687,959 , GRCh37.p13 chr6: 17,426,373-17,688,190 NUP153, LOC101928491, 6 more genes
    nsv6636333copy number variation1nstd102humanPathogenic GRCh37 chr6: 12,005,630-22,849,647 , GRCh38.p12 chr6: 12,005,397-22,849,418 SOX4, MDH1P2, 136 more genes
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