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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5728195mobile element insertion1nstd211human GRCh38 chr17: 34,287,705-34,287,705 , GRCh37.p13 chr17: 32,614,724-32,614,724 CCL11
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5374903translocation1nstd200human GRCh38 chr17: 34,287,540-34,287,540 , GRCh38 chr17: 34,287,242-34,287,242 , GRCh37.p13 chr17: 32,614,261-32,614,261 , GRCh37.p13 chr17: 32,614,559-32,614,559 CCL11
    nsv5184887mobile element insertion1nstd203human GRCh38 chr17: 34,287,689-34,287,705 , GRCh37.p13 chr17: 32,614,708-32,614,724 CCL11
    nsv5029040copy number variation1nstd200human GRCh38 chr17: 33,729,995-34,320,708 , GRCh37.p13 chr17: 32,057,014-32,647,727 , LOC107985038, 12 more genes
    nsv5029039copy number variation1nstd200human GRCh38 chr17: 33,631,491-34,610,756 , GRCh37.p13 chr17: 31,958,510-32,937,775 , TLK2P1, 18 more genes
    nsv5016105copy number variation1nstd200human GRCh38 chr17: 34,285,405-34,285,551 , GRCh37.p13 chr17: 32,612,424-32,612,570 CCL11
    nsv5016104copy number variation1nstd200human GRCh38 chr17: 34,284,090-34,287,541 , GRCh37.p13 chr17: 32,611,109-32,614,560 CCL11
    nsv4864615copy number variation1nstd200human GRCh37 chr17: 32,057,014-32,647,727 , GRCh38.p12 chr17: 33,729,995-34,320,708 , LOC107987247, 12 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4621313copy number variation1nstd183human GRCh37 chr17: 31,959,395-32,938,034 , GRCh38.p12 chr17: 33,632,376-34,611,015 , LOC105371735, 18 more genes
    nsv4505162mobile element insertion1nstd166human GRCh37.p13 chr17: 32,615,767-32,615,767 , GRCh38.p12 chr17: 34,288,748-34,288,748 CCL11
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 more genes
    nsv4457359copy number variation1nstd102humanUncertain significance GRCh37 chr17: 31,957,257-32,944,153 , GRCh38.p12 chr17: 33,630,238-34,617,134 TLK2P1, CCL8, 17 more genes
    nsv4436271copy number variation1nstd102humanUncertain significance GRCh37 chr17: 31,889,285-33,557,612 , GRCh38.p12 chr17: 33,562,266-35,230,593 LOC105371739, CCL7, 33 more genes
    nsv4425531copy number variation1nstd174human GRCh37 chr17: 31,957,151-32,944,152 , GRCh38.p12 chr17: 33,630,132-34,617,133 , CCL2, 18 more genes
    nsv4384972copy number variation1nstd173human GRCh37 chr17: 27,710,978-33,392,085 , GRCh38.p12 chr17: 29,383,960-35,065,066 , LOC105371737, 137 more genes
    nsv4372464copy number variation1nstd173human GRCh37 chr17: 31,959,227-32,937,658 , GRCh38.p12 chr17: 33,632,208-34,610,639 , LINC01989, 18 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4236239copy number variation1nstd166human GRCh37.p13 chr17: 31,958,510-32,937,775 , GRCh38.p12 chr17: 33,631,491-34,610,756 , LOC105371738, 18 more genes
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