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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    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
    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
    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
    nsv4234046copy number variation1nstd166human GRCh37.p13 chr17: 30,657,307-33,838,598 , GRCh38.p12 chr17: 32,330,288-35,511,579 , PSMD11, 65 more genes
    nsv3917235copy number variation1nstd102humanLikely benign GRCh37 chr17: 31,998,125-32,922,906 , GRCh38 chr17: 33,671,106-34,595,887 , NCBI36 chr17: 29,022,238-29,947,019 LOC107987247, CCL8, 17 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3910771copy number variation1nstd102humanLikely benign GRCh37 chr17: 31,998,116-32,923,001 , GRCh38 chr17: 33,671,097-34,595,982 , NCBI36 chr17: 29,022,229-29,947,114 TMEM132E-DT, LOC105371735, 17 more genes
    nsv3909912copy number variation1nstd102humanUncertain significance NCBI36 chr17: 28,993,827-29,900,343 , GRCh37 chr17: 31,969,714-32,876,230 , GRCh38 chr17: 33,642,695-34,549,211 RNA5SP438, CCL11, 15 more genes
    nsv3909026copy number variation1nstd102humanUncertain significance GRCh37 chr17: 31,982,779-32,917,705 , GRCh38.p12 chr17: 33,655,760-34,590,686 LOC107987247, CCL2, 17 more genes
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