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Items: 1 to 20 of 187

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094921copy number variation1nstd102humanUncertain significance GRCh37 chr17: 76,851,749-78,367,298 , GRCh38.p12 chr17: 78,855,667-80,393,498 RNF213-AS1, EIF4A3, 25 more genes
    nsv6993964copy number variation1nstd229human GRCh38 chr17: 78,767,102-79,347,128 , GRCh37.p13 chr17: 76,763,184-77,343,210 CYTH1, C1QTNF1-AS1, 9 more genes
    nsv6993667copy number variation1nstd229human GRCh38 chr17: 78,709,580-81,173,842 , GRCh37.p13 chr17: 76,705,662-79,147,642 C1QTNF1-AS1, NPTX1, 47 more genes
    nsv6988338copy number variation1nstd229human GRCh38 chr17: 79,010,779-79,043,253 , GRCh37.p13 chr17: 77,006,861-77,039,335 C1QTNF1, C1QTNF1-AS1
    nsv6624116copy number variation1nstd224human GRCh37 chr17: 76,921,790-77,051,253 , GRCh38.p12 chr17: 78,925,708-79,055,171 TIMP2, LGALS3BP, 3 more genes
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6529265copy number variation1nstd223human GRCh38 chr17: 78,919,705-79,477,438 , GRCh37.p13 chr17: 76,915,787-77,412,076 CANT1, C1QTNF1-AS1, 5 more genes
    nsv6517656copy number variation1nstd223human GRCh38 chr17: 79,022,064-79,022,674 , GRCh37.p13 chr17: 77,018,146-77,018,756 C1QTNF1-AS1, C1QTNF1
    nsv6315182copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323 DUS1L, PVALEF, 252 more genes
    nsv6314181copy number variation1nstd102humanUncertain significance GRCh37 chr17: 76,770,309-77,174,429 , GRCh38.p12 chr17: 78,774,227-79,178,347 LGALS3BP, CYTH1, 9 more genes
    nsv6291550copy number variation1nstd102humanUncertain significance GRCh37 chr17: 76,852,379-77,297,300 , GRCh38.p12 chr17: 78,856,297-79,301,218 LGALS3BP, ENGASE, 6 more genes
    nsv6133425copy number variation1nstd213human GRCh37 chr17: 76,360,000-77,240,001 , GRCh38.p12 chr17: 78,363,919-79,243,919 LGALS3BP, PGS1, 18 more genes
    nsv6133371copy number variation1nstd213human GRCh37 chr17: 76,980,000-77,230,001 , GRCh38.p12 chr17: 78,983,918-79,233,919 ENGASE, C1QTNF1, 3 more genes
    nsv5014073copy number variation1nstd200human GRCh38 chr17: 78,919,633-79,477,545 , GRCh37.p13 chr17: 76,915,715-77,412,183 TIMP2, LGALS3BP, 5 more genes
    nsv4729773copy number variation1nstd102humanUncertain significance GRCh37 chr17: 76,852,029-77,297,898 , GRCh38.p12 chr17: 78,855,947-79,301,816 C1QTNF1, CANT1, 6 more genes
    nsv4676104copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963 LLGL2, TSEN54, 165 more genes
    nsv4457695copy number variation2nstd102humanUncertain significance GRCh37 chr17: 76,857,398-77,308,782 , GRCh38.p12 chr17: 78,861,316-79,312,700 CEP295NL, C1QTNF1-AS1, 6 more genes
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4271462copy number variation1nstd166human GRCh37.p13 chr17: 77,022,301-77,026,768 , GRCh38.p12 chr17: 79,026,219-79,030,686 C1QTNF1-AS1, C1QTNF1
    nsv4262229copy number variation1nstd166human GRCh37.p13 chr17: 76,649,383-77,059,909 , GRCh38.p12 chr17: 78,653,301-79,063,827 , CEP295NL, 9 more genes
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