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Items: 1 to 20 of 281

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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
    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
    nsv6579076inversion1nstd223human GRCh38 chr17: 78,989,246-78,989,931 , GRCh37.p13 chr17: 76,985,328-76,986,013 CANT1
    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
    nsv6524279copy number variation1nstd223human GRCh38 chr17: 79,008,401-79,010,600 , GRCh37.p13 chr17: 77,004,483-77,006,682 CANT1
    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
    nsv6259102mobile element insertion1nstd215human GRCh38 chr17: 79,009,887-79,009,887 , GRCh37.p13 chr17: 77,005,969-77,005,969 CANT1
    nsv6201129copy number variation1nstd214human GRCh38 chr17: 79,009,144-79,009,196 , GRCh37.p13 chr17: 77,005,226-77,005,278 CANT1
    nsv6192994copy number variation1nstd214human GRCh38 chr17: 79,009,175-79,009,227 , GRCh37.p13 chr17: 77,005,257-77,005,309 CANT1
    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
    nsv6095199insertion1nstd212human GRCh38 chr17: 79,004,436-79,004,436 , GRCh37.p13 chr17: 77,000,518-77,000,518 CANT1
    nsv6092168insertion1nstd212human GRCh38 chr17: 79,005,127-79,005,127 , GRCh37.p13 chr17: 77,001,209-77,001,209 CANT1
    nsv6039328copy number variation1nstd212human GRCh38 chr17: 79,004,280-79,004,563 , GRCh37.p13 chr17: 77,000,362-77,000,645 CANT1
    nsv6034931copy number variation1nstd212human GRCh38 chr17: 79,009,173-79,009,228 , GRCh37.p13 chr17: 77,005,255-77,005,310 CANT1
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