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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141660insertion1nstd232human GRCh37.p13 chr3: 179,288,029-179,288,029 , GRCh38.p12 chr3: 179,570,241-179,570,241 ACTL6A
    nsv7139401copy number variation1nstd232human GRCh37.p13 chr3: 179,294,514-179,294,610 , GRCh38.p12 chr3: 179,576,726-179,576,822 ACTL6A
    nsv7055432inversion1nstd229human GRCh38 chr3: 178,407,350-179,923,018 , GRCh37.p13 chr3: 178,125,138-179,640,806 H3P13, ZMAT3, 20 more genes
    nsv6735415copy number variation1nstd229human GRCh38 chr3: 179,223,847-179,566,269 , GRCh37.p13 chr3: 178,941,635-179,284,057 ZNF639, MTHFD2P7, 7 more genes
    nsv6735339copy number variation1nstd229human GRCh38 chr3: 179,565,455-179,565,499 , GRCh37.p13 chr3: 179,283,243-179,283,287 ACTL6A
    nsv6734493copy number variation1nstd229human GRCh38 chr3: 179,394,501-179,680,800 , GRCh37.p13 chr3: 179,112,289-179,398,588 MFN1, ACTL6A, 7 more genes
    nsv6634512copy number variation1nstd102humanPathogenic GRCh38 chr3: 179,547,548-182,152,788 , GRCh37.p13 chr3: 179,265,336-181,870,576 LOC105374243, RNF13P1, 34 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6574885inversion1nstd223human GRCh38 chr3: 179,566,704-179,567,164 , GRCh37.p13 chr3: 179,284,492-179,284,952 ACTL6A
    nsv6574360inversion1nstd223human GRCh38 chr3: 179,578,449-179,579,018 , GRCh37.p13 chr3: 179,296,237-179,296,806 ACTL6A
    nsv6574018inversion1nstd223human GRCh38 chr3: 179,566,759-179,567,378 , GRCh37.p13 chr3: 179,284,547-179,285,166 ACTL6A
    nsv6562224inversion1nstd223human GRCh38 chr3: 179,584,465-179,585,109 , GRCh37.p13 chr3: 179,302,253-179,302,897 ACTL6A
    nsv6291110copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 168,118,411-179,867,071 , GRCh38.p12 chr3: 168,400,623-180,149,283 ACTL6A, ECT2, 141 more genes
    nsv6290246copy number variation1nstd102humanPathogenic GRCh37 chr3: 175,119,199-187,592,480 , GRCh38.p12 chr3: 175,401,410-187,874,692 RPL39L, MCF2L2, 220 more genes
    nsv6260059mobile element insertion1nstd215human GRCh38 chr3: 179,574,220-179,574,220 , GRCh37.p13 chr3: 179,292,008-179,292,008 ACTL6A
    nsv6134795copy number variation1nstd213human GRCh37 chr3: 178,940,000-180,410,001 , GRCh38.p12 chr3: 179,222,212-180,692,213 NDUFB5, PIK3CA, 21 more genes
    nsv5896500copy number variation1nstd209human GRCh38 chr3: 171,525,972-180,293,041 , GRCh37.p13 chr3: 171,243,761-180,010,829 , RNU6-1120P, 95 more genes
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5225286copy number variation1nstd204human GRCh38.p13 chr3: 179,580,197-179,581,396 , GRCh37.p13 chr3: 179,297,985-179,299,184 ACTL6A
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
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