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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112688copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,154,188-128,324,987 , GRCh38.p12 chr3: 120,435,341-128,606,144 OR7E130P, DUTP1, 171 more genes
    nsv5973212inversion1nstd209human GRCh38 chr3: 121,858,185-122,522,926 , GRCh37.p13 chr3: 121,577,032-122,241,773 CASR, CD86, 12 more genes
    nsv5621891insertion1nstd207human GRCh38 chr3: 122,333,540-122,333,540 , GRCh37.p13 chr3: 122,052,387-122,052,387 CSTA
    nsv5560039inversion1nstd206human GRCh38 chr3: 119,854,156-122,655,800 , GRCh37.p13 chr3: 119,573,003-122,374,647 CD86, CSTA, 55 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 TMEM108-AS1, RN7SL172P, 801 more genes
    nsv5031637inversion1nstd200human GRCh38 chr3: 112,181,184-125,673,487 , GRCh37.p13 chr3: 111,900,031-125,392,331 GOLGB1, ARHGAP31, 218 more genes
    nsv4453697copy number variation1nstd102humanUncertain significance GRCh37 chr3: 121,384,741-123,672,180 , GRCh38.p12 chr3: 121,665,894-123,953,333 ILDR1, CCDC14, 36 more genes
    nsv4317801inversion1nstd166human GRCh37.p13 chr3: 106,160,269-123,476,086 , GRCh38.p12 chr3: 106,441,422-123,757,239 , CD86, 270 more genes
    nsv4079002copy number variation1nstd166human GRCh37.p13 chr3: 122,043,941-122,045,743 , GRCh38.p12 chr3: 122,325,094-122,326,896 CSTA
    nsv4072651copy number variation1nstd166human GRCh37.p13 chr3: 122,045,837-122,045,956 , GRCh38.p12 chr3: 122,326,990-122,327,109 CSTA
    nsv3924082copy number variation1nstd102humanPathogenic NCBI36 chr3: 119,875,435-127,742,263 , GRCh38 chr3: 118,673,898-126,540,730 , GRCh37 chr3: 118,392,745-126,259,573 MTCO2P29, LOC100420144, 169 more genes
    nsv3923097copy number variation1nstd102humanPathogenic NCBI36 chr3: 120,318,703-127,122,267 , GRCh37 chr3: 118,836,013-125,639,577 , GRCh38 chr3: 119,117,166-125,920,734 CD86, LOC107984000, 144 more genes
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 MIR12124, LOC105374039, 815 more genes
    nsv3919464copy number variation1nstd102humanPathogenic GRCh37 chr3: 113,841,409-124,251,221 , GRCh38 chr3: 114,122,562-124,532,374 , NCBI36 chr3: 115,324,099-125,733,911 RPL10P7, CD86, 151 more genes
    nsv3919094copy number variation1nstd102humanPathogenic GRCh37 chr3: 114,737,921-122,232,245 , GRCh38 chr3: 115,019,074-122,513,398 , NCBI36 chr3: 116,220,611-123,714,935 BZW1P2, LINC02049, 110 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 LOC100421154, NPM1P29, 1517 more genes
    nsv3918661copy number variation1nstd102humanPathogenic GRCh37 chr3: 93,605,515-122,935,530 , NCBI36 chr3: 95,088,205-124,418,220 , GRCh38 chr3: 93,886,671-123,216,683 HNRNPKP4, PLCXD2, 415 more genes
    nsv3918094copy number variation1nstd102humanPathogenic NCBI36 chr3: 113,822,514-129,935,667 , GRCh38 chr3: 112,620,977-128,734,134 , GRCh37 chr3: 112,339,824-128,452,977 PRR20G, KALRN, 292 more genes
    nsv3913250copy number variation1nstd102humanPathogenic NCBI36 chr3: 123,126,684-127,983,782 , GRCh38 chr3: 121,925,147-126,782,249 , GRCh37 chr3: 121,643,994-126,501,092 SEC22A, KLF15, 108 more genes
    nsv3909926copy number variation1nstd102humanPathogenic GRCh38 chr3: 121,644,209-125,676,353 , NCBI36 chr3: 122,845,746-126,877,887 , GRCh37 chr3: 121,363,056-125,395,197 LOC105374076, MIR5092, 68 more genes
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