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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142069insertion1nstd232human GRCh37.p13 chr12: 125,574,734-125,574,734 , GRCh38.p12 chr12: 125,090,188-125,090,188 AACS
    nsv7137283insertion1nstd232human GRCh37.p13 chr12: 125,574,754-125,574,754 , GRCh38.p12 chr12: 125,090,208-125,090,208 AACS
    nsv7074643inversion1nstd229human GRCh38 chr12: 123,471,880-125,706,144 , GRCh37.p13 chr12: 123,956,427-126,190,690 DHX37, RNU6-927P, 44 more genes
    nsv7074199inversion1nstd229human GRCh38 chr12: 123,186,434-132,825,682 , GRCh37.p13 chr12: 123,670,981-133,402,268 PIWIL1, FZD10-AS1, 187 more genes
    nsv6937432copy number variation1nstd229human GRCh38 chr12: 125,107,794-125,113,325 , GRCh37.p13 chr12: 125,592,340-125,597,871 AACS
    nsv6936871copy number variation1nstd229human GRCh38 chr12: 125,090,700-125,090,733 , GRCh37.p13 chr12: 125,575,246-125,575,279 AACS
    nsv6935804copy number variation1nstd229human GRCh38 chr12: 125,059,501-125,065,600 , GRCh37.p13 chr12: 125,544,047-125,550,146 AACS, LOC105370052
    nsv6935412copy number variation1nstd229human GRCh38 chr12: 125,122,101-125,136,543 , GRCh37.p13 chr12: 125,606,647-125,621,089 AACS
    nsv6929311copy number variation1nstd229human GRCh38 chr12: 125,063,676-125,089,274 , GRCh37.p13 chr12: 125,548,222-125,573,820 AACS, LOC105370052
    nsv6928116copy number variation1nstd229human GRCh38 chr12: 125,106,265-125,106,405 , GRCh37.p13 chr12: 125,590,811-125,590,951 AACS
    nsv6924954copy number variation1nstd229human GRCh38 chr12: 125,108,962-125,109,529 , GRCh37.p13 chr12: 125,593,508-125,594,075 AACS
    nsv6923392copy number variation1nstd229human GRCh38 chr12: 125,059,854-125,170,623 , GRCh37.p13 chr12: 125,544,400-125,655,169 LOC105370053, AACS, 1 more genes
    nsv6918147copy number variation1nstd229human GRCh38 chr12: 125,141,030-125,141,414 , GRCh37.p13 chr12: 125,625,576-125,625,960 AACS
    nsv6638030copy number variation1nstd102humanUncertain significance GRCh37 chr12: 125,346,689-126,135,525 , GRCh38.p12 chr12: 124,862,143-125,650,979 MIR5188, TRD-GTC2-10, 19 more genes
    nsv6587406inversion1nstd223human GRCh38 chr12: 125,083,830-125,084,259 , GRCh37.p13 chr12: 125,568,376-125,568,805 AACS, LOC105370052
    nsv6581741inversion1nstd223human GRCh38 chr12: 123,471,879-125,706,143 , GRCh37.p13 chr12: 123,956,426-126,190,689 LOC105370042, TMEM132B, 44 more genes
    nsv6493032copy number variation1nstd223human GRCh38 chr12: 125,120,156-125,126,203 , GRCh37.p13 chr12: 125,604,702-125,610,749 AACS
    nsv6485808copy number variation1nstd223human GRCh38 chr12: 125,097,341-125,097,945 , GRCh37.p13 chr12: 125,581,887-125,582,491 AACS
    nsv6479611copy number variation1nstd223human GRCh38 chr12: 125,073,952-125,074,965 , GRCh37.p13 chr12: 125,558,498-125,559,511 AACS, LOC105370052
    nsv6290239copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 117,461,902-133,841,395 , GRCh38.p12 chr12: 117,024,097-133,264,809 ACADS, BCL7A, 356 more genes
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