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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148095copy number variation1nstd102humanUncertain significance GRCh37 chr12: 121,341,598-124,103,434 , GRCh38.p12 chr12: 120,903,795-123,618,887 ANAPC5, MLXIP, 82 more genes
    nsv7094203copy number variation1nstd102humanUncertain significance GRCh37 chr12: 122,277,634-124,242,579 , GRCh38.p12 chr12: 121,839,728-123,758,032 SBNO1, MIR9902-1, 58 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
    nsv7071183inversion1nstd229human GRCh38 chr12: 122,804,561-124,735,813 , GRCh37.p13 chr12: 123,289,108-125,220,359 TMED2, GTF2H3, 41 more genes
    nsv7060673inversion1nstd229human GRCh38 chr12: 123,243,001-123,542,078 , GRCh37.p13 chr12: 123,727,548-124,026,625 KMT5A, SNRNP35, 11 more genes
    nsv7058574inversion1nstd229human GRCh38 chr12: 122,435,128-123,376,948 , GRCh37.p13 chr12: 122,919,675-123,861,495 RNA5SP375, HCAR1, 23 more genes
    nsv6934866copy number variation1nstd229human GRCh38 chr12: 119,918,701-123,974,100 , GRCh37.p13 chr12: 120,356,505-124,458,647 RNU6-1088P, LOC105370042, 130 more genes
    nsv6934489copy number variation1nstd229human GRCh38 chr12: 123,150,901-123,311,500 , GRCh37.p13 chr12: 123,635,448-123,796,047 SBNO1, MTRFR, 3 more genes
    nsv6934455copy number variation1nstd229human GRCh38 chr12: 123,232,501-123,974,100 , GRCh37.p13 chr12: 123,717,048-124,458,647 MPHOSPH9, MIR8072, 27 more genes
    nsv6934445copy number variation1nstd229human GRCh38 chr12: 123,136,242-123,305,528 , GRCh37.p13 chr12: 123,620,789-123,790,075 PITPNM2, MTRFR, 4 more genes
    nsv6931612copy number variation1nstd229human GRCh38 chr12: 123,168,201-123,595,200 , GRCh37.p13 chr12: 123,652,748-124,079,747 SBNO1, MIR3908, 13 more genes
    nsv6930301copy number variation1nstd229human GRCh38 chr12: 123,261,802-123,265,194 , GRCh37.p13 chr12: 123,746,349-123,749,741 CDK2AP1
    nsv6924793copy number variation1nstd229human GRCh38 chr12: 123,177,605-123,324,885 , GRCh37.p13 chr12: 123,662,152-123,809,432 CDK2AP1, MTRFR, 3 more genes
    nsv6924517copy number variation1nstd229human GRCh38 chr12: 123,240,585-123,418,041 , GRCh37.p13 chr12: 123,725,132-123,902,588 SBNO1, CDK2AP1, 7 more genes
    nsv6923985copy number variation1nstd229human GRCh38 chr12: 123,155,001-123,808,300 , GRCh37.p13 chr12: 123,639,548-124,292,847 TMED2-DT, EIF2B1, 24 more genes
    nsv6922314copy number variation1nstd229human GRCh38 chr12: 123,175,344-123,268,795 , GRCh37.p13 chr12: 123,659,891-123,753,342 CDK2AP1, MTRFR, 1 more genes
    nsv6583876inversion1nstd223human GRCh38 chr12: 118,054,469-123,705,974 , GRCh37.p13 chr12: 118,492,274-124,190,521 RPL11P5, RPL17P37, 159 more genes
    nsv6492143copy number variation1nstd223human GRCh38 chr12: 123,234,685-123,276,571 , GRCh37.p13 chr12: 123,719,232-123,761,118 MTRFR, CDK2AP1, 1 more genes
    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
    nsv6132219copy number variation1nstd213human GRCh37 chr12: 123,360,000-123,870,001 , GRCh38.p12 chr12: 122,875,453-123,385,454 SBNO1, KMT5A, 13 more genes
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