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Items: 1 to 20 of 345

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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
    nsv7071183inversion1nstd229human GRCh38 chr12: 122,804,561-124,735,813 , GRCh37.p13 chr12: 123,289,108-125,220,359 TMED2, GTF2H3, 41 more genes
    nsv7071037inversion1nstd229human GRCh38 chr12: 122,803,823-122,809,385 , GRCh37.p13 chr12: 123,288,370-123,293,932 CCDC62
    nsv7058574inversion1nstd229human GRCh38 chr12: 122,435,128-123,376,948 , GRCh37.p13 chr12: 122,919,675-123,861,495 RNA5SP375, HCAR1, 23 more genes
    nsv6935578copy number variation1nstd229human GRCh38 chr12: 122,801,773-122,849,881 , GRCh37.p13 chr12: 123,286,320-123,334,428 CCDC62, HIP1R
    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
    nsv6933168copy number variation1nstd229human GRCh38 chr12: 122,778,172-122,842,916 , GRCh37.p13 chr12: 123,262,719-123,327,463 CCDC62, HIP1R
    nsv6929788copy number variation1nstd229human GRCh38 chr12: 122,824,607-122,824,633 , GRCh37.p13 chr12: 123,309,154-123,309,180 CCDC62
    nsv6928193copy number variation1nstd229human GRCh38 chr12: 122,781,973-122,784,765 , GRCh37.p13 chr12: 123,266,520-123,269,312 CCDC62
    nsv6924408copy number variation1nstd229human GRCh38 chr12: 122,644,242-123,080,927 , GRCh37.p13 chr12: 123,128,789-123,565,474 VPS37B, MIR9902-1, 13 more genes
    nsv6921268copy number variation1nstd229human GRCh38 chr12: 122,802,319-122,802,422 , GRCh37.p13 chr12: 123,286,866-123,286,969 CCDC62
    nsv6637402copy number variation1nstd102humanUncertain significance GRCh37 chr12: 122,737,779-123,265,478 , GRCh38.p12 chr12: 122,253,232-122,780,931 HCAR3, MIR9902-1, 13 more genes
    nsv6590645inversion1nstd223human GRCh38 chr12: 122,782,546-122,782,947 , GRCh37.p13 chr12: 123,267,093-123,267,494 CCDC62
    nsv6590583inversion1nstd223human GRCh38 chr12: 122,782,560-122,783,017 , GRCh37.p13 chr12: 123,267,107-123,267,564 CCDC62
    nsv6589116inversion1nstd223human GRCh38 chr12: 122,827,862-122,828,393 , GRCh37.p13 chr12: 123,312,409-123,312,940 CCDC62
    nsv6583876inversion1nstd223human GRCh38 chr12: 118,054,469-123,705,974 , GRCh37.p13 chr12: 118,492,274-124,190,521 RPL11P5, RPL17P37, 159 more genes
    nsv6583229inversion1nstd223human GRCh38 chr12: 122,814,298-122,814,526 , GRCh37.p13 chr12: 123,298,845-123,299,073 CCDC62
    nsv6581458inversion1nstd223human GRCh38 chr12: 122,817,119-122,818,036 , GRCh37.p13 chr12: 123,301,666-123,302,583 CCDC62
    nsv6581163inversion1nstd223human GRCh38 chr12: 122,804,344-122,804,984 , GRCh37.p13 chr12: 123,288,891-123,289,531 CCDC62
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