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Items: 19

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    Number of Variants: 19

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3923612copy number variation1nstd102humanPathogenic GRCh38 chr12: 120,718,786-127,500,215 , GRCh37 chr12: 121,156,589-127,984,760 , NCBI36 chr12: 119,640,972-126,550,713 CAMKK2, NCOR2, 161 more genes
    nsv3921651copy number variation1nstd102humanPathogenic NCBI36 chr12: 119,426,254-121,510,218 , GRCh37 chr12: 120,941,871-122,944,265 , GRCh38 chr12: 120,504,068-122,459,718 CAMKK2, ACADS, 58 more genes
    nsv3904242copy number variation1nstd102humanPathogenic GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309 CAMKK2, RNA5SP369, 2454 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 CAMKK2, LOH12CR2, 2452 more genes
    nsv3897722copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059 CAMKK2, RNU4ATAC16P, 2452 more genes
    nsv3914194copy number variation1nstd102humanPathogenic NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807 CAMKK2, BTG1P1, 2451 more genes
    nsv3904719copy number variation1nstd102humanPathogenic GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532 CAMKK2, OR5BT1P, 2441 more genes
    nsv3913894copy number variation1nstd102humanPathogenic NCBI36 chr12: 113,190,591-132,287,975 , GRCh38 chr12: 114,268,403-133,201,316 , GRCh37 chr12: 114,706,208-133,777,902 CAMKK2, TAOK3, 386 more genes
    nsv3924220copy number variation1nstd102humanPathogenic GRCh38 chr12: 115,131,583-133,166,920 , NCBI36 chr12: 114,053,771-132,253,579 , GRCh37 chr12: 115,569,388-133,743,506 CAMKK2, LOC105370080, 376 more genes
    nsv3920557copy number variation1nstd102humanPathogenic GRCh37 chr12: 118,603,264-133,758,908 , GRCh38 chr12: 118,165,459-133,182,322 , NCBI36 chr12: 117,087,647-132,268,981 CAMKK2, TMED2, 339 more genes
    nsv3896575copy number variation1nstd102humanPathogenic GRCh37 chr12: 120,367,241-133,777,645 , GRCh38.p12 chr12: 119,929,437-133,201,059 CAMKK2, LOC107984448, 306 more genes
    nsv3923347copy number variation1nstd102humanPathogenic NCBI36 chr12: 119,619,858-132,289,149 , GRCh37 chr12: 121,135,475-133,779,076 , GRCh38 chr12: 120,697,672-133,202,490 CAMKK2, LOC105370044, 273 more genes
    nsv6290239copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 117,461,902-133,841,395 , GRCh38.p12 chr12: 117,024,097-133,264,809 CAMKK2, ACADS, 356 more genes
    nsv3914229copy number variation1nstd102humanLikely benign NCBI36 chr12: 120,033,179-120,248,060 , GRCh37 chr12: 121,548,796-121,763,677 , GRCh38 chr12: 121,110,993-121,325,874 CAMKK2, ANAPC5, 4 more genes
    nsv6637167copy number variation1nstd102humanUncertain significance GRCh37 chr12: 121,551,496-121,771,295 , GRCh38.p12 chr12: 121,113,693-121,333,492 CAMKK2, ANAPC5, 4 more genes
    nsv3922077copy number variation1nstd102humanUncertain significance NCBI36 chr12: 118,209,081-121,689,052 , GRCh38 chr12: 119,286,893-122,638,552 , GRCh37 chr12: 119,724,698-123,123,099 CAMKK2, RPS20P31, 94 more genes
    nsv7148095copy number variation1nstd102humanUncertain significance GRCh37 chr12: 121,341,598-124,103,434 , GRCh38.p12 chr12: 120,903,795-123,618,887 CAMKK2, ANAPC5, 82 more genes
    nsv3890662copy number variation1nstd102humanUncertain significance GRCh37 chr12: 121,441,298-122,107,345 , GRCh38.p12 chr12: 121,003,495-121,669,439 CAMKK2, MORN3, 17 more genes
    nsv3910686copy number variation1nstd102humanUncertain significance NCBI36 chr12: 119,868,295-120,506,227 , GRCh37.p13 chr12: 121,383,912-122,021,844 , GRCh38.p12 chr12: 120,946,109-121,583,939 CAMKK2, LOC105370030, 15 more genes
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