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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3149402copy number variation1nstd151human GRCh37 (hg19) chr12: 111,290,756-111,358,338 , GRCh38 (hg38) chr12: 110,852,952-110,920,534 MYL2, CCDC63
    nsv3140753copy number variation1nstd151human GRCh37 (hg19) chr12: 109,967,692-111,786,134 , GRCh38 (hg38) chr12: 109,529,887-111,348,330 ATP2A2, MYL2, 41 more genes
    nsv3140672copy number variation1nstd151human GRCh37 (hg19) chr12: 111,317,707-111,358,338 , GRCh38 (hg38) chr12: 110,879,903-110,920,534 MYL2, CCDC63
    nsv2778199copy number variation1nstd37humanLikely pathogenic GRCh37 (hg19) chr12: 103,044,333-111,639,805 , GRCh38 (hg38) chr12: 102,650,555-111,202,001 , NCBI36 (hg18) chr12: 101,568,463-110,124,188 GLTP, SSH1, 156 more genes
    nsv2770609copy number variation3nstd37humanPathogenic GRCh37 (hg19) chr12: 173,787-133,777,902 , GRCh38 (hg38) chr12: 64,621-133,201,316 , NCBI36 (hg18) chr12: 44,048-132,287,975 HOXC11, CUX2, 2519 more genes
    nsv2768213copy-neutral loss of heterozygosity1nstd125human GRCh38 (hg38) chr12: 109,335,169-113,005,376 , GRCh37 (hg19) chr12: 109,772,974-113,443,181 ALDH2, ATP2A2, 80 more genes
    esv3868871copy number variation1estd219human GRCh37 (hg19) chr12: 111,286,859-111,418,188 , GRCh38 (hg38) chr12: 110,849,055-110,980,384 LINC01405, MYL2, 2 more genes
    nsv2740531copy number variation1nstd130human NCBI36 (hg18) chr12: 49,559,698-128,874,436 , GRCh37 (hg19) chr12: 51,273,431-130,308,483 , GRCh38 (hg38) chr12: 50,879,648-129,823,938 ACACB, ACADS, 1470 more genes
    nsv2739875copy number variation1nstd130human NCBI36 (hg18) chr12: 83,709,527-131,568,361 , GRCh37 (hg19) chr12: 85,185,396-133,058,288 , GRCh38 (hg38) chr12: 84,791,617-132,481,702 ALDH2, ARL1, 861 more genes
    nsv2735999copy number variation1nstd130human NCBI36 (hg18) chr12: 64,079-132,288,869 , GRCh37 (hg19) chr12: 282,465-133,778,796 , GRCh38 (hg38) chr12: 84,652-133,202,210 ABCD2, AQP6, 2519 more genes
    nsv2732862copy number variation1nstd130human NCBI36 (hg18) chr12: 83,150,928-132,289,191 , GRCh37 (hg19) chr12: 84,626,797-133,779,118 , GRCh38 (hg38) chr12: 84,233,018-133,202,532 NT5DC3, CLLU1, 893 more genes
    nsv2731470copy number variation1nstd130human NCBI36 (hg18) chr12: 180,595-132,288,869 , GRCh37 (hg19) chr12: 310,334-133,778,796 , GRCh38 (hg38) chr12: 201,168-133,202,210 UTP20, HTR1DP1, 2515 more genes
    nsv2730709copy number variation1nstd130human NCBI36 (hg18) chr12: 2,290,505-132,223,513 , GRCh37 (hg19) chr12: 2,420,244-133,713,440 , GRCh38 (hg38) chr12: 2,311,078-133,136,854 RPL10P12, LOC724085, 2473 more genes
    nsv1689253short tandem repeat3nstd128human GRCh37 (hg19) chr12: 111,350,103-111,350,115 , GRCh38 (hg38) chr12: 110,912,299-110,912,311 MYL2
    nsv1666769short tandem repeat1nstd128human GRCh37 (hg19) chr12: 111,351,551-111,351,575 , GRCh38 (hg38) chr12: 110,913,747-110,913,771 MYL2
    nsv1664269short tandem repeat4nstd128human GRCh37 (hg19) chr12: 111,355,295-111,355,325 , GRCh38 (hg38) chr12: 110,917,491-110,917,521 MYL2
    nsv1664268short tandem repeat3nstd128human GRCh37 (hg19) chr12: 111,354,644-111,354,668 , GRCh38 (hg38) chr12: 110,916,840-110,916,864 MYL2
    nsv1664267short tandem repeat3nstd128human GRCh37 (hg19) chr12: 111,351,950-111,351,981 , GRCh38 (hg38) chr12: 110,914,146-110,914,177 MYL2
    nsv1663921short tandem repeat1nstd128human GRCh37 (hg19) chr12: 111,354,142-111,354,163 , GRCh38 (hg38) chr12: 110,916,338-110,916,359 MYL2
    nsv1663920short tandem repeat1nstd128human GRCh37 (hg19) chr12: 111,350,364-111,350,380 , GRCh38 (hg38) chr12: 110,912,560-110,912,576 MYL2
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