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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3047981copy number variation1nstd140human GRCh38 (hg38) chr1: 219,941,517-219,941,590 , GRCh37 (hg19) chr1: 220,114,859-220,114,932 SLC30A10
    nsv2800659copy number variation1nstd137human GRCh38 (hg38) chr1: 219,941,481-219,941,552 , GRCh37 (hg19) chr1: 220,114,823-220,114,894 SLC30A10
    nsv2778339copy number variation3nstd37humanLikely benign GRCh37 (hg19) chr1: 220,089,258-220,100,436 , GRCh38 (hg38) chr1: 219,915,916-219,927,094 , NCBI36 (hg18) chr1: 218,155,881-218,167,059 SLC30A10
    nsv2772868copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr1: 849,467-249,224,684 , GRCh38 (hg38) chr1: 914,087-248,930,485 , NCBI36 (hg18) chr1: 839,330-247,191,307 AKT3, MIR942, 2723 more genes
    nsv2770490copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr1: 195,483,439-249,213,000 , GRCh38 (hg38) chr1: 195,514,309-248,918,801 , NCBI36 (hg18) chr1: 193,750,062-247,179,623 AKT3, C1orf132, 535 more genes
    nsv2770253copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr1: 214,697,099-249,224,684 , GRCh38 (hg38) chr1: 214,523,756-248,930,485 , NCBI36 (hg18) chr1: 212,763,722-247,191,307 AKT3, BTNL10, 319 more genes
    nsv2770146copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr1: 144,764,751-247,199,719 , GRCh37 (hg19) chr1: 146,053,394-249,233,096 , GRCh38 (hg38) chr1: 120,836,007-248,938,897 AKT3, MIR190B, 1326 more genes
    nsv2768399copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr1: 144,475,856-247,199,719 , GRCh37 (hg19) chr1: 145,764,499-249,233,096 , GRCh38 (hg38) chr1: 120,836,007-248,938,897 AKT3, MIR190B, 1329 more genes
    nsv1483203short tandem repeat2nstd128human GRCh37 (hg19) chr1: 220,125,519-220,125,541 , GRCh38 (hg38) chr1: 219,952,177-219,952,199 SLC30A10
    nsv1483202short tandem repeat3nstd128human GRCh37 (hg19) chr1: 220,104,771-220,104,785 , GRCh38 (hg38) chr1: 219,931,429-219,931,443 SLC30A10
    nsv1483201short tandem repeat3nstd128human GRCh37 (hg19) chr1: 220,102,868-220,102,879 , GRCh38 (hg38) chr1: 219,929,526-219,929,537 SLC30A10
    nsv1408900short tandem repeat4nstd128human GRCh37 (hg19) chr1: 220,130,006-220,130,036 , GRCh38 (hg38) chr1: 219,956,664-219,956,694 SLC30A10
    nsv1408899short tandem repeat1nstd128human GRCh37 (hg19) chr1: 220,126,946-220,126,979 , GRCh38 (hg38) chr1: 219,953,604-219,953,637 SLC30A10
    nsv1408898short tandem repeat3nstd128human GRCh37 (hg19) chr1: 220,125,065-220,125,097 , GRCh38 (hg38) chr1: 219,951,723-219,951,755 SLC30A10
    nsv1408897short tandem repeat1nstd128human GRCh37 (hg19) chr1: 220,124,293-220,124,307 , GRCh38 (hg38) chr1: 219,950,951-219,950,965 SLC30A10
    nsv1408896short tandem repeat1nstd128human GRCh37 (hg19) chr1: 220,123,090-220,123,129 , GRCh38 (hg38) chr1: 219,949,748-219,949,787 SLC30A10
    nsv1408894short tandem repeat2nstd128human GRCh37 (hg19) chr1: 220,097,402-220,097,429 , GRCh38 (hg38) chr1: 219,924,060-219,924,087 SLC30A10
    nsv1408893short tandem repeat10nstd128human GRCh37 (hg19) chr1: 220,095,215-220,095,247 , GRCh38 (hg38) chr1: 219,921,873-219,921,905 SLC30A10
    nsv1408892short tandem repeat1nstd128human GRCh37 (hg19) chr1: 220,093,961-220,093,975 , GRCh38 (hg38) chr1: 219,920,619-219,920,633 SLC30A10
    nsv1408891short tandem repeat1nstd128human GRCh37 (hg19) chr1: 220,087,259-220,087,273 , GRCh38 (hg38) chr1: 219,913,917-219,913,931 SLC30A10
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