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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5013282copy number variation1nstd200human GRCh38 chr20: 55,997,907-55,998,066 , GRCh37.p13 chr20: 54,572,963-54,573,122 CBLN4
    nsv5013281copy number variation1nstd200human GRCh38 chr20: 55,995,536-55,996,863 , GRCh37.p13 chr20: 54,570,592-54,571,919 CBLN4
    nsv4853973copy number variation1nstd200human GRCh37 chr20: 54,570,592-54,571,919 , GRCh38.p12 chr20: 55,995,536-55,996,863 CBLN4
    nsv4570293mobile element insertion1nstd166human GRCh37.p13 chr20: 54,571,437-54,571,437 , GRCh38.p12 chr20: 55,996,381-55,996,381 CBLN4
    nsv4357849copy number variation1nstd102humanPathogenic GRCh37 chr20: 54,143,747-62,194,881 , GRCh38.p12 chr20: 55,568,689-63,563,528 RBM38, LAMA5, 192 more genes
    nsv4278503copy number variation1nstd166human GRCh37.p13 chr20: 54,570,635-54,571,919 , GRCh38.p12 chr20: 55,995,579-55,996,863 CBLN4
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 MIR3646, NPEPL1, 1310 more genes
    nsv3918295copy number variation1nstd102humanPathogenic GRCh38 chr20: 54,594,888-58,190,583 , NCBI36 chr20: 52,644,834-56,199,045 , GRCh37 chr20: 53,211,427-56,765,639 MTRNR2L3, LOC105372687, 59 more genes
    nsv3915005copy number variation1nstd102humanPathogenic NCBI36 chr20: 42,849,759-62,379,118 , GRCh37 chr20: 43,416,345-62,908,674 , GRCh38 chr20: 44,787,704-64,277,321 FTLP1, RNA5SP487, 472 more genes
    nsv3912982copy number variation1nstd102humanLikely pathogenic NCBI36 chr20: 53,639,062-58,949,658 , GRCh37 chr20: 54,220,678-59,516,263 , GRCh38 chr20: 55,630,597-60,941,207 ATP5F1E, BMP7, 103 more genes
    nsv3910818copy number variation1nstd102humanUncertain significance NCBI36 chr20: 25,616,026-62,435,964 , GRCh37.p13 chr20: 25,668,026-62,965,520 , GRCh38.p12 chr20: 25,687,390-64,334,167 RNA5SP481, LOC105372625, 855 more genes
    nsv3910223copy number variation1nstd102humanLikely pathogenic NCBI36 chr20: 51,286,111-62,385,999 , GRCh37 chr20: 51,852,704-62,915,555 , GRCh38 chr20: 53,236,165-64,284,202 ATP5F1E, BMP7, 253 more genes
    nsv3905072copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435 LRRN4, SNRPB, 1313 more genes
    nsv3901084copy number variation1nstd102humanUncertain significance GRCh37 chr20: 54,541,125-55,162,415 , GRCh38.p12 chr20: 55,966,069-56,587,359 FAM209B, RPL39P, 13 more genes
    nsv3896520copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110 COMMD7, RNU7-6P, 1311 more genes
    nsv3895314copy number variation2nstd102humanPathogenic GRCh37 chr20: 61,569-62,915,555 , GRCh38.p12 chr20: 80,928-64,284,202 PKIG, LINC01523, 1311 more genes
    nsv3894116copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 51,542,616-62,915,555 , GRCh38.p12 chr20: 52,926,077-64,284,202 ATP5F1E, BMP7, 254 more genes
    nsv3892750copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941 TGIF2-RAB5IF, LOC105372609, 1314 more genes
    esv4010589copy number variation1estd233human GRCh37 chr20: 52,535,000-56,724,000 , GRCh38.p12 chr20: 53,918,461-58,148,944 , BMP7, 67 more genes
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