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Items: 1 to 20 of 162

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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
    nsv5875876copy number variation1nstd209human GRCh38 chr20: 62,536,869-62,550,324 , GRCh37.p13 chr20|NW_003571063.2: 80,387-93,842 MIR1-1HG, LOC105376995, 1 more genes
    nsv5381223copy number variation2nstd102humanUncertain significance GRCh37 chr20: 60,831,241-62,664,346 , GRCh38.p12 chr20: 62,256,185-64,032,993 KCNQ2-AS1, HAR1B, 100 more genes
    nsv5289201copy number variation1nstd204human GRCh38.p13 chr20: 62,058,601-62,909,300 , GRCh37.p13 chr20: 60,633,657-61,540,652 , LOC105372716, 47 more genes
    nsv5286355copy number variation1nstd204human GRCh38.p13 chr20: 62,445,901-62,672,900 , GRCh37.p13 chr20: 61,020,957-61,304,252 , GRCh37.p13 chr20|NW_003571063.2: 1-179,899 GATA5, SLCO4A1, 11 more genes
    nsv5025804copy number variation1nstd200human GRCh38 chr20: 62,515,332-62,643,111 , GRCh37.p13 chr20|NW_003571063.2: 58,850-179,899 , GRCh37.p13 chr20: 61,090,388-61,267,733 SLCO4A1, MIR1-1, 6 more genes
    nsv5025801copy number variation1nstd200human GRCh38 chr20: 62,359,844-62,584,783 , GRCh37.p13 chr20|NW_003571063.2: 1-128,301 , GRCh37.p13 chr20: 61,031,539-61,181,990 LOC105372709, MIR1-1HG, 13 more genes
    nsv4676332copy number variation1nstd102humanPathogenic GRCh37 chr20: 55,743,522-62,032,989 , GRCh38.p12 chr20: 57,168,466-63,401,636 BMP7, MIR298, 153 more genes
    nsv4676181copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,788,101-62,762,405 , GRCh38.p12 chr20: 58,213,045-64,131,052 LOC105372697, MIR647, 174 more genes
    nsv4457856copy number variation1nstd102humanUncertain significance GRCh37 chr20: 61,033,338-61,412,941 , GRCh38.p12 chr20: 62,458,282-62,781,589 RPL7P3, GATA5, 13 more genes
    nsv4457810copy number variation1nstd102humanUncertain significance GRCh37 chr20: 60,946,209-61,975,606 , GRCh38.p12 chr20: 62,371,153-63,344,254 SLCO4A1-AS2, ARFGAP1, 51 more genes
    nsv4436326complex substitution1nstd102humanUncertain significance GRCh37 chr20: 60,885,242-61,929,348 , GRCh38.p12 chr20: 62,310,186-63,297,996 COL9A3, LAMA5, 52 more genes
    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
    nsv3961013copy number variation1nstd168human GRCh38 chr20: 62,477,793-62,553,392 , GRCh37.p13 chr20|NW_003571063.2: 21,311-96,910 , GRCh37.p13 chr20: 61,052,849-61,150,599 CRMA, LOC105372711, 3 more genes
    nsv3953143insertion1nstd167human GRCh37 chr20: 61,147,929-61,147,929 , GRCh38.p12 chr20: 62,550,722-62,550,722 MIR1-1HG, CRMA
    nsv3924353copy number variation1nstd102humanPathogenic NCBI36 chr20: 59,335,000-62,379,123 , GRCh38 chr20: 61,326,549-64,277,326 , GRCh37 chr20: 59,901,605-62,908,679 PPDPF, CRMA, 126 more genes
    nsv3922590copy number variation1nstd102humanPathogenic NCBI36 chr20: 60,553,022-62,343,283 , GRCh38 chr20: 62,545,370-64,241,486 , GRCh37 chr20: 61,142,577-62,872,839 RPL7P3, BHLHE23, 95 more genes
    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
    nsv3916789copy number variation1nstd102humanPathogenic GRCh37 chr20: 57,617,021-62,908,674 , GRCh38 chr20: 59,041,966-64,277,321 , NCBI36 chr20: 57,050,416-62,379,118 RNU7-141P, UCKL1, 153 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
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