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Items: 1 to 20 of 102

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4143037copy number variation1nstd166human GRCh37.p13 chr6: 156,868,361-156,880,037 , GRCh38.p12 chr6: 156,547,227-156,558,903 NMTRV-TAC1-1
    esv3385832copy number variation1estd59human NCBI36 chr6: 156,910,725-156,910,929 , GRCh37.p13 chr6: 156,869,033-156,869,237 , GRCh38.p12 chr6: 156,547,899-156,548,103 NMTRV-TAC1-1
    esv2831556insertion1estd209human GRCh37 chr6: 156,868,443-156,868,443 , GRCh38.p12 chr6: 156,547,309-156,547,309 NMTRV-TAC1-1
    nsv7049729inversion1nstd229human GRCh38 chr6: 156,547,755-156,551,331 , GRCh37.p13 chr6: 156,868,889-156,872,465 NMTRV-TAC1-1
    nsv2450187short tandem repeat2nstd128human GRCh37 chr6: 156,868,601-156,868,629 , GRCh38.p12 chr6: 156,547,467-156,547,495 NMTRV-TAC1-1
    nsv6807074copy number variation1nstd229human GRCh38 chr6: 156,485,976-156,575,653 , GRCh37.p13 chr6: 156,807,110-156,896,787 NMTRV-TAC1-1, LOC105378073
    nsv6136479copy number variation1nstd213human GRCh37 chr6: 156,710,000-156,920,001 , GRCh38.p12 chr6: 156,388,866-156,598,867 NMTRV-TAC1-1, LOC105378073
    nsv3911475copy number variation1nstd102humanPathogenic GRCh38 chr6: 152,793,402-170,610,394 , GRCh37 chr6: 153,114,537-170,919,482 , NCBI36 chr6: 153,156,230-170,761,407 SNORA116, PRR18, 275 more genes
    nsv3913213copy number variation1nstd102humanPathogenic GRCh38 chr6: 154,118,058-170,602,152 , NCBI36 chr6: 154,480,885-170,753,165 , GRCh37 chr6: 154,439,193-170,911,240 LDHAL6FP, QKI, 258 more genes
    nsv3921695copy number variation1nstd102humanPathogenic GRCh38 chr6: 154,539,655-170,714,507 , NCBI36 chr6: 154,902,481-170,865,520 , GRCh37 chr6: 154,860,789-171,023,595 LOC105378128, LOC105378102, 255 more genes
    nsv6313530copy number variation1nstd102humanPathogenic GRCh37 chr6: 153,207,930-164,322,346 , GRCh38.p12 chr6: 152,886,795-163,901,314 RSPH3, FBXO5, 144 more genes
    nsv3916405copy number variation1nstd102humanPathogenic NCBI36 chr6: 150,744,068-159,894,974 , GRCh38 chr6: 150,381,239-159,553,952 , GRCh37 chr6: 150,702,375-159,974,984 LOC112267968, ARMT1, 126 more genes
    nsv3916251copy number variation1nstd102humanPathogenic GRCh38 chr6: 155,378,049-163,133,499 , NCBI36 chr6: 155,740,875-163,474,521 , GRCh37 chr6: 155,699,183-163,554,531 MAP3K4, LOC112267977, 99 more genes
    nsv7148221copy number variation1nstd102humanPathogenic GRCh38 chr6: 150,905,553-158,511,926 , GRCh37.p13 chr6: 151,226,689-158,932,958 RNU6-824P, LOC105378067, 97 more genes
    nsv3903110copy number variation1nstd102humanPathogenic GRCh37 chr6: 153,647,248-158,255,989 , GRCh38.p12 chr6: 153,326,113-157,834,957 MTCO2P31, RNU6-824P, 49 more genes
    nsv3897252copy number variation1nstd102humanPathogenic GRCh37 chr6: 155,525,920-159,889,169 , GRCh38.p12 chr6: 155,204,786-159,468,137 NMTRV-TAC1-1, SNX9, 60 more genes
    nsv6291028copy number variation1nstd102humanPathogenic GRCh37 chr6: 153,584,880-157,203,309 , GRCh38.p12 chr6: 153,263,745-156,882,175 NMTRV-TAC1-1, MTND4LP20, 40 more genes
    nsv5381779copy number variation1nstd102humanPathogenic GRCh37 chr6: 155,308,263-158,394,005 , GRCh38.p12 chr6: 154,987,129-157,972,973 TFB1M, ARID1B, 30 more genes
    nsv4675220copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr6: 156,654,463-157,964,661 , GRCh38.p12 chr6: 156,333,329-157,543,629 H3P28, LOC115308161, 14 more genes
    nsv3910176copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,353,632-157,449,782 , NCBI36 chr6: 156,716,458-157,790,802 , GRCh37 chr6: 156,674,766-157,870,814 LOC105378073, ZDHHC14, 13 more genes
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