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Items: 1 to 20 of 29

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4674989copy number variation1nstd102humanUncertain significance GRCh37 chr6: 155,405,078-155,584,960 , GRCh38.p12 chr6: 155,083,944-155,263,826 TFB1M, TIAM2, 1 more genes
    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 TFB1M, SNORA116, 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 TFB1M, LDHAL6FP, 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 TFB1M, LOC105378128, 255 more genes
    nsv6313530copy number variation1nstd102humanPathogenic GRCh37 chr6: 153,207,930-164,322,346 , GRCh38.p12 chr6: 152,886,795-163,901,314 TFB1M, RSPH3, 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 TFB1M, LOC112267968, 126 more genes
    nsv7148221copy number variation1nstd102humanPathogenic GRCh38 chr6: 150,905,553-158,511,926 , GRCh37.p13 chr6: 151,226,689-158,932,958 TFB1M, RNU6-824P, 97 more genes
    nsv3903110copy number variation1nstd102humanPathogenic GRCh37 chr6: 153,647,248-158,255,989 , GRCh38.p12 chr6: 153,326,113-157,834,957 TFB1M, MTCO2P31, 49 more genes
    nsv3897252copy number variation1nstd102humanPathogenic GRCh37 chr6: 155,525,920-159,889,169 , GRCh38.p12 chr6: 155,204,786-159,468,137 TFB1M, NMTRV-TAC1-1, 60 more genes
    nsv6291028copy number variation1nstd102humanPathogenic GRCh37 chr6: 153,584,880-157,203,309 , GRCh38.p12 chr6: 153,263,745-156,882,175 TFB1M, NMTRV-TAC1-1, 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
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 TFB1M, LOC105378061, 2914 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 TFB1M, RNU6-411P, 2910 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 TFB1M, SOD1P1, 2905 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 TFB1M, ITPR3, 2905 more genes
    nsv3911993copy number variation1nstd102humanPathogenic NCBI36 chr6: 133,900,102-166,209,023 , GRCh38 chr6: 133,537,271-165,875,545 , GRCh37 chr6: 133,858,409-166,289,033 TFB1M, LOC105369171, 418 more genes
    nsv3915150copy number variation1nstd102humanPathogenic NCBI36 chr6: 124,322,082-156,156,864 , GRCh37.p13 chr6: 124,280,383-156,115,172 , GRCh38.p12 chr6: 123,959,238-155,794,038 TFB1M, KATNA1, 422 more genes
    nsv3920975copy number variation1nstd102humanPathogenic GRCh37 chr6: 141,454,127-169,739,666 , GRCh38 chr6: 141,132,990-169,339,571 , NCBI36 chr6: 141,495,820-169,481,591 TFB1M, UST-AS2, 394 more genes
    nsv3908622copy number variation1nstd102humanPathogenic GRCh37 chr6: 150,284,435-170,919,470 , GRCh38.p12 chr6: 149,963,299-170,610,382 TFB1M, LOC105378120, 319 more genes
    nsv3911164copy number variation1nstd102humanPathogenic NCBI36 chr6: 135,720,981-155,817,943 , GRCh37 chr6: 135,679,288-155,776,251 , GRCh38 chr6: 135,358,150-155,455,117 TFB1M, HYMAI, 263 more genes
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