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Items: 19

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    Number of Variants: 19

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4350212copy number variation1nstd102humanPathogenic GRCh37 chr6: 135,239,633-146,997,510 , GRCh38.p12 chr6: 134,918,495-146,676,374 AIG1, LOC100131041, 146 more genes
    nsv3891146copy number variation1nstd102humanPathogenic GRCh37 chr6: 139,513,020-150,389,231 , GRCh38.p12 chr6: 139,191,883-150,068,095 AIG1, UST, 131 more genes
    nsv3904441copy number variation1nstd102humanPathogenic GRCh37 chr6: 133,077,239-143,761,582 , GRCh38.p12 chr6: 132,756,100-143,440,445 AIG1, SNORD101, 147 more genes
    nsv3916499copy number variation1nstd102humanPathogenic NCBI36 chr6: 136,359,437-146,708,473 , GRCh37.p13 chr6: 136,317,744-146,666,780 , GRCh38.p12 chr6: 135,996,606-146,345,644 AIG1, SLC35D3, 127 more genes
    nsv3912178copy number variation1nstd102humanPathogenic NCBI36 chr6: 142,070,748-145,748,578 , GRCh37.p13 chr6: 142,029,055-145,706,885 , GRCh38.p12 chr6: 141,707,918-145,385,749 AIG1, GJE1, 40 more genes
    nsv7097046copy number variation1nstd102humanPathogenic GRCh37 chr6: 142,623,467-144,508,628 , GRCh38.p12 chr6: 142,302,330-144,187,491 AIG1, ZC2HC1B, 26 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 AIG1, LOC105378061, 2914 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 AIG1, RNU6-411P, 2910 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 AIG1, SOD1P1, 2905 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 AIG1, 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 AIG1, 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 AIG1, 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 AIG1, UST-AS2, 394 more genes
    nsv3913689copy number variation1nstd102humanPathogenic NCBI36 chr6: 121,373,749-146,289,101 , GRCh37.p13 chr6: 121,332,050-146,247,408 , GRCh38.p12 chr6: 121,010,904-145,926,272 AIG1, TPD52L1, 316 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 AIG1, HYMAI, 263 more genes
    nsv6313714copy number variation1nstd102humanPathogenic GRCh37 chr6: 143,331,663-145,817,051 , GRCh38.p12 chr6: 143,010,526-145,495,915 AIG1, LOC100131041, 31 more genes
    nsv3909706copy number variation1nstd102humanUncertain significance GRCh37 chr6: 143,204,211-143,689,813 , GRCh38.p12 chr6: 142,883,074-143,368,676 AIG1, HIVEP2, 4 more genes
    nsv6636975copy number variation1nstd102humanUncertain significance GRCh37 chr6: 143,645,794-143,860,372 , GRCh38.p12 chr6: 143,324,657-143,539,235 AIG1, VDAC1P8, 10 more genes
    nsv4683714copy number variation1nstd102humanUncertain significance GRCh37 chr6: 143,654,419-143,832,771 , GRCh38.p12 chr6: 143,333,282-143,511,634 AIG1, ADAT2, 9 more genes
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