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Items: 1 to 20 of 124

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5689783mobile element insertion1nstd211human GRCh38 chr6: 25,921,803-25,921,803 , GRCh37.p13 chr6: 25,922,031-25,922,031 SLC17A2
    nsv5537934insertion1nstd206human GRCh38 chr6: 25,921,803-25,921,842 , GRCh37.p13 chr6: 25,922,031-25,922,070 SLC17A2
    nsv5472360copy number variation1nstd206human GRCh38 chr6: 25,927,317-25,927,914 , GRCh37.p13 chr6: 25,927,545-25,928,142 SLC17A2
    nsv5114008mobile element insertion1nstd203human GRCh38 chr6: 25,921,791-25,921,803 , GRCh37.p13 chr6: 25,922,019-25,922,031 SLC17A2
    nsv5036471inversion1nstd200human GRCh38 chr6: 25,888,426-29,704,316 , GRCh37.p13 chr6: 25,888,654-29,672,093 , OR11A1, 368 more genes
    nsv4940460copy number variation1nstd200human GRCh38 chr6: 25,927,317-25,927,914 , GRCh37.p13 chr6: 25,927,545-25,928,142 SLC17A2
    nsv4940459copy number variation1nstd200human GRCh38 chr6: 25,903,429-25,910,835 , GRCh37.p13 chr6: 25,903,657-25,911,063 SLC17A2
    nsv4879678inversion1nstd200human GRCh37 chr6: 25,888,654-29,672,093 , GRCh38.p12 chr6: 25,888,426-29,704,316 , H1-4, 368 more genes
    nsv4815671copy number variation1nstd200human GRCh37 chr6: 25,903,657-25,911,063 , GRCh38.p12 chr6: 25,903,429-25,910,835 SLC17A2
    nsv4495146mobile element insertion1nstd166human GRCh37.p13 chr6: 25,922,019-25,922,019 , GRCh38.p12 chr6: 25,921,791-25,921,791 SLC17A2
    nsv4456351copy number variation1nstd102humanUncertain significance GRCh37 chr6: 25,896,585-26,287,389 , GRCh38.p12 chr6: 25,896,357-26,287,161 H3P26, H1-6, 44 more genes
    nsv4121805copy number variation1nstd166human GRCh37.p13 chr6: 25,927,545-25,928,142 , GRCh38.p12 chr6: 25,927,317-25,927,914 SLC17A2
    nsv3922819copy number variation1nstd102humanUncertain significance NCBI36 chr6: 23,360,729-26,075,484 , GRCh37 chr6: 23,252,750-25,967,505 , GRCh38 chr6: 23,252,522-25,967,277 KAAG1, ACOT13, 52 more genes
    nsv3920564copy number variation1nstd102humanPathogenic GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946 PRELID1P2, RPL7AP7, 785 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
    nsv3888702copy number variation1nstd102humanUncertain significance GRCh37 chr6: 25,851,789-26,319,486 , GRCh38.p12 chr6: 25,851,561-26,319,258 TRIM38, TRR-TCG4-1, 54 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 RNU6-411P, LOC107986611, 2910 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 LOC105378061, MIR4640, 2914 more genes
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