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Items: 1 to 20 of 955

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057368inversion1nstd229human GRCh38 chr2: 167,316,020-167,323,766 , GRCh37.p13 chr2: 168,172,530-168,180,276 B3GALT1
    nsv7057182inversion1nstd229human GRCh38 chr2: 167,836,093-168,417,213 , GRCh37.p13 chr2: 168,692,603-169,273,723 LOC105373734, B3GALT1-AS1, 4 more genes
    nsv7055393inversion1nstd229human GRCh38 chr2: 167,309,966-167,309,992 , GRCh37.p13 chr2: 168,166,476-168,166,502 B3GALT1
    nsv7054506inversion1nstd229human GRCh38 chr2: 167,383,555-167,424,243 , GRCh37.p13 chr2: 168,240,065-168,280,753 B3GALT1
    nsv7053047inversion1nstd229human GRCh38 chr2: 167,765,218-167,770,301 , GRCh37.p13 chr2: 168,621,728-168,626,811 B3GALT1
    nsv7052913inversion1nstd229human GRCh38 chr2: 167,394,968-167,395,022 , GRCh37.p13 chr2: 168,251,478-168,251,532 B3GALT1
    nsv7051472inversion1nstd229human GRCh38 chr2: 167,676,115-167,765,504 , GRCh37.p13 chr2: 168,532,625-168,622,014 CTAGE14P, B3GALT1
    nsv7051273inversion1nstd229human GRCh38 chr2: 167,316,080-167,316,180 , GRCh37.p13 chr2: 168,172,590-168,172,690 B3GALT1
    nsv7050884inversion1nstd229human GRCh38 chr2: 167,323,597-167,327,692 , GRCh37.p13 chr2: 168,180,107-168,184,202 B3GALT1
    nsv7050331inversion1nstd229human GRCh38 chr2: 167,316,076-167,323,763 , GRCh37.p13 chr2: 168,172,586-168,180,273 B3GALT1
    nsv7046991inversion1nstd229human GRCh38 chr2: 167,316,083-167,327,692 , GRCh37.p13 chr2: 168,172,593-168,184,202 B3GALT1
    nsv7044892inversion1nstd229human GRCh38 chr2: 167,381,881-167,403,565 , GRCh37.p13 chr2: 168,238,391-168,260,075 B3GALT1
    nsv6697987copy number variation1nstd229human GRCh38 chr2: 167,585,516-167,587,226 , GRCh37.p13 chr2: 168,442,026-168,443,736 B3GALT1
    nsv6697739copy number variation1nstd229human GRCh38 chr2: 167,387,801-167,504,000 , GRCh37.p13 chr2: 168,244,311-168,360,510 B3GALT1
    nsv6697616copy number variation1nstd229human GRCh38 chr2: 167,635,112-167,645,071 , GRCh37.p13 chr2: 168,491,622-168,501,581 B3GALT1
    nsv6697608copy number variation1nstd229human GRCh38 chr2: 167,431,018-167,607,970 , GRCh37.p13 chr2: 168,287,528-168,464,480 B3GALT1
    nsv6697414copy number variation1nstd229human GRCh38 chr2: 167,514,023-167,762,454 , GRCh37.p13 chr2: 168,370,533-168,618,964 CTAGE14P, RNU7-148P, 1 more genes
    nsv6697236copy number variation1nstd229human GRCh38 chr2: 167,461,201-167,466,800 , GRCh37.p13 chr2: 168,317,711-168,323,310 B3GALT1
    nsv6696628copy number variation1nstd229human GRCh38 chr2: 167,432,495-167,793,253 , GRCh37.p13 chr2: 168,289,005-168,649,763 RNU7-148P, CTAGE14P, 1 more genes
    nsv6696400copy number variation1nstd229human GRCh38 chr2: 167,516,427-167,525,261 , GRCh37.p13 chr2: 168,372,937-168,381,771 B3GALT1
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