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Items: 1 to 20 of 958

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141065copy number variation1nstd232human GRCh37.p13 chr2: 154,966,785-154,966,858 , GRCh38.p12 chr2: 154,110,272-154,110,345 GALNT13
    nsv7140349copy number variation1nstd232human GRCh37.p13 chr2: 155,155,099-155,155,206 , GRCh38.p12 chr2: 154,298,586-154,298,693 GALNT13
    nsv7139314insertion1nstd232human GRCh37.p13 chr2: 154,891,194-154,891,194 , GRCh38.p12 chr2: 154,034,681-154,034,681 GALNT13
    nsv7138756insertion1nstd232human GRCh37.p13 chr2: 155,200,875-155,200,875 , GRCh38.p12 chr2: 154,344,363-154,344,363 GALNT13
    nsv7056508inversion1nstd229human GRCh38 chr2: 154,357,245-154,362,190 , GRCh37.p13 chr2: 155,213,757-155,218,702 GALNT13
    nsv7055310inversion1nstd229human GRCh38 chr2: 154,252,266-154,300,807 , GRCh37.p13 chr2: 155,108,779-155,157,320 PHB1P4, GALNT13
    nsv7055067inversion1nstd229human GRCh38 chr2: 154,060,120-154,069,630 , GRCh37.p13 chr2: 154,916,633-154,926,143 GALNT13
    nsv7053722inversion1nstd229human GRCh38 chr2: 154,164,839-154,164,938 , GRCh37.p13 chr2: 155,021,352-155,021,451 GALNT13
    nsv7053155inversion1nstd229human GRCh38 chr2: 154,031,993-154,133,469 , GRCh37.p13 chr2: 154,888,506-154,989,982 GALNT13
    nsv7052534inversion1nstd229human GRCh38 chr2: 154,063,550-154,069,624 , GRCh37.p13 chr2: 154,920,063-154,926,137 GALNT13
    nsv7049659inversion1nstd229human GRCh38 chr2: 154,441,588-154,441,632 , GRCh37.p13 chr2: 155,298,100-155,298,144 GALNT13, GALNT13-AS1
    nsv7048871inversion1nstd229human GRCh38 chr2: 154,172,011-154,172,117 , GRCh37.p13 chr2: 155,028,524-155,028,630 GALNT13
    nsv7040074inversion1nstd229human GRCh38 chr2: 154,060,128-154,063,697 , GRCh37.p13 chr2: 154,916,641-154,920,210 GALNT13
    nsv7038090inversion1nstd229human GRCh38 chr2: 152,079,952-160,943,714 , GRCh37.p13 chr2: 152,936,466-161,800,225 , ITGB6, 105 more genes
    nsv6697273copy number variation1nstd229human GRCh38 chr2: 154,208,635-154,208,670 , GRCh37.p13 chr2: 155,065,148-155,065,183 GALNT13
    nsv6695990copy number variation1nstd229human GRCh38 chr2: 154,055,527-154,055,579 , GRCh37.p13 chr2: 154,912,040-154,912,092 GALNT13
    nsv6695753copy number variation1nstd229human GRCh38 chr2: 153,904,841-153,909,317 , GRCh37.p13 chr2: 154,761,354-154,765,830 GALNT13
    nsv6695389copy number variation1nstd229human GRCh38 chr2: 154,287,509-154,291,742 , GRCh37.p13 chr2: 155,144,022-155,148,255 GALNT13, PHB1P4
    nsv6694962copy number variation1nstd229human GRCh38 chr2: 154,143,656-154,158,016 , GRCh37.p13 chr2: 155,000,169-155,014,529 GALNT13
    nsv6694900copy number variation1nstd229human GRCh38 chr2: 154,294,762-154,298,915 , GRCh37.p13 chr2: 155,151,275-155,155,428 GALNT13
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