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Items: 1 to 20 of 225

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7078067inversion1nstd229human GRCh38 chr22: 30,287,061-38,012,264 , GRCh37.p13 chr22: 30,683,050-38,408,271 LINC02885, RN7SL20P, 203 more genes
    nsv7068065inversion1nstd229human GRCh38 chr22: 27,585,838-32,538,391 , GRCh37.p13 chr22: 27,981,799-32,934,377 LOC105372995, NEFH, 147 more genes
    nsv7065500inversion1nstd229human GRCh38 chr22: 29,260,563-37,652,385 , GRCh37.p13 chr22: 29,656,552-38,048,392 RFPL1, PATZ1, 217 more genes
    nsv7033735copy number variation1nstd229human GRCh38 chr22: 31,654,801-31,657,800 , GRCh37.p13 chr22: 32,050,787-32,053,786 PISD
    nsv7033026copy number variation1nstd229human GRCh38 chr22: 31,641,445-31,642,829 , GRCh37.p13 chr22: 32,037,431-32,038,815 PISD
    nsv7032105copy number variation1nstd229human GRCh38 chr22: 31,641,584-31,642,873 , GRCh37.p13 chr22: 32,037,570-32,038,859 PISD
    nsv7032023copy number variation1nstd229human GRCh38 chr22: 31,604,001-31,627,000 , GRCh37.p13 chr22: 31,999,987-32,022,986 SFI1, MIR7109, 1 more genes
    nsv7030210copy number variation1nstd229human GRCh38 chr22: 31,642,223-31,642,812 , GRCh37.p13 chr22: 32,038,209-32,038,798 PISD
    nsv7025245copy number variation1nstd229human GRCh38 chr22: 31,659,875-31,669,762 , GRCh37.p13 chr22: 32,055,861-32,065,748 PISD
    nsv7024636copy number variation1nstd229human GRCh38 chr22: 31,630,515-31,631,195 , GRCh37.p13 chr22: 32,026,501-32,027,181 PISD
    nsv7018931copy number variation1nstd229human GRCh38 chr22: 31,651,980-31,656,125 , GRCh37.p13 chr22: 32,047,966-32,052,111 PISD
    nsv6599153inversion1nstd223human GRCh38 chr22: 31,640,905-31,641,809 , GRCh37.p13 chr22: 32,036,891-32,037,795 PISD
    nsv6599052inversion1nstd223human GRCh38 chr22: 31,660,520-31,660,950 , GRCh37.p13 chr22: 32,056,506-32,056,936 PISD
    nsv6598271inversion1nstd223human GRCh38 chr22: 31,650,832-31,651,137 , GRCh37.p13 chr22: 32,046,818-32,047,123 PISD
    nsv6552473copy number variation1nstd223human GRCh38 chr22: 31,641,601-31,642,822 , GRCh37.p13 chr22: 32,037,587-32,038,808 PISD
    nsv6549312copy number variation1nstd223human GRCh38 chr22: 31,636,630-31,640,590 , GRCh37.p13 chr22: 32,032,616-32,036,576 PISD
    nsv6544203copy number variation1nstd223human GRCh38 chr22: 31,640,601-31,644,500 , GRCh37.p13 chr22: 32,036,587-32,040,486 PISD
    nsv6537168copy number variation1nstd223human GRCh38 chr22: 31,634,577-31,634,906 , GRCh37.p13 chr22: 32,030,563-32,030,892 PISD
    nsv6311263copy number variation1nstd102humanUncertain significance GRCh37 chr22: 29,083,885-34,046,674 , GRCh38.p12 chr22: 28,687,897-33,650,688 SNORD125, LOC107985533, 145 more genes
    nsv6220081copy number variation1nstd214human GRCh38 chr22: 31,624,684-31,624,759 , GRCh37.p13 chr22: 32,020,670-32,020,745 PISD
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