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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4455613copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,935,248-57,958,159 , GRCh38.p12 chr16: 57,901,344-57,924,255 CNGB1
    nsv7094590copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,935,236-57,957,304 , GRCh38.p12 chr16: 57,901,332-57,923,400 CNGB1
    nsv4683487copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,937,726-57,945,779 , GRCh38.p12 chr16: 57,903,822-57,911,875 CNGB1
    nsv7095034copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,937,706-57,938,799 , GRCh38.p12 chr16: 57,903,802-57,904,895 CNGB1
    nsv6310013copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,951,152-57,951,400 , GRCh38.p12 chr16: 57,917,248-57,917,496 CNGB1
    nsv4681193copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,951,172-57,951,380 , GRCh38.p12 chr16: 57,917,268-57,917,476 CNGB1
    nsv4769256copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 57,984,349-57,989,077 , GRCh38 chr16: 57,950,445-57,955,173 CNGB1
    nsv7094680copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 57,938,618-57,957,304 , GRCh38.p12 chr16: 57,904,714-57,923,400 CNGB1
    nsv7094855copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 57,931,281-57,946,918 , GRCh38.p12 chr16: 57,897,377-57,913,014 CNGB1
    nsv4681249copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 57,983,257-57,984,444 , GRCh38.p12 chr16: 57,949,353-57,950,540 CNGB1
    nsv6314614delins1nstd102humanLikely pathogenic GRCh38 chr16: 57,900,360-57,901,354 , GRCh37 chr16: 57,934,264-57,935,258 CNGB1
    nsv3894397copy number variation1nstd102humanBenign GRCh37 chr16: 57,965,720-58,000,714 , GRCh38.p12 chr16: 57,931,816-57,966,810 CNGB1
    nsv7095035copy number variation1nstd102humanUncertain significance GRCh37 chr16: 57,965,600-58,001,190 , GRCh38.p12 chr16: 57,931,696-57,967,286 CNGB1
    nsv6112822copy number variation1nstd102humanUncertain significance GRCh38 chr16: 57,903,821-57,931,878 , GRCh37.p13 chr16: 57,937,725-57,965,782 CNGB1
    nsv3916542copy number variation1nstd102humanPathogenic GRCh38 chr16: 55,457,477-63,841,622 , NCBI36 chr16: 54,048,890-62,433,027 , GRCh37 chr16: 55,491,389-63,875,526 CNGB1, CES1, 139 more genes
    nsv3908644copy number variation1nstd102humanPathogenic GRCh37 chr16: 56,950,941-60,203,590 , GRCh38.p12 chr16: 56,917,029-60,169,686 CNGB1, ADGRG1, 75 more genes
    nsv7095031copy number variation2nstd102humanPathogenic GRCh37 chr16: 56,226,148-58,768,132 , GRCh38.p12 chr16: 56,192,236-58,734,228 CNGB1, MT1B, 92 more genes
    nsv7094589copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,016,057-58,768,132 , GRCh38.p12 chr16: 56,982,145-58,734,228 CNGB1, SLC38A7, 58 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 CNGB1, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 CNGB1, LOC100128079, 1879 more genes
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