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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7136984copy number variation1nstd102humanUncertain significance GRCh37 chr16: 46,940,888-46,965,210 , GRCh38.p12 chr16: 46,906,976-46,931,298 GPT2
    nsv7094672copy number variation1nstd102humanUncertain significance GRCh37 chr16: 46,694,384-48,258,199 , GRCh38.p12 chr16: 46,660,472-48,224,288 LOC100420642, ITFG1-AS1, 26 more genes
    nsv6988320copy number variation1nstd229human GRCh38 chr16: 46,928,901-46,931,200 , GRCh37.p13 chr16: 46,962,813-46,965,112 GPT2
    nsv6987978copy number variation1nstd229human GRCh38 chr16: 46,905,211-46,908,948 , GRCh37.p13 chr16: 46,939,123-46,942,860 GPT2
    nsv6987126copy number variation1nstd229human GRCh38 chr16: 46,896,191-46,954,526 , GRCh37.p13 chr16: 46,930,103-46,988,438 GPT2, DNAJA2
    nsv6986102copy number variation1nstd229human GRCh38 chr16: 46,914,801-46,916,500 , GRCh37.p13 chr16: 46,948,713-46,950,412 GPT2
    nsv6986060copy number variation1nstd229human GRCh38 chr16: 46,929,560-46,967,083 , GRCh37.p13 chr16: 46,963,472-47,000,995 GPT2, DNAJA2
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 LINC02140, LOC100130602, 279 more genes
    nsv6504398copy number variation1nstd223human GRCh38 chr16: 46,896,191-46,954,526 , GRCh37.p13 chr16: 46,930,103-46,988,438 DNAJA2, GPT2
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6291594copy number variation1nstd102humanUncertain significance GRCh37 chr16: 46,503,328-47,004,071 , GRCh38.p12 chr16: 46,469,416-46,970,159 ANKRD26P1, RNU6-845P, 13 more genes
    nsv6271475copy number variation1nstd214human GRCh38 chr16: 46,907,936-46,908,095 , GRCh37.p13 chr16: 46,941,848-46,942,007 GPT2
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6132991copy number variation1nstd213human GRCh37 chr16: 46,460,000-48,129,895 , GRCh38.p12 chr16: 46,426,088-48,095,984 CKBP1, PHKB, 31 more genes
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv6024952copy number variation1nstd212human GRCh38 chr16: 46,915,423-46,915,594 , GRCh37.p13 chr16: 46,949,335-46,949,506 GPT2
    nsv5525386copy number variation1nstd206human GRCh38 chr16: 46,920,733-46,920,909 , GRCh37.p13 chr16: 46,954,645-46,954,821 GPT2
    nsv5522573copy number variation1nstd206human GRCh38 chr16: 46,386,400-46,898,682 , GRCh37.p13 chr16: 46,420,312-46,932,594 C16orf87, GPT2, 12 more genes
    nsv5150611mobile element insertion1nstd203human GRCh38 chr16: 46,885,833-46,885,848 , GRCh37.p13 chr16: 46,919,745-46,919,760 GPT2, SNORD148
    nsv5005643copy number variation1nstd200human GRCh38 chr16: 46,896,191-46,954,526 , GRCh37.p13 chr16: 46,930,103-46,988,438 GPT2, DNAJA2
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