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Items: 1 to 20 of 229

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076079inversion1nstd229human GRCh38 chr16: 9,015,595-14,846,246 , GRCh37.p13 chr16: 9,109,452-14,940,103 LOC105371093, RNU6-633P, 100 more genes
    nsv6977393copy number variation1nstd229human GRCh38 chr16: 11,790,016-11,793,021 , GRCh37.p13 chr16: 11,883,872-11,886,877 ZC3H7A
    nsv6975402copy number variation1nstd229human GRCh38 chr16: 11,772,208-11,773,841 , GRCh37.p13 chr16: 11,866,064-11,867,697 ZC3H7A
    nsv6972753copy number variation1nstd229human GRCh38 chr16: 11,616,748-11,854,058 , GRCh37.p13 chr16: 11,710,604-11,947,915 LITAF, ZC3H7A, 5 more genes
    nsv6972675copy number variation1nstd229human GRCh38 chr16: 11,729,457-11,754,447 , GRCh37.p13 chr16: 11,823,313-11,848,303 TXNDC11, ZC3H7A
    nsv6960587copy number variation1nstd229human GRCh38 chr16: 11,697,619-12,319,744 , GRCh37.p13 chr16: 11,791,475-12,413,601 RSL1D1-DT, UBL5P4, 11 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    nsv6637308copy number variation1nstd102humanUncertain significance GRCh37 chr16: 10,423,631-12,176,517 , GRCh38.p12 chr16: 10,329,774-12,082,660 LOC400499, RSL1D1, 46 more genes
    nsv6623365copy number variation1nstd224human GRCh37 chr16: 11,868,029-11,901,557 , GRCh38.p12 chr16: 11,774,173-11,807,701 ZC3H7A
    nsv6623312copy number variation1nstd224human GRCh37 chr16: 11,431,919-13,207,154 , GRCh38.p12 chr16: 11,338,062-13,113,297 TNFRSF17, RSL1D1, 29 more genes
    nsv6590579inversion1nstd223human GRCh38 chr16: 11,772,170-11,772,730 , GRCh37.p13 chr16: 11,866,026-11,866,586 ZC3H7A
    nsv6588333inversion1nstd223human GRCh38 chr16: 11,778,449-11,778,719 , GRCh37.p13 chr16: 11,872,305-11,872,575 ZC3H7A
    nsv6581421inversion1nstd223human GRCh38 chr16: 11,785,100-11,785,643 , GRCh37.p13 chr16: 11,878,956-11,879,499 ZC3H7A
    nsv6575787inversion1nstd223human GRCh38 chr16: 11,771,814-11,772,076 , GRCh37.p13 chr16: 11,865,670-11,865,932 ZC3H7A
    nsv6511469copy number variation1nstd223human GRCh38 chr16: 11,772,201-11,773,800 , GRCh37.p13 chr16: 11,866,057-11,867,656 ZC3H7A
    nsv6502290copy number variation1nstd223human GRCh38 chr16: 11,778,301-11,829,300 , GRCh37.p13 chr16: 11,872,157-11,923,157 ZC3H7A, BCAR4
    nsv6499255copy number variation1nstd223human GRCh38 chr16: 11,747,777-11,748,899 , GRCh37.p13 chr16: 11,841,633-11,842,755 ZC3H7A
    nsv6313996copy number variation1nstd102humanUncertain significance GRCh37 chr16: 11,364,838-13,592,668 , GRCh38.p12 chr16: 11,270,981-13,498,811 LOC100420951, RSL1D1-DT, 36 more genes
    nsv6133278copy number variation2nstd213human GRCh37 chr16: 60,000-14,990,001 , GRCh38.p12 chr16: 10,001-14,896,144 , ABAT, 446 more genes
    nsv6132977copy number variation1nstd213human GRCh37 chr16: 11,640,000-11,980,001 , GRCh38.p12 chr16: 11,546,144-11,886,144 GSPT1, SNN, 6 more genes
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