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Items: 1 to 20 of 269

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969472inversion1nstd209human GRCh38 chr16: 16,657,579-18,701,513 , GRCh37.p13 chr16: 16,751,436-18,712,835 , XYLT1, 28 more genes
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5943157copy number variation1nstd209human GRCh38 chr16: 17,132,531-17,132,590 , GRCh37.p13 chr16: 17,226,388-17,226,447 LOC102723692, XYLT1
    nsv5940711copy number variation1nstd209human GRCh38 chr16: 17,132,481-17,132,535 , GRCh37.p13 chr16: 17,226,338-17,226,392 LOC102723692, XYLT1
    nsv5928138copy number variation1nstd209human GRCh38 chr16: 15,180,124-18,091,718 , GRCh37.p13 chr16: 15,273,981-18,185,575 , LOC102723692, 42 more genes
    nsv5666478inversion1nstd207human GRCh38 chr16: 16,632,193-18,073,542 , GRCh37.p13 chr16: 16,726,050-18,167,399 XYLT1, RPL7P47, 6 more genes
    nsv5648751insertion1nstd207human GRCh38 chr16: 17,132,531-17,132,531 , GRCh37.p13 chr16: 17,226,388-17,226,388 XYLT1, LOC102723692
    nsv5596538copy number variation1nstd207human GRCh38 chr16: 17,132,481-17,132,535 , GRCh37.p13 chr16: 17,226,338-17,226,392 LOC102723692, XYLT1
    nsv5530940copy number variation1nstd206human GRCh38 chr16: 17,138,974-17,139,031 , GRCh37.p13 chr16: 17,232,831-17,232,888 LOC102723692, XYLT1
    nsv5274445copy number variation1nstd204human GRCh38.p13 chr16: 17,044,801-17,631,300 , GRCh37.p13 chr16: 17,138,658-17,725,157 LOC105371106, TCERG1P2, 3 more genes
    nsv5002992copy number variation1nstd200human GRCh38 chr16: 17,136,693-17,137,976 , GRCh37.p13 chr16: 17,230,550-17,231,833 XYLT1, LOC102723692
    nsv4994505copy number variation1nstd200human GRCh38 chr16: 17,044,735-17,410,967 , GRCh37.p13 chr16: 17,138,592-17,504,824 XYLT1, LOC102723692, 1 more genes
    nsv4864033copy number variation1nstd200human GRCh37 chr16: 17,138,592-17,504,824 , GRCh38.p12 chr16: 17,044,735-17,410,967 , GRCh38.p12 chr16|NW_019805500.1: 45,996-412,228 LOC102723692, XYLT1, 1 more genes
    nsv4754659inversion1nstd199human GRCh37 chr16: 16,726,089-18,732,830 , GRCh38.p12 chr16: 16,632,232-18,721,508 , XYLT1, 28 more genes
    nsv4737394copy number variation1nstd199human GRCh37 chr16: 17,226,371-17,226,426 , GRCh38.p12 chr16: 17,132,514-17,132,569 , GRCh38.p12 chr16|NW_019805500.1: 133,775-133,830 LOC102723692, XYLT1
    nsv4730208inversion9nstd198human GRCh38 chr16: 16,118,120-18,828,979 , GRCh37.p13 chr16: 16,211,977-18,840,301 , ABCC6, 48 more genes
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 NPIPB9, TMEM219, 597 more genes
    nsv4729445copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,375,911-18,198,455 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-2,659,700 , GRCh38.p12 chr16: 15,282,054-18,104,598 BMERB1, RNU6-213P, 38 more genes
    nsv4729435copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 15,316,618-18,164,698 , GRCh38.p12 chr16: 15,222,761-18,070,841 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-2,659,700 ABCC6, ABCC1, 37 more genes
    nsv4728906copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 15,481,920-18,164,698 , GRCh38.p12 chr16: 15,388,063-18,070,841 , GRCh38.p12 chr16|NT_187607.1: 1,046,027-2,659,700 ABCC6, ABCC1, 35 more genes
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