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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148080copy number variation1nstd102humanPathogenic GRCh37 chr2: 111,335,152-113,127,204 , GRCh38.p12 chr2: 110,577,575-112,369,627 MIR4771-2, BUB1, 33 more genes
    nsv7148068copy number variation1nstd102humanUncertain significance GRCh37 chr2: 111,395,541-113,090,065 , GRCh38.p12 chr2: 110,637,964-112,332,488 NDUFB4P6, SLC30A6P1, 28 more genes
    nsv7098850copy number variation1nstd102humanUncertain significance GRCh37 chr2: 111,368,292-113,191,030 , GRCh38.p12 chr2: 110,610,715-112,433,453 MERTK, MIR4435-2HG, 33 more genes
    nsv6696827copy number variation1nstd229human GRCh38 chr2: 111,162,859-111,163,076 , GRCh37.p13 chr2: 111,920,436-111,920,653 BCL2L11
    nsv6694585copy number variation1nstd229human GRCh38 chr2: 111,126,873-111,134,034 , GRCh37.p13 chr2: 111,884,450-111,891,611 BCL2L11
    nsv6685382copy number variation1nstd229human GRCh38 chr2: 111,125,617-111,128,521 , GRCh37.p13 chr2: 111,883,194-111,886,098 BCL2L11
    nsv6683728copy number variation1nstd229human GRCh38 chr2: 111,159,047-111,161,929 , GRCh37.p13 chr2: 111,916,624-111,919,506 BCL2L11
    nsv6682350copy number variation1nstd229human GRCh38 chr2: 111,131,267-111,142,192 , GRCh37.p13 chr2: 111,888,844-111,899,769 BCL2L11
    nsv6678618copy number variation1nstd229human GRCh38 chr2: 111,144,090-111,144,270 , GRCh37.p13 chr2: 111,901,667-111,901,847 BCL2L11
    nsv6637066copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 111,397,786-113,111,856 , GRCh38.p12 chr2: 110,640,209-112,354,279 BUB1, BCL2L11, 29 more genes
    nsv6636824copy number variation1nstd102humanPathogenic GRCh37 chr2: 111,366,256-113,127,751 , GRCh38.p12 chr2: 110,608,679-112,370,174 PAFAH1B1P2, BUB1, 33 more genes
    nsv6636588copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 111,365,996-113,111,856 , GRCh38.p12 chr2: 110,608,419-112,354,279 BUB1, BCL2L11, 32 more genes
    nsv6636225copy number variation1nstd102humanPathogenic GRCh37 chr2: 111,369,264-113,142,794 , GRCh38.p12 chr2: 110,611,687-112,385,217 RPL34P8, SNORD132, 32 more genes
    nsv6627672copy number variation1nstd224human GRCh37 chr2: 111,395,603-113,217,630 , GRCh38.p12 chr2: 110,638,026-112,460,053 ACOXL, TMEM87B, 30 more genes
    nsv6627671copy number variation2nstd224human GRCh37 chr2: 111,395,603-113,093,928 , GRCh38.p12 chr2: 110,638,026-112,336,351 BUB1, PAFAH1B1P2, 28 more genes
    nsv6627497copy number variation2nstd224human GRCh37 chr2: 111,399,346-113,103,748 , GRCh38.p12 chr2: 110,641,769-112,346,171 BUB1, MERTK, 29 more genes
    nsv6353255copy number variation1nstd223human GRCh38 chr2: 111,159,047-111,161,927 , GRCh37.p13 chr2: 111,916,624-111,919,504 BCL2L11
    nsv6337274copy number variation1nstd223human GRCh38 chr2: 111,125,001-111,128,500 , GRCh37.p13 chr2: 111,882,578-111,886,077 BCL2L11
    nsv6315442copy number variation1nstd102humanPathogenic GRCh37 chr2: 111,365,995-113,199,850 , GRCh38.p12 chr2: 110,608,418-112,442,273 MIR4435-2HG, LOC105373553, 33 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
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