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Items: 1 to 20 of 295

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7046049inversion1nstd229human GRCh38 chr2: 96,997,023-97,135,627 , GRCh37.p13 chr2: 97,662,760-97,801,364 LOC100420569, RN7SL313P, 6 more genes
    nsv7038758inversion1nstd229human GRCh38 chr2: 97,057,081-97,647,910 , GRCh37.p13 chr2: 97,722,818-98,264,373 GPAT2P2, LOC107985920, 14 more genes
    nsv6691602copy number variation1nstd229human GRCh38 chr2: 97,081,101-97,082,300 , GRCh37.p13 chr2: 97,746,838-97,748,037 FAHD2B, GPAT2P2
    nsv6636315copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 95,341,388-100,340,514 , GRCh38.p12 chr2: 94,675,663-99,724,052 ADRA2B, ATP5F1BP1, 130 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6628429copy number variation1nstd224human GRCh37 chr2: 96,747,466-98,186,298 , GRCh38.p12 chr2: 96,081,718-97,569,835 ARID5A, IGKV2OR2-2, 42 more genes
    nsv6628179copy number variation1nstd224human GRCh37 chr2: 96,721,808-98,186,298 , GRCh38.p12 chr2: 96,056,060-97,569,835 ADRA2B, IGKV2OR2-10, 43 more genes
    nsv6547092inversion1nstd223human GRCh38 chr2: 96,007,660-97,097,743 , GRCh37.p13 chr2: 96,673,408-97,763,480 CNNM4, DUSP2, 34 more genes
    nsv6352319copy number variation1nstd223human GRCh38 chr2: 97,073,801-97,132,400 , GRCh37.p13 chr2: 97,739,538-97,798,137 FAHD2B, ANKRD36, 2 more genes
    nsv6348609copy number variation1nstd223human GRCh38 chr2: 97,082,401-97,107,500 , GRCh37.p13 chr2: 97,748,138-97,773,237 RN7SL313P, GPAT2P2, 1 more genes
    nsv6341717copy number variation1nstd223human GRCh38 chr2: 97,054,001-97,081,200 , GRCh37.p13 chr2: 97,719,738-97,746,937 GPAT2P2, FAHD2B
    nsv6340789copy number variation1nstd223human GRCh38 chr2: 97,070,401-97,090,900 , GRCh37.p13 chr2: 97,736,138-97,756,637 GPAT2P2, FAHD2B
    nsv6339526copy number variation1nstd223human GRCh38 chr2: 97,070,301-97,114,200 , GRCh37.p13 chr2: 97,736,038-97,779,937 GPAT2P2, FAHD2B, 2 more genes
    nsv6339262copy number variation1nstd223human GRCh38 chr2: 97,081,201-97,082,200 , GRCh37.p13 chr2: 97,746,938-97,747,937 GPAT2P2, FAHD2B
    nsv6336550copy number variation1nstd223human GRCh38 chr2: 97,076,401-97,114,800 , GRCh37.p13 chr2: 97,742,138-97,780,537 FAHD2B, ANKRD36, 2 more genes
    nsv6336493copy number variation1nstd223human GRCh38 chr2: 97,063,801-97,178,800 , GRCh37.p13 chr2: 97,729,538-97,844,537 RN7SL313P, FAHD2B, 2 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6300569copy number variation1nstd186human GRCh37 chr2: 97,728,515-97,860,737 , GRCh38.p12 chr2: 97,062,778-97,195,000 FAHD2B, ANKRD36, 2 more genes
    nsv6295466copy number variation1nstd186human GRCh37 chr2: 97,715,744-97,951,534 , GRCh38.p12 chr2: 97,050,007-97,285,797 IGKV2OR2-2, FAHD2B, 4 more genes
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