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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 LOC105377327, LOC105377324, 214 more genes
    nsv7054609inversion1nstd229human GRCh38 chr4: 95,257,712-104,152,159 , GRCh37.p13 chr4: 96,178,863-105,073,316 SLC39A8, PABPC1P7, 96 more genes
    nsv7052845inversion1nstd229human GRCh38 chr4: 97,450,222-102,053,198 , GRCh37.p13 chr4: 98,371,373-102,974,355 RNU6-462P, LOC105377345, 58 more genes
    nsv7052661inversion1nstd229human GRCh38 chr4: 96,912,053-103,991,076 , GRCh37.p13 chr4: 97,833,204-104,912,233 MIR1255A, LOC107986297, 86 more genes
    nsv7046928inversion1nstd229human GRCh38 chr4: 95,051,434-103,882,549 , GRCh37.p13 chr4: 95,972,585-104,803,706 PABPC1P7, RN7SL728P, 95 more genes
    nsv7040929inversion1nstd229human GRCh38 chr4: 98,629,276-99,014,611 , GRCh37.p13 chr4: 99,550,427-99,935,762 LOC112267901, NDUFS5P4, 11 more genes
    nsv6757208copy number variation1nstd229human GRCh38 chr4: 98,734,601-98,740,100 , GRCh37.p13 chr4: 99,655,752-99,661,251 BTF3P13
    nsv6575060inversion1nstd223human GRCh38 chr4: 98,741,848-98,742,348 , GRCh37.p13 chr4: 99,662,999-99,663,499 BTF3P13
    nsv6559166inversion1nstd223human GRCh38 chr4: 98,629,274-99,014,615 , GRCh37.p13 chr4: 99,550,425-99,935,766 TBCAP3, TSPAN5, 11 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6291428copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 95,490,755-109,977,216 , GRCh38.p12 chr4: 94,569,604-109,056,060 ADH1A, ADH1B, 157 more genes
    nsv6135628copy number variation1nstd213human GRCh37 chr4: 99,460,000-99,660,001 , GRCh38.p12 chr4: 98,538,849-98,738,850 TSPAN5, BTF3P13, 3 more genes
    nsv6135624copy number variation1nstd213human GRCh37 chr4: 94,300,000-108,550,001 , GRCh38.p12 chr4: 93,378,849-107,628,845 , ADH1A, 146 more genes
    nsv6135091copy number variation1nstd213human GRCh37 chr4: 94,310,000-108,550,001 , GRCh38.p12 chr4: 93,388,849-107,628,845 , ADH1A, 146 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5311203copy number variation1nstd204human GRCh38.p13 chr4: 98,465,397-99,287,870 , GRCh37.p13 chr4: 99,386,548-100,209,027 TBCAP3, ADH5, 19 more genes
    nsv5239886copy number variation1nstd204human GRCh38.p13 chr4: 98,506,801-99,288,000 , GRCh37.p13 chr4: 99,427,952-100,209,157 TSPAN5, PCNAP1, 19 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4943767copy number variation1nstd200human GRCh38 chr4: 98,465,400-99,287,861 , GRCh37.p13 chr4: 99,386,551-100,209,018 ADH5, TSPAN5, 19 more genes
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