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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096482copy number variation1nstd102humanPathogenic GRCh37 chr4: 100,239,320-100,528,137 , GRCh38.p12 chr4: 99,318,163-99,606,980 ADH1B, ADH1C, 5 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
    nsv7054570inversion1nstd229human GRCh38 chr4: 99,506,447-99,514,336 , GRCh37.p13 chr4: 100,427,604-100,435,493 C4orf17
    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
    nsv7044544inversion1nstd229human GRCh38 chr4: 98,964,941-108,185,877 , GRCh37.p13 chr4: 99,886,092-109,107,033 LOC102725220, TACR3, 117 more genes
    nsv6755344copy number variation1nstd229human GRCh38 chr4: 99,540,229-99,709,776 , GRCh37.p13 chr4: 100,461,386-100,630,933 MTTP, C4orf17, 2 more genes
    nsv6394606copy number variation1nstd223human GRCh38 chr4: 99,512,872-99,513,393 , GRCh37.p13 chr4: 100,434,029-100,434,550 C4orf17
    nsv6388953copy number variation1nstd223human GRCh38 chr4: 99,539,501-99,540,600 , GRCh37.p13 chr4: 100,460,658-100,461,757 C4orf17
    nsv6388487copy number variation1nstd223human GRCh38 chr4: 99,535,754-99,537,093 , GRCh37.p13 chr4: 100,456,911-100,458,250 C4orf17
    nsv6387591copy number variation1nstd223human GRCh38 chr4: 99,508,201-99,518,500 , GRCh37.p13 chr4: 100,429,358-100,439,657 C4orf17
    nsv6381733copy number variation1nstd223human GRCh38 chr4: 99,529,101-99,533,100 , GRCh37.p13 chr4: 100,450,258-100,454,257 C4orf17
    nsv6377433copy number variation1nstd223human GRCh38 chr4: 99,529,601-99,531,300 , GRCh37.p13 chr4: 100,450,758-100,452,457 C4orf17
    nsv6311812copy number variation1nstd102humanUncertain significance GRCh37 chr4: 100,239,320-100,544,005 , GRCh38.p12 chr4: 99,318,163-99,622,848 C4orf17, ADH1B, 5 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
    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
    nsv6134728copy number variation1nstd213human GRCh37 chr4: 100,310,000-100,840,001 , GRCh38.p12 chr4: 99,388,843-99,918,844 ADH7, MTTP, 7 more genes
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