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Items: 1 to 20 of 429

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7054962inversion1nstd229human GRCh38 chr4: 46,025,567-46,034,939 , GRCh37.p13 chr4: 46,027,584-46,036,956 GABRG1
    nsv7048465inversion1nstd229human GRCh38 chr4: 46,044,677-46,044,749 , GRCh37.p13 chr4: 46,046,694-46,046,766 GABRG1
    nsv7044914inversion1nstd229human GRCh38 chr4: 44,885,626-46,661,497 , GRCh37.p13 chr4: 44,887,643-46,663,514 LOC100419154, GABRA2, 8 more genes
    nsv7044426inversion1nstd229human GRCh38 chr4: 46,030,287-46,034,751 , GRCh37.p13 chr4: 46,032,304-46,036,768 GABRG1
    nsv7041619inversion1nstd229human GRCh38 chr4: 45,342,295-46,673,045 , GRCh37.p13 chr4: 45,344,312-46,675,062 GABRA2, RN7SKP199, 4 more genes
    nsv6735822copy number variation1nstd229human GRCh38 chr4: 43,303,724-46,592,616 , GRCh37.p13 chr4: 43,305,741-46,594,633 LINC02475, RN7SL193P, 27 more genes
    nsv6733865copy number variation1nstd229human GRCh38 chr4: 45,360,948-46,450,757 , GRCh37.p13 chr4: 45,362,965-46,452,774 RN7SKP199, GABRA2, 3 more genes
    nsv6731956copy number variation1nstd229human GRCh38 chr4: 46,122,757-46,129,988 , GRCh37.p13 chr4: 46,124,774-46,132,005 GABRG1
    nsv6731500copy number variation1nstd229human GRCh38 chr4: 46,113,451-46,138,394 , GRCh37.p13 chr4: 46,115,468-46,140,411 GABRG1
    nsv6730126copy number variation1nstd229human GRCh38 chr4: 45,977,941-46,051,636 , GRCh37.p13 chr4: 45,979,958-46,053,653 GABRG1, RN7SKP199
    nsv6727887copy number variation1nstd229human GRCh38 chr4: 45,628,925-46,076,361 , GRCh37.p13 chr4: 45,630,942-46,078,378 GABRG1, RN7SKP199
    nsv6727119copy number variation1nstd229human GRCh38 chr4: 46,101,144-46,101,475 , GRCh37.p13 chr4: 46,103,161-46,103,492 GABRG1
    nsv6724965copy number variation1nstd229human GRCh38 chr4: 46,120,843-46,121,243 , GRCh37.p13 chr4: 46,122,860-46,123,260 GABRG1
    nsv6719704copy number variation1nstd229human GRCh38 chr4: 45,796,772-46,556,891 , GRCh37.p13 chr4: 45,798,789-46,558,908 GABRA2, RN7SKP199, 2 more genes
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6629870copy number variation1nstd224human GRCh37 chr4: 46,027,834-46,043,232 , GRCh38.p12 chr4: 46,025,817-46,041,215 GABRG1
    nsv6395346copy number variation1nstd223human GRCh38 chr4: 46,114,801-46,116,100 , GRCh37.p13 chr4: 46,116,818-46,118,117 GABRG1
    nsv6395304copy number variation1nstd223human GRCh38 chr4: 46,043,686-46,044,301 , GRCh37.p13 chr4: 46,045,703-46,046,318 GABRG1
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