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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5710350mobile element insertion1nstd211human GRCh38 chr7: 143,337,695-143,337,695 , GRCh37.p13 chr7: 143,034,788-143,034,788 CLCN1
    nsv5673925copy number variation1nstd102humanPathogenic GRCh38 chr7: 143,316,257-143,321,158 , GRCh37 chr7: 143,013,350-143,018,251 CLCN1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5486239copy number variation1nstd206human GRCh38 chr7: 143,329,388-143,329,520 , GRCh37.p13 chr7: 143,026,481-143,026,613 CLCN1
    nsv5118216mobile element insertion1nstd203human GRCh38 chr7: 143,325,499-143,325,513 , GRCh37.p13 chr7: 143,022,592-143,022,606 CLCN1
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4966938copy number variation1nstd200human GRCh38 chr7: 143,335,945-143,338,054 , GRCh37.p13 chr7: 143,033,038-143,035,147 CLCN1
    nsv4966937copy number variation1nstd200human GRCh38 chr7: 143,333,924-143,335,430 , GRCh37.p13 chr7: 143,031,017-143,032,523 CLCN1
    nsv4966936copy number variation1nstd200human GRCh38 chr7: 143,316,260-143,321,159 , GRCh37.p13 chr7: 143,013,353-143,018,252 CLCN1
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4827270copy number variation1nstd200human GRCh37 chr7: 143,013,354-143,018,258 , GRCh38.p12 chr7: 143,316,261-143,321,165 CLCN1
    nsv4683443copy number variation1nstd102humanPathogenic GRCh37 chr7: 143,021,494-143,028,755 , GRCh38.p12 chr7: 143,324,401-143,331,662 CLCN1
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 RPL26P23, ST13P17, 887 more genes
    nsv4675615copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,414,604-159,126,310 , GRCh38.p12 chr7: 131,729,845-159,333,620 ATG9B, OR10AC1, 603 more genes
    nsv4652564copy number variation1nstd186human GRCh37 chr7: 143,022,518-143,023,361 , GRCh38.p12 chr7: 143,325,425-143,326,268 CLCN1
    nsv4494645mobile element insertion1nstd166human GRCh37.p13 chr7: 143,022,592-143,022,592 , GRCh38.p12 chr7: 143,325,499-143,325,499 CLCN1
    nsv4457314copy number variation1nstd102humanUncertain significance GRCh37 chr7: 141,751,875-147,105,208 , GRCh38.p12 chr7: 142,052,075-147,408,116 ARHGEF5, FAM131B-AS2, 195 more genes
    nsv4455493copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,592,554-159,119,707 , GRCh38.p12 chr7: 130,907,795-159,327,017 OR2A1, LOC101027084, 614 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4450468copy number variation1nstd102humanUncertain significance GRCh37 chr7: 143,047,445-143,049,078 , GRCh38 chr7: 143,350,352-143,351,985 CLCN1, FAM131B
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