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Items: 1 to 20 of 412

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7137044copy number variation1nstd102humanUncertain significance GRCh37 chrX: 19,564,040-19,954,016 , GRCh38.p12 chrX: 19,545,922-19,935,898 BCLAF3, SH3KBP1
    nsv7098359copy number variation1nstd102humanUncertain significance GRCh37 chrX: 18,525,053-20,284,750 , GRCh38.p12 chrX: 18,506,933-20,266,632 PPEF1, PDHA1, 23 more genes
    nsv7086124copy number variation1nstd229human GRCh38 chrX: 19,985,094-19,991,294 , GRCh37.p13 chrX: 20,003,212-20,009,412 BCLAF3, LOC729609
    nsv7086123copy number variation1nstd229human GRCh38 chrX: 19,980,701-19,990,700 , GRCh37.p13 chrX: 19,998,819-20,008,818 BCLAF3, LOC729609
    nsv7086122copy number variation1nstd229human GRCh38 chrX: 19,958,541-19,958,677 , GRCh37.p13 chrX: 19,976,659-19,976,795 BCLAF3
    nsv7086121copy number variation1nstd229human GRCh38 chrX: 19,955,436-19,976,477 , GRCh37.p13 chrX: 19,973,554-19,994,595 BCLAF3
    nsv7086120copy number variation1nstd229human GRCh38 chrX: 19,952,101-19,952,293 , GRCh37.p13 chrX: 19,970,219-19,970,411 BCLAF3
    nsv7086119copy number variation1nstd229human GRCh38 chrX: 19,938,878-19,939,206 , GRCh37.p13 chrX: 19,956,996-19,957,324 BCLAF3
    nsv7086118copy number variation1nstd229human GRCh38 chrX: 19,938,463-20,028,227 , GRCh37.p13 chrX: 19,956,581-20,046,345 MAP7D2, MIR23C, 2 more genes
    nsv7086117copy number variation1nstd229human GRCh38 chrX: 19,936,533-19,938,127 , GRCh37.p13 chrX: 19,954,651-19,956,245 BCLAF3
    nsv7086116copy number variation1nstd229human GRCh38 chrX: 19,932,680-19,935,645 , GRCh37.p13 chrX: 19,950,798-19,953,763 BCLAF3
    nsv7086115copy number variation1nstd229human GRCh38 chrX: 19,928,718-19,928,746 , GRCh37.p13 chrX: 19,946,836-19,946,864 BCLAF3
    nsv7086101copy number variation1nstd229human GRCh38 chrX: 19,663,657-28,237,068 , GRCh37.p13 chrX: 19,681,775-28,255,185 MAGEB18, RPS6KA3, 89 more genes
    nsv7086099copy number variation1nstd229human GRCh38 chrX: 19,654,658-19,989,900 , GRCh37.p13 chrX: 19,672,776-20,008,018 SH3KBP1, LOC729609, 1 more genes
    nsv7086095copy number variation1nstd229human GRCh38 chrX: 19,614,989-19,927,633 , GRCh37.p13 chrX: 19,633,107-19,945,751 SH3KBP1, BCLAF3
    nsv7086093copy number variation1nstd229human GRCh38 chrX: 19,598,545-20,102,184 , GRCh37.p13 chrX: 19,616,663-20,120,302 SH3KBP1, BCLAF3, 3 more genes
    nsv7086090copy number variation1nstd229human GRCh38 chrX: 19,542,301-19,937,000 , GRCh37.p13 chrX: 19,560,419-19,955,118 SH3KBP1, BCLAF3
    nsv7086086copy number variation1nstd229human GRCh38 chrX: 19,521,108-20,478,041 , GRCh37.p13 chrX: 19,539,226-20,496,159 LOC729609, BCLAF3, 8 more genes
    nsv7085539copy number variation1nstd229human GRCh38 chrX: 15,461,305-24,177,792 , GRCh37.p13 chrX: 15,479,428-24,195,909 LOC105373146, PIR-FIGF, 104 more genes
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