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Items: 1 to 20 of 285

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137705copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,419,493-40,774,118 , GRCh38.p12 chr9: 61,281,967-67,217,006 , GRCh38.p12 chr9: 36,419,496-39,445,729 ZNF658B, LOC105379814, 208 more genes
    nsv6137704copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,426,622-38,787,479 , GRCh38.p12 chr9: 36,426,625-38,787,482 MELK, SLC25A51, 55 more genes
    nsv6137700copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,088,563-39,092,820 , GRCh38.p12 chr9: 36,088,566-39,092,823 SNX18P3, VN1R48P, 69 more genes
    nsv5912956copy number variation1nstd209human GRCh38 chr9: 38,555,863-38,565,086 , GRCh37.p13 chr9: 38,555,860-38,565,083 ANKRD18A
    nsv5851343copy number variation1nstd209human GRCh38 chr9: 38,590,459-38,592,849 , GRCh37.p13 chr9: 38,590,456-38,592,846 ANKRD18A
    nsv5726636mobile element insertion1nstd211human GRCh38 chr9: 38,575,313-38,575,313 , GRCh37.p13 chr9: 38,575,310-38,575,310 ANKRD18A
    nsv5701905mobile element insertion2nstd211human GRCh38 chr9: 38,614,244-38,614,244 , GRCh37.p13 chr9: 38,614,241-38,614,241 ANKRD18A
    nsv5631520insertion1nstd207human GRCh38 chr9: 38,589,680-38,589,680 , GRCh37.p13 chr9: 38,589,677-38,589,677 ANKRD18A
    nsv5631108insertion1nstd207human GRCh38 chr9: 38,574,446-38,574,446 , GRCh37.p13 chr9: 38,574,443-38,574,443 ANKRD18A
    nsv5626251insertion1nstd207human GRCh38 chr9: 38,572,753-38,572,753 , GRCh37.p13 chr9: 38,572,750-38,572,750 ANKRD18A
    nsv5603379copy number variation1nstd207human GRCh38 chr9: 38,570,189-38,571,001 , GRCh37.p13 chr9: 38,570,186-38,570,998 ANKRD18A
    nsv5600604copy number variation1nstd207human GRCh38 chr9: 38,582,763-38,583,027 , GRCh37.p13 chr9: 38,582,760-38,583,024 ANKRD18A
    nsv5598099copy number variation1nstd207human GRCh38 chr9: 38,596,884-38,597,000 , GRCh37.p13 chr9: 38,596,881-38,596,997 ANKRD18A
    nsv5594824copy number variation1nstd207human GRCh38 chr9: 38,566,857-38,566,999 , GRCh37.p13 chr9: 38,566,854-38,566,996 ANKRD18A, SNX18P3
    nsv5590712copy number variation1nstd207human GRCh38 chr9: 38,599,888-38,599,946 , GRCh37.p13 chr9: 38,599,885-38,599,943 ANKRD18A
    nsv5585651copy number variation1nstd207human GRCh38 chr9: 38,608,791-38,609,180 , GRCh37.p13 chr9: 38,608,788-38,609,177 ANKRD18A
    nsv5555672sequence alteration1nstd206human GRCh38 chr9: 38,596,809-38,596,858 , GRCh37.p13 chr9: 38,596,806-38,596,855 ANKRD18A
    nsv5490534copy number variation1nstd206human GRCh38 chr9: 38,498,789-38,685,381 , GRCh37.p13 chr9: 38,498,786-38,685,378 CYP4F33P, ANKRD18A, 8 more genes
    nsv5481462copy number variation1nstd206human GRCh38 chr9: 38,564,000-38,576,000 , GRCh37.p13 chr9: 38,563,997-38,575,997 SNX18P3, ANKRD18A
    nsv5476353copy number variation1nstd206human GRCh38 chr9: 38,555,863-38,565,063 , GRCh37.p13 chr9: 38,555,860-38,565,060 ANKRD18A
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