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Items: 1 to 20 of 669

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098676copy number variation1nstd102humanUncertain significance GRCh37 chrX: 76,763,829-77,381,327 , GRCh38.p12 chrX: 77,508,351-78,125,830 C4orf46P2, ATRX, 8 more genes
    nsv7098675copy number variation1nstd102humanUncertain significance GRCh37 chrX: 76,763,829-76,972,740 , GRCh38.p12 chrX: 77,508,351-77,717,263 ATRX
    nsv7098569copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 76,937,002-76,972,730 , GRCh38.p12 chrX: 77,681,510-77,717,253 ATRX
    nsv7098568copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,763,829-76,776,414 , GRCh38.p12 chrX: 77,508,351-77,520,936 ATRX
    nsv7098330copy number variation1nstd102humanUncertain significance GRCh37 chrX: 76,972,588-77,084,752 , GRCh38.p12 chrX: 77,717,111-77,829,255 FABP5P15, MAGT1, 1 more genes
    nsv7098329copy number variation2nstd102humanUncertain significance GRCh37 chrX: 76,888,675-77,264,780 , GRCh38.p12 chrX: 77,633,187-78,009,283 MAGT1, ATRX, 7 more genes
    nsv7093210copy number variation1nstd102humanUncertain significance GRCh37 chrX: 76,760,355-76,778,729 , GRCh38.p12 chrX: 77,504,877-77,523,251 ATRX
    nsv7089187copy number variation1nstd229human GRCh38 chrX: 77,777,035-77,777,074 , GRCh37.p13 chrX: 77,032,521-77,032,560 , GRCh37.p13 chrX|NW_003871101.3: 334,297-334,336 ATRX
    nsv7089186copy number variation1nstd229human GRCh38 chrX: 77,773,737-77,781,795 , GRCh37.p13 chrX: 77,029,219-77,037,281 , GRCh37.p13 chrX|NW_003871101.3: 330,999-339,057 ATRX
    nsv7089185copy number variation1nstd229human GRCh38 chrX: 77,771,696-77,977,376 , GRCh37.p13 chrX|NW_003871101.3: 328,958-534,638 , GRCh37.p13 chrX: 77,027,177-77,232,872 ATP7A, RN7SL460P, 6 more genes
    nsv7089184copy number variation1nstd229human GRCh38 chrX: 77,771,101-77,818,300 , GRCh37.p13 chrX: 77,026,582-77,073,797 , GRCh37.p13 chrX|NW_003871101.3: 328,363-375,562 ATRX
    nsv7089183copy number variation1nstd229human GRCh38 chrX: 77,756,138-77,761,196 , GRCh37.p13 chrX|NW_003871101.3: 313,400-318,458 , GRCh37.p13 chrX: 77,011,619-77,016,677 ATRX
    nsv7089182copy number variation1nstd229human GRCh38 chrX: 77,745,970-77,752,205 , GRCh37.p13 chrX|NW_003871101.3: 303,232-309,467 , GRCh37.p13 chrX: 77,001,451-77,007,686 ATRX
    nsv7089181copy number variation1nstd229human GRCh38 chrX: 77,743,118-77,752,206 , GRCh37.p13 chrX|NW_003871101.3: 300,380-309,468 , GRCh37.p13 chrX: 76,998,599-77,007,687 ATRX
    nsv7089180copy number variation1nstd229human GRCh38 chrX: 77,740,735-77,745,022 , GRCh37.p13 chrX: 76,996,214-77,000,503 , GRCh37.p13 chrX|NW_003871101.3: 297,997-302,284 ATRX
    nsv7089179copy number variation1nstd229human GRCh38 chrX: 77,739,715-77,740,013 , GRCh37.p13 chrX|NW_003871101.3: 296,977-297,275 , GRCh37.p13 chrX: 76,995,192-76,995,490 ATRX
    nsv7089178copy number variation1nstd229human GRCh38 chrX: 77,729,998-77,733,941 , GRCh37.p13 chrX: 76,985,476-76,989,418 , GRCh37.p13 chrX|NW_003871101.3: 287,260-291,203 ATRX
    nsv7089177copy number variation1nstd229human GRCh38 chrX: 77,729,401-77,740,200 , GRCh37.p13 chrX|NW_003871101.3: 286,663-297,462 , GRCh37.p13 chrX: 76,984,879-76,995,679 ATRX
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