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Items: 1 to 20 of 324

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142534insertion1nstd232human GRCh37.p13 chrX: 77,158,267-77,158,267 , GRCh38.p12 chrX: 77,902,770-77,902,770 COX7B
    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
    nsv7098677copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,084,697-77,268,629 , GRCh38.p12 chrX: 77,829,200-78,013,132 ATP7A, COX7B, 5 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
    nsv7098548copy number variation1nstd102humanUncertain significance GRCh37 chrX: 77,150,786-77,289,339 , GRCh38.p12 chrX: 77,895,289-78,033,841 ATP7A, C4orf46P2, 3 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
    nsv7089197copy number variation1nstd229human GRCh38 chrX: 77,899,384-77,899,566 , GRCh37.p13 chrX|NW_003871101.3: 456,646-456,828 , GRCh37.p13 chrX: 77,154,881-77,155,063 COX7B
    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
    nsv7089172copy number variation1nstd229human GRCh38 chrX: 77,652,101-78,132,700 , GRCh37.p13 chrX: 76,907,591-77,388,197 , GRCh37.p13 chrX|NW_003871101.3: 209,363-689,962 COX7B, PGAM4, 9 more genes
    nsv7036395inversion1nstd229human GRCh38 chrX: 77,632,403-78,132,717 , GRCh37.p13 chrX: 76,887,891-77,388,214 , GRCh37.p13 chrX|NW_003871101.3: 189,665-689,979 RN7SL460P, ATRX, 9 more genes
    nsv7033525inversion1nstd229human GRCh38 chrX: 77,852,956-78,523,514 , GRCh37.p13 chrX: 77,108,453-77,450,502 , GRCh37.p13 chrX|NW_003871101.3: 410,218-752,267 MAGT1, HMGN1P34, 10 more genes
    nsv7026063inversion1nstd229human GRCh38 chrX: 76,257,068-80,095,987 , GRCh37.p13 chrX: 75,477,467-77,450,502 ATRX, MAGEE1, 40 more genes
    nsv7018633inversion1nstd229human GRCh38 chrX: 76,256,859-80,096,106 , GRCh37.p13 chrX: 75,477,258-77,450,502 LDHBP2, ATP7A, 40 more genes
    nsv6636566copy number variation1nstd102humanUncertain significance GRCh37 chrX: 76,646,315-77,386,337 , GRCh38.p12 chrX: 77,425,852-78,130,840 PGK1, TAF9B, 10 more genes
    nsv6636337copy number variation1nstd102humanUncertain significance GRCh37 chrX: 75,463,914-77,297,280 , GRCh38.p12 chrX: 76,243,515-78,041,782 MAGEE1, MIR384, 20 more genes
    nsv6634329copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,794,355-119,282,836 , GRCh38.p12 chrX: 77,538,874-120,148,930 NXF4, RHOXF1P1, 489 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6315393copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383 H2BP8, LOC101060199, 2151 more genes
    nsv6315389copy number variation1nstd102humanPathogenic GRCh37 chrX: 11,522,765-155,233,731 , GRCh38.p12 chrX: 11,504,645-156,004,066 RBMX, LOC100129144, 2042 more genes
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