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Items: 1 to 20 of 301

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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
    nsv7089205copy number variation1nstd229human GRCh38 chrX: 77,968,401-78,133,800 , GRCh37.p13 chrX: 77,223,898-77,389,297 , GRCh37.p13 chrX|NW_003871101.3: 525,663-691,062 PGK1, TAF9B, 2 more genes
    nsv7089204copy number variation1nstd229human GRCh38 chrX: 77,944,402-78,187,315 , GRCh37.p13 chrX: 77,199,899-77,442,812 , GRCh37.p13 chrX|NW_003871101.3: 501,664-744,577 FNDC3CP, TAF9B, 4 more genes
    nsv7089198copy number variation1nstd229human GRCh38 chrX: 77,908,036-78,168,542 , GRCh37.p13 chrX|NW_003871101.3: 465,298-725,804 , GRCh37.p13 chrX: 77,163,533-77,424,039 C4orf46P2, PGAM4, 4 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
    nsv6636666copy number variation1nstd102humanUncertain significance GRCh37 chrX: 77,274,160-77,491,039 , GRCh38.p12 chrX: 78,018,663-78,235,542 FNDC3CP, TAF9B, 3 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
    nsv6636339copy number variation1nstd102humanUncertain significance GRCh37 chrX: 77,263,244-77,501,532 , GRCh38.p12 chrX: 78,007,747-78,246,035 TAF9B, ATP7A, 3 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
    nsv6315332copy number variation1nstd102humanPathogenic GRCh37 chrX: 62,685,885-155,233,731 , GRCh38.p12 chrX: 63,466,005-156,004,066 MAGT1, TAFAZZIN, 1337 more genes
    nsv6315331copy number variation4nstd102humanPathogenic GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 PLAC1, PGK1P1, 2154 more genes
    nsv6313464copy number variation1nstd102humanUncertain significance GRCh37 chrX: 72,095,006-88,455,505 , GRCh38.p12 chrX: 72,875,172-89,200,506 LOC105373285, LOC105373288, 170 more genes
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