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Items: 1 to 20 of 335

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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
    nsv7098221copy number variation1nstd102humanPathogenic GRCh37 chrX: 123,494,030-123,499,653 , GRCh38.p12 chrX: 124,360,180-124,365,803 SH2D1A
    nsv7098113copy number variation1nstd102humanPathogenic GRCh37 chrX: 123,499,591-123,499,694 , GRCh38.p12 chrX: 124,365,741-124,365,844 SH2D1A
    nsv7097986copy number variation1nstd102humanUncertain significance GRCh37 chrX: 123,480,147-123,505,241 , GRCh38.p12 chrX: 124,346,297-124,371,391 SH2D1A
    nsv7083677copy number variation1nstd229human GRCh38 chrX: 124,368,416-124,368,516 , GRCh37.p13 chrX: 123,502,266-123,502,366 SH2D1A
    nsv7083676copy number variation1nstd229human GRCh38 chrX: 124,365,943-125,159,438 , GRCh37.p13 chrX: 123,499,793-124,293,287 RPS26P57, LOC105373331, 2 more genes
    nsv7083675copy number variation1nstd229human GRCh38 chrX: 124,363,349-124,363,540 , GRCh37.p13 chrX: 123,497,199-123,497,390 SH2D1A
    nsv7083674copy number variation1nstd229human GRCh38 chrX: 124,355,720-124,355,905 , GRCh37.p13 chrX: 123,489,570-123,489,755 SH2D1A
    nsv7083673copy number variation1nstd229human GRCh38 chrX: 124,348,917-124,431,870 , GRCh37.p13 chrX: 123,482,767-123,565,720 SH2D1A, LOC105373331, 1 more genes
    nsv7083671copy number variation1nstd229human GRCh38 chrX: 124,327,201-124,350,600 , GRCh37.p13 chrX: 123,461,051-123,484,450 TEX13D, SH2D1A
    nsv7083670copy number variation1nstd229human GRCh38 chrX: 124,323,639-124,590,014 , GRCh37.p13 chrX: 123,457,489-123,723,864 TEX13D, SH2D1A, 2 more genes
    nsv7083371copy number variation1nstd229human GRCh38 chrX: 121,591,286-126,454,661 , GRCh37.p13 chrX: 120,725,140-125,588,644 RNU7-69P, SH2D1A, 31 more genes
    nsv7048896inversion1nstd229human GRCh38 chrX: 124,356,566-124,666,581 , GRCh37.p13 chrX: 123,490,416-123,800,431 TENM1, LOC105373331, 1 more genes
    nsv6634565copy number variation1nstd102humanPathogenic GRCh37 chrX: 123,499,618-123,499,776 , GRCh38 chrX: 124,365,768-124,365,926 SH2D1A
    nsv6634554copy number variation1nstd102humanPathogenic GRCh38 chrX: 124,346,562-124,365,760 , GRCh37.p13 chrX: 123,480,412-123,499,610 SH2D1A
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6315429copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,670,699-155,233,731 , GRCh38.p12 chrX: 78,415,202-156,004,066 H2AB1, GPR174, 1081 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
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