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Items: 1 to 20 of 422

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148203copy number variation1nstd102humanPathogenic GRCh38 chrX: 111,250,820-111,333,251 , GRCh37.p13 chrX: 110,494,048-110,576,479 CAPN6, DCX
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7136969copy number variation1nstd102humanPathogenic GRCh37 chrX: 110,653,301-110,653,993 , GRCh38 chrX: 111,410,073-111,410,765 DCX
    nsv7098492copy number variation1nstd102humanUncertain significance GRCh37 chrX: 110,544,915-110,544,991 , GRCh38.p12 chrX: 111,301,687-111,301,763 DCX
    nsv7098215copy number variation1nstd102humanPathogenic GRCh37 chrX: 110,576,259-110,576,401 , GRCh38.p12 chrX: 111,333,031-111,333,173 DCX
    nsv7098214copy number variation1nstd102humanUncertain significance GRCh37 chrX: 109,919,459-111,003,227 , GRCh38.p12 chrX: 110,676,231-111,759,999 RNU6-496P, FCF1P4, 11 more genes
    nsv7082398copy number variation1nstd229human GRCh38 chrX: 111,400,931-111,401,288 , GRCh37.p13 chrX: 110,644,159-110,644,516 DCX
    nsv7082397copy number variation1nstd229human GRCh38 chrX: 111,366,601-111,370,018 , GRCh37.p13 chrX: 110,609,829-110,613,246 DCX
    nsv7082396copy number variation1nstd229human GRCh38 chrX: 111,349,500-111,349,584 , GRCh37.p13 chrX: 110,592,728-110,592,812 DCX
    nsv7082395copy number variation1nstd229human GRCh38 chrX: 111,342,965-111,371,809 , GRCh37.p13 chrX: 110,586,193-110,615,037 DCX
    nsv7082394copy number variation1nstd229human GRCh38 chrX: 111,306,999-111,307,210 , GRCh37.p13 chrX: 110,550,227-110,550,438 DCX
    nsv7082393copy number variation1nstd229human GRCh38 chrX: 111,292,431-111,292,660 , GRCh37.p13 chrX: 110,535,659-110,535,888 DCX
    nsv7044993inversion1nstd229human GRCh38 chrX: 104,618,913-113,302,073 , GRCh37.p13 chrX: 103,863,594-112,545,300 NCBP2L, TEX13B, 92 more genes
    nsv7044117inversion1nstd229human GRCh38 chrX: 111,342,903-111,342,936 , GRCh37.p13 chrX: 110,586,131-110,586,164 DCX
    nsv6636712copy number variation1nstd102humanPathogenic GRCh37 chrX: 108,922,296-111,549,785 , GRCh38.p12 chrX: 109,679,067-112,306,557 M6PRP1, HMGB1P12, 27 more genes
    nsv6636543copy number variation1nstd102humanPathogenic GRCh37 chrX: 93,805,850-118,913,329 , GRCh38.p12 chrX: 94,550,851-119,779,366 TRPC5OS, LOC105373314, 351 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
    nsv6633565copy number variation1nstd224human GRCh37 chrX: 107,804,808-114,879,367 , GRCh38.p12 chrX: 108,561,578-115,645,047 DCX, IL13RA2, 80 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
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