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Items: 1 to 20 of 345

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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
    nsv7098224copy number variation2nstd102humanPathogenic GRCh37 chrX: 12,885,698-13,787,227 , GRCh38.p12 chrX: 12,867,579-13,769,108 GPM6B, MIR6086, 21 more genes
    nsv7077089copy number variation1nstd229human GRCh38 chrX: 13,316,134-13,744,822 , GRCh37.p13 chrX: 13,334,253-13,762,941 TCEANC, RPL30P15, 12 more genes
    nsv7076782copy number variation1nstd229human GRCh38 chrX: 13,291,112-13,329,523 , GRCh37.p13 chrX: 13,309,231-13,347,642 ATXN3L, GS1-600G8.3, 1 more genes
    nsv7074049copy number variation1nstd229human GRCh38 chrX: 13,221,611-13,939,189 , GRCh37.p13 chrX: 13,239,730-13,957,308 GPX1P1, LINC01203, 14 more genes
    nsv7073171copy number variation1nstd229human GRCh38 chrX: 12,908,154-13,642,785 , GRCh37.p13 chrX: 12,926,273-13,660,904 LOC105373134, TLR8-AS1, 13 more genes
    nsv7071676copy number variation1nstd229human GRCh38 chrX: 13,306,701-13,311,500 , GRCh37.p13 chrX: 13,324,820-13,329,619 GS1-600G8.3
    nsv7066985copy number variation1nstd229human GRCh38 chrX: 12,854,465-13,549,089 , GRCh37.p13 chrX: 12,872,584-13,567,208 TMSB4X, GS1-600G8.3, 10 more genes
    nsv7066843copy number variation1nstd229human GRCh38 chrX: 13,006,444-13,544,442 , GRCh37.p13 chrX: 13,024,563-13,562,561 LOC105373133, LOC105373134, 6 more genes
    nsv7064892copy number variation1nstd229human GRCh38 chrX: 13,070,979-13,598,020 , GRCh37.p13 chrX: 13,089,098-13,616,139 LOC105373134, LINC01203, 9 more genes
    nsv7064242copy number variation1nstd229human GRCh38 chrX: 13,115,594-13,744,822 , GRCh37.p13 chrX: 13,133,713-13,762,941 ATXN3L, RPL30P15, 14 more genes
    nsv7030183inversion1nstd229human GRCh38 chrX: 9,810,086-13,425,949 , GRCh37.p13 chrX: 9,778,126-13,444,068 EIF5P1, ATXN3L, 32 more genes
    nsv6636165copy number variation1nstd102humanPathogenic GRCh37 chrX: 2,703,633-14,515,021 , GRCh38.p12 chrX: 2,785,592-14,496,899 GPX1P1, XG, 108 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6634135copy number variation1nstd224human GRCh37 chrX: 2,700,157-26,836,730 , GRCh38.p12 chrX: 2,782,116-26,818,613 AMELX, ARSF, 258 more genes
    nsv6633774copy number variation1nstd224human GRCh37 chrX: 13,288,751-13,355,937 , GRCh38.p12 chrX: 13,270,632-13,337,818 GS1-600G8.3, LINC02154, 2 more genes
    nsv6315577complex substitution1nstd102humanPathogenic GRCh37 chrX: 590,376-56,315,041 , GRCh38.p12 chrX: 629,641-56,288,608 ACTG1P10, NR0B1, 778 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
    nsv6315331copy number variation4nstd102humanPathogenic GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 PLAC1, PGK1P1, 2154 more genes
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