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Items: 1 to 20 of 343

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148181copy number variation1nstd102humanPathogenic GRCh38 chr7: 98,454,022-100,723,798 , GRCh37.p13 chr7: 98,083,334-100,321,421 LAMTOR4, PTCD1, 107 more genes
    nsv7098147copy number variation1nstd102humanUncertain significance GRCh37 chr7: 98,507,659-100,860,555 , GRCh38.p12 chr7: 98,910,036-101,217,274 SLC12A9, LOC105375423, 127 more genes
    nsv7098146copy number variation1nstd102humanUncertain significance GRCh37 chr7: 98,478,774-98,779,708 , GRCh38.p12 chr7: 98,881,151-99,182,085 SMURF1, MIR3609, 5 more genes
    nsv7097766copy number variation1nstd102humanUncertain significance GRCh37 chr7: 98,478,774-98,493,463 , GRCh38.p12 chr7: 98,881,151-98,895,840 MIR3609, SCARNA28, 1 more genes
    nsv7052776inversion1nstd229human GRCh38 chr7: 96,709,838-100,726,550 , GRCh37.p13 chr7: 96,339,150-100,324,173 TMEM225B, PILRB, 141 more genes
    nsv7045433inversion1nstd229human GRCh38 chr7: 98,960,933-98,961,032 , GRCh37.p13 chr7: 98,558,556-98,558,655 TRRAP
    nsv7043964inversion1nstd229human GRCh38 chr7: 98,873,163-98,876,901 , GRCh37.p13 chr7|NW_003571041.1: 242,345-246,083 , GRCh37.p13 chr7: 98,470,786-98,474,524 TRRAP
    nsv6835192copy number variation1nstd229human GRCh38 chr7: 98,908,560-98,908,588 , GRCh37.p13 chr7|NW_003571041.1: 277,742-277,770 , GRCh37.p13 chr7: 98,506,183-98,506,211 TRRAP
    nsv6833782copy number variation1nstd229human GRCh38 chr7: 98,846,126-98,927,990 , GRCh37.p13 chr7: 98,443,749-98,525,613 , GRCh37.p13 chr7|NW_003571041.1: 215,308-297,172 MIR3609, TRRAP, 2 more genes
    nsv6832123copy number variation1nstd229human GRCh38 chr7: 98,983,340-98,983,530 , GRCh37.p13 chr7: 98,580,963-98,581,153 TRRAP
    nsv6830739copy number variation1nstd229human GRCh38 chr7: 98,915,626-98,915,701 , GRCh37.p13 chr7: 98,513,249-98,513,324 , GRCh37.p13 chr7|NW_003571041.1: 284,808-284,883 TRRAP
    nsv6829089copy number variation1nstd229human GRCh38 chr7: 98,803,126-98,968,206 , GRCh37.p13 chr7|NW_003571041.1: 172,308-327,774 , GRCh37.p13 chr7: 98,400,749-98,556,215 MIR3609, TRRAP, 2 more genes
    nsv6828132copy number variation1nstd229human GRCh38 chr7: 98,667,290-99,135,243 , GRCh37.p13 chr7: 98,296,602-98,556,215 , GRCh37.p13 chr7|NW_003571041.1: 36,472-327,774 SMURF1, TRRAP, 7 more genes
    nsv6827492copy number variation1nstd229human GRCh38 chr7: 99,000,729-99,003,209 , GRCh37.p13 chr7: 98,598,352-98,600,832 TRRAP
    nsv6825456copy number variation1nstd229human GRCh38 chr7: 98,873,723-98,880,438 , GRCh37.p13 chr7|NW_003571041.1: 242,905-249,620 , GRCh37.p13 chr7: 98,471,346-98,478,061 MIR3609, SCARNA28, 1 more genes
    nsv6823894copy number variation1nstd229human GRCh38 chr7: 98,880,601-98,880,797 , GRCh37.p13 chr7|NW_003571041.1: 249,783-249,979 , GRCh37.p13 chr7: 98,478,224-98,478,420 TRRAP, SCARNA28, 1 more genes
    nsv6822030copy number variation1nstd229human GRCh38 chr7: 98,865,322-99,195,183 , GRCh37.p13 chr7: 98,556,216-98,792,806 TMEM130, SCARNA28, 6 more genes
    nsv6821677copy number variation1nstd229human GRCh38 chr7: 98,880,235-98,880,290 , GRCh37.p13 chr7|NW_003571041.1: 249,417-249,472 , GRCh37.p13 chr7: 98,477,858-98,477,913 TRRAP, SCARNA28, 1 more genes
    nsv6821396copy number variation1nstd229human GRCh38 chr7: 98,953,048-98,953,081 , GRCh37.p13 chr7|NW_003571041.1: 322,230-322,263 , GRCh37.p13 chr7: 98,550,671-98,550,704 TRRAP
    nsv6820665copy number variation1nstd229human GRCh38 chr7: 98,953,301-98,979,000 , GRCh37.p13 chr7: 98,556,216-98,576,623 TRRAP
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