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Items: 1 to 20 of 668

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140505insertion1nstd232human GRCh37.p13 chrX: 151,351,125-151,351,125 , GRCh38.p12 chrX: 152,182,653-152,182,653 GABRA3
    nsv7139266insertion1nstd232human GRCh37.p13 chrX: 151,351,210-151,351,210 , GRCh38.p12 chrX: 152,182,738-152,182,738 GABRA3
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098869copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,586,015-154,774,957 , GRCh38.p12 chrX: 140,503,850-155,545,296 MAGEA6, LOC101928832, 303 more genes
    nsv7079631copy number variation1nstd229human GRCh38 chrX: 152,434,060-152,434,258 , GRCh37.p13 chrX: 151,602,532-151,602,730 GABRA3
    nsv7079630copy number variation1nstd229human GRCh38 chrX: 152,420,477-152,421,216 , GRCh37.p13 chrX: 151,588,949-151,589,688 GABRA3
    nsv7079629copy number variation1nstd229human GRCh38 chrX: 152,396,868-152,398,246 , GRCh37.p13 chrX: 151,565,340-151,566,718 GABRA3
    nsv7079628copy number variation1nstd229human GRCh38 chrX: 152,390,416-152,407,315 , GRCh37.p13 chrX: 151,558,888-151,575,787 MIR105-1, MIR767, 2 more genes
    nsv7079627copy number variation1nstd229human GRCh38 chrX: 152,369,394-152,587,299 , GRCh37.p13 chrX: 151,537,866-151,734,489 MAGEA3-DT, MIR105-2, 4 more genes
    nsv7079626copy number variation1nstd229human GRCh38 chrX: 152,328,641-152,331,643 , GRCh37.p13 chrX: 151,497,113-151,500,115 GABRA3
    nsv7079625copy number variation1nstd229human GRCh38 chrX: 152,313,613-152,313,959 , GRCh37.p13 chrX: 151,482,085-151,482,431 GABRA3
    nsv7079624copy number variation1nstd229human GRCh38 chrX: 152,305,245-152,317,906 , GRCh37.p13 chrX: 151,473,717-151,486,378 GABRA3
    nsv7079623copy number variation1nstd229human GRCh38 chrX: 152,305,209-152,308,459 , GRCh37.p13 chrX: 151,473,681-151,476,931 GABRA3
    nsv7079622copy number variation1nstd229human GRCh38 chrX: 152,304,883-152,305,591 , GRCh37.p13 chrX: 151,473,355-151,474,063 GABRA3
    nsv7079621copy number variation1nstd229human GRCh38 chrX: 152,302,101-152,308,752 , GRCh37.p13 chrX: 151,470,573-151,477,224 GABRA3
    nsv7079620copy number variation1nstd229human GRCh38 chrX: 152,300,363-152,308,603 , GRCh37.p13 chrX: 151,468,835-151,477,075 GABRA3
    nsv7079619copy number variation1nstd229human GRCh38 chrX: 152,281,960-152,282,780 , GRCh37.p13 chrX: 151,450,432-151,451,252 GABRA3
    nsv7079618copy number variation1nstd229human GRCh38 chrX: 152,275,502-152,275,911 , GRCh37.p13 chrX: 151,443,974-151,444,383 GABRA3
    nsv7079617copy number variation1nstd229human GRCh38 chrX: 152,265,401-152,266,500 , GRCh37.p13 chrX: 151,433,873-151,434,972 GABRA3
    nsv7079616copy number variation1nstd229human GRCh38 chrX: 152,264,528-152,792,675 , GRCh37.p13 chrX: 151,433,000-151,734,489 CSAG2, MAGEA2, 17 more genes
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