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Items: 1 to 20 of 348

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148053copy number variation1nstd102humanUncertain significance GRCh37 chrX: 48,417,285-48,631,851 , GRCh38.p12 chrX: 48,558,897-48,773,435 LOC107985695, VN1R110P, 8 more genes
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098786copy number variation1nstd102humanPathogenic GRCh37 chrX: 46,466,387-51,241,672 , GRCh38.p12 chrX: 46,606,952-51,498,820 LOC100419232, LOC791091, 172 more genes
    nsv7098666copy number variation1nstd102humanPathogenic GRCh37 chrX: 48,542,243-48,652,571 , GRCh38.p12 chrX: 48,683,854-48,794,164 GATA1, SUV39H1, 5 more genes
    nsv7098319copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chrX: 48,368,209-51,241,672 , GRCh38.p12 chrX: 48,509,821-51,498,820 GRIPAP1, ASMER2, 92 more genes
    nsv7098318copy number variation3nstd102humanUncertain significance GRCh37 chrX: 47,001,716-50,659,607 , GRCh38.p12 chrX: 47,142,317-50,916,607 PYY3, CCDC120, 148 more genes
    nsv7098317copy number variation1nstd102humanPathogenic GRCh37 chrX: 46,466,387-50,659,607 , GRCh38.p12 chrX: 46,606,952-50,916,607 PLP2, RN7SL262P, 160 more genes
    nsv7087999copy number variation1nstd229human GRCh38 chrX: 48,774,059-48,774,210 , GRCh37.p13 chrX|NW_004070880.2: 1,013,488-1,013,639 , GRCh37.p13 chrX: 48,632,475-48,632,626 ACAA2P1, GLOD5
    nsv7087998copy number variation1nstd229human GRCh38 chrX: 48,771,969-48,774,482 , GRCh37.p13 chrX|NW_004070880.2: 1,011,398-1,013,911 , GRCh37.p13 chrX: 48,630,385-48,632,898 ACAA2P1, GLOD5
    nsv7087997copy number variation1nstd229human GRCh38 chrX: 48,769,987-48,773,244 , GRCh37.p13 chrX|NW_004070880.2: 1,009,416-1,012,673 , GRCh37.p13 chrX: 48,628,403-48,631,660 GLOD5
    nsv7087996copy number variation1nstd229human GRCh38 chrX: 48,769,775-48,772,034 , GRCh37.p13 chrX|NW_004070880.2: 1,009,204-1,011,463 , GRCh37.p13 chrX: 48,628,192-48,630,450 GLOD5
    nsv7087995copy number variation1nstd229human GRCh38 chrX: 48,765,128-48,768,357 , GRCh37.p13 chrX: 48,623,532-48,626,774 , GRCh37.p13 chrX|NW_004070880.2: 1,004,557-1,007,786 GLOD5
    nsv7087994copy number variation1nstd229human GRCh38 chrX: 48,758,001-48,766,200 , GRCh37.p13 chrX|NW_004070880.2: 997,430-1,005,629 , GRCh37.p13 chrX: 48,616,404-48,624,605 GLOD5
    nsv7087992copy number variation1nstd229human GRCh38 chrX: 48,742,072-48,770,576 , GRCh37.p13 chrX|NW_004070880.2: 981,501-1,010,005 , GRCh37.p13 chrX: 48,600,478-48,628,992 GLOD5
    nsv7028188inversion1nstd229human GRCh38 chrX: 48,271,055-52,545,048 , GRCh37.p13 chrX|NW_004070877.1: 1-2,258,163 SSXP8, CACNA1F, 141 more genes
    nsv6637069copy number variation1nstd102humanPathogenic GRCh37 chrX: 39,525,562-52,832,596 , GRCh38.p12 chrX: 39,666,308-52,803,572 LOC100419238, NDP, 312 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 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
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