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Items: 1 to 20 of 292

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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
    nsv7098218copy number variation1nstd102humanUncertain significance GRCh37 chrX: 118,708,675-119,761,021 , GRCh38.p12 chrX: 119,574,712-120,627,166 RHOXF2B, RHOXF1P3, 33 more genes
    nsv7098217copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chrX: 117,629,935-119,761,021 , GRCh38.p12 chrX: 118,495,972-120,627,166 HNRNPA1P28, RNU7-86P, 59 more genes
    nsv7057233inversion1nstd229human GRCh38 chrX: 117,599,215-122,918,174 , GRCh37.p13 chrX: 116,733,178-122,052,027 NUDT19P1, RHOXF1P2, 89 more genes
    nsv7053551inversion1nstd229human GRCh38 chrX: 119,787,766-120,266,058 , GRCh37.p13 chrX|NW_004070886.1: 1-318,488 , GRCh37.p13 chrX: 119,081,534-119,399,913 TMEM255A, RHOXF2B, 20 more genes
    nsv7053106inversion1nstd229human GRCh38 chrX: 118,857,141-120,493,178 , GRCh37.p13 chrX: 117,991,104-119,627,033 LINC03098, RNF113A, 49 more genes
    nsv7049773inversion1nstd229human GRCh38 chrX: 118,660,648-122,841,710 , GRCh37.p13 chrX: 117,794,611-121,975,563 NUDT19P6, MRPS17P9, 83 more genes
    nsv7048267inversion1nstd229human GRCh37.p13 chrX|NW_004070886.1: 86,406-257,835 , GRCh38 chrX: 120,033,976-120,205,405 , GRCh37.p13 chrX: 119,167,941-119,339,254 RHOXF1, RHOXF1-AS1, 4 more genes
    nsv7040030inversion1nstd229human GRCh37.p13 chrX|NW_004070886.1: 90,641-272,029 , GRCh38 chrX: 120,038,211-120,219,599 , GRCh37.p13 chrX: 119,172,176-119,353,447 SFR1P1, RHOXF2B, 5 more genes
    nsv7038305inversion1nstd229human GRCh38 chrX: 118,464,002-122,855,541 , GRCh37.p13 chrX: 117,597,965-121,989,394 UBE2V1P16, RNY3P16, 84 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 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
    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
    nsv6315332copy number variation1nstd102humanPathogenic GRCh37 chrX: 62,685,885-155,233,731 , GRCh38.p12 chrX: 63,466,005-156,004,066 MAGT1, TAFAZZIN, 1337 more genes
    nsv6315331copy number variation4nstd102humanPathogenic GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 PLAC1, PGK1P1, 2154 more genes
    nsv6290694copy number variation1nstd102humanUncertain significance GRCh37 chrX: 119,173,583-119,330,572 , GRCh38.p12 chrX: 120,039,618-120,196,722 RHOXF1-AS1, RHOXF2, 3 more genes
    nsv6290546copy number variation1nstd102humanPathogenic GRCh37 chrX: 119,173,583-126,584,360 , GRCh38.p12 chrX: 120,039,618-127,450,379 FBLIM1P1, PNPLA10P, 81 more genes
    nsv6137629copy number variation1nstd213human GRCh37 chrX: 66,030,000-152,230,001 , GRCh38.p12 chrX: 66,810,158-153,061,271 ABCB7, AGTR2, 1162 more genes
    nsv6137579copy number variation1nstd213human GRCh37 chrX: 114,940,000-134,860,001 , GRCh38.p12 chrX: 115,705,680-135,719,285 AGTR2, SLC25A5, 295 more genes
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