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Items: 1 to 20 of 311

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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
    nsv7082312copy number variation1nstd229human GRCh38 chrX: 110,331,682-110,332,287 , GRCh37.p13 chrX: 109,574,910-109,575,515 LOC105373312, AMMECR1
    nsv7082311copy number variation1nstd229human GRCh38 chrX: 110,319,528-110,320,015 , GRCh37.p13 chrX: 109,562,756-109,563,243 AMMECR1, LOC105373312
    nsv7082309copy number variation1nstd229human GRCh38 chrX: 110,291,366-110,685,524 , GRCh37.p13 chrX: 109,534,594-109,928,752 RTL9, GNG5B, 5 more genes
    nsv7082295copy number variation1nstd229human GRCh38 chrX: 110,147,666-110,458,509 , GRCh37.p13 chrX: 109,390,894-109,701,737 LOC105373312, SNORD96B, 4 more genes
    nsv7052621inversion1nstd229human GRCh38 chrX: 103,826,879-110,334,422 , GRCh37.p13 chrX: 103,081,809-109,577,650 CSGALNACT2P2, LOC107985662, 82 more genes
    nsv7050472inversion1nstd229human GRCh38 chrX: 110,323,875-110,324,020 , GRCh37.p13 chrX: 109,567,103-109,567,248 AMMECR1, LOC105373312
    nsv7046525inversion1nstd229human GRCh38 chrX: 110,330,048-110,330,090 , GRCh37.p13 chrX: 109,573,276-109,573,318 LOC105373312, AMMECR1
    nsv7044993inversion1nstd229human GRCh38 chrX: 104,618,913-113,302,073 , GRCh37.p13 chrX: 103,863,594-112,545,300 NCBP2L, TEX13B, 92 more genes
    nsv7041719inversion1nstd229human GRCh38 chrX: 105,592,744-110,464,662 , GRCh37.p13 chrX: 104,836,737-109,707,890 LOC105373312, PPP6CP, 59 more genes
    nsv6636712copy number variation1nstd102humanPathogenic GRCh37 chrX: 108,922,296-111,549,785 , GRCh38.p12 chrX: 109,679,067-112,306,557 M6PRP1, HMGB1P12, 27 more genes
    nsv6636543copy number variation1nstd102humanPathogenic GRCh37 chrX: 93,805,850-118,913,329 , GRCh38.p12 chrX: 94,550,851-119,779,366 TRPC5OS, LOC105373314, 351 more genes
    nsv6636492copy number variation1nstd102humanUncertain significance GRCh37 chrX: 109,520,211-109,929,010 , GRCh38.p12 chrX: 110,276,983-110,685,782 GNG5B, CRIPTO3, 5 more genes
    nsv6634329copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,794,355-119,282,836 , GRCh38.p12 chrX: 77,538,874-120,148,930 NXF4, RHOXF1P1, 489 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6633566copy number variation1nstd224human GRCh37 chrX: 108,792,848-109,795,316 , GRCh38.p12 chrX: 109,549,619-110,552,088 ACSL4, CRIPTO3, 13 more genes
    nsv6633565copy number variation1nstd224human GRCh37 chrX: 107,804,808-114,879,367 , GRCh38.p12 chrX: 108,561,578-115,645,047 DCX, IL13RA2, 80 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
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