U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 282

    loading data ...

    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
    nsv7084155copy number variation1nstd229human GRCh38 chrX: 135,103,682-135,210,325 , GRCh37.p13 chrX: 134,237,712-134,344,256 , GRCh37.p13 chrX|NW_004070887.1: 34,826-141,469 SMIM10L2B-AS1, ETDB, 4 more genes
    nsv7052528inversion1nstd229human GRCh38 chrX: 135,035,595-135,257,899 , GRCh37.p13 chrX|NW_004070887.1: 1-189,043 , GRCh37.p13 chrX: 134,202,887-134,391,847 LOC100419791, LOC728470, 10 more genes
    nsv7047939inversion1nstd229human GRCh38 chrX: 135,061,353-135,263,134 , GRCh37.p13 chrX|NW_004070887.1: 1-194,278 , GRCh37.p13 chrX: 134,202,887-134,397,081 ETDA, LOC650024, 9 more genes
    nsv7044060inversion1nstd229human GRCh38 chrX: 134,736,748-136,484,102 , GRCh37.p13 chrX|NW_004070887.1: 1-1,045,622 , GRCh37.p13 chrX: 133,870,778-135,566,261 ETDA, SAGE3P, 57 more genes
    nsv7039688inversion1nstd229human GRCh38 chrX: 134,719,241-135,187,875 , GRCh37.p13 chrX: 133,853,271-134,202,886 LOC100419791, MOSPD1, 17 more genes
    nsv7039420inversion1nstd229human GRCh38 chrX: 134,755,627-135,206,647 , GRCh37.p13 chrX: 133,889,657-134,202,886 RTL8B, RTL8C, 18 more genes
    nsv6636407copy number variation1nstd102humanPathogenic GRCh37 chrX: 124,749,464-155,233,731 , GRCh38.p12 chrX: 125,615,468-156,004,066 RN7SKP31, LOC728470, 539 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6634203copy number variation1nstd224human GRCh37 chrX: 134,220,715-134,457,426 , GRCh38.p12 chrX: 135,086,685-135,323,500 ZNF75D, LOC650024, 10 more genes
    nsv6633775copy number variation1nstd224human GRCh37 chrX: 133,906,202-135,831,362 , GRCh38.p12 chrX: 134,772,172-136,749,203 GAPDHP67, VGLL1, 63 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
    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
    nsv6137409copy number variation1nstd213human GRCh37 chrX: 73,710,000-151,990,001 , GRCh38.p12 chrX: 74,490,165-152,821,457 ABCB7, AGTR2, 991 more genes
    nsv6137362copy number variation1nstd213human GRCh37 chrX: 104,480,000-134,870,001 , GRCh38.p12 chrX: 105,235,316-135,719,285 AGTR2, SLC25A5, 423 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center