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Items: 1 to 20 of 296

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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
    nsv7137047copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 105,066,840-106,486,528 , GRCh38.p12 chrX: 105,822,847-107,243,298 SERPINA7, CLDN2, 19 more genes
    nsv7098107copy number variation1nstd102humanPathogenic GRCh37 chrX: 106,046,084-108,868,249 , GRCh38.p12 chrX: 106,802,854-109,625,020 VSIG1, NXT2, 32 more genes
    nsv7078250copy number variation1nstd229human GRCh38 chrX: 106,898,373-106,901,673 , GRCh37.p13 chrX: 106,141,603-106,144,903 CLDN2, RIPPLY1
    nsv7078249copy number variation1nstd229human GRCh38 chrX: 106,898,004-106,905,558 , GRCh37.p13 chrX: 106,141,234-106,148,788 RIPPLY1, CLDN2
    nsv7078247copy number variation1nstd229human GRCh38 chrX: 106,865,199-106,930,986 , GRCh37.p13 chrX: 106,108,429-106,174,216 TBC1D8B, CLDN2, 1 more genes
    nsv7078240copy number variation1nstd229human GRCh38 chrX: 106,772,993-106,909,209 , GRCh37.p13 chrX: 106,016,223-106,152,439 TBC1D8B, RNF128, 2 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
    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
    nsv6636905copy number variation1nstd102humanUncertain significance GRCh37 chrX: 105,730,612-107,162,289 , GRCh38.p12 chrX: 106,487,382-107,919,059 NUP62CL, MID2, 21 more genes
    nsv6636839copy number variation1nstd102humanUncertain significance GRCh37 chrX: 105,652,108-106,324,639 , GRCh38.p12 chrX: 106,408,878-107,081,409 TBC1D8B, NAP1L4P2, 9 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
    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
    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
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