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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
    nsv7083614copy number variation1nstd229human GRCh38 chrX: 123,785,001-123,960,200 , GRCh37.p13 chrX: 122,918,851-123,094,050 STAG2, CHCHD2P1, 5 more genes
    nsv7083613copy number variation1nstd229human GRCh38 chrX: 123,781,658-123,918,077 , GRCh37.p13 chrX: 122,915,508-123,051,927 RNU6-122P, PARD6BP1, 3 more genes
    nsv7083611copy number variation1nstd229human GRCh38 chrX: 123,749,401-123,960,700 , GRCh37.p13 chrX: 122,883,251-123,094,550 STAG2-AS1, STAG2, 7 more genes
    nsv7083609copy number variation1nstd229human GRCh38 chrX: 123,738,801-123,898,000 , GRCh37.p13 chrX: 122,872,651-123,031,850 PARD6BP1, MEMO1P4, 5 more genes
    nsv7083608copy number variation1nstd229human GRCh38 chrX: 123,734,301-123,834,400 , GRCh37.p13 chrX: 122,868,151-122,968,250 RN7SL190P, RNU7-69P, 2 more genes
    nsv7083607copy number variation1nstd229human GRCh38 chrX: 123,733,401-123,961,700 , GRCh37.p13 chrX: 122,867,251-123,095,550 STAG2, THOC2, 8 more genes
    nsv7083604copy number variation1nstd229human GRCh38 chrX: 123,696,801-123,970,000 , GRCh37.p13 chrX: 122,830,651-123,103,850 STAG2-AS1, PARD6BP1, 8 more genes
    nsv7083599copy number variation1nstd229human GRCh38 chrX: 123,669,413-123,854,432 , GRCh37.p13 chrX: 122,803,264-122,988,282 RNU7-69P, THOC2, 3 more genes
    nsv7083596copy number variation1nstd229human GRCh38 chrX: 123,638,050-123,909,984 , GRCh37.p13 chrX: 122,771,901-123,043,834 XIAP, RN7SL190P, 6 more genes
    nsv7083371copy number variation1nstd229human GRCh38 chrX: 121,591,286-126,454,661 , GRCh37.p13 chrX: 120,725,140-125,588,644 RNU7-69P, SH2D1A, 31 more genes
    nsv7042376inversion1nstd229human GRCh38 chrX: 123,759,737-123,823,983 , GRCh37.p13 chrX: 122,893,587-122,957,833 CHCHD2P1, RN7SL190P, 2 more genes
    nsv6637110copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 122,773,699-123,323,939 , GRCh38.p12 chrX: 123,639,848-124,190,089 XIAP, STAG2, 9 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6633759copy number variation1nstd224human GRCh37 chrX: 122,536,930-122,999,047 , GRCh38.p12 chrX: 123,403,079-123,865,197 XIAP, GRIA3, 9 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
    nsv6315380copy number variation1nstd102humanPathogenic GRCh37 chrX: 122,855,926-123,438,005 , GRCh38.p12 chrX: 123,722,076-124,304,155 PARD6BP1, STAG2-AS1, 11 more genes
    nsv6315346copy number variation1nstd102humanPathogenic GRCh37 chrX: 122,845,829-123,288,831 , GRCh38.p12 chrX: 123,711,979-124,154,981 RNU7-69P, RN7SL190P, 8 more genes
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