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Items: 1 to 20 of 385

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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
    nsv7097991copy number variation1nstd102humanPathogenic GRCh37 chrX: 135,730,408-136,113,833 , GRCh38.p12 chrX: 136,648,249-137,031,674 RPL7P56, RAB28P5, 11 more genes
    nsv7084311copy number variation1nstd229human GRCh38 chrX: 136,764,486-136,768,430 , GRCh37.p13 chrX: 135,846,645-135,850,589 ARHGEF6
    nsv7084310copy number variation1nstd229human GRCh38 chrX: 136,757,901-136,776,900 , GRCh37.p13 chrX: 135,840,060-135,859,059 ARHGEF6, RNU6-972P
    nsv7084309copy number variation1nstd229human GRCh38 chrX: 136,719,809-136,725,525 , GRCh37.p13 chrX: 135,801,968-135,807,684 ARHGEF6
    nsv7084308copy number variation1nstd229human GRCh38 chrX: 136,706,783-136,794,233 , GRCh37.p13 chrX: 135,788,942-135,876,392 ARHGEF6, LOC100422685, 2 more genes
    nsv7084307copy number variation1nstd229human GRCh38 chrX: 136,661,810-136,665,449 , GRCh37.p13 chrX: 135,743,969-135,747,608 ARHGEF6
    nsv7084303copy number variation1nstd229human GRCh38 chrX: 136,622,176-137,342,517 , GRCh37.p13 chrX: 135,704,335-136,424,676 RPL7P56, RAB28P5, 12 more genes
    nsv7084302copy number variation1nstd229human GRCh38 chrX: 136,614,398-136,681,354 , GRCh37.p13 chrX: 135,696,557-135,763,513 CD40LG, ARHGEF6, 1 more genes
    nsv7084288copy number variation1nstd229human GRCh38 chrX: 136,430,040-137,211,313 , GRCh37.p13 chrX: 135,512,199-136,293,472 VGLL1, GPR101, 17 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
    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
    nsv6313037copy number variation3nstd102humanPathogenic GRCh37 chrX: 135,067,662-136,652,229 , GRCh38.p12 chrX: 135,985,503-137,570,070 GPR101, SRRM1P3, 26 more genes
    nsv6290578copy number variation1nstd102humanPathogenic GRCh37 chrX: 135,767,906-136,348,117 , GRCh38.p12 chrX: 136,685,747-137,265,958 SNORD61, SRRM1P3, 10 more genes
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