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Items: 1 to 20 of 283

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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
    nsv7084295copy number variation1nstd229human GRCh38 chrX: 136,493,958-136,494,306 , GRCh37.p13 chrX: 135,576,117-135,576,465 BRS3
    nsv7084294copy number variation1nstd229human GRCh38 chrX: 136,487,329-136,507,553 , GRCh37.p13 chrX: 135,569,488-135,589,712 HTATSF1, BRS3
    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
    nsv6290488copy number variation1nstd102humanUncertain significance GRCh38 chrX: 136,487,348-136,507,517 , GRCh37.p13 chrX: 135,569,507-135,589,676 BRS3, HTATSF1
    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
    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
    nsv6137376copy number variation1nstd213human GRCh37 chrX: 134,930,000-152,230,001 , GRCh38.p12 chrX: 135,766,029-153,061,271 BCYRN1P1, BRS3, 246 more genes
    nsv6137375copy number variation1nstd213human GRCh37 chrX: 134,920,000-152,230,001 , GRCh38.p12 chrX: 135,751,569-153,061,271 BCYRN1P1, BRS3, 247 more genes
    nsv6137221copy number variation1nstd213human GRCh37 chrX: 66,020,000-152,230,001 , GRCh38.p12 chrX: 66,800,158-153,061,271 ABCB7, AGTR2, 1162 more genes
    nsv6137215copy number variation3nstd213human GRCh37 chrX: 61,730,000-152,230,001 , GRCh38.p12 chrX: 62,510,530-153,061,271 ABCB7, AGTR2, 1217 more genes
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