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Items: 1 to 20 of 357

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148274copy number variation1nstd102humanUncertain significance GRCh38 chrX: 136,209,840-136,213,009 , GRCh37.p13 chrX: 135,291,999-135,295,168 FHL1, MAP7D3
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7084252copy number variation1nstd229human GRCh38 chrX: 136,150,608-136,152,340 , GRCh37.p13 chrX: 135,232,767-135,234,499 FHL1
    nsv7084251copy number variation1nstd229human GRCh38 chrX: 136,131,825-136,146,376 , GRCh37.p13 chrX: 135,213,984-135,228,535 FHL1
    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
    nsv7039291inversion1nstd229human GRCh38 chrX: 136,154,540-136,154,554 , GRCh37.p13 chrX: 135,236,699-135,236,713 FHL1
    nsv6636956copy number variation1nstd102humanUncertain significance GRCh37 chrX: 135,017,562-135,489,217 , GRCh38.p12 chrX: 135,935,403-136,407,058 SLC9A6, ADGRG4, 7 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
    nsv6315227copy number variation1nstd102humanUncertain significance GRCh37 chrX: 135,229,558-135,293,519 , GRCh38.p12 chrX: 136,147,399-136,211,360 MAP7D3, FHL1
    nsv6313316copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 135,292,010-135,292,184 , GRCh38.p12 chrX: 136,209,851-136,210,025 FHL1
    nsv6313315copy number variation1nstd102humanUncertain significance GRCh37 chrX: 135,288,592-135,292,184 , GRCh38.p12 chrX: 136,206,433-136,210,025 FHL1
    nsv6313140copy number variation1nstd102humanUncertain significance GRCh37 chrX: 135,289,169-135,292,189 , GRCh38.p12 chrX: 136,207,010-136,210,030 FHL1
    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
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