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Items: 1 to 20 of 338

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137666copy number variation1nstd102humanPathogenic GRCh37 chrX: 91,829,757-113,050,225 , GRCh38.p12 chrX: 92,574,758-113,806,943 TCEAL8, MTND5P26, 272 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5976619copy number variation1nstd209human GRCh38 chrX: 100,724,252-100,730,731 , GRCh37.p13 chrX: 99,979,233-99,985,719 SYTL4
    nsv5880646copy number variation1nstd209human GRCh38 chrX: 100,724,910-100,774,493 , GRCh37.p13 chrX: 99,979,898-100,029,482 SYTL4
    nsv5669139copy number variation1nstd207human GRCh38 chrX: 100,723,965-100,724,014 , GRCh37.p13 chrX: 99,978,946-99,978,995 SYTL4
    nsv5666966copy number variation1nstd207human GRCh38 chrX: 100,723,890-100,724,113 , GRCh37.p13 chrX: 99,978,871-99,979,094 SYTL4
    nsv5416089copy number variation1nstd206human GRCh38 chrX: 100,724,910-100,774,496 , GRCh37.p13 chrX: 99,979,898-100,029,485 SYTL4
    nsv5184988mobile element insertion1nstd203human GRCh38 chrX: 100,716,450-100,716,484 , GRCh37.p13 chrX: 99,971,445-99,971,463 SYTL4
    nsv5183691mobile element insertion1nstd203human GRCh38 chrX: 100,704,330-100,704,339 , GRCh37.p13 chrX: 99,959,326-99,959,335 SYTL4
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4905806copy number variation1nstd200human GRCh38 chrX: 100,593,602-100,773,219 , GRCh37.p13 chrX: 99,848,599-100,028,208 LOC105373298, SRPX2, 3 more genes
    nsv4905804copy number variation1nstd200human GRCh38 chrX: 100,363,871-100,949,127 , GRCh37.p13 chrX: 99,618,869-100,204,116 NSA2P3, SRPX2, 12 more genes
    nsv4782216copy number variation1nstd200human GRCh37 chrX: 99,848,599-100,028,208 , GRCh38.p12 chrX: 100,593,602-100,773,219 TNMD, SYTL4, 3 more genes
    nsv4771985copy number variation1nstd200human GRCh37 chrX: 99,929,323-99,949,979 , GRCh38.p12 chrX: 100,674,326-100,694,982 SYTL4, SRPX2
    nsv4769250copy number variation1nstd201human GRCh37 chrX: 96,096,220-155,208,244 , GRCh38.p12 chrX: 96,841,221-155,978,579 , AGTR2, 959 more genes
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
    nsv4728644copy number variation1nstd102humanUncertain significance GRCh37 chrX: 99,581,496-100,047,228 , GRCh38.p12 chrX: 100,326,498-100,792,239 PCDH19, TNMD, 4 more genes
    nsv4728601copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,514,079-127,770,854 , GRCh38.p12 chrX: 78,258,582-128,636,876 PHB1P10, SNORA35, 565 more genes
    nsv4728533copy number variation1nstd102humanPathogenic GRCh37 chrX: 94,264,404-155,233,731 , GRCh38.p12 chrX: 95,009,405-156,004,066 CT45A10, MIR224, 968 more genes
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