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Items: 1 to 20 of 225

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130670insertion1nstd186human GRCh37 chr22: 43,578,052-43,578,102 , GRCh38.p12 chr22: 43,182,046-43,182,096 TTLL12
    nsv5978361insertion1nstd209human GRCh38 chr22: 43,166,074-43,166,074 , GRCh37.p13 chr22: 43,562,080-43,562,080 TTLL12
    nsv5971493insertion1nstd209human GRCh38 chr22: 43,182,045-43,182,045 , GRCh37.p13 chr22: 43,578,051-43,578,051 TTLL12
    nsv5673276copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,440,000-43,780,000 , GRCh38.p12 chr22: 42,043,996-43,383,994 RPL5P34, ARFGAP3, 48 more genes
    nsv5669614insertion1nstd207human GRCh38 chr22: 43,173,308-43,173,308 , GRCh37.p13 chr22: 43,569,314-43,569,314 TTLL12
    nsv5666100insertion1nstd207human GRCh38 chr22: 43,181,999-43,181,999 , GRCh37.p13 chr22: 43,578,005-43,578,005 TTLL12
    nsv5558119sequence alteration1nstd206human GRCh38 chr22: 42,902,305-43,295,409 , GRCh37.p13 chr22: 43,298,311-43,691,415 BIK, MCAT, 9 more genes
    nsv5551823copy number variation1nstd206human GRCh38 chr22: 43,172,914-43,175,858 , GRCh37.p13 chr22: 43,568,920-43,571,864 TTLL12
    nsv5549983insertion1nstd206human GRCh38 chr22: 43,182,046-43,182,096 , GRCh37.p13 chr22: 43,578,052-43,578,102 TTLL12
    nsv5549256copy number variation1nstd206human GRCh38 chr22: 43,185,250-43,185,305 , GRCh37.p13 chr22: 43,581,256-43,581,311 TTLL12
    nsv5548298copy number variation1nstd206human GRCh38 chr22: 43,184,980-43,185,097 , GRCh37.p13 chr22: 43,580,986-43,581,103 TTLL12
    nsv5542874insertion1nstd206human GRCh38 chr22: 43,173,327-43,173,359 , GRCh37.p13 chr22: 43,569,333-43,569,365 TTLL12
    nsv5381149copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,333,802-51,195,728 , GRCh38.p12 chr22: 41,937,798-50,757,300 WBP2NL, RN7SKP80, 210 more genes
    nsv5381088copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,356,886-43,684,002 , GRCh38.p12 chr22: 41,960,882-43,287,996 CYP2D8P, SCUBE1, 49 more genes
    nsv5175451mobile element insertion1nstd203human GRCh38 chr22: 43,173,308-43,173,327 , GRCh37.p13 chr22: 43,569,314-43,569,333 TTLL12
    nsv5164513mobile element insertion1nstd203human GRCh38 chr22: 43,173,312-43,173,327 , GRCh37.p13 chr22: 43,569,318-43,569,333 TTLL12
    nsv5160769mobile element insertion1nstd203human GRCh38 chr22: 43,173,313-43,173,327 , GRCh37.p13 chr22: 43,569,319-43,569,333 TTLL12
    nsv5033755copy number variation1nstd200human GRCh38 chr22: 43,123,022-43,166,322 , GRCh37.p13 chr22: 43,519,028-43,562,328 TSPO, BIK, 2 more genes
    nsv5032425inversion1nstd200human GRCh38 chr22: 41,452,969-44,153,937 , GRCh37.p13 chr22: 41,848,973-44,549,817 , LOC101927393, 95 more genes
    nsv4872369copy number variation1nstd200human GRCh37 chr22: 43,519,028-43,562,328 , GRCh38.p12 chr22: 43,123,022-43,166,322 TTLL12, MCAT, 2 more genes
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