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Items: 1 to 20 of 337

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098415copy number variation1nstd102humanPathogenic GRCh37 chrX: 43,515,590-44,970,656 , GRCh38.p12 chrX: 43,656,342-45,111,411 RPSAP61, RPL19P20, 16 more genes
    nsv7098314copy number variation2nstd102humanPathogenic GRCh37 chrX: 43,515,590-43,817,891 , GRCh38.p12 chrX: 43,656,342-43,958,645 NDP, MAOA, 2 more genes
    nsv7087519copy number variation1nstd229human GRCh38 chrX: 43,818,631-43,951,183 , GRCh37.p13 chrX: 43,677,878-43,810,429 MAOB, NDP, 1 more genes
    nsv7087513copy number variation1nstd229human GRCh38 chrX: 43,777,701-44,141,600 , GRCh37.p13 chrX: 43,636,948-44,000,846 MAOB, NDP, 2 more genes
    nsv7087502copy number variation1nstd229human GRCh38 chrX: 43,595,421-44,016,474 , GRCh37.p13 chrX: 43,454,669-43,875,720 MAOA, NDP, 2 more genes
    nsv7031878inversion1nstd229human GRCh38 chrX: 43,947,825-43,947,898 , GRCh37.p13 chrX: 43,807,071-43,807,144 NDP-AS1, NDP
    nsv7027413inversion1nstd229human GRCh38 chrX: 43,879,125-43,995,043 , GRCh37.p13 chrX: 43,738,371-43,854,289 MAOB, NDP-AS1, 1 more genes
    nsv7026678inversion1nstd229human GRCh38 chrX: 43,954,737-43,954,773 , GRCh37.p13 chrX: 43,813,983-43,814,019 NDP-AS1, NDP
    nsv7023393inversion1nstd229human GRCh38 chrX: 43,855,971-43,954,559 , GRCh37.p13 chrX: 43,715,217-43,813,805 NDP, MAOB, 1 more genes
    nsv6637069copy number variation1nstd102humanPathogenic GRCh37 chrX: 39,525,562-52,832,596 , GRCh38.p12 chrX: 39,666,308-52,803,572 LOC100419238, NDP, 312 more genes
    nsv6636684copy number variation1nstd102humanPathogenic GRCh37 chrX: 41,350,855-44,616,591 , GRCh38.p12 chrX: 41,491,602-44,757,345 PINCR, YWHAZP10, 31 more genes
    nsv6636476copy number variation1nstd102humanUncertain significance GRCh37 chrX: 43,615,734-44,011,605 , GRCh38.p12 chrX: 43,756,487-44,152,359 RBM39P1, EFHC2, 3 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6315577complex substitution1nstd102humanPathogenic GRCh37 chrX: 590,376-56,315,041 , GRCh38.p12 chrX: 629,641-56,288,608 ACTG1P10, NR0B1, 778 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
    nsv6315331copy number variation4nstd102humanPathogenic GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 PLAC1, PGK1P1, 2154 more genes
    nsv6315330copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-57,841,304 , GRCh38.p12 chrX: 251,879-57,814,871 NPM1P9, UBE2E4P, 799 more genes
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