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Items: 1 to 20 of 323

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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
    nsv7091433copy number variation1nstd229human GRCh38 chrX: 34,131,527-34,134,849 , GRCh37.p13 chrX: 34,149,644-34,152,966 FAM47A
    nsv7091427copy number variation1nstd229human GRCh38 chrX: 34,070,661-34,145,725 , GRCh37.p13 chrX: 34,088,778-34,163,842 FTH1P14, FAM47A, 1 more genes
    nsv7091414copy number variation1nstd229human GRCh38 chrX: 34,005,411-34,577,989 , GRCh37.p13 chrX: 34,023,528-34,596,106 FTH1P14, FAM47A, 3 more genes
    nsv7091404copy number variation1nstd229human GRCh38 chrX: 33,937,098-34,579,318 , GRCh37.p13 chrX: 33,955,215-34,597,435 FAM47A, FTH1P14, 3 more genes
    nsv7091353copy number variation1nstd229human GRCh38 chrX: 33,601,442-34,346,042 , GRCh37.p13 chrX: 33,619,559-34,364,159 LOC105373153, LOC107985674, 2 more genes
    nsv7091347copy number variation1nstd229human GRCh38 chrX: 33,528,487-34,134,632 , GRCh37.p13 chrX: 33,546,604-34,152,749 FAM47A, LOC105373153
    nsv7087189copy number variation1nstd229human GRCh38 chrX: 32,918,935-34,173,163 , GRCh37.p13 chrX: 32,937,052-34,191,280 TBCAP1, FTH1P14, 4 more genes
    nsv7087186copy number variation1nstd229human GRCh38 chrX: 32,905,340-34,319,606 , GRCh37.p13 chrX: 32,923,457-34,337,723 TBCAP1, FTH1P14, 4 more genes
    nsv7087091copy number variation1nstd229human GRCh38 chrX: 32,431,799-34,356,692 , GRCh37.p13 chrX: 32,449,916-34,374,809 MIR548F5, LOC107985674, 7 more genes
    nsv6636670copy number variation1nstd102humanPathogenic GRCh37 chrX: 32,419,533-37,487,291 , GRCh38.p12 chrX: 32,401,416-37,628,038 FAM47B, FAM47A, 36 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
    nsv6313340copy number variation1nstd102humanUncertain significance GRCh37 chrX: 33,906,163-35,902,937 , GRCh38.p12 chrX: 33,888,046-35,884,820 LOC105373153, SIAH1P1, 12 more genes
    nsv6290594copy number variation1nstd102humanUncertain significance GRCh37 chrX: 32,990,095-34,190,399 , GRCh38.p12 chrX: 32,971,978-34,172,282 TBCAP1, LOC646506, 4 more genes
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