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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv6637094copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,613,883-155,233,731 , GRCh38.p12 chrX: 154,385,523-156,004,066 FAM3A, TAFAZZIN, 65 more genes
    nsv6636961copy number variation1nstd102humanUncertain significance GRCh37 chrX: 154,617,565-155,233,731 , GRCh38.p12 chrX: 155,387,916-156,004,066 H2AB3, ELOCP24, 10 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
    nsv6636221copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 154,697,070-155,233,731 , GRCh38.p12 chrX: 155,467,409-156,004,066 AMD1P2, IL9R, 7 more genes
    nsv6636057copy number variation1nstd102humanUncertain significance GRCh37 chrY: 16,203,971-59,336,737 , GRCh38.p12 chrY: 14,092,091-57,190,586 RBMY2YP, FAM8A9P, 324 more genes
    nsv6636003copy number variation1nstd102humanPathogenic GRCh37 chrY: 14,370,813-59,373,566 , GRCh38.p12 chrY: 12,250,109-57,217,415 RBMY2FP, PRORY, 357 more genes
    nsv6634391copy number variation1nstd102humanPathogenic GRCh37 chrX: 142,401,540-155,233,731 , GRCh38.p12 chrX: 143,313,746-156,004,066 CSAG4, LOC112268308, 279 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6634094copy number variation4nstd224human GRCh37 chrY: 1-59,373,566 , GRCh38.p12 chrY: 10,001-57,217,415 ASMT, ASS1P6, 570 more genes
    nsv6315439copy number variation2nstd102humanPathogenic GRCh37 chrX: 152,372,767-155,233,731 , GRCh38.p12 chrX: 153,106,941-156,004,066 SNORA36A, VBP1, 126 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
    nsv6315229copy number variation1nstd102humanPathogenic GRCh37 chrY: 1-59,373,566 , GRCh38.p12 chrY: 10,001-57,217,415 RBMY2VP, RFTN1P1, 570 more genes
    nsv6314891copy number variation2nstd102humanPathogenic GRCh38 chrX: 153,427,468-156,004,919 , GRCh37.p13 chrX|NW_003871103.3: 861,451-3,110,903 , GRCh37.p13 chrX: 152,692,926-154,906,585 BGN, MIR3202-1, 114 more genes
    nsv6290583copy number variation1nstd102humanPathogenic GRCh38 chrX: 154,612,552-156,038,495 , GRCh37.p13 chrX|NW_003871103.3: 2,046,531-3,110,903 , GRCh37.p13 chrX: 153,840,805-154,906,585 LOC105373387, VAMP7, 48 more genes
    nsv6139014copy number variation1nstd206human GRCh38 chrX: 155,695,000-156,010,500 , GRCh37.p13 chrX: 154,924,661-155,240,165 AMD1P2, IL9R, 5 more genes
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