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Items: 1 to 20 of 268

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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
    nsv7092375copy number variation1nstd229human GRCh38 chrX: 65,104,915-65,548,999 , GRCh37.p13 chrX: 64,324,795-64,768,879 CCT4P2, MORF4L1P5, 7 more genes
    nsv7092296copy number variation1nstd229human GRCh38 chrX: 64,660,651-65,563,284 , GRCh37.p13 chrX: 63,880,531-64,783,164 LOC100533843, GRPEL2P2, 11 more genes
    nsv7081347copy number variation1nstd229human GRCh38 chrX: 65,546,883-65,599,947 , GRCh37.p13 chrX: 64,766,763-64,819,827 MSN, FRMD8P1
    nsv7081345copy number variation1nstd229human GRCh38 chrX: 65,510,301-65,601,800 , GRCh37.p13 chrX: 64,730,181-64,821,680 LAS1L, MSN, 1 more genes
    nsv7081341copy number variation1nstd229human GRCh38 chrX: 65,500,304-65,649,296 , GRCh37.p13 chrX: 64,720,184-64,869,160 LAS1L, ZC3H12B, 2 more genes
    nsv7081339copy number variation1nstd229human GRCh38 chrX: 65,446,707-66,134,477 , GRCh37.p13 chrX: 64,666,587-65,354,319 NANOGP9, EIF4BP9, 11 more genes
    nsv7081326copy number variation1nstd229human GRCh38 chrX: 65,375,750-66,393,455 , GRCh37.p13 chrX: 64,595,630-65,613,297 ETF1P3, CCNYL5, 14 more genes
    nsv6636229copy number variation1nstd102humanUncertain significance GRCh37 chrX: 64,490,318-64,853,602 , GRCh38.p12 chrX: 65,270,438-65,633,723 ZC3H12B, AP1M2P1, 7 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 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
    nsv6314857copy number variation1nstd102humanUncertain significance GRCh38 chrX: 65,104,915-65,548,999 , GRCh37.p13 chrX: 64,324,795-64,768,879 LOC100533843, AP1M2P1, 7 more genes
    nsv6313346copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,974,855-79,123,671 , GRCh38.p12 chrX: 62,755,385-79,868,171 RPS7P14, RNY4P23, 280 more genes
    nsv6313230copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,877,278-79,123,671 , GRCh38.p12 chrX: 62,657,808-79,868,171 SSBL2P, LOC105373239, 280 more genes
    nsv6290495copy number variation1nstd102humanUncertain significance GRCh37 chrX: 64,348,107-65,038,267 , GRCh38.p12 chrX: 65,128,227-65,818,425 ETF1P3, ZC3H12B, 11 more genes
    nsv6137626copy number variation1nstd213human GRCh37 chrX: 61,730,000-73,580,001 , GRCh38.p12 chrX: 62,510,530-74,360,166 AR, ARR3, 210 more genes
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