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Items: 1 to 20 of 286

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148073copy number variation1nstd102humanUncertain significance GRCh37 chrX: 70,373,327-70,524,150 , GRCh38.p12 chrX: 71,153,477-71,304,300 NONO, NLGN3, 5 more genes
    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
    nsv7098544copy number variation1nstd102humanUncertain significance GRCh37 chrX: 70,327,586-70,683,896 , GRCh38.p12 chrX: 71,107,736-71,464,046 LOC107985688, TAF1, 11 more genes
    nsv7098325copy number variation1nstd102humanUncertain significance GRCh37 chrX: 69,748,945-70,644,108 , GRCh38.p12 chrX: 70,529,095-71,424,258 SOCS5P4, SNX12, 23 more genes
    nsv7088675copy number variation1nstd229human GRCh38 chrX: 71,289,997-71,368,424 , GRCh37.p13 chrX: 70,509,847-70,588,274 NONO, ITGB1BP2, 3 more genes
    nsv7035556inversion1nstd229human GRCh38 chrX: 71,297,928-71,347,244 , GRCh37.p13 chrX: 70,517,778-70,567,094 NONO, ZCRB1P1, 1 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6315446copy number variation1nstd102humanUncertain significance GRCh37 chrX: 70,471,177-70,511,530 , GRCh38.p12 chrX: 71,251,327-71,291,680 ZMYM3, NONO, 1 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
    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
    nsv6290401copy number variation1nstd102humanUncertain significance GRCh37 chrX: 69,917,640-70,638,292 , GRCh38.p12 chrX: 70,697,790-71,418,442 ZMYM3, GJB1, 23 more genes
    nsv6137775copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 70,511,796-70,512,102 , GRCh38 chrX: 71,291,946-71,292,252 NONO
    nsv6137629copy number variation1nstd213human GRCh37 chrX: 66,030,000-152,230,001 , GRCh38.p12 chrX: 66,810,158-153,061,271 ABCB7, AGTR2, 1162 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
    nsv6137403copy number variation1nstd213human GRCh37 chrX: 61,730,000-103,250,001 , GRCh38.p12 chrX: 62,510,530-103,995,433 ABCB7, AR, 529 more genes
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