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Items: 1 to 20 of 272

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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
    nsv7089094copy number variation1nstd229human GRCh38 chrX: 76,997,018-77,003,711 , GRCh37.p13 chrX: 76,217,443-76,224,136 , GRCh37.p13 chrX|NW_003871100.1: 1,016,438-1,023,131 MIR325HG, MIR325
    nsv7089059copy number variation1nstd229human GRCh38 chrX: 76,642,918-77,057,568 , GRCh37.p13 chrX|NW_003871100.1: 662,338-1,076,988 , GRCh37.p13 chrX: 75,863,322-76,277,996 MIR384, RNA5SP508, 3 more genes
    nsv7089048copy number variation1nstd229human GRCh38 chrX: 76,615,098-77,016,935 , GRCh37.p13 chrX|NW_003871100.1: 634,518-1,036,355 , GRCh37.p13 chrX: 75,835,502-76,237,360 TRAPPC13P1, MIR325, 3 more genes
    nsv7036954inversion1nstd229human GRCh38 chrX: 76,891,365-77,881,765 , GRCh37.p13 chrX|NW_003871100.1: 910,785-1,461,188 , GRCh37.p13 chrX: 76,111,790-77,137,262 RNU6-854P, FGF16, 9 more genes
    nsv7036257inversion1nstd229human GRCh38 chrX: 76,689,677-77,390,248 , GRCh37.p13 chrX|NW_003871100.1: 709,097-1,409,668 , GRCh37.p13 chrX: 75,910,075-76,610,711 MIR325, SPRYD7P1, 4 more genes
    nsv7026063inversion1nstd229human GRCh38 chrX: 76,257,068-80,095,987 , GRCh37.p13 chrX: 75,477,467-77,450,502 ATRX, MAGEE1, 40 more genes
    nsv7023006inversion1nstd229human GRCh38 chrX: 76,882,925-77,139,096 , GRCh37.p13 chrX|NW_003871100.1: 902,345-1,158,516 , GRCh37.p13 chrX: 76,103,350-76,359,551 MIR325, MIR325HG, 3 more genes
    nsv7018633inversion1nstd229human GRCh38 chrX: 76,256,859-80,096,106 , GRCh37.p13 chrX: 75,477,258-77,450,502 LDHBP2, ATP7A, 40 more genes
    nsv6636337copy number variation1nstd102humanUncertain significance GRCh37 chrX: 75,463,914-77,297,280 , GRCh38.p12 chrX: 76,243,515-78,041,782 MAGEE1, MIR384, 20 more genes
    nsv6636208copy number variation1nstd102humanUncertain significance GRCh37 chrX: 74,946,710-76,904,755 , GRCh38.p12 chrX: 75,726,875-77,649,265 FGF16, SPRYD7P1, 19 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
    nsv6313464copy number variation1nstd102humanUncertain significance GRCh37 chrX: 72,095,006-88,455,505 , GRCh38.p12 chrX: 72,875,172-89,200,506 LOC105373285, LOC105373288, 170 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
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