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Items: 1 to 20 of 292

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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
    nsv7088976copy number variation1nstd229human GRCh38 chrX: 76,172,124-76,172,184 , GRCh37.p13 chrX|NW_003871100.1: 191,544-191,604 , GRCh37.p13 chrX: 75,391,959-75,392,019 PBDC1
    nsv7088974copy number variation1nstd229human GRCh38 chrX: 76,155,501-76,207,600 , GRCh37.p13 chrX: 75,375,336-75,427,442 , GRCh37.p13 chrX|NW_003871100.1: 174,921-227,020 PBDC1
    nsv7088969copy number variation1nstd229human GRCh38 chrX: 76,104,462-76,527,749 , GRCh37.p13 chrX: 75,324,297-75,748,160 , GRCh37.p13 chrX|NW_003871100.1: 123,882-547,169 PBDC1, MAGEE1, 4 more genes
    nsv7088956copy number variation1nstd229human GRCh38 chrX: 75,969,306-76,970,155 , GRCh37.p13 chrX|NW_003871100.1: 1-989,575 , GRCh37.p13 chrX: 75,200,416-76,190,580 MMADHCP1, MIR325HG, 9 more genes
    nsv7088944copy number variation1nstd229human GRCh38 chrX: 75,840,245-76,178,332 , GRCh37.p13 chrX: 75,200,416-75,398,167 , GRCh37.p13 chrX|NW_003871100.1: 1-197,752 PBDC1, ARL5AP5, 1 more genes
    nsv7029790inversion1nstd229human GRCh38 chrX: 76,149,148-76,233,558 , GRCh37.p13 chrX|NW_003871100.1: 168,568-252,978 , GRCh37.p13 chrX: 75,368,983-75,453,957 PBDC1, MMADHCP1
    nsv7021820inversion1nstd229human GRCh38 chrX: 76,141,868-76,231,916 , GRCh37.p13 chrX|NW_003871100.1: 161,288-251,336 , GRCh37.p13 chrX: 75,361,703-75,452,315 MMADHCP1, PBDC1
    nsv7021197inversion1nstd229human GRCh38 chrX: 76,148,985-76,212,020 , GRCh37.p13 chrX|NW_003871100.1: 168,405-231,440 , GRCh37.p13 chrX: 75,368,820-75,431,819 PBDC1
    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
    nsv6290541copy number variation1nstd102humanUncertain significance GRCh37 chrX: 75,373,284-76,555,631 , GRCh38.p12 chrX: 76,153,449-77,335,168 TRAPPC13P1, MMADHCP1, 11 more genes
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