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Items: 1 to 20 of 294

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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
    nsv7092872copy number variation1nstd229human GRCh38 chrX: 93,671,958-93,672,631 , GRCh37.p13 chrX: 92,926,957-92,927,630 NAP1L3, FAM133A
    nsv7092871copy number variation1nstd229human GRCh38 chrX: 93,671,886-93,672,060 , GRCh37.p13 chrX: 92,926,885-92,927,059 NAP1L3, FAM133A
    nsv7092870copy number variation1nstd229human GRCh38 chrX: 93,657,696-94,049,471 , GRCh37.p13 chrX: 92,912,695-93,304,470 FAM133A, RNU6-332P, 1 more genes
    nsv7092869copy number variation1nstd229human GRCh38 chrX: 93,652,701-93,682,900 , GRCh37.p13 chrX: 92,907,700-92,937,899 NAP1L3, FAM133A
    nsv7092825copy number variation1nstd229human GRCh38 chrX: 93,273,244-94,089,091 , GRCh37.p13 chrX: 92,528,243-93,344,090 FAM133A, NT5DC1P1, 4 more genes
    nsv7092691copy number variation1nstd229human GRCh38 chrX: 90,583,822-99,472,797 , GRCh37.p13 chrX: 89,838,821-98,727,795 RNU2-26P, KRT18P11, 57 more genes
    nsv7045405inversion1nstd229human GRCh38 chrX: 93,478,022-94,001,532 , GRCh37.p13 chrX: 92,733,021-93,256,531 RPL7P55, NAP1L3, 1 more genes
    nsv7044358inversion1nstd229human GRCh38 chrX: 93,599,521-94,001,365 , GRCh37.p13 chrX: 92,854,520-93,256,364 FAM133A, NAP1L3
    nsv6637108copy number variation1nstd102humanUncertain significance GRCh37 chrX: 92,667,113-93,429,578 , GRCh38.p12 chrX: 93,412,114-94,174,579 RNU6-332P, NAP1L3, 2 more genes
    nsv6636889copy number variation1nstd102humanUncertain significance GRCh37 chrX: 87,082,472-95,826,084 , GRCh38.p12 chrX: 87,827,472-96,571,085 PABPC5-AS1, KAT7P1, 57 more genes
    nsv6634400copy number variation1nstd102humanPathogenic GRCh37 chrX: 90,868,186-99,828,437 , GRCh38.p12 chrX: 91,613,187-100,573,440 LOC100420872, LOC100420955, 55 more genes
    nsv6634329copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,794,355-119,282,836 , GRCh38.p12 chrX: 77,538,874-120,148,930 NXF4, RHOXF1P1, 489 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 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
    nsv6313385copy number variation1nstd102humanUncertain significance GRCh37 chrX: 92,453,752-92,979,462 , GRCh38.p12 chrX: 93,198,753-93,724,463 ST13P18, NT5DC1P1, 4 more genes
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