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Items: 1 to 20 of 289

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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
    nsv7097991copy number variation1nstd102humanPathogenic GRCh37 chrX: 135,730,408-136,113,833 , GRCh38.p12 chrX: 136,648,249-137,031,674 RPL7P56, RAB28P5, 11 more genes
    nsv7084333copy number variation1nstd229human GRCh38 chrX: 137,024,196-137,029,199 , GRCh37.p13 chrX: 136,106,355-136,111,358 GPR101
    nsv7084332copy number variation1nstd229human GRCh38 chrX: 137,004,969-137,668,434 , GRCh37.p13 chrX: 136,087,128-136,750,593 RN7SL325P, ZFYVE9P1, 3 more genes
    nsv7084303copy number variation1nstd229human GRCh38 chrX: 136,622,176-137,342,517 , GRCh37.p13 chrX: 135,704,335-136,424,676 RPL7P56, RAB28P5, 12 more genes
    nsv7084288copy number variation1nstd229human GRCh38 chrX: 136,430,040-137,211,313 , GRCh37.p13 chrX: 135,512,199-136,293,472 VGLL1, GPR101, 17 more genes
    nsv6636407copy number variation1nstd102humanPathogenic GRCh37 chrX: 124,749,464-155,233,731 , GRCh38.p12 chrX: 125,615,468-156,004,066 RN7SKP31, LOC728470, 539 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
    nsv6313037copy number variation3nstd102humanPathogenic GRCh37 chrX: 135,067,662-136,652,229 , GRCh38.p12 chrX: 135,985,503-137,570,070 GPR101, SRRM1P3, 26 more genes
    nsv6290578copy number variation1nstd102humanPathogenic GRCh37 chrX: 135,767,906-136,348,117 , GRCh38.p12 chrX: 136,685,747-137,265,958 SNORD61, SRRM1P3, 10 more genes
    nsv6242985mobile element insertion1nstd215human GRCh38 chrX: 137,031,296-137,031,296 , GRCh37.p13 chrX: 136,113,455-136,113,455 GPR101
    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
    nsv6137588copy number variation1nstd213human GRCh37 chrX: 136,060,000-136,190,001 , GRCh38.p12 chrX: 136,977,841-137,107,842 GPR101, SRRM1P3, 1 more genes
    nsv6137409copy number variation1nstd213human GRCh37 chrX: 73,710,000-151,990,001 , GRCh38.p12 chrX: 74,490,165-152,821,457 ABCB7, AGTR2, 991 more genes
    nsv6137376copy number variation1nstd213human GRCh37 chrX: 134,930,000-152,230,001 , GRCh38.p12 chrX: 135,766,029-153,061,271 BCYRN1P1, BRS3, 246 more genes
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