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Items: 1 to 20 of 264

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148175copy number variation1nstd102humanPathogenic GRCh38 chr1: 230,178,121-243,646,135 , GRCh37.p13 chr1: 230,313,867-243,809,437 AGT, MAP10, 221 more genes
    nsv7137173copy number variation1nstd102humanPathogenic GRCh38 chr1: 233,502,994-236,105,019 , GRCh37.p13 chr1: 233,638,740-236,268,319 ARID4B, MTND3P8, 58 more genes
    nsv7099266copy number variation1nstd231human GRCh38.p12 chr1: 226,993,371-235,936,592 , GRCh37 chr1: 227,181,072-236,099,892 ACTA1, AGT, 223 more genes
    nsv7093371copy number variation1nstd102humannot provided GRCh37 chr1: 224,230,307-243,181,599 , GRCh38.p12 chr1: 224,042,605-243,018,297 RPL36P6, MTND4LP21, 377 more genes
    nsv7050233inversion1nstd229human GRCh38 chr1: 233,627,622-233,631,232 , GRCh37.p13 chr1: 233,763,368-233,766,978 KCNK1
    nsv7048727inversion1nstd229human GRCh38 chr1: 231,257,209-234,326,619 , GRCh37.p13 chr1: 231,392,955-234,462,365 LOC105373171, LINC01744, 44 more genes
    nsv7048010inversion1nstd229human GRCh38 chr1: 233,396,223-235,667,657 , GRCh37.p13 chr1: 233,531,969-235,830,957 RN7SL668P, LINC02961, 52 more genes
    nsv7044310inversion1nstd229human GRCh38 chr1: 230,890,958-235,370,433 , GRCh37.p13 chr1: 231,026,704-235,533,748 TARBP1, LOC105373170, 86 more genes
    nsv7040126inversion1nstd229human GRCh38 chr1: 233,623,274-233,627,894 , GRCh37.p13 chr1: 233,759,020-233,763,640 MIR4427, KCNK1
    nsv6675874copy number variation1nstd229human GRCh38 chr1: 232,900,608-233,617,904 , GRCh37.p13 chr1: 233,036,354-233,753,650 RPS7P3, MAP3K21, 7 more genes
    nsv6675008copy number variation1nstd229human GRCh38 chr1: 233,624,901-233,630,500 , GRCh37.p13 chr1: 233,760,647-233,766,246 KCNK1
    nsv6671536copy number variation1nstd229human GRCh38 chr1: 233,488,326-233,925,294 , GRCh37.p13 chr1: 233,624,072-234,061,040 SLC35F3, KCNK1, 2 more genes
    nsv6666177copy number variation1nstd229human GRCh38 chr1: 233,665,571-233,665,608 , GRCh37.p13 chr1: 233,801,317-233,801,354 KCNK1
    nsv6661083copy number variation1nstd229human GRCh38 chr1: 233,635,176-233,645,602 , GRCh37.p13 chr1: 233,770,922-233,781,348 KCNK1
    nsv6659222copy number variation1nstd229human GRCh38 chr1: 233,609,716-233,641,903 , GRCh37.p13 chr1: 233,745,462-233,777,649 KCNK1, MIR4427
    nsv6637109copy number variation1nstd102humanUncertain significance GRCh37 chr1: 232,895,447-238,787,061 , GRCh38.p12 chr1: 232,759,701-238,623,761 RPL9P10, LOC105373207, 105 more genes
    nsv6637037copy number variation1nstd102humanUncertain significance GRCh37 chr1: 232,827,966-240,750,334 , GRCh38.p12 chr1: 232,692,220-240,587,034 RNU1-74P, EDARADD, 123 more genes
    nsv6636794copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,972,939-249,224,684 , GRCh38.p12 chr1: 223,785,237-248,930,485 SEPTIN7P13, WNT3A, 546 more genes
    nsv6636265copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 227,992,928-236,659,905 , GRCh38.p12 chr1: 227,805,227-236,496,605 ACTA1, AGT, 211 more genes
    nsv6636217copy number variation1nstd102humanPathogenic GRCh37 chr1: 232,732,121-243,338,216 , GRCh38.p12 chr1: 232,596,375-243,174,914 LINC01347, LOC100130331, 169 more genes
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