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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7056306inversion1nstd229human GRCh38 chr2: 216,152,063-216,313,649 , GRCh37.p13 chr2: 217,016,786-217,178,372 MARCHF4, POLHP1, 4 more genes
    nsv7056189inversion1nstd229human GRCh38 chr2: 216,110,969-216,267,091 , GRCh37.p13 chr2: 216,975,692-217,131,814 LOC100421349, MARCHF4, 3 more genes
    nsv7047048inversion1nstd229human GRCh38 chr2: 216,286,412-216,579,954 , GRCh37.p13 chr2: 217,151,135-217,444,677 RPL37A-DT, RPL37A, 8 more genes
    nsv6697933copy number variation1nstd229human GRCh38 chr2: 216,115,509-216,266,324 , GRCh37.p13 chr2: 216,980,232-217,131,047 MARCHF4, POLHP1, 3 more genes
    nsv6696976copy number variation1nstd229human GRCh38 chr2: 216,308,401-216,311,600 , GRCh37.p13 chr2: 217,173,124-217,176,323 MARCHF4, LOC107985983
    nsv6693817copy number variation1nstd229human GRCh38 chr2: 216,273,902-216,304,305 , GRCh37.p13 chr2: 217,138,625-217,169,028 MARCHF4, LOC107985983
    nsv6693433copy number variation1nstd229human GRCh38 chr2: 216,350,452-216,360,122 , GRCh37.p13 chr2: 217,215,175-217,224,845 MARCHF4
    nsv6693115copy number variation1nstd229human GRCh38 chr2: 216,241,518-216,280,130 , GRCh37.p13 chr2: 217,106,241-217,144,853 MARCHF4
    nsv6692578copy number variation1nstd229human GRCh38 chr2: 216,304,001-216,309,800 , GRCh37.p13 chr2: 217,168,724-217,174,523 LOC107985983, MARCHF4
    nsv6691902copy number variation1nstd229human GRCh38 chr2: 216,358,201-216,360,638 , GRCh37.p13 chr2: 217,222,924-217,225,361 MARCHF4
    nsv6691360copy number variation1nstd229human GRCh38 chr2: 216,349,501-216,360,100 , GRCh37.p13 chr2: 217,214,224-217,224,823 MARCHF4
    nsv6690736copy number variation1nstd229human GRCh38 chr2: 216,303,053-216,305,987 , GRCh37.p13 chr2: 217,167,776-217,170,710 LOC107985983, MARCHF4
    nsv6688891copy number variation1nstd229human GRCh38 chr2: 216,271,506-216,277,551 , GRCh37.p13 chr2: 217,136,229-217,142,274 MARCHF4
    nsv6688826copy number variation1nstd229human GRCh38 chr2: 216,293,625-216,294,004 , GRCh37.p13 chr2: 217,158,348-217,158,727 MARCHF4
    nsv6685966copy number variation1nstd229human GRCh38 chr2: 216,286,401-216,589,900 , GRCh37.p13 chr2: 217,151,124-217,454,623 LINC01280, RPL37A-DT, 9 more genes
    nsv6684599copy number variation1nstd229human GRCh38 chr2: 216,262,332-216,787,882 , GRCh37.p13 chr2: 217,127,055-217,652,605 LOC107985983, RPL31P14, 14 more genes
    nsv6681685copy number variation1nstd229human GRCh38 chr2: 216,259,744-216,264,353 , GRCh37.p13 chr2: 217,124,467-217,129,076 MARCHF4
    nsv6679309copy number variation1nstd229human GRCh38 chr2: 216,313,401-216,319,700 , GRCh37.p13 chr2: 217,178,124-217,184,423 LOC107985983, MARCHF4
    nsv6678667copy number variation1nstd229human GRCh38 chr2: 216,274,415-216,276,991 , GRCh37.p13 chr2: 217,139,138-217,141,714 MARCHF4
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