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Items: 1 to 20 of 323

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146378copy number variation1nstd232human GRCh37.p13 chr5: 148,401,433-148,401,590 , GRCh38.p12 chr5: 149,021,870-149,022,027 SH3TC2
    nsv7138720copy number variation1nstd232human GRCh37.p13 chr5: 148,385,841-148,385,939 , GRCh38.p12 chr5: 149,006,278-149,006,376 SH3TC2
    nsv7097514copy number variation1nstd102humanPathogenic GRCh37 chr5: 148,426,859-148,427,552 , GRCh38.p12 chr5: 149,047,296-149,047,989 SH3TC2
    nsv7097513copy number variation1nstd102humanUncertain significance GRCh37 chr5: 147,774,340-149,681,936 , GRCh38.p12 chr5: 148,394,777-150,302,373 CSNK1A1, SLC26A2, 39 more genes
    nsv7053998inversion1nstd229human GRCh38 chr5: 148,749,982-154,424,819 , GRCh37.p13 chr5: 148,129,545-153,804,379 HMGXB3, RN7SL868P, 102 more genes
    nsv7053584inversion1nstd229human GRCh38 chr5: 144,534,922-150,861,041 , GRCh37.p13 chr5: 143,914,485-150,240,603 SMIM3, NAMPTP2, 102 more genes
    nsv7045608inversion1nstd229human GRCh38 chr5: 142,902,498-151,105,008 , GRCh37.p13 chr5: 142,282,063-150,484,569 FBXO38-DT, POU4F3, 126 more genes
    nsv7038217inversion1nstd229human GRCh38 chr5: 142,898,166-151,101,968 , GRCh37.p13 chr5: 142,277,731-150,481,529 RPS20P4, PPARGC1B, 126 more genes
    nsv6795370copy number variation1nstd229human GRCh38 chr5: 149,006,281-149,006,377 , GRCh37.p13 chr5: 148,385,844-148,385,940 SH3TC2
    nsv6790714copy number variation1nstd229human GRCh38 chr5: 149,034,216-149,041,075 , GRCh37.p13 chr5: 148,413,779-148,420,638 SH3TC2
    nsv6787694copy number variation1nstd229human GRCh38 chr5: 149,012,446-149,046,609 , GRCh37.p13 chr5: 148,392,009-148,426,172 SH3TC2
    nsv6783504copy number variation1nstd229human GRCh38 chr5: 149,045,464-149,045,970 , GRCh37.p13 chr5: 148,425,027-148,425,533 SH3TC2
    nsv6781407copy number variation1nstd229human GRCh38 chr5: 149,019,308-149,019,346 , GRCh37.p13 chr5: 148,398,871-148,398,909 SH3TC2
    nsv6780678copy number variation1nstd229human GRCh38 chr5: 149,038,953-149,041,060 , GRCh37.p13 chr5: 148,418,516-148,420,623 SH3TC2
    nsv6779184copy number variation1nstd229human GRCh38 chr5: 149,063,489-149,066,560 , GRCh37.p13 chr5: 148,443,052-148,446,123 SH3TC2, SH3TC2-DT
    nsv6778231copy number variation1nstd229human GRCh38 chr5: 149,059,688-149,064,646 , GRCh37.p13 chr5: 148,439,251-148,444,209 SH3TC2-DT, SH3TC2, 1 more genes
    nsv6636986copy number variation1nstd102humanPathogenic GRCh37 chr5: 147,164,969-149,315,489 , GRCh38.p12 chr5: 147,785,406-149,935,926 GRPEL2-AS1, PDE6A, 43 more genes
    nsv6636012copy number variation1nstd102humanUncertain significance GRCh38 chr5: 149,006,277-149,006,376 , GRCh37 chr5: 148,385,840-148,385,939 SH3TC2
    nsv6407817copy number variation1nstd223human GRCh38 chr5: 149,063,489-149,066,559 , GRCh37.p13 chr5: 148,443,052-148,446,122 SH3TC2-DT, SH3TC2
    nsv6405566copy number variation1nstd223human GRCh38 chr5: 149,036,101-149,038,300 , GRCh37.p13 chr5: 148,415,664-148,417,863 SH3TC2
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