sh3kbp1[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6289886	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 19,667,630-19,886,572 , GRCh38.p12 chrX: 19,649,512-19,868,454	SH3KBP1
nsv3903085	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 19,695,151-19,900,092 , NCBI36 chrX: 19,605,072-19,810,013 , GRCh38 chrX: 19,677,033-19,881,974	SH3KBP1
nsv3913487	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chrX: 19,520,147-19,671,846 , GRCh37.p13 chrX: 19,610,226-19,761,925 , GRCh38.p12 chrX: 19,592,108-19,743,807	SH3KBP1
nsv7098363	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 19,764,416-19,764,579 , GRCh38.p12 chrX: 19,746,298-19,746,461	SH3KBP1
nsv6313156	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 19,564,020-19,905,428 , GRCh38.p12 chrX: 19,545,902-19,887,310	SH3KBP1
nsv6313155	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 19,554,535-19,587,326 , GRCh38.p12 chrX: 19,536,417-19,569,208	SH3KBP1
nsv3889286	copy number variation	1	nstd102	human	Benign	GRCh37 chrX: 19,561,853-19,949,936 , GRCh38.p12 chrX: 19,543,735-19,931,818	SH3KBP1, BCLAF3
nsv3870891	copy number variation	1	nstd102	human	Benign	GRCh37 chrX: 19,515,847-19,825,756 , GRCh38.p12 chrX: 19,497,729-19,807,638	SH3KBP1, MAP3K15
nsv3919812	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chrX: 19,460,053-19,878,919 , GRCh37.p13 chrX: 19,550,132-19,968,998 , GRCh38.p12 chrX: 19,532,014-19,950,880	SH3KBP1, BCLAF3
nsv6636078	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 19,560,496-19,971,546 , GRCh38.p12 chrX: 19,542,378-19,953,428	SH3KBP1, BCLAF3
nsv4454046	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 19,560,561-19,952,212 , GRCh38.p12 chrX: 19,542,443-19,934,094	SH3KBP1, BCLAF3
nsv6636112	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 19,560,496-19,951,834 , GRCh38.p12 chrX: 19,542,378-19,933,716	SH3KBP1, BCLAF3
nsv6313403	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 19,560,561-19,951,834 , GRCh38.p12 chrX: 19,542,443-19,933,716	SH3KBP1, BCLAF3
nsv7137044	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 19,564,040-19,954,016 , GRCh38.p12 chrX: 19,545,922-19,935,898	SH3KBP1, BCLAF3
nsv4450961	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 19,665,569-19,942,210 , GRCh38.p12 chrX: 19,647,451-19,924,092	SH3KBP1, BCLAF3
nsv4674517	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 19,167,477-19,595,672 , GRCh38.p12 chrX: 19,149,359-19,577,554	SH3KBP1, EIF5P2, 2 more genes
nsv3904162	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 10,001-156,030,895 , GRCh37 chrX: 60,001-155,260,560 , NCBI36 chrX: 1-154,913,754	SH3KBP1, NANOGNBP3, 2154 more genes
nsv3913255	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chrX: 701-154,913,754 , GRCh37.p13 chrX: 60,701-155,260,560 , GRCh38.p12 chrX: 10,701-156,030,895	SH3KBP1, NHS-AS1, 2154 more genes
nsv3907094	copy number variation	4	nstd102	human	Pathogenic	GRCh38 chrX: 10,679-156,022,206 , GRCh37 chrX: 60,679-155,251,871 , NCBI36 chrX: 679-154,905,065	SH3KBP1, GPR119, 2153 more genes
nsv3878553	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chrX: 60,262-155,245,765 , GRCh38.p12 chrX: 10,262-156,016,100	SH3KBP1, H2AB2, 2152 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 180

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Number of Variants: 20

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