b4galt5[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3912455	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr20: 47,545,606-47,688,365 , GRCh37.p13 chr20: 48,112,199-48,254,958 , GRCh38.p12 chr20: 49,495,662-49,638,421	B4GALT5, LOC101927486, 2 more genes
nsv6290315	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 42,985,044-48,599,046 , GRCh38.p12 chr20: 44,356,404-49,982,509	B4GALT5, PABPC1L, 170 more genes
nsv3908507	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 47,627,844-52,045,480 , GRCh38.p12 chr20: 49,011,307-53,428,941	B4GALT5, LOC100419570, 93 more genes
nsv3892750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941	B4GALT5, TGIF2-RAB5IF, 1314 more genes
nsv3905072	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435	B4GALT5, LRRN4, 1313 more genes
nsv3895314	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr20: 61,569-62,915,555 , GRCh38.p12 chr20: 80,928-64,284,202	B4GALT5, PKIG, 1311 more genes
nsv3896520	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110	B4GALT5, COMMD7, 1311 more genes
nsv3920218	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118	B4GALT5, MIR3646, 1310 more genes
nsv3915005	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 42,849,759-62,379,118 , GRCh37 chr20: 43,416,345-62,908,674 , GRCh38 chr20: 44,787,704-64,277,321	B4GALT5, FTLP1, 472 more genes
nsv3907741	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 47,726,521-50,427,649 , GRCh38.p12 chr20: 49,109,984-51,811,110	B4GALT5, CEBPB, 70 more genes
nsv1398389	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 47,682,662-49,884,981 , GRCh38.p12 chr20: 49,066,125-51,268,444	B4GALT5, CEBPB, 65 more genes
nsv4457555	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 48,023,123-48,581,111 , GRCh38.p12 chr20: 49,406,586-49,964,574	B4GALT5, MIR12122, 16 more genes
nsv3910818	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr20: 25,616,026-62,435,964 , GRCh37.p13 chr20: 25,668,026-62,965,520 , GRCh38.p12 chr20: 25,687,390-64,334,167	B4GALT5, RNA5SP481, 855 more genes
nsv3874236	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 46,962,638-50,647,699 , GRCh38.p12 chr20: 48,333,895-52,031,160	B4GALT5, MIR645, 85 more genes

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